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Post by aqt on Sept 4, 2011 11:00:55 GMT -5
Lily's information on bacteriorhodopsin A method of preparing an analog of bacteriorhodopsin in which organic cations selectively replace calcium and magnesium cations. The method comprises preparing a cation-free blue membrane and incubating the blue membrane with an organic cation selected from the group consisting of monovalent quaternary ammonium cations, bolaform cations and pyridinal cations. www.patentstorm.us/patents/5922843.html
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Post by aqt on Sept 4, 2011 11:06:26 GMT -5
Smart dust, says Montemagno, is based on bacteriorhodopsin, the protein in heliobacter and certain other bacteria that allows them to be photosynthetic. NASA wants to use smart dust on Mars to look for likely sites where life albeit equally tiny might exist. Even smarter dust could have a diagnostic and therapeutic function, seeking out and treating pathogens in plants. Or people.www.news.cornell.edu/chronicle/00/10.12.00/ss-molecules_of_life.htmlbacteriorhodopsin Bacteriorhodopsin is a protein used by Archaea, the most notable one being Halobacteria. It acts as a proton pump; that is, it captures light energy and uses it to move protons across the membrane out of the cell.[1] The resulting proton gradient is subsequently converted into chemical energy.[2] Bacteriorhodopsin is an integral membrane protein usually found in two-dimensional crystalline patches known as "purple membrane", which can occupy up to nearly 50% of the surface area of the archaeal cell. The repeating element of the hexagonal lattice is composed of three identical protein chains, each rotated by 120 degrees relative to the others. Each chain has seven transmembrane alpha helices and contains one molecule of retinal buried deep within, the typical structure for retinylidene proteins It is the retinal molecule that changes its conformation when absorbing a photon, resulting in a conformational change of the surrounding protein and the proton pumping action.[3] It is covalently linked to Lys216 in the chromophore by Schiff base action. After photoisomerization of the retinal molecule, Asp85 becomes a proton acceptor of the donor proton from the retinal molecule. This releases a proton from a "holding site" into the extracellular side (EC) of the membrane. Reprotonation of the retinal molecule by Asp96 restores its original isomerized form. This results in a second proton being released to the EC side. Asp85 releases its proton into the "holding site," where a new cycle may begin. The bacteriorhodopsin molecule is purple and is most efficient at absorbing green light (wavelength 500-650 nm, with the absorption maximum at 568 nm). Bacteriorhodopsin belongs to a family of bacterial proteins related to vertebrate rhodopsins, the pigments that sense light in the retina. Rhodopsins also contain retinal; however, the functions of rhodopsin and bacteriorhodopsin are different, and there is only slight homology in their amino acid sequences. Both rhodopsin and bacteriorhodopsin belong to the 7TM receptor family of proteins, but rhodopsin is a G protein-coupled receptor and bacteriorhodopsin is not. In the first use of electron crystallography to obtain an atomic-level protein structure, the structure of bacteriorhodopsin was resolved in 1990. It was then used as a template to build models of G protein-coupled receptors before crystallographic structures were also available for these proteins. Many molecules have homology to bacteriorhodopsin, including the light-driven chloride pump halorhodopsin (for which the crystal structure is also known), and some directly light-activated channels like channelrhodopsin. All other photosynthetic systems in bacteria, algae, and plants use chlorophylls or bacteriochlorophylls rather than bacteriorhodopsin. These also produce a proton gradient, but in a quite different and more indirect way involving an electron transfer chain consisting of several other proteins. Furthermore, chlorophylls are aided in capturing light energy by other pigments known as "antennas"; these are not present in bacteriorhodopsin-based systems. Last, chlorophyll-based photosynthesis is coupled to carbon fixation (the incorporation of carbon dioxide into larger organic molecules); this is not true for bacteriorhodopsin-based system. Thus, it is likely that photosynthesis independently evolved at least twice, once in bacteria and once in archaeaen.wikipedia.org/wiki/Bacteriorhodopsin
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Post by aqt on Sept 4, 2011 11:08:46 GMT -5
www.docstoc.com/docs/42652561/Photoelectric-Transducer-Having-Photosensitive-Chromoprotein-Film-Ie-Bacteriorhodopsin---Patent-5107104 A photoelectric transducer which comprises a photoresponsive electrode, which is provided with an oriented film of a photosensitive chromoprotein at the interface of an electrically conductive electrode substrate and an electrolyte, combined with a counter electrode.electrolytes? to be used in us?
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Post by aqt on Sept 4, 2011 11:11:22 GMT -5
www.faqs.org/patents/app/20110171747BACTERIORHODOPSIN-BASED PHOTOCHROMIC SENSOR FOR DETECTION OF CHEMICAL AND ENVIRONMENTAL TOXINS Read more: www.faqs.org/patents/app/20110171747#ixzz1X06c3xweA bacteriorhodopsin based chemical sensing architecture based upon the collective response of bacteriorhodopsin and a number of its mutants; the wild type protein and a selection of genetically-engineered variants was able to respond differentially to a selection of amines. The observable response to the presence of a target chemical was manifested through a modulation of bacteriorhodopsin's photokinetic properties, which are monitored through pump-probe techniques using a custom prototype flash photolysis system. Differential responsivity exists at two levels; (1) bacteriorhodopsin proteins (wild-type and genetically-engineered variants) respond differentially upon exposure of a target chemical, and (2) the response pattern exhibited by the proteins differs from chemical to chemical. This dichotomy forms the basis for a BR-mediated chemical sensing technology that is highly sensitive and selective and may therefore discriminate between different chemicals. Read more: www.faqs.org/patents/app/20110171747#ixzz1X06nomwo
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Post by aqt on Sept 4, 2011 11:29:52 GMT -5
This is the story of Barb Metcalf......Connecticut Barb Metcalf, a Morgellons sufferer in Connecticut, who lives only 30 miles from the US Army’s top secret Plum Island research facility, felt differently. Metcalf’s story is incredible, and is presented here in her own words. Recounts Metcalf: “It was December 8, 1998 a beautiful 72F winter day in Manchester, Connecticut. The weather was most unusual, we had had snow and several hard frosts, but this day was like a Spring day. I was outdoors at a party, standing under a large oak tree. I felt something inside my shirt; I never considered it to be a bug because nothing should have survived the winter weather. When I removed my shirt that night, it was very clear that I had been bitten at least 8 times on my back. There was a leg left behind in the struggle, so I placed it in a bag for identification. The next day, I had a major allergic attack with signs of oncoming breathing difficulties. I went to the doctor who did nothing more than a Lyme disease test, although there were no obvious signs that it was a tick. “I took the leg to an entomologist at University of Connecticut who identified it as coming from an arthropod. By leg size, mouth size, he determined that it was not a tick, but could not otherwise determine the exact type of bug. Living in here is always reason enough to be checked for insect bites, living so close and in the migratory bird path of Old Lyme, Connecticut, just 12 miles from Plum Island, the world’s depository of infectious diseases of all types. Old Lyme is just 42 miles from my home, and about 30 miles ’as the crow flies’ or any other species of insect, birds, geese, etc. that take the migratory bird path that literally goes over Plum Island. “Three months to the day, I felt as though I was being bitten all over again! I was screaming in horror and pain and could see nothing attacking me. After careful examination, my husband could see crystals sticking out of my back! He removed several of them with tweezers — they were all alike: triangular in shape, with one side serrated the other two rather straight, and all had either a black or red dot in the center. Once the crystal was removed the pain ceased immediately. Along with some of these crystals pieces of black material also was removed to find later that they were actually pieces of an insect’s leg. This cycle happened like clockwork every 3 months, leaving behind scars of white pox-like marks, red striated lines, red dots, and tender skin. “Visits to specialists of Infectious Disease, was the least helpful. They would not look at the samples, nor listen to how I became ill. Then, other symptoms became apparent. Abdominal bloating and severe pain, upper right quadrant pain and swelling; difficulty swallowing, headaches, muscle pain, no apparent lesions or other marks on my body except for those lines and red dots. I was tested for Lyme disease, and both tests were negative. “Having been married to a microbiologist for the EPA and having worked in the lab alongside my husband, studying what he studied, made me wonder just what had attacked me and why. I got out my old microscope and could see that there was more there than met the eye. Insect pieces, pieces that looked like crystal, and when dissected, appeared to be very interesting indeed. It was time I invested in another piece of equipment and found a child’s toy - Digital Blue; a digital microscope for about $100 solved the problem immediately. From that day forward, I documented everything that I found unusual coming from my body. Cataloguing by date, location in the body where the specimen came from, i.e. oral, nasal, head, other body parts, stool...I have compiled a digital microscopy library of over 300,000 photographs in color and b & w, including videos of microbes and various bacterial specimens from my own body. “Getting more ill as time went on, I literally begged my rheumatoid specialist to help me find out what this disease was. I was tested and the results were startling. From being a relatively healthy 54 year old, active female business woman, to have positive test results for: fibromyalgia, diabetes, chronic fatigue syndrome, IBS, and Rheumatoid arthritis. All in just a few months’ time! “When the bugs, worms and large strange specimens began coming from my body, none of my doctors would have anything to do with me. They shunned me in total disbelief! I was mortified to say the least that someone they had trusted to be knowledgeable in the past 10 years had suddenly told them of worms, insects, and God-know-what coming from her body! I was told to see a psychiatrist, which shocked me to no end. I was not crazy, nor was I delusional - you can’t photograph a delusion. “I searched the internet endless hours for photographs of specimens in all areas of medicine and veterinary medicine that looked like mine, to no avail. The disease got worse. I could no longer sleep, the pain increased to where I could no longer walk without a cane, and needed assistance from my family to do simple, everyday chores around the house and maintain my own body. “Being of a medically scientific mindset, I just knew there had to be an answer out there. But after several years of not finding anything similar, I began to be more than frustrated. I called on several scientific friends and associates for help and they too were stymied by the change in my appearance, I had lost more than 50 pounds within 3 months...and did not sleep more than a couple hours a day. Without sleep, the body cannot produce Serotonin, which it needs to repair and maintain a healthy system. “Then in 2005, I needed water to be replaced in my swimming pool. I called for a delivery and asked where it was coming from - a local reservoir. When I first went into the pool, I noticed hundreds of small snails along the surface of the pool. I had never seen anything like this in the previous years. Then the large slugs began to be seen in the early morning hours...some as large as 4-5" long. Knowing better, I still picked up hundreds of these snails in my hands to dispose of them. “In April 2006 I went to Florida to visit my son and his family only to begin feeling ill just 3 days into the visit. I left earlier than planned, and within one day of my return to CT I became extremely ill. Vomiting, diarrhea (with obvious worm-like specimens which I saved for future observance), and then within 2 days had a fever of 104F. I collapsed and was admitted into the ICU at a local hospital. All manner of specialists were called in, including infectious disease, cardiology, immunology, pulmonary, and dermatology. With a raging fever for 8 days, nothing was determined except that I was diagnosed with bilateral pneumonia...of unknown origin. Upon discharge, the disease worsened, especially the abdominal bloating, abdominal pain, diarrhea and vomiting. I brought samples of these worms to the specialists along with other unidentifiable specimens that looked like undeveloped insects, and they refused to even consider them, and threw them away. They would ask me, "Can you part with them?" I was treated as though I was some type of idiot, let loose on the street. I was incensed to say the least! “I took literally hundreds of preserved samples to a university Microbiology Department in another state, where specialists - all PhDs in various specialties: microbiology, parasitological, entomology, biology, marine biology, virology. They selected an obvious egg specimen that they all agreed was a Schistosoma mansoni egg and tested it with stain. It did not respond in the normal manner. They did another ... same results. They were surprised to say the least. When the Department head asked why they thought this had happened, to a person, the response was, "It’s genetically modified". “’Genetically modified’ appears to be an understatement at this point in time. This was not the first time that my interests were being challenged. In September, 2008 I woke to check my pool to find thousands of beige/khaki colored threads all over my deck and the roof of my home. I couldn’t imagine where they had come from. I picked them up in my hands and put them in a bag for disposal, then vacuumed the area still wondering where they had come from. Curious, I put one under the microscope only to be shocked again. These fibers were not normal threads at all, but were twists and braided forms of fibers with many types of organisms literally woven into the pattern. What shocked me most was that some of these specimens I saw were the very same specimens I had seen come out of my own body. I double-checked my photographs to be certain I was not in error. I wasn’t. The next day, the same thing happened again. I checked the neighborhood by walking the street to see if there were more threads, but did not find any. “A year later in September, 2009, the threads appeared again. Same type of thread, same type of organisms entwined within the fibers. By coincidence, just a few days later, I was lying on a raft in my pool, looking up into the sky, and saw something floating down from the sky where there were no trees. I jumped out of the pool and caught it before it hit the ground! It was one of those same threads! No doubt about it. I ran into the house and put it under the scope - and sure enough even though it was a year later, this lone thread blew into my yard, just like those before it, with what looked like the colored threads of red, black, blue and white of what I became to know as Morgellons Disease or the Fiber Disease! “So, where had they come from? To this day, I have no idea, but they didn’t just fly in on their own. “From about that same time, I was studying what I found to be called Morgellons Disease from an ABC Special that showed these same fiber masses that I had photographed! A friend called me and asked me why I had given my material and photographs to ABC. I told her I hadn’t; she said they are on TV right now! And, yes, those there looked like my very own photos. I was overwhelmed to say the least. A whole new world of investigation opened for me. “I’ve contacted medical facilities all over the country looking for help, to no avail, until I found an infectious disease facility in Boston MA who finally took me on as a patient, after checking me for DOP [Delusions of Parasitosis], and I submitted samples from my body sometimes within 30 minutes! They had never seen anything like it. I brought and sent in many digital photographs of the specimens from my body, and none could be identified - even in this area of the country known for its excellence in medicine and new technology. I asked about Morgellons...they had not heard of it. However, I could match what came out of my body with photographs published by others. I was finally given medicine to help remove these parasites from my body, along with extensive testing of my brain, abdomen, chest, lungs, etc. and blood. No conclusive findings or diagnosis was found and no etiology of what was in my body. They agreed to advise me if anyone else came to their facility with my same symptoms in the future. I must have faith in what they try to do...until I learn more. “It is now 2 months since I took the medicine that was prescribed, and I am still producing fungus gnats, flies, from my nasal cavities, eggs and worms and various other strange specimens in my stool. My abdomen is again bloating and in pain, and the vicious circle of this debilitating disease goes on. “Many strange incidents have happened since I contracted Morgellons Disease; my computer has been broken/hacked into and only certain information, including my book that I had been writing for more than 10 years, was removed. While discussing Morgellons with another Morgy, we were both viewing the same site, when both our computers went black! We were also on the phone at the time. He lives in another state and does not have the same ISP; his computer came back on, mine did not. I took my computer to experts to verify what had happened. “I have no doubt that this disease has killed more people than we are aware of; we are getting no support from anyone; we are researching daily; many victims have lost their jobs, their homes, their families, support from their friends and families, and most of all from the lack of care from the medical community at large. They are all waiting for what the CDC finds in their Kaiser Permanente Investigation that has been a long time coming. In the meanwhile, people have been dying from this disease or complications of this disease, or have committed suicide because they no longer are able to fight the daily horrors and pain this horrific disease does to mind and body.” Source: www.voltairenet.org/article165822.htmlvector borne also aqt
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Post by aqt on Sept 4, 2011 11:34:57 GMT -5
Ode to Wonderland Where went the hormone estrogen that Elwood sought to trace? The nucleus was where it hid, a most unlikely place.
And mightn't it act upon the genes? a molecular Director The curiouser of curious paths; t'was a nuclear receptor.
In tandem with Le Grand Fromage in search of mother lodes... we riddled out the means by which the DNA decodes.
The time has come, the lipids screamed to cease your mad conniption a superfamily was revealed that modulates transcription.
The rabbit hole through which we fell put us through our paces to puzzle out the secret of physiologic homeostasis.www.nature.com/nm/journal/v10/n10/full/nm1004-1022.htmlplease follow trhe above link aqt
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Post by aqt on Sept 4, 2011 12:20:19 GMT -5
Lily knows her stuff....for sure!! The present invention relates to the discovery of novel insect receptor polypeptides, which, when complexed with certain ligands, or otherwise activated by certain compounds, modulate transcription of certain genes by binding to cognate response elements associated with the promoters of the genes. The novel receptors of the invention are substantially similar to previously discovered mammalian receptors which are activated to modulate transcription of certain genes in cells, when the cells are exposed to retinoic acid. The invention provides DNAs encoding the novel receptors, including expression vectors for expression of the receptors in cells; cells transformed with such expression vectors; cells co-transformed with such expression vectors and with reporter vectors to monitor activation of the receptors to modulate transcription, when the cells are exposed to ligand for the invention receptor; and methods of using such co-transformed cells in screening for compounds which are capable of leading to activation of the receptors and for compounds which are capable of interfering with such activation and, as such, are potentially potent insecticides. The invention also provides DNA and RNA probes for identifying DNA's encoding related receptors, of insects and other animals, of the class, to which the novel receptors of the invention belong. www.patents.com/us-5641652.html
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Post by aqt on Sept 4, 2011 12:30:07 GMT -5
BIOLOGICAL ADHESIVESUsed to make something ADHERE to cell tissue organ ect... ? www.patentstorm.us/applications/20100003329/claims.htmlClaims 1. A composition comprising a biologically compatible polymer functionalized with at least two species of reactive moiety, wherein one reactive moiety binds to a biological surface. 2. The composition according to claim 1, wherein said polymer comprises at least ten monomelic units. 3. The composition according to claim 1, wherein one said reactive moiety is selected from group consisting of methacrylates, ethacrylates, itaconates and acrylamides. 4. The composition according to claim 3, wherein said reactive moiety is methacrylate. 5. The composition according to claim 1, wherein one said reactive moiety is an aldehyde. 6. The composition according to claim 1, wherein said polymer is functionalized through one or more thio, carboxylic acid or alcohol moieties. 7. A composition comprising the composition of claim 1 and a biological surface. 8. The composition of claim 7, wherein said biological surface is on a cell, tissue or organ. 9. The composition of claim 8, wherein said tissue is ocular tissue. 10. The composition of claim 8, wherein said tissue comprises an intervertebral disc. 11. A composition comprising the composition of claim 1 and a hydrogel functionalized with a reactive moiety. 12. The composition of claim 11, wherein said hydrogel comprises poly(ethylene oxide) diacrylate. 13. The composition of claim 11, wherein said hydrogel further comprises a biocompatible polymer. 14. The composition of claim 13, wherein said biocompatible polymer is hyaluronic acid. 15. The composition of claim 11, wherein said hydrogel comprises a biologically active agent. 16. A composition comprising the composition of claim 1 and a polyfunctional bridging molecule reactive therewith. 17. The composition of claim 16, wherein said bridging molecule reacts with said reactive moiety which reacts with a biological surface. 18. The composition of claim 16, wherein said biologically compatible polymer comprises a second reactive moiety, wherein said bridging molecule reacts with said second reactive moiety. 19. The composition of claim 16, wherein said polyfunctional bridging molecule comprises multiple amine groups. 20. A composition comprising the composition of claim 16 and a biological surface. 21. The composition of claim 20, wherein said biological surface is on a cell, tissue or organ. 22. The composition of claim 21, wherein said tissue is ocular tissue. 23. A composition comprising the composition of claim 1 and a support. 24. The composition of claim 23, wherein said support is an inert carrier. 25. The composition of claim 16, wherein said polymer comprises a film and said bridging molecule comprises a film, wherein said films are stacked on each other. 26. The composition of claim 25, comprising a third film comprising a biologically compatible polymer, stacked onto said film comprising said bridging molecule. 27. The composition of 26, further comprising a support. 28. The composition of claim 27, wherein said support is an inert carrier. 29. A composition comprising the composition of claim 23 and a biological surface. 30. The composition of claim 29, wherein said biological surface is on a cell, tissue or organ. 31. The composition of claim 30, wherein said tissue is ocular tissue. 32. A composition comprising the composition of claim 16 and a support. 33. The composition of claim 32, wherein said support is an inert carrier. www.patentstorm.us/applications/20100003329/claims.html
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Post by aqt on Sept 4, 2011 12:47:18 GMT -5
Quantum dot memory cell Abstract A channel layer and a spacer layer form a heterojunction therebetween. A V-shaped groove is formed in the spacer layer. The sharp bottom of the V-shaped is located above the heterojunction interface. On the bottom of the V-shaped groove a plurality of quantum dots are formed in a line and discretely. A gate electrode is formed above the quantum dots. A source electrode is connected to the heterojunction interface to form an ohmic contact therebetween. A drain electrode is connected to the heterojunction interface to form an ohmic contact therebetween. The quantum dots are arranged between the source and drain electrodes. BACKGROUND OF THE INVENTION The present invention relates to a memory cell that is a constituent element of a semiconductor memory cell array, and more specifically to a structure thereof. There is little room for further improvements in packing density, capacity and power dissipation of semiconductor memory cell arrays by scaling down the dimensions of memory cells of conventional structures. To overcome this, the advent of memory cells having novel structures and operating principles has been expected. One of such memory cells is a quantum dot memory cell. We claim: 1. A memory cell comprising: a channel layer of a first semiconductor; a spacer layer formed on the channel layer, the spacer layer comprising of a second semiconductor that is dissimilar to the first semiconductor-to form a heterojunction interface therebetween; a V-shaped groove formed in the spacer layer, the bottom of the V-shaped groove being located above the heterojunction interface between the channel layer and the spacer layer; a gate oxide formed in the V-shaped groove; a plurality of quantum dots buried in the gate oxide; a gate electrode formed on the gate oxide; a source electrode connected to the heterojunction interface to form an ohmic contact therebetween; and a drain electrode connected to the heterojunction interface to form an ohmic contact therebetween, the drain electrode being spaced away from the source electrode so that the quantum dots are arranged therebetween. 2. The memory cell according to claim 1, wherein the first semiconductor is n-type SiGe, the second semiconductor is n-type silicon, the gate oxide is silicon oxide, and the quantum dots are made of silicon (Si). 3. The memory cell according to claim 2, wherein the gate electrode is made of n.sup.+ -poly-Si. 4. The memory cell according to claim 1, wherein the first semiconductor is strained p-type Si formed on relaxed p-type SiGe, the second semiconductor is relaxed p-type SiGe, the gate oxide is silicon oxide, and the quantum dots are made of silicon. 5. The memory cell according to claim 4, wherein the gate electrode is made of n.sup.+ -poly-Si. www.patents.com/us-5923046.html
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Post by aqt on Sept 4, 2011 12:51:21 GMT -5
Regulating gene expression using retinoids with CH.sub.2 OH or related groups at the side chain terminal position Abstract For the first time, certain retinoids with a side chain terminal CH.sub.2 OH group or ester or ether thereof or aldehyde rather than a side chain terminal COOH group and substitution at the 4-position have been indicated to bind to nuclear receptors and to be biologically active in inducing cell differentiation of normal and tumor cells. These compounds activate gene expression through binding to nuclear receptor proteins. These compounds induce differentiation in normal and cancer cells and are useful for treating leukemias, and lymphomas, squamous cell carcinomas, deep (cystic) acne, psoriasis and photodamaged or aging skin. These compounds have stability and in vitro half-life advantages over and solubility differences from all-trans-retinoic acid and activity advantages over 13-cis retinoic acid.honing their skills..... www.patents.com/us-5962534.html
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Post by aqt on Sept 4, 2011 13:11:16 GMT -5
13 cis-isomer medconditions.net/13-cis-isomer-isotretinoin-zinc-salt.html13 cis Isomer Isotretinoin Zinc Salt: A topical dermatologic agent that is used in the treatment of acne vulgaris and several other skin diseases. The drug has teratogenic and other adverse effects. medconditions.net/tretinoin-zinc-salt.htmlTretinoin Zinc Salt: An important regulator of gene expression, particularly during growth and development and in neoplasms. Retinoic acid derived from maternal vitamin A is essential for normal gene expression during embryonic development and either a deficiency or an excess can be teratogenic. It is also a topical dermatologic agent which is used in the treatment of psoriasis, acne vulgaris, and several other skin diseases. It has also been approved for use in promyelocytic leukemia. expressing genes through use of topical creams? never even thought of that route..until now aqt teratogenic effects: abnormalities of physiological development.... of course...if we are changing the expression of the genes, the physiological development would be abnormal...stands to reason..no?
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Post by aqt on Sept 4, 2011 13:22:33 GMT -5
heterobiopolysaccharides A composition according to claim 1 wherein the heterobiopolysaccharide is soluble in water and comprises at least glucose, mannose and glucuronic or galacturonic acid units in its structure. www.patents.com/us-4871530.html
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Post by skyship on Sept 4, 2011 15:48:40 GMT -5
It is in the environment.
The earth is being dumped upon, and then cleansed.
There are specifics to Morgellons though, and by observations we will get there.
So, it is everyone's efforts.
We are covering a wide range again, which takes us way out in to neverland.
We have narrowed some of this down.
We know that an egg, an embryo, a germling, mucous itself, oligomers, nanos, yet, viruses are still used, Morgellons is not all the above.
Morgellons is specific........ meaning it effects specific people.
Not everyone has this. Those who say everyone has this, do not understand the replicator, at all.
Those who have just he wires, are not effect, it has been perfected, this was a process.
So, lets get back to the filament, the sphere, the hexagon, the organism and the freqs.
Otherwise we are going over and over the same things.
We have been trying to piece this together on this board, but, no one seems to be reading it!
We have narrowed this down, very much so, knowing that iron is involved, the blood cell itself, the fibers are different, are from podospora prions, then became nanowires, then became amphiphiles and bolaamphiphiles. These began with chimeras of natural genes and proteins and enzymes and membrane proteins, an organism was created, a multicellular eukaryotic minicell, this is the core of the organism. The spheres are the minispheres.......and so on, but, our work has been tossed aside, to bring in an rehash what we have already covered.
This has been covered here, on LB, biology on line, till we got to the truth, and we got kicked off.
Ms. Lily should know all about that.
Skyship
Skyship
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Post by kritters on Sept 7, 2011 19:17:14 GMT -5
This Lily person is beyond scary brilliant and super-ultimately informed!!!
I wonder who she is!!!
She's fabulous!!! And she has a huge heart as we all here do.
She has come from the universe to help form all that we here are also helping to create with positive energy and specific information.
I just overcame something that has plagued me financially for two years because of Wallace Waddles' book, "the Science of Growing Rich" which is the book "The Secret" is based upon. That guy wrote it in like, 1929 and it has moved miracles for me and will continue to do so with what we are fighting right now. Trust me on this.
It's in play and there are enough of us that will make a difference.
p.s. the book is NOT about growing 'rich' but about letting the universe and the force (God or whatever you might call it) do the thing you expect it to do because it's all about love and that power is incredible.
xoxoKritts
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Post by skyship on Sept 13, 2011 10:02:18 GMT -5
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Post by skyship on Sept 13, 2011 10:16:06 GMT -5
the biological computer: www.patentstorm.us/patents/5922843.htmlso, we have to separate out that a biological computer is made from proteins. This is not the computer in the human. It is not the Interface, there has to be an interface. And they only way humans affected is by viral mutation. To mutate a live wire into the body system, is what had to be done. That live wire, the sup35, makes prions, unfolds proteins in us, folds in the artificial computer. heat shock proteins is the evolutionary capcitor. Can be put on head of a pin. Natural selection is correct, artificial selection is what is happening, many are accepting the artificial, many are not, there is a reason for this. We have pre condition biological native genes that will not cooperate. We suffer, we reject the nanowires. The nanowires have the quantum dots in them. These are like LEDs, Electronic Engineering 07 * Electronic Engineering 07's Notes (0) Subscribe * Electronic Engineering 07's Notes LED Wrisv spotch Technology In Human Skin by Electronic Engineering 07 on Friday, March 18, 2011 at 12:31pm After the great performance of LED in the field of Interior designing.Now this technology is used in human beings.Yes, i am talking about the electric watch inside the human skin.Strange but true.Here the question arises that how led technology can be used in human beings.A LED wrisv spotch is placed inside the human skin.Some people called this watch as electric tattoo which is implanted under your skin.Best thing about this watch is that it does not require batteries but it needs to be charged.This watch is powered by kinetic energy of our body.One more thing is that it illuminates only when you turn your wrist towards your face.It is the best we can have because it works with our body movements and needs no battery. www.facebook.com/note.php?note_id=171020582947559================================== Varying ratios of wavelengths in dual wavelength LED photomodulation alters gene expression profiles in human skin fibroblasts. McDaniel DH, Weiss RA, Geronemus RG, Mazur C, Wilson S, Weiss MA. Source Laser Skin & Vein Center of Virginia, Institute of Anti-Aging Research; Virginia Beach, Virginia 23462, USA. mail@lsvcv.com Abstract BACKGROUND AND OBJECTIVE: LED photomodulation has been shown to profoundly influence cellular behavior. A variety of parameters with LED photomodulation can alter cellular response in vitro. The effects of one visible and one infrared wavelength were evaluated to determine the optimal ratio to produce a net increase in dermal collagen by altering the ratio of total energy output of each wavelength. The ratio between the two wavelengths (590 and 870 nm) was shifted in 25% increments. Cell metabolism and gene expression can be altered by simultaneous exposure to multiple wavelengths of low energy light. Varying the ratios of specific wavelength intensity in both visible and near infrared light therapy can strongly influence resulting fibroblast gene expression patterns. www.ncbi.nlm.nih.gov/pubmed/20662030==================================== The LED’s that produced near-infrared light used in NASA’s research were shown to stimulate the basic energy processes by activating color sensitive chemicals within the cells. DNA synthesis in fibroblasts and muscle cells had been quintupled. The light absorbed by the cells stimulated the metabolism in muscle and bone as well as skin and subcutaneous tissue. What people and animals had felt through utilizing this technology in real life, NASA was proving to be true in the laboratory. LED-ENHANCEMENT OF CELL GROWTH Studies on cells exposed to microgravity and hypergravity indicate that human cells need gravity to stimulate growth. As the gravitational force increases or decreases, the cell function responds in a linear fashion. This poses significant health risks for astronauts in long-term space flight. The application of light therapy with the use of NASA LEDs will significantly improve the medical care that is available to astronauts on long-term space missions. NASA LEDs stimulate the basic energy processes in the mitochondria (energy compartments) of each cell, particularly when near-infrared light is used to activate the color sensitive chemicals (chromospheres, cytochrome systems) inside. Optimal LED wavelengths include 680, 730 and 880 nm and their laboratory has improved the healing of wounds in laboratory animals by using both LED light and hyperbaric oxygen. Furthermore, DNA synthesis in fibroblasts and muscle cells has been quintupled using NASA LED light alone, in a single application combining 680, 730 and 880 nm each at 4 Joules per centimeter squared. Muscle and bone atrophy are well documented in astronauts, and various minor injuries occurring in space have been reported not to heal until landing on Earth. An LED blanket device may be used for the prevention of bone and muscle atrophy in astronauts. The depth of near-infrared light penetration into human tissue has been measured spectroscopically (Chance, et al., 1988). Spectra taken from the wrist flexor muscles in the forearm and muscles in the calf of the leg demonstrate that most of the light photons at wavelengths between 630-800 nm travel 23 cm through the surface tissue and muscle between input and exit at the photon detector. The light is absorbed by mitochondria where it stimulates energy metabolism in muscle and bone, as well as skin and subcutaneous tissue. hymbas.com/dplledNasa.htmlskyship
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Post by skyship on Sept 13, 2011 10:25:02 GMT -5
Mention of DRAM: The Central Processor in Living Cells So let me leave the big DRAM memory now and look at some of the other parts. Let's look at the microprocessor, the ribosome, several thousand of them scattered around the cell, they are all built alike, and they all have two levels of cache memory. Let's look first at the cache memories, L1 and L2, as we computer people talk. Let's look at L2. This is called messenger RNA in the biological lingo. Messenger RNA copies an entire subroutine out of the big DRAM memory and moves it close to the processor for fast access. How big is this? It's tens of thousands of bits long. That's comfortable for us. That sounds like an L2 memory. How about the L1 memory? Well, it takes small pieces out of the L2 memory and moves it into the microprocessor for translation of instructions. This is called transfer RNA. The Role of Transfer RNA Well, what size pieces does it take? It's pretty interesting because this reminds me of the old days. The biologist says first of all that the binary data in the big DRAM is paired, called base pairs. Base pairs, two bits. And for this purpose, three base pairs in a row is treated as an entity, a base pair triplet. In other words, six bits. And that's what's taken, one six-bit field at a time, out of the L2 memory and moved into the microprocessor. I can remember when we built computers with six-bit codes. That was before the ASCII committee. Apparently the biological system never got the word. And so they're still using six bits in our biological system. The six-bit codes get translated in sequence to choose amino acids to make a protein molecule. One by one, they get assembled, the whole subroutine gets read, and we generate protein molecules, and we send it off to do whatever it's going to do, and we run the subroutine again and we make another one. And we keep doing this until we have all the protein molecules we want, and then we reprogram the microprocessor with a different subroutine. So that sounds pretty familiar. americanhistory.si.edu/collections/comphist/montic/cray.htm#cr7skyship
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Post by skyship on Sept 13, 2011 10:49:44 GMT -5
RNA is the human messenger. "Previous research has presented other ways to modify the genetic code, but what is really unique about our method is that it is at the RNA level and it is site specific. We can express the artificial guide RNA in a cell and direct it to make a modification at a single site and only that site," said Yu. Altering messenger RNA in this way may be another mechanism human cells use to create many different types of proteins. Given our complexity, humans have surprisingly few genes. While it is well established that the majority of human genes code for more than one protein, mRNA modification may be an unrealized way that humans are able to do this. Scientists Override Errant Form of Genetic Signaling for First Time: Changing Genetic 'Red Light' to Green Holds Promise for Treating Disease www.sciencedaily.com/releases/2011/06/110615132019.htm=================================== Artificial RNA, protein: November 21, 2003 Researchers Design and Build First Artificial Protein computer-generated image of the artificial protein, Top7. Using sophisticated computer algorithms running on standard desktop computers, researchers have designed and constructed a novel functional protein that is not found in nature. The achievement should enable researchers to explore larger questions about how proteins evolved and why nature “chose” certain protein folds over others. The ability to specify and design artificial proteins also opens the way for researchers to engineer artificial protein enzymes for use as medicines or industrial catalysts, said the study's lead author, Howard Hughes Medical Institute investigator David Baker at the University of Washington. Baker and colleagues Brian Kuhlman, who is now at the University of North Carolina, Chapel Hill, and graduate student Gautam Dantas at the University of Washington, published their studies in the November 21, 2003, issue of the journal Science . The scientists collaborated on the studies with other researchers at the University of Washington and the Fred Hutchinson Cancer Research Center in Seattle. Proteins are initially synthesized as long chains of amino acids and they cannot function properly until they fold into intricate globular structures. Understanding and predicting the rules that govern this complex folding process—involving the folding of the main backbone and the packing of the molecular side chains of the amino acids—is one of the central problems of biology. According to Baker, the ability to specify a desired folded protein structure and then to create that protein offers powerful scientific and practical benefits. “First, specifying a protein fold and then designing that protein is a very stringent test of our current understanding of the forces and energetics of macromolecular systems,” he said. “Because designing something that's completely new means you can't copy any aspect from nature. “Secondly, if one can design completely new structures, one can potentially design novel molecular machines—proteins for carrying out new functions as therapeutics, catalysts, etc. And finally, there's the evolutionary question of whether the folds that are sampled in nature are the limit of what's possible; or whether there are quite different folds that are also possible,” he said. “Basically, we want to understand whether nature only sampled a subset of what's possible,” said Baker. The challenges of designing an amino acid sequence to fold into a new structure were considerable, said Baker. “If you draw on the back of an envelope some arbitrary protein structure, it might be that there is simply no amino acid sequence that will fold up to that structure. We had to develop methods to computationally sample possible structures similar to the one drawn on the back of the envelope, searching for a conformation for which there exists a very low energy amino acid sequence,” he said. Baker and his colleagues took advantage of methods for sampling alternative protein structures that they have been developing for some time as part of the Rosetta ab initio protein structure prediction methodology. “Indeed, the integration of protein design algorithms (to identify low energy amino acid sequences for a fixed protein structure) with protein structure-prediction algorithms (which identify low energy protein structures for a fixed amino acid sequence) was a key ingredient of our success,” Baker said. He likened the problem to the three-dimensional version of attempting to create a specified outline for a jigsaw puzzle, given only a certain number of pieces—the equivalent of the 20 known amino acids in nature. In addition, he said, these amino acids can rotate into a number of different conformations. “At each position, you can have one of the twenty amino acids, and for each of those amino acids you can have on the order of ten different shapes,” he said. “So, you have two hundred different possible shapes for each piece. With those restrictions, it may be that there are some outlines to this jigsaw puzzle that you just cannot achieve. So you need to have a way of changing the boundary to find a protein that can actually be made, because the main constraint is that the side chains fit together perfectly in the interior of the protein. “Thus, the problem is that the number of alternatives can be huge. Even for one fixed backbone conformation, you have an astronomical number of possible amino acid sequences,” said Baker. “So, we needed a computational approach to search the huge space of possible conformations and possible amino acid sequences efficiently.” In their design and construction effort, the scientists chose a version of a globular protein of a type called an alpha/beta conformation that was not found in nature. “We chose this conformation because there are many of this type that are currently found in nature, but there are glaring examples of possible folds that haven't been seen yet,” he said. “We chose a fold that has not been observed in nature.” www.hhmi.org/news/baker3.htmlOligonucleotide synthesis From Wikipedia, the free encyclopedia Jump to: navigation, search Oligonucleotide synthesis is the chemical synthesis of relatively short fragments of nucleic acids with defined chemical structure (sequence). The technique is extremely useful in current laboratory practice because it provides a rapid and inexpensive access to custom-made oligonucleotides of the desired sequence. Whereas enzymes synthesize DNA and RNA in a 5' to 3' direction, chemical oligonucleotide synthesis is carried out in the opposite, 3' to 5' direction. Currently, the process is implemented as solid-phase synthesis using phosphoramidite method and phosphoramidite building blocks derived from protected 2'-deoxynucleosides (dA, dC, dG, and T), ribonucleosides (A, C, G, and U), or chemically modified nucleosides, e.g. LNA. To obtain the desired oligonucleotide, the building blocks are sequentially coupled to the growing oligonucleotide chain in the order required by the sequence of the product (see Synthetic cycle below). The process has been fully automated since the late 1970s. Upon the completion of the chain assembly, the product is released from the solid phase to solution, deprotected, and collected. The occurrence of side reactions sets practical limits for the length of synthetic oligonucleotides (up to about 200 nucleotide residues) because the number of errors accumulates with the length of the oligonucleotide being synthesized.[1] Products are often isolated by HPLC to obtain the desired oligonucleotides in high purity. Typically, synthetic oligonucleotides are single-stranded DNA or RNA molecules around 15–25 bases in length. They are most commonly used as antisense oligonucleotides, small interfering RNA, primers for DNA sequencing and amplification, probes for detecting complementary DNA or RNA via molecular hybridization, tools for the targeted introduction of mutations and restriction sites, and for the synthesis of artificial genes. en.wikipedia.org/wiki/Oligonucleotide_synthesis============================================== skyship
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Post by skyship on Sept 13, 2011 11:42:37 GMT -5
Lily,
Can you come on here and discuss some of this?
Some patents can be found to be used in products, as you say, but Morgellons itself has to be related to some viral component, don't you think?
Would like some feedback from you.
Come on board.
You have covered a vast array of products, and I am finding that many of these buckyballs were used in products as well as in so many other areas.
The cage sheds its coat and the sphere remains, in foods, env. people etc.
That microsphere could be the NgCAM.
Skyship
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Post by skyship on Sept 13, 2011 11:46:55 GMT -5
Erasmus Darwin called it the Microscopic ens. He also wrote poetry in reference to Evolution: " By firm immutable immortal laws Impress'd on Nature by the GREAT FIRST CAUSE, Say, MUSE! how rose from elemental strife Organic forms, and kindled into life.Darwin's iconoclastic poem, subtitled The Origin of Society, seeks eventually to explain From what fair fountain mortal life arose, Whence the fine nerve to move and feel assign'd, Contractile fibre, and ethereal mind. (1: 216–18)" ........ "The fountain metaphor turns out to be especially apt, as Darwin surmises that “Nurs'd by warm sun-beams in primeval caves / Organic Life began beneath the waves” (1: 233–34). Moreover, life arises not from the special act of a deity, but as a result of natural processes already in motion: “Hence without parent by spontaneous birth / Rise the first specks of animated earth” (1: 247–48). These specks gradually develop into more complex, but still relatively simple and asexually reproducing forms, two of Darwin's chief examples being the fungus—“So the lone Truffle, lodged beneath the earth, / Shoots from paternal roots the tuberous birth”—and the oyster: “Unknown to sex the pregnant oyster swells, / And coral-insects build their radiate shells” (2: 71–2, 89–90). The development of highly complex organic beings—like us—requires sexual differentiation and with it all the advantages that sexual reproduction has over cloning. But this takes place again by means of natural, accretive processes unassisted by divine intervention. No definitive line divides the human being from the oyster, the oyster from the fungus, or the fungus from the original animate specks. All living beings, including “Imperious man,” “Arose from rudiments of form and sense, / An embryon point, or microscopic ens!” (1: 313–14)." dev.alexanderstreet.com/romr/romr.object.details.aspx?id=1002133751&browseurl=ABI&searchurl=2TNQThis theory was basis for the current Evolutionary theory, meaning mans genes are everywhere in nature, nature is in man, however, evolution fails to address the problem of circular DNA, only through SV40 viral component, that is the "original animate specks" What are those specks? found in SV40? Quantum dots not taking the place of those "animate specks"....... ~~~~~~~~~~~~~~~~~~~~~~~~~~ Virus means "veleno". Viruses are basically a way a form of genetic information insures its continued survival. They are entities which reproduces their DNA/RNA within living cells utilizing mechanisms of cells for this. ...""FILTERABLE VIRUS". We now know that viruses range in size from 20 nm (10-9 meters) to 250 nm. We also know that some of the smallest bacteria such as the chlamydia and mycoplasma are almost as small as the largest viruses and that they too can pass through filters that retard 99% of the other bacteria. By the early 1900 diseases like foot-mouth-disease in cattle, some cancers (in animals) and yellow fever in humans had been demonstrated to be caused by filterable viruses. The scientific community knew that it had a new group of dangerous pathogens to contend with. The term "VIRUSES" became permanently associated with this life form. You have previously seen that bacterial viruses (view the "Single Burst Graph Animation") or #bacteriophage (phage) were discovered in 1915 & 1917. Viruses, however were not "seen" until the electron microscope was developed in the late 1930s. This site contains electron micrographs of many bacteriophage; view the P2, lambda and P4 phage. T-Even Phage Figure 2. T-EVEN PHAGE. This is a large bacteriophage. It happens to be one of the most complex viruses. Not all phage are large; some are composed of only 7 genes. This is an E. coli phage and it has been studied intensely and much is known about it. Click here for another picture of a bacteriophage. We now know that viruses exist that attack perhaps every form of cellular life on this planet. I haven't seen references to thermophilic phage, but I would be surprised if they didn't exist. We are discovering new viruses all the time and most virologists feel we have only scratched the surface of viral variety. For example, when sea water is concentrated and examined under the electron microscope it teems with VIRUS-LIKE PARTICLES and we have no idea what they are or where they come from or what their hosts are?"............... www.slic2.wsu.edu:82/hurlbert/micro101/pages/Chap11.html=================================== What are those virus-like particles? Valeno: Etymology The word is from the Latin virus referring to poison and other noxious substances, first used in English in 1392.[9] Virulent, from Latin virulentus (poisonous), dates to 1400.[10] A meaning of " agent that causes infectious disease" is first recorded in 1728,[9] before the discovery of viruses by Dmitry Ivanovsky in 1892. The plural is viruses. The adjective viral dates to 1948.[11] The term virion is also used to refer to a single infective viral particle. The origins of viruses in the evolutionary history of life are unclear: some may have evolved from plasmids – pieces of DNA that can move between cells – while others may have evolved from bacteria. In evolution, viruses are an important means of horizontal gene transfer, which increases genetic diversity.[7] Viruses spread in many ways; viruses in plants are often transmitted from plant to plant by insects that feed on the sap of plants, such as aphids; viruses in animals can be carried by blood-sucking insects. These disease-bearing organisms are known as vectors. Influenza viruses are spread by coughing and sneezing. Norovirus and rotavirus, common causes of viral gastroenteritis, are transmitted by the faecal-oral route and are passed from person to person by contact, entering the body in food or water. HIV is one of several viruses transmitted through sexual contact and by exposure to infected blood. The range of host cells that a virus can infect is called its "host range". This can be narrow or, as when a virus is capable of infecting many species, broad en.wikipedia.org/wiki/Virusskyship
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Post by skyship on Sept 13, 2011 12:26:59 GMT -5
Lily or AQT,
I do wonder about the use of this (viral phenomenon) for evolutionary change, and when that happens, there is certain species extinction that takes place. Morgellons is causing one of them. There are others.
That spark of life becomes the quantum dot, that is artificial evolution.
That spark of life that was original "junk dna" has found a way to become immune to host.
So, now that quantum enters picture to integrate into the human, through the junk dna, then that host protection is taken away. The virus become active. And the introduced quantum dot technology inside the oligomers becomes the controller/expression of dna.
Morgellons in end is viral vectorial pathogen. The vector moves in. Whether it is quantum dot RNA, or SV40, the spark is activated, by em, microwave, or radio wave.
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So "the law of attraction" does that......... signals, not made by you but outside of you.
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The signal is in environment both outside of cell, in extracellular spaces, and outside the human body.
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Viruses do that.
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Viruses are the mutators to change RNA and DNA.
Then along came the artificial signal to do the same thing.
This is Evolution toward the Artificial.
The Alpha and Omega.
Alpha is used for the new Evolution. Starting over again, but, this time artificial/synthetic is brought in, using Biology/chemistry/geology/physics/microbiology is where the answers lie.
The smallest thing. Reductionism. The "microscopic ens".......
skyship
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Post by skyship on Sept 13, 2011 12:52:58 GMT -5
There are 4 chemicals that make up a cell. What are those chemicals? ======================== Overview • Hydrogen, oxygen, nitrogen, carbon, sulfur, and phosphorus normally makeup more than 99% of the mass of living cells. • Ninety-nine percent of the molecules inside living cells are water molecules. • Cells normally contain more protein than DNA. • Homogenous polymers are noninformational. • All non-essential lipids can be generated from acetyl-CoA. • Like certain amino acids and unsaturated fatty acids, various inorganic elements are dietarily "essential". • Most all diseases in animals are manifestations of abnormalities in biomolecules, chemical reactions, or biochemical pathways. All living organisms, from microbes to mam- mals, are composed of chemical substances from both the inorganic and organic world, that appear in roughly the same proportions, and perform the same general tasks. Hydrogen, oxygen, nitrogen, carbon, phosphorus, and sulfur normally make up more than 99% of the mass of living cells, and when combined in various ways, form virtually all known organic biomolecules. They are initially utilized in the synthesis of a small number of building blocks that are, in turn, used in the construction of a vast array of vital macromolecules (Fig 1-1). www.tetonnm.com/pics/IndependentSamplePages/1-893441-42-3.pdf
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Post by kritters on Sept 13, 2011 18:01:20 GMT -5
Shipster,
I see yu as one very brilliant chickster.
I'm becoming aware that everything seems to evolve around the proteins.
what's up with that?
You are tanacious and agressive in your pursuit of knowledge and answeres and I so admire you.
Kritts
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Post by aqt on Sept 15, 2011 14:46:53 GMT -5
more from Lily...trying to keep up with all of this!!
Review Hoffman and LaRoche patent 4267382 using dichloro. This toxic poison makes the zig zag chain reaction and is derived from clostridium teuranum and chloroplast. They cause metabolic reactions and are known as capacitors. Learn terms such as actuator, capacitors, molecular motors, ligands, residues (for which Dr. Vicotr Mellul, dermatologist stated I was suffering from residues but would not elaborate on what that meant).
These agents can accept or change discharged electrons. They are using tetrahedra configurations. Look on wikipedia and chemical data bases and will show ball and stick of these molecules and how they connect. Proteins are pigments and are being used from drugs, cosmetics to paints at nanolevel. Propene used is a gas and produces nano crystal needles that are being ejected and makes this a bioweapon. Pubmed 8157082 will explain the hazards and potent reaction of tetrazol and how it causes brain damage.
It is highly explosive and is discourage from being used in drugs as are stereoisomers, yet there are thousands of patents using them. Dichloro causes blue lips, nails and skin and confusion, convulsions, dizziness, shortness of breath, headaches, redness and pain of eyes and abdominal pain as well as many of the other agents used in Renova 0.05%.
One toxic agent on a hypersensitive person can be deadly let alone the numerous toxic agents used in this cream and creams and drugs like it. Review patent 4877805 you will see toxic chemicals being used like trimenthylphenyl, propene, tetrazol, xanthum gum (explosive and used in TNT gel patent), napthalene (pesticide moth balls), hexatrienyl, butadiene, inden, ethylsulfony, benzyl alcohol, hydroxy, thienyl, didehydroretinoic acid, octatrienoic acid, TTNP, tetramenthyl, 2,4,6,8 and 5,6,7,8 tetrahydro (pesticides), 2,3-dihydro, nanoactetraenoic acid, benzoic acid, cyclohexane, dichloro, 3,7-dimenthyl and many other toxic poisonous compounds.
Who caused my health issues and those millions of people who were prescribed these drugs from cancer to skin disorders and when the patents expired gave corps. like Avon, Estee Lauder, Loreal, Unilever and hundreds of others the right to put them in over the counter products from makeup, antiaging creams to sunblock lotions that will cause skin cancer and other cancers. Time for the so call researchers of Morgellons, chronic fatigue, hepatitis B epidemic, Epstein Barr epidemic to work together as it is the agents being misused by all to be punished and exposed.
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Post by aqt on Sept 15, 2011 14:47:04 GMT -5
Again, I ask to excuse typo errors and misspellings as I don’t see well do to coagulase neg. staph and Keratitis from these retinoid Vitamin A derivatives that were prescribed by Dr. Booth Durham and his colleagues left me to suffer and not be cultured or biopsied or treated for this known adverse event that Seeger and Weiss and other attorneys are representing certain chosen clients and not, which effects the true statistics of drug injury cases. I am trying very hard to educate those who want to know what is causing their health issues and condensing six years into these blogs, while someone is busy trying to delete them and preventing your from knowning the total truth.
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Post by aqt on Sept 15, 2011 14:49:11 GMT -5
In above blogs I informed you how they are using cnidocytes and nemacysts as stinging capsules in cosmetics and tattooing and that these agents shoot off hairlike threads as weapons to catch their prey, see wikipedia cnidocytes. You know need not look for textile threads any longer Mr. Wymore and need to concentrate on biological threads of marine parasites and liquid cholesteric benzoates and hairlike organelles known as whips. As a professor of pharmaceutical and biology you show be aware of the misuse of these agents in pharmaceutical and cosmetic products. They are using whole organisms in these products as well as in vitamin patents. Why people will have parts of insects coming through their skin and stools. Because pharmaceutical corps are putting them in their products. They are using the umbrella structures of the jellyfish and using the tentacles. Patent 6406709, Nematocyst discharge, assignee Nanocyte Inc., Wilmington DE, Patents 6337389 and 5714582 Bioscience L.L.C., Norfolk VA using the jellyfish for collagen used in pharmaceuticals and cosmetics and its coils. Dimethicone and cyclomethicone used to enhance shine. The many uses of the bacteriorhodopsin purple membrane 13-cis retinoic acid are patents 4711815 Recording medium, 5628934 Photochromic color, Patent 5922843 Analog bacteriorhodopsin molecules, Robert Birge, Patent 6461594 Robert Birge Syracuse University, Patent 6190677 and 6224884. www.alct.com/publications/pt3.pdf “Thread” will inform you about liquid crystals as well as the wikipedia by using liquid crystal as search engine. The various phases and the hedghog and how crystallography and microscopy tools can view these agents as well as the OSU microscopy donated by the NSF via your tax dollars, which should entitle you to free of charge for analysis of samples to prove what has infected and invaded your body. Lipid membranes of these various species used in biologoy as biomimetic to mimic nature. These agents flip and flop known as flipase and flopase. Patents 5922843, 6140012 and 5223355 are more the bacteriorhodopsin patents. Read US District Court Master File NO CV-92-P10000-s and see the toxicity of liquid silicone and how it was not to be used on humans, yet Johnson and Johnson’s own patent is using it directly on the face in the cream Renova 0.05%. The fumes will burn the eyes and respiratory system. The DMSO will penetrate the membrane of the skin and allow entry of this toxic agent into the body and bloodstream and when it goes to the lungs and solidifies and causes silicosis of the lungs and there is no antedote for this disease that use to occur in miners and now women from breast implants to people have TMJ implants to now being used in retinoids and shampoos. Reasrch leukocytosis, Sezary Syndrome (leukemia and caused by chemicals in Renova and other retinoid products and pesticides due to benzene). Phtlates and pyrolles are poisonous agents and used in these products. Phttlates are used to make plastic soften like gel used in these products and it is the feeling of a gel that I can feel falling from my hair over my face. See how many lawsuits are against Johnson and Johnson for false advertising as Renova was falsely advertised and they were only given a warning letter in 2002, a few years too late for those of us that used it in 1999 and before that date. Where are the whistleblowers to inform us of the truth and why are these whistleblowers being given large sums of settlements for telling the truth, and why did they wait so long in doing so? The settlements should be given to the sufferers and nothing to anyone else. Attorneys for drug injury cases knew for decades how dangerous these agents of retinoids and toxic agents used with were and they wait till there is enough injuries before advertising to the public and then they only accept cases they want to accept and leaver others to suffer. This is an outrage and insult to the Constitutional rights of all citizens of this country and it is discrimination. When adults stop lying and stop extorting and stop murdering one another then maybe our children will have a chance. A this point in time they can’t trust adults in any manner. Your children hear and see and learn from your behavior. They hear your phone conversation that you think they are not listening to. They hear your prejudice and your abusive language and they mimic it, just as these biological agents are being used to mimic nature. Kandy Griffin mentions NASA biologist Lucid in above article, I called her name up in search engine of free patents to see what I could find on her inventions. What I was amazed that came up was patents 20080199538 and 5507716 which were patents on Compounds to enhance lucid erotic dreams assigned to Lucidity Institute. They even have chemicals to make you have erotic dreams and for which is a mind control agent. What prevents this person who is have these dreams to wake and carry out these erotic acts on a innocent child or person? As I stated above they can chemicals to make you do anything they want you to do. Don’t take anything until you research it and research every chemical and don’t leave anything out. Trust has been taken and it will take a long time to regain it. Physicians need to wise up fast because their profession will suffer forever and then they can see what it is like to be unemployed and not be able to care for your family. Many have lost everything they ever worked for do to this profession poisoning its trusted patients.
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Post by aqt on Sept 15, 2011 14:51:04 GMT -5
Daniel Bellvaneeden, Silentsuperbug emailed an article to me toady on another microbiologists being infected with bacteria (yersinia pestis) in a Chicago lab. One died from the bacillus cereus infection two years ago in this lab.
Man can’t leave nature alone, it has to mess with it and alter it and wants to be the creator of agents that cause death. Then we have those who pretend they are heroic human beings trying to help the less fortunate sufferers of a disease caused by this monsters called biologists. A heroic person doesn’t charge to help another person. They don’t extort money and call them donations and then only do tests for the ones with the highest donations, yet don’t ever really give them the answer to what caused or who caused their health issues. They don’t make promises to help and put it in writing and then when they get the documentations and samples of evidence turn their back on the person to whom they stated would help. They don’t falsely advertise that they can do hair samples for metal toxicity and parasites and then cash a check paying in advance and they don’t do the analysis promised. They don’t steal someone’s research and then make it into their own research publications.
Honest ethical people give credit to who deserves and gives help to all who need it. For years I read so many publications and found so many supposed researchers stating they can help and are researching a new emerging disease. No one hears from Mary Leitao, Ginger Savely, Dr. Staninger, nor Randy Wymore in the past few years. No one knows how many true sufferers there are in this new emerging disease and we only hear of a few who are getting testing done, including Kaisar Permanente.
All univrsities have the tools to analyzed for nanotechnology, proteins, viruses and all had the capability of having these agents tested. The above samples per Kandy Griffin, have the inventors names on them and those individiuals can should be held responsible for causing harm to the individuals they were taken from. Ligands and retinoids carry the crypted encoded transcript to aler genetics. The human race is in serious trouble right, and not one researcher or self proclaimed toxicologist or scientist with ethics should be playing games with anyone’s life nor charging them.
A woman who stated she was an advocate for Dr. Staninger, Theresa Brown and Gwen Simmons (infectious disease nurse) contacted me via biology-online, after I gave my knowledge from researching chemicals in Renova 0.05%. They pretended that they used retinoids as suffered the same adverse events. Then they wanted my research and that Dr. Staninger wanted my samples as well as Randy Wymore. Theresa Brown brought her knowledge of the yersinia pestis and the Andy Coyle story (which no one hears from him anymore and he states he was set up by both women to meet a man that would help him, and who per Andy was a Monsanto personnel and stole his documents). She asked for my password on my email as was going to create an email to Dr. Randy Gaugler, at Rutgers who created and released this transgenic yersinia pestis nematode. She sent an email to this man at Rutgers using my email address of my old email that I haven’t used since it was hacked and all my emails pertaining to her and Sunny were delted an to others. Those emails had been sent to my other emails address before that time and were printed out. I print ever email concerning my conditions and those who I have consulted with. It is called CYA.
Yesterday, I received an email from that old email address to my new email address and where I found my blogs being deleted from this website. This person sent this email to Sunny (Gwen Simmons) and to another person I had been in contact with upto last year. Maybe these people don’t realized that hacking a computer and sending fictious emails using another person’s email is a criminal act and falls under fraud. The the govt can track back to who is doing it. Having these people who have stated this new disease has been tracked back to NASA, per Staninger publications, Gwen Simmons statements and Theresa Brown statements. That this had to do with electronics and nanotechnology.
They are able to trace anything and everything they want to trace. The bacteriorhodopsin (purple retina membrane known as smart dust) is a retinoid (vitamin A polypeptide) used as an optical recording medium and known for its memory storage. The retinoid known as 13-cis retinoic acid. My entire life I believe in doctors as healers. My entire life I told that Salk cure polio. Now I find out that Salk created new cancers by putting the sv40 simian virus in this oral poliovaccine. Do you know how many people I have lost to cancer who fall into the age group that would have been given this oral polio vaccine? I now find out that pharmaceutical corps. are causing cancer, MRSA, and other life threatening health issues with this 13-cis retinoic acid and other retinoids known as vitamin A; as well as comestic corps. from Avon to Loreal to Unilever and many others.
I don’t find this funny and I don’t find false advocates funny. If any of you have had a child you would not find this amusing that innocent children are being misused in torturous experiments. That this vitamin A derivatives cause cranial facial deformities, blindness, death. Be a parent of a child who is severely suffering from a toxic poison put in a drug that you took that caused this and were never informed of the dangers to your children or their children. Be a parent has to endure the pain and heartache of watching their child suffer. The heartache of worrying who will take care of that child when you are gone or become disabled and can’t care for them. This is not about suing a person, this is about having those people who invented these agents punished and put far away from human beings so they can’t hurt another person or animal or our food supply.
Maybe, someday all will wake up to realize that the longer you prolong exposing these people and taking the physical evidence to the proper authorities with witnesses, you are helping in causing the alteration of the human race and creating mutants and cancers that will consume all inhabitants.
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Post by aqt on Sept 15, 2011 14:53:47 GMT -5
Sad, again people are trying to delete the truth and don't want Morgellon sufferers to know the truth and where their disease truly has come from. If the person who has spent time deleting a week worth of blogs furnishing needed information to the public wants to make speculations of nanotechnology and protein and crystals found on samples, please take the samples I have a test them the way that you tested the above mentioned samples. I have an unopened package returned by the FBI several years ago, who refused to test the samples and stated it was situation for state officials. Now, knowning the knowledge I gained from patents, chemical data banks and protein data banks, pubmed, articles written about AM Kligman and the MKNAOMI Projects, and medical publications and nanotechnology over the past six years, these samples would prove who and what is major developer of nanotechnology crystal protein robotics and that is Johnson and Johnson, AM Kligman now deceased and unpunished, Univer of Penn and those individuals from the FDA and CDC who approved this drug Renova 0.05% and Renova 0.02%. The name of this cream was changed from Renuva 0.05% to the hi-scientific name Renova (definition is repeating small atomic explosions). Fact they are using explosive chemicals and combustible chemicals in this cream, ligands, crystals, proteins, microorganisms used in cloning, viruse engineered by chemists and purchased from the other known corrupt pharmaceutical corps Hoffman and LaRoche known for light emitting diodes derived from liquid cholesterol. As stated above liquid crystal that builds walls, reservoirs, wells, uses hinges and binders and creates threads when defected. Liquid cholesterol are fatty acids. Retinoids are chemodrugs and can be verified at www.chemocare.com/bio/ and on this website you can look up isotretinoin 13-cis retinoic acid (Accutane), tretnoin, all trans retinoic acid and click each drug listed on this data bank and it will bring you to descriptions of each of these Vitamin A agents and their toxicities and that the adverse reactions are the same as the Morgellon suffers from headaches, high lipid counts, high glucose, vision problems, intestinal pain (Crohns), hepatic disorders, swelling of feet and hands, rashes, blisters, loss of hair, heart problems, respiratory problems, sinus problems and severe itching. Morgellons is caused not just from chem trails that the above and other researchers want you to think it is just chemtrails and it is not. The pesicides sprayed in chemtrails are also used in these retinoid drugs and cancer drugs and they were used as biowarfare agents and contain mustard gases and other toxic agents that are poisons. These agents are being put in cosmetics as Avon and Loreal have retinoid patents as there are hundreds and hundreds of retinoids patents out there. Vitamins are toxic and should only be taken in small quantities via natural food supply, not supplements. Johnson and Johnson and Hoffman and LaRoche are large vitamin suppliers and are causing severe vitamin poisoning in people with these supplements and synthetic vitamins used in these drugs and hand lotions. Carbon nano tubes are used in antiaging creams and that is per ICTA own publication on nanotechnology and knew that they cause asbestosis of the lungs. \\ If these researchers truly want to prove their statements, I have the cream, hair samples and photos that prove what they created in this product Renova. Photos are the only true tool used to prove what they created and photos don't lie and can see into invisible light. To whom is deleting vital blogs that you asked people to comment on, you are violating a Constitutional Right of freedom of speech and preventing people from knowning the truth. You want the truth analyze the samples. These blogs have been printed, scanned and sent to others, as this website was copied and pasted and sent to others, so all you are proving is that you want to prevent the truth from being known. Johnson and Johnson, NASA, Merck, UMD-NJ, Rutgers, Bell/Lucent Labs, and MIT, DOE, NIH and others are in a joint venture in creating nano protein robots and bioengineered tisse and THE CANDIDATE is just one publication of many on Rutgers Aerospace projects. The space shuttle explosions, drugs, pesticides and cosmetics are the ways that humans, animals and our food supply are being contaminated with these toxic poisons.
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Post by aqt on Sept 15, 2011 14:55:37 GMT -5
To verify to you that retinoids are chemodrugs go to www.chemocare.com/bio/ and it will take you to the website and give you a list of chemotheraphy drugs. First on the list is 13-cis-retinoic acid and generic name is isotretinoin and trade name is Accutane. You will find tretinoin and all trans retinoic acid and list of many other drug names. Click each name and it will inform you of doctors using chemo drugs for anything they may feel would benefit you and not inform you that they are chemodrugs and the known side effects. You will find a list of the known side effects listed under each drug you call up by scrolling downward and you will side that the side effects listed are the same effects felt by Morgellons and the same abnormal lab results that are starting to be exposed from high lipids, glucose, neutrophil and easinophil etc. etc. There are now articles appearing on occupational workers who mixed and prepared chemodrugs coming down with cancer diseases. Amazing that these toxic mustard gases used in WWI for biowarfare are being used as chemotheraphy drugs to cure cancer when they cause cancer and what a web of deceit this has been. The occupational worker in danger, the one who is administering these agents in danger, the patient and what about the caretakers and family members who are touching these patients who are exposed to these toxic agents, radiation agents and microbial agents used in this cocktail of poisons? I find where advocates for the publica sue these corporation are getting settlements, but where are the settlements for the patient who is suffering and was given no choices on what these agents were about. Now, we find they are used in creams for antiaging and cosmetics and causing health issues and death to all of us unknowning of this. Drug injury attorneys knew this was going on as well as Congress Stupak, CDC and FDA personnel and advocates of the people, yet it was allowed to happen and none are helping the true innocent victims. These agents can and will cause impaired fertility (a way of sterilization of the human race without your knowledge and consent and a violation of your Constitutional Rights to conceive and reproduce a healthy child) and to cause you life long health issues that a physician will prevent you from knowning. Drug injury attorneys are picking and chosing who they want to represent and not informing the client of the entire extent of their injuries and what these chemodrugs are really made of. The FDA will not expose to you under the FOIA act what the trade secrets are in these patents of pharmaceutical manufacturers. They will black out certain information as we seen in Hank Albarelli’s documents from the FDA. How is that freedom of information if it is blacked out from you knowning what has poisoned you? Dr. James Bowen is a witnessed in Johnson and Johnson’s false advertising of spenda and has stated that splenda is a deadly poisoned and it is carbon tetrachloride and methylene chloride and they were used in Renova. Johnson and Johnson was giving warnings for falsely advertising Renova as a device to use instead of a facelift in a Martha Stewart magazine which was the article in the dermatologist office that attracted my husband and when he asked me to ask the dermatologist about it. Lured in with lies and false advertising and false labeling of a drug that was nothing more than a chemodrug used for people who had no other options being used as an antiwrinkle device that would cause life long health issues and even death because of the fatty long chain acids used that clog arteries and cause myocardial infarctions, fecal impactions, intestinal obstructions from the aluminum used and other heavy toxic metals and gases. Who is there for us? Why the game being played when all knew carbon nano tubes were being used in antiwrinkle creams, toxic metals, microorganisms and toxic gases? To find out if your hair has been altered to what Dr. Staninger stated in an email as pseudo hair, is just put hair under a microscope to find out whether the bulb has been damage or altered. That is all Dr. Janet Hull had to do and report and was specifically asked to do in my request for hair analysis along with a report on microorganisms (parasite pathogens).
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Post by skyship on Sept 15, 2011 19:42:28 GMT -5
Little ms Lily,
Now, calm down here. Many of us never used Renova. And the newer adaptations are in Chemtrails.
The Older ones, no. Some of us have the actual organic nanotubes, the organic chimeras in us.
This was before Chemtrails and before Renova.
You said,
"Morgellons is caused not just from chem trails that the above and other researchers want you to think it is just chemtrails and it is not. .....
I never claimed that it was just Chemtrails. It is in the foods. I do claim it is nano, which it is.
There are organic nanos and inorganic nanos. These are evolutionary adaptive products.
So, your claim if for the Rentinoid A.
Do you have Morgellons?
That is the question. You want us to sue. It is too late for that. Because, we will be dead before anything happens. And the real truth will remain intact as a lie. The GMOs need to stop. The best revolutionary act we could do, would be to break into the SEED BANK and get back our rightful crop seeds.
Skyship
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