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Post by skyship on Feb 19, 2014 23:57:14 GMT -5
Thanks for input from DonZ, Jdp7100, Kritters, and especially Lil Sis and others who have posted in the past. Revisiting many posts, and info from others has brought us to this point. The hidden journals which one has to pay for, can be found with limited info, but enough to tell the story. I have dug where others may have not had the time to go, and it has all been from the heart. I do this for the Morgie community. Many have found protocols that work, and thankfully they have gone on with their lives.
Others of us suffer continually due to the variations of our own dnas and our specific adaptations that have worked in the past. But, when those variations are open to the environmental onslaughts perpetuated by new tech options which can destroy those carrying the adaptations that worked, they are left open for destruction. No thought was ever given as to what would happen when variations are exposed, and those which lead to perfection or immortality are chosen, and that the adaptations we have already made were necessary to produce wellness. Nature itself took care of that, plus our knowledge on the subject of genetics. When that shield is taken away we are left to the wild and the genetic info is in the hands of these New Creators, who made themselves "gods" reinstating the power of the "gods" while destroying the real God.
We understand the powers of this dark side of humanity. What is the saying? "Be Wise as Serpents, (gentle)innocent as Doves".....
Healing is one thing, staying alive is another. The Movie, Avatar comes to mind. Those who are immortal, may find that something was amiss all along, but to your advantage you may have won, but have you really? True History tells the story, and you left a trail, in plain sight. The Pilgrim's Progress still applies and those pilgrims can see the details. We took the narrow road, more detail, more pure nature, more connection to nature. We have felt its presence all along. We know its powers, for we have slithered over its landscape and understood its beauty, you only saw it as hybrid monies, as control. You didn't watch over nature, but as gods of old, you revived its darkness. So even though we lose our skins, we renew ourselves everytime we lose something. You can't do that. You can only brag of your immortality. You had no thick skin to lose. You were thin skinned, yellow and used drones, and super tech to overcome the natural cycles. You changed our carbon~! You altered our adaptions that kept us alive.
You have chosen your crew, but, we are not done yet~! We are assembling as well. And the majority rules, not the minority. We listen to you, but you do not rule. We do~! You are so secret you cannot show yourselves. You hide in the Shadows, and the fake illuminated light is just that. When the blinding light of Truth is shone in your faces, you will cower in fear, as you have made us do. We are not looking for paybacks, or revenge, that destroys the purpose. No, we want Truth and we are finding it, despite your efforts to hide it, as you always have done. Our last breaths will be heard. Yours won't, unless you relent and tell us your secrets, especially those who will benefit especially, the poorest among us. We still love you and that means faith and hope are always possible as some liberated souls know.
So, Morgies we got work to do. We can overcome. We can find ways to bat this inferrance upon us. We can adapt with higher powers. I just have to find them. LOL..... What are your strongest qualities, genes, body parts which seem not to get infected with this darkness? These C4 carbons or C60 carbons (which can and should be replaced with gold dust, manna) are not healthy. These C4 carbons rob us of Carbon and evidence is showing up that it takes the oxygen with the Carbon. Or sometimes leaves the new carbon with the old carbon and takes the oxygen. All in the name of curing the earth of CO2. Stop lying folks, you had a bigger agenda and us truth seekers know this, us Morgies feel the change, and it is not good for us. We suffer from the toxic polymers used, the RuBisCO which is now showing to be dangerous, not only to humans but plants.
So, if we can capture this light of healing, we can use the protocols available, the Rife, the grape juice or wine spits, to get them out of teeth, and gargle with it gets them out of throat. DonZ has one here as does jdp7100, Dr. Gwen Scott, our own thoughts and intentions for bringing in the white light to heal, can work, a placing of hands in area of pain, movement and disturbance.
These people who have hurt us will come up with a solution, but, it will be worse than any we have come up with. How can we put our trust in those who have condemned us? They are evil. So, walk a mile with the snake and see what it sees. The smallest things are revealed to you, and that too is the place where these small things can walk right into our systems, but they can bring in the self assembling of evil, rather than good. At the same time you can see how low the serpent will go, and can live in mounds and can go into places we can't go. They can hide, they can sneak up, they can bite, they wrap around you and squeeze, they do shed skins. So, then be gentle as a dove, and know they are appreciated somewhere, somehow, but can be used as evil symbols and gods for imposing the dark upon us.
If gold dust particles (manna) can heal; why not rain down the gold particles? Then the tin, platinum, nickel, ruthenium or palladium can rust and the dark matter of fullerenes can be blasted out of the body. Even some who worked on them, have died from cancer from these nanocarbons. At least we will have iron for energy to carry on our own enlightened endeavors to heal others who suffer so badly. You see, we care, you don't~! That is our noble variation. And those who know that gold dust heals, also know this. So amongst you caring folks at the top who have not fallen over the cliff into the darkness, contact us. We got a job for you.
Skyship
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Post by kritters on Feb 20, 2014 5:37:35 GMT -5
Brilliant, eloquent and profound, Sky!!!
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Post by jdp7100 on Feb 20, 2014 14:43:23 GMT -5
If gold dust particles (manna) can heal; Hi Skyship, Have spent a small fortune on supplements many years ago. The single best one I ever used was m-iridium. Best way to describe is it lit up my brain. I was recommended to this brand as being very good and it worked for me at the time. www.oceanalchemy.com/M-Rhodium may be an interesting one in that the highest concentrations of m-rhodium found in red grapes. I wonder if this information ties into pulling material from mouth using red wine/grape juice. M-rhodium greatly assists in healing cancers and part of reason why juicing carrots works well for cancer treatment... carrots contain large amounts of m-rhodium. With that said, ormus is a gas. I went to free methods. While many use this method www.cherokeegold.net/mawatr.html I personally strongly believe that the classical radionic box helps to trap ormus which I use and posted before and after healing of morgellons non healing lesion. The water needs to be used quickly once taken off the classical radionic box as ormus is a gas and will leave the water. ----------------------------------------------------------------------------------------------- ----------------------------------------------------------------------------------------------- ----------------------------------------------------------------------------------------------- Once it was mentioned about the Antoine Priore device used for healing. For scalar/longitudinal waves for treatment with morgellons. In general, the scalar waves while it did not heal morgellons directly, does have a healing effect. electromedicine.wordpress.com/2013/01/31/a-non-technical-and-technical-description-of-the-priore-process/There is a study I have showing increased immune system function using scalar waves. Here is a video. www.dailymotion.com/video/x7xsqg_scalar-energy-in-healing-from-the-h_techI use a device called SG-1 to emit scalar waves www.royalrife.com/QE-3_order.html which when sitting next to it will emit strong scalar waves that can be detected in about an 18 inch radius but can go up to about 5 feet and which I have before and after pictures of strawberries taking much longer to go bad when using such technology. Plasma bulbs I also believe are able to emit scalar waves as well and used in many Rife equipment.
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Post by kritters on Feb 21, 2014 15:53:43 GMT -5
Well, this Ormus and m-rodium is BA-LOWING MY MIND!!! First, thanks for tolerating me here. I'm like a fly on the wall drop-jawed and so appreciative of all this incredible knowledge and information. I feel like the little yippie mascot jumping up and down and asking about things I don't understand! Hopefully I am providing some light distraction for some well deserved mental breaks.
I have never heard of this! Evidently, this Ormus thing is fairly new conceptually? Sky, weren't we talking on this forum a long while back about the dead sea? Is this how it's significant?
Also, I'd like to back up a bit and ask a seemingly stupid question: who was it that had the idea to use the wine swish and spit test for Morgs? What made him/her think to try this? I mean, did someone get really drunk on wine one night and spit in the sink and see the Morg strings and say, Ureka, what a great test! ? Reason I ask is that I'm wondering if anyone tried using sugar and blue food coloring to swish. I'm wondering if it's the sugar in (did they use cheap, sweet wine in which sugar was added?) the wine that lured the critters out of the teeth, gums and tongue and the red wine just stained it. I'm thinking, on an aside, that the most effective treatments might be a combination of sugars for feeding frenzy and then a solution to trap and kill the suckers. Like what I just did in my mouse traps.
Also, does anyone know if wine is made from seeded or seedless grapes? I would assume the quality wine would come from grapes with seeds intact. I go to whole foods to buy grapes with seeds so I can get the benefits, although I usually stay away from fruit because of my candida. But I figure, while I eat some of them, the grape seed extract might kill them. Thus my theory on the trap and kill LOL.
Also the bioflavinoids in the grape skins, which are used to make red wine. How would they come into play?
Anyway, thanks for that info you all seem to take in stride about Ormus. That is an amazing and seemingly untapped source for important health information.
Best, Kritts
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Post by kritters on Feb 21, 2014 16:31:54 GMT -5
www.subtleenergies.com/ormus/tw/variation.htmHudson also reported tHudson also reported that the m-state rhodium is the material which would "disappear in a flash of light" if it was left out in the sun. Two other researchers have reported similar experiences with the m-state rhodium.hat the m-state rhodium is the material which would "disappear in a flash of light" if it was left out in the sun. Two other researchers have reported similar experiences with the m-state rhodium. WONDER WHY THAT WOULD BE? (QUICK OFFERING FROM GOD OR SOME OTHER ALIEN, TAKEN AWAY TO OFFER ANOTHER IF NOT USED QUICKLY ENOUGH? LOL) 80% of rhodium passes through in the urine. WONDER WHY THAT WOULD BE? Rhodium is associated with the thymus. When you take rhodium over a period of a month and a half, the thymus grows by 40%. I REMEMBER READING A BOOK ABOUT 40 YEARS AGO, NOT SURE OF THE TITLE, BUT 'THUMP THE THYMUS' WAS THE FOCUS. What I am telling you, last night, is that over 5%, by dry matter weight, of your brain and nervous tissue, is made up of rhodium and iridium in the high-spin state. And, literally, you have light flowing in your body right now. MAYBE THIS ELEMENT IS THE GOD ELEMENT I've heard of people drinking macro amounts of carrot juice and curing cancer. Well rhodium is the cancer cure. WELL, THIS MIGHT PROVE MY TRAP AND ZAP THEORY OF CURING LOL. I KNOW CARROTS ARE HIGH IN NATURAL SUGAR AND I STAY AWAY FROM THEM IN LARGE AMOUNTS. HIGH GLYCEMIC VALUE. Flax oil has rhodium and iridium. Almond seeds also have it. Apricot seeds have it. Grape juice has it as does grape seed. Water cress has a lot in it. LAETRILE/AMYGDALIN...FROM APRICOT SEEDS. WELL, WE ALL KNOW THIS CURES CANCER. The other researcher says that the Wet Method m-state gold precipitate occurs in the following amounts for the following water sources: Dead Sea water: 70% Great Salt Lake: 19% Pacific Ocean: 8-14% BASHAR: Specifically it is strong in that direction. Even the energy field itself, around the monoatomic gold will impart the idea of increased longevity. If the m-gold is abundant in Dead Sea water (and salt) then it is the most easily isolated of the m-state elements. OKAY, so now, I'm really curious about iridium.
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Post by kritters on Feb 21, 2014 17:40:41 GMT -5
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Post by kritters on Feb 21, 2014 18:32:58 GMT -5
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Post by kritters on Feb 21, 2014 19:27:33 GMT -5
www.spagyricus.com/articles/oil-of-gold-and-three-kings-elixirs-of-life-history-and-usesthe more I research and read about quantum physics, string theory, etc.... (not that I understand it, mind you), the more I realize that there just might be something to stuff in the bible, albeit misinterpreted in many ways in order to confuse and deter people from true understanding. I am of the firm belief at this time that we are in fact infiltrated by aliens from other planets. I also believe that God, in fact, might be as well, but not sure. I do know that we have aliens among us. The tall whites, greys, whatever. Who knows what all this means? I certainly will never know in my lifetime but I'm so intrigued at what has, in fact, been revealed to me that I am hopeful that future generations will pick up the ball and run to score, and I believe they will. It's because of people like those on this forum that it will happen. Kritts
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Post by skyship on Feb 23, 2014 18:44:53 GMT -5
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Post by skyship on Feb 23, 2014 23:33:46 GMT -5
The RNA problem, even NIH now has some RNA studies in the COMMON FUND. That would be for us common folk, ya know~!~! After they gave it to us. Gotta cleanup the damage? Morgellons is listed here: rarediseases.info.nih.gov/gard/browse-by-first-letter/MBut, because we know Morgellons is not a disease, we will back up one page to this: Click on Disease on this page: rarediseases.info.nih.gov/research/pages/27/undiagnosed-diseases-programThen Click on the second blue highlighted page that says this: FDA approved medical products: rarediseases.info.nih.gov/gard/diseases-with-medical-products/AFirst off, on letter A note how may forms of ALS: then go to M. Morgellons not listed. Means they are not done with us yet, right? More FDA products needed to up the ante? Some other pages: rarediseasesnetwork.epi.usf.edu/rarediseases.info.nih.gov/research/pages/41/rare-diseases-clinical-research-networkthis may apply to us: the ncRNA, or any mRNA or tRNA. but,...........Notice what the link is. Leishmaniasis.....our little protomyxzoa? under the BioFilm? which is under the wax ester? Just curious here~! ......Several non coding RNA biosynthesis? ====================================== Agenda - Office of Rare Diseases - National Institutes of Health File Format: PDF/Adobe Acrobat Several Non-Coding RNA (ncRNA) Biosynthesis. Gautam Chaudhuri, Professor, Meharry Medical College, Nashville, Tennessee, USA. 11:30 – 11:45. rarediseases. info.nih.gov/.../Leishmainia%20Agenda%20NIAID%202009.pdf
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Post by skyship on Feb 24, 2014 0:13:31 GMT -5
I am having a hard time posting, Will have to check those (redirects) out. Meanwhile These reports need to be seen. ========================= ============================= Here if you can imagine it, trying to make a quad (Kurzweil definition- square) out of a round cell, or oblong once it is unfolded and the artificial is folded in, it becomes a square which hold the cruciform, or the Cloverleaf. Do you feel lucky? It is a four leafer~!================================== The crystal: www.technologyreview.com/view/419703/a-step-closer-to-perfect-3-d-data-storage/?ref=rss==================================================== ================================================= www.rayandterry.com/transcend/kurzweilai.php======================================== Please Note who the first RNA image is from~! Why would there be interest in this on K's part? Remember he and former Darpa head now work for Google~! ========================================= RNAImage Courtesy : kurzweilai.net/images/RNA_square.jpg image: shows structure of RNAclip_image004image: www.yourarticlelibrary.com/rna/rna-structure-and-functions-of-rna-explained/12247/====================================== More images next post, can only post 3 images/post. skyship
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Post by skyship on Feb 24, 2014 0:23:01 GMT -5
Well, we are tracked, but, oh well we knew that anyway. Images from above RNA info link: Credit to this link L-from model of tRNAtRNA the adaptor moleculewww.yourarticlelibrary.com/rna/rna-structure-and-functions-of-rna-explained/12247/***************************************************************** ************************************* Transfer RNA - Definition Transfer RNA www.wordiq.com/knowledge/images/1/15/TRNA2.pngTransfer RNA (abbreviated tRNA) is a small RNA chain (74-93 nucleotides) that transfers a specific amino acid to a growing polypeptide chain at the ribosomal site of protein synthesis during translation. It has sites for amino-acid attachment and codon (a particular sequence of 3 bases) recognition. The codon recognition is different for each tRNA and is determined by the anticodon region, which contains the complementary bases to the ones encountered on the mRNA. Each tRNA molecule binds only one type of amino acid, but because the genetic code is degenerate, more than one codon exists for each amino acid. Transfer RNA is the "adaptor" molecule hypothesized by Francis Crick, which mediates recognition of the codon sequence in mRNA and allows its translation into the appropriate amino acid. Contents [hide] 1 Structure of tRNA 1.1 Features 1.2 Aminoacylation2 External links
Structure of tRNAtRNA has primary structure (the order of nucleotides from 5' to 3'), secondary structure (usually visualized as the cloverleaf structure), and tertiary structure (all tRNAs have a similar L-shaped 3D structure that allows them to fit into the P and A sites of the ribosome).Features The 5'-terminal phosphate. The acceptor stem (also called the amino acid stem) is a 7-bp stem that incudes the 5'-terminal nucleotide and the 3'-terminal nucleotide with the 3'-terminal OH group (which can bind the amino acid). The acceptor stem may contain non-Watson-Crick base pairs. The CCA tail is a CCA sequence added to the 3' end of the tRNA molecule. This sequence is important for the recognition of tRNA by enzymes critical in translation. The D arm is a 4 bp stem ending in a loop that often contains dihydrouridine. The anticodon arm is a 5-bp stem containing the anticodon. Each tRNA contains a specific anticodon triplet sequence that can base-pair to one or more codons for an amino acid. For example, one codon for lysine is AAA; the anticodon of a lysine tRNA might be UUU (some anticodons can pair with more than one codon due to a phenomenon know as wobble). The T arm is a 5 bp stem containing the sequence TψC. Modified bases are several bases contained in tRNA that are not "canonical" bases, i.e. that are modified forms of the standard adenine, guanine, cytosine, and uracil bases. AminoacylationAminoacylation is the process of adding an aminoacyl group to a compound.Each tRNA is aminoacylated (or charged) with a specific amino acid by an aminoacyl tRNA synthetase. There is often just one aminoacyl tRNA synthetase for each amino acid, despite the fact that there can be more than one tRNA, and more than one anticodon, for an amino acid. Recognition of the approriate tRNA by the synthetases in not mediated solely by the anticodon, and the acceptor stem often plays a prominent role.Reaction:
amino acid + ATP → aminoacyl-AMP + PPi aminoacyl-AMP + tRNA → aminoacyl-tRNA + AMP External links tRNA could be the cause of heart attackwww.wordiq.com/definition/Transfer_RNA******************************************** Truth is definitely a day at the beach~! WHEN IT IS RAINING~!~!~!
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Post by skyship on Feb 24, 2014 1:44:34 GMT -5
Last Updated: Friday, 22 October, 2004, Single gene link to heart healthDNA DNA could hold the key to cardiovascular health A single gene fault could hold the key to a range of disorders linked to heart disease and stroke, a study has found. A team from Yale University School of Medicine found the defect was linked to conditions such as high blood pressure and high cholesterol. It affects the genes of the mitochondria - the energy-producing 'power plants' of the cell that are passed from mother to offspring.
The research is published online by the magazine Science. This doesn't answer the big questions, but it does give us a new place to start looking Professor Hugh Watkins, Oxford University Experts hope the finding will lead to greater understanding of the causes of such disorders. The US team's discovery stemmed from the study of one woman who had hypertension - high blood pressure - and low blood magnesium levels.Low magnesium is relatively rare, so researchers tested her for known mutations that they had previously associated with that trait.The woman said a number of other female relatives in her family also had low magnesium levels, which researchers said suggested there was a particular genetic condition affecting her family which had not been seen before.
They studied 142 women in the family and found there was a high frequency of high cholesterol and high blood pressure. Around half had all three conditions. This suggested there was a defect in the mitochondrial genome, because those genes are uniquely passed down by the mother.New linkThe researchers then carried out detailed analysis of the mitochondrial genomes of family members and found that all those who were affected had a defect within a gene linked to a specific transfer RNA (tRNA) in the mitochondria.
Transfer RNAs are involved in the construction of proteins in cells.
The family's genetic defect affected the tRNA that transports the amino acid isoleucine. Since many proteins normally contain isoleucine, this could contribute to a broad range of cell malfunctions. Researchers found members of the family were also affected by other conditions linked to mitochondrial malfunction, such as hearing loss and migraines.Dr Richard Lifton, who led the research, said: "There has never before been a report of a common genetic link among any of the three traits we found - low magnesium, hypertension and high cholesterol."This raises the general question of whether the more common forms of these traits might arise from abnormal mitochondrial function as well." He said that, since not all family members who had the mutation had all three conditions, there must be other genetic or environmental factors which influenced whether or not someone would be affected. He said: "It was particularly striking that the complex pattern of clustering that we see arising from this single mutation has many of the hallmarks of the kinds of clustering that we see in the general population." However, he added: "We have identified this defect and linked it with these traits, but there remains a complex black box in between. We don't know the mechanism that links the two."'Early stages'Hugh Watkins, professor of Cardiovascular Medicine at Oxford University, told BBC News Online: "This doesn't answer the big questions, but it does give us a new place to start looking. "Never before has a link been made between mitochondrial DNA defects and low magnesium levels, high cholesterol or high blood pressure." He added: "We are still in the very early stages of this research and we are very far from treatment." But Professor Watkins said a similar discovery of a rare genetic defect which affected how the liver handled cholesterol eventually informed work on statins, which are now widely used to reduce cholesterol levels. news.bbc.co.uk/2/hi/health/3762664.stm
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Post by skyship on Feb 24, 2014 2:01:12 GMT -5
So, it appears that variations where to be weeded out. Thinking along lines of directed variation diseases and this was accomplished using tRNA. One question is, when did it begin? When were the first tRNAs induced into the human genome? If these are mito, then we are talking about altering our given inherited genes. This is troubling. Not only is directed variation taking place, but, selection seems to be involved as well. If all are to be the same, then our inherited genes from ancestors are being altered. Was it Enki that did that once before? In fact how many times has this "Great Work" of Illumination Alchemy been done? Oh, lets see the fall of Atlantis, the fall of Babylon I and so on.
So what other reactions are showing up in clinics due to this "Great Work" of re genesis?
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Post by skyship on Feb 24, 2014 2:11:53 GMT -5
tRNA in OMIM Online Mendelian NEW syndromes due to induction of tRNAs changing mitochondria, hence producing new mitochondria syndromes. Remember from past post the way to alter our genome was by cloning or modifying/altering the variations of mitochondrial cells, ones that make us different, ones that identify our heredity. CLONING Aminoacyl-tRNA synthetases perform an essential function in protein synthesis by catalyzing the esterification of an amino acid to its cognate tRNA. These enzymes are necessarily present in each cell and must properly recognize the tRNA and the amino acid in order to maintain fidelity of translation. From the primary structures, 2 distinct classes of synthetases have been recognized, with similarity of certain structural features, amino acid attachment sites, and other properties between members of a class. Certain aminoacyl-tRNA synthetases are autoantigens in patients with the idiopathic inflammatory myopathies, polymyositis, and dermatomyositis. Autoantibodies reactive with synthetases are found almost exclusively in these conditions, with individuals usually having autoantibodies to only a single synthetase.
Most commonly they are directed at histidyl-tRNA synthetase (142810), labeled 'anti-Jo-1' autoantibodies. Ge et al. (1994) used a cDNA encoding the human form of glycyl-tRNA synthetase for isolation of corresponding cDNAs. Shiba et al. (1994) likewise cloned a class II human glycyl-tRNA synthetase and compared its structure with that of the bacterial counterpart from which it was found to diverge widely. Williams et al. (1995) also cloned the human GARS cDNA. The predicted 685-amino acid protein showed approximately 45% identity to the yeast protein. The recombinantly expressed protein was immunoprecipitated with human serum containing autoantibodies to glycyl-tRNA synthetase and was shown to catalyze the aminoacylation of tRNA.omim.org/entry/600783
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Post by skyship on Feb 24, 2014 2:30:19 GMT -5
This is why there are so many variations to Morgellons. This is just one clone with this histidyl-tRNA.
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ABOUT TIME~!~!~!~!~!~!~!~! IT IS STILL RAINING~!~!~!~!
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Post by skyship on Feb 24, 2014 2:43:01 GMT -5
So, do we have evidence folks? There is much more.
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Post by skyship on Feb 24, 2014 3:38:33 GMT -5
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Post by skyship on Feb 25, 2014 19:09:59 GMT -5
If you were to reconstruct the cytoskeletal cells, what would you do? First off accept that there are 3 dominions of life. Now, there are no cultured archaea. Why is that, yet we are to believe these have been in our body system all along. The big Lie. They have not. None were cultured and the work published for a reason. These involve the so called heat shock proteins. It took me a while to get here on this thread, but, there is a reason for that. We are going from the big picture, with all the lies from CSH,(the molecular machine) from those who hid Archaea under the rug, to those who incorporated pruvate into many gmo crops and other things, to altering DNA through rRNA and tRNA, using archaea to incorporate and destroy ancient DNA. The objective was to get rid of the so called "selfish gene"....... What is that "selfish gene", once gone does it eliminate all info regarding our hidden ancestry? Bet it does~! In their minds, but the image is still there. So, we need to light up the image. I suppose Rife or Priore or even Oxygen tabs could do that? Again, whatever protocol we take we have to be consistent with it and maintain somehow. Once, variations of human genome were found, they set about eliminating them. So, we are all the same. There goes our uniqueness, or individuality on a genome level. There goes the "junk DNA" which is gold to some of us. But, this can be events that weed out, just like the imperfections of a cow, or plant, or water itself. So, the norm becomes abnormal. Therein is the dis ease. The adaptor tRNA can select, delete, or enhance. But, what is the signal that would do the selection? Are they called Selectins? ================================= "Selectins are a family of transmembrane molecules, expressed on the surface of leukocytes and activated endothelial cells. Selectins contain an N-terminal extracellular domain with structural homology to calcium-dependent lectins, followed by a domain homologous to epidermal growth factor, and two to nine consensus repeats (CR) similiar to sequences found in complement regulatory proteins. Each of these adhesion receptors is inserted via a hydrophobic transmembrane domain and possesses a short cytoplasmic tail. The initial attachment of leukocytes, during inflammation, from the blood stream is afforded by the selectin family, and causes a slow downstream movement of leukocytes along the endothelium via transient, reversible, adhesive interactions called leukocyte rolling. Each of the three selectins can mediate leukocyte rolling given the appropriate conditions. L-selectin is the smallest of the vascular selectins, and can be found on most leukocytes. P-selectin, the largest selectin, is expressed on activated platelets and endothelial cells primarily. E-selectin is expressed on activated endothelium with chemically or cytokine-induced inflammation." bme.virginia.edu/ley/selectins.html============================ With the polymorphisms of Morgellons, it seems that serum is involved. But how? In conclusion, we showed that SELP polymorphisms strongly influence the concentration and the familial aggregation of P-selectin. After adjusting for the effect of SELP polymorphisms, the familial correlation of P-selectin levels between biological relatives still remained of great magnitude (r = 0.33), suggesting that other genetic or shared environmental factors could be involved in the determinism of P-selectin variability. onlinelibrary.wiley.com/doi/10.1111/j.1538-7836.2008.02952.x/full================ So from the environment? ? ..." genetic or shared environmental factors could be involved in the determinism of P-selectin variability." ======================= =============================== Well, some scientists are looking at not just nurture(behavioral) but environment itself. ============================== The resulting tendency to focus on the genes does not necessarily lead to less effort to understand the environmental contributors by any means, but it can have that effect. Known genetic involvement even of a single-gene single-trait type clearly does not mean that a particular outcome is unavoidable (any more so than in cases referred to as “environmentally determined”). Such examples can still be amenable to environmental and behavioral interventions, and the monogenic “genetic” disease PKU is a good case in point. Eliminating the indigestible amino acid from the diet currently provides the best treatment. The particulars of each problem determine how best it can be handled, so, in the future, some problems thought of as environmentally determined may be best dealt with through gene therapies. (For now, those therapies appear to remain distant possibilities.) Moore also notes that, although it is inherently less likely to lead to the stuck-with-it do-nothing outcome that has sometimes resulted from genetic determinism, environmental determinism is problematic too. After all, environmental interventions operate on organisms built in part by genes, and they continue to be affected by genes through gene products. Even features that seem largely controlled by environmental factors for almost everyone are influenced by genes, and can be very different given enough of a change in the genome. An obvious example for behavior analysts is learning, in the case of PKU or Down syndrome, with their documented genetic contributions. But more subtle examples exist too, and behavioral interventions may sometimes fail to work because of unrecognized genetic factors (see, e.g., Manuck, Flory, Ferrell, & Muldoon, 2004; Suomi, 2002, 2003). Knowledge of such genetic involvement would be very helpful even without the existence of gene therapies. If they were to exist, the known presence in an individual of genetic predispositions for alcoholism or autism, for example, means that behavioral and other environmental countermeasures could be targeted at an early age. The presence of interactions means that the predispositions might be problematic only in particular environments to begin with...... ......... Conclusion The 21st century brings a revolution in our understanding of nature–nurture relations, one that clearly goes far beyond the mapping of the human genome. As The Dependent Gene documents, genes and environmental factors interact at all levels in very complex ways. The more dissemination of this spectrum of findings, the better for fields like behavior analysis that are focused on behavior–environment principles that do not always get the same respect as genetics. Ironically, many geneticists do recognize the important role of the environment (e.g., Moore; Morange, 2001), although that message has not always been well publicized. Similarly, behavior analysts have always recognized the importance of genetic involvement in the phenomena they study (and now the practical implications are growing). But that fact has not always been acknowledged either: As Morris, Lazo, and Smith (2004) documented, although B. F. Skinner wrote amply about biological, genetic, and evolutionary involvement in behavior, he was and continues to be frequently accused of neglect. Behavior analysts can be proactive by talking knowledgeably about their science's relation to the larger life sciences—and the pivotal role of the behavior processes they study and apply. Awareness of the nature–nurture relations described in The Dependent Gene can provide support as well as illumination......... The Tangled Tale of Genes and Environment: Moore's The Dependent Gene: The Fallacy of “nature VS. Nurture” europepmc.org/articles/PMC2223161/reload=0;jsessionid=oJh8bGxCFytY8MZ9YMv2.10===================
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Post by skyship on Feb 25, 2014 20:17:30 GMT -5
So, in America didn't we combine both? Why these same things seen in Germany and Russia now showing up here, in a Trojan manner? Nature vs. Nurture, or environmental determination. the environment, at large. Changing and deleting genetics from the air or space ie: Space station, satellites, laser on moon etc. =============================
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But, what have we done?
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But, who was controlling all of this? behind Nazism, behind Communism and now Technoism, Geneticism and Environmentalism..........
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Post by skyship on Feb 26, 2014 4:24:46 GMT -5
Well, we have arrived or at least I have. This is often hard to explain, but, if you think of it as the human body plan. Now, this is a great endeavor. Updating the Human Genome, the whole purpose to fit it into the evolutionary paradigm. In other words, undo what the junk dna stored. Show that all the human body parts are the same as what is in the environment, but, one mistake, how did the archaea get in there? After all, they came from under the earths crust, from volcanoes, hydrovents, geysers, under the sea etc. These items where not on the earth's crust, they were under the earth. Have the hidden dna express itself, hidden in X chromosome which has been altered. You are carriers of certain diseases, that you do not get, that means your junk dna discarded it for your benefit, yet stored it in the "junk dna". It does not harm you but you carry it. Your body plan in this new paradigm, has genes that can be identified in other plants and animals, and the new archaen proteins which were never in our genome. So, a gene from a fly, mouse, snake, spinach, tomato, zebra fish, you name it all fit into the human body parts. Universal one with Gaia. One with the earth. From the environment came the Mobile Genetic Element, like a chemical altered the RNA and DNA. 6 things were going on:1. Acetylation 2. Methylation 3. phosphorylation 4. Ubiquitinylation 5. Sumolation 6. ADP Ribosylation and much more. I will be putting this together in full form, then in summarized form for the MRG website if I can. As far as peer reviewed papers, I am like this author who will: Write the Science Right. This has not been done. We were never told what was going on, only through our persistent digging, because they love to post their papers, we have been able to decipher their mumble jumble, use of Alphabet groups and Greek symbols, which now they want to change to Latin. Ex. the beta symbol, the Alpha symbol and the Psych symbol or psi symbol, etc. So much involved but one of the Epigenetic changes was what Karen suffered from: p53, plus organ growth and many other elements as well. We have different symptoms, depending on what was stored in the silent X, it was opened up, and ncRNA was there as well, and those were either deleted or opened up. and heat shock proteins insured another protein from the environment was added in.(archaean) =================================================================================================== We begin with the whole Epigenetic Program. The 2 main components of the Epigenetic code are:DNA Methylation Histone Modification universe-review.ca/I10-33-epigenetic.jpg================================ Universal Code is what they were after, and sought high and low for proteins from all walks of life and inorganic as well. For one thing H was substituted with CH3 and this is in outerspace. " Epigenetic mechanisms includes histone modification, DNA methylation (replacing H with CH3), and RNA interference. "............universe-review.ca/F11-monocell13.htm========================================
Histone modification DNA methylation (replacing H with CH3) RNA interference=============================== All that we have said on this board in many posts, reviewed posts, all from morgie sufferers and some who have died, all for an "idea" that gained footing through secret science and coverups of the risks and the damage that has been done to the human population.
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Post by skyship on Feb 26, 2014 4:50:10 GMT -5
Epigenetic Diseases: Click on images to see larger versionsWhat Is Epigenetics? How Do Epigenetic Changes Affect Genes?This triangle-shaped diagram shows that three systems can interact to silence genes in cells. Arranged as points on the triangle, the systems are DNA methylation, histone modification, and RNA. From each of the systems, arrows point to the interior of the triangle, indicating that these systems may produce heritable silencing, though RNA-associated silencing in higher organisms has not yet been established. View Full-Size ImageFigure 1 Epigenetics involves genetic control by factors other than an individual's DNA sequence. Epigenetic changes can switch genes on or off and determine which proteins are transcribed.Epigenetics is involved in many normal cellular processes. Consider the fact that our cells all have the same DNA, but our bodies contain many different types of cells: neurons, liver cells, pancreatic cells, inflammatory cells, and others. How can this be? In short, cells, tissues, and organs differ because they have certain sets of genes that are "turned on" or expressed, as well as other sets that are "turned off" or inhibited. Epigenetic silencing is one way to turn genes off, and it can contribute to differential expression. Silencing might also explain, in part, why genetic twins are not phenotypically identical. In addition, epigenetics is important for X-chromosome inactivation in female mammals, which is necessary so that females do not have twice the number of X-chromosome gene products as males (Egger et al., 2004). Thus, the significance of turning genes off via epigenetic changes is readily apparent.However, inactivating them when they contain a "junk dna" defect is another reason they are shut off. But, here the were shut on to reveal the VARIATIONS in the X and this involves mitochondria as wellWithin cells, there are three systems that can interact with each other to silence genes: DNA methylation, histone modifications, and RNA-associated silencing (Figure 1; Egger et al., 2004).
Read more here:Epigenetic Influences and Disease By: Danielle Simmons, Ph.D. (Write Science Right) © 2008 Nature Education Citation: Simmons, D. (2008) Epigenetic influence and disease. Nature Education 1(1):6
The behavior of a person's genes doesn't just depend on the genes' DNA sequence - it's also affected by so-called epigenetic factors. Changes in these factors can play a critical role in disease.www.nature.com/scitable/topicpage/Epigenetic-Influences-and-Disease-895#====================================== Diseases and elements involved......p53 is there....... Attachment DeletedTable 1: Epigenetic diseases and their causes and symptoms Epigenetic changes are responsible for human diseases, including Fragile X syndrome, Angelman’s syndrome, Prader-Willi syndrome, and various cancers. Abbreviations: ATR-X syndrome, alpha-thalassaemia, mental retardation syndrome, X linked; BWS, Beckwith–Wiedemann syndrome; CREB, cAMP-response-element-binding protein; HAT, histone acetyltransferase; HMT, histone methyltransferase; ICF, immunodeficiency, centromeric region instability and facial anomalies syndrome; UTR, untranslated region.© 2004 Nature Publishing Group Egger, G. et al. Epigenetics in human disease and prospects for epigenetic therapy. Nature 429, 459 (2004). All rights reserved. ATR-X syndrome has symptoms that include intellectual disabilities and alpha-thalassaemia. Its etiology involves mutations in the ATRX gene and hypomethylation of certain repeat and satellite sequences. Fragile X syndrome has symptoms that include chromosome instability and intellectual disabilities. Its etiology involves expansion and methylation of a CGG repeat in the fragile X mental retardation 1 (FMR1) five-prime (5’) UTR and promoter methylation. ICF syndrome has symptoms that include chromosome instability and immunodeficiency. Its etiology involves DNA methyltransferase 3b (DNMT3b) mutations and DNA hypomethylation. Angelman’s syndrome has symptoms that include intellectual disabilities. Its etiology involves deregulation of one or more imprinted genes at 15q11–13 (maternal). Prader–Willi syndrome has symptoms that include obesity www.nature.com/scitable/topicpage/Epigenetic-Influences-and-Disease-895#==================== The important thing here is that the mutation came from the environment:===========================
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Post by skyship on Feb 26, 2014 5:49:41 GMT -5
What is the environmental transposable element that could have accomplished these genetic disruptions?
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Post by skyship on Feb 27, 2014 23:45:48 GMT -5
Okay these TEs' come from:Gene mutations New Gene Formation Chromosome RearrangementsGene mutations would be the DNA Methylation, this opens the gene New Gene Formation would be the RNAi RNA interference proteins Chromosome Rearrangements: means Histone Modification Now how could these three things have been done? By the three new amino acids? We always had 20. 21.Selenocysteine 22.Pyrrolysine23.Not Phenylalanine, (see below), exact name of #23. N-formylmethionine ......(one previously used could have been a pseudo -phenylalanine which has the capacity to make toxic fibrils related to amyloids. So, this could have been one of the mistakes when it was altered or mimicked.) ============================================================================ Nonprotein amino acids:...... Definition by negationTechnically, any organic compound with an amine (-NH2) and a carboxylic acid (-COOH) functional group is an amino acid. The proteinogenic amino acids are small subset of this group that possess central carbon atom (α- or 2-) bearing an amino group, a carboxyl group, a side chain and an α-hydrogen levo conformation, with the exception of glycine, which is achiral, and proline, whose amine group is a secondary amine and is consequently frequently referred to as an imino acid for traditional reasons, albeit not an imino. The genetic code encodes 20 standard amino acids. However, there are three extra proteinogenic amino acids: selenocysteine, pyrrolysine and N-formylmethionine. The former two do not have a dedicated codon, but are added in place of a stop codon when a specific sequence is present, UGA codon and SECIS element for selenocysteine, UAG PYLIS downstream sequence for pyrrolysine.[2][3] Formylmethionine is an amino acid encoded by the start codon AUG in bacteria, mitochondria and chloroplasts, but is often removed posttranslationaly.[4] en.wikipedia.org/wiki/Non-proteinogenic_amino_acids======================================== Now, in the Expanded genetic code, if SECIS element(selenocysteine), UAG PYLIS-(Pyrrolysine) and N-Formylmethionine(AUG) in bacteria, mitochondria and chloroplasts, would perform the functions? Would they relate to the following functions if extending the code and what would they do? functions: Dna methylation, (removes the H and substitutes CH3-methyl) RNAinterference (RNAi, ncRNA, mRNA etc) and Histone modification (chromosome alterations).=================================== What is SECIS made of, what does this element do? www.ncbi.nlm.nih.gov/pmc/articles/PMC3541580/=============== = www.ncbi.nlm.nih.gov/pmc/articles/PMC3541580/figure/F2/=== www.ncbi.nlm.nih.gov/pmc/articles/PMC3541580/figure/F4/============= There are mutations and there are problems, but, what is the delivery system? Something is able to read our dna and what integrates this into the human body?
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Post by skyship on Feb 28, 2014 1:46:07 GMT -5
Now we can see what may be going on.
www.ncbi.nlm.nih.gov/pmc/articles/PMC3541580/
The unit structure and its components and element is very evasive. It is hard to find what was actually used to create this and info on how it was delivered to the human is non existent.
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Post by skyship on Feb 28, 2014 16:11:09 GMT -5
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Post by skyship on Feb 28, 2014 16:56:56 GMT -5
This why these are unidentifiable. Like a trojan horse (vectors) plants animals air. etc. Transposable elements, unseen unidentified, uncultured. Now, use of lucerifase, jelly fish proteins and others bring in colors, but in telechelic polymers a dye could be used for the colored filaments, resins and epoxies etc. rubber, vinyl etc. Along with Smart Meters, can read anything electrical: you have Smart Polymers: The combination of polymers with nano- or microsized solid materials displays novel and often enhancedproperties compared to the traditional materials. They can open up possibilities for new technologicalapplications. Materials whose physical properties can be varied by application of magnetic fields belongto a specific class of smart materials. The broad family of magnetic field-controllable soft materialsincludes ferrofluids, magneto-rheological fluids, magnetic gels, and magnetic elastomers. The magneticgels and elastomers (magnetoelasts) represent a new type of composite and consist of small magneticparticles, usually in the nanometer to micron range, dispersed in a highly elastic polymeric matrix.The magnetic particles can be incorporated into the elastic body either randomly or in ordered structure.If a uniform magnetic field is applied to the reactive mixture during the cross-linking process, particlechains form and become locked into the elastomer. The resulting composites exhibit anisotropic properties. Combination of magnetic and elastic properties leads to a number of striking phenomena that areexhibited in response to impressed magnetic fields. The magnetic particles couple the shape and the elasticmodulus with the external magnetic field. Giant deformational effects, high elasticity, anisotropic elasticand swelling properties, and quick response to magnetic fields open new opportunities for using such materialsfor various applications. Since the magnetic fields are convenient stimuli from the point of signal control,the magnetoelasts are promising smart materials in engineering due to their real-time controllable elasticproperties. More recently, increasing interest has been devoted to exploration of multiresponsive magnetic polymers,which exhibit sensitivity to several external stimuli. Micro- and nanospheres that combine both magnetic,temperature, and pH sensitivity were also elaborated and studied. These new results provide novel possibilitiesfor preparation of more complex magnetic field-responsive materials like membranes with on/off switchingcontrol. In this article, we review recent advances in mechanical and swelling behavior of magnetic field-responsivesoft materials, including flexible polymer networks and gels. Oligomers - Polymer Composites - Molecular Imprinting Oligomers - Polymer Composites - Molecular link.springer.com/chapter/10.1007/12_2006_104link.springer.com/book/10.1007/978-3-540-46830-1======================================
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Post by skyship on Mar 1, 2014 1:50:47 GMT -5
With the 3 addition amino acid units using archarea, would explain the organisms. With the 3 functins going on: DNA methylation, histone modification and RNAi.... And then along comes Biodegradable telechelic oligomers. These are polypeptides: these look like what I have recently found under my microscope: ================ [/b] www.imc.cas.cz/sympo/43micros/pc02i2.jpgwww.imc.cas.cz/sympo/43micros/posters.htm================================================= Aggregation of these bundles found on my face: Under a small lump. The end of the pink turned red filament in my aggregated bundle: Image by Kathryn (Skyship)The Aggregated Bundle: Notice the prongs at the ends of the black one, in this case an extended Telechelic Polymer. Image by Kathryn (Skyship)======================= These could be Biodegradable Polymer, but, it seems the PLGA is the one that is important in aggregating. What would be their purpose, since they do have elongation factors?
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Post by skyship on Mar 1, 2014 2:43:51 GMT -5
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Post by skyship on Mar 1, 2014 3:12:54 GMT -5
Polymersomes created by hydrophilic block of amphiphilic block copolymers I FOUND ONE OF THESE SUCKERS.... I have an image (blue) of one with this same kind of end. If this is not one and the same, These are polymersomes used for gene delivery~! Wonder if they are delivered in phages? Air? My image: Image by Kathryn (Skyship)Polymersomes: a. the same type I have found, from my microscope~! Click on images for larger view~!~! www.rsc.org/ej/JM/2009/b818869f/b818869f-f12.gifProvided the right hydrophilic/hydrophobic balance can be achieved , amphiphilic block copolymers are able to assemble in water into membranes. These membranes can enclose forming spheres with an aqueous core. Such structures, known as polymer vesicles or polymersomes (from the Greek “-some” = “body of”), have sizes that vary from tens to thousands of nanometers. The wholly synthetic nature of block copolymers affords control over parameters such as the molar mass and composition which ultimately determine the structure and properties of the species in solution. By varying the copolymer molecular mass it is possible to adjust the mechanical properties and permeability of the polymersomes, while the synthetic nature of copolymers allows the design of interfaces containing various biochemically-active functional groups. In particular, non-fouling and non-antigenic polymers have been combined with hydrophobic polymers in the design of biocompatible nano-carriers that are expected to exhibit very long circulation times. Stimulus-responsive block copolymers have also been used to exploit the possibility to trigger the disassembly of polymersomes in response to specific external stimuli such as pH, oxidative species, and enzyme degradation. Such bio-inspired ‘bottom-up’ supramolecular design principles offer outstanding advantages in engineering structures at a molecular level, using the same long-studied principles of biological molecules. Thanks to their unique properties, polymersomes have already been reported and studied as delivery systems for both drugs, genes, and image contrast agents as well as nanometer-sized reactors.
Polymersomes: nature inspired nanometer sized compartments pubs.rsc.org/en/content/articlelanding/2009/jm/b818869f#!divAbstract ============================== WE got these SOBs.......Supermolecular design and they circulate in the ECM. Extra cellular matrix and they aggregate around the PANCREAS...JOINTS....NEUROMUSCULAR JUNCTIONS.....TENDON areas....etc. you name it. CONNECTIVE TISSUE and more....encrypted.google.com/search?tbm=isch&q=Polymersomes%20created%20by%20hydrophilic%20block%20of%20amphiphilic%20block%20copolymers&tbs=imgo:1#facrc=_&imgrc=gaTc_nwVsAuQRM%253A%3BEPFyok6qu6KWWM%3Bhttp%253A%252F%252Fwww.rsc.org%252Fej%252FJM%252F2009%252Fb818869f%252Fb818869f-f12.gif%3Bhttp%253A%252F%252Fpubs.rsc.org%252Fen%252Fcontent%252Farticlehtml%252F2009%252FJM%252FB818869F%3B594%3B540
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