"The new technique builds on this earlier work, and is based on a protein called TRPV4, which is sensitive to both temperature and stretching forces. These stimuli open its central pore, allowing electrical current to flow through the cell membrane; this evokes nervous impulses that travel into the spinal cord and then up to the brain ."
"Güler and his colleagues reasoned that magnetic torque (or rotating) forces might activate TRPV4 by tugging open its central pore, and so they used genetic engineering to fuse the protein to the paramagnetic region of ferritin , together with short DNA sequences that signal cells to transport proteins to the nerve cell membrane and insert them into it."
"When they introduced this genetic construct into human embryonic kidney cells growing in Petri dishes, the cells synthesized the ‘Magneto’ protein and inserted it into their membrane . Application of a magnetic field activated the engineered TRPV1 protein"
" Next, the researchers inserted the Magneto DNA sequence into the genome of a virus .. Using microelectrodes, they then showed that applying a magnetic field to the brain slices activated Magneto so that the cells produce nervous impulses."
⬆️ Do we even know whether this magneto DNA sequence has or has not been inserted into the genome of the SARSCoV2 virus? We don't. It could have been. The virus could be part 1, the injection part 2, the booster part 3.
“Previous attempts [ using magnets to control neuronal activity ] needed multiple components for the system to work – injecting magnetic particles [THE "VACCINE"?], injecting a virus that expresses a heat-sensitive channel [THE BOOSTER?], [or] head-fixing the animal so that a coil could induce changes in magnetism,” he explains. “The problem with having a multi-component system is that there’s so much room for each individual piece to break down.”
"This system is a single, elegant virus [SARSCoV2?] that can be injected anywhere in the brain [SPIKE CROSSES BLOOD BRAIN BARRIER?], which makes it technically easier and less likely for moving bells and whistles to break down,” he adds, “and their behavioral equipment was cleverly designed to contain magnets where appropriate [THE "VACCINE"?] so that the animals could be freely moving around"
WE ARE TALKING MAGNETOGENETICS HERE.
" Magnetogenetics ’ is therefore an important addition to neuroscientists’ tool box, which will undoubtedly be developed further, and provide researchers with new ways of studying brain development and function."
https://www.theguardian.com/science/neurophilosophy/2016/mar/24/magneto-remotely-controls-brain-and-behaviour
" Magnetogenetics ’ is therefore an important addition to neuroscientists’ tool box, which will undoubtedly be developed further, and provide researchers with new ways of studying brain development and function."
https://www.theguardian.com/science/neurophilosophy/2016/mar/24/magneto-remotely-controls-brain-and-behaviour
the Guardian
Genetically engineered 'Magneto' protein remotely controls brain and behaviour
“Badass” new method uses a magnetised protein to activate brain cells rapidly, reversibly, and non-invasively
"Genetically targeted magnetic control of the nervous system - PubMed
We have overcome these disadvantages by synthesizing a single-component, magnetically sensitive actuator, "Magneto," comprising the cation channel TRPV4 [ ⚠️LOOK AT WHAT TRPV4 DOES IN THE NEXT ARTICLE⚠️ ] fused to the paramagnetic protein ferritin . We validated noninvasive magnetic control over neuronal activity by demonstrating remote stimulation of cells using in vitro calcium imaging assays, electrophysiological recordings in brain slices, in vivo electrophysiological recordings in the brains of freely moving mice, and behavioral outputs in zebrafish and mice. As proof of concept, we used Magneto to delineate a causal role of striatal dopamine receptor 1 neurons in mediating reward behavior in mice. Together our results present Magneto as an actuator capable of remotely controlling circuits associated with complex animal behaviors."
https://pubmed.ncbi.nlm.nih.gov/26950006/
We have overcome these disadvantages by synthesizing a single-component, magnetically sensitive actuator, "Magneto," comprising the cation channel TRPV4 [ ⚠️LOOK AT WHAT TRPV4 DOES IN THE NEXT ARTICLE⚠️ ] fused to the paramagnetic protein ferritin . We validated noninvasive magnetic control over neuronal activity by demonstrating remote stimulation of cells using in vitro calcium imaging assays, electrophysiological recordings in brain slices, in vivo electrophysiological recordings in the brains of freely moving mice, and behavioral outputs in zebrafish and mice. As proof of concept, we used Magneto to delineate a causal role of striatal dopamine receptor 1 neurons in mediating reward behavior in mice. Together our results present Magneto as an actuator capable of remotely controlling circuits associated with complex animal behaviors."
https://pubmed.ncbi.nlm.nih.gov/26950006/
PubMed
Genetically targeted magnetic control of the nervous system - PubMed
Optogenetic and chemogenetic actuators are critical for deconstructing the neural correlates of behavior. However, these tools have several limitations, including invasive modes of stimulation or slow on/off kinetics. We have overcome these disadvantages…
"TRPV4 is the temperature-sensitive ion channel of human sperm | eLife
Ion channels control the ability of human sperm to fertilize the egg by triggering hyperactivated motility, which is regulated by membrane potential..Here, we functionally characterize DSper, the Depolarizing Channel of Sperm, as the temperature-activated channel TRPV4 . It is functionally expressed at both mRNA and protein levels, while other temperature-sensitive TRPV channels are not functional in human sperm . DSper currents are activated by warm temperatures and mediate cation conductance, that shares a pharmacological profile reminiscent of TRPV4. Together, these results suggest that TRPV4 activation triggers initial membrane depolarization, facilitating both CatSper and Hv1 gating and, consequently, sperm hyperactivation."
https://elifesciences.org/articles/35853
Ion channels control the ability of human sperm to fertilize the egg by triggering hyperactivated motility, which is regulated by membrane potential..Here, we functionally characterize DSper, the Depolarizing Channel of Sperm, as the temperature-activated channel TRPV4 . It is functionally expressed at both mRNA and protein levels, while other temperature-sensitive TRPV channels are not functional in human sperm . DSper currents are activated by warm temperatures and mediate cation conductance, that shares a pharmacological profile reminiscent of TRPV4. Together, these results suggest that TRPV4 activation triggers initial membrane depolarization, facilitating both CatSper and Hv1 gating and, consequently, sperm hyperactivation."
https://elifesciences.org/articles/35853
eLife
TRPV4 is the temperature-sensitive ion channel of human sperm
The molecular identity of the temperature-sensitive ion channel of human sperm that ensures depolarization is TRPV4.
⬆️ All the above indicates the scientific knowledge of how to control both brain activity & potential to reproduce remotely through electro-magnetic wave action. Remember, I am sharing published science in highly reputable journals in the above train of thought I am sharing on this channel. I am beginning to see something here. Save all of the links above in case they are removed. 🚫💉🧲
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The short video version of many of the scientific articles shared above.
Forwarded from SDB
I presume you know that toxoplasma is known to influence behavior in its hosts. Mice lose fear of cats and possible link to schizophrenia in humans. Also causes severe birth problems from mother to unborn infant (congenital) https://www.livescience.com/56529-strange-facts-about-toxoplasma-gondii-parasite.html
livescience.com
7 Strange Facts about the 'Mind-Control' Parasite Toxoplasma Gondii
A single-cell parasite, Toxoplasma gondii, is perhaps best-known for its connection to cats. The parasite can move from its feline host to humans, most commonly through contact with cat feces. And while the parasite typically only causes mild infection (people…
⬆️ Anti-parasitic drug Ivermectin anyone? Is this why they are so keen to prevent us getting hold of any? Most of my twitter bans happened when I mentioned Ivermectin. It's almost as if it spoils their plans entirely..?
"Conclusion: These results indicate that ivermectin significantly inhibited replication of the tachyzoites of Toxoplasma gondii RH strain ."
https://www.researchgate.net/publication/265517420_In_Vitro_Effects_of_Ivermectin_and_Sulphadiazine_on_Toxoplasma_gondii
https://www.researchgate.net/publication/265517420_In_Vitro_Effects_of_Ivermectin_and_Sulphadiazine_on_Toxoplasma_gondii
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Anybody who has been "vaccinated" should consider taking IVERMECTIN. This is because some "vaccines" may be contaminated by the parasite TOXOPLASMA GONDII. See end of this video.
"Conclusion: These results indicate that ivermectin significantly inhibited replication of the tachyzoites of Toxoplasma gondii RH strain ."
https://www.researchgate.net/publication/265517420_In_Vitro_Effects_of_Ivermectin_and_Sulphadiazine_on_Toxoplasma_gondii
"Conclusion: These results indicate that ivermectin significantly inhibited replication of the tachyzoites of Toxoplasma gondii RH strain ."
https://www.researchgate.net/publication/265517420_In_Vitro_Effects_of_Ivermectin_and_Sulphadiazine_on_Toxoplasma_gondii
BioActive Carbon & NAC (N-acetyl cysteine):
"A potent tool to bind and eliminate harmful heavy metals is BioActive Carbon. But NAC may help in this area too.
Due to its chemical structure, NAC can bind heavy metals like cadmium, lead, and mercury. That enables you to excrete them, including via your urine."
https://microbeformulas.com/blogs/microbe-formulas/top-12-health-benefits-of-n-acetyl-cysteine-nac
"A potent tool to bind and eliminate harmful heavy metals is BioActive Carbon. But NAC may help in this area too.
Due to its chemical structure, NAC can bind heavy metals like cadmium, lead, and mercury. That enables you to excrete them, including via your urine."
https://microbeformulas.com/blogs/microbe-formulas/top-12-health-benefits-of-n-acetyl-cysteine-nac
Microbeformulas
Can't Find What You're Looking For? - Microbe Formulas™
N-Acetylcysteine (NAC) to Combat COVID-19: An Evidence Review:
"The gut is the largest immune organ we have, carrying 70% of all lymphocytes in the body. Absorbed in the small intestine, oral NAC interacts with epithelial cells and immune cells, potentially boosting our immune system to combat virus infection. One capsule of 600 mg NAC can reach a level of 16 μM NAC in the peripheral blood in half an hour after administration..To protect those who have not contracted SARS-Cov-2, oral NAC (600 mg, bid) could be an effective and economical measurement to modulate their immune systems against potential infection. Once onset symptoms appear, such as fever or dry cough, oral NAC (1200 mg, bid) could be taken to alleviate symptoms and accelerate recovery from virus infection."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649937/
"The gut is the largest immune organ we have, carrying 70% of all lymphocytes in the body. Absorbed in the small intestine, oral NAC interacts with epithelial cells and immune cells, potentially boosting our immune system to combat virus infection. One capsule of 600 mg NAC can reach a level of 16 μM NAC in the peripheral blood in half an hour after administration..To protect those who have not contracted SARS-Cov-2, oral NAC (600 mg, bid) could be an effective and economical measurement to modulate their immune systems against potential infection. Once onset symptoms appear, such as fever or dry cough, oral NAC (1200 mg, bid) could be taken to alleviate symptoms and accelerate recovery from virus infection."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649937/
PubMed Central (PMC)
N-Acetylcysteine to Combat COVID-19: An Evidence Review
The novel coronavirus disease (COVID-19) is caused by a virus (SARS-Cov-2) and is known for inducing multisystem organ dysfunction associated with significant morbidity and mortality. Current therapeutic strategies for COVID-19 have failed to effectively…
Suramin Inhibits SARS-CoV-2 Infection in Cell Culture by Interfering with Early Steps of the Replication Cycle:
"Time-of-addition and plaque reduction assays performed on Vero E6 cells showed that suramin acts on early steps of the replication cycle, possibly preventing binding or entry of the virus. In a primary human airway epithelial cell culture model, suramin also inhibited the progression of infection."
https://aac.asm.org/content/64/8/e00900-20
"Time-of-addition and plaque reduction assays performed on Vero E6 cells showed that suramin acts on early steps of the replication cycle, possibly preventing binding or entry of the virus. In a primary human airway epithelial cell culture model, suramin also inhibited the progression of infection."
https://aac.asm.org/content/64/8/e00900-20
There is no "Indian variant". It's another lie folks..
https://pib.gov.in/PressReleasePage.aspx?PRID=1717876
https://pib.gov.in/PressReleasePage.aspx?PRID=1717876