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An intact human heart, rendered transparent. Because disease doesn't happen in 2D. Whole-organ tissue clearing + microscopy reveal coronary vessels (magenta) and atherosclerotic plaques (gold) across the intact organ. More at: 🫀🔬#FluorescenceFriday!

13,008 görüntüleme • 1 ay önce •via X (Twitter)

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🚀 We’re hiring! Staff Scientist / Postdoc – Tissue Clearing & 3D Image Analysis (m/f/d) (LMU Munich) Are you a great fit, or do you know someone outstanding, please reach out 🔁 If you want to at the frontier of whole-organ / whole-body 3D imaging, and help generate truly beautiful datasets that drive major biological discoveries and therapeutic development, see below ✨ We’re building the next-generation pipeline for tissue clearing + light-sheet microscopy + quantitative 3D analysis in the SyNergy Excellence Cluster (Mesoscale Hub) and we’re looking for someone excited to push this forward with us. 🧠🔬📈 🎥 I’m also attaching a short video showing the kind of high-quality imaging and datasets you’d be working with. What you’ll do 🛠️ 🔹 Lead and evolve tissue clearing + light-sheet workflows across collaborative SyNergy projects 🔹 Turn complex 3D datasets into robust quantitative insights (visualization, atlas registration, readouts) 🔹 Develop new methods and analysis pipelines together with our AI team 🤖 🔹 Maintain and optimize cutting-edge light-sheet systems (optional: support animal license writing) What we’re looking for 🎯 ✅ Strong hands-on experience in tissue clearing and/or fluorescence microscopy ✅ Solid experience with light-sheet microscopy and 3D imaging workflows ✅ Familiarity with 3D tools like Imaris / arivis Vision4D, stitching (e.g., BigStitcher), and quantitative analysis in cleared tissues ✅ Service mindset, great organization, and strong scientific English How to apply 📩 Apply via the LMU Klinikum online application form Please also send your application to: [email protected] CC: [email protected] 📎 Include one PDF: short cover letter, CV, 2–3 referees, and earliest start date. 📍 Campus Großhadern (Munich) and Helmholtz Munich | 🕒 Full-time | 📅 Start: 01 January 2026 If you love high-quality imaging, cutting-edge biology, and building something that will matter, we’d love to hear from you. 🌍✨ #hiring #StaffScientist #Postdoc #TissueClearing #LightSheetMicroscopy #ImageAnalysis #SpatialBiology #Neuroscience #SyNergy #LMU #Munich

Ali Max Erturk

14,781 görüntüleme • 8 ay önce

Excited to share TERRA, a tissue world model 🧬 Over ~1.5 years we ran a large data-generation + modelling effort to build a world model for human tissues, pretrained on 112M cells from spatial transcriptomics (mostly Xenium 5000-plex + public data). It's built on one of the largest human spatial transcriptomics corpora assembled to date, spanning 20 tissues across development, health and 26 disease conditions, ~two-thirds newly generated in-house. Why a "world model" for tissue? Images have universal representations (ViT/DINOv3), so do proteins (ESM, Alex Rives) and pathology (UNI, Faisal Mahmood). We've worked hard to build something similar for human tissue: one model that captures its multi-scale logic, genes → cells → their native microenvironments. Like the JEPA approach Yann LeCun has championed, TERRA learns by prediction in embedding space, but for human tissue. How it works: it tokenises each cell together with its nearest neighbours into one sequence while keeping every gene's identity, then masks part of a neighbourhood and predicts the representation of the hidden part, not raw noisy counts. From one backbone it reads out three scales, gene embeddings (what a gene is doing in a cell and its niche), cell embeddings (cell type and state) and neighbourhood embeddings (the niche), and because it keeps gene-level resolution it can knock a gene out in silico and predict the response. Applied entirely zero-shot, TERRA maps and perturbs human tissue across unseen organs, diseases and technologies, outperforming existing spatial approaches. Three take-homes: 1️⃣ One model, any tissue. A single pretrained backbone provides tissue representations zero-shot, handling genes, cells and niches across organs and platforms, off the shelf. 2️⃣ New biology, development to clinic. We built a new spatial atlas of the developing human pancreas and found an islet-associated capillary state that looks like a precursor of mature islet vasculature. In kidney, TERRA's in silico knockouts predicted the tissue-injury programme from cancer immunotherapy (checkpoint blockade), confirmed in treated kidneys, detected in blood, and linked to declining kidney function. 3️⃣ A grammar of tissue architecture. By coupling each cell's state to its niche, TERRA defines recurring cross-organ "archetypes" of macrophage neighbourhoods, including a tumour-boundary niche that tracks poor survival in kidney cancer. TERRA is already in use: it powered our recent skin atlas of hidden immune-memory niches ( with more studies coming soon. This was an amazing collaboration between clinicians, machine-learning scientists and cell biologists 🙏 Led by Sebastian Birk, Vali Sanian Amirhosein Vahidi, Samuel Ogden, Daniyal Jafree, Adib Miraki, Carlo Leonardi and Arpit Merchant, with Lassi Paavolainen, Menna Clatworthy, Omer Ali Bayraktar, Muzlifah Haniffa, Tom Mitchell and Mostafa Bakhti. Huge thanks too to everyone who shared data and helped along the way. What excites me most is seeing how the community builds on this. The model, code and tutorials are all public, so anyone can run TERRA on their own tissues, extend it, or build new models on top. Huge thanks to the whole team across Wellcome Sanger Institute and our many collaborators. 📄 Paper: 💻 Code: 🤗 Model: #SpatialTranscriptomics #SpatialGenomics #FoundationModels #AI4Science #MachineLearning #ComputationalBiology #SingleCell #WorldModels

Mo Lotfollahi

50,313 görüntüleme • 17 gün önce

Blood Isn't Charity...It Is A 48 Billion Dollar Industry That's In High Demand. Dr Lee Merritt, MD Serious Ethical Lines Are Erased, As People Seek Out 'Young Blood' To Reverse Aging. The Practice Of Harvesting Organs & Tissue Is More Dark & Sinister Than Anyone Wants To Admit. Most people think blood donation is all charity…but it’s actually a billion-dollar industry. There are even studies discussing how infusing younger blood benefits older people — a concept that raises serious ethical questions. And when it comes to controversial topics like organ & tissue markets, the story is far bigger & darker than what we’re told. From The Study: Young Blood Rejuvenates Old Bodies: Exploited natural resources such as gold & oil have often been external to human beings, but now they may become internal. Previously people worked in factories, now they may become factories. No doubt, biological material has been conceived of as waste or natural resources previously, but that was mainly excess material such as tissue samples & removed tumors. Hence, the rejuvenating effect of blood may result in a commodification of blood & disrupt well-established traditions of altruism-based donation, undermining the well-established organization of blood donation. Young blood is sought after because it has demonstrated its potential in mitigating aging-related symptoms, promoting cell growth & repair, & restraining age-associated chronic inflammation & fibrosis in older individuals. Young blood effectively reverses age-related gene expressions in a diverse range of cell types (51 in total) derived from the 20 main organs & tissues of the elderly. From The Study: Trafficking In Human Organs: The desperate need for organ transplantation surgeries has given rise to a lucrative, transnational criminal enterprise that enables organ seekers to purchase organs from donors. This enterprise, commonly referred to as organ trafficking, is a global phenomenon. Even though it is illegal in most countries, trafficked organs account for billions into the trillions of dollars. “Organ Trafficking” is an umbrella term that covers a number of unethical & illegal practices. It consists of any of the following activities: Removing organs from living donors without valid consent. Transportation, manipulation, transplantation or other use of such organs. Healthcare professional, public official, or employee of a private sector entity to facilitate or perform such removal or use. Soliciting or recruiting donors or recipients, where carried out for financial gain or comparative advantage. “Trafficking in persons for the purpose of organ removal” The recruitment, transportation, transfer, harbouring, or receipt of persons, by means of the threat or use of force or other forms of coercion, of abduction, of fraud, of deception, of the abuse of power or of a position of vulnerability, or of the giving or receiving of payments or benefits to achieve the consent of a person having control over another person, for the purpose of the removal of organs. 👇Human Trafficking For The Removal Of Organs👇 👇Trafficking In Human Organs: An Overview👇 👇Young Blood Rejuvenates Aging Organs👇 Speaker: Dr Lee Merritt, MD Video: WR

Valerie Anne Smith

130,862 görüntüleme • 11 ay önce

"There Were 4 Drugs That Were Being Tested For Ebola...Remdesivir Killed More People Than Placebo" Dr Paul Marik, MD "The Data Safety Monitoring Board Actually Stopped The Study" "53% Of The Patients Died In The Failed Ebola Trial" Remdesivir Was Fauci's 'Covid Drug Of Choice' In the halted Ebola trial, Remdesivir mortality was 53% overall & 85% mortality in those with high viral load. Fauci took the failed Ebola drug, Remdesivir (Veklury), & made it the mandatory treatment as an unelected bureaucrat to be used at every hospital for the treatment of COVID in the United States. Not only does the drug not cure COVID it kills people by causing multi organ failure, yet the FDA approved the drug based on expert opinions from Big Pharma industry insiders who used to work at the CDC & FDA. Remdesivir (Veklury) continues to be used in hospitals today as 1st line treatment across ALL age groups. Recently FDA & CDC approved to be used for the treatment in neonate newborns, less than 28 days old, weighing at least 3 lbs. All of the doctors, nurses & hospitals know at this point...Nurses even coined Remdesivir's nickname 'Run...Death...Is...Near.' Hospital administration continues on. Their bosses make more money when patients with organ failure hit the ICU. It is well known that Remdesivir does not work for COVID or any other illness & is in fact a death sentence to the majority of the people it's given to. Remdesivir Causes Multi Organ Failure By Harming The Kidneys, Liver & Heart... Kidney Damage...Those treated with Remdesivir (Veklury) suffered 2.8X times greater Acute Kidney Injury (AKI) & subsequent permanent renal damage. Liver Damage...Remdesivir, on a cellular level, has been demonstrated to be toxic to human hepatocytes, causing drug induced permanent liver damage. Heart Damage...Continuous cardiac monitoring is recommended for those receiving remdesivir because of documented cases of Cardiac arrest, Heart block, Torsade de pointes (fatal arrhythmia), Sinus bradycardia (slow heart rate), T-wave abnormalities, Prolonged QT interval, Ventricular fibrillation Hospitals murdered COVID patients. The more they kill, the more money they make. When the hospitals test for COVID, they get paid more. When they admit patients for COVID, they get paid more. When they put people on Remdesivir, they get paid more. And when they put loved ones on a ventilator, they get paid more. 👇2019 Ebola Drug Trial Research Documents👇 👇Remdesivir (Veklury) Package Insert👇 👇Remdesivir Causes Kidney Failure👇 👇Remdesivir Causes Heart Failure👇 Video: Vaxxed 3: Authorized To Kill Documentary Credit: Children’s Health Defense

Valerie Anne Smith

34,071 görüntüleme • 9 ay önce

Yoga and improved skin health and hair growth? India’s pseudoscience poster boy, Ranveer, aka Beerbiceps gets it embarrassingly wrong. Let us break it down. I am sorry this is lengthy, because – as per Brandolini's Law (aka the Bullshit Asymmetry Principle): It takes a lot more energy to refute bullshit than to produce it. Check out this video. In it, Ranveer “pseudoscience peddler” Allahbadia with over 8 million followers on YouTube and Instagram bullshits everyone in just 35 seconds. He showcases some major female movie celebrities and tells the viewers that the secret to their skin and hair is that they perform Yoga every day, especially a Yoga pose called the “Sarvangasana” or shoulder-stand or candle pose. His “scientific” explanation? The stance increases blood flow the scalp and head, and improves skin health and hair growth. This is utter nonsense. What happens to the blood flow, heart, head, and brain region when someone takes an upside-down stance? For that, you must know the meaning of one word – Homeostasis. Homeostasis is a self-regulating process by which human body maintains internal stability in its organ functions while adjusting to changing external conditions. This is also consists of “autoregulation,” the method by which an organ or tissue maintains blood flow despite a change in perfusion due to external (eg: body position changes) or internal (block in blood vessels) conditions. For example, we are normally supposed to walk on two legs or rest by sitting down or lying down. The heart rate, blood flow to all organs including scalp and brain is all maintained depending on the importance and metabolic activity of that organ. For example, at rest, highest proportion of blood flow is received by the liver (nearly 25% of cardiac output) which is 100ml/min per 100g liver weight. The brain receives 50ml/min per 100g weight, while the skin receives 1 to 3ml per 100g per minute. Organ tissues are usually considered as blood supply-dependent (e.g., heart and brain) and blood supply-independent (e.g., abdominal organs, kidneys, skin, and resting muscle) for oxygen delivery – meaning the latter WILL receive fixed amounts to maintain its functioning while the former requires changes to blood flow depending on various unusual situations. For example, in massive blood loss, the body will try to maintain blood flow into heart and brain rather than skin and muscle to maintain life. The blood flow is set in the body for proper functioning of organs and every time we try to change that flow, a healthy body will re-align that flow depending on the importance of the organ systems functions. So, when you do a shoulder stand or candle pose, the initial sudden change to the body position will be caught by the receptors in the blood vessels and heart which will re-align the flow to organs of importance, thereby maintaining critical functions that are required for health. Which means, the blood flow to the skin including the scalp, will be re-aligned to its required flow and DOES NOT increase to face and scalp or brain as India’s pseudoscience peddler mentions. In heavy aerobic exercise and changes to temperature related sweating or certain disease conditions, the skin blood can increase. Yoga is not a proper exercise as it is not an aerobic activity. Now Sarvangasana and blood flow – a study showed that heart and blood flow responses were NOT AFFECTED with this pose in healthy people. Even a complete head stand, called Sirsasana does not increase blood flow to the brain, forget the scalp skin, because of blood delivery homeostasis due to autoregulatory mechanisms. The claims for effects of Yoga on specific organs are complete bluff – a public duping started by B K S Iyengar who took Yoga to the international stage. Even in his authoritative books, he does not mention shoulder stand or candle pose to be useful for hair growth. In fact, he [nonsensically] mentions that shoulder stand will improve “thyroid health” (it does not), controls asthma (it does not), reduces disease of the throat (it does not) and prevents common cold (it does not, because common cold is caused by a virus, and not dependent on whether you stand, sit, lie down, and hang yourself upside down). Also, note that Sarvangasana (shoulder stand), Sirsasana (head stand) and Padmasana (lotus position) are the most common Yoga poses reported to cause an injury. In those with high blood pressure or heart disease, these poses may become life threatening. You can see those here here and here Yoga, especially shoulder or head stands do not improve skin health or increase hair growth by increasing blood flow. In fact, Yoga does nothing specific for organ systems functions since such evidence does not exist. A lot of pseudoscience peddlers who sympathize with Yoga will mislead you with many such magical benefits. So then, what specific exercise or action improves hair growth? We do not really know. There is some evidence, even though weak, for standardized scalp massages: good evidence for scalp cooling (prevents hair loss, may promote regrowth especially in chemotherapy patients) Speak with your Dermatologist on skin and hair health queries and not National-level baby-face poster boys of misinformation.

TheLiverDoc™

496,182 görüntüleme • 3 yıl önce

I’m so grateful that more and more people are starting to talk about this. 🙏🏻 But it’s only the beginning of a much bigger conversation about how technology and human biology are starting to intersect. Whistleblowers like Psinergy-solafide have been warning about this for years: ⚠️ The government has the ability to remotely log in to your body. They access something called your biofield. It’s as physical as any other organ in your body but you can’t see it. And it’s been used for decades to broadcast signals through a WBAN (wireless body area network). 🌐 See, most people were never taught that the human body is electrical. Your nervous system, your heart, and your cells are constantly communicating through bioelectric signals. 🔌 And as technology evolves, we need to understand how these systems interact with the human body and how to protect the body’s natural design. 🧬 That’s exactly why I’m hosting the Transhumanism Solutions Summit. We’re going to break down, in very simple terms: • How the body’s electrical systems work • What emerging technologies are interacting with biology • What researchers like Maria Crisler are observing 🔬 • And most importantly, how to strengthen and detox your body Because the goal isn’t fear. The goal is awareness, resilience, and protecting the divine design of the human body. Here’s the link to save your seat! Stay informed. Stay human. Dr. Edward Group, DC

Dr. Edward Group, DC

22,091 görüntüleme • 5 ay önce

Outrageous...Bayer's 'Glyphosate Free' Roundup Is 200X More Toxic. Bayer Removed Glyphosate & Replaced It With Even More Poisonous Diquat. Diquat Causes Cancer, Is A Neurotoxin & Increases Parkinson's Disease 126%. Banned In Other Countries For Causing Multiple Organ Failure. It’s been 7 years since Germany’s Bayer bought US agrochemical giant Monsanto, inheriting not only the company’s vast portfolio of seeds & pesticide products, but also more than 100,000 lawsuits against Monsanto’s Roundup herbicide with Glyphosate. To stop further lawsuits, Bayer replaced Glyphosate with Diquat & claimed it 'safe & effective' for home & landscape use. The facts reveal Diquat is 200 times more toxic than glyphosate in chronic exposure. 45 times more toxic in acute exposure. And increases Parkinson' Disease in humans & pets by 126%. Diquat is an herbicide that causes multi-organ failure, due to oxidative stress & cellular damage. While it is most toxic to the kidneys & gastrointestinal system, exposure leads to damage in every organ system. Here is what Diquat does to the body... Kidneys: The kidneys are the primary target organ for diquat toxicity. Diquat accumulates in the kidneys & causes acute kidney failure by damaging the renal tubules. Kidney damage is a leading cause of death in fatal diquat poisoning cases. Gastrointestinal tract: As the main entry point for poisoning, the digestive tract is immediately & severely affected. Diquat causes burning, ulceration & inflammation of the mouth, esophagus & stomach. Gut microbiome: Diquat significantly damages the gut lining, causing intestinal inflammation & killing beneficial bacteria like Lactobacillus. The resulting imbalance amplifies systemic toxicity to other organs. Lungs: Diquat causes lung damage, leading to pulmonary edema, respiratory failure & even lung fibrosis. Central nervous system (CNS): Diquat toxicity affects the brain & central nervous system. Neurological effects range from restlessness & disorientation to seizures, coma & brain damage, which proves fatal. Research shows, living within 3 miles of Diquat being used on lawn & landscapes, increases Parkinson's Disease by 126% in humans & family pets. Liver: The liver is vulnerable to oxidative stress from diquat, which disrupts mitochondrial function & triggers inflammation. Liver damage is common. Heart: Diquat poisoning causes damage to the heart muscle, a condition known as toxic cardiomyopathy. This leads to myocardial injury, myocardial necrosis & cardiocirculatory collapse. Skeletal muscles: Diquat poisoning causes rhabdomyolysis, the breakdown of skeletal muscle tissue. This releases myoglobin & other substances that can further damage the kidneys. The US House Interior-Environment Appropriations bill AB-453... Nicknamed the "Monsanto Protection Act," tucked quietly into AB-453 is complete broad immunity for pesticide & herbicide companies. Already passed thru one set of votes & headed for the final vote in 2026. A final passing vote will cause grave harm... Total pesticide immunity: AB-453 provides broad immunity for pesticide companies, including Monsanto (Bayer), from lawsuits that challenge their failure to disclose known harm caused by their products. Blocks states from adding warnings: The provision prevents states from requiring additional product warning labels beyond what the Environmental Protection Agency (EPA) has already approved. Undermines consumer & farmer rights: This legislation leaves individuals harmed by pesticides without legal recourse for "failure to warn" claims. The chemical industry is attempting to protect itself from litigation, such as the numerous lawsuits linking Roundup to non-Hodgkin's lymphoma. Controversial lobbying efforts: The legislation is a result of chemical companies' lobbying efforts to end costly litigation over their products. 👇Diquat Causes 126% More Parkinson's Disease👇 👇Diquat Poisoning & Multi Organ Failure👇 👇Diquat Toxic Effects On Gut Microbiome Health👇 Speaker: Dani Klass

Valerie Anne Smith

243,312 görüntüleme • 10 ay önce

A caller asks Dave Ramsey what to do with required minimum distributions from his 401k that he doesn't need. His gut tells him to invest in gold. Dave's response is immediate and emphatic: "No, no, no, no, we don't put anything in gold." His reasoning starts with the math. "Gold is much more volatile. If you look at the price of gold on a chart, it's way up and way down, much more than the stock market is. It is a lot riskier, and it does not yield a good net return; the average annual rate of return on gold sucks." But Dave doesn't stop at performance. He wants to explain "why" gold underperforms. And this is where the conversation gets interesting. "Gold is a commodity; it's a rock that is yellow." He explains that commodities, whether barrels of oil, precious metals, or corn, are all traded 100% based on people's perception of shortage. If the perception is that there's too much of it, the price goes down. Compare that to a real investment: "An investment that creates revenue is a company that's running and making a profit, like Home Depot, Microsoft, or Apple. Their stock goes up because they are creating revenue. Gold, corn, and oil do not create revenue; they only trade based on scarcity and the psychology of the marketplace, greed and fear." In other words, when gold prices rise, the gold itself hasn't become more valuable. Dave puts it plainly: "If a whole bunch of people rush towards gold, it creates a shortage and the price goes up, but the gold did not become more valuable, just more people were chasing fewer bars." He extends the logic to income-producing real estate, which is priced based on the income it creates, not because it's a "golden rock." And he takes a swipe at diamonds while he's at it: "Diamonds are not necessarily a girl's best friend; that is a marketing slogan. Diamonds do not go up in value; there is no actual investment return on them." Then Dave addresses the headlines designed to scare people into gold, stories about the dollar being threatened by China, Russia, or Brazil: "You can't run to gold because there is nothing magical about it." His geopolitical take is sharp: "While Russia and Brazil are large landmasses, they are not large economies. Texas has a larger gross domestic production than Brazil; Texas is a bigger economy. These countries are going to have to do business with the '800-pound gorilla,' and we do business in dollars, so they are still going to be at our mercy." His advice to the caller? Pull the required distribution out of the 401k as the law demands, and move it into good mutual funds in the process.

Black Edge

83,185 görüntüleme • 3 ay önce

"There's absolutely no question that this was not an accident...the fact that we have one-third DNA product and two-thirds RNA product [in the C19 jabs] is, for whatever reason, the ratio that the makers wanted it to be. They have lied to us in the extreme." Canadian Comprehensive Physician Dr. Chris Shoemaker (@CShoemakerMD) describes for the RAIR Foundation (RAIR Foundation USA) how the DNA contamination of the COVID injections "was not an accident." Shoemaker notes that "They have lied to us in the extreme" and "We are in danger in the extreme, not just in the short term." "There's absolutely no question that this was not an accident. There's absolutely no question that it was carefully and scientifically accomplished," Shoemaker says. "And the fact that we have one-third DNA product and two-thirds RNA product is, for whatever reason, the ratio that the makers wanted it to be." "What's the difference [if there is] DNA is in [the jabs] instead of just mRNA? The difference is that...the DNA, functionally, once in the nucleus, can influence the nucleus, [and] can produce mRNA near the nucleus and have that mRNA migrate out into the cytoplasm of the cell," Shoemaker says. "And once that's done, what should be, at worst, an 8-month process inside your body is, in fact, an 8- to 10-year process inside your body because of the nefarious decision to allow DNA in these shots." Partial transcription of clip: "There's absolutely no question that this was not an accident. There's absolutely no question that it was carefully and scientifically accomplished. And the fact that we have one-third DNA product and two-thirds RNA product is, for whatever reason, the ratio that the makers wanted it to be. They have lied to us in the extreme. "We are in danger in the extreme, not just in the short term. We know the 2 percent, 3 percent of people who passed away suddenly and surprisingly and that's way more than should happen. But the long term effect on the ability to fight cancer or for a cancer to perhaps be a turbo cancer, all these are being influenced by both DNA and RNA that is within us. "The key thing is that it makes the whole process last longer. If it was only mRNA, it would probably be 8 to 12 months only that mRNA would seed out into your body and be repeatedly creating spike, repeatedly creating spike. Remember, the end-product is the most dangerous part of this human engineered genome. The spike protein is the thing that congeals blood cells against each other. The spike protein is the thing that, if it's in your liver, is waving a flag saying, Hey, I'm not your liver. I'm not a human liver. I've got this strange created spike protein. You can identify that I'm not your liver, and you can attack it, and you can make hepatitis for this person because it's not even their liver. "This is what mRNA does is create a flag so that you're attacking through your healthy immune system. Your healthy immune system is going after it in organ after organ after organ. For some people, it's just a specific organ that was already a bit weak to begin with. And for other people, it's a different organ. But either way, mRNA produces a spike flag, which your immune system attacks. "To return to your question about DNA, what's the difference that DNA is in there instead of just mRNA? The difference is that the DNA can, for years, not just 8 to 12 months. The DNA, functionally, once in the nucleus, can influence the nucleus, can produce mRNA near the nucleus and have that mRNA migrate out into the cytoplasm of the cell. And once that's done, what should be, at worst, an 8-month process inside your body is, in fact, an 8 to 10 year process inside your body because of the nefarious decision to allow DNA in these shots."

Sense Receptor

95,273 görüntüleme • 1 yıl önce

🚨BREAKING NEWS🚨 Twice-Censored Landmark COVID-19 Vaccine Autopsy Study Fully Peer-Reviewed and Published •After enduring relentless censorship, our systematic review linking COVID-19 vaccines to death is now available for the entire world to read  by: NICOLAS HULSCHER, MPH Nicolas Hulscher, MPH NOV 17, 2024 •The largest COVID-19 vaccine autopsy study to-date, providing robust evidence that COVID-19 vaccines can cause death, has been officially republished following successful peer-review in the journal Science, Public Health Policy, and the Law: A Systematic Review Of Autopsy Findings In Deaths After COVID-19 Vaccination •This comes after unethical censorship on two occasions: first, removal from Preprints with the Lancetand later, withdrawal by Elsevier after publication in Forensic Science International •Background: The rapid development of COVID-19 vaccines, combined with a high number of adverse event reports, have led to concerns over possible mechanisms of injury including systemic lipid nanoparticle (LNP) and mRNA distribution, Spike protein-associated tissue damage, thrombogenicity, immune system dysfunction, and carcinogenicity •The aim of this systematic review is to investigate possible causal links between COVID-19 vaccine administration and death using autopsies and post-mortem analysis •Methods: We searched PubMed and ScienceDirect for all published autopsy and organ-restricted autopsy reports relating to COVID-19 vaccination up until May 18th, 2023 •All autopsy and organ-restricted autopsy studies that included COVID-19 vaccination as an antecedent exposure were included •Because the state of knowledge has advanced since the time of the original publications, three physicians independently reviewed each case and adjudicated whether or not COVID-19 vaccination was the direct cause or contributed significantly to death •Results: We initially identified 678 studies and, after screening for our inclusion criteria, included 44 papers that contained 325 autopsy cases and one organ-restricted autopsy case (heart) •The mean age of death was 70.4 years •The most implicated organ system among cases was the cardiovascular (49%), followed by hematological (17%), respiratory (11%), and multiple organ systems (7%) •Three or more organ systems were affected in 21 cases •The mean time from vaccination to death was 14.3 days •Most deaths occurred within a week from last vaccine administration •A total of 240 deaths (73.9%) were independently adjudicated as directly due to or significantly contributed to by COVID-19 vaccination, of which the primary causes of death include sudden cardiac death (35%), pulmonary embolism (12.5%), myocardial infarction (12%), VITT (7.9%), myocarditis (7.1%), multisystem inflammatory syndrome (4.6%), and cerebral hemorrhage (3.8%) •Conclusions: The consistency seen among cases in this review with known COVID-19 vaccine mechanisms of injury and death, coupled with autopsy confirmation by physician adjudication, suggests there is a high likelihood of a causal link between COVID-19 vaccines and death •Further urgent investigation is required for the purpose of clarifying our findings •Our study indicates that the COVID-19 injectable products must undergo an immediate Class I recall by the FDA to protect public safety •The U.S. Food and Drug Administration defines a Class I recall as: “A situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.” •The censorship and retraction of studies that show COVID-19 mRNA injection harms is deeply concerning •First, this study was inappropriately removed from Preprints with the Lancet (SSRN) •The paper was posted on the server on July 5th, 2023 and censored in less than 24 hours after receiving massive numbers of downloads and reads, "because the study's conclusions are not supported by the study methodology."

Lyndsey, RN 💜🐭

153,138 görüntüleme • 1 yıl önce

Human Chromosome Number 2 were fused together about 200,000 years ago and it not clear what did this, but it gave us the human brain of logic, empathy and creativity. — “But what they’re showing is that we showed up about 200,000 years ago. Now there’s a little evidence that may have been back as far as 300,000. But the kicker is that we can now look at the DNA and reverse engineer it and say, what did it take to get where we are? And what scientists are now calling the smoking gun. And there’s still a lot of controversy around this is human chromosome number 2. Human chromosome number 2 is the second largest chromosome in every cell of the body. It’s got about 1200 or so genes in that chromosome. And just one of them, gene tbr number one, is responsible for most of the brain that we have for our neocortex. So our humanness, our empathy, sympathy, compassion, love, our cognitive abilities, the mirror neurons, all these kinds of things are because that one gene. Well, where this gets really interesting is where did chromosome 2 come from? And scientists have the answer, but they don’t like the answer because chromosome 2 is the product of a fusion. Proceedings from National Academy of Sciences. The volume Genetics says this very clearly. We conclude that the origin of human chromosome 2 is the product of an ancestral fusion of telomere to telomere. Fusion of two pre existing chromosomes. That does not happen in nature. It can’t happen in nature. So here’s what they’re saying. You got two fully formed, fully functional chromosomes, and on the end are the telomeres that protect those chromosomes when the cells divide. And that’s why they’re on the end, they take the hit. It’s a trauma in a cell when those chromosomes are pulled apart and some of the DNA doesn’t make it. So nature puts telomeres on the end to take the hit, so the good DNA remains intact, and that’s why it’s on the ends. Human chromosome two, those telomeres are right in the middle of the chromosome where they shouldn’t be, because those chromosomes were fused together about 200,000 years ago when we appeared”

Brian Roemmele

165,400 görüntüleme • 10 ay önce

Davis Once Again Confirms the Wilson/Davis Notes. Also, Mary Elizabeth Elliot Illegally Leaked Him Info. about Intact Craft at Wright Patt AFB (OK, here's the little tidbit I was talking about earlier today. Did anybody pick up on it? Let's go to the Wilson/Davis notes...) Davis to Wilson: "I will keep mouth shut (about the meeting with Admiral Wilson)." Davis Writing: I told Wilson about Mary Elizabeth Elliot - the TRW story, Ingo’s story and the 1974 RVer woman at WPAFB (Wright Patterson Air Force Base ~Joe). Wilson: "Mary Elliot sounds like real deal based on her info and behavior with attorney (Jeffrey W. Griffith). She probably will only come totally clean on her deathbed thirty years from now." (I've tried to get more information on MEE (and so have others) but it's not easy. OmniTalk Radio. Davis added some details to her story today.) Matt - The Good Trouble Show with Matt Ford: "As far as your work at NIDS...were you ever privy to any classified information that would give you a clue that the Roswell did happen?" Dr. Eric Davis: "Not Roswell, specifically. I was given leaked classified information by someone (This is Mary Elizabeth Elliot) who was an executive administrative assistant and field security officer for one of the Legacy aerospace companies (TRW ~Joe) that no longer exists. It got absorbed by one of the other Legacy aerospace companies after 2000 or about that period of time." (TRW was acquired by Northrop Grumman in December of 2002.) Davis: "And that individual (MEE) revealed that Wright Patterson Air Force Base, where they had a facility at - her company that employed her - and they had intact craft there that they were trying to reverse engineer." (Intact craft sounds plural. Not an intact craft, but intact craft.) Davis: "And so, that I knew about, that was illegal information she shouldn't have told me, but I didn't have security clearances with the need-to-know to get that. (This may be why info. on MEE is so hard to come by: She was/is being protected because she may have broken the law. I hope she shares all that she knows one day before she passes.) Davis: "That was leaked, and that was kept very quiet until the leak of the Wilson notes, in which elements of her story, of that woman (MEE) - that's a woman - that individual's story were included as context to provide context to the Wilson notes. It was just kind of glommed on to the Wilson transcript to provide context to the crash retrieval's absurd security measures to keep it hidden." (That's Davis confirming, AGAIN, that he wrote the W/D notes. I don't think we've heard the last of the MEE story and what they may have discovered when working on that (or those) intact craft.)

Joe Murgia

81,298 görüntüleme • 1 ay önce

Excited to share our new work on building a multimodal atlas of human skin in health and inflammatory disease — a project I’m especially proud of, bringing together AI, high-throughput genomics, and clinical science to accelerate discovery. Over the past decade, single-cell genomics has transformed how we map cells in human tissues. But a major challenge remains: can we systematically decode how cells organize into functional niches in situ — including those invisible to standard histopathology? To address this, we integrated large-scale scRNA-seq, spatial transcriptomics, histopathology, and AI-driven modeling frameworks to build an in situ atlas of human skin across health and disease. Led by Lloyd Steele, an MD/PhD student working between Haniffa Lab and my lab at Wellcome Sanger Institute and Cambridge University . Another amazing collaboration with Muzz Haniffa, the mastermind behind the work as part of Human Cell Atlas. A key part of this study is that we didn’t build everything from scratch — we leveraged and combined AI methods that actually work! and showed how they can be used together to extract biological insight at scale. We used: • scArches to build and map into a reference scRNA-seq atlas of human skin: • NicheCompass to identify and characterize spatial niches: • MINT-Flow to extract microenvironment-induced cell states and gene programs: Together, these enabled an end-to-end workflow from atlas construction to spatial mapping, niche discovery, and cell state decoding. At scale, we integrated ~5 million cells and 100+ spatial sections, enabling a systematic view of tissue organization. Using this framework, we identified 26 niches in skin, including known histopathologic structures as well as hidden disease-associated niches not visible on H&E. Among the most striking findings were a resident memory T cell-rich sebaceous gland niche and a plasma cell-rich sweat gland niche, suggesting that appendageal structures act as active immunological microenvironments and may contribute to inflammatory memory and disease persistence. Importantly, this atlas is not just descriptive — it is usable. It can support mapping of new datasets, resolve finer cell types and niches, extract microenvironment-driven programs, and enable predictive analyses at scale. More broadly, this work shows what becomes possible when AI, spatial genomics, and atlas-scale data are integrated end-to-end: not just mapping tissues, but systematically decoding them. This was a massive collaboration, and I’m very grateful to the amazing scientists April Foster, Kenny Roberts, and Chloe Admane. Lloyd is an amazing scientist, and I’m especially excited for the community to see more of his work soon — stay tuned. The data and pre-trained models will be released soon. Preprint:

Mo Lotfollahi

11,813 görüntüleme • 4 ay önce