Video yükleniyor...

Video Yüklenemedi

Ana Sayfaya Dön

Scientists are one step closer to creating “designer babies” after they precisely edited human embryo genes for the first time, according to the New York Times. Dr. Dieter Egli at Columbia University was reportedly able to replace individual genetic letters in sequences of DNA. “But the edits were still...

CollinRugg's profile picture

Collin Rugg

2,877,945 subscribers

331,317 görüntüleme • 3 ay önce •via X (Twitter)

Bilim & Teknoloji
LIVE

Anya Rossi• Live Now

Private livecam show

0 Yorum

Yorum bulunmuyor

Orijinal gönderinin yorumları burada görünecek

Benzer Videolar

OpenAI CEO Sam Altman and His Husband Are Funding the Creation of Genetically Engineered Babies By merging AI with CRISPR, they aim to “fix” humans while offshoring early embryo testing to evade oversight. First iterations of GMO children will endure immense suffering. Zuccaro et al already tested CRISPR gene edits on real human embryos: entire chromosomes were deleted, DNA shattered, and the embryo collapsed into genetic chaos.
1:27

OpenAI CEO Sam Altman and His Husband Are Funding the Creation of Genetically Engineered Babies By merging AI with CRISPR, they aim to “fix” humans while offshoring early embryo testing to evade oversight. First iterations of GMO children will endure immense suffering. Zuccaro et al already tested CRISPR gene edits on real human embryos: entire chromosomes were deleted, DNA shattered, and the embryo collapsed into genetic chaos.

Nicolas Hulscher, MPH

98,283 görüntüleme • 7 ay önce

Herasight advisor and genetics professor Alex Strudwick Young says that in the future, we may be able to create gametes from non-gamete adult cells and stack that with gene editing to remove disease-causing variants: "In vitro gametogenesis is a technology to create gametes — so sperm and eggs, eggs is what would be more useful generally — from adult cells that are not gamete cells." "That could potentially create thousands of embryos." "Then there's also gene editing. You can use CRISPR or a technology like that to go into an embryo and edit particular base pairs, remove some disease-causing variant, or maybe more controversially enhance some ability." "My idea for the future of this space could be that you have a stack, where you have in vitro gametogenesis that creates thousands of embryos. Then you can get the genome data, do the predictions of the disease risks and traits from that, select a few promising embryos, and then do some edits in them."
1:16

Herasight advisor and genetics professor Alex Strudwick Young says that in the future, we may be able to create gametes from non-gamete adult cells and stack that with gene editing to remove disease-causing variants: "In vitro gametogenesis is a technology to create gametes — so sperm and eggs, eggs is what would be more useful generally — from adult cells that are not gamete cells." "That could potentially create thousands of embryos." "Then there's also gene editing. You can use CRISPR or a technology like that to go into an embryo and edit particular base pairs, remove some disease-causing variant, or maybe more controversially enhance some ability." "My idea for the future of this space could be that you have a stack, where you have in vitro gametogenesis that creates thousands of embryos. Then you can get the genome data, do the predictions of the disease risks and traits from that, select a few promising embryos, and then do some edits in them."

TBPN

21,726 görüntüleme • 5 ay önce

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.
6:34

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.

You

574,563 görüntüleme • 2 yıl önce

GENETIC MIRACLE: DIRE WOLVES BORN FROM 72,000-YEAR-OLD DNA The process began with two dire wolf fossils: a 13,000-year-old bone and a 72,000-year-old inner ear. Scientists extracted viable DNA, sequenced their genomes, and identified the gene differences that made dire wolves unique from modern wolves. With that blueprint, Colossal edited 14 genes in gray wolf DNA—adjusting for size, coat, vocalization, and other distinct traits. That edited DNA was placed into egg cells, grown into embryos, and implanted into surrogate hound dogs. On October 1, 2024, twin pups Romulus and Remus were born. Source: Time
6:57

GENETIC MIRACLE: DIRE WOLVES BORN FROM 72,000-YEAR-OLD DNA The process began with two dire wolf fossils: a 13,000-year-old bone and a 72,000-year-old inner ear. Scientists extracted viable DNA, sequenced their genomes, and identified the gene differences that made dire wolves unique from modern wolves. With that blueprint, Colossal edited 14 genes in gray wolf DNA—adjusting for size, coat, vocalization, and other distinct traits. That edited DNA was placed into egg cells, grown into embryos, and implanted into surrogate hound dogs. On October 1, 2024, twin pups Romulus and Remus were born. Source: Time

Mario Nawfal

489,338 görüntüleme • 1 yıl önce

NEW: Guest blows Joe Rogan’s mind when he reveals that China has ALREADY genetically modified children. Biotech founder Ben Lamm explained how Chinese scientists cloned embryos and then edited them to make babies immune to HIV. But it gets worse. Lamm said there’s growing debate over whether those same babies were also genetically enhanced for increased INTELLIGENCE. The science is still unclear, but he warned the intent is very real. He pointed to BGI (Beijing Genomics Institute), a Chinese genetics company that he claims used the COVID-19 pandemic as an opportunity to collect global DNA. According to Lamm, BGI offered free COVID testing to countries around the world—not just as a humanitarian gesture, but as a way to gather genetic data on entire populations. He claimed BGI has openly stated its goal is to sequence as much of the global population as possible in search of genes linked to intelligence—and act on what they find. “They are openly saying we are sequencing as much as we can of the world population looking for genes for intelligence.” “How old are these [genetically modified] kids now?” Rogan asked. “Are they already winning chess tournaments?”
2:58

NEW: Guest blows Joe Rogan’s mind when he reveals that China has ALREADY genetically modified children. Biotech founder Ben Lamm explained how Chinese scientists cloned embryos and then edited them to make babies immune to HIV. But it gets worse. Lamm said there’s growing debate over whether those same babies were also genetically enhanced for increased INTELLIGENCE. The science is still unclear, but he warned the intent is very real. He pointed to BGI (Beijing Genomics Institute), a Chinese genetics company that he claims used the COVID-19 pandemic as an opportunity to collect global DNA. According to Lamm, BGI offered free COVID testing to countries around the world—not just as a humanitarian gesture, but as a way to gather genetic data on entire populations. He claimed BGI has openly stated its goal is to sequence as much of the global population as possible in search of genes linked to intelligence—and act on what they find. “They are openly saying we are sequencing as much as we can of the world population looking for genes for intelligence.” “How old are these [genetically modified] kids now?” Rogan asked. “Are they already winning chess tournaments?”

The Vigilant Fox 🦊

2,703,305 görüntüleme • 1 yıl önce

The mark of the beast, known as 666.. Is a DNA seal placed on 6th base tone of DNA strand 1, 6th base tone of DNA strand 5, and 6th base tone of DNA strand 6, known as the Templar (Stargate )-Axion Seal which was originally applied to the Sirian-Annunaki who refused to uphold the Sacred Law of One so that distorted DNA codes could not enter into 5D earth Tara. (Protect the purity of the higher dimensions of Earth) - 666 became part of much of the human genetic code through interbreeding with visiting Annunaki, who created the hybrid races Nephillim and Annu. - Through following the Sacred Law of One teachings one can rehabilitate their DNA in preparation for ascension. - The same off planet beings are still messing with human DNA. Be mindful before you inject anything into your body that it maintains the purity of your original celestial human DNA. ~ Samuel Lee ✨🙌🏽💫
3:24

The mark of the beast, known as 666.. Is a DNA seal placed on 6th base tone of DNA strand 1, 6th base tone of DNA strand 5, and 6th base tone of DNA strand 6, known as the Templar (Stargate )-Axion Seal which was originally applied to the Sirian-Annunaki who refused to uphold the Sacred Law of One so that distorted DNA codes could not enter into 5D earth Tara. (Protect the purity of the higher dimensions of Earth) - 666 became part of much of the human genetic code through interbreeding with visiting Annunaki, who created the hybrid races Nephillim and Annu. - Through following the Sacred Law of One teachings one can rehabilitate their DNA in preparation for ascension. - The same off planet beings are still messing with human DNA. Be mindful before you inject anything into your body that it maintains the purity of your original celestial human DNA. ~ Samuel Lee ✨🙌🏽💫

🧬Maxpein🧬

17,013 görüntüleme • 6 ay önce

🚨EPSTEIN FILES STATE THE CREATED NEANDERTHALS CLONES Clones of Neanderthals were created in underground tunnels as stated in the Epstein files released by the DOJ government in 2026. It is impossible to ignore the truth at this point. The truth is stranger than fiction and we have not heard anything stranger than this happening in real life. Per Charlie T Griffen The first studies of Neanderthal DNA focused on the genetic sequences of mitochondria, the microscopic organelles that convert food to energy within cells. In 2005, however, 454 began a collaborative project with the Max Planck Institute in Leipzig, Germany, to sequence the full genetic code of a Neanderthal woman who died in Croatia's Vindija cave 30,000 years ago. As the Neanderthal genome is painstakingly sequenced, the archaeologists and biologists who study it will be faced with an opportunity that seemed like science fiction just 10 years ago. They will be able to look at the genetic blueprint of humankind's nearest relative and understand its biology as intimately as our own. In addition to giving scientists the ability to answer questions about Neanderthals' relationship to our own species--did we interbreed, are we separate species, who was smarter--the Neanderthal genome may be useful in researching medical treatments. Newly developed techniques could make cloning Neanderthal cells or body parts a reality within a few years. The ability to use the genes of extinct hominins is going to force the field of paleoanthropology into some unfamiliar ethical territory. There are still technical obstacles, but soon it could be possible to use that long-extinct genome to safely create a healthy, living Neanderthal clone. Should it be done? At the 454 Life Sciences offices, Gerald Irzyk, Jason Affourtit, and Thomas Jarvie explain the process they use to read the chemicals that made up Neanderthal DNA and the genes that determined a large part of their biology. DNA has a shape, called a double helix, that makes it look like a twisted ladder. Each rung on the ladder is called a base-pair. The rungs are made up of a pair of chemicals called nucleotides--adenine, thymine, cytosine, and guanine, which are usually referred to by their first initials. The sequence of the nucleotides in the DNA determines what genes an organism has and how they function. Max Planck Institute initially chose 454 because it had come up with a way to read hundreds of thousands of DNA sequences at a time. Genome-sequencing technology is advancing at a rate comparable to computer processing power. Putting the fragments themselves in order can be a little tricky. "At first glance, it's just this completely random assemblage of As, Ts, Cs, and Gs," says Irzyk. "But it turns out there are patterns and motifs, and sometimes these are very specific to a group of organisms." For the Neanderthal sample, the human and chimpanzee genomes were used as references for checking the sequence. Working with ancient DNA can be much more problematic than sequencing genetic material from living species. Within hours of death, cells begin to break down in a process called apoptosis. The dying cells release enzymes that chop up DNA into tiny pieces. In a human cell, this means that the entire three-billion-base-pair genome is reduced to fragments a few hundred base-pairs long or shorter. The DNA also goes through chemical changes that alter the nucleotides as it ages--C changes into T, and G turns into A--which can cause the gene sequence to be interpreted incorrectly. In the case of the Neanderthal sample, somewhere between 90 and 99 percent of the DNA came from bacteria and other contaminants that had found their way into the bone as it sat in the ground and in storage. The contaminant DNA has to be identified and eliminated. Given the similarity between Neanderthal and modern human DNA, this can be especially difficult when the contamination comes from the people who excavated or analyzed the bone.
2:28

🚨EPSTEIN FILES STATE THE CREATED NEANDERTHALS CLONES Clones of Neanderthals were created in underground tunnels as stated in the Epstein files released by the DOJ government in 2026. It is impossible to ignore the truth at this point. The truth is stranger than fiction and we have not heard anything stranger than this happening in real life. Per Charlie T Griffen The first studies of Neanderthal DNA focused on the genetic sequences of mitochondria, the microscopic organelles that convert food to energy within cells. In 2005, however, 454 began a collaborative project with the Max Planck Institute in Leipzig, Germany, to sequence the full genetic code of a Neanderthal woman who died in Croatia's Vindija cave 30,000 years ago. As the Neanderthal genome is painstakingly sequenced, the archaeologists and biologists who study it will be faced with an opportunity that seemed like science fiction just 10 years ago. They will be able to look at the genetic blueprint of humankind's nearest relative and understand its biology as intimately as our own. In addition to giving scientists the ability to answer questions about Neanderthals' relationship to our own species--did we interbreed, are we separate species, who was smarter--the Neanderthal genome may be useful in researching medical treatments. Newly developed techniques could make cloning Neanderthal cells or body parts a reality within a few years. The ability to use the genes of extinct hominins is going to force the field of paleoanthropology into some unfamiliar ethical territory. There are still technical obstacles, but soon it could be possible to use that long-extinct genome to safely create a healthy, living Neanderthal clone. Should it be done? At the 454 Life Sciences offices, Gerald Irzyk, Jason Affourtit, and Thomas Jarvie explain the process they use to read the chemicals that made up Neanderthal DNA and the genes that determined a large part of their biology. DNA has a shape, called a double helix, that makes it look like a twisted ladder. Each rung on the ladder is called a base-pair. The rungs are made up of a pair of chemicals called nucleotides--adenine, thymine, cytosine, and guanine, which are usually referred to by their first initials. The sequence of the nucleotides in the DNA determines what genes an organism has and how they function. Max Planck Institute initially chose 454 because it had come up with a way to read hundreds of thousands of DNA sequences at a time. Genome-sequencing technology is advancing at a rate comparable to computer processing power. Putting the fragments themselves in order can be a little tricky. "At first glance, it's just this completely random assemblage of As, Ts, Cs, and Gs," says Irzyk. "But it turns out there are patterns and motifs, and sometimes these are very specific to a group of organisms." For the Neanderthal sample, the human and chimpanzee genomes were used as references for checking the sequence. Working with ancient DNA can be much more problematic than sequencing genetic material from living species. Within hours of death, cells begin to break down in a process called apoptosis. The dying cells release enzymes that chop up DNA into tiny pieces. In a human cell, this means that the entire three-billion-base-pair genome is reduced to fragments a few hundred base-pairs long or shorter. The DNA also goes through chemical changes that alter the nucleotides as it ages--C changes into T, and G turns into A--which can cause the gene sequence to be interpreted incorrectly. In the case of the Neanderthal sample, somewhere between 90 and 99 percent of the DNA came from bacteria and other contaminants that had found their way into the bone as it sat in the ground and in storage. The contaminant DNA has to be identified and eliminated. Given the similarity between Neanderthal and modern human DNA, this can be especially difficult when the contamination comes from the people who excavated or analyzed the bone.

SANTINO

54,154 görüntüleme • 6 ay önce

Dr. Sucharit Bhakdi, a renowned microbiologist and immunologist, is issuing a dire warning to humanity about the dangers of mRNA vaccines. He claims that the integration of foreign genes into human chromosomes through these vaccines poses catastrophic risks—not only to individuals but to future generations. According to Dr. Bhakdi, the introduction of bacterial plasmids and foreign DNA into human cells via mRNA vaccines is a reckless experiment that could lead to permanent genetic alterations. "Any foreign gene integrated into your chromosome can trigger cancer immediately, cause widespread cellular dysfunction, and be passed down to your offspring," Dr. Bhakdi warns. He emphasizes that once these genetic changes occur, they are irreversible, transforming the very blueprint of human biology. Every cell altered by these foreign genes, he argues, is "doomed," setting the stage for unpredictable and potentially devastating health consequences. Dr. Bhakdi asserts that global health authorities like the WHO, CDC, and FDA are pushing these vaccines without fully acknowledging their risks. He points to the presence of bacterial-derived plasmids in mRNA vaccines, which he claims can infiltrate human cells and wreak havoc on genetic stability. This, he says, is not a theoretical concern but a reality already unfolding with the rollout of these vaccines worldwide. This is not a message of fear but a call to awareness. Dr. Bhakdi urges people to question the narrative, demand transparency, and protect their health and future generations from what he describes as a dangerous overreach by global health institutions. "We are at a crossroads," he declares. "The genetic integrity of humanity is at stake."
1:50

Dr. Sucharit Bhakdi, a renowned microbiologist and immunologist, is issuing a dire warning to humanity about the dangers of mRNA vaccines. He claims that the integration of foreign genes into human chromosomes through these vaccines poses catastrophic risks—not only to individuals but to future generations. According to Dr. Bhakdi, the introduction of bacterial plasmids and foreign DNA into human cells via mRNA vaccines is a reckless experiment that could lead to permanent genetic alterations. "Any foreign gene integrated into your chromosome can trigger cancer immediately, cause widespread cellular dysfunction, and be passed down to your offspring," Dr. Bhakdi warns. He emphasizes that once these genetic changes occur, they are irreversible, transforming the very blueprint of human biology. Every cell altered by these foreign genes, he argues, is "doomed," setting the stage for unpredictable and potentially devastating health consequences. Dr. Bhakdi asserts that global health authorities like the WHO, CDC, and FDA are pushing these vaccines without fully acknowledging their risks. He points to the presence of bacterial-derived plasmids in mRNA vaccines, which he claims can infiltrate human cells and wreak havoc on genetic stability. This, he says, is not a theoretical concern but a reality already unfolding with the rollout of these vaccines worldwide. This is not a message of fear but a call to awareness. Dr. Bhakdi urges people to question the narrative, demand transparency, and protect their health and future generations from what he describes as a dangerous overreach by global health institutions. "We are at a crossroads," he declares. "The genetic integrity of humanity is at stake."

Camus

56,601 görüntüleme • 1 yıl önce

NEW: California couples break down in tears after an Orange County fertility doctor allegedly stole their embryos and took them to Bakersfield. 26 patients have now launched a lawsuit against Dr. Brian David Acacio for "kidnapping" their embryos. "I feel like they were kidnapped. I don't know where they are," said Bernice Cervantes. "We've gone through multiple retrievals, multiple transfers, and this man does not care about us. We've been through so much. We just need him to be accountable. We want our embryos," said Christina Chandler. The lawsuit claims Acacio failed to pay over $240,000 in rent. Once he was evicted, he took the embryos to Bakersfield without notifying any of the patients.
1:08

NEW: California couples break down in tears after an Orange County fertility doctor allegedly stole their embryos and took them to Bakersfield. 26 patients have now launched a lawsuit against Dr. Brian David Acacio for "kidnapping" their embryos. "I feel like they were kidnapped. I don't know where they are," said Bernice Cervantes. "We've gone through multiple retrievals, multiple transfers, and this man does not care about us. We've been through so much. We just need him to be accountable. We want our embryos," said Christina Chandler. The lawsuit claims Acacio failed to pay over $240,000 in rent. Once he was evicted, he took the embryos to Bakersfield without notifying any of the patients.

Collin Rugg

526,010 görüntüleme • 6 ay önce

Evolution says you can turn anything into anything if you tweak it long enough. But that house of cards collapses immediately when you realize what it takes to make even a single cell. They say new cell types arise one mutation at a time. Is that plausible? Here is the issue: Different cell types are created through a massive coordinated stack of genetic information, and it's not all just about DNA sequences. First you need a whole suite of new genetic systems related to the cell: new genes for the cell’s internal systems, instructions for its specific functional role in the body, the regulators that coordinate everything, markers to tell them where to go and when, and the controls that keep the wrong programs off. But the DNA structure itself must also be manipulated. You see, every cell in your body contains the DNA instructions to make any other cell. So how does a bone cell become a bone cell instead of a skin cell? Because of how the DNA is folded. DNA is folded in certain ways for different cell types, so that only the "bone cell instructions" are able to be read by the "cell construction program." The DNA fold decides which programs are open for each cell type. This is critical. If DNA is not folded properly so that specific cell-type information can be read, catastrophe ensues. Then you need placement blueprints, so the cells form in the right place, in the right number, and lock together to form a functional tissue. These developmental instructions are passed from parent to offspring - but research shows that tweaking these master developmental programs ends badly for the child. One mutation at a time cannot invent that entire programming stack and keep it coordinated. Research has confirmed this. To convert one cell type into another in the lab, researchers have to force many changes to happen at the same time in coordination. And even when directed by the researcher, cell conversion almost always fails. Change the sequence without the fold and you cannot get a new cell type. Fold the DNA without the new systems and you can only rearrange old programs. Make the cell without the map and it shows up in the wrong place. Break one layer in the stack and the others do not patiently wait - they fail. So creating a new cell type is not simply "tweak a gene one at a time." It requires a coordinated stack of entirely new programmed instructions: > New suite of internal systems, programmed into the DNA > New functional DNA fold so only the right systems are activated > New mapping blueprints so everything goes where it's needed Step-by-step mutation does not coordinate those layers. It produces broken cells before it produces new ones. Coordination of this level of complexity has only ever been known to come from one place: Intelligence.
0:29

Evolution says you can turn anything into anything if you tweak it long enough. But that house of cards collapses immediately when you realize what it takes to make even a single cell. They say new cell types arise one mutation at a time. Is that plausible? Here is the issue: Different cell types are created through a massive coordinated stack of genetic information, and it's not all just about DNA sequences. First you need a whole suite of new genetic systems related to the cell: new genes for the cell’s internal systems, instructions for its specific functional role in the body, the regulators that coordinate everything, markers to tell them where to go and when, and the controls that keep the wrong programs off. But the DNA structure itself must also be manipulated. You see, every cell in your body contains the DNA instructions to make any other cell. So how does a bone cell become a bone cell instead of a skin cell? Because of how the DNA is folded. DNA is folded in certain ways for different cell types, so that only the "bone cell instructions" are able to be read by the "cell construction program." The DNA fold decides which programs are open for each cell type. This is critical. If DNA is not folded properly so that specific cell-type information can be read, catastrophe ensues. Then you need placement blueprints, so the cells form in the right place, in the right number, and lock together to form a functional tissue. These developmental instructions are passed from parent to offspring - but research shows that tweaking these master developmental programs ends badly for the child. One mutation at a time cannot invent that entire programming stack and keep it coordinated. Research has confirmed this. To convert one cell type into another in the lab, researchers have to force many changes to happen at the same time in coordination. And even when directed by the researcher, cell conversion almost always fails. Change the sequence without the fold and you cannot get a new cell type. Fold the DNA without the new systems and you can only rearrange old programs. Make the cell without the map and it shows up in the wrong place. Break one layer in the stack and the others do not patiently wait - they fail. So creating a new cell type is not simply "tweak a gene one at a time." It requires a coordinated stack of entirely new programmed instructions: > New suite of internal systems, programmed into the DNA > New functional DNA fold so only the right systems are activated > New mapping blueprints so everything goes where it's needed Step-by-step mutation does not coordinate those layers. It produces broken cells before it produces new ones. Coordination of this level of complexity has only ever been known to come from one place: Intelligence.

Divinely Designed

22,570 görüntüleme • 23 gün önce

Zach Bush explains why the completion of the human genome project was so embarrassing for scientists and reveals how your genes compare to a flea "Then we start in 1992. We set out to decode the human genome. And we thought, well, this is going to be amazing. It's going to be a 40-year project because we knew how many genes we could decode each year with our genetic sequencers. So we thought we were going to have to find 400,000 genes because we knew by this time that we had 400,000 different proteins in the human body." "1996 rolls around, and the team finishes 25 years ahead of schedule because there were not 400,000 genes. There was 25,000 genes. Everybody laughed, said, you screwed it up. Three more teams finished over the next two years. There was not 25,000 genes. There was 19,000 genes." "We have less than 20,000 human genes that make a human body. The reason why that's so embarrassing is because a flea has 30,000 genes. A fruit fly has 13,000 genes. So you sit somewhere between a flea and a fruit fly genetically. In fact, you're a little closer to the fruit fly than the flea. That's probably why the flea can jump 40 times its height and you can't."
1:12

Zach Bush explains why the completion of the human genome project was so embarrassing for scientists and reveals how your genes compare to a flea "Then we start in 1992. We set out to decode the human genome. And we thought, well, this is going to be amazing. It's going to be a 40-year project because we knew how many genes we could decode each year with our genetic sequencers. So we thought we were going to have to find 400,000 genes because we knew by this time that we had 400,000 different proteins in the human body." "1996 rolls around, and the team finishes 25 years ahead of schedule because there were not 400,000 genes. There was 25,000 genes. Everybody laughed, said, you screwed it up. Three more teams finished over the next two years. There was not 25,000 genes. There was 19,000 genes." "We have less than 20,000 human genes that make a human body. The reason why that's so embarrassing is because a flea has 30,000 genes. A fruit fly has 13,000 genes. So you sit somewhere between a flea and a fruit fly genetically. In fact, you're a little closer to the fruit fly than the flea. That's probably why the flea can jump 40 times its height and you can't."

Rad

57,201 görüntüleme • 1 ay önce

🚨🚨🚨🚨 Oh-oh! First experiments of genetic vaccines getting absorbed by human cells completed - Prof Sucharit Bhakdi reveals. ----------------------------- Our two lady scientists who are just brilliant, they took cells, human cells, and immersed these cells in the vaccine and they found, and these are the first experiments that have ever been done, okay, that the human cells immediately took up the vaccines and the DNA and the chromosomes, and the chromosomes, bacterial chromosomes, entered the cells and these cells immediately started making the spike protein in horrendous quantity and they have quantified this, they have shown what happens to the spike protein, that it is stable, that it is shed into the blood, into the circulation, they have shown that they can measure this in the blood, they can measure this anywhere actually, and they have shown that the plasmid and the spike production goes on for many, many days. So, what did our girls do? They sent their human cells that had been transfected to Kevin McKernan, begging the question, Kevin, can you find any chromosomal integration of bacterial DNA in the human cell chromosomes? Do you know the answer? He put it up in his substack one week ago, and the answer is yes. He's found it. ------------------------------------- Kevin McKernan
5:27

🚨🚨🚨🚨 Oh-oh! First experiments of genetic vaccines getting absorbed by human cells completed - Prof Sucharit Bhakdi reveals. ----------------------------- Our two lady scientists who are just brilliant, they took cells, human cells, and immersed these cells in the vaccine and they found, and these are the first experiments that have ever been done, okay, that the human cells immediately took up the vaccines and the DNA and the chromosomes, and the chromosomes, bacterial chromosomes, entered the cells and these cells immediately started making the spike protein in horrendous quantity and they have quantified this, they have shown what happens to the spike protein, that it is stable, that it is shed into the blood, into the circulation, they have shown that they can measure this in the blood, they can measure this anywhere actually, and they have shown that the plasmid and the spike production goes on for many, many days. So, what did our girls do? They sent their human cells that had been transfected to Kevin McKernan, begging the question, Kevin, can you find any chromosomal integration of bacterial DNA in the human cell chromosomes? Do you know the answer? He put it up in his substack one week ago, and the answer is yes. He's found it. ------------------------------------- Kevin McKernan

aussie17

333,911 görüntüleme • 2 yıl önce

“I don’t think it’s exaggerating to say that this is the future of medicine.” For years, Dr. Rebecca Ahrens-Nicklas treated babies with rare genetic diseases knowing palliative care was often the only option. In 2023, she partnered with gene-editing researcher Dr. Kiran Musunuru to try something new: using CRISPR to correct disease-causing mutations before the damage became irreversible. In 2025, doctors delivered the first successful personalized CRISPR therapy, pointing to a future where gene therapies are custom-built for patients who once had no options. See the full TIME100 Health list of leaders, scientists, doctors, and more here:
1:23

“I don’t think it’s exaggerating to say that this is the future of medicine.” For years, Dr. Rebecca Ahrens-Nicklas treated babies with rare genetic diseases knowing palliative care was often the only option. In 2023, she partnered with gene-editing researcher Dr. Kiran Musunuru to try something new: using CRISPR to correct disease-causing mutations before the damage became irreversible. In 2025, doctors delivered the first successful personalized CRISPR therapy, pointing to a future where gene therapies are custom-built for patients who once had no options. See the full TIME100 Health list of leaders, scientists, doctors, and more here:

TIME

19,885 görüntüleme • 7 ay önce

NEW: Florida couple launches lawsuit after DNA test revealed that their baby girl wasn't actually theirs. The couple says they used their own egg and sperm to create three viable embryos at the IVF Life, Inc. D/B/A Fertility Center. In March 2025, an embryo was implanted in the woman, which resulted in a successful pregnancy. After the birth of the child, the couple, identified as 'John and Jane Doe,' became suspicious after noticing the baby did not have the same skin color as them. "While we are beyond grateful to have her in our lives and love her immeasurably, we also recognize that we have a moral obligation to find her genetic parents," they said. "Our joy over her birth is further complicated by the devastating reality that her genetic parents, whom we do not yet know, or possibly another family entirely, may have received our genetic embryo. We are heartbroken, devastated, and confused." The couple says the clinic has been "entirely uncooperative" with them. "Until yesterday, the clinic has been entirely uncooperative and refused to provide any verifiable information or a timeline as to when such information would be provided," the couple said. "Faced with the prospect of a court order at yesterday’s hearing, the clinic has now promised cooperation, but that promise has not yet been fulfilled. We hope it will be." Insane.
1:22

NEW: Florida couple launches lawsuit after DNA test revealed that their baby girl wasn't actually theirs. The couple says they used their own egg and sperm to create three viable embryos at the IVF Life, Inc. D/B/A Fertility Center. In March 2025, an embryo was implanted in the woman, which resulted in a successful pregnancy. After the birth of the child, the couple, identified as 'John and Jane Doe,' became suspicious after noticing the baby did not have the same skin color as them. "While we are beyond grateful to have her in our lives and love her immeasurably, we also recognize that we have a moral obligation to find her genetic parents," they said. "Our joy over her birth is further complicated by the devastating reality that her genetic parents, whom we do not yet know, or possibly another family entirely, may have received our genetic embryo. We are heartbroken, devastated, and confused." The couple says the clinic has been "entirely uncooperative" with them. "Until yesterday, the clinic has been entirely uncooperative and refused to provide any verifiable information or a timeline as to when such information would be provided," the couple said. "Faced with the prospect of a court order at yesterday’s hearing, the clinic has now promised cooperation, but that promise has not yet been fulfilled. We hope it will be." Insane.

Collin Rugg

418,856 görüntüleme • 7 ay önce

REPORT: Guest blows Joe Rogan’s mind when he reveals that China ALREADY has genetically modified children. Biotech founder Ben Lamm explained how Chinese scientists cloned embryos and then edited them to make babies immune to HIV. But it gets worse. Lamm said there’s growing debate over whether those same babies were also genetically enhanced for increased INTELLIGENCE. The science is still unclear, but he warned the intent is very real. He pointed to BGI (Beijing Genomics Institute), a Chinese genetics company that he claims used the COVID-19 pandemic as an opportunity to collect global DNA. According to Lamm, BGI offered free COVID testing to countries around the world—not just as a humanitarian gesture, but as a way to gather genetic data on entire populations. He claimed BGI has openly stated its goal is to sequence as much of the global population as possible in search of genes linked to intelligence—and act on what they find. “They are openly saying we are sequencing as much as we can of the world population looking for genes for intelligence.” “How old are these [genetically modified] kids now?” Rogan asked. “Are they already winning chess tournaments?” If one country starts genetically modifying its population, others won’t stand by and watch. It’ll set off a global arms race—not with missiles or drones, but with DNA to see who can engineer the smartest, most advanced generation of humans on the planet. And once that race begins, there’s no going back. Watch give her take on the whole situation:
7:40

REPORT: Guest blows Joe Rogan’s mind when he reveals that China ALREADY has genetically modified children. Biotech founder Ben Lamm explained how Chinese scientists cloned embryos and then edited them to make babies immune to HIV. But it gets worse. Lamm said there’s growing debate over whether those same babies were also genetically enhanced for increased INTELLIGENCE. The science is still unclear, but he warned the intent is very real. He pointed to BGI (Beijing Genomics Institute), a Chinese genetics company that he claims used the COVID-19 pandemic as an opportunity to collect global DNA. According to Lamm, BGI offered free COVID testing to countries around the world—not just as a humanitarian gesture, but as a way to gather genetic data on entire populations. He claimed BGI has openly stated its goal is to sequence as much of the global population as possible in search of genes linked to intelligence—and act on what they find. “They are openly saying we are sequencing as much as we can of the world population looking for genes for intelligence.” “How old are these [genetically modified] kids now?” Rogan asked. “Are they already winning chess tournaments?” If one country starts genetically modifying its population, others won’t stand by and watch. It’ll set off a global arms race—not with missiles or drones, but with DNA to see who can engineer the smartest, most advanced generation of humans on the planet. And once that race begins, there’s no going back. Watch give her take on the whole situation:

The Vigilant Fox 🦊

507,015 görüntüleme • 1 yıl önce

🚨 Kevin McKernan broke down how Pfizer BURIED the truth about parts of their Covid shots. “They omitted some of these components in the disclosure to the FDA … ” And that convinced him that Pfizer knew they were being completely “reckless.” “There are recommendations for how much DNA can be in a vaccine.” “But they have never considered… how do those change when you have a lipid nanoparticle around?” “They get DNA into the cells a hundredfold more effectively than a vaccine.” “A Warp Speed artifact of Pfizer… left some of these components in the plasmid.” “They quickly grabbed a plasmid from the gene therapy department, threw the spike into it, and raced that to market.” “One [sequence] is a nuclear targeting sequence, which means it drives DNA into the nucleus.” “When you introduce [extracellular] DNA to the cell… it’s a stimulator of interferon genes.” “If you do that repeatedly, it can lead to cancer.” “Moderna’s own patents speak to this being a risk.” “I think we’re looking at something that is a Swiss army knife of problems.” Kevin McKernan MAHA Institute
3:08

🚨 Kevin McKernan broke down how Pfizer BURIED the truth about parts of their Covid shots. “They omitted some of these components in the disclosure to the FDA … ” And that convinced him that Pfizer knew they were being completely “reckless.” “There are recommendations for how much DNA can be in a vaccine.” “But they have never considered… how do those change when you have a lipid nanoparticle around?” “They get DNA into the cells a hundredfold more effectively than a vaccine.” “A Warp Speed artifact of Pfizer… left some of these components in the plasmid.” “They quickly grabbed a plasmid from the gene therapy department, threw the spike into it, and raced that to market.” “One [sequence] is a nuclear targeting sequence, which means it drives DNA into the nucleus.” “When you introduce [extracellular] DNA to the cell… it’s a stimulator of interferon genes.” “If you do that repeatedly, it can lead to cancer.” “Moderna’s own patents speak to this being a risk.” “I think we’re looking at something that is a Swiss army knife of problems.” Kevin McKernan MAHA Institute

Children’s Health Defense

32,381 görüntüleme • 6 ay önce