Lifeboat Foundation

It’s not everyday that you see some of the worlds leading cancer scientists attending a scientific forum put on by a hospital from Mexico. But CHIPSA hospital isn’t your average hospital and the scientists showed presenting their research, much of which they are working on with CHIPSA.

Take for instance Dr. Franco Marincola. The fa med former chief of immunogenetics for the NIH, editor of 9 peer reviewed publications and co-author of the textbook mosts oncologists use for immunotherapy reference. Dr. Marincola joined the CHIPSA Scientific advisory board in June and speaks highly of their work and passion for translational science.

Or Dr. Vijay Mahant, who did his post doctorate at MD Anderson in 1985 and invented the prostate cancer test that is widely used today. He also co-founded auto-genomics a leading liquid biopsy company that is studying diagnosing cancer through the blood.

In a new paper, researchers describe their new model that is genetically a lab mouse, but has the microbiome of a wild mouse.

In a paper published in the July 31 issue of Science Translational Medicine, researchers at Fred Hutchinson Cancer Research Center used CRISPR-Cas9 to edit long-lived blood stem cells to reverse the clinical symptoms observed with several blood disorders, including sickle cell disease and beta-thalassemia.

It’s the first time that scientists have specifically edited the genetic makeup of a specialized subset of adult blood stem cells that are the source of all cells in the blood and immune system.

The proof-of-principle study suggests that efficient modification of targeted stem cells could reduce the costs of gene-editing treatments for blood disorders and other diseases while decreasing the risks of unwanted effects that can occur with a less discriminating approach.

FAIRY-SIZED astronauts will become humanity’s weapon of choice when it comes to exploring the universe.

That’s the shock claim made by one expert, who reckons by the end of the century we’ll be creating tiny people with wings to travel to new worlds for us.

Dr Ian Pearson, a “futurologist” – someone who specialises in predicting future tech trends – says we’ll soon be able to genetically engineer folk of all shapes and sizes.

Mr. Epstein’s vision reflected his longstanding fascination with what has become known as transhumanism: the science of improving the human population through technologies like genetic engineering and artificial intelligence. Critics have likened transhumanism to a modern-day version of eugenics, the discredited field of improving the human race through controlled breeding.

Mr. Epstein, the accused sex trafficker, was fascinated by eugenics. He told scientists and others of his vision of using his New Mexico ranch to impregnate women.

Working with mouse and human tissue, Johns Hopkins Medicine researchers report new evidence that a protein pumped out of some—but not all—populations of “helper” cells in the brain, called astrocytes, plays a specific role in directing the formation of connections among neurons needed for learning and forming new memories.

Using mice genetically engineered and bred with fewer such connections, the researchers conducted proof-of-concept experiments that show they could deliver corrective proteins via nanoparticles to replace the missing protein needed for “road repairs” on the defective neural highway.

Since such connective networks are lost or damaged by neurodegenerative diseases such as Alzheimer’s or certain types of intellectual disability, such as Norrie disease, the researchers say their findings advance efforts to regrow and repair the networks and potentially restore normal brain function.

Victoria Gray, 34, of Forest, Miss., has volunteered for one of the most anticipated medical experiments in decades: the first attempt to use the gene-editing technique CRISPR to treat a genetic disorder in the U.S. Meredith Rizzo/NPR hide caption.

But getting human cells to grow in another species is not easy. Nakauchi and colleagues announced at the 2018 American Association for the Advancement of Science meeting in Austin, Texas that they had put human iPS cells into sheep embryos that had been engineered not to produce a pancreas. But the hybrid embryos, grown for 28 days, contained very few human cells, and nothing resembling organs. This is probably because of the genetic distance between humans and sheep, says Nakauchi.

The research could eventually lead to new sources of organs for transplant, but ethical and technical hurdles need to be overcome.