Accordingly, we used uH2A, as well as a previously generated ubiquitylated H2B, in chaperone-coupled nucleosome stability assays to demonstrate that the direct effect of ubiquitylated histones on ...

⊥Present address: Department of Chemistry, University of Southern California, Los Angeles, CA 90089. Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 ...

Gene Hackman, Wes Anderson, Bill Murray on the set of 2001's 'The Royal Tenenbaums' Buena Vista Pictures/Courtesy Everett Collection Ahead of the Cannes premiere of his latest film, The Phoenician ...

Doctors announced this week that they have treated a newborn baby with a rare genetic disease using the world’s first personalized gene editing therapy. Geoff Bennett discussed the treatment and ...

A baby born with a rare genetic disease is "growing and thriving" after getting bespoke gene therapy. It's the first time anyone in the world has been given an experimental gene-editing treatment ...

News broke yesterday that researchers in Philadelphia appear to have successfully treated a 6-month-old baby boy, called KJ, with a personalized CRISPR gene-editing therapy. The treatment corrects ...

The treatment, described in a new study published in The New England Journal of Medicine and presented at the American Society of Gene and Cell Therapy meeting, relies on a complex therapy known ...

They would use a technology known as CRISPR, a personalized gene-editing therapy, to find the one uniquely mutated gene out of 20,000 in his little body, and fix it. KJ subsequently received three ...

This baby boy was treated with the first personalized gene-editing drug Doctors say they constructed a bespoke gene-editing treatment in less than seven months and used it to treat a baby with a ...

A Japanese research team led by Kyushu University professor Hiroyuki Sasaki has said it discovered a gene that determines the color patterns of the tricolored calico cat, known in Japan as mike neko.

A US infant with a rare condition has become history's first patient to be treated with a personalized gene-editing technique that raises hopes for other people with obscure illnesses, doctors said ...