Conclusions: The frequency of NOD2 gene variants was lower in genetically homogenous Finns than in other populations. The 1007fs variant was associated with CD. The occurrence of CARD15 variants ...

Putting the uniquely human version of a certain gene into mice changed the way that ... but humans have a unique variant. Yoko Tajima, a postdoctoral associate in Darnell's lab, led an effort ...

A new study shows that giving mice the human version of a gene changes their squeak ... but humans have a unique variant. Yoko Tajima, a postdoctoral associate in Darnell's lab, led an effort ...

He was interested in a different gene called NOVA1, which he has studied for over two decades. NOVA1 is active in the brain, where it produces a protein that can affect the activity of other genes.

Recent research takes aim at the a variant in gene SCN1B, which causes a severe form of developmental epileptic encephalopathy. Dravet syndrome and other developmental epileptic encephalopathies ...