General Discharge on MSN15 小时
The Neanderthal Autism Link? | Ancient Man
Hey Hunters, With DNA sequencing technology developing we have found a different picture of the History of Ancient Man.
The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human DNA by first breaking it into small pieces -- short reads. Scientists found ...
Smithsonian Magazine on MSN11 小时
Why Is Every Human Being Riddled With Genetic Errors?
Your body is a collection of cells carrying thousands of genetic mistakes accrued over a lifetime—many harmless, some bad and ...
Information on tumor mutational status was limited before the development of NGS because traditional Sanger sequencing and ...
Scientists have discovered a surprising mechanism by which the inherited genetic mutation known to cause Huntington's disease leads to the death of brain cells. The findings change the understanding ...
The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human ...
New research shows that the mutation is, surprisingly, harmless for decades. But it quietly grows into a larger mutation — ...
One type of co-excluder bacteria, called Faecalibacterium, stood out as particularly important. It produces chemicals called short-chain fatty acids by breaking down a variety of fibres in our diet.
Archimed, KKR and Novo Holdings are among the PE firms investing in pharma research, development and sales for genetic medicine.
A new search to solve the Loch Ness Monster mystery is being planned by the scientist who revealed Nessie could be a giant ...
The field of biomolecular research has expanded dramatically over recent decades, particularly in the areas of DNA, RNA, and protein studies. The vast ...