Protein tail mutation may cause rare genetic diseases Researchers from Germany found that a change in a protein’s charge disrupts cellular self-organization, resulting in an extremely rare hereditary developmental disorder called brachyphalangy-polydactyly-tibial aplasia/hypoplasia syndrome (BPTAS).Read More
MicroRNAs strongly associated with type 2 diabetes in study Scientists at the NIH’s National Human Genome Research Institute (NHGRI) have found a set of small RNA molecules, called microRNAs, in human pancreatic cells that are strongly associated with type 2 diabetes.Read More
Tiny but mighty gene fragments maintain blood glucose levels Researchers have discovered that tiny gene fragments called microexons are prevalent in pancreatic islets – tissues that host beta cells which produce insulin. The findings, published February 9 in Nature Metabolism, indicate that microexons may constitute new therapeutic targets for diabetes treatment.Read More
Vaccine effectiveness against Omicron variants may change over time Researchers from The Chinese University of Hong Kong and the Harvard T.H. Chan School of Public Health in Boston, Massachusetts collaborated on a case-control study and found that two vaccines were generally effective over time against severe outcomes from SARS-CoV-2 Omicron infection. The research, published February 3 in the journal JAMA Network Open, also showed that protection among older individuals was more likely to wane six months after the second dose.Read More
Genes for coronary artery disease identified University of Virginia researchers and their collaborators have identified genes that play a key role in the development of coronary artery disease, the number one cause of death worldwide. The research, published recently in Circulation Research, may provide scientists with promising therapeutic targets as they work to develop new and improved treatments.Read More