6don MSN
New method reveals how mutations drive transthyretin amyloidosis and guides precision drug design
An international research team reveals new molecular mechanisms associated with pathogenic mutations in the protein ...
Mutations in the tumor suppressor TP53 are a common cause of cancer, making the altered protein an attractive target for ...
Most mutations that cause disease by swapping one amino acid out for another do so by making the protein less stable, according to a major study of human protein variants that was published in Nature ...
CONNECTICUT — Close gatherings over the Thanksgiving holiday could cause an uptick in emergency room visits in Connecticut due to a trio of respiratory illnesses that typically rise this time of year, ...
3don MSN
Scientists report new immune insights and targets into LRRK2 mutations in Parkinson's disease
Parkinson's disease (PD) is a debilitating and progressive neurodegenerative disorder caused by the loss of ...
Influenza cases are down across the United States, but a new flu strain mutation identified in August is causing a spike in ...
Researchers at the Translational Genomics Research Institute (TGen) have identified a genomic mutation that causes physical abnormalities and developmental delays in children. Upon analyzing the ...
X-linked adrenoleukodystrophy is a rare genetic condition that causes problems with the white matter in your nervous system and adrenal glands. X-linked adrenoleukodystrophy (X-ALD) is a genetic ...
Sickle cell disease is a hereditary condition, which means a person inherits it from their biological parents. The condition occurs when a person inherits two copies of the hemoglobin beta (HBB) gene ...
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