Most cancers are not driven by a single gene mutation, but rather an accumulation of mutations that develop over the evolution of tumor growth. While mouse models are useful for identifying cancer ...
Please provide your email address to receive an email when new articles are posted on . NASHVILLE, Tenn. — An analysis of germline susceptibility to renal cell carcinoma revealed considerable ...
Forty-five years ago adult AL was incurable. Since then we have discovered the striking heterogeneity of AL and its importance in selecting therapy, resulting in cure of increasing numbers of patients ...
A comprehensive single-cell atlas of AML uncovers regulatory networks and age-dependent molecular differences to advance the understanding of disease mechanisms and enable subtype-specific therapeutic ...
A new study links telomere length genetics to IPF risk, showing how rare variants and polygenic scores may guide future screening and precision care.
Type 2 diabetes and high blood pressure share a genetic link, according to new research from the University of Surrey, U.K., ...
New study shows that autism is not one condition, but four, each driven by different genes and brain development patterns, helping to reshape diagnosis and care. Study: Decomposition of phenotypic ...
Hypermobile Ehlers–Danlos syndrome (hEDS) is one of the most common heritable connective tissue disorders. Early estimates have reported that this genetic disorder affects at least one in 5,000 ...
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