Hermansky–Pudlak syndrome (HPS) is a genetically heterogeneous autosomal recessive disorder characterised by oculocutaneous albinism, bleeding diathesis and, in certain subtypes, immunodeficiency, ...
Schizophrenia arises from the complex interplay of numerous genetic variants, each contributing modestly to overall risk, alongside rare high-penetrance alterations. Large-scale genome-wide studies ...
In a recent study published in Frontiers in Pediatrics, researchers discuss the psychological and physiological impacts of obesity on pediatric populations, as well as possible intervention strategies ...
A landmark study uncovers how a specific lung gene, FOXP4, raises the risk of persistent symptoms after COVID-19, providing fresh insight into why some people are more susceptible to long COVID than ...
Researchers analyzed pancreatic islets from 299 donors and found that differences in alpha, beta, and delta cell composition ...
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