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Background: The purpose of this study is to determine the mutation frequencies of key driver genes in uveal melanoma (UM) in… Expand Background: Uveal melanoma (UM), a rare cancer of the eye, is characterized by initiating mutations in the genes G-protein… Expand To explore the implications of lipid catabolism-associated genes in gastrointestinal stromal tumors, we reappraised… Expand Auriculocondylar syndrome, mainly characterized by micrognathia, small mandibular condyle, and question mark ears, is a rare… Expand Next generation sequencing of uveal melanoma (UM) samples has identified a number of recurrent oncogenic or loss-of-function… Expand Auriculo‐Condylar Syndrome (ACS) is a craniofacial malformation syndrome characterized by external ear anomalies, hypoplasia of… Expand Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis affecting infants and young children. Coronary… Expand Gene expression microarrays are widely used to investigate molecular targets in cancers, including lung cancer. In this study, we… Expand Auriculocondylar syndrome (ACS) is a rare, autosomal-dominant craniofacial malformation syndrome characterized by variable… Expand Purpose Primary open-angle glaucoma is a leading cause of blindness worldwide. We previously identified a region on chromosome… Expand