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PLCB4 gene

Known as: PLCB4, PHOSPHOLIPASE C, BETA-4, PLC-BETA-4 
 
National Institutes of Health

Papers overview

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2019
2019
BACKGROUND Uveal melanoma (UM), a rare cancer of the eye, is characterized by initiating mutations in the genes G-protein subunit… Expand
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2019
2019
Background: The purpose of this study is to determine the mutation frequencies of key driver genes in uveal melanoma (UM) in… Expand
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2017
2017
To explore the implications of lipid catabolism-associated genes in gastrointestinal stromal tumors, we reappraised… Expand
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2017
2017
Auriculocondylar syndrome, mainly characterized by micrognathia, small mandibular condyle, and question mark ears, is a rare… Expand
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Highly Cited
2016
Highly Cited
2016
Next generation sequencing of uveal melanoma (UM) samples has identified a number of recurrent oncogenic or loss-of-function… Expand
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2016
2016
Auriculo-Condylar Syndrome (ACS) is a craniofacial malformation syndrome characterized by external ear anomalies, hypoplasia of… Expand
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2015
2015
Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis affecting infants and young children. Coronary… Expand
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2014
2014
Gene expression microarrays are widely used to investigate molecular targets in cancers, including lung cancer. In this study, we… Expand
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2012
2012
Auriculocondylar syndrome (ACS) is a rare, autosomal-dominant craniofacial malformation syndrome characterized by variable… Expand
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2008
2008
PURPOSE Primary open-angle glaucoma is a leading cause of blindness worldwide. We previously identified a region on chromosome… Expand
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