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P2RY14 gene

Known as: KIAA0001, purinergic receptor P2Y14, PURINERGIC RECEPTOR P2Y, G PROTEIN-COUPLED, 14 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Identification of key genes related to high-risk gastrointestinal stromal tumors using bioinformatics analysis
Aim: The purpose of this study was to identify predictive biomarkers used for clinical therapy and prognostic evaluation of high… 
2018
2018
Abstract 3554: The role of P2RY14 in acute leukemia
Leukemia is a group of blood cancers that originate in the bone marrow and involves uncontrolled proliferation of different types… 
2017
2017
Role of the g-protein-coupled receptor p2ry14 in acute leukemia
Leukemia involves uncontrolled proliferation of different types of blood cells. Accordingly, it is classified as Acute myeloid… 
2015
2015
UTP activates small conductance Ca 2 +-activated K + ( SK ) channels in 1 murine detrusor PDGFRα + cells
14 Purines induce transient contraction and prolonged relaxation of detrusor muscles. 15 Transient contraction is likely due to… 
2013
2013
Transcriptome Analysis of Genes Regulated by Cholesterol Loading in Two Strains of Mouse Macrophages Associates Lysosome Pathway and ER Stress Response with Atherosclerosis Susceptibility
Cholesterol loaded macrophages in the arterial intima are the earliest histological evidence of atherosclerosis. Studies of mouse… 
2009
2009
The UDP-Glucose Receptor P2RY14 Triggers Innate Mucosal Immunity in the Female Reproductive Tract by Inducing IL-81
Innate mucosal immune responses, including recognition of pathogen-associated molecular patterns through Toll-like receptors… 
2009
2009
Gene expression signature of chronic lymphocytic leukaemia with Trisomy 12
Background  The prognosis of chronic lymphocytic leukaemia (CLL) patients is largely determined by the karyotype of the malignant… 
2000
2000
A sequence-ready map of the Usher syndrome type III critical region on chromosome 3q.
Usher syndrome type 3 (USH3; MIM 276902) is an autosomal recessive disorder associated with progressive hearing loss and retinal… 
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