GPR179 gene

Known as: GPR179, G PROTEIN-COUPLED RECEPTOR 179, CSNB1E 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2012-2016
012320122016

Papers overview

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2016
2016
Cacna1s encodes the α1S subunit (Cav1.1) of voltage-dependent calcium channels, and is required for normal skeletal and cardiac… (More)
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2016
2016
In vertebrate retina, light responses generated by the rod photoreceptors are transmitted to the second-order neurons, the ON… (More)
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2015
2015
Mutations in LRIT3 lead to complete congenital stationary night blindness (cCSNB). The exact role of LRIT3 in ON-bipolar cell… (More)
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2014
2014
Parallel visual pathways are initiated at the first retinal synapse by signaling between the rod and cone photoreceptors and two… (More)
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2013
2013
OBJECTIVE To investigate the relative frequency of the genetic causes of the Schubert-Bornschein type of congenital stationary… (More)
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2013
2013
Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous retinal disorder. Two forms can be… (More)
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2013
2013
PURPOSE Mutations in GPR179, which encodes the G protein-coupled receptor 179, lead to autosomal recessive complete (c… (More)
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2013
2013
PURPOSE Complete congenital stationary night blindness (CSNB1) is characterized by loss of night vision due to a defect in the… (More)
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2012
2012
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders… (More)
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2012
2012
The extent and temporal characteristics of G protein-coupled receptor (GPCR) signaling are shaped by the regulator of G protein… (More)
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