NR2E3 gene

Known as: rd7, RP37, PNR 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2016
024620002016

Papers overview

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2008
2008
Neural developmental programs require a high level of coordination between the decision to exit cell cycle and acquisition of… (More)
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2007
2007
"Autosomal dominant retinitis pigmentosa" (adRP) refers to a genetically heterogeneous group of retinal dystrophies, in which 54… (More)
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2007
2007
PURPOSE Mutations in the orphan nuclear receptor gene NR2E3 have been found to cause both recessive and dominant retinopathies… (More)
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2006
2006
Rod and cone photoreceptors in mammalian retina are generated from common pool(s) of neuroepithelial progenitors. NRL, CRX and… (More)
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2006
2006
The transcription factor Nr2e3 is an essential component for development and specification of rod and cone photoreceptors… (More)
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Highly Cited
2004
Highly Cited
2004
NR2E3, a photoreceptor-specific orphan nuclear receptor, is believed to play a pivotal role in the differentiation of… (More)
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2004
2004
PURPOSE To study the physiological function of NR2E3 and possible molecular mechanisms underlying enhanced short-wavelength cone… (More)
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Highly Cited
2002
Highly Cited
2002
Normal human retinal development involves orderly generation of rods and cones by complex mechanisms. Cell-fate specification… (More)
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Highly Cited
2001
Highly Cited
2001
The rd7 mouse is a model for hereditary retinal degeneration characterized clinically by retinal spotting throughout the fundus… (More)
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Highly Cited
2000
Highly Cited
2000
Hereditary human retinal degenerative diseases usually affect the mature photoreceptor topography by reducing the number of cells… (More)
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