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NR2E3 gene
Known as:
rd7
, RP37
, PNR
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National Institutes of Health
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Related topics
1 relation
NR2E3 protein, human
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations
F. Collison
,
Jason C. Park
,
G. Fishman
,
E. Stone
,
J. McAnany
Documenta Ophthalmologica
2016
Corpus ID: 21194272
PurposeThe purpose of this study was to evaluate pupillary light reflexes (PLRs) mediated by rod, cone, and intrinsically…
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2016
2016
A transcription factor network controls cell migration and fate decisions in the developing zebrafish pineal complex
Sataree Khuansuwan
,
Joshua A. Clanton
,
Benjamin J. Dean
,
J. G. Patton
,
J. Gamse
Development
2016
Corpus ID: 5010230
The zebrafish pineal complex consists of four cell types (rod and cone photoreceptors, projection neurons and parapineal neurons…
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2016
2016
Manipulating photoreceptor gene expression with putative Nr2e3 modulators
Paul A Nakamura
,
Shibing Tang
,
Sheng Ding
,
T. Reh
2016
Corpus ID: 90865449
2013
2013
Novel mutations in enhanced S-cone syndrome.
K. Kuniyoshi
,
Takaaki Hayashi
,
+5 authors
Y. Shimomura
Ophthalmology (Rochester, Minn.)
2013
Corpus ID: 28085559
2011
2011
A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome
A. Rocha-Sousa
,
Takaaki Hayashi
,
+7 authors
F. Falcão-Reis
Graefe's Archive for Clinical and Experimental…
2011
Corpus ID: 14679342
BackgroundEnhanced S-cone syndrome (ESCS) is an autosomal recessive retinal disorder characterized by an increased number of S…
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2010
2010
Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese population.
Yaping Yang
,
Xin Zhang
,
+7 authors
C. Pang
Investigative Ophthalmology and Visual Science
2010
Corpus ID: 21671175
Purpose. Mutations in the NR2E3 and NRL genes have been implicated in both autosomal dominant and autosomal recessive retinitis…
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2010
2010
Helicoid subretinal fibrosis associated with a novel recessive NR2E3 mutation p.S44X.
Arif O. Khan
,
Mohammed A. Aldahmesh
,
E. Al-Harthi
,
F. Alkuraya
A M A Archives of Ophthalmology
2010
Corpus ID: 39174990
OBJECTIVES To describe a unique pattern of helicoid subretinal fibrosis associated with a novel recessive NR2E3 mutation and to…
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2009
2009
The Nuclear Receptor Gene Nr1d1 Functions With Nr2e3 to Regulate the Expression of Photoreceptor-Specific Genes
N. Mollema
,
A. Nystuen
,
N. Haider
2009
Corpus ID: 83457592
2008
2008
A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3rd7/rd7 retinas
A. Nystuen
,
A. Sachs
,
Yang Yuan
,
L. Heuermann
,
N. Haider
Mammalian Genome
2008
Corpus ID: 25940426
The nmf193 mutant was generated by a large-scale ENU mutagenesis screen and originally described as having a dominantly inherited…
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1990
1990
Analyse en CLHP des substances produites par le palmier à huile au cours de l'infection par le Fusarium oxysporum f. sp. elaeidis: perspectives pour la sélection
B. Taquet
,
S. Diabaté
,
J. Renard
,
H. Franqueville
,
P. Reiser
1990
Corpus ID: 132368958
Le principe de la technique de chromatographie liquide a haute performance (HPLC) reside en la separation fine et en la…
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