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NYX gene
Known as:
CLRP
, NYCTALOPIN
, CSNB1A
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National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Night Blindness, Congenital Stationary, Type 1A
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
NYX mutations in four families with high myopia with or without CSNB1
Lin Zhou
,
Tuo Li
,
Xiu-sheng Song
,
Yin Li
,
Hongyan Li
,
Handong Dan
Molecular Vision
2015
Corpus ID: 17793658
Purpose Mutations in the NYX gene are known to cause complete congenital stationary night blindness (CSNB1), which is always…
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2013
2013
Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.
J. Klooster
,
M. V. van Genderen
,
+6 authors
M. Kamermans
Investigative Ophthalmology and Visual Science
2013
Corpus ID: 20241991
PURPOSE Complete congenital stationary night blindness (CSNB1) is characterized by loss of night vision due to a defect in the…
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2012
2012
Topological Analysis of Small Leucine-Rich Repeat Proteoglycan Nyctalopin
Pasano Bojang
,
R. Gregg
PLoS ONE
2012
Corpus ID: 6274241
Nyctalopin is a small leucine rich repeat proteoglycan (SLRP) whose function is critical for normal vision. The absence of…
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2006
2006
CSNB1 in Chinese families associated with novel mutations inNYX
Xueshan Xiao
,
Xiao-yun Jia
,
Xiangming Guo
,
Shi-qiang Li
,
Zhikuan Yang
,
Qingjiong Zhang
Journal of Human Genetics
2006
Corpus ID: 10267552
AbstractX-linked congenital stationary night blindness (CSNB) and NYX mutation have not been reported in Chinese. Here, two…
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Review
2005
Review
2005
Focus on molecules: nyctalopin.
S. Poopalasundaram
,
L. Erskine
,
M. Cheetham
,
A. Hardcastle
Experimental Eye Research
2005
Corpus ID: 526951
2005
2005
Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat protein.
E. O'Connor
,
B. Eisenhaber
,
+5 authors
D. Trump
Human Molecular Genetics
2005
Corpus ID: 24239463
Mutations in the gene NYX, which encodes nyctalopin, lead to the retinal disorder congenital stationary night blindness which is…
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2003
2003
NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.
C. Zeitz
,
H. Scherthan
,
+4 authors
W. Berger
Investigative Ophthalmology and Visual Science
2003
Corpus ID: 7969480
PURPOSE The complete type of X-linked congenital stationary night blindness (CSNB1) in human and mouse is caused by mutations in…
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2003
2003
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina.
K. Pesch
,
C. Zeitz
,
+5 authors
B. Wissinger
Investigative Ophthalmology and Visual Science
2003
Corpus ID: 1235431
PURPOSE It has been shown recently that mutations in NYX (nyctalopin on chromosome X), encoding a novel protein associated with…
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2003
2003
Nyctalopin Is Required for Signaling Through Depolarizing Bipolar Cells in the Murine Retina
R. Gregg
,
P. Lukasiewicz
,
N. Peachey
,
B. Sagdullaev
,
M. McCall
2003
Corpus ID: 83020462
1992
1992
Anaerobic Production of Extracellular Polysaccharide by Butyrivibrio fibrisolvens nyx
D. Wachenheim
,
J. Patterson
Applied and Environmental Microbiology
1992
Corpus ID: 9458798
Anaerobic production of extracellular polysaccharide (EP) was examined, using a previously uncharacterized, obligately anaerobic…
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