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NYX gene

Known as: CLRP, NYCTALOPIN, CSNB1A 
National Institutes of Health

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.
Review
2015
Review
2015
Synthesis and analytical applications of molecularly imprinted polymers on the surface of carbon nanotubes: a review
AbstractThis review (with 142 references) summarize the state of the art in molecularly imprinting technology as applied to the… 
Highly Cited
2011
Highly Cited
2011
TRPM1 Forms Complexes with Nyctalopin In Vivo and Accumulates in Postsynaptic Compartment of ON-Bipolar Neurons in mGluR6-Dependent Manner
Synaptic transmission between light-sensory photoreceptor cells and downstream ON-bipolar neurons plays an important role for… 
Highly Cited
2011
Highly Cited
2011
A Role for Nyctalopin, a Small Leucine-Rich Repeat Protein, in Localizing the TRP Melastatin 1 Channel to Retinal Depolarizing Bipolar Cell Dendrites
Expression of channels to specific neuronal sites can critically impact their function and regulation. Currently, the molecular… 
Review
2010
Review
2010
Drug delivery systems: Advanced technologies potentially applicable in personalized treatments
Advanced drug delivery systems (DDS) present indubitable benefits for drug administration. Over the past three decades, new… 
Highly Cited
2006
Highly Cited
2006
Failure to Maintain Eye-Specific Segregation in nob, a Mutant with Abnormally Patterned Retinal Activity
Highly Cited
2005
Highly Cited
2005
Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness.
Retinal on-pathway dysfunction is implicated in human complete-type congenital stationary night blindness (CSNB1), a Mendelian… 
Highly Cited
2003
Highly Cited
2003
Immunohistochemical analysis of the outer plexiform layer in the nob mouse shows no abnormalities
In the nob mouse, a mutation in nyctalopin results in a loss of signal transmission from photoreceptors to depolarizing bipolar… 
2001
2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
PURPOSE To study the slow and fast rod signals of the scotopic 15-Hz flicker ERG in patients carrying mutations in the NYX gene… 
Highly Cited
2000
Highly Cited
2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
During development, visual photoreceptors, bipolar cells and other neurons establish connections within the retina enabling the… 
Highly Cited
2000
Highly Cited
2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
X-linked congenital stationary night blindness (XLCSNB) is characterized by impaired scotopic vision with associated ocular… 
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