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Nyctalopin
Recessive Mutations of the Gene TRPM1 Abrogate on Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans
Two Novel NYX Gene Mutations in the Chinese Families with X-Linked
A Role for Nyctalopin, a Small Leucine-Rich Repeat Protein, in Localizing the TRP Melastatin 1 Channel to Retinal Depolarizing Bipolar Cell Dendrites
Thirty Distinct CACNA1F Mutations in 33 Families with Incomplete Type of XLCSNB and Cacna1f Expression Profiling in Mouse Retina
Resisting Drugs New Light on Night Blindness
Human Recombinant Protein – TP316019
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Agricultural University of Athens
Congenital Disorder of Glycosylation Due to Phosphomannomutase Deficiency
In Vivo Development of Retinal ON-Bipolar Cell Axonal Terminals Visualized in Nyx::MYFP Transgenic Zebrafish
(Nyctalopin on Chromosome X), the Gene Mutated in Congenital Stationary Night Blindness, Encodes a Cell Surface Protein
V13a36-Zhang Pgmkr
Nyctalopin Is Essential for Synaptic Transmission in the Cone Dominated Zebrafish Retina
Small Leucine-Rich Proteoglycans (Slrps) in the Retina
Mouse Models Neal S. Peachey Cole Eye Institute, Cleveland
'Genotyping Microarray for CSNB-Associated Genes'
A Novel Gene, TRPM1 Is Mutated in Patients with Complete Autosomal
BII – Gene Function Prediction Publications 157 Goh F, Zhang MM, Lim TR, Low KN, Nge CE, Heng E, Yeo WL, Sirota FL, Crasta S
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Elucidating the Genetic Basis of Canine Progressive Retinal Atrophies in Several Breeds of Dog
Molecular Genetics of Infantile-Onset Retinal Dystrophies
11521.Full.Pdf
Two R7 Regulator of G-Protein Signaling Proteins Shape Retinal Bipolar Cell Signaling
Molecular Pathology of Autosomal Recessive Retinal Disease
The Familial Dementia Gene Revisited: a Missense Mutation Revealed By
NYX Mutations in Four Families with High Myopia with Or Without CSNB1
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Product Datasheet Qprest
NYX Gene Nyctalopin
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency
(12) Patent Application Publication (10) Pub. No.: US 2015/0366997 A1 Guild Et Al
Outer Retinal Structural Anomaly Due to Frameshift Mutation in CACNA1F Gene 1 Ahmed Y, Schimel AM, Pathengay A, Colyer MH, Flynn HW Jr
Isolation of the Mouse Nyctalopin Gene Nyx and Expression Studies in Mouse and Rat Retina
LRIT3 Is Required for Nyctalopin Expression and Normal on and OFF Pathway Signaling in the 2 Retina 3 4 Nazarul Hasan1,Gobinda Pangeni2 ,Thomas A
Topology and Function of Nyctalopin in Yeast and In-Vitro Translation Systems
LRIT3 Is Required for Nyctalopin Expression and Normal on and OFF Pathway Signaling in the Retina
Identification and Functional Characterization of Gene Defects Underlying Congenital Stationary Night Blindness (Csnb) Marion Neuille
TRPM1 Is Required for the Depolarizing Light Response in Retinal ON-Bipolar Cells