Nyctalopin Expression in Retinal Bipolar Cells Restores Visual Function in a Mouse Model of Complete X-Linked Congenital Stationary Night Blindness
Gregg et al.
J. Neurophysiol. 2007;98:3023-3033.
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A Novel CACNA1F Gene Mutation Causes Aland Island Eye Disease
Jalkanen et al.
IOVS 2007;48:2498-2502.
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Keratoconus associated with CSNB1
Nguyen et al.
Br. J. Ophthalmol. 2007;91:116-117.
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X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene
Jalkanen et al.
J. Med. Genet. 2006;43:699-704.
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Different amino Acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
Neidhardt et al.
IOVS 2006;47:1630-1635.
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Unilateral electronegative ERG of non-vascular aetiology
Robson et al.
Br. J. Ophthalmol. 2005;89:1620-1626.
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Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram
Zeitz et al.
IOVS 2005;46:4328-4335.
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Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina
Mansergh et al.
Hum Mol Genet 2005;14:3035-3046.
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Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat protein
O'Connor et al.
Hum Mol Genet 2005;14:1877-1887.
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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation
Hemara-Wahanui et al.
Proc. Natl. Acad. Sci. USA 2005;102:7553-7558.
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Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6
Dryja et al.
Proc. Natl. Acad. Sci. USA 2005;102:4884-4889.
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Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness
Khan et al.
J. Neurophysiol. 2005;93:481-492.
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Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance
Kabanarou et al.
Br. J. Ophthalmol. 2004;88:1018-1022.
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Genotype-phenotype correlation in British families with X linked congenital stationary night blindness
Allen et al.
Br. J. Ophthalmol. 2003;87:1413-1420.
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NYX (Nyctalopin on Chromosome X), the Gene Mutated in Congenital Stationary Night Blindness, Encodes a Cell Surface Protein
Zeitz et al.
IOVS 2003;44:4184-4191.
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Retinal and Optic Disc Atrophy Associated With a CACNA1F Mutation in a Japanese Family
Nakamura et al.
Arch Ophthalmol 2003;121:1028-1033.
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Isolation of the Mouse Nyctalopin Gene Nyx and Expression Studies in Mouse and Rat Retina
Pesch et al.
IOVS 2003;44:2260-2266.
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Identification of the Gene and the Mutation Responsible for the Mouse nob Phenotype
Gregg et al.
IOVS 2003;44:378-384.
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Role of the {beta}2 Subunit of Voltage-Dependent Calcium Channels in the Retinal Outer Plexiform Layer
Ball et al.
IOVS 2002;43:1595-1603.
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Preservation of Retinal Morphology and Functions in Royal College Surgeons Rat by Nilvadipine, a Ca2+ Antagonist
Yamazaki et al.
IOVS 2002;43:919-926.
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Slow and Fast Rod ERG Pathways in Patients with X-Linked Complete Stationary Night Blindness Carrying Mutations in the NYX Gene
Scholl et al.
IOVS 2001;42:2728-2736.
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Localization of the {alpha}1F Calcium Channel Subunit in the Rat Retina
Morgans
IOVS 2001;42:2414-2418.
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Novel CACNA1F Mutations in Japanese Patients with Incomplete Congenital Stationary Night Blindness
Nakamura et al.
IOVS 2001;42:1610-1616.
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Multifocal ERG Findings in Complete Type Congenital Stationary Night Blindness
Kondo et al.
IOVS 2001;42:1342-1348.
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Abnormalities of the Photoreceptor-Bipolar Cell Synapse in a Substrain of C57BL/10 Mice
Ruether et al.
IOVS 2000;41:4039-4047.
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Localization of the Mouse nob (no b-wave) Gene to the Centromeric Region of the X Chromosome
Candille et al.
IOVS 1999;40:2748-2751.
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Blue-on-Yellow Perimetry in the Complete Type of Congenital Stationary Night Blindness
Terasaki et al.
IOVS 1999;40:2761-2764.
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Electrophysiological evaluation of visual loss in Muller cell sheen dystrophy
Kellner et al.
Br. J. Ophthalmol. 1998;82:650-654.
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