Abnormal Cone Structure in Foveal Schisis Cavities in X-Linked Retinoschisis from Mutations in Exon 6 of the RS1 Gene
Duncan et al.
IOVS 2011;52:9614-9623.
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Tyrosinase Is the Modifier of Retinoschisis in Mice
Johnson et al.
Genetics 2010;186:1337-1344.
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Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis
Sergeev et al.
Hum Mol Genet 2010;19:1302-1313.
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Null Retinoschisin-Protein Expression from an RS1 c354del1-ins18 Mutation Causing Progressive and Severe XLRS in a Cross-Sectional Family Study
Vijayasarathy et al.
IOVS 2009;50:5375-5383.
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Macular spectral-domain optical coherence tomography in patients with X linked retinoschisis
Gregori et al.
Br J Ophthalmol 2009;93:373-378.
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Genetic Modification of the Schisis Phenotype in a Mouse Model of X-Linked Retinoschisis
Johnson et al.
Genetics 2008;178:1785-1794.
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Retinoschisin Gene Therapy and Natural History in the Rs1h-KO Mouse: Long-term Rescue from Retinal Degeneration
Kjellstrom et al.
IOVS 2007;48:3837-3845.
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X-linked retinoschisis: an update
Sikkink et al.
J. Med. Genet. 2007;44:225-232.
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Novel Phenotypic and Genotypic Findings in X-Linked Retinoschisis
Tsang et al.
Arch Ophthalmol 2007;125:259-267.
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Molecular pathology of X linked retinoschisis: mutations interfere with retinoschisin secretion and oligomerisation
Wang et al.
Br J Ophthalmol 2006;90:81-86.
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X-linked retinoschisis: clinical phenotype and RS1 genotype in 86 UK patients
Pimenides et al.
J. Med. Genet. 2005;42:e35-e35.
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RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis
Zeng et al.
IOVS 2004;45:3279-3285.
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A Retinal Neuronal Developmental Wave of Retinoschisin Expression Begins in Ganglion Cells during Layer Formation
Takada et al.
IOVS 2004;45:3302-3312.
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Multifocal Electroretinograms in X-Linked Retinoschisis
Piao et al.
IOVS 2003;44:4920-4930.
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Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families
Simonelli et al.
Br J Ophthalmol 2003;87:1130-1134.
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Defective Discoidin Domain Structure, Subunit Assembly, and Endoplasmic Reticulum Processing of Retinoschisin are Primary Mechanisms Responsible for X-linked Retinoschisis
Wu and Molday
J. Biol. Chem. 2003;278:28139-28146.
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Retinoschisin, a Photoreceptor-Secreted Protein, and Its Interaction with Bipolar and Muller Cells
Reid et al.
J. Neurosci. 2003;23:6030-6040.
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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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High-Frequency Attenuation of the Cone ERG and ON-Response Deficits in X-linked Retinoschisis
Alexander et al.
IOVS 2001;42:2094-2101.
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Expression of X-Linked Retinoschisis Protein RS1 in Photoreceptor and Bipolar Cells
Molday et al.
IOVS 2001;42:816-825.
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ON-Response Deficit in the Electroretinogram of the Cone System in X-Linked Retinoschisis
Alexander et al.
IOVS 2001;42:453-459.
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Phenotypic Expression of Juvenile X-linked Retinoschisis in Swedish Families With Different Mutations in the XLRS1 Gene
Eksandh et al.
Arch Ophthalmol 2000;118:1098-1104.
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Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells
Grayson et al.
Hum Mol Genet 2000;9:1873-1879.
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X-Linked Retinoschisis With Point Mutations in the XLRS1 Gene
Inoue et al.
Arch Ophthalmol 2000;118:93-96.
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Optical Cross-sectional Imaging of the Macula With the Retinal Thickness Analyzer in X-linked Retinoschisis
Tanna et al.
Arch Ophthalmol 1998;116:1036-1041.
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Familial Internal Limiting Membrane Dystrophy: A New Sheen Retinal Dystrophy
Polk et al.
Arch Ophthalmol 1997;115:878-885.
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Clinical Features in Affected Males With X-Linked Retinoschisis
George et al.
Arch Ophthalmol 1996;114:274-280.
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A{degrees}land Island Eye Disease (Forsius-Eriksson Syndrome) Associated With Contiguous Deletion Syndrome at Xp21: Similarity to Incomplete Congenital Stationary Night Blindness
Weleber et al.
Arch Ophthalmol 1989;107:1170-1179.
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