Clinical and Genetic Heterogeneity in Multifocal Vitelliform Dystrophy
Boon et al.
Arch Ophthalmol 2007;125:1100-1106.
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Differential Macular and Peripheral Expression of Bestrophin in Human Eyes and Its Implication for Best Disease
Mullins et al.
IOVS 2007;48:3372-3380.
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Fundus autofluorescence in exudative age-related macular degeneration
McBain et al.
Br. J. Ophthalmol. 2007;91:491-496.
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VMD2 Promoter Requires Two Proximal E-box Sites for Its Activity in Vivo and Is Regulated by the MITF-TFE Family
Esumi et al.
J. Biol. Chem. 2007;282:1838-1850.
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The Light Peak of the Electroretinogram Is Dependent on Voltage-gated Calcium Channels and Antagonized by Bestrophin (Best-1)
Marmorstein et al.
J. Gen. Physiol. 2006;127:577-589.
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Late Development of Vitelliform Lesions and Flecks in a Patient With Best Disease: Clinicopathologic Correlation
Mullins et al.
Arch Ophthalmol 2005;123:1588-1594.
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Looking Chloride Channels Straight in the Eye: Bestrophins, Lipofuscinosis, and Retinal Degeneration
Hartzell et al.
Physiology 2005;20:292-302.
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The Retinal Pigment Epithelium in Visual Function
Strauss
Physiol. Rev. 2005;85:845-881.
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Structure and Function of CLCA Proteins
Loewen and Forsyth
Physiol. Rev. 2005;85:1061-1092.
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Quantitative Phenotyping of Chromatic Dysfunction in Best Macular Dystrophy
Campos et al.
Arch Ophthalmol 2005;123:944-949.
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Nutritional Manipulation of Primate Retinas, II: Effects of Age, n-3 Fatty Acids, Lutein, and Zeaxanthin on Retinal Pigment Epithelium
Leung et al.
IOVS 2004;45:3244-3256.
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Analysis of the VMD2 Promoter and Implication of E-box Binding Factors in Its Regulation
Esumi et al.
J. Biol. Chem. 2004;279:19064-19073.
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Structure-Function Analysis of the Bestrophin Family of Anion Channels
Tsunenari et al.
J. Biol. Chem. 2003;278:41114-41125.
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The genetics of inherited macular dystrophies
Michaelides et al.
J. Med. Genet. 2003;40:641-650.
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Bestrophin Interacts Physically and Functionally with Protein Phosphatase 2A
Marmorstein et al.
J. Biol. Chem. 2002;277:30591-30597.
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The vitelliform macular dystrophy protein defines a new family of chloride channels
Sun et al.
Proc. Natl. Acad. Sci. USA 2002;99:4008-4013.
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Biosynthetic Studies of A2E, a Major Fluorophore of Retinal Pigment Epithelial Lipofuscin
Ben-Shabat et al.
J. Biol. Chem. 2002;277:7183-7190.
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Blue Light-Induced Apoptosis of A2E-Containing RPE: Involvement of Caspase-3 and Protection by Bcl-2
Sparrow and Cai
IOVS 2001;42:1356-1362.
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Photodamage to Human RPE Cells by A2-E, a Retinoid Component of Lipofuscin
Schütt et al.
IOVS 2000;41:2303-2308.
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Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease
Lois et al.
Br. J. Ophthalmol. 2000;84:741-745.
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Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration
Lotery et al.
IOVS 2000;41:1291-1296.
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A2E, a Lipofuscin Fluorophore, in Human Retinal Pigmented Epithelial Cells in Culture
Sparrow et al.
IOVS 1999;40:2988-2995.
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Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope
Lois et al.
Br. J. Ophthalmol. 1999;83:276-279.
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Cone-Rod Dystrophy With Serpentine-like Retinal Deposits
Kellner
Arch Ophthalmol 1998;116:1307-1313.
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Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6q
Reichel et al.
Br. J. Ophthalmol. 1998;82:1162-1168.
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A Gene Map of the Best's Vitelliform Macular Dystrophy Region in Chromosome 11q12-q13.1
Stöhr et al.
Genome Res. 1998;8:48-56.
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Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium
Marmorstein et al.
Proc. Natl. Acad. Sci. USA 2000;97:12758-12763.
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