BACKGROUND: DBA/2J (D2) mice develop an age-related form of glaucoma. Their eyes progressively develop iris pigment dispersion and iris atrophy followed by increased intraocular pressure (IOP) and glaucomatous optic nerve damage. Mutant alleles of the Gpnmb and Tyrp1 genes are necessary for the iris disease, but it is unknown whether alleles of other D2 gene(s) are necessary for the distinct later stages of disease. We initiated a study of congenic strains to further define the genetic requirements and disease mechanisms of the D2 glaucoma. RESULTS: To further understand D2 glaucoma, we created congenic strains of mice on the C57BL/6J (B6) genetic background. B6 double-congenic mice carrying D2-derived Gpnmb and Tyrp1 mutations de...
PURPOSE: Mutations in the gene encoding collagen type IV alpha 1 (COL4A1) cause multisystem disorder...
Purpose: The DBA/2J (D2) mouse carries mutations in two of its genes, Tyrp1 and Gpnmb. These alterat...
BACKGROUND: The molecular mechanisms causing pigment dispersion syndrome (PDS) and the pathway(s) by...
BACKGROUND: The glaucomas are a common but incompletely understood group of diseases. DBA/2J mice de...
A variety of inherited animal models with different genetic causes and distinct genetic backgrounds ...
BACKGROUND: Glaucoma is a common disease but its molecular etiology is poorly understood. It involve...
Abstract Background The glaucomas are a common but incompletely understood group of diseases. DBA/2J...
Abstract Background Glaucoma is a common disease but its molecular etiology is poorly understood. It...
A variety of inherited animal models with different genetic causes and distinct genetic backgrounds ...
Glaucomas are a major cause of blindness. Visual loss typically involves retinal ganglion cell death...
Pigmentary glaucoma is a significant cause of human blindness. Abnormally liberated iris pigment and...
PURPOSE. In this study parameters relevant for glaucoma in DBA/2J (D2J) mice were compared with thos...
PURPOSE: To characterize ocular abnormalities associated with iris atrophy in DBA/2J mice and to det...
The glaucomas are neurodegenerative diseases involving death of retinal ganglion cells and optic ner...
BackgroundThe molecular mechanisms causing pigment dispersion syndrome (PDS) and the pathway(s) by w...
PURPOSE: Mutations in the gene encoding collagen type IV alpha 1 (COL4A1) cause multisystem disorder...
Purpose: The DBA/2J (D2) mouse carries mutations in two of its genes, Tyrp1 and Gpnmb. These alterat...
BACKGROUND: The molecular mechanisms causing pigment dispersion syndrome (PDS) and the pathway(s) by...
BACKGROUND: The glaucomas are a common but incompletely understood group of diseases. DBA/2J mice de...
A variety of inherited animal models with different genetic causes and distinct genetic backgrounds ...
BACKGROUND: Glaucoma is a common disease but its molecular etiology is poorly understood. It involve...
Abstract Background The glaucomas are a common but incompletely understood group of diseases. DBA/2J...
Abstract Background Glaucoma is a common disease but its molecular etiology is poorly understood. It...
A variety of inherited animal models with different genetic causes and distinct genetic backgrounds ...
Glaucomas are a major cause of blindness. Visual loss typically involves retinal ganglion cell death...
Pigmentary glaucoma is a significant cause of human blindness. Abnormally liberated iris pigment and...
PURPOSE. In this study parameters relevant for glaucoma in DBA/2J (D2J) mice were compared with thos...
PURPOSE: To characterize ocular abnormalities associated with iris atrophy in DBA/2J mice and to det...
The glaucomas are neurodegenerative diseases involving death of retinal ganglion cells and optic ner...
BackgroundThe molecular mechanisms causing pigment dispersion syndrome (PDS) and the pathway(s) by w...
PURPOSE: Mutations in the gene encoding collagen type IV alpha 1 (COL4A1) cause multisystem disorder...
Purpose: The DBA/2J (D2) mouse carries mutations in two of its genes, Tyrp1 and Gpnmb. These alterat...
BACKGROUND: The molecular mechanisms causing pigment dispersion syndrome (PDS) and the pathway(s) by...