The clinical and histologic features are reported of an autosomal dominant mouse cataract that was first observed as a new mutation in a cross between BALB/cJ and AKR/J. In the homozygous state, the eyes were microphthalmic, and a dense white cataract was present when the eyes opened at day 12. Histologic changes were apparent from birth and as early as 18 days\u27 gestation. Liquefaction started by day 4, and herniation of lens contents posteriorly was seen at day 11. Heterozygous mice had variable expression depending both on their genetic background and age. When the single gene was expressed fully, the cataract appeared as a fetal nuclear white opacity; partial expression gave a nuclear haze to snowflake nuclear opacities. Lo...
Congenital cataract is a leading cause of visual disability among children worldwide, it has a heter...
During an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an autosomal do...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
PURPOSE. The purpose of this study was the characterization of eight new dominant cataract mutations...
During the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominant cataracts. ...
peer reviewedDuring the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominan...
During the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominant cataracts. ...
This study was initiated to identify causal mutations responsible for autosomal recessive congenital...
We established a recessive cataract model from a spontaneous mutation in the KUNMING outbred mice. L...
A mouse mutant expressing a bilateral nuclear and radial cataract was found after paternal treatment...
Mouse mutants are a long-lasting, valuable tool to identify genes underlying eye diseases, because t...
peer reviewedDuring an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an...
We analyzed the offspring of paternally N-ethyl-N-nitrosourea (ENU) treated C57BL/6J mice for eye-si...
A dominant induced mutation in the mouse, tightly associated with a reciprocal chromosomal transloca...
Congenital cataract is a leading cause of visual disability among children worldwide, it has a heter...
During an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an autosomal do...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
PURPOSE. The purpose of this study was the characterization of eight new dominant cataract mutations...
During the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominant cataracts. ...
peer reviewedDuring the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominan...
During the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominant cataracts. ...
This study was initiated to identify causal mutations responsible for autosomal recessive congenital...
We established a recessive cataract model from a spontaneous mutation in the KUNMING outbred mice. L...
A mouse mutant expressing a bilateral nuclear and radial cataract was found after paternal treatment...
Mouse mutants are a long-lasting, valuable tool to identify genes underlying eye diseases, because t...
peer reviewedDuring an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an...
We analyzed the offspring of paternally N-ethyl-N-nitrosourea (ENU) treated C57BL/6J mice for eye-si...
A dominant induced mutation in the mouse, tightly associated with a reciprocal chromosomal transloca...
Congenital cataract is a leading cause of visual disability among children worldwide, it has a heter...
During an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an autosomal do...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...