The murine mutation, Cat Fraser (Cat(Fr)), causes dominantly inherited ocular cataracts. Lenses of adult mice bearing this mutation contain reduced amounts of all seven γ-crystallin proteins and their corresponding transcripts. Levels of other lens proteins and transcripts appear normal and no extra-ocular effects of the mutation have been observed. The selective effect of this mutation on the γ-crystallins is consistent with the possibility that the site at which it occurs is involved in the coordinated regulation of the family of genes which encodes them. We have shown that several restriction fragment length polymorphisms in the γ-crystallin genes segregate independently of the Cat(Fr) mutation. Therefore, despite its selective effect on...
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...
A novel ENU-induced mutation in the mouse leading to a nuclear and cortical opacity of the eye lens ...
PURPOSE: A previous study had found a mouse mutant to have bilateral nuclear cataract with zonular o...
A number of murine cataract mutations have been localized to chromosome 1 close to the γ-crystallin ...
During a large-scale ENU mutagenesis screen, a mouse mutant with a dominant cataract was detected an...
peer reviewedDuring a large-scale ENU mutagenesis screen, a mouse mutant with a dominant cataract wa...
During a large-scale ENU mutagenesis screen, a mouse mutant with a dominant cataract was detected an...
During the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominant cataracts. ...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
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. ...
Mice bearing the mutant gene Cat:Fr have dominantly inherited congenital cataracts, which are more e...
SummaryDespite the fact that cataracts constitute the leading cause of blindness worldwide, the mech...
PURPOSE: During an ethylnitrosourea (ENU) mutagenesis screen, mice were tested for the occurrence of...
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...
A novel ENU-induced mutation in the mouse leading to a nuclear and cortical opacity of the eye lens ...
PURPOSE: A previous study had found a mouse mutant to have bilateral nuclear cataract with zonular o...
A number of murine cataract mutations have been localized to chromosome 1 close to the γ-crystallin ...
During a large-scale ENU mutagenesis screen, a mouse mutant with a dominant cataract was detected an...
peer reviewedDuring a large-scale ENU mutagenesis screen, a mouse mutant with a dominant cataract wa...
During a large-scale ENU mutagenesis screen, a mouse mutant with a dominant cataract was detected an...
During the mouse ENU mutagenesis screen, mice were tested for the occurrence of dominant cataracts. ...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
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. ...
Mice bearing the mutant gene Cat:Fr have dominantly inherited congenital cataracts, which are more e...
SummaryDespite the fact that cataracts constitute the leading cause of blindness worldwide, the mech...
PURPOSE: During an ethylnitrosourea (ENU) mutagenesis screen, mice were tested for the occurrence of...
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...
A novel ENU-induced mutation in the mouse leading to a nuclear and cortical opacity of the eye lens ...