This study was initiated to identify causal mutations responsible for autosomal recessive congenital cataracts in consanguineous familial cases. in embryonic and postnatal mice lens was investigated with TaqMan probe. in mouse lens as early as embryonic day 15 (E15) that increased significantly until postnatal day 6 (P6) with steady level of expression thereafter. associated with autosomal recessive congenital nuclear cataracts
The clinical and histologic features are reported of an autosomal dominant mouse cataract that was f...
Studies on hereditary congenital cataracts have led to the identification of genes involved in forma...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in ...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in ...
<div><p>Purpose</p><p>This study was performed to investigate the genetic determinants of autosomal ...
<div><p>Purpose</p><p>To identify the molecular basis of non-syndromic autosomal recessive congenita...
PurposeTo investigate the genetic basis of autosomal recessive congenital cataracts (arCC) in a larg...
Cataracts (opacities of the lens) are frequent in the elderly, but rare in paediatric practice. Cong...
A mouse mutant expressing a bilateral nuclear and radial cataract was found after paternal treatment...
We established a recessive cataract model from a spontaneous mutation in the KUNMING outbred mice. L...
PURPOSE: A previous study had found a mouse mutant to have bilateral nuclear cataract with zonular o...
PURPOSE: A new mouse mutant with small lenses was identified within a mutagenesis screen. The aim of...
PURPOSE. The purpose of this study was the characterization of eight new dominant cataract mutations...
The clinical and histologic features are reported of an autosomal dominant mouse cataract that was f...
Studies on hereditary congenital cataracts have led to the identification of genes involved in forma...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in ...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in ...
<div><p>Purpose</p><p>This study was performed to investigate the genetic determinants of autosomal ...
<div><p>Purpose</p><p>To identify the molecular basis of non-syndromic autosomal recessive congenita...
PurposeTo investigate the genetic basis of autosomal recessive congenital cataracts (arCC) in a larg...
Cataracts (opacities of the lens) are frequent in the elderly, but rare in paediatric practice. Cong...
A mouse mutant expressing a bilateral nuclear and radial cataract was found after paternal treatment...
We established a recessive cataract model from a spontaneous mutation in the KUNMING outbred mice. L...
PURPOSE: A previous study had found a mouse mutant to have bilateral nuclear cataract with zonular o...
PURPOSE: A new mouse mutant with small lenses was identified within a mutagenesis screen. The aim of...
PURPOSE. The purpose of this study was the characterization of eight new dominant cataract mutations...
The clinical and histologic features are reported of an autosomal dominant mouse cataract that was f...
Studies on hereditary congenital cataracts have led to the identification of genes involved in forma...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...