Add to ORKGGenetic variations in ephrin type-A receptor 2 (EPHA2) have been associated with inherited and age-related forms of cataract in humans. Here, we have characterized the eye lens phenotype and transcript profile of germlin
The cellular and molecular mechanisms underlying the pathogenesis of cataracts leading to visual imp...
<p>(<b>A</b>) Schematic diagram showing the domains of EPHA2 receptor and the locations of four SAM ...
<div><p>The mammalian eye lens expresses a high concentration of crystallins (α, β and γ-crystallins...
Purpose: Age-related cataract is the leading cause of blindness worldwide. Variants in the EPHA2 gen...
Purpose: Age-related cataract is the leading cause of blindness worldwide. Variants in the EPHA2...
Purpose: Congenital cataract is a leading cause of childhood blindness. Mutations in the EPHA2 gene ...
Age-related cataract is the major cause of blindness worldwide. Both genetic and environmental facto...
Purpose: Our studies in mouse eye lenses demonstrate that ephrin-A5 and EphA2 are needed for normal ...
Purpose: Cataract is the major cause of vision-related disability worldwide. Mutations in the crysta...
PURPOSE: During an ethylnitrosourea (ENU) mutagenesis screen, mice were tested for the occurrence of...
<div><p>Rare germ-line mutations in the coding regions of the human EPHA2 gene (<i>EPHA2</i>) have b...
<div><p>The cellular and molecular mechanisms underlying the pathogenesis of cataracts leading to vi...
PURPOSE: A previous study had found a mouse mutant to have bilateral nuclear cataract with zonular o...
PURPOSE: This study analyzed genes associated with the morphology and regulation of ethylnitrosourea...
PURPOSE: A new mouse mutant with small lenses was identified within a mutagenesis screen. The aim of...
The cellular and molecular mechanisms underlying the pathogenesis of cataracts leading to visual imp...
<p>(<b>A</b>) Schematic diagram showing the domains of EPHA2 receptor and the locations of four SAM ...
<div><p>The mammalian eye lens expresses a high concentration of crystallins (α, β and γ-crystallins...
Purpose: Age-related cataract is the leading cause of blindness worldwide. Variants in the EPHA2 gen...
Purpose: Age-related cataract is the leading cause of blindness worldwide. Variants in the EPHA2...
Purpose: Congenital cataract is a leading cause of childhood blindness. Mutations in the EPHA2 gene ...
Age-related cataract is the major cause of blindness worldwide. Both genetic and environmental facto...
Purpose: Our studies in mouse eye lenses demonstrate that ephrin-A5 and EphA2 are needed for normal ...
Purpose: Cataract is the major cause of vision-related disability worldwide. Mutations in the crysta...
PURPOSE: During an ethylnitrosourea (ENU) mutagenesis screen, mice were tested for the occurrence of...
<div><p>Rare germ-line mutations in the coding regions of the human EPHA2 gene (<i>EPHA2</i>) have b...
<div><p>The cellular and molecular mechanisms underlying the pathogenesis of cataracts leading to vi...
PURPOSE: A previous study had found a mouse mutant to have bilateral nuclear cataract with zonular o...
PURPOSE: This study analyzed genes associated with the morphology and regulation of ethylnitrosourea...
PURPOSE: A new mouse mutant with small lenses was identified within a mutagenesis screen. The aim of...
The cellular and molecular mechanisms underlying the pathogenesis of cataracts leading to visual imp...
<p>(<b>A</b>) Schematic diagram showing the domains of EPHA2 receptor and the locations of four SAM ...
<div><p>The mammalian eye lens expresses a high concentration of crystallins (α, β and γ-crystallins...