Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

CRYGA gene

Known as: crystallin gamma A, CRY-g-A, CRYGA 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Genes are transcribed in irregular pulses of activity termed transcriptional bursts. Cellular differentiation requires… Expand
  • figure 8
  • figure 11
2018
2018
Congenital cataract (CC) is a significant cause of childhood blindness worldwide. CC is a genetically heterogeneous disease… Expand
2010
2010
Purpose Identification of causal mutation in the crystallin, connexin, and paired box gene 6 (PAX6) genes associated with… Expand
  • table 1
  • table 1
  • figure 1
  • figure 2
  • figure 4
2010
2010
Primary cataracts (CAT) are characterized as any form of opacities of the eye lenses and are not accompanied by other diseases… Expand
  • figure 1
  • table 1
  • table 2
  • table 4
2009
2009
Aim: Polymorphisms in γ-crystallins (CRYG) can serve as markers for lens differentiation and eye disorders leading to cataract… Expand
2006
2006
OBJECTIVE To identify genetic defects associated with autosomal dominant congenital golden crystal nuclear cataract (ADCC) in a… Expand
2005
2005
PURPOSE To identify genetic defects associated with nuclear golden crystal autosomal dominant congenital cataract (ADCC) in a… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
2000
2000
Abstract. We have summarized our extensive series of mutagenesis experiments to isolate dominant mutations in the mouse that… Expand
  • table 1
  • table 2
1997
1997
Based upon DNA sequence analysis of the promoters from six gamma-crystallin genes (cryga-->crygf) a 36-bp DNA fragment was… Expand
Highly Cited
1996
Highly Cited
1996
Cataract is one of the major causes of blindness in humans. We describe here an autosomal dominant polymorphic congenital… Expand