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Coppock-Like Cataract
Also Known As:
Cataract, Coppock-Like; Cataract, Embryonic Nuclear
Networked:
4
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Eye Diseases: 3522
Lens Diseases: 7
Cataract: 28071
Coppock-Like Cataract: 4
Related Diseases
1.
Cataract (Cataracts)
Experts
1.
Liang, Jack J-N
: 2 articles (12/2008 - 09/2004)
2.
Hanson, Mark
: 1 article (12/2008)
3.
Liu, Bing-Fen
: 1 article (12/2008)
4.
Song, Shuhua
: 1 article (12/2008)
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Coppock-Like Cataract:
1.
gamma-Crystallins
IBA
02/01/1994 - "
Reactivation of the psi gamma E gene and concomitant overexpression of the gamma-crystallin fragment could be the cause of the Coppock-like cataract.
"
02/01/1994 - "
The locus for the hereditary human Coppock-like cataract (CCL) is closely linked to a particular combination of polymorphic TaqI sites within the human gamma-crystallin gene cluster.
"
01/01/1987 - "
The absolute correlation between the presence of haplotype P and cataract within this family shows that the gamma-crystallin gene cluster and the locus for the Coppock-like cataract are closely linked [logarithm of odds (lod) score of 7.58 at its maximum at phi = 0].
"
2.
Crystallins (Crystallin)
IBA
12/01/2008 - "
The human lens crystallin gene CRYGC T5P is associated with Coppock-like cataract and has a phenotype of a dust-like opacity of the fetal lens nucleus and deep cortical region.
"
09/01/2004 - "
Together with previous results obtained with a two-hybrid system assay of interactions between alphaA- and gammaC-crystallin, the present FRET and chaperone results indicate that loss of interactions of T5P mutant with other crystallins may play a larger role than the protection afforded by chaperone-like activity in Coppock-like cataract.
"
09/01/2004 - "
T5P gammaC-crystallin mutation is associated with Coppock-like cataract, one of the autosomal dominant congenital cataracts.
"
3.
crystallin gammaE
IBA
02/01/1994 - "
Activation of the gamma E-crystallin pseudogene in the human hereditary Coppock-like cataract.
"