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Protein-protein interactions involving congenital cataract T5P γC-crystallin mutant: A confocal fluorescence microscopy study

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. Previous in vitro mutation studies indicate that the protein has changed conformation, solubility, and stability, which may...

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Detalhes bibliográficos
Main Authors: Liu, Bing-Fen, Song, Shuhua, Hanson, Mark, Liang, Jack J-N
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2644446/
https://ncbi.nlm.nih.gov/pubmed/18926820
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2008.08.021
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