In vivo lens deficiency of the R49C alphaA-crystallin mutant.
about
In vivo substrates of the lens molecular chaperones αA-crystallin and αB-crystallinExpression of the HSF4 DNA binding domain-EGFP hybrid gene recreates early childhood lamellar cataract in transgenic miceA knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataracts.PON-Sol: prediction of effects of amino acid substitutions on protein solubility.Differential role of arginine mutations on the structure and functions of α-crystallin.Truncation attenuates molecular chaperoning and apoptosis inhibition by p26, a small heat shock protein from Artemia franciscana.Quantitative biometric phenotype analysis in mouse lenses.Autophagy and UPR in alpha-crystallin mutant knock-in mouse models of hereditary cataractsActivation of the unfolded protein response by a cataract-associated αA-crystallin mutation.SODA: prediction of protein solubility from disorder and aggregation propensity.
P2860
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P2860
In vivo lens deficiency of the R49C alphaA-crystallin mutant.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
In vivo lens deficiency of the R49C alphaA-crystallin mutant.
@en
type
label
In vivo lens deficiency of the R49C alphaA-crystallin mutant.
@en
prefLabel
In vivo lens deficiency of the R49C alphaA-crystallin mutant.
@en
P2860
P1476
In vivo lens deficiency of the R49C alphaA-crystallin mutant
@en
P2093
Matthew A Reilly
Usha P Andley
P2860
P304
P356
10.1016/J.EXER.2010.02.009
P577
2010-02-23T00:00:00Z