Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
about
Folding mechanism of the metastable serpin α1-antitrypsin.Substrate recognition in nuclear protein quality control degradation is governed by exposed hydrophobicity that correlates with aggregation and insolubility.Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants.Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy.Functional analysis of novel alpha-1 antitrypsin variants G320R and V321F.
P2860
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@en
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@nl
type
label
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@en
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@nl
prefLabel
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@en
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@nl
P2093
P2860
P356
P1433
P1476
Retarded protein folding of deficient human alpha 1-antitrypsin D256V and L41P variants.
@en
P2093
P2860
P304
P356
10.1110/PS.03356604
P577
2004-02-06T00:00:00Z