ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome.
about
Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiencyThe structural basis of XRCC1-mediated DNA repairRole of ALADIN in human adrenocortical cells for oxidative stress response and steroidogenesisNeuroprotection resulting from insufficiency of RANBP2 is associated with the modulation of protein and lipid homeostasis of functionally diverse but linked pathways in response to oxidative stress.Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.Mutation of the zebrafish nucleoporin elys sensitizes tissue progenitors to replication stress.Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanismDNA polymerase β contains a functional nuclear localization signal at its N-terminus.Oxidative stress and adrenocortical insufficiency.Transcriptional profile of primary astrocytes expressing ALS-linked mutant SOD1.Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD).Importin 7 and Nup358 promote nuclear import of the protein component of human telomerase.Decreased Expression of a Gene Caused by a T-DNA Insertion in an Adjacent Gene in Arabidopsis.The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formation.Deficiency of ALADIN impairs redox homeostasis in human adrenal cells and inhibits steroidogenesis.The roles of the nuclear pore complex in cellular dysfunction, aging and disease.Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.Triple A syndrome in Japan.ALADIN is required for the production of fertile mouse oocytes.Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.Compensation for chronic oxidative stress in ALADIN null mice.
P2860
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P2860
ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome.
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@ast
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@en
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@nl
type
label
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@ast
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@en
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@nl
prefLabel
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@ast
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@en
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@nl
P2093
P2860
P356
P1476
ALADINI482S causes selective f ...... e stress in triple A syndrome.
@en
P2093
Akira Yasui
Hirohide Asai
Makito Hirano
Satoshi Ueno
Yoshiko Furiya
P2860
P304
P356
10.1073/PNAS.0505598103
P407
P577
2006-02-07T00:00:00Z