Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism
about
Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiencyThe molecular biology, biochemistry, and physiology of human steroidogenesis and its disordersRole of ALADIN in human adrenocortical cells for oxidative stress response and steroidogenesisOxidative stress and adrenocortical insufficiency.Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD).Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73.The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formation.Regulation of neuronal ferritin heavy chain, a new player in opiate-induced chemokine dysfunctionIdentification of a novel putative interaction partner of the nucleoporin ALADIN.Deficiency of ALADIN impairs redox homeostasis in human adrenal cells and inhibits steroidogenesis.Nucleoporin genes in human diseases.The roles of the nuclear pore complex in cellular dysfunction, aging and disease.Genes for iron metabolism influence circadian rhythms in Drosophila melanogaster.ALADIN is required for the production of fertile mouse oocytes.Clinical and genetic characterisation of a series of patients with triple A syndrome.Compensation for chronic oxidative stress in ALADIN null mice.FHC, an NS4B-interacting Protein, Enhances Classical Swine Fever Virus Propagation and Acts Positively in Viral Anti-apoptosis.Serum ferritin is an important inflammatory disease marker, as it is mainly a leakage product from damaged cells
P2860
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P2860
Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@ast
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@en
Deficiency of ferritin heavy-c ...... the primary disease mechanism.
@nl
type
label
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@ast
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@en
Deficiency of ferritin heavy-c ...... the primary disease mechanism.
@nl
prefLabel
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@ast
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@en
Deficiency of ferritin heavy-c ...... the primary disease mechanism.
@nl
P2093
P2860
P356
P1476
Deficiency of ferritin heavy-c ...... the primary disease mechanism
@en
P2093
Adrian J L Clark
Angela Huebner
Barbara Kind
David A Parfitt
Helen L Storr
Katrin Koehler
P2860
P304
P356
10.1210/ME.2009-0056
P50
P577
2009-10-23T00:00:00Z