α-Galactosidase a Deficiency in Fabry Disease Leads to Extensive Dysregulated Cellular Signaling Pathways in Human Podocytes.
Fabry disease
podocytes
proteome analysis
sphingolipids
α-galactosidase A-deficiency
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
20 Oct 2021
20 Oct 2021
Historique:
received:
24
08
2021
revised:
08
10
2021
accepted:
14
10
2021
entrez:
13
11
2021
pubmed:
14
11
2021
medline:
4
1
2022
Statut:
epublish
Résumé
Fabry disease (FD) is caused by mutations in the α-galactosidase A (
Identifiants
pubmed: 34768768
pii: ijms222111339
doi: 10.3390/ijms222111339
pmc: PMC8583658
pii:
doi:
Substances chimiques
alpha-Galactosidase
EC 3.2.1.22
ASAH1 protein, human
EC 3.5.1.23
Acid Ceramidase
EC 3.5.1.23
rab11 protein
EC 3.6.1.-
rab GTP-Binding Proteins
EC 3.6.5.2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Dr. Werner Jackstädt foundation
ID : XXX
Organisme : Innovative Medical Research
ID : LE211702
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