Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency.
BRET
PEX26
edgetic perturbations
network medicine
peroxisome
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2021
2021
Historique:
received:
16
06
2021
accepted:
18
10
2021
entrez:
22
11
2021
pubmed:
23
11
2021
medline:
23
11
2021
Statut:
epublish
Résumé
Peroxisomes share metabolic pathways with other organelles and peroxisomes are embedded into key cellular processes. However, the specific function of many peroxisomal proteins remains unclear and restricted knowledge of the peroxisomal protein interaction network limits a precise mapping of this network into the cellular metabolism. Inborn peroxisomal disorders are autosomal or X-linked recessive diseases that affect peroxisomal biogenesis (PBD) and/or peroxisomal metabolism. Pathogenic variants in the
Identifiants
pubmed: 34804114
doi: 10.3389/fgene.2021.726174
pii: 726174
pmc: PMC8600046
doi:
Types de publication
Journal Article
Langues
eng
Pagination
726174Informations de copyright
Copyright © 2021 Lotz-Havla, Woidy, Guder, Schmiesing, Erdmann, Waterham, Muntau and Gersting.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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