Increased burden of mitochondrial DNA deletions and point mutations in early-onset age-related hearing loss in mitochondrial mutator mice.
Aging
Hearing loss
Mitochondrial DNA mutations
Mitochondrial disease
Journal
Experimental gerontology
ISSN: 1873-6815
Titre abrégé: Exp Gerontol
Pays: England
ID NLM: 0047061
Informations de publication
Date de publication:
01 10 2019
01 10 2019
Historique:
received:
14
01
2019
revised:
14
07
2019
accepted:
20
07
2019
pubmed:
26
7
2019
medline:
17
7
2020
entrez:
26
7
2019
Statut:
ppublish
Résumé
Mitochondrial DNA (mtDNA) mutations are thought to have a causal role in a variety of age-related neurodegenerative diseases, including age-related hearing loss (AHL). In the current study, we investigated the roles of mtDNA deletions and point mutations in AHL in mitochondrial mutator mice (Polg
Identifiants
pubmed: 31344454
pii: S0531-5565(19)30035-X
doi: 10.1016/j.exger.2019.110675
pmc: PMC6857812
mid: NIHMS1536253
pii:
doi:
Substances chimiques
DNA, Mitochondrial
0
DNA Polymerase gamma
EC 2.7.7.7
Polg protein, mouse
EC 2.7.7.7
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
110675Subventions
Organisme : NIDCD NIH HHS
ID : R01 DC012552
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG028740
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK063491
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG055518
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG028748
Pays : United States
Organisme : NIDCD NIH HHS
ID : R01 DC014437
Pays : United States
Organisme : NIA NIH HHS
ID : K08 AG032873
Pays : United States
Organisme : NIDCD NIH HHS
ID : R03 DC011840
Pays : United States
Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.
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