Phosphorylation of Lamin A/C at serine 22 modulates Na
Lamin phosphorylation
Nav1.5
cardiac conduction disease
Journal
Physiological reports
ISSN: 2051-817X
Titre abrégé: Physiol Rep
Pays: United States
ID NLM: 101607800
Informations de publication
Date de publication:
11 2021
11 2021
Historique:
revised:
29
10
2021
received:
02
07
2021
accepted:
31
10
2021
entrez:
22
11
2021
pubmed:
23
11
2021
medline:
17
3
2022
Statut:
ppublish
Résumé
Variants in the LMNA gene, which encodes for Lamin A/C, are associated with cardiac conduction disease (CCD). We previously reported that Lamin A/C variants p.R545H and p.A287Lfs*193, which were identified in CCD patients, decreased peak I
Identifiants
pubmed: 34806324
doi: 10.14814/phy2.15121
pmc: PMC8606869
doi:
Substances chimiques
LMNA protein, human
0
Lamin Type A
0
NAV1.5 Voltage-Gated Sodium Channel
0
SCN5A protein, human
0
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
e15121Subventions
Organisme : NCI NIH HHS
ID : R01 CA211866
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL093056
Pays : United States
Informations de copyright
© 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.
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