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Suppression of Activated FOXO Transcription Factors in the Heart Prolongs Survival in a Mouse Model of Laminopathies

RATIONALE: Mutations in the LMNA gene, encoding nuclear inner membrane protein Lamin A/C, cause distinct phenotypes, collectively referred to as laminopathies. Heart failure, conduction defects, and arrhythmias are the common causes of death in laminopathies. OBJECTIVE: To identify and therapeutical...

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Bibliografske podrobnosti
izdano v:Circ Res
Main Authors: Auguste, Gaelle, Gurha, Priyatansh, Lombardi, Raffaella, Coarfa, Cristian, Willerson, James T., Marian, Ali J.
Format: Artigo
Jezik:Inglês
Izdano: 2018
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5834384/
https://ncbi.nlm.nih.gov/pubmed/29317431
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.117.312052
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