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AKT controls protein synthesis and oxidative metabolism via combined mTORC1 and FOXO1 signalling to...

AKT controls protein synthesis and oxidative metabolism via combined mTORC1 and FOXO1 signalling to...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_762fe12f3fe3495f9e5c9957980465ca

AKT controls protein synthesis and oxidative metabolism via combined mTORC1 and FOXO1 signalling to govern muscle physiology

About this item

Full title

AKT controls protein synthesis and oxidative metabolism via combined mTORC1 and FOXO1 signalling to govern muscle physiology

Publisher

Germany: John Wiley & Sons, Inc

Journal title

Journal of Cachexia, Sarcopenia and Muscle, 2022-02, Vol.13 (1), p.495-514

Language

English

Formats

Publication information

Publisher

Germany: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Background
Skeletomuscular diseases result in significant muscle loss and decreased performance, paralleled by a loss in mitochondrial and oxidative capacity. Insulin and insulin‐like growth factor‐1 (IGF‐1) are two potent anabolic hormones that activate a host of signalling intermediates including the serine/threonine kinase AKT to influence sk...

Alternative Titles

Full title

AKT controls protein synthesis and oxidative metabolism via combined mTORC1 and FOXO1 signalling to govern muscle physiology

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_762fe12f3fe3495f9e5c9957980465ca

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_762fe12f3fe3495f9e5c9957980465ca

Other Identifiers

ISSN

2190-5991

E-ISSN

2190-6009

DOI

10.1002/jcsm.12846

How to access this item