4E‐BP1 and 4E‐BP2 double knockout mice are protected from aging‐associated sarcopenia-Reference-Cited by-同舟云学术

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4E‐BP1 and 4E‐BP2 double knockout mice are protected from aging‐associated sarcopenia

Published:2019-03-29 Issue:3 Volume:10 Page:696-709
ISSN:2190-5991
Container-title:Journal of Cachexia, Sarcopenia and Muscle
language:en
Short-container-title:Journal of Cachexia, Sarcopenia and Muscle

Author:

Le Bacquer Olivier¹,Combe Kristell¹,Patrac Véronique¹,Ingram Brian²,Combaret Lydie¹,Dardevet Dominique¹,Montaurier Christophe¹,Salles Jérôme¹,Giraudet Christophe¹,Guillet Christelle¹,Sonenberg Nahum³,Boirie Yves¹⁴,Walrand Stéphane¹

Affiliation:

1. INRA, UMR1019 Université Clermont Auvergne, UNH, Unité de Nutrition Humaine CRNH Auvergne Clermont‐Ferrand France

2. Metabolon Inc. Morrisville NC USA

3. Department of Biochemistry McGill University Montreal QC Canada

4. CHU Clermont‐Ferrand, Service Nutrition Clinique Clermont‐Ferrand France

Funder

Région Auvergne-Rhône-Alpes

Publisher

Wiley

Subject

Physiology (medical),Orthopedics and Sports Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcsm.12412

Reference53 articles.

1. mTOR Signaling in Growth, Metabolism, and Disease

2. Insulin-dependent stimulation of protein synthesis by phosphorylation of a regulator of 5'-cap function

3. 4E-BP3, a New Member of the Eukaryotic Initiation Factor 4E-binding Protein Family

4. Repression of cap-dependent translation by 4E-binding protein 1: competition with p220 for binding to eukaryotic initiation factor-4E.

5. Regulation of 4E-BP1 phosphorylation: a novel two-step mechanism

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