The role and regulation of MAFbx/atrogin-1 and MuRF1 in skeletal muscle atrophy

VC Foletta, LJ White, AE Larsen, B Léger… - … -European Journal of …, 2011 - Springer
Skeletal muscle atrophy occurs in many chronic diseases and disuse conditions. Its severity
reduces patient recovery, independence and quality of life. The discovery of two muscle …

Anabolic and catabolic pathways regulating skeletal muscle mass

JJ McCarthy, KA Esser - Current Opinion in Clinical Nutrition & …, 2010 - journals.lww.com
Anabolic and catabolic pathways regulating skeletal muscle m... : Current Opinion in Clinical
Nutrition & Metabolic Care Anabolic and catabolic pathways regulating skeletal muscle mass …

[PDF][PDF] Molecular mechanisms of muscle plasticity with exercise

H Hoppeler, O Baum, G Lurman, M Mueller - Compr Physiol, 2011 - academia.edu
The skeletal muscle phenotype is subject to considerable malleability depending on use.
Lowintensity endurance type exercise leads to qualitative changes of muscle tissue …

Olig2-lineage astrocytes: a distinct subtype of astrocytes that differs from GFAP astrocytes

K Tatsumi, A Isonishi, M Yamasaki, Y Kawabe… - Frontiers in …, 2018 - frontiersin.org
Astrocytes are the most abundant glia cell type in the central nervous system (CNS), and are
known to constitute heterogeneous populations that differ in their morphology, gene …

Signals mediating skeletal muscle remodeling by resistance exercise: PI3-kinase independent activation of mTORC1

A Philp, DL Hamilton, K Baar - Journal of Applied …, 2011 - journals.physiology.org
For over 10 years, we have known that the activation of the mammalian target of rapamycin
complex 1 (mTORC1) has correlated with the increase in skeletal muscle size and strength …

Muscle protein synthesis, mTORC1/MAPK/Hippo signaling, and capillary density are altered by blocking of myostatin and activins

JJ Hulmi, BM Oliveira, M Silvennoinen… - American Journal …, 2013 - journals.physiology.org
Loss of muscle mass and function occurs in various diseases. Myostatin blocking can
attenuate muscle loss, but downstream signaling is not well known. Therefore, to elucidate …

Altered REDD1, myostatin, and Akt/mTOR/FoxO/MAPK signaling in streptozotocin-induced diabetic muscle atrophy

JJ Hulmi, M Silvennoinen, M Lehti… - American Journal …, 2012 - journals.physiology.org
Type 1 diabetes, if poorly controlled, leads to skeletal muscle atrophy, decreasing the quality
of life. We aimed to search highly responsive genes in diabetic muscle atrophy in a common …

Decreased specific force and power production of muscle fibers from myostatin-deficient mice are associated with a suppression of protein degradation

CL Mendias, E Kayupov, JR Bradley… - Journal of applied …, 2011 - journals.physiology.org
Myostatin (MSTN) is a member of the transforming growth factor-β superfamily of cytokines
and is a negative regulator of skeletal muscle mass. Compared with MSTN+/+ mice, the …

Tamoxifen improves glucose tolerance in a delivery-, sex-, and strain-dependent manner in mice

AM Ceasrine, N Ruiz-Otero, EE Lin… - …, 2019 - academic.oup.com
Tamoxifen, a selective estrogen-receptor modulator, is widely used in mouse models to
temporally control gene expression but is also known to affect body composition. We report …

Inducible liver-specific knockdown of protein tyrosine phosphatase 1B improves glucose and lipid homeostasis in adult mice

C Owen, EK Lees, L Grant, DJ Zimmer, N Mody… - Diabetologia, 2013 - Springer
Aims/hypothesis Protein tyrosine phosphatase 1B (PTP1B) is a key negative regulator of
insulin signalling. Hepatic PTP1B deficiency, using the Alb-Cre promoter to drive Ptp1b …