Cullin-3 intervenes in muscle atrophy in the elderly by mediating the degradation of nAchRs ubiquitination

Neuromuscular junction pathology is correlated with differential motor unit vulnerability in spinal and bulbar muscular atrophy

(2022) Elana Molotsky et al.   Acta Neuropathologica Communications

The Ubiquitin Proteasome System in Neuromuscular Disorders: Moving Beyond Movement

(2020) Sara Bachiller et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Sarcopenia – Molecular mechanisms and open questions

(2020) Petra Wiedmer et al.   AGEING RESEARCH REVIEWS

Sarcopenia and its association with falls and fractures in older adults: A systematic review and meta‐analysis

(2019) Suey S.Y. Yeung et al.   Journal of Cachexia Sarcopenia and Muscle

CUL3 Deficiency Causes Social Deficits and Anxiety-like Behaviors by Impairing Excitation-Inhibition Balance through the Promotion of Cap-Dependent Translation

(2019) Zhaoqi Dong et al.   NEURON

Opposed Actions of PKA Isozymes (RI and RII) and PKC Isoforms (cPKCβI and nPKCε) in Neuromuscular Developmental Synapse Elimination

(2019) Garcia et al.   Cells

Hepatocyte growth factor regulates miR-206-HDAC4 cascade to control the neurogenic muscle atrophy following surgical denervation in mice

(2018) Wooshik Choi et al.   Molecular Therapy-Nucleic Acids

Identification of candidate genes and proteins in aging skeletal muscle (sarcopenia) using gene expression and structural analysis

(2018) Gita Shafiee et al.   PeerJ

Sarcopenia: Aging-Related Loss of Muscle Mass and Function

(2018) Lars Larsson et al.   PHYSIOLOGICAL REVIEWS

Cullin E3 Ligase Activity Is Required for Myoblast Differentiation

(2017) Jordan Blondelle et al.   JOURNAL OF MOLECULAR BIOLOGY

Age-related deficits in skeletal muscle recovery following disuse are associated with neuromuscular junction instability and ER stress, not impaired protein synthesis

(2016) Leslie M. Baehr et al.   Aging-US

Biomarkers in sarcopenia: A multifactorial approach

(2016) Francesco Curcio et al.   EXPERIMENTAL GERONTOLOGY

Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting

(2015) Lionel A. Tintignac et al.   PHYSIOLOGICAL REVIEWS

Cullin Family Proteins and Tumorigenesis: Genetic Association and Molecular Mechanisms

(2015) Zhi Chen et al.   Journal of Cancer

KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy

(2014) Ankit Garg et al.   JOURNAL OF CLINICAL INVESTIGATION

The Neuromuscular Junction: Aging at the Crossroad between Nerves and Muscle

(2014) Marta Gonzalez-Freire et al.   Frontiers in Aging Neuroscience

Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy

(2013) Vandana A. Gupta et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Protein breakdown in muscle wasting: Role of autophagy-lysosome and ubiquitin-proteasome

(2013) Marco Sandri   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

Misregulation of autophagy and protein degradation systems in myopathies and muscular dystrophies

(2013) M. Sandri et al.   JOURNAL OF CELL SCIENCE

Regulation and physiological roles of the calpain system in muscular disorders

(2012) H. Sorimachi et al.   CARDIOVASCULAR RESEARCH

Signaling and aging at the neuromuscular synapse: lessons learnt from neuromuscular diseases

(2012) Anna Rostedt Punga et al.   CURRENT OPINION IN PHARMACOLOGY

Cellular and molecular mechanisms of muscle atrophy

(2012) P. Bonaldo et al.   Disease Models & Mechanisms

Genomic and Proteomic Profiling Reveals Reduced Mitochondrial Function and Disruption of the Neuromuscular Junction Driving Rat Sarcopenia

(2012) C. Ibebunjo et al.   MOLECULAR AND CELLULAR BIOLOGY

Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy

(2010) Sebahattin Cirak et al.   BRAIN

Further Characterisation of the Molecular Signature of Quiescent and Activated Mouse Muscle Satellite Cells

(2009) Viola F. Gnocchi et al.   PLoS One