Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2H

Functional interactions between ubiquitin E2 enzymes and TRIM proteins

(2011) Luisa M. Napolitano et al.   BIOCHEMICAL JOURNAL

The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype

(2011) E. Kudryashova et al.   HUMAN MOLECULAR GENETICS

TRIM32 Protein Sensitizes Cells to Tumor Necrosis Factor (TNFα)-induced Apoptosis via Its RING Domain-dependent E3 Ligase Activity against X-linked Inhibitor of Apoptosis (XIAP)

(2011) Yeung Sook Ryu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Losartan Restores Skeletal Muscle Remodeling and Protects Against Disuse Atrophy in Sarcopenia

(2011) T. N. Burks et al.   Science Translational Medicine

Autophagy in health and disease. 3. Involvement of autophagy in muscle atrophy

(2010) Marco Sandri   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice

(2010) Alessandra Sacco et al.   CELL

Autosomal recessive muscular dystrophy in Manitoba Hutterites*

(2010) M. H. K. Shokeir et al.   CLINICAL GENETICS

Signaling pathways perturbing muscle mass

(2010) David J Glass   CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE

Forty-eight hours of unloading and 24 h of reloading lead to changes in global gene expression patterns related to ubiquitination and oxidative stress in humans

(2010) Kimberly A. Reich et al.   JOURNAL OF APPLIED PHYSIOLOGY

PIASy stimulates HIF1α SUMOylation and negatively regulates HIF1α activity in response to hypoxia

(2010) X Kang et al.   ONCOGENE

Prevention of Muscle Aging by Myofiber-Associated Satellite Cell Transplantation

(2010) J. K. Hall et al.   Science Translational Medicine

Post-translational modification by SUMO

(2010) Zara Hannoun et al.   TOXICOLOGY

The impact of sarcopenia and exercise training on skeletal muscle satellite cells

(2009) Tim Snijders et al.   AGEING RESEARCH REVIEWS

SUMOylation and cell signalling

(2009) Artemisia M. Andreou et al.   Biotechnology Journal

Molecular aging and rejuvenation of human muscle stem cells

(2009) Morgan E. Carlson et al.   EMBO Molecular Medicine

Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic component

(2009) Elena Kudryashova et al.   HUMAN MOLECULAR GENETICS

TRIM32 is an E3 ubiquitin ligase for dysbindin

(2009) Matthew Locke et al.   HUMAN MOLECULAR GENETICS

Intragenic deletion ofTRIM32in compound heterozygotes with sarcotubular myopathy/LGMD2H

(2009) Kristian Borg et al.   HUMAN MUTATION

During muscle atrophy, thick, but not thin, filament components are degraded by MuRF1-dependent ubiquitylation

(2009) Shenhav Cohen et al.   JOURNAL OF CELL BIOLOGY

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H

(2009) Mireille Cossée et al.   NEUROMUSCULAR DISORDERS

Replicative aging down-regulates the myogenic regulatory factors in human myoblasts

(2008) Anne Bigot et al.   BIOLOGY OF THE CELL

Tripartite Motif Protein 32 Facilitates Cell Growth and Migration via Degradation of Abl-Interactor 2

(2008) S. Kano et al.   CANCER RESEARCH

Non-Smad pathways in TGF-β signaling

(2008) Ying E Zhang   CELL RESEARCH

Current Topics in DNA Double-Strand Break Repair

(2008) Junya KOBAYASHI et al.   JOURNAL OF RADIATION RESEARCH

Noncanonical E2 Variant-Independent Function of UBC13 in Promoting Checkpoint Protein Assembly

(2008) M. S. Y. Huen et al.   MOLECULAR AND CELLULAR BIOLOGY

Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H

(2007) Valentina Saccone et al.   HUMAN MUTATION