The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy

Carfilzomib: A second-generation proteasome inhibitor for the treatment of multiple myeloma

(2015) A. McBride et al.   AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY

The E3 ubiquitin ligase TRIM32 regulates myoblast proliferation by controlling turnover of NDRG2

(2015) Ekaterina I. Mokhonova et al.   HUMAN MOLECULAR GENETICS

TRIM-NHL proteins in development and disease

(2015) Cristina Tocchini et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Treatment-related symptom management in patients with multiple myeloma: a review

(2015) Kathleen Colson   SUPPORTIVE CARE IN CANCER

Bortezomib Partially Improves Laminin α2 Chain–Deficient Muscular Dystrophy

(2014) Zandra Körner et al.   AMERICAN JOURNAL OF PATHOLOGY

Unveiling the degradative route of the V247M α-sarcoglycan mutant responsible for LGMD-2D

(2014) Elisa Bianchini et al.   HUMAN MOLECULAR GENETICS

Pharmacologic Management of Duchenne Muscular Dystrophy: Target Identification and Preclinical Trials

(2014) J. N. Kornegay et al.   ILAR JOURNAL

Trim32 reduces PI3K–Akt–FoxO signaling in muscle atrophy by promoting plakoglobin–PI3K dissociation

(2014) Shenhav Cohen et al.   JOURNAL OF CELL BIOLOGY

Immunoproteasome in animal models of Duchenne muscular dystrophy

(2014) Chiao-nan Joyce Chen et al.   JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY

Involvement of oxidative stress, Nuclear Factor kappa B and the Ubiquitin proteasomal pathway in dysferlinopathy

(2014) Dhanarajan Rajakumar et al.   LIFE SCIENCES

Muscle atrophy, ubiquitin-proteasome, and autophagic pathways in dysferlinopathy

(2014) Marina Fanin et al.   MUSCLE & NERVE

Proteasome inhibitors increase missense mutated dysferlin in patients with muscular dystrophy

(2014) B. A. Azakir et al.   Science Translational Medicine

The physiological response of protease inhibition in dystrophic muscle

(2013) K. Hollinger et al.   Acta Physiologica

Molecular Architecture and Assembly of the Eukaryotic Proteasome

(2013) Robert J. Tomko et al.   Annual Review of Biochemistry

Muscular dystrophy

(2013) Eugenio Mercuri et al.   CURRENT OPINION IN PEDIATRICS

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

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

A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation

(2013) M. Neri et al.   NEUROMUSCULAR DISORDERS

Bortezomib (PS-341) Treatment Decreases Inflammation and Partially Rescues the Expression of the Dystrophin-Glycoprotein Complex in GRMD Dogs

(2013) Karla P. C. Araujo et al.   PLoS One

Proteasomal Inhibition Restores Biological Function of Mis-sense Mutated Dysferlin in Patient-derived Muscle Cells

(2012) Bilal A. Azakir et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Ubiquitylation by Trim32 causes coupled loss of desmin, Z-bands, and thin filaments in muscle atrophy

(2012) Shenhav Cohen et al.   JOURNAL OF CELL BIOLOGY

HECT and RING finger families of E3 ubiquitin ligases at a glance

(2012) M. B. Metzger et al.   JOURNAL OF CELL SCIENCE

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

(2012) Elena Kudryashova et al.   JOURNAL OF CLINICAL INVESTIGATION

Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota Hutterite

(2012) Teerin Liewluck et al.   NEUROMUSCULAR DISORDERS

TRIM32 Regulates Skeletal Muscle Stem Cell Differentiation and Is Necessary for Normal Adult Muscle Regeneration

(2012) Sarah Nicklas et al.   PLoS One

The Ubiquitin Ligase Nedd4-1 Participates in Denervation-Induced Skeletal Muscle Atrophy in Mice

(2012) Preena Nagpal et al.   PLoS One

Regulation of the calpain and ubiquitin-proteasome systems in a canine model of muscular dystrophy

(2011) Kristine M. Wadosky et al.   MUSCLE & NERVE

Therapeutic Potential of Proteasome Inhibition in Duchenne and Becker Muscular Dystrophies

(2010) Elisabetta Gazzerro et al.   AMERICAN JOURNAL OF PATHOLOGY

Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance

(2010) Verena Arndt et al.   CURRENT BIOLOGY

Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice

(2010) Virginie Carmignac et al.   HUMAN MOLECULAR GENETICS

Regulation of the Psoriatic Chemokine CCL20 by E3 Ligases Trim32 and Piasy in Keratinocytes

(2010) Yuangang Liu et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Recognition and Processing of Ubiquitin-Protein Conjugates by the Proteasome

(2009) Daniel Finley   Annual Review of Biochemistry

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

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

Inhibition of Proteasome Activity Promotes the Correct Localization of Disease-Causing α-Sarcoglycan Mutants in HEK-293 Cells Constitutively Expressing β-, γ-, and δ-Sarcoglycan

(2008) Stefano Gastaldello et al.   AMERICAN JOURNAL OF PATHOLOGY

Effect of calpain and proteasome inhibition on Ca2+-dependent proteolysis and muscle histopathology in the mdx mouse

(2008) Alexandre Briguet et al.   FASEB JOURNAL

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

(2007) Valentina Saccone et al.   HUMAN MUTATION