Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy
Authors
Keywords
-
Journal
JOURNAL OF CELL BIOLOGY
Volume 207, Issue 1, Pages 139-158
Publisher
Rockefeller University Press
Online
2014-10-14
DOI
10.1083/jcb.201402079
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mitotic Asynchrony Induces Transforming Growth Factor-β1 Secretion from Airway Epithelium
- (2014) Sarah E. Alcala et al. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
- Sparing of the Dystrophin-Deficient Cranial Sartorius Muscle Is Associated with Classical and Novel Hypertrophy Pathways in GRMD Dogs
- (2013) Peter P. Nghiem et al. AMERICAN JOURNAL OF PATHOLOGY
- VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects
- (2013) Christopher R. Heier et al. EMBO Molecular Medicine
- Dystrophin-deficient pigs provide new insights into the hierarchy of physiological derangements of dystrophic muscle
- (2013) Nikolai Klymiuk et al. HUMAN MOLECULAR GENETICS
- Toll-Like Receptor 4 Signaling Augments Transforming Growth Factor-β Responses
- (2012) Swati Bhattacharyya et al. AMERICAN JOURNAL OF PATHOLOGY
- LTBP4genotype predicts age of ambulatory loss in duchenne muscular dystrophy
- (2012) Kevin M. Flanigan et al. ANNALS OF NEUROLOGY
- TGFβ signaling
- (2012) Elizabeth M. MacDonald et al. CURRENT OPINION IN RHEUMATOLOGY
- TGFβ Signaling in Liver Regeneration
- (2012) Sofia Karkampouna et al. CURRENT PHARMACEUTICAL DESIGN
- MicroRNAs, transforming growth factor beta-1, and tissue fibrosis
- (2012) Timothy Bowen et al. JOURNAL OF PATHOLOGY
- Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies
- (2012) Joe N. Kornegay et al. MAMMALIAN GENOME
- Targeting the TGFβ signalling pathway in disease
- (2012) Rosemary J. Akhurst et al. NATURE REVIEWS DRUG DISCOVERY
- Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
- (2012) L. Bello et al. NEUROLOGY
- The Paradox of Muscle Hypertrophy in Muscular Dystrophy
- (2012) Joe N. Kornegay et al. Physical Medicine and Rehabilitation Clinics of North America
- Novel Approaches to Corticosteroid Treatment in Duchenne Muscular Dystrophy
- (2012) Eric P. Hoffman et al. Physical Medicine and Rehabilitation Clinics of North America
- Glucocorticoid-Treated Mice Are an Inappropriate Positive Control for Long-Term Preclinical Studies in the mdx Mouse
- (2012) Arpana Sali et al. PLoS One
- Passing the baton: the HIF switch
- (2012) Mei Yee Koh et al. TRENDS IN BIOCHEMICAL SCIENCES
- Elevated levels of active matrix metalloproteinase-9 cause hypertrophy in skeletal muscle of normal and dystrophin-deficient mdx mice
- (2011) Saurabh Dahiya et al. HUMAN MOLECULAR GENETICS
- Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers
- (2011) Daigo Miyazaki et al. HUMAN MOLECULAR GENETICS
- Osteopontin-Stimulated Expression of Matrix Metalloproteinase-9 Causes Cardiomyopathy in the mdx Model of Duchenne Muscular Dystrophy
- (2011) S. Dahiya et al. JOURNAL OF IMMUNOLOGY
- Immune Response and Mitochondrial Metabolism Are Commonly Deregulated in DMD and Aging Skeletal Muscle
- (2011) Daniel Baron et al. PLoS One
- Asthmatic Airway Epithelium Is Intrinsically Inflammatory and Mitotically Dyssynchronous
- (2010) Robert J. Freishtat et al. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
- Elevated satellite cell number in Duchenne muscular dystrophy
- (2010) Michael Kottlors et al. CELL AND TISSUE RESEARCH
- Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy
- (2010) M’Hammed Aguennouz et al. NEUROBIOLOGY OF AGING
- SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy
- (2010) E. Pegoraro et al. NEUROLOGY
- Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
- (2009) Katharine Bushby et al. LANCET NEUROLOGY
- caBIG™ VISDA: Modeling, visualization, and discovery for cluster analysis of genomic data
- (2008) Yitan Zhu et al. BMC BIOINFORMATICS
- Duration of chronic inflammation alters gene expression in muscle from untreated girls with juvenile dermatomyositis
- (2008) Yi-Wen Chen et al. BMC IMMUNOLOGY
- Crosstalk Between Vascular Endothelial Growth Factor, Notch, and Transforming Growth Factor-β in Vascular Morphogenesis
- (2008) Matthew T. Holderfield et al. CIRCULATION RESEARCH
- Shifts in macrophage phenotypes and macrophage competition for arginine metabolism affect the severity of muscle pathology in muscular dystrophy
- (2008) S. A. Villalta et al. HUMAN MOLECULAR GENETICS
- Transforming growth factor-β and myostatin signaling in skeletal muscle
- (2007) Helen D. Kollias et al. JOURNAL OF APPLIED PHYSIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation