Cargando…

GRMD cardiac and skeletal muscle metabolism gene profiles are distinct

BACKGROUND: Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, which codes for the dystrophin protein. While progress has been made in defining the molecular basis and pathogenesis of DMD, major gaps remain in understanding mechanisms that contribute to the marked delay in car...

Descripción completa

Detalles Bibliográficos
Autores principales:	Markham, Larry W., Brinkmeyer-Langford, Candice L., Soslow, Jonathan H., Gupte, Manisha, Sawyer, Douglas B., Kornegay, Joe N., Galindo, Cristi L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385041/ https://www.ncbi.nlm.nih.gov/pubmed/28390424 http://dx.doi.org/10.1186/s12920-017-0257-2

Ejemplares similares

Translating golden retriever muscular dystrophy microarray findings to novel biomarkers for cardiac/skeletal muscle function in Duchenne Muscular Dystrophy
por: Galindo, Cristi L., et al.
Publicado: (2015)

Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever Model
por: Brinkmeyer-Langford, Candice, et al.
Publicado: (2013)

Levels of α7 integrin and laminin-α2 are increased following prednisone treatment in the mdx mouse and GRMD dog models of Duchenne muscular dystrophy
por: Wuebbles, Ryan D., et al.
Publicado: (2013)

Genome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophy
por: Brinkmeyer-Langford, Candice, et al.
Publicado: (2016)

Oxidative damage to urinary proteins from the GRMD dog and mdx mouse as biomarkers of dystropathology in Duchenne muscular dystrophy
por: Terrill, Jessica R., et al.
Publicado: (2020)

Expression profiling of disease progression in canine model of Duchenne muscular dystrophy
por: Brinkmeyer-Langford, Candice, et al.
Publicado: (2018)

Correction: Expression profiling of disease progression in canine model of Duchenne muscular dystrophy
por: Brinkmeyer-Langford, Candice, et al.
Publicado: (2020)

Identification in GRMD dog muscle of critical miRNAs involved in pathophysiology and effects associated with MuStem cell transplantation
por: Robriquet, Florence, et al.
Publicado: (2016)

Short-term treatment of golden retriever muscular dystrophy (GRMD) dogs with rAAVrh74.MHCK7.GALGT2 induces muscle glycosylation and utrophin expression but has no significant effect on muscle strength
por: Martin, Paul T., et al.
Publicado: (2021)

Increased Number of Circulating CD8/CD26 T Cells in the Blood of Duchenne Muscular Dystrophy Patients Is Associated with Augmented Binding of Adenosine Deaminase and Higher Muscular Strength Scores
por: Soslow, Jonathan H., et al.
Publicado: (2017)

Effects of an Immunosuppressive Treatment in the GRMD Dog Model of Duchenne Muscular Dystrophy
por: Barthélémy, Inès, et al.
Publicado: (2012)

Predictive markers of clinical outcome in the GRMD dog model of Duchenne muscular dystrophy
por: Barthélémy, Inès, et al.
Publicado: (2014)

Early detection of contractile dysfunction in GRMD dogs by post-processing of standard cine FLASH-MRI
por: Gilles, Raymond, et al.
Publicado: (2011)

Bortezomib (PS-341) Treatment Decreases Inflammation and Partially Rescues the Expression of the Dystrophin-Glycoprotein Complex in GRMD Dogs
por: Araujo, Karla P. C., et al.
Publicado: (2013)

Aging Shapes the Population-Mean and -Dispersion of Gene Expression in Human Brains
por: Brinkmeyer-Langford, Candice L., et al.
Publicado: (2016)

Using MRI to quantify skeletal muscle pathology in Duchenne muscular dystrophy: A systematic mapping review
por: Alic, Lejla, et al.
Publicado: (2021)

Dystrophin-deficient dogs with reduced myostatin have unequal muscle growth and greater joint contractures
por: Kornegay, Joe N., et al.
Publicado: (2016)

Neuregulin (NRG-1β) Is Pro-Myogenic and Anti-Cachectic in Respiratory Muscles of Post-Myocardial Infarcted Swine
por: Galindo, Cristi L., et al.
Publicado: (2022)

Left ventricular function by echocardiography correlates poorly with cardiac MRI measures in Duchenne muscular dystrophy
por: Soslow, Jonathan H, et al.
Publicado: (2014)

Antagonism of the Thromboxane‐Prostanoid Receptor as a Potential Therapy for Cardiomyopathy of Muscular Dystrophy
por: West, James D., et al.
Publicado: (2019)

Myostatin promotes distinct responses on protein metabolism of skeletal and cardiac muscle fibers of rodents
por: Manfredi, L.H., et al.
Publicado: (2017)

3D Co-culture of hiPSC-Derived Cardiomyocytes With Cardiac Fibroblasts Improves Tissue-Like Features of Cardiac Spheroids
por: Beauchamp, Philippe, et al.
Publicado: (2020)

Assessment of brain-derived neurotrophic factor and osteopontin in a healthy pediatric population
por: Chew, Joshua D, et al.
Publicado: (2018)

Identification of distinct non-myogenic skeletal-muscle-resident mesenchymal cell populations
por: Leinroth, Abigail P., et al.
Publicado: (2022)

Aberrant Gene Expression in Humans
por: Zeng, Yong, et al.
Publicado: (2015)

Osteopontin is linked with AKT, FoxO1, and myostatin in skeletal muscle cells
por: Nghiem, Peter P., et al.
Publicado: (2017)

Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
por: Kerkis, Irina, et al.
Publicado: (2008)

Regional 4D Cardiac Magnetic Resonance Strain Predicts Cardiomyopathy Progression in Duchenne Muscular Dystrophy
por: Earl, Conner C., et al.
Publicado: (2023)

Distinct roles of UVRAG and EGFR signaling in skeletal muscle homeostasis
por: Kim, Min Jeong, et al.
Publicado: (2021)

Myocardial strain imaging in Duchenne muscular dystrophy
por: Earl, Conner C., et al.
Publicado: (2022)

Comprehensive cardiac magnetic resonance T1, T2, and extracellular volume mapping to define Duchenne cardiomyopathy
por: Sunthankar, Sudeep D., et al.
Publicado: (2023)

Cardiomyocyte SMAD4-Dependent TGF-β Signaling is Essential to Maintain Adult Heart Homeostasis
por: Umbarkar, Prachi, et al.
Publicado: (2019)

T1 mapping is abnormal before decline in EF in patients with Becker and Duchenne muscular dystrophy
por: Soslow, Jonathan H, et al.
Publicado: (2013)

A Comparative Study of N-glycolylneuraminic Acid (Neu5Gc) and Cytotoxic T Cell (CT) Carbohydrate Expression in Normal and Dystrophin-Deficient Dog and Human Skeletal Muscle
por: Martin, Paul T., et al.
Publicado: (2014)

RNA-seq of serial kidney biopsies obtained during progression of chronic kidney disease from dogs with X-linked hereditary nephropathy
por: Chu, Candice P., et al.
Publicado: (2017)

Author Correction: RNA-seq of serial kidney biopsies obtained during progression of chronic kidney disease from dogs with X-linked hereditary nephropathy
por: Chu, Candice P., et al.
Publicado: (2020)

The BDNF rs6265 Polymorphism is a Modifier of Cardiomyocyte Contractility and Dilated Cardiomyopathy
por: Raucci, Frank J., et al.
Publicado: (2020)

Towards ‘Eternal Youth’ of cardiac and skeletal muscle
por: Yacoub, Magdi, et al.
Publicado: (2015)

Anserine is expressed in human cardiac and skeletal muscles
por: de Souza Gonçalves, Lívia, et al.
Publicado: (2023)

miR-27 and miR-125 Distinctly Regulate Muscle-Enriched Transcription Factors in Cardiac and Skeletal Myocytes
por: Lozano-Velasco, Estefania, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_7nfkqktt3ed8q0jn93q2el54q2