[PDF][PDF] Influence of the MuSK-system on muscle pathology in the mdx mouse model of Duchenne Muscular Dystrophy
B Beqaj - 2020 - core.ac.uk
As discussed in the introduction chapter, the TA muscles of mdx mice are heavier than those
of the age-matched wild type genetic background strain (C57BL/10 ScSn). Furthermore …
of the age-matched wild type genetic background strain (C57BL/10 ScSn). Furthermore …
Methods and compositions for treating muscular dystrophy
RJ Hajjar, RA Li, OT Wong - US Patent App. 18/260,456, 2024 - Google Patents
DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid; trioxomolybdenum Chemical
compound O=[Mo](= O)= OO=[Mo](= O)= OO=[Mo](= O)= OO=[Mo](= O)= OO=[Mo](= O) …
compound O=[Mo](= O)= OO=[Mo](= O)= OO=[Mo](= O)= OO=[Mo](= O)= OO=[Mo](= O) …
[引用][C] Functional Characterization of Myosin Binding Protein-C Slow in Health and Disease
JG Hauserman - 2019 - University of Maryland, Baltimore
Functional characterization of Myosin Binding Protein-C slow in health and disease
J Geist Hauserman - 2019 - archive.hshsl.umaryland.edu
Myosin Binding Protein-C (MyBP-C) comprises a family of proteins with structural and
regulatory roles in muscle. There are three MyBP-C isoforms in the family, encoded by …
regulatory roles in muscle. There are three MyBP-C isoforms in the family, encoded by …
[HTML][HTML] Integrative Cardiovascular Physiology and Pathophysiology: Exacerbation of dystrophic cardiomyopathy by phospholamban deficiency mediated chronically …
ML Law, KW Prins, ME Olander… - American Journal of …, 2018 - ncbi.nlm.nih.gov
Cardiomyopathy is a significant contributor to morbidity and mortality in Duchenne muscular
dystrophy (DMD). Membrane instability, leading to intracellular Ca 2+ mishandling and …
dystrophy (DMD). Membrane instability, leading to intracellular Ca 2+ mishandling and …
La communication os-muscle dans la dystrophie musculaire: une interaction musculaire hors triade pour l'ostéoprotégérine
A Boulanger Piette - 2019 - library-archives.canada.ca
La dystrophie musculaire de Duchenne est caractérisée par une dégénérescence
musculaire progressive accompagnée d'une fragilité osseuse exacerbée par la norme de …
musculaire progressive accompagnée d'une fragilité osseuse exacerbée par la norme de …
Evidence for a Reversible, Redox-Mediated Component to Eccentric Contraction-Induced Force Loss in Dystrophin-Deficient Skeletal Muscle
JT Olthoff - 2018 - search.proquest.com
Duchenne muscular dystrophy (DMD) is one of the most common and severe forms of
muscular dystrophy. To better understand eccentric contraction-induced force loss in …
muscular dystrophy. To better understand eccentric contraction-induced force loss in …
[PDF][PDF] Characterization of Grp78/BiP Protein Complexes in Skeletal Muscle Using Affinity Mass Spectrometry
D Chen, DAG Mázala, Y Wang… - Journal of Medical …, 2017 - e-discoverypublication.com
1Department of Kinesiology, School of Public Health, University of Maryland, College Park,
MD 20740 2Proteomics Core Facility, University of Maryland, College Park, MD 20740 …
MD 20740 2Proteomics Core Facility, University of Maryland, College Park, MD 20740 …
Does Sarcolipin Ablation Alter Deflazacort Treatment Effects in mdx Mice?
C Bellissimo - 2017 - uwspace.uwaterloo.ca
Duchenne Muscular Dystrophy (DMD) and the murine model mdx are degenerative
diseases that are characterized by the absence of the protein dystrophin causing membrane …
diseases that are characterized by the absence of the protein dystrophin causing membrane …
Effect of novel ryanodine receptor modulators in mouse and human models of Duchenne muscular dystrophy
G Aldanondo Aristizabal - 2017 - addi.ehu.es
Ahulken (AHK) is a novel family of small molecules (triazoles) specifically designed to
stabilise the interaction between ryanodine receptor 1 (RyR1) and calstabin 1 (Calst1) in …
stabilise the interaction between ryanodine receptor 1 (RyR1) and calstabin 1 (Calst1) in …