Misregulation of calcium-handling proteins promotes hyperactivation of calcineurin–NFAT signaling in skeletal muscle of DM1 mice
A Ravel-Chapuis, G Bélanger, J Côté… - Human Molecular …, 2017 - academic.oup.com
Abstract Myotonic Dystrophy type 1 (DM1) is caused by an expansion of CUG repeats in
DMPK mRNAs. This mutation affects alternative splicing through misregulation of RNA …
DMPK mRNAs. This mutation affects alternative splicing through misregulation of RNA …
Saturation of SERCA's lipid annulus may protect against its thermal inactivation
VA Fajardo, N Trojanowski, LM Castelli… - Biochemical and …, 2017 - Elsevier
The sarco (endo) plasmic reticulum Ca 2+-ATPase (SERCA) pumps are integral membrane
proteins that catalyze the active transport of Ca 2+ into the sarcoplasmic reticulum, thereby …
proteins that catalyze the active transport of Ca 2+ into the sarcoplasmic reticulum, thereby …
[PDF][PDF] Advances in the Application of Protein Mass Spectrometry to Skeletal Muscle Biology
D Chen, RQ Landers-Ramos… - Journal of Medical …, 2017 - researchgate.net
Protein mass spectrometry has been emerging as a powerful technology in the studies of
human diseases. The advances in this technology, such as instrumentation, sample …
human diseases. The advances in this technology, such as instrumentation, sample …
[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 - euskadi.osasuna.ezagutzarenataria …
La distrofia muscular de Duchenne (DMD) es una enfermedad hereditaria ligada al
cromosoma X queafecta a uno de cada 3500 varones. Esta enfermedad se caracteriza por …
cromosoma X queafecta a uno de cada 3500 varones. Esta enfermedad se caracteriza por …
Effect of novel ryanodine receptor modulators in mouse and human models of duchenne muscular dystrophy
GA Aristizabal - 2017 - dialnet.unirioja.es
La distrofia muscular de Duchenne (DMD) es una enfermedad hereditaria ligada al
cromosoma X queafecta a uno de cada 3500 varones. Esta enfermedad se caracteriza por …
cromosoma X queafecta a uno de cada 3500 varones. Esta enfermedad se caracteriza por …