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期刊名:Journal of muscle research and cell motility

缩写:J MUSCLE RES CELL M

ISSN:0142-4319

e-ISSN:1573-2657

IF/分区:2.2/Q4

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共收录本刊相关文章索引551条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Karolina Cseri,János Vincze,Julianna Cseri et al. Karolina Cseri et al.
The High-Mobility Group Box 1 protein (HMGB1) is a known nuclear protein which may be released from the nucleus into the cytoplasm and the extracellular space. It is believed that the mobilized HMGB1 plays role in the autoimmune processes a...
Benjamin T Barnes,Amy L Confides,Mark M Rich et al. Benjamin T Barnes et al.
Critical illness myopathy (CIM) is associated with severe muscle atrophy and fatigue in affected patients. Apoptotic signaling is involved in atrophy and is elevated in muscles from patients with CIM. In this study we investigated underlyin...
Daiki Watanabe,Keita Kanzaki,Mai Kuratani et al. Daiki Watanabe et al.
The aim of this study was to examine whether prolonged low-frequency force depression (PLFFD) that occurs in situ is the result of decreased myofibrillar Ca(2+) sensitivity and/or reduced sarcoplasmic reticulum (SR) Ca(2+) release. Intact r...
Hanna Drzymała-Celichowska,Piotr Krutki Hanna Drzymała-Celichowska
The aim of the study was to investigate sex-related differences in contractile properties, parameters of action potentials, and mechanisms of force regulation of motor units in the rat soleus muscle, which is a frequent experimental model i...
Manuela Lavorato,Tai-Qin Huang,Venkat Ramesh Iyer et al. Manuela Lavorato et al.
In cardiac muscle, calmodulin (CaM) regulates the activity of several membrane proteins involved in Ca(2+) homeostasis (CaV1.2; RyR2, SERCA2, PMCA). Three engineered amino acid substitutions in the CaM binding site of the cardiac ryanodine ...
Jennifer Manning,Dervla O&#x;Malley Jennifer Manning
Duchenne muscular dystrophy (DMD) is a fatal X-chromosome linked recessive disorder caused by the truncation or deletion of the dystrophin gene. The most widely used animal model of this disease is the dystrophin-deficient mdx mouse which w...
Yi-Chen Chen,Marius P Sumandea,Lars Larsson et al. Yi-Chen Chen et al.
Skeletal muscles are the most abundant tissues in the human body. They are composed of a heterogeneous collection of muscle fibers that perform various functions. Skeletal muscle troponin (sTn) regulates skeletal muscle contraction and rela...
Magdolna Kósa,Kitti Brinyiczki,Philip van Damme et al. Magdolna Kósa et al.
The sarcoplasmic/endoplasmic reticulum calcium ATPase 1 (SERCA1) has two muscle specific splice isoforms; SERCA1a in fast-type adult and SERCA1b in neonatal and regenerating skeletal muscles. At the protein level the only difference between...
Jana Viskupicova,Magdalena Majekova,Lubica Horakova Jana Viskupicova
The effect of lipophilic rutin derivatives (acylated with fatty acid chain length of 16-22) on sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA1 isoform) compared to the parent molecule rutin was evaluated. Rutin derivatives caused concentr...