Muscular Dystrophy, DuchenneIsoenzymesGlucoseDrosophila ProteinsRyanodine Receptor Calcium Release ChannelRegional Blood FlowIn the past five years, skeletal muscle has emerged as a paradigm of "nitric oxide" (NO) function and redox-related signaling in biology. All major nitric oxide synthase (NOS) ...
Boys with Duchenne muscular dystrophy (DMD) experience a progressive loss of functional muscle mass, with fibrosis and lipid accumulation. Accurate evaluation of whole-body functional muscle mass (MM) in DMD patients has not p...
12. Detail Contents: Genetic disorders -- Immune deficiencies -- Breast cancer -- Colon cancer -- Melanoma -- Cystic fibrosis -- Hemophilia -- Liver disease -- Cardiovascular disease -- Muscular dystrophy -- Alzheimer's disease -- Parkinson's disease -- Huntington's disease -- Viruses: the...
Cross-bridge cycling is the mechanism by which skeletal muscle contracts. At the beginning of this cycle, myosin is bound tightly to actin in a step termed rigor. In the absence of basic physiologic energy, such as in death, this is a semi-permanent state called rigor mortis. In living ti...
Dr. Christopher Perry, York University and Dr. Homira Osman, Muscular Dystrophy Canada answer questions from a recent webinar on how the integration of clinical, industrial, and not-for-profit advocacy partners with preclinical research labs offers great potential to improve our research impact. ...
期刊名称:《The Journal of Physiology》 | 2014年第Pt 21期 5.Nitric oxide synthase deficiency and the pathophysiology of muscular dystrophy 机译:一氧化氮合酶缺乏症与肌肉营养不良的病理生理学 作者:James G Tidball;*;Michelle Wehling-Henricks;* 期刊名称:《The Journal of Physiology》 | 2014年第Pt...
Calcium Excitation–contraction coupling Muscular dystrophy RyR1 Skeletal muscle Access this article Subscribe and save €32.70 /Month Get 10 units per month Download Article/Chapter or eBook 1 Unit = 1 Article or 1 Chapter Cancel anytime
Aartsma-Rus, A. et al. Development of exon skipping therapies for Duchenne muscular dystrophy: a critical review and a perspective on the outstanding issues.Nucleic Acid. Ther.27, 251–259 (2017). ArticleCASPubMedPubMed CentralGoogle Scholar ...
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G). Hum Mol Genet. 2014;23(15):4103–10. 95. Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, Rogelj B, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral ...
WD Willis,DR Kenshalo,RB Leonard - 《Journal of Comparative Neurology》 被引量: 612发表: 1979年 Swallowing in myotonic muscular dystrophy: A videofluoroscopic study Leonard RJ, Kendall KA, Johnson R, McKenzie S. Swallowing in myotonic muscular dystrophy: a videofluoroscopic study. Arch Phys Med...