By John Lynn Jefferies, Burns Blaxall, Jeffrey Towbin MD, Jeffrey Robbins

ISBN-10: 0128000406

ISBN-13: 9780128000403

ISBN-10: 0128005807

ISBN-13: 9780128005804

Cardioskeletal Myopathies in kids and younger Adults specializes in plaques that kill humans of their 40’s-50’s and how they begin to shape in younger maturity. The Annals of kinfolk Medicine record that nearly half teens have at the very least one heart problems threat issue (Mar 2010), and a rise in cardiovascular mortality premiums in teens was once substantiated in a research at Northwestern drugs (Nov 2011).

Given the expanding popularity of genetic triggers at the back of every kind of heart problems, and the starting to be inhabitants of teenagers with basic or received myocardial illness, the necessity has arisen for a reference that gives a accomplished method of the certainty of uncomplicated, translational, and medical elements of particular muscle illnesses whereas making the hyperlink among younger grownup and grownup healthiness.

  • Reveals the hyperlink among cardiac muscle sickness and skeletal muscle disease
  • Explains how genetics and environmental elements impact muscle functionality of numerous origins
  • Designates present and novel healing innovations that concentrate on either cardiac and skeletal muscle systems

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Additional info for Cardioskeletal Myopathies in Children and Young Adults

Sample text

Alpha 1 syntrophin is present throughout the muscle fiber plasma membrane and plays a role in mediating the anchoring of neuronal nitric synthase (nNOS) to the DAPC, while beta 2 syntrophin is restricted to the neuromuscular junction. The carboxyl terminus of dystrophin contains two binding sites for syntrophin and there are two more binding sites on α-dystrobrevin, which is a cytoplasmic protein that shares significant homology with the carboxy-terminal domains of dystrophin. This arrangement is thought to confer the DAPC with a role in regulating various intracellular signaling pathways.

Hum Mol Genet 1999;8:1589–98. [41] Coral-Vazquez R, Cohn RD, Moore SA, Hill JA, Weiss RM, Davisson RL, et al. Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell 1999;98:465–74. [42] Crosbie RH, Lebakken CS, Holt KH, Venzke DP, Straub V, Lee JC, et al. Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex. J Cell Biol 1999;145:153–65. [43] Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, et al.

28] Labeit S, Ottenheijm CA, Granzier H. Nebulin, a major player in muscle health and disease. FASEB J 2011;25:822–9. [29] Brendza RP, O’Brien C, Simmons K, McKeel DW, Bales KR, Paul SM, et al. PDAPP; YFP double transgenic mice: a tool to study amyloid-beta associated changes in axonal, dendritic, and synaptic structures. J Comp Neurol 2003;456:375–83. [30] Dulhunty AF, Franzini-Armstrong C. The relative contributions of the folds and caveolae to the surface membrane of frog skeletal muscle fibres at different sarcomere lengths.

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Cardioskeletal Myopathies in Children and Young Adults by John Lynn Jefferies, Burns Blaxall, Jeffrey Towbin MD, Jeffrey Robbins

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