Produktbild: Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy

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Methods and Protocols, Methods in Molecular Biology 1687

ISBN: 1493984667
ISBN 13: 9781493984664
Herausgeber: Camilla Bernardini
Verlag: Humana Press
Umfang: xii, 287 S., 15 s/w Illustr., 34 farbige Illustr., 287 p. 49 illus., 34 illus. in color.
Erscheinungsdatum: 23.08.2018
Auflage: 1/2018
Produktform: Kartoniert
Einband: Kartoniert

This volume explores experimental approaches used to study Duchenne muscular dystrophy (DMD), an X-linked degenerative skeletal muscle disease caused by mutations in the dystrophin gene. Including the latest progress and scientific achievements, the book covers recent discoveries achieved through in vivo gene editing which have proven to be promising in restoring dystrophin expression, at least in ameliorating skeletal muscle symptoms, and the contents focus on „Omics“ techniques in gene expression, protein expression, miRNAs, and long non-coding RNA analysis, as well as experimental studies of the structural/functional changes affecting the skeletal and cardiac muscles and ongoing preclinical studies and clinical trials. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.  Authoritative and practical, Duchenne Muscular Dystrophy: Methods and Protocols serves as a guide for researchers exploring the complicated nature of dystrophin in the hope of helping the victims of this disorder.

Artikelnummer: 6778657 Kategorie:

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Humana Press in Springer Science + Business Media
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14197 Berlin
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E-Mail: juergen.hartmann@springer.com

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