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Titlebook: Gene Expression in Muscle; Richard C. Strohman,Stewart Wolf Book 1985 The Editor(s) (if applicable) and The Author(s), under exclusive lic

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書目名稱Gene Expression in Muscle
編輯Richard C. Strohman,Stewart Wolf
視頻videohttp://file.papertrans.cn/382/381927/381927.mp4
叢書名稱Advances in Experimental Medicine and Biology
圖書封面Titlebook: Gene Expression in Muscle;  Richard C. Strohman,Stewart Wolf Book 1985 The Editor(s) (if applicable) and The Author(s), under exclusive lic
描述This volume contains the edited transcript of an interdisci- plinary colloquium held at Totts Gap Medical Research Laboratories, Bangor, Pennsylvania on October 12-14, 1983 under the sponsorship of the Muscular Dystrophy Association. The aim was to illuminate the pathogenic mechanism of Duchenne Muscular Dystrophy through a synthesis of available data on gene expression in muscle. In the informal give and take ot the collo- quium, the participants found themselves engaged in mutual education and enlightenment as they attempted to put together what is known and to highlight what is not known about the subject. Significant research into muscle as a tissue and muscle disease began only about 50 years ago although the description of muscular dystrophy by Guillaume Benjamin Amand Duchenne de Boulogne had been published in 1862. By 1943 it was clear that Duchenne muscular dystrophy was an X-linked genetic disorder. Up to the present, however, the offending gene has not been identified although its location on the short arm of the X chromosome has been approximately determined. The gene product associated with the initial disturbance in skeletal muscle has also remained elusive up to now.
出版日期Book 1985
關(guān)鍵詞chromosome; gene expression; genes
版次1
doihttps://doi.org/10.1007/978-1-4684-4907-5
isbn_softcover978-1-4684-4909-9
isbn_ebook978-1-4684-4907-5Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
The information of publication is updating

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Myosin Isoforms in Normal and Dystrophic Human and Murine Muscleswork and heat, The rate of energy transduction is a function of the kinetics of myosin as a mechano-enzyme. Myosin exists as a large family of isoenzymic forms differing from each other in subunit composition, ATPase activity and consequently the rate of energy transduction. The functional significa
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Distribution of Slow Myosin in Dystrophic Chicken Musclel, histochemical, and biochemical methods have demonstrated clear dystrophic abnormalities in the posterior latisslmus dorsi (PLD) while the anterior latissimus dorsi (ALD), a slow tonic muscle, is unaffected by the disease (216,219). Most of this research has been performed on normal and dystrophic
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Trophic and Myogenic Effects with Special Reference to Transferrinract (EE). However, they do not grow, when incubated with a medium composed of Eagle’s MEM and horse serum (basal medium). This indicates that EE contains essential substance(s) for chick myogenic cell growth, which is contained in neither the artificial medium nor horse serum.
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Control of Myosin Isozymes during Myogenesis in the Ratmuscle fibers (367, 368) with different physiological and metabolic properties. For example, fast and slow twitch fibers contain both different myosin heavy chain and myosin light chain complements; and among the fast twitch fibers, IIa and IIb fibers contain myosins with qualitatively distinct myos
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