Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle-Reference-Cited by-同舟云学术

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

Published:1996-05 Issue:1 Volume:13 Page:63-69
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Poetter Karl,Jiang He,Hassanzadeh Shahin,Master Stephen R.,Chang Anthony,Dalakas Marinos C.,Rayment Ivan,Sellers James R.,Fananapazir Lameh,Epstein Neal D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0596-63.pdf

Reference45 articles.

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2. Huxley, H.E. The mechanism of muscular contraction. Science 164, 1356–1366 (1969).

3. Rayment, I. et al. Three-dimensional structure of myosin subfragment-1: a molecular motor. Science 261, 50–58 (1993).

4. Xie, X. et al. Structure of the regulatory domain of scallop myosin at 2.8 Å resolution. Nature 368, 306–312 (1994).

5. Houdusse, A. & Cohen, C. Structure of the regulatory domain of scallop myosin at 2 resolution:implications for regulation. Structure 4, 21–32 (1996).

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