Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart-Reference-Cited by-同舟云学术

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Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart

Published:1993-08-23 Issue:1-2 Volume:329 Page:227-231
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Iwata Yuko,Nakamura Hiroshi,Mizuno Yuji,Yoshida Mikiharu,Ozawa Eijro,Shigekawa Munekazu

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(93)80227-L/fullpdf

Reference20 articles.

1. MYOPATHY OF HAMSTER DYSTROPHY: HISTORY AND MORPHOLOGIC ASPECTS

2. Catecholamines, calcium and cardiomyopathy

3. Dystrophin: The protein product of the duchenne muscular dystrophy locus

4. Dystrophin, the protein product of the Duchenne/Becker muscular dystrophy gene

5. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide

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1. Blockade of TRPV2 is a Novel Therapy for Cardiomyopathy in Muscular Dystrophy;International Journal of Molecular Sciences;2019-08-07

2. Molecular Therapies for Muscular Dystrophies;Current Treatment Options in Neurology;2018-06-21

3. Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy;Molecular & Cellular Proteomics;2016-06

4. The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle;Computational and Structural Biotechnology Journal;2016

5. Sarcospan: a small protein with large potential for Duchenne muscular dystrophy;Skeletal Muscle;2013-01-03

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