Specific increase of genetic expression of parvalbumin in fast skeletal muscles of mdx mice-Reference-Cited by-同舟云学术

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Specific increase of genetic expression of parvalbumin in fast skeletal muscles of mdx mice

Published:1993-07-01 Issue:1-3 Volume:326 Page:272-274
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Gailly Ph.,Hermans E.,Octave J.N.,Gillis J.M.

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(93)81806-B/fullpdf

Reference32 articles.

1. Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular Dystrophy

2. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

3. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

4. Muscle development in mdx mutant mice

5. Dystrophin: A clinical perspective

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2. Eccentric exercise in aging and diseased skeletal muscle: good or bad?;Journal of Applied Physiology;2014-06-01

3. TRP channels in normal and dystrophic skeletal muscle;Current Opinion in Pharmacology;2012-06

4. Altered calcium pump and secondary deficiency of γ-sarcoglycan and microspan in sarcoplasmic reticulum membranes isolated from δ-sarcoglycan knockout mice;Cell Calcium;2010-07

5. Role of TRPC1 channel in skeletal muscle function;American Journal of Physiology-Cell Physiology;2010-01

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