Activity of Polyribosomes from the Muscle of Normal and Dystrophic Mice in Cell-Free Amino-Acid Incorporation
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1975.tb02214.x/fullpdf
Reference15 articles.
1. Biochemical changes in progressive muscular dystrophy. VII. Studies on the biosynthesis of protein and RNA in various cellular fractions of the muscle of normal and dystrophic mice
2. Biochemical Changes in Progressive Muscular Dystrophy. IX. Synthesis of Native Myosin, Actin, and Tropomyosin in the Skeletal Muscle of Mouse as a Function of Muscular Dystrophy
3. A new approach for carrier detection in Duchenne muscular dystrophy: Protein synthesis of niuscle polyribosomes in vitro
4. Ribosomal protein synthesis in Duchenne muscular dystrophy
5. Identification of carriers of Duchenne muscular dystrophy by muscle protein synthesis
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2. The expression of glycogen phosphorylase in normal and dystrophic muscle;Biochemical Journal;1991-08-15
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4. The effect of stretch removal on muscle weight and proteolytic enzyme activity in normal and dystrophic chicken muscles;Muscle & Nerve;1984-07
5. The 60S ribosomal subunit is altered in the skeletal muscle of dystrophic hamsters;Biochemical and Biophysical Research Communications;1983-08
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