Literature DB >> 998168

Detection of carriers and genetic counseling in duchenne muscular dystrophy by ribosomal protein synthesis.

V Ionasescu, H Zellweger, L Burmeister.   

Abstract

The in vitro protein synthesis by polyribosomes extracted from biopsied muscle (vastus lateralis) was studied in 47 known carriers, 87 possible carriers and in 60 normal females. A significant increase in specific activity of monomeric ribosomes, total polyribosomes and collagen synthesis was found in 46 (97.8 per cent) known carriers and 47 (54 per cent) possible carriers of Duchenne muscular dytrophy. The latter showed an increase in ribosomal protein synthesis in 10 (52.6 per cent) of 19 mothers of isolated cases, 31 (53.3 per cent) of 58 sisters, and 6 (60 per cent) of other female relatives. Serum creatine phosphokinase was increased in 30 (63.8 per cent) of 47 known carriers.

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Year:  1976        PMID: 998168     DOI: 10.1111/j.1600-0404.1976.tb04376.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  3 in total

1.  Defective myoblasts identified in Duchenne muscular dystrophy.

Authors:  H M Blau; C Webster; G K Pavlath
Journal:  Proc Natl Acad Sci U S A       Date:  1983-08       Impact factor: 11.205

2.  Detection of Duchenne muscular dystrophy carriers: quantitative echography and creatine kinasemia.

Authors:  G Schapira; P Laugier; J Rochette; G Berger; P Katz; J Perrin
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

3.  Detection of carriers for Duchenne muscular dystrophy. Quality control of creatine kinase assay.

Authors:  H Plauchu; C Junien; I Maire; R Said; R Gozlan; J M Lalouel
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

  3 in total

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