Literature DB >> 1874604

Hereditary human myopathies in muscle culture.

G Meola1.   

Abstract

In this article I illustrated the use of regenerating human muscle cultures for studying the hereditary human myopathies. Although some of the data are still controversial, they do point up the great potential of this "in vitro system". For hereditary myopathies due to developmentally regulated proteins that are expressed only at a more advanced stage of muscle differentiation, the use of highly differentiated nerve-muscle cocultures might contribute significantly to a better understanding of their developmental pathogenesis. More advanced techniques (permanent human muscle cell lines, heterokaryons, myoblast transfer, gene transfer, myogenic conversion of human non-muscle cells, cybrid clones) may provide a great deal of information at molecular level and may also have practical applications in the diagnosis or even in the treatment of hereditary human myopathies.

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Year:  1991        PMID: 1874604     DOI: 10.1007/bf02337773

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  50 in total

1.  Differential expression of nuclear genes for cytochrome c oxidase during myogenesis.

Authors:  M I Lomax; E Coucouvanis; E A Schon; K F Barald
Journal:  Muscle Nerve       Date:  1990-04       Impact factor: 3.217

2.  Differential expression of creatine kinase and phosphoglycerate mutase isozymes during development in aneural and innervated human muscle culture.

Authors:  A F Miranda; E R Peterson; E B Masurovsky
Journal:  Tissue Cell       Date:  1988       Impact factor: 2.466

3.  Reincarnation in cultured muscle of mitochondrial abnormalities. Two patients with epilepsy and lactic acidosis.

Authors:  V Askanas; W K Engel; D E Britton; B T Adornato; R M Eiben
Journal:  Arch Neurol       Date:  1978-12

4.  Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.

Authors:  K Sato; F Imai; I Hatayama; R I Roelofs
Journal:  Biochem Biophys Res Commun       Date:  1977-09-23       Impact factor: 3.575

5.  Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients.

Authors:  T Mongini; D Ghigo; C Doriguzzi; F Bussolino; G Pescarmona; B Pollo; D Schiffer; A Bosia
Journal:  Neurology       Date:  1988-03       Impact factor: 9.910

6.  Properties of acetylcholine-receptor activation in human Duchenne muscular dystrophy myotubes.

Authors:  E Mancinelli; A Sardini; A D'Aumiller; G Meola; G Martucci; G Cossu; E Wanke
Journal:  Proc R Soc Lond B Biol Sci       Date:  1989-07-22

7.  A case of mitochondrial myopathy, lactic acidosis and complex I deficiency.

Authors:  L Bet; N Bresolin; M Moggio; G Meola; A Prelle; A H Schapira; T Binzoni; A Chomyn; F Fortunato; P Cerretelli
Journal:  J Neurol       Date:  1990-11       Impact factor: 4.849

8.  In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.

Authors:  A Chomyn; G Meola; N Bresolin; S T Lai; G Scarlato; G Attardi
Journal:  Mol Cell Biol       Date:  1991-04       Impact factor: 4.272

9.  Muscle carnitine deficiency: fatty acid metabolism in cultured fibroblasts and muscle cells.

Authors:  J Avigan; V Askanas; W K Engel
Journal:  Neurology       Date:  1983-08       Impact factor: 9.910

10.  Human--rat muscle somatic cell hybrids form myotubes and express human muscle gene products.

Authors:  C A Quinn; P N Goodfellow; S Povey; F S Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  1981-08       Impact factor: 11.205

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