Literature DB >> 329151

[Neuromuscular interactions--tendencies toward a biochemical-genetic analysis].

H Jockusch.   

Abstract

The analysis of hereditary neuro-muscular diseases in the mouse and in other vertebrates may contribute to our understanding of the developmental interactions between spinal cord and sceletal muscle. Meaningful biochemical analysis must be preceded by "biological mixing experiments" to demonstrate whether a given mutation is cell-autonomous, and, if so, which cell type caries the primary defect. Techniques are available to carry out the critical experiment in vivo (artificial chimaeras) or in culture.

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Year:  1977        PMID: 329151     DOI: 10.1007/bf00438298

Source DB:  PubMed          Journal:  Naturwissenschaften        ISSN: 0028-1042


  25 in total

1.  Acetylcholine receptor antibodies in myasthenia gravis.

Authors:  S H Appel; R R Almon; N Levy
Journal:  N Engl J Med       Date:  1975-10-09       Impact factor: 91.245

2.  Mouse chimaeras developed from fused eggs.

Authors:  A K TARKOWSKI
Journal:  Nature       Date:  1961-06-03       Impact factor: 49.962

Review 3.  Gene control of mammalian differentiation.

Authors:  B Mintz
Journal:  Annu Rev Genet       Date:  1974       Impact factor: 16.830

4.  Expression of the dystrophia muscularis (dy) recessive gene in mice.

Authors:  R Parsons
Journal:  Nature       Date:  1974-10-18       Impact factor: 49.962

5.  Trophic functions of the neuron. IV. Clinical disorders of trophic functions muscular dystrophy? Sick motoneurons and muscle disease.

Authors:  A J McComas; R E Sica; A R Upton; F Petito
Journal:  Ann N Y Acad Sci       Date:  1974-03-22       Impact factor: 5.691

6.  Chimaera mouse study shows absence of disease in genetically dystrophic muscle.

Authors:  A C Peterson
Journal:  Nature       Date:  1974-04-12       Impact factor: 49.962

7.  Innervation in cultures of fetal rodent skeletal muscle by organotypic explants of spinal cord from different animals.

Authors:  E R Peterson; S M Crain
Journal:  Z Zellforsch Mikrosk Anat       Date:  1970

8.  CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM).

Authors:  L W DUCHEN; S J STRICH; D S FALCONER
Journal:  Brain       Date:  1964-06       Impact factor: 13.501

9.  MED myopathy. A new hereditary myopathy.

Authors:  S I Zacks; M F Sheff; M Rhodes; A Saito
Journal:  Lab Invest       Date:  1969-08       Impact factor: 5.662

10.  Fate of ganglionic synapses and ganglion cell axons during normal and induced cell death.

Authors:  L Landmesser; G Pilar
Journal:  J Cell Biol       Date:  1976-02       Impact factor: 10.539

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  2 in total

1.  Calcium-binding protein, parvalbumin, is reduced in mutant mammalian muscle with abnormal contractile properties.

Authors:  I Stuhlfauth; J Reininghaus; H Jockusch; C W Heizmann
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

2.  Hereditary motor endplate disease (med) of the mouse: observations on dissociated myogenic cells and their development in culture.

Authors:  H Jockusch; W Burkart; M M Burger
Journal:  Cell Tissue Res       Date:  1980       Impact factor: 5.249

  2 in total

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