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Literature DB >> 6197859

Axonal transport dysfunction in dystrophia myotonica.

M I Behrens, G Torrealba, J Court, M A Soza, B U Ramírez.

Abstract

Axonal transport of acetylcholinesterase (AChE) was measured in the median and sural nerves of a subject who suffered from dystrophia myotonica and in a control subject. It was found that the basal activity of AChE was increased in myotonic nerves while its proximodistal transport was inhibited.

Entities: Disease Gene

Mesh：

Substances：
Acetylcholinesterase

Year: 1983 PMID： 6197859 DOI： 10.1007/bf00684935

Source DB: PubMed Journal: Acta Neuropathol ISSN： 0001-6322 Impact factor: 17.088

10 in total

1. A new and rapid colorimetric determination of acetylcholinesterase activity.

Authors: G L ELLMAN; K D COURTNEY; V ANDRES; R M FEATHER-STONE
Journal: Biochem Pharmacol Date: 1961-07 Impact factor: 5.858

2. Fast axoplasmic transport of acetylcholinesterase in mammalian nerve fibres.

Authors: N Ranish; S Ochs
Journal: J Neurochem Date: 1972-11 Impact factor: 5.372

3. 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

4. A definition of irreversible coma. Report of the Ad Hoc Committee of the Harvard Medical School to Examine the Definition of Brain Death.

Authors:
Journal: JAMA Date: 1968-08-05 Impact factor: 56.272

Review 5. Smooth endoplasmic reticulum and axonal transport.

Authors: A Rambourg; B Droz
Journal: J Neurochem Date: 1980-07 Impact factor: 5.372

Review 6. On axoplasmic flow.

Authors: L Lubińska
Journal: Int Rev Neurobiol Date: 1975 Impact factor: 3.230

1 in total

1. Neural control of the expression of a Ca(2+)-activated K+ channel involved in the induction of myotonic-like characteristics.

Authors: B U Ramírez; M I Behrens; C Vergara
Journal: Cell Mol Neurobiol Date: 1996-02 Impact factor: 5.046

1 in total

Axonal transport dysfunction in dystrophia myotonica.

1. A new and rapid colorimetric determination of acetylcholinesterase activity.

2. Fast axoplasmic transport of acetylcholinesterase in mammalian nerve fibres.

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

4. A definition of irreversible coma. Report of the Ad Hoc Committee of the Harvard Medical School to Examine the Definition of Brain Death.

Review 5. Smooth endoplasmic reticulum and axonal transport.

Review 6. On axoplasmic flow.

7. Rapid axoplasmic transport in dystrophic mice.

8. Dystrophia myotonica. Peripheral nerve involvement and pathogenetic implications.

9. Axonal transport of dopamine- -hydroxylase by human sural nerves in vitro.

10. Reduced axonal transport of 10S acetylcholinesterase in dystrophic mice.

1. Neural control of the expression of a Ca(2+)-activated K+ channel involved in the induction of myotonic-like characteristics.