Literature DB >> 7865504

A simple test to monitor the motor dysfunction in a transgenic mouse model of amyotrophic lateral sclerosis.

J F Collard1, J P Julien.   

Abstract

We reported recently that transgenic mice overexpressing human neurofilament heavy (NF-H) proteins develop a progressive neurological disorder with pathological features resembling those found in amyotrophic lateral sclerosis (ALS) (Côté et al 1993). A simple behavioral test, the grasping ability, has been used here for evaluating the motor dysfunction during aging of NF-H transgenic mice. Transgenic mice overexpressing NF-H proteins are normal at birth but they progressively fail to uphold their weight when tested for their grasping ability. The deficits in motor function during aging correlate with a progressive disruption of peripheral nerve function as evidenced by the atrophy and degeneration of distal axons.

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Year:  1995        PMID: 7865504      PMCID: PMC1188660     

Source DB:  PubMed          Journal:  J Psychiatry Neurosci        ISSN: 1180-4882            Impact factor:   6.186


  10 in total

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Authors:  D C Gajdusek
Journal:  N Engl J Med       Date:  1985-03-14       Impact factor: 91.245

Review 2.  Axonal transport in neurological disease.

Authors:  J W Griffin; D F Watson
Journal:  Ann Neurol       Date:  1988-01       Impact factor: 10.422

3.  Proximal axonal enlargement in motor neuron disease.

Authors:  S Carpenter
Journal:  Neurology       Date:  1968-09       Impact factor: 9.910

4.  Alterations in neurofilament mRNA in hereditary canine spinal muscular atrophy.

Authors:  N A Muma; L C Cork
Journal:  Lab Invest       Date:  1993-10       Impact factor: 5.662

5.  Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease.

Authors:  Z Xu; L C Cork; J W Griffin; D W Cleveland
Journal:  Cell       Date:  1993-04-09       Impact factor: 41.582

6.  Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis.

Authors:  F Côté; J F Collard; J P Julien
Journal:  Cell       Date:  1993-04-09       Impact factor: 41.582

7.  Fine structural observations of neurofilamentous changes in amyotrophic lateral sclerosis.

Authors:  A Hirano; H Donnenfeld; S Sasaki; I Nakano
Journal:  J Neuropathol Exp Neurol       Date:  1984-09       Impact factor: 3.685

8.  Swellings of proximal axons in a case of motor neuron disease.

Authors:  S Sasaki; S Maruyama; K Yamane; H Sakuma; M Takeishi
Journal:  Ann Neurol       Date:  1989-05       Impact factor: 10.422

9.  Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Authors:  D R Rosen; T Siddique; D Patterson; D A Figlewicz; P Sapp; A Hentati; D Donaldson; J Goto; J P O'Regan; H X Deng
Journal:  Nature       Date:  1993-03-04       Impact factor: 49.962

10.  Phosphate dependent and independent neurofilament epitopes in the axonal swellings of patients with motor neuron disease and controls.

Authors:  M L Schmidt; M J Carden; V M Lee; J Q Trojanowski
Journal:  Lab Invest       Date:  1987-03       Impact factor: 5.662

  10 in total
  1 in total

1.  Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment.

Authors:  A Pramatarova; J Laganière; J Roussel; K Brisebois; G A Rouleau
Journal:  J Neurosci       Date:  2001-05-15       Impact factor: 6.167

  1 in total

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