Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment. (Q48874060)

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7 November 2019

title

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

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7 November 2019

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A Pramatarova

1

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7 November 2019

J Laganière

2

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7 November 2019

J Roussel

3

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7 November 2019

K Brisebois

4

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7 November 2019

G A Rouleau

5

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7 November 2019

language of work or name

English

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publication date

1 May 2001

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7 November 2019

published in

Journal of Neuroscience

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7 November 2019

volume

21

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7 November 2019

page(s)

3369-3374

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7 November 2019

issue

10

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Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis

7 November 2019

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in management.

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12 December 2020

Neuronal-specific expression of human copper-zinc superoxide dismutase gene in transgenic mice: animal model of gene dosage effects in Down's syndrome

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12 December 2020

A rapid and simple method for introducing specific mutations into any position of DNA leaving all other positions unaltered

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12 December 2020

Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate

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12 December 2020

Motor neuron degeneration induced by excitotoxin agonists has features in common with those seen in the SOD-1 transgenic mouse model of amyotrophic lateral sclerosis

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12 December 2020

Familial adult motor neuron disease: amyotrophic lateral sclerosis

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12 December 2020

Restricted expression of G86R Cu/Zn superoxide dismutase in astrocytes results in astrocytosis but does not cause motoneuron degeneration

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12 December 2020

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

1 reference

12 December 2020

Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity

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12 December 2020

Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

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12 December 2020

Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis

1 reference

12 December 2020

Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome

1 reference

12 December 2020

Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).

1 reference

12 December 2020

Somatic expression of herpes thymidine kinase in mice following injection of a fusion gene into eggs

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12 December 2020

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

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12 December 2020

Multiple neuron-specific enhancers in the gene coding for the human neurofilament light chain

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12 December 2020

Decreased neurofilament gene expression is an index of selective axonal hypotrophy in ageing.

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12 December 2020

A distinct pattern of trophic factor expression in myelin-deficient nerves of Trembler mice: implications for trophic support by Schwann cells.

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12 December 2020

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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12 December 2020

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease

1 reference

12 December 2020

Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

1 reference

12 December 2020

Glutamate neurotoxicity and diseases of the nervous system

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12 December 2020

Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

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12 December 2020

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

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12 December 2020

Superoxide radical and superoxide dismutases

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12 December 2020

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

1 reference

12 December 2020

10.1523/JNEUROSCI.21-10-03369.2001

Identifiers

DOI

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7 November 2019

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7 November 2019

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