(Q28267385)

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Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

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Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis (English)

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amyotrophic lateral sclerosis

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neurodegeneration

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author name string

C L Lin

1

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L A Bristol

2

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L Jin

3

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M Dykes-Hoberg

4

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T Crawford

5

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L Clawson

6

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J D Rothstein

7

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language of work or name

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publication date

March 1998

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20

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3

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589-602

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Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis

1 reference

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Evidence for autoimmunity in amyotrophic lateral sclerosis

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Functional comparisons of three glutamate transporter subtypes cloned from human motor cortex

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Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis

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A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group

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Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis

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Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis

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Glutamate transporter gene expression in amyotrophic lateral sclerosis motor cortex

1 reference

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El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

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Superoxide dismutase and familial amyotrophic lateral sclerosis: new insights into mechanisms and treatments

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Mechanisms of selective motor neuron death in ALS: insights from transgenic mouse models of motor neuron disease

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NMDA and kainate induce internucleosomal DNA cleavage associated with both apoptotic and necrotic cell death in the neonatal rat brain

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In vitro kainate injury to large, SMI-32(+) spinal neurons is Ca2+ dependent.

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Cell culture evidence for neuronal degeneration in amyotrophic lateral sclerosis being linked to glutamate AMPA/kainate receptors

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DNA strand breaks induced by sustained glutamate excitotoxicity in primary neuronal cultures.

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Intron retention generates a novel isoform of the murine vitamin D receptor that acts in a dominant negative way on the vitamin D signaling pathway

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An excitatory amino-acid transporter with properties of a ligand-gated chloride channel

1 reference

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Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980997-6

7 January 2021

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Increased 3-nitrotyrosine and oxidative damage in mice with a human copper/zinc superoxide dismutase mutation.

1 reference

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The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

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Cellular and synaptic localization of the neuronal glutamate transporters excitatory amino acid transporter 3 and 4.

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Benefit of vitamin E, riluzole, and gabapentin in a transgenic model of familial amyotrophic lateral sclerosis

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Genomic organization, promoter analysis, and chromosomal localization of the gene for the mouse glial high-affinity glutamate transporter Slc1a3.

1 reference

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Brain glutamate transporter proteins form homomultimers

1 reference

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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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Parvalbumin and calbindin D-28k in the human motor system and in motor neuron disease

1 reference

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An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease).

1 reference

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Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II

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7 January 2021

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A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease

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Differential expression of two glial glutamate transporters in the rat brain: quantitative and immunocytochemical observations

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The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

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7 January 2021

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Genomic organization of the human excitatory amino acid transporter gene GLT-1.

1 reference

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Placebo-controlled trial of gabapentin in patients with amyotrophic lateral sclerosis. WALS Study Group. Western Amyotrophic Lateral Sclerosis Study Group

1 reference

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smg mutants affect the expression of alternatively spliced SR protein mRNAs in Caenorhabditis elegans

1 reference

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Excitotoxicity hypothesis

1 reference

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7 January 2021

based on heuristic

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Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

1 reference

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

1 reference

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Chronic inhibition of glutamate uptake produces a model of slow neurotoxicity

1 reference

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7 January 2021

based on heuristic

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Localization of neuronal and glial glutamate transporters

1 reference

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based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

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Excitotoxicity and motor neurone disease: a review of the evidence

1 reference

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inferred from DOI database lookup

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

CSF and plasma amino acid levels in motor neuron disease: elevation of CSF glutamate in a subset of patients

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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based on heuristic

inferred from DOI database lookup

Serum antibodies to L-type calcium channels in patients with amyotrophic lateral sclerosis

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1 reference

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1 reference

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Peroxynitrite inhibits glutamate transporter subtypes

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inferred from DOI database lookup

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10.1016/S0896-6273(00)80997-6

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