Amyotrophic lateral sclerosis: human challenge for neuroscience (Q34598050)

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English	Amyotrophic lateral sclerosis: human challenge for neuroscience	scientific article

Statements

instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

7877963

retrieved

3 August 2017

review article

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Europe PubMed Central

title

Amyotrophic lateral sclerosis: human challenge for neuroscience (English)

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Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

main subject

amyotrophic lateral sclerosis

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author name string

Rowland LP

series ordinal

1

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Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

language of work or name

English

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publication date

1 February 1995

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Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

published in

Proceedings of the National Academy of Sciences of the United States of America

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stated in

Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

volume

92

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stated in

Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

issue

5

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Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

page(s)

1251-1253

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Europe PubMed Central

PubMed publication ID

7877963

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3 August 2017

cites work

Motor neurone disease and animal models

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

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

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

Neurofilament-deficient axons and perikaryal aggregates in viable transgenic mice expressing a neurofilament-beta-galactosidase fusion protein

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

Down-regulation of copper/zinc superoxide dismutase causes apoptotic death in PC12 neuronal cells

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

Chronic inhibition of superoxide dismutase produces apoptotic death of spinal neurons

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

New pathological findings in amyotrophic lateral sclerosis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

Cytopathology of amyotrophic lateral sclerosis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

Transgenic mice with increased Cu/Zn-superoxide dismutase activity are resistant to N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

7 July 2018

Superoxide dismutase, catalase, and glutathione peroxidase activities in copper/zinc-superoxide dismutase transgenic mice

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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7 July 2018

Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

26 October 2018

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

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26 October 2018

Autosomal dominant amyotrophic lateral sclerosis: a novel mutation in the Cu/Zn superoxide dismutase-1 gene

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42496

retrieved

26 October 2018

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofilament light and polyadenylated mRNA levels are decreased in amyotrophic lateral sclerosis motor neurons

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

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Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

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Did radicals strike Lou Gehrig?

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased cerebrospinal-fluid superoxide dismutase in amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

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Amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

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Identification of a novel SOD1 mutation in an apparently sporadic amyotrophic lateral sclerosis patient and the detection of Ile113Thr in three others

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A two basepair deletion in the SOD 1 gene causes familial amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ALS, SOD and peroxynitrite

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutant mice, Cu,Zn superoxide dismutase, and motor neuron degeneration

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cu/Zn superoxide dismutase free radicals, and motoneuron disease

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cu/Zn superoxide dismutase (SOD1) mutations and sporadic amyotrophic lateral sclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Red blood cell Cu/Zn superoxide dismutase activity in sporadic amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Response

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A transgenic-mouse model of amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superoxide dismutase and ALS

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decrease in Cu/Zn- and Mn-superoxide dismutase activities in brain and spinal cord of patients with amyotrophic lateral sclerosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild ALS in Japan associated with novel SOD mutation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

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Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

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A study of apoptosis in normal and pathologic nervous tissue after in situ end-labeling of DNA strand breaks

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of superoxide dismutase activity by the polarographic method of catalytic currents in the cerebrospinal fluid of aging brain and neurologic degenerative diseases

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7877963

retrieved

12 December 2020

based on heuristic

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Identifiers

DOI

10.1073/PNAS.92.5.1251

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7877963

retrieved

3 August 2017

ADS bibcode

1995PNAS...92.1251R

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PMC publication ID

42496

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7877963

retrieved

3 August 2017

PubMed publication ID

7877963

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7877963

retrieved

3 August 2017

ResearchGate publication ID

15321191

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