Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase (Q71990868)

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scientific article published on 01 May 1995

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English	Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase	scientific article published on 01 May 1995

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

title

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

main subject

amyotrophic lateral sclerosis

1 reference

based on heuristic

inferred from title

homozygosity

1 reference

based on heuristic

inferred from title

homozygote

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

author name string

P. M. Andersen

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

P. Nilsson

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

V. Ala-Hurula

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

M. L. Keränen

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

I. Tarvainen

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

T. Haltia

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

L. Nilsson

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

M. Binzer

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

L. Forsgren

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

S. L. Marklund

series ordinal

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647793

retrieved

14 July 2024

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

7647793

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7647793

retrieved

14 July 2024

publication date

1 May 1995

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

full work available at URL

http://www.nature.com/articles/ng0595-61

1 reference

stated in

Crossref

DOI

10.1038/NG0595-61

reference URL

https://api.crossref.org/works/10.1038/NG0595-61

retrieved

14 July 2024

http://www.nature.com/articles/ng0595-61.pdf

file format

Portable Document Format

1 reference

stated in

Crossref

DOI

10.1038/NG0595-61

reference URL

https://api.crossref.org/works/10.1038/NG0595-61

retrieved

14 July 2024

published in

Nature Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

volume

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

page(s)

61-66

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

cites work

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

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

based on heuristic

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

1 reference

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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Mild ALS in Japan associated with novel SOD mutation

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7 January 2021

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SOD1 missense mutation in an Italian family with ALS

1 reference

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

based on heuristic

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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

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis

1 reference

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

based on heuristic

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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

based on heuristic

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

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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Human copper-containing superoxide dismutase of high molecular weight

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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inferred from DOI database lookup

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

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase.

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7 January 2021

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Plasma extracellular superoxide dismutase and erythrocyte Cu,Zn-containing superoxide dismutase in alcoholics treated with disulfiram

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7 January 2021

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Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. I.

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7 January 2021

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Phenotypic and genotypic heterogeneity of dominantly inherited amyotrophic lateral sclerosis

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7 January 2021

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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

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Population studies in northern Sweden. VI. Polymorphism of superoxide dismutase

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Superoxide Dismutase. A Population Study

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Genetics of human superoxide dismutase

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Epidemiology of motor neuron disease in northern Sweden

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7 January 2021

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Determination and analysis of the 2 A-structure of copper, zinc superoxide dismutase

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Crossref

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https://api.crossref.org/works/10.1038%2FNG0595-61

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7 January 2021

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Conserved patterns in the Cu,Zn superoxide dismutase family.

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Crossref

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7 January 2021

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ALS, SOD and peroxynitrite

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Crossref

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7 January 2021

based on heuristic

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Criteria for diagnosis of familial amyotrophic lateral sclerosis. European FALS Collaborative Group

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Confounding and effect-modification

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Crossref

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Concordance for amyotrophic lateral sclerosis in a pair of dizygous twins of consanguineous parents

series ordinal

25

1 reference

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Crossref

DOI

10.1038/NG0595-61

reference URL

https://api.crossref.org/works/10.1038/NG0595-61

retrieved

14 July 2024

Identifiers

DOI

10.1038/NG0595-61

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

PubMed publication ID

7647793

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7647793

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647793%20AND%20SRC:MED&resulttype=core&format=json

retrieved

22 October 2019

 

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