(Q74622805)

English

Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation

scientific article published on 01 October 2001

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scholarly article

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Europe PubMed Central

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12 November 2019

Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11602336%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

amyotrophic lateral sclerosis

1 reference

based on heuristic

inferred from title

1 reference

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inferred from title

author name string

M Kato

1

1 reference

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12 November 2019

M Aoki

2

1 reference

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12 November 2019

M Ohta

3

1 reference

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12 November 2019

M Nagai

4

1 reference

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12 November 2019

F Ishizaki

5

1 reference

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12 November 2019

S Nakamura

6

1 reference

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12 November 2019

Y Itoyama

7

1 reference

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12 November 2019

publication date

1 October 2001

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12 November 2019

number of pages

4

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inferred from page(s)

Neuroscience Letters

1 reference

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12 November 2019

312

1 reference

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12 November 2019

3

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12 November 2019

165-168

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12 November 2019

Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI 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

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

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

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

SOD1 aggregates in ALS: cause, correlate or consequence?

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Reevaluation of assay methods and establishment of kit for superoxide dismutase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902212-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0304-3940(01)02212-1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11602336%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11602336%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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