Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27 (Q24680250)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9042918%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27 (English)

1 reference

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1 November 2019

2 references

parkinsonian syndrome

1 reference

Matsumine H

1

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1 November 2019

Saito M

2

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1 November 2019

Shimoda-Matsubayashi S

3

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1 November 2019

Tanaka H

4

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1 November 2019

Ishikawa A

5

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1 November 2019

Nakagawa-Hattori Y

6

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1 November 2019

Yokochi M

7

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1 November 2019

Kobayashi T

8

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1 November 2019

Igarashi S

9

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1 November 2019

Takano H

10

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1 November 2019

Sanpei K

11

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1 November 2019

Koike R

12

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1 November 2019

Mori H

13

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1 November 2019

Kondo T

14

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1 November 2019

Mizutani Y

15

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1 November 2019

Schäffer AA

16

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1 November 2019

Yamamura Y

17

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1 November 2019

Nakamura S

18

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1 November 2019

Kuzuhara S

19

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1 November 2019

Tsuji S

20

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1 November 2019

Mizuno Y

21

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1 November 2019

language of work or name

English

0 references

publication date

1 March 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9042918%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

1 November 2019

published in

1 reference

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1 November 2019

volume

60

1 reference

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1 November 2019

issue

3

1 reference

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1 November 2019

page(s)

588-596

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 November 2019

cites work

1 reference

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The 1993-94 Généthon human genetic linkage map

7 April 2017

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Faster sequential genetic linkage computations

7 April 2017

1 reference

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Easy calculations of lod scores and genetic risks on small computers

7 April 2017

1 reference

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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

7 April 2017

1 reference

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Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

7 April 2017

1 reference

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Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

28 September 2017

1 reference

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Human Mn superoxide dismutase cDNA sequence

28 September 2017

1 reference

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Isolation of cDNAs encoding human manganese superoxide dismutase

28 September 2017

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Biosynthesis and regulation of superoxide dismutases

28 September 2017

1 reference

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Familial juvenile parkinsonism: clinical and pathologic study in a family

28 September 2017

1 reference

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Integrating Parallelization Strategies for Linkage Analysis

30 May 2018

1 reference

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Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease

30 May 2018

1 reference

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Sublocalization of the gene encoding manganese superoxide dismutase (MnSOD/SOD2) to 6q25 by fluorescence in situ hybridization and somatic cell hybrid mapping

30 May 2018

1 reference

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Absence of electron transport (Rho 0 state) restores growth of a manganese-superoxide dismutase-deficient Saccharomyces cerevisiae in hyperoxia. Evidence for electron transport as a major source of superoxide generation in vivo.

30 May 2018

1 reference

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Report of the Second International Workshop on Human Chromosome 6.

28 November 2018

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Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

28 November 2018

1 reference

12 December 2020

A selective increase in particulate superoxide dismutase activity in parkinsonian substantia nigra

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12 December 2020

Purification of DNA from formaldehyde fixed and paraffin embedded human tissue

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12 December 2020

Inhibition of mitochondrial NADH-ubiquinone oxidoreductase activity by 1-methyl-4-phenylpyridinium ion

1 reference

12 December 2020

Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease

1 reference

12 December 2020

1-Methyl-4-phenylpyridinium (MPP+) induces NADH-dependent superoxide formation and enhances NADH-dependent lipid peroxidation in bovine heart submitochondrial particles

1 reference

12 December 2020

Linkage analysis of juvenile parkinsonism to tyrosine hydroxylase gene locus on chromosome 11

1 reference

12 December 2020

[Early-onset parkinsonism with diurnal fluctuation--clinical and pathological studies]

1 reference

12 December 2020

Prevalence of Parkinson's disease in the elderly: The Rotterdam Study

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12 December 2020

[A 62-year-old man with familial parkinsonism with the onset at 24 years of the age]

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12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Identifiers

4168321

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

4168321

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9042918%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

9042918

2 references

Consolidated OpenCitations Corpus – April 2017

4168321