(Q33737269)

29 July 2017

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title

Role of mitochondria in Parkinson disease (English)

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29 July 2017

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Kösel S

1

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29 July 2017

Hofhaus G

2

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29 July 2017

Maassen A

3

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29 July 2017

Vieregge P

4

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29 July 2017

Graeber MB

5

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29 July 2017

publication date

1 July 1999

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29 July 2017

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29 July 2017

volume

380

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29 July 2017

issue

7-8

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29 July 2017

page(s)

865-870

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Sequence and organization of the human mitochondrial genome

29 July 2017

cites work

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Glial pathology but absence of apoptotic nigral neurons in long-standing Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer's and Parkinson's diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease.

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

The apoptosis-necrosis paradox. Apoptogenic proteases activated after mitochondrial permeability transition determine the mode of cell death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Point mutations of mitochondrial genome in Parkinson's disease

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

The mitochondrial permeability transition in cell death: a common mechanism in necrosis, apoptosis and autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

The ubiquitin pathway in Parkinson's disease

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Quantitation of a mitochondrial DNA deletion in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Effects of isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on mitochondrial respiration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Mitochondria as regulators of apoptosis: doubt no more.

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Origin and functional consequences of the complex I defect in Parkinson's disease

21 January 2018

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https://api.crossref.org/works/10.1515%2FBC.1999.106

Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Diseases of the mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Maternal inheritance in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: Localization to Chromosome 7q32 and identification of a pseudogene on 11pl5

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.106

21 January 2018

Identifiers

DOI

10.1515/BC.1999.106

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29 July 2017

1 reference