(Q77905916)

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Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population

scientific article published on 01 July 1999

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scholarly article

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9 December 2019

Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population (English)

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9 December 2019

author name string

P Chagnon

1

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9 December 2019

M Gee

2

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9 December 2019

M Filion

3

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9 December 2019

Y Robitaille

4

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9 December 2019

M Belouchi

5

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9 December 2019

D Gauvreau

6

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9 December 2019

publication date

1 July 1999

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9 December 2019

American Journal of Medical Genetics Part A

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9 December 2019

85

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9 December 2019

1

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9 December 2019

20-30

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9 December 2019

Sequence and organization of the human mitochondrial genome

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

1 reference

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21 January 2018

Structure and function of cytochrome c oxidase

1 reference

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21 January 2018

Increased risk of dementia in mothers of Alzheimer's disease cases: evidence for maternal inheritance

1 reference

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21 January 2018

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

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21 January 2018

Intercorrelations of regional cerebral glucose metabolic rates in Alzheimer's disease.

1 reference

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21 January 2018

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy

1 reference

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21 January 2018

Abnormalities of Glucose Metabolism in Alzheimer's Disease

1 reference

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21 January 2018

Glucose metabolism as the site of the primary abnormality in early-onset dementia of Alzheimer type?

1 reference

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21 January 2018

A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

1 reference

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21 January 2018

Cytochrome b mutations in Leber hereditary optic neuropathy

1 reference

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21 January 2018

Diagnosis of Alzheimer's disease

1 reference

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21 January 2018

Brain Cytochrome Oxidase in Alzheimer's Disease

1 reference

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21 January 2018

No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's disease.

1 reference

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21 January 2018

A familial Alzheimer's disease locus on chromosome 1.

1 reference

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21 January 2018

Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains

1 reference

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21 January 2018

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

1 reference

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21 January 2018

Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease

1 reference

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21 January 2018

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

1 reference

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21 January 2018

Cytochrome oxidase deficiency in Alzheimer's disease

1 reference

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21 January 2018

Cytochrome c oxidase in Alzheimer's disease brain: purification and characterization

1 reference

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21 January 2018

Electron transport chain defects in Alzheimer's disease brain.

1 reference

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21 January 2018

Alterations in calcium content and biochemical processes in cultured skin fibroblasts from aged and Alzheimer donors

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21 January 2018

Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease

1 reference

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21 January 2018

Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

1 reference

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21 January 2018

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

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21 January 2018

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

1 reference

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21 January 2018

Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders

1 reference

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21 January 2018

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

1 reference

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21 January 2018

Mitochondrial DNA and Disease

1 reference

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21 January 2018

Mitochondrial DNA mutations in diseases of energy metabolism

1 reference

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21 January 2018

Mitochondrial DNA mutations in human degenerative diseases and aging

1 reference

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21 January 2018

Cytochrome oxidase: an endogenous metabolic marker for neuronal activity

1 reference

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21 January 2018

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant.

1 reference

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21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19990702)85:1<20::AID-AJMG6>3.0.CO;2-K

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10377009%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10377009%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

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