(Q44915866)

English

Mutations in mitochondrial-encoded cytochrome c oxidase subunits I, II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Mutations in mitochondrial-encoded cytochrome c oxidase subunits I, II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Alzheimer's disease

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author name string

Natasha S Hamblet

1

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Brian Ragland

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Mervat Ali

3

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Barbara Conyers

4

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Frank J Castora

5

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

publication date

1 February 2006

1 reference

Europe PubMed Central

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7 December 2017

Electrophoresis

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Europe PubMed Central

PubMed publication ID

7 December 2017

27

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Europe PubMed Central

PubMed publication ID

7 December 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

398-408

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Europe PubMed Central

PubMed publication ID

7 December 2017

Reduced platelet cytochrome c oxidase activity in Alzheimer's disease.

1 reference

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Electron transport chain defects in Alzheimer's disease brain.

1 reference

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Elevated levels of the Kearns-Sayre syndrome mitochondrial DNA deletion in temporal cortex of Alzheimer's patients

1 reference

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21 January 2018

Decreased pyruvate dehydrogenase complex activity in Huntington and Alzheimer brain

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7 January 2021

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Mitochondrial function in brain tissue in primary degenerative dementia.

1 reference

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7 January 2021

based on heuristic

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Cytochrome oxidase deficiency in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500420

7 January 2021

based on heuristic

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Brain Cytochrome Oxidase in Alzheimer's Disease

1 reference

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7 January 2021

based on heuristic

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A "mitochondrial cascade hypothesis" for sporadic Alzheimer's disease

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

1 reference

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Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication

1 reference

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7 January 2021

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High activity of alpha-glycerophosphate oxidation by human placental mitochondria

1 reference

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7 January 2021

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Cloning of human mitochondrial DNA in Escherichia coli

1 reference

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7 January 2021

based on heuristic

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Sequence and organization of the human mitochondrial genome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500420

7 January 2021

based on heuristic

inferred from DOI database lookup

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

1 reference

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How sensitive is PCR-SSCP?

1 reference

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7 January 2021

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The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

1 reference

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based on heuristic

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Detection of single nucleotide mutations in wheat using single strand conformation polymorphism gels

1 reference

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7 January 2021

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

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7 January 2021

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Mitochondrial genome variation and the origin of modern humans

1 reference

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7 January 2021

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Evidence for mtDNA admixture between the Finns and the Saami

1 reference

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7 January 2021

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Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

1 reference

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7 January 2021

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Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

1 reference

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7 January 2021

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Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome

1 reference

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7 January 2021

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

1 reference

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7 January 2021

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Correction: Mitochondrial DNA Variation in Amerindians.

1 reference

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7 January 2021

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A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy

1 reference

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7 January 2021

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Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations

1 reference

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7 January 2021

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

1 reference

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7 January 2021

based on heuristic

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Aberrations of the p53 tumor suppressor gene in human epithelial ovarian carcinoma

1 reference

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7 January 2021

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Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500420

7 January 2021

based on heuristic

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Evolution of human mitochondrial DNA: evidence for departure from a pure neutral model of populations at equilibrium

1 reference

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7 January 2021

based on heuristic

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A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene.

1 reference

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based on heuristic

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Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy

1 reference

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7 January 2021

based on heuristic

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Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families

1 reference

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7 January 2021

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Identifiers

10.1002/ELPS.200500420

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

ResearchGate publication ID

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