(Q30654181)

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Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region

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Europe PubMed Central

PubMed publication ID

26 June 2017

Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

mitochondrial DNA

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1 reference

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author name string

Finnilä S

1

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Europe PubMed Central

PubMed publication ID

26 June 2017

Hassinen IE

2

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Europe PubMed Central

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26 June 2017

Majamaa K

3

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Europe PubMed Central

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26 June 2017

language of work or name

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publication date

1 June 2001

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Europe PubMed Central

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26 June 2017

Mutation Research

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26 June 2017

458

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Europe PubMed Central

PubMed publication ID

26 June 2017

1-2

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Europe PubMed Central

PubMed publication ID

26 June 2017

31-39

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

Mutation accumulation in transfer RNAs: molecular evidence for Muller's ratchet in mitochondrial genomes

1 reference

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7 January 2021

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Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction

1 reference

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7 January 2021

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Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

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Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype

1 reference

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7 January 2021

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inferred from DOI database lookup

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

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inferred from DOI database lookup

Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

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based on heuristic

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The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct.

1 reference

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7 January 2021

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Interrater reliability of an etiologic classification of ischemic stroke.

1 reference

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Phylogeography of mitochondrial DNA in western Europe

1 reference

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7 January 2021

based on heuristic

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Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Convenient single-step, one tube purification of PCR products for direct sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

based on heuristic

inferred from DOI database lookup

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

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Mitochondrial DNA mutations associated with aging and degenerative diseases

1 reference

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based on heuristic

inferred from DOI database lookup

Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations

1 reference

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Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

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Secondary structure of the large subunit ribosomal RNA from Escherichia coli, Zea mays chloroplast, and human and mouse mitochondrial ribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

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inferred from DOI database lookup

The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

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based on heuristic

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Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

based on heuristic

inferred from DOI database lookup

An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2801%2900012-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1383-5726(01)00012-7

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

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