(Q34145261)

English

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

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scholarly article

1 reference

Europe PubMed Central

31 July 2017

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

1 reference

Europe PubMed Central

31 July 2017

electrophoresis

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1 reference

based on heuristic

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author name string

Finnilä S

1

1 reference

Europe PubMed Central

31 July 2017

Hassinen IE

2

1 reference

Europe PubMed Central

31 July 2017

Ala-Kokko L

3

1 reference

Europe PubMed Central

31 July 2017

Majamaa K

4

1 reference

Europe PubMed Central

31 July 2017

language of work or name

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publication date

1 March 2000

1 reference

Europe PubMed Central

31 July 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

31 July 2017

66

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Europe PubMed Central

31 July 2017

1017-1026

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Europe PubMed Central

31 July 2017

3

1 reference

Europe PubMed Central

31 July 2017

Mitochondrial DNA analysis: polymorphisms and pathogenicity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

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

1 reference

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5 July 2018

Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Messages from an isolate: lessons from the Finnish gene pool

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Classification of European mtDNAs from an analysis of three European populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Comparison between the complete mitochondrial DNA sequences of Homo and the common chimpanzee based on nonchimeric sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Paleolithic and neolithic lineages in the European mitochondrial gene pool

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Mitochondrial portraits of human populations using median networks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Detection of mismatched bases in double stranded DNA by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Disease gene mapping in isolated human populations: the example of Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Sequence-specific "gene signatures" can be obtained by PCR with single specific primers at low stringency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Mitochondrial DNA sequence variation in human evolution and disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Length heteroplasmy in the first hypervariable segment of the human mtDNA control region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Mechanism of somatic mitochondrial DNA mutations associated with age and diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

5 July 2018

Phylogeography of mitochondrial DNA in western Europe.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

28 October 2018

Genes and languages in Europe: an analysis of mitochondrial lineages.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288139

28 October 2018

The detection of mitochondrial DNA mutations using single stranded conformation polymorphism (SSCP) analysis and heteroduplex analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of human mitochondrial DNA fragments corresponding to the genes for ATPase, cytochrome C oxidase, and nine tRNAs in a denaturing gradient gel electrophoresis system

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification of mitochondrial DNA from human cell cultures and placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of sequence polymorphisms in the human mitochondrial DNA control region by polymerase chain reaction and single-strand conformation analysis in mutation detection enhancement gels

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SSCP analysis: A blind sensitivity trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial Disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10712215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

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