249 related articles for article (PubMed ID: 10712215)
1. Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis.
Finnilä S; Hassinen IE; Ala-Kokko L; Majamaa K
Am J Hum Genet; 2000 Mar; 66(3):1017-26. PubMed ID: 10712215
[TBL] [Abstract][Full Text] [Related]
2. Phylogenetic network for European mtDNA.
Finnilä S; Lehtonen MS; Majamaa K
Am J Hum Genet; 2001 Jun; 68(6):1475-84. PubMed ID: 11349229
[TBL] [Abstract][Full Text] [Related]
3. Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region.
Finnilä S; Hassinen IE; Majamaa K
Mutat Res; 2001 Jun; 458(1-2):31-9. PubMed ID: 11406419
[TBL] [Abstract][Full Text] [Related]
4. Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J.
Moilanen JS; Finnila S; Majamaa K
Mol Biol Evol; 2003 Dec; 20(12):2132-42. PubMed ID: 12949126
[TBL] [Abstract][Full Text] [Related]
5. Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population.
Finnilä S; Majamaa K
J Hum Genet; 2001; 46(2):64-9. PubMed ID: 11281414
[TBL] [Abstract][Full Text] [Related]
6. Frequency distribution of mitochondrial DNA haplogroups in Corsica and Sardinia.
Morelli L; Grosso MG; Vona G; Varesi L; Torroni A; Francalacci P
Hum Biol; 2000 Aug; 72(4):585-95. PubMed ID: 11048788
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
Annunen-Rasila J; Finnilä S; Mykkänen K; Moilanen JS; Veijola J; Pöyhönen M; Viitanen M; Kalimo H; Majamaa K
Neurogenetics; 2006 Jul; 7(3):185-94. PubMed ID: 16807713
[TBL] [Abstract][Full Text] [Related]
8. SNaPshot minisequencing to resolve mitochondrial macro-haplogroups found in Africa.
Schlebusch CM; Naidoo T; Soodyall H
Electrophoresis; 2009 Nov; 30(21):3657-64. PubMed ID: 19810027
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial DNA variability in Poles and Russians.
Malyarchuk BA; Grzybowski T; Derenko MV; Czarny J; Woźniak M; Miścicka-Sliwka D
Ann Hum Genet; 2002 Jul; 66(Pt 4):261-83. PubMed ID: 12418968
[TBL] [Abstract][Full Text] [Related]
10. The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.
Lahermo P; Sajantila A; Sistonen P; Lukka M; Aula P; Peltonen L; Savontaus ML
Am J Hum Genet; 1996 Jun; 58(6):1309-22. PubMed ID: 8651309
[TBL] [Abstract][Full Text] [Related]
11. Evidence for mtDNA admixture between the Finns and the Saami.
Meinilä M; Finnilä S; Majamaa K
Hum Hered; 2001; 52(3):160-70. PubMed ID: 11588400
[TBL] [Abstract][Full Text] [Related]
12. An update on conformation sensitive gel electrophoresis.
Ganguly A
Hum Mutat; 2002 Apr; 19(4):334-42. PubMed ID: 11933188
[TBL] [Abstract][Full Text] [Related]
13. Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.
Herrnstadt C; Elson JL; Fahy E; Preston G; Turnbull DM; Anderson C; Ghosh SS; Olefsky JM; Beal MF; Davis RE; Howell N
Am J Hum Genet; 2002 May; 70(5):1152-71. PubMed ID: 11938495
[TBL] [Abstract][Full Text] [Related]
14. Phylogenetic classification of Japanese mtDNA assisted by complete mitochondrial DNA sequences.
Nohira C; Maruyama S; Minaguchi K
Int J Legal Med; 2010 Jan; 124(1):7-12. PubMed ID: 19066930
[TBL] [Abstract][Full Text] [Related]
15. Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: a comparison of fluorescent and manual techniques.
Hashemi Soteh M; Peake IR; Marsden L; Anson J; Batlle J; Meyer D; Fressinaud E; Mazurier C; Goudemand J; Eikenboom J; Goodeve A;
Haematologica; 2007 Apr; 92(4):550-3. PubMed ID: 17488667
[TBL] [Abstract][Full Text] [Related]
16. Microevolution in prehistoric Andean populations: chronologic mtDNA variation in the desert valleys of northern Chile.
Moraga M; Santoro CM; Standen VG; Carvallo P; Rothhammer F
Am J Phys Anthropol; 2005 Jun; 127(2):170-81. PubMed ID: 15503344
[TBL] [Abstract][Full Text] [Related]
17. High resolution analysis and phylogenetic network construction using complete mtDNA sequences in sardinian genetic isolates.
Fraumene C; Belle EM; Castrì L; Sanna S; Mancosu G; Cosso M; Marras F; Barbujani G; Pirastu M; Angius A
Mol Biol Evol; 2006 Nov; 23(11):2101-11. PubMed ID: 16901986
[TBL] [Abstract][Full Text] [Related]
18. A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease.
Soini HK; Väisänen A; Kärppä M; Hinttala R; Kytövuori L; Moilanen JS; Uusimaa J; Majamaa K
BMC Med Genet; 2017 Feb; 18(1):14. PubMed ID: 28187756
[TBL] [Abstract][Full Text] [Related]
19. A sensitive denaturing gradient-Gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region.
Tully LA; Parsons TJ; Steighner RJ; Holland MM; Marino MA; Prenger VL
Am J Hum Genet; 2000 Aug; 67(2):432-43. PubMed ID: 10873789
[TBL] [Abstract][Full Text] [Related]
20. Sequence polymorphisms of the mitochondrial DNA control region and phylogenetic analysis of mtDNA lineages in the Japanese population.
Maruyama S; Minaguchi K; Saitou N
Int J Legal Med; 2003 Aug; 117(4):218-25. PubMed ID: 12845447
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]