Majamaa K - Search Results

1

Somatic point mutations in mtDNA control region are influenced by genetic background and associated with healthy aging: a GEHA study.

Rose G, Romeo G, Dato S, Crocco P, Bruni AC, Hervonen A, Majamaa K, Sevini F, Franceschi C, Passarino G; GEnetics of Healthy Ageing Project Consortium. Rose G, et al. Among authors: majamaa k. PLoS One. 2010 Oct 14;5(10):e13395. doi: 10.1371/journal.pone.0013395. PLoS One. 2010. PMID: 20976236 Free PMC article.

2

The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific.

Raule N, Sevini F, Li S, Barbieri A, Tallaro F, Lomartire L, Vianello D, Montesanto A, Moilanen JS, Bezrukov V, Blanché H, Hervonen A, Christensen K, Deiana L, Gonos ES, Kirkwood TB, Kristensen P, Leon A, Pelicci PG, Poulain M, Rea IM, Remacle J, Robine JM, Schreiber S, Sikora E, Eline Slagboom P, Spazzafumo L, Antonietta Stazi M, Toussaint O, Vaupel JW, Rose G, Majamaa K, Perola M, Johnson TE, Bolund L, Yang H, Passarino G, Franceschi C. Raule N, et al. Among authors: majamaa k. Aging Cell. 2014 Jun;13(3):401-7. doi: 10.1111/acel.12186. Epub 2013 Dec 17. Aging Cell. 2014. PMID: 24341918 Free PMC article.

3

Mitochondrial DNA polymorphisms associated with longevity in a Finnish population.

Niemi AK, Hervonen A, Hurme M, Karhunen PJ, Jylhä M, Majamaa K. Niemi AK, et al. Among authors: majamaa k. Hum Genet. 2003 Jan;112(1):29-33. doi: 10.1007/s00439-002-0843-y. Epub 2002 Oct 17. Hum Genet. 2003. PMID: 12483296

4

A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects.

Niemi AK, Moilanen JS, Tanaka M, Hervonen A, Hurme M, Lehtimäki T, Arai Y, Hirose N, Majamaa K. Niemi AK, et al. Among authors: majamaa k. Eur J Hum Genet. 2005 Feb;13(2):166-70. doi: 10.1038/sj.ejhg.5201308. Eur J Hum Genet. 2005. PMID: 15483642

5

Phylogenetic network for European mtDNA.

Finnilä S, Lehtonen MS, Majamaa K. Finnilä S, et al. Among authors: majamaa k. Am J Hum Genet. 2001 Jun;68(6):1475-84. doi: 10.1086/320591. Epub 2001 May 10. Am J Hum Genet. 2001. PMID: 11349229 Free PMC article.

6

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

Finnilä S, Hassinen IE, Majamaa K. Finnilä S, et al. Among authors: majamaa k. Mutat Res. 1999 Aug;406(2-4):109-14. doi: 10.1016/s1383-5726(99)00007-2. Mutat Res. 1999. PMID: 10479727

7

Haplotype-matched controls as a tool to discriminate polymorphisms from pathogenic mutations in mtDNA.

Lehtonen MS, Meinilä M, Hassinen IE, Majamaa K. Lehtonen MS, et al. Among authors: majamaa k. Hum Genet. 1999 Nov;105(5):513-4. doi: 10.1007/s004390051139. Hum Genet. 1999. PMID: 10598821

8

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

Uimonen S, Moilanen JS, Sorri M, Hassinen IE, Majamaa K. Uimonen S, et al. Among authors: majamaa k. Hum Genet. 2001 Apr;108(4):284-9. doi: 10.1007/s004390100475. Hum Genet. 2001. PMID: 11379873

9

The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.

Kervinen M, Hinttala R, Helander HM, Kurki S, Uusimaa J, Finel M, Majamaa K, Hassinen IE. Kervinen M, et al. Among authors: majamaa k. Hum Mol Genet. 2006 Sep 1;15(17):2543-52. doi: 10.1093/hmg/ddl176. Epub 2006 Jul 18. Hum Mol Genet. 2006. PMID: 16849371

10

Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.

Lindroos MM, Pärkkä JP, Taittonen MT, Iozzo P, Kärppä M, Hassinen IE, Knuuti J, Nuutila P, Majamaa K. Lindroos MM, et al. Among authors: majamaa k. J Inherit Metab Dis. 2016 Jan;39(1):67-74. doi: 10.1007/s10545-015-9865-1. Epub 2015 Jun 26. J Inherit Metab Dis. 2016. PMID: 26112752

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