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European Journal of Human Genetics : EJHG|August 27, 2003
Lack of a modulative factor in locus 8p23 in a Finnish family with nonsyndromic sensorineural hearing loss associated with the 1555A>G mitochondrial DNA mutationSaara Finnilä, Kari MajamaaJournal of Molecular Evolution|June 29, 2005
Sequence variation in the tRNA genes of human mitochondrial DNATiina Vilmi, Jukka S Moilanen, Saara Finnilä, et al.BMC Medical Genetics|July 23, 2013
Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitusHeidi K Soini, Jukka S Moilanen, Tiina Vilmi-Kerälä, et al.Pediatrics|August 3, 2004
Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) genesJohanna Uusimaa, Saara Finnilä, Anne M Remes, et al.Human Genetics|April 27, 2004
Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementiaJaana Autere, Jukka S Moilanen, Saara Finnilä, et al.Mitochondrion|February 6, 2007
Cytoskeletal structure in cells harboring two mutations: R133C in NOTCH3 and 5650G>A in mitochondrial DNAJohanna Annunen-Rasila, Mikko Kärppä, Saara Finnilä, et al.Pediatrics|March 4, 2003
A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like diseaseJohanna Uusimaa, Saara Finnilä, Leena Vainionpää, et al.Mitochondrion|March 4, 2010
Analysis of functional consequences of haplogroup J polymorphisms m.4216T>C and m.3866T>C in human MT-ND1: mutagenesis of homologous positions in Escherichia coliReetta Hinttala, Marko Kervinen, Johanna Uusimaa, et al.BMC Neurology|May 5, 2010
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotypeTuomas Komulainen, Reetta Hinttala, Mikko Kärppä, et al.Neurogenetics|June 30, 2006
Mitochondrial DNA sequence variation and mutation rate in patients with CADASILJohanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, et al.Pageof 2