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Methods (San Diego, Calif.)|April 14, 2010
Mouse models of mtDNA replication diseasesHenna Tyynismaa, Anu SuomalainenEMBO Reports|January 17, 2009
Mouse models of mitochondrial DNA defects and their relevance for human diseaseHenna Tyynismaa, Anu SuomalainenHuman Molecular Genetics|April 24, 2010
High mitochondrial DNA copy number has detrimental effects in miceEmil Ylikallio, Henna Tyynismaa, Hiroyuki Tsutsui, et al.American Journal of Human Genetics|August 12, 2009
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletionsHenna Tyynismaa, Emil Ylikallio, Mehul Patel, et al.Human Molecular Genetics|October 31, 2008
Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stallingSteffi Goffart, Helen M Cooper, Henna Tyynismaa, et al.Journal of Inherited Metabolic Disease|July 6, 2023
Disease models of mitochondrial aminoacyl-tRNA synthetase defectsHenna TyynismaaNucleic Acids Research|August 21, 2010
Ribonucleotide reductase is not limiting for mitochondrial DNA copy number in miceEmil Ylikallio, Jennifer L Page, Xia Xu, et al.The Journal of Clinical Endocrinology and Metabolism|December 3, 2010
Liver fat but not other adiposity measures influence circulating FGF21 levels in healthy young adult twinsHenna Tyynismaa, Taneli Raivio, Antti Hakkarainen, et al.Proceedings of the National Academy of Sciences of the United States of America|November 23, 2005
Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in miceHenna Tyynismaa, Katja Peltola Mjosund, Sjoerd Wanrooij, et al.Neurology|July 20, 2014
Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophySofia Ahola, Pirjo Isohanni, Liliya Euro, et al.Pageof 21