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Journal of Inherited Metabolic Disease|July 6, 2023
Disease models of mitochondrial aminoacyl-tRNA synthetase defectsHenna TyynismaaMethods (San Diego, Calif.)|April 14, 2010
Mouse models of mtDNA replication diseasesHenna Tyynismaa, Anu SuomalainenMolecular Genetics and Metabolism|February 26, 2013
Mitochondrial aminoacyl-tRNA synthetases in human diseaseSvetlana Konovalova, Henna TyynismaaEMBO Reports|January 17, 2009
Mouse models of mitochondrial DNA defects and their relevance for human diseaseHenna Tyynismaa, Anu SuomalainenEMBO Molecular Medicine|January 30, 2014
Mixing and matching mitochondrial aminoacyl synthetases and their tRNAs: a new way to treat respiratory chain disorders?Henna Tyynismaa, Eric A SchonCurrent Protocols in Toxicology|August 1, 2018
Analysis of Mitochondrial Protein Synthesis: De Novo Translation, Steady-State Levels, and Assembled OXPHOS ComplexesTaru Hilander, Svetlana Konovalova, Mügen Terzioglu, et al.Human Mutation|June 10, 2016
Splicing Defect in Mitochondrial Seryl-tRNA Synthetase Gene Causes Progressive Spastic Paresis Instead of HUPRA SyndromeTarja Linnankivi, Nirajan Neupane, Uwe Richter, et al.Human Molecular Genetics|April 24, 2010
High mitochondrial DNA copy number has detrimental effects in miceEmil Ylikallio, Henna Tyynismaa, Hiroyuki Tsutsui, et al.Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesisEmil Ylikallio, Elisa Rahikkala, Riikka Keski-Filppula, et al.European Journal of Human Genetics : EJHG|November 4, 2005
Genetic background of HSH in three Polish families and a patient with an X;9 translocationReetta Jalkanen, Ewa Pronicka, Henna Tyynismaa, et al.Pageof 9