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European Journal of Human Genetics : EJHG|April 12, 2007
Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European foundersAnna H Hakonen, Guido Davidzon, Renato Salemi, et al.European Journal of Nutrition|September 11, 2025
Bone and mineral metabolism in 2-7-year-old Finnish children and their caregivers following vegan, vegetarian, and omnivorous dietsSuvi T Itkonen, Topi Hovinen, Elina Kettunen, et al.Cells|August 26, 2022
Varied Responses to a High m.3243A>G Mutation Load and Respiratory Chain Dysfunction in Patient-Derived CardiomyocytesSanna Ryytty, Shalem R Modi, Nikolay Naumenko, et al.Circulation|December 2, 2025
Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart AssociationJessica L Fetterman, Patrick F Chinnery, Rebecca McClellan, et al.Cell Metabolism|August 3, 2017
mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy ProgressionNahid A Khan, Joni Nikkanen, Shuichi Yatsuga, et al.Neurology. Genetics|July 9, 2020
Genetic background of ataxia in children younger than 5 years in FinlandErika Ignatius, Pirjo Isohanni, Max Pohjanpelto, et al.Plos One|July 11, 2013
The overexpression of Twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in miceAtsushi Tanaka, Tomomi Ide, Takeo Fujino, et al.Journal of Community Genetics|April 6, 2020
Attitudes towards genetic testing and information: does parenthood shape the views?Antti Saastamoinen, Virva Hyttinen, Mika Kortelainen, et al.Human Molecular Genetics|February 20, 2010
Ketogenic diet slows down mitochondrial myopathy progression in miceSofia Ahola-Erkkilä, Christopher J Carroll, Katja Peltola-Mjösund, 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 16