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Life Science Alliance|January 27, 2019
Mitochondrial stress response triggered by defects in protein synthesis quality controlUwe Richter, Kah Ying Ng, Fumi Suomi, et al.Communications Biology|January 3, 2024
Recessive TMOD1 mutation causes childhood cardiomyopathyCatalina Vasilescu, Mert Colpan, Tiina H Ojala, et al.Cell Metabolism|September 17, 2019
Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA DeletionsSaara Forsström, Christopher B Jackson, Christopher J Carroll, et al.Cell Metabolism|October 8, 2019
Regulation of Mother-to-Offspring Transmission of mtDNA HeteroplasmyAna Latorre-Pellicer, Ana Victoria Lechuga-Vieco, Iain G Johnston, et al.Human Molecular Genetics|October 5, 2018
Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathyEwen W Sommerville, Xiao-Long Zhou, Monika Oláhová, et al.Neurology|June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactateAnna-Kaisa Anttonen, Taru Hilander, Tarja Linnankivi, et al.Nature Communications|October 13, 2019
TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytesJason W Miklas, Elisa Clark, Shiri Levy, et al.Nature Communications|May 10, 2020
Author Correction: TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytesJason W Miklas, Elisa Clark, Shiri Levy, et al.Neurology|October 30, 2016
FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disordersJenni M Lehtonen, Saara Forsström, Emanuela Bottani, et al.Science Advances|August 9, 2023
TNIK is a conserved regulator of glucose and lipid metabolism in obesityT C Phung Pham, Lucile Dollet, Mona S Ali, et al.Pageof 16