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FEBS Open Bio|May 5, 2022
Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1Aleksi Sutinen, Giang Thi Tuyet Nguyen, Arne Raasakka, et al.Nucleic Acids Research|December 12, 2017
Editing activity for eliminating mischarged tRNAs is essential in mammalian mitochondriaTaru Hilander, Xiao-Long Zhou, Svetlana Konovalova, et al.Redox Biology|August 12, 2018
Redox regulation of GRPEL2 nucleotide exchange factor for mitochondrial HSP70 chaperoneSvetlana Konovalova, Xiaonan Liu, Pooja Manjunath, et al.Frontiers in Neurology|June 16, 2016
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle DiseasePäivi Piirilä, Minna E Similä, Johanna Palmio, et al.Human Molecular Genetics|October 29, 2004
Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy numberHenna Tyynismaa, Hiroshi Sembongi, Monika Bokori-Brown, et al.Human Molecular Genetics|September 23, 2011
Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletionsHenna Tyynismaa, Ren Sun, Sofia Ahola-Erkkilä, et al.Plos Biology|February 7, 2019
TRIM2, a novel member of the antiviral family, limits New World arenavirus entryNicolas Sarute, Nouhou Ibrahim, Bani Medegan Fagla, et al.Frontiers in Neurology|March 7, 2022
Serum Creatine, Not Neurofilament Light, Is Elevated in CHCHD10-Linked Spinal Muscular AtrophyJulius Järvilehto, Sandra Harjuhaahto, Edouard Palu, et al.Plos One|March 31, 2015
Overexpression of TFAM or twinkle increases mtDNA copy number and facilitates cardioprotection associated with limited mitochondrial oxidative stressMasataka Ikeda, Tomomi Ide, Takeo Fujino, et al.Human Gene Therapy|August 15, 2012
Capsid-modified adenoviral vectors for improved muscle-directed gene therapyKilian Guse, Masataka Suzuki, Gautam Sule, et al.Pageof 9