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Cell Reports|May 17, 2025
De novo serine biosynthesis is protective in mitochondrial diseaseChristopher B Jackson, Anastasiia Marmyleva, Geoffray Monteuuis, et al.Nature Communications|December 3, 2025
Vacuolar-type H<sup>+</sup>-ATPase-mediated extra-organellar buffering resolves mitochondrial dysfunctionGeoffray Monteuuis, Ryan Awadhpersad, Daan van der Kolk, et al.Human Molecular Genetics|July 27, 2010
Mitochondrial myopathy induces a starvation-like responseHenna Tyynismaa, Christopher J Carroll, Nuno Raimundo, et al.Human Molecular Genetics|July 27, 2012
Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathyJenni M Elo, Srujana S Yadavalli, Liliya Euro, et al.Mitochondrion|February 23, 2018
A urinary biosignature for mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS)Karien Esterhuizen, J Zander Lindeque, Shayne Mason, et al.Journal of the American College of Cardiology|November 3, 2018
Genetic Basis of Severe Childhood-Onset CardiomyopathiesCatalina Vasilescu, Tiina H Ojala, Virginia Brilhante, et al.Iscience|July 17, 2024
Supernumerary proteins of the human mitochondrial ribosomal small subunit are integral for assembly and translationTaru Hilander, Ryan Awadhpersad, Geoffray Monteuuis, 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.Clinical Genetics|July 30, 2022
HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H-TM proteinMinna Kraatari-Tiri, Leila Soikkonen, Matti Myllykoski, et al.Pageof 5