Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases
Na Cai, Aurora Gómez-Durán, Ekaterina Yonova‐Doing, Kousik Kundu, A I Burgess, Zoe Golder, Claudia Calabrese, Marc Jan Bonder, Marta Camacho, Rachael A. Lawson, Lixin Li, Caroline H. Williams‐Gray, ICICLE-PD Study Group, Emanuele Di Angelantonio, David J. Roberts, Nick Watkins, Willem H. Ouwehand, Adam S. Butterworth, Isobel D. Stewart, Maik Pietzner, Nicholas J. Wareham, Claudia Langenberg, John Danesh, Klaudia Walter, Peter M. Rothwell, Joanna M. M. Howson, Oliver Stegle, Patrick F. Chinnery, Nicole Soranzo
Topics & Concepts
ProteostasisMitochondrial DNABiologyHaplogroupGeneticsMitochondrionHuman mitochondrial DNA haplogroupHuman mitochondrial geneticsCell biologyGeneHaplotypeAlleleMitochondrial Function and PathologyMetabolism and Genetic DisordersLipid metabolism and biosynthesis