Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kristian Want"'
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Friedreich’s ataxia (FRDA) is the most prevalent autosomic recessive ataxia and is associated with a severe cardiac hypertrophy and less frequently diabetes. It is caused by mutations in the gene encoding frataxin (FXN), a small mitochondrial prote
Externí odkaz:
https://doaj.org/article/5740df41d66c45fa9eca949aab5d60e1
Autor:
Batoul Srour, Sylvain Gervason, Maren Hellen Hoock, Beata Monfort, Kristian Want, Djabir Larkem, Nadine Trabelsi, Gautier Landrot, Andrea Zitolo, Emiliano Fonda, Emilien Etienne, Guillaume Gerbaud, Christina Sophia Müller, Jonathan Oltmanns, Jesse B. Gordon, Vishal Yadav, Malgorzata Kleczewska, Marcin Jelen, Michel B. Toledano, Rafal Dutkiewicz, David P. Goldberg, Volker Schünemann, Bruno Guigliarelli, Bénédicte Burlat, Christina Sizun, Benoit D’Autréaux
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, 2022, 144 (38), pp.17496-17515. ⟨10.1021/jacs.2c06338⟩
Journal of the American Chemical Society, 2022, 144 (38), pp.17496-17515. ⟨10.1021/jacs.2c06338⟩
International audience; Iron−sulfur (Fe−S) clusters are prosthetic groups of proteins biosynthesized on scaffold proteins by highly conserved multi-protein machineries. Biosynthesis of Fe−S clusters into the ISCU scaffold protein is initiated b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09f1e62412505c0e54f958b4c5b661c5
https://doi.org/10.1021/jacs.2c06338
https://doi.org/10.1021/jacs.2c06338
Publikováno v:
Frontiers in Neuroscience. 16
Friedreich’s ataxia (FRDA) is the most prevalent autosomic recessive ataxia and is associated with a severe cardiac hypertrophy and less frequently diabetes. It is caused by mutations in the gene encoding frataxin (FXN), a small mitochondrial prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1408bf728b0a0df07e18a0a759f9496