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Metabolic switch from fatty acid oxidation to glycolysis in knock-in mouse model of Barth syndrome.
Chowdhury A, Boshnakovska A, Aich A, Methi A, Vergel Leon AM, Silbern I, Lüchtenborg C, Cyganek L, Prochazka J, Sedlacek R, Lindovsky J, Wachs D, Nichtova Z, Zudova D, Koubkova G, Fischer A, Urlaub H, Brügger B, Katschinski DM, Dudek J, Rehling P. Chowdhury A, et al. Among authors: rehling p. EMBO Mol Med. 2023 Sep 11;15(9):e17399. doi: 10.15252/emmm.202317399. Epub 2023 Aug 3. EMBO Mol Med. 2023. PMID: 37533404 Free PMC article.
Moving proteins from the cytosol into mitochondria.
Chacinska A, Rehling P. Chacinska A, et al. Among authors: rehling p. Biochem Soc Trans. 2004 Nov;32(Pt 5):774-6. doi: 10.1042/BST0320774. Biochem Soc Trans. 2004. PMID: 15494012 Review.
The mitochondrial import machinery for preproteins.
Rehling P, Wiedemann N, Pfanner N, Truscott KN. Rehling P, et al. Crit Rev Biochem Mol Biol. 2001;36(3):291-336. doi: 10.1080/20014091074200. Crit Rev Biochem Mol Biol. 2001. PMID: 11450972 Review.
Pex17p of Saccharomyces cerevisiae is a novel peroxin and component of the peroxisomal protein translocation machinery.
Huhse B, Rehling P, Albertini M, Blank L, Meller K, Kunau WH. Huhse B, et al. Among authors: rehling p. J Cell Biol. 1998 Jan 12;140(1):49-60. doi: 10.1083/jcb.140.1.49. J Cell Biol. 1998. PMID: 9425153 Free PMC article.
The Saccharomyces cerevisiae pex17-1 mutant was isolated from a screen to identify mutants defective in peroxisome biogenesis. pex17-1 and pex17 null mutants fail to import matrix proteins into peroxisomes via both PTS1- and PTS2-dependent pathways. The PEX17 gene (formerly PAS9; …
The Saccharomyces cerevisiae pex17-1 mutant was isolated from a screen to identify mutants defective in peroxisome biogenesis. pex17-1 and p …
150 results