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Mitochondrial Complexome Profiling.
Giese H, Meisterknecht J, Heidler J, Wittig I. Giese H, et al. Among authors: heidler j. Methods Mol Biol. 2021;2192:269-285. doi: 10.1007/978-1-0716-0834-0_19. Methods Mol Biol. 2021. PMID: 33230779
Supercomplex-associated Cox26 protein binds to cytochrome c oxidase.
Strecker V, Kadeer Z, Heidler J, Cruciat CM, Angerer H, Giese H, Pfeiffer K, Stuart RA, Wittig I. Strecker V, et al. Among authors: heidler j. Biochim Biophys Acta. 2016 Jul;1863(7 Pt A):1643-52. doi: 10.1016/j.bbamcr.2016.04.012. Epub 2016 Apr 16. Biochim Biophys Acta. 2016. PMID: 27091403 Free PMC article.
Coi1 is a novel assembly factor of the yeast complex III-complex IV supercomplex.
Singhal RK, Kruse C, Heidler J, Strecker V, Zwicker K, Düsterwald L, Westermann B, Herrmann JM, Wittig I, Rapaport D. Singhal RK, et al. Among authors: heidler j. Mol Biol Cell. 2017 Aug 9;28(20):2609-22. doi: 10.1091/mbc.E17-02-0093. Online ahead of print. Mol Biol Cell. 2017. PMID: 28794267 Free PMC article.
Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I.
Alahmad A, Nasca A, Heidler J, Thompson K, Oláhová M, Legati A, Lamantea E, Meisterknecht J, Spagnolo M, He L, Alameer S, Hakami F, Almehdar A, Ardissone A, Alston CL, McFarland R, Wittig I, Ghezzi D, Taylor RW. Alahmad A, et al. Among authors: heidler j. EMBO Mol Med. 2020 Nov 6;12(11):e12619. doi: 10.15252/emmm.202012619. Epub 2020 Sep 24. EMBO Mol Med. 2020. PMID: 32969598 Free PMC article.
Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue.
Winter L, Wittig I, Peeva V, Eggers B, Heidler J, Chevessier F, Kley RA, Barkovits K, Strecker V, Berwanger C, Herrmann H, Marcus K, Kornblum C, Kunz WS, Schröder R, Clemen CS. Winter L, et al. Among authors: heidler j. Acta Neuropathol. 2016 Sep;132(3):453-73. doi: 10.1007/s00401-016-1592-7. Epub 2016 Jul 8. Acta Neuropathol. 2016. PMID: 27393313 Free PMC article.
Acyl modification and binding of mitochondrial ACP to multiprotein complexes.
Angerer H, Schönborn S, Gorka J, Bahr U, Karas M, Wittig I, Heidler J, Hoffmann J, Morgner N, Zickermann V. Angerer H, et al. Among authors: heidler j. Biochim Biophys Acta Mol Cell Res. 2017 Oct;1864(10):1913-1920. doi: 10.1016/j.bbamcr.2017.08.006. Epub 2017 Aug 9. Biochim Biophys Acta Mol Cell Res. 2017. PMID: 28802701 Free article.
Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency.
Alston CL, Heidler J, Dibley MG, Kremer LS, Taylor LS, Fratter C, French CE, Glasgow RIC, Feichtinger RG, Delon I, Pagnamenta AT, Dolling H, Lemonde H, Aiton N, Bjørnstad A, Henneke L, Gärtner J, Thiele H, Tauchmannova K, Quaghebeur G, Houstek J, Sperl W, Raymond FL, Prokisch H, Mayr JA, McFarland R, Poulton J, Ryan MT, Wittig I, Henneke M, Taylor RW. Alston CL, et al. Among authors: heidler j. Am J Hum Genet. 2018 Oct 4;103(4):592-601. doi: 10.1016/j.ajhg.2018.08.013. Epub 2018 Sep 20. Am J Hum Genet. 2018. PMID: 30245030 Free PMC article.
91 results