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Wittig I, Braun HP, Schägger H. Wittig I, et al. Nat Protoc. 2006;1(1):418-28. doi: 10.1038/nprot.2006.62. Nat Protoc. 2006. PMID: 17406264
Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency.
Alston CL, Veling MT, Heidler J, Taylor LS, Alaimo JT, Sung AY, He L, Hopton S, Broomfield A, Pavaine J, Diaz J, Leon E, Wolf P, McFarland R, Prokisch H, Wortmann SB, Bonnen PE, Wittig I, Pagliarini DJ, Taylor RW. Alston CL, et al. Among authors: wittig i. Am J Hum Genet. 2020 Jan 2;106(1):92-101. doi: 10.1016/j.ajhg.2019.12.001. Epub 2019 Dec 19. Am J Hum Genet. 2020. PMID: 31866046 Free PMC article.
Bioenergetic consequences from xenotopic expression of a tunicate AOX in mouse mitochondria: Switch from RET and ROS to FET.
Szibor M, Gainutdinov T, Fernandez-Vizarra E, Dufour E, Gizatullina Z, Debska-Vielhaber G, Heidler J, Wittig I, Viscomi C, Gellerich F, Moore AL. Szibor M, et al. Among authors: wittig i. Biochim Biophys Acta Bioenerg. 2020 Feb 1;1861(2):148137. doi: 10.1016/j.bbabio.2019.148137. Epub 2019 Dec 9. Biochim Biophys Acta Bioenerg. 2020. PMID: 31825809 Free article.
Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease.
Key J, Maletzko A, Kohli A, Gispert S, Torres-Odio S, Wittig I, Heidler J, Bárcena C, López-Otín C, Lei Y, West AP, Münch C, Auburger G. Key J, et al. Among authors: wittig i. Neurogenetics. 2020 Jul;21(3):187-203. doi: 10.1007/s10048-020-00609-2. Epub 2020 Apr 28. Neurogenetics. 2020. PMID: 32342250 Free PMC article.
Identification of two proteins associated with mammalian ATP synthase.
Meyer B, Wittig I, Trifilieff E, Karas M, Schägger H. Meyer B, et al. Among authors: wittig i. Mol Cell Proteomics. 2007 Oct;6(10):1690-9. doi: 10.1074/mcp.M700097-MCP200. Epub 2007 Jun 17. Mol Cell Proteomics. 2007. PMID: 17575325 Free article.
186 results