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Gazing at translocation in the mitochondrion.
Walsh S, Koehler CM. Walsh S, et al. Among authors: koehler cm. Cell. 2008 Aug 8;134(3):382-3. doi: 10.1016/j.cell.2008.07.024. Cell. 2008. PMID: 18692459 Free article.
MTCH2/MIMP is a major facilitator of tBID recruitment to mitochondria.
Zaltsman Y, Shachnai L, Yivgi-Ohana N, Schwarz M, Maryanovich M, Houtkooper RH, Vaz FM, De Leonardis F, Fiermonte G, Palmieri F, Gillissen B, Daniel PT, Jimenez E, Walsh S, Koehler CM, Roy SS, Walter L, Hajnóczky G, Gross A. Zaltsman Y, et al. Among authors: koehler cm. Nat Cell Biol. 2010 Jun;12(6):553-562. doi: 10.1038/ncb2057. Epub 2010 May 2. Nat Cell Biol. 2010. PMID: 20436477 Free PMC article.
New developments in mitochondrial assembly.
Koehler CM. Koehler CM. Annu Rev Cell Dev Biol. 2004;20:309-35. doi: 10.1146/annurev.cellbio.20.010403.105057. Annu Rev Cell Dev Biol. 2004. PMID: 15473843 Review.
Correcting human mitochondrial mutations with targeted RNA import.
Wang G, Shimada E, Zhang J, Hong JS, Smith GM, Teitell MA, Koehler CM. Wang G, et al. Among authors: koehler cm. Proc Natl Acad Sci U S A. 2012 Mar 27;109(13):4840-5. doi: 10.1073/pnas.1116792109. Epub 2012 Mar 12. Proc Natl Acad Sci U S A. 2012. PMID: 22411789 Free PMC article.
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
von Ameln S, Wang G, Boulouiz R, Rutherford MA, Smith GM, Li Y, Pogoda HM, Nürnberg G, Stiller B, Volk AE, Borck G, Hong JS, Goodyear RJ, Abidi O, Nürnberg P, Hofmann K, Richardson GP, Hammerschmidt M, Moser T, Wollnik B, Koehler CM, Teitell MA, Barakat A, Kubisch C. von Ameln S, et al. Among authors: koehler cm. Am J Hum Genet. 2012 Nov 2;91(5):919-27. doi: 10.1016/j.ajhg.2012.09.002. Epub 2012 Oct 18. Am J Hum Genet. 2012. PMID: 23084290 Free PMC article.
101 results