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Barth syndrome mutations that cause tafazzin complex lability.
Claypool SM, Whited K, Srijumnong S, Han X, Koehler CM. Claypool SM, et al. Among authors: koehler cm. J Cell Biol. 2011 Feb 7;192(3):447-62. doi: 10.1083/jcb.201008177. J Cell Biol. 2011. PMID: 21300850 Free PMC article.
Defining functional classes of Barth syndrome mutation in humans.
Lu YW, Galbraith L, Herndon JD, Lu YL, Pras-Raves M, Vervaart M, Van Kampen A, Luyf A, Koehler CM, McCaffery JM, Gottlieb E, Vaz FM, Claypool SM. Lu YW, et al. Among authors: koehler cm. Hum Mol Genet. 2016 May 1;25(9):1754-70. doi: 10.1093/hmg/ddw046. Epub 2016 Feb 16. Hum Mol Genet. 2016. PMID: 26908608 Free PMC article.
The complexity of cardiolipin in health and disease.
Claypool SM, Koehler CM. Claypool SM, et al. Among authors: koehler cm. Trends Biochem Sci. 2012 Jan;37(1):32-41. doi: 10.1016/j.tibs.2011.09.003. Epub 2011 Oct 17. Trends Biochem Sci. 2012. PMID: 22014644 Free PMC article. Review.
99 results