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Ketones and inborn errors of metabolism: old friends revisited.
Wüst RC, Visser G, Wanders RJ, Houtkooper RH. Wüst RC, et al. Among authors: houtkooper rh. J Inherit Metab Dis. 2017 Jan;40(1):3-4. doi: 10.1007/s10545-016-9997-y. J Inherit Metab Dis. 2017. PMID: 27830424 No abstract available.
Identification and characterization of human cardiolipin synthase.
Houtkooper RH, Akbari H, van Lenthe H, Kulik W, Wanders RJ, Frentzen M, Vaz FM. Houtkooper RH, et al. FEBS Lett. 2006 May 29;580(13):3059-64. doi: 10.1016/j.febslet.2006.04.054. Epub 2006 Apr 27. FEBS Lett. 2006. PMID: 16678169 Free article.
Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome.
Houtkooper RH, Rodenburg RJ, Thiels C, van Lenthe H, Stet F, Poll-The BT, Stone JE, Steward CG, Wanders RJ, Smeitink J, Kulik W, Vaz FM. Houtkooper RH, et al. Anal Biochem. 2009 Apr 15;387(2):230-7. doi: 10.1016/j.ab.2009.01.032. Epub 2009 Jan 31. Anal Biochem. 2009. PMID: 19454236
The enigmatic role of tafazzin in cardiolipin metabolism.
Houtkooper RH, Turkenburg M, Poll-The BT, Karall D, Pérez-Cerdá C, Morrone A, Malvagia S, Wanders RJ, Kulik W, Vaz FM. Houtkooper RH, et al. Biochim Biophys Acta. 2009 Oct;1788(10):2003-14. doi: 10.1016/j.bbamem.2009.07.009. Epub 2009 Jul 18. Biochim Biophys Acta. 2009. PMID: 19619503 Free article. Review.
Barth syndrome: cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation.
Gonzalvez F, D'Aurelio M, Boutant M, Moustapha A, Puech JP, Landes T, Arnauné-Pelloquin L, Vial G, Taleux N, Slomianny C, Wanders RJ, Houtkooper RH, Bellenguer P, Møller IM, Gottlieb E, Vaz FM, Manfredi G, Petit PX. Gonzalvez F, et al. Among authors: houtkooper rh. Biochim Biophys Acta. 2013 Aug;1832(8):1194-206. doi: 10.1016/j.bbadis.2013.03.005. Epub 2013 Mar 20. Biochim Biophys Acta. 2013. PMID: 23523468 Free article.
Fatty acid oxidation flux predicts the clinical severity of VLCAD deficiency.
Diekman EF, Ferdinandusse S, van der Pol L, Waterham HR, Ruiter JP, Ijlst L, Wanders RJ, Houten SM, Wijburg FA, Blank AC, Asselbergs FW, Houtkooper RH, Visser G. Diekman EF, et al. Among authors: houtkooper rh. Genet Med. 2015 Dec;17(12):989-94. doi: 10.1038/gim.2015.22. Epub 2015 Apr 2. Genet Med. 2015. PMID: 25834949 Free article.
184 results