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Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis.
Heindryckx B, Neupane J, Vandewoestyne M, Christodoulou C, Jackers Y, Gerris J, Van den Abbeel E, Van Coster R, Deforce D, De Sutter P. Heindryckx B, et al. Among authors: vandewoestyne m. Mitochondrion. 2014 Sep;18:12-7. doi: 10.1016/j.mito.2014.08.005. Epub 2014 Aug 23. Mitochondrion. 2014. PMID: 25159128
Assessment of nuclear transfer techniques to prevent the transmission of heritable mitochondrial disorders without compromising embryonic development competence in mice.
Neupane J, Vandewoestyne M, Ghimire S, Lu Y, Qian C, Van Coster R, Gerris J, Deroo T, Deforce D, De Sutter P, Heindryckx B. Neupane J, et al. Among authors: vandewoestyne m. Mitochondrion. 2014 Sep;18:27-33. doi: 10.1016/j.mito.2014.09.003. Epub 2014 Sep 16. Mitochondrion. 2014. PMID: 25229667
Cellular Heterogeneity in the Level of mtDNA Heteroplasmy in Mouse Embryonic Stem Cells.
Neupane J, Ghimire S, Vandewoestyne M, Lu Y, Gerris J, Van Coster R, Deroo T, Deforce D, Vansteelandt S, De Sutter P, Heindryckx B. Neupane J, et al. Among authors: vandewoestyne m. Cell Rep. 2015 Nov 17;13(7):1304-1309. doi: 10.1016/j.celrep.2015.10.019. Epub 2015 Nov 5. Cell Rep. 2015. PMID: 26549459 Free article.
Detailed method description for noninvasive monitoring of differentiation status of human embryonic stem cells.
Scheerlinck E, Van Steendam K, Vandewoestyne M, Lepez T, Gobin V, Meert P, Vossaert L, Van Nieuwerburgh F, Van Soom A, Peelman L, Heindryckx B, De Sutter P, Dhaenens M, Deforce D. Scheerlinck E, et al. Among authors: vandewoestyne m. Anal Biochem. 2014 Sep 15;461:60-6. doi: 10.1016/j.ab.2014.05.026. Epub 2014 Jun 5. Anal Biochem. 2014. PMID: 24909445 Free article.
38 results