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Stem cells in reproductive medicine: ready for the patient?ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: preliminary assessment of data from January 1997 to September 1998. ESHRE PGD Consortium Steering Committee.ESHRE PGD Consortium data collection IV: May-December 2001.ESHRE PGD Consortium data collection V: cycles from January to December 2002 with pregnancy follow-up to October 2003.ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004.ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006.Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the Automated Laser Fluorescence DNA Sequencer.Preimplantation genetic diagnosis for myotonic dystrophy type 1: upon request to childPreimplantation genetic diagnosis for fragile Xa syndrome: difficult but not impossible.Concurrent whole-genome haplotyping and copy-number profiling of single cells.Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage.Higher-Density Culture in Human Embryonic Stem Cells Results in DNA Damage and Genome Instability.PGD for monogenic disorders: aspects of molecular biology.Creation of a registry for human embryonic stem cells carrying an inherited defect: joint collaboration between ESHRE and hESCreg.Current controversies in prenatal diagnosis 1: is stem cell therapy ready for human fetuses?CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic DystrophyGenome engineering through CRISPR/Cas9 technology in the human germline and pluripotent stem cells.The role of methylation, DNA polymorphisms and microRNAs on HLA-G expression in human embryonic stem cells.Female human pluripotent stem cells rapidly lose X chromosome inactivation marks and progress to a skewed methylation pattern during culture.The Role of D4Z4-Encoded Proteins in the Osteogenic Differentiation of Mesenchymal Stromal Cells Isolated from Bone Marrow.Preimplantation genetic screening 2.0: the theoryThe why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologistsHuman embryonic stem cells show low-grade microsatellite instability.Mitotic spindle disruption in human preimplantation embryos activates the spindle assembly checkpoint but not apoptosis until Day 5 of development.Role of BMP signaling in pancreatic progenitor differentiation from human embryonic stem cells.FGF signaling via MAPK is required early and improves Activin A-induced definitive endoderm formation from human embryonic stem cells.Establishment of hESC lines from the inner cell mass of blastocyst-stage embryos and single blastomeres of 4-cell stage embryos.Human embryonic stem cell lines derived from single blastomeres of two 4-cell stage embryos.Characterization of CD30 expression in human embryonic stem cell lines cultured in serum-free media and passaged mechanically.Markers that define stemness in ESC are unable to identify the totipotent cells in human preimplantation embryos.CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation.Efficient differentiation of human embryonic stem cells into a homogeneous population of osteoprogenitor-like cells.Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders.Characterisation of a cDNA for porcine PDH-E1 alpha and comparison with the human cDNA.Novel universal approach for preimplantation genetic diagnosis of beta-thalassaemia in combination with HLA matching of embryos.Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos.Review: preimplantation diagnosis of inherited disease.Chromosome constitution of human embryos generated after in vitro maturation including 3-isobutyl-1-methylxanthine in the oocyte collection medium.Recent advances and prospects in the differentiation of pancreatic cells from human embryonic stem cells.PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.
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researcher ORCID ID = 0000-0002-2311-9034
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wetenschapper
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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Karen Sermon
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P31
P496
0000-0002-2311-9034