Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bert, van der Reijden"'
Autor:
Huan Zhang, Marten Hansen, Franca di Summa, Marieke von Lindern, Nynke Gillemans, Wilfred F.J. van IJcken, Arthur Flohr Svendsen, Sjaak Philipsen, Bert van der Reijden, Eszter Varga, Emile van den Akker
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Differentiation of induced pluripotent stem cells (iPSCs) into hematopoietic lineages offers great therapeutic potential. During embryogenesis, hemogenic endothelium (HE) gives rise to hematopoietic stem and progenitor cells through the endothelial-t
Externí odkaz:
https://doaj.org/article/844b71922450425d8dc141a667fe69d7
Autor:
Marten Hansen, Eszter Varga, Tatjana Wüst, Clemens Mellink, Anne-Marie van der Kevie-Kersemaekers, Anne E. Marneth, Marieke von Lindern, Bert van der Reijden, Emile van den Akker
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 34-37 (2017)
Peripheral blood mononuclear cells were isolated from an individual harboring a heterozygous c.859C → T p.Q287* mutation in GFI1B, causing an autosomal dominant bleeding disorder, platelet type, 17 (BDPLT17). PBMCs were differentiated to erythrobla
Externí odkaz:
https://doaj.org/article/91a2cfd943dd436f9e9a8fa9f4e6c4e8
Autor:
Branco Heuts, Saioa Arza-Apalategi, Sinna Alkema, Esther Tijchon, Laura Jussen, Saskia Bergevoet, Bert van der Reijden, Joost H. A. Martens
A t(9;11)(p22;q23) translocation produces the MLL-AF9 fusion protein, which is found in up to 25% of de novo AML cases in children. Despite major advances, obtaining a comprehensive understanding of context-dependent MLL-AF9-mediated gene programs du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af6664e2950a51ae1d66deb9b6d711c1
https://doi.org/10.21203/rs.3.rs-2521405/v1
https://doi.org/10.21203/rs.3.rs-2521405/v1
Autor:
Julia van Leersum, Norah M. van Mello, Bert van der Reijden, Callista L. Mulder, Thessa N. Koorenhof-Scheele, Ron Peek, Catharina C. M. Beerendonk, Didi D.M. Braat, Lotte L Eijkenboom
Publikováno v:
Journal of Assisted Reproduction and Genetics
Eijkenboom, L, Mulder, C, van der Reijden, B, van Mello, N, van Leersum, J, Koorenhof-Scheele, T, Braat, D, Beerendonk, C & Peek, R 2021, ' Purging human ovarian cortex of contaminating leukaemic cells by targeting the mitotic catastrophe signalling pathway ', Journal of Assisted Reproduction and Genetics, vol. 38, no. 6, pp. 1571-1588 . https://doi.org/10.1007/s10815-021-02081-9
Journal of Assisted Reproduction and Genetics, 38(6), 1571-1588. Springer New York
Journal of assisted reproduction and genetics, 38(6), 1571-1588. Springer New York
Journal of Assisted Reproduction and Genetics, 38, 6, pp. 1571-1588
Journal of Assisted Reproduction and Genetics, 38, 1571-1588
Eijkenboom, L, Mulder, C, van der Reijden, B, van Mello, N, van Leersum, J, Koorenhof-Scheele, T, Braat, D, Beerendonk, C & Peek, R 2021, ' Purging human ovarian cortex of contaminating leukaemic cells by targeting the mitotic catastrophe signalling pathway ', Journal of Assisted Reproduction and Genetics, vol. 38, no. 6, pp. 1571-1588 . https://doi.org/10.1007/s10815-021-02081-9
Journal of Assisted Reproduction and Genetics, 38(6), 1571-1588. Springer New York
Journal of assisted reproduction and genetics, 38(6), 1571-1588. Springer New York
Journal of Assisted Reproduction and Genetics, 38, 6, pp. 1571-1588
Journal of Assisted Reproduction and Genetics, 38, 1571-1588
Purpose Is it possible to eliminate metastasised chronic myeloid leukaemia (CML) and acute myeloid leukaemia (AML) cells from ovarian cortex fragments by inhibition of Aurora B/C kinases (AURKB/C) without compromising ovarian tissue or follicles? Met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52d438225ec6925496c5219e15b8f40b
http://europepmc.org/articles/PMC8266964
http://europepmc.org/articles/PMC8266964
Autor:
Marian J, Stevens-Kroef, Daniel, Olde Weghuis, Najat, ElIdrissi-Zaynoun, Bert, van der Reijden, Eline M P, Cremers, Canan, Alhan, Theresia M, Westers, Heleen A, Visser-Wisselaar, Dana A, Chitu, Sonia M, Cunha, Edo, Vellenga, Saskia K, Klein, Pierre, Wijermans, Georgine E, de Greef, M Ron, Schaafsma, Petra, Muus, Gert J, Ossenkoppele, Arjan A, van de Loosdrecht, Joop H, Jansen
Publikováno v:
Genes, chromosomescancer. 56(7)
Karyotyping is considered as the gold standard in the genetic subclassification of myelodysplastic syndrome (MDS). Oligo/SNP-based genomic array profiling is a high-resolution tool that also enables genome wide analysis. We compared karyotyping with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6844d0fb1cddab8185dc511f4070d7b
https://pubmed.ncbi.nlm.nih.gov/28236351
https://pubmed.ncbi.nlm.nih.gov/28236351
Autor:
Nona Shayegi, Andre Willasch, Peter Bader, Selim Kuçi, Hermann Kreyenberg, Gerrit Weber, Dietrich Niethammer, Gaby Schneider, Thomas Klingebiel, Bert Van Der Reijden, Britta Sofia Reincke
Publikováno v:
Laboratory Hematology, 13, 73-84
Laboratory Hematology, 13, 3, pp. 73-84
Laboratory Hematology, 13, 3, pp. 73-84
Sequence polymorphisms (SPs) can serve as genetic markers for quantitative polymerase chain reactions (qPCR) for chimerism analysis, providing a significantly higher sensitivity compared to short tandem repeat PCR. In this study, a panel of 29 select
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4cc3bc55d09272950f7738a4e1e5924
https://doi.org/10.1532/lh96.07004
https://doi.org/10.1532/lh96.07004