Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Anne Marie van der Kevie-Kersemaekers"'
Autor:
Sabina Kersting, Mark-David Levin, Julie Dubois, Yvette van Norden, Johan Dobber, Yvonne Jauw, Anne-Marie van der Kevie-Kersemaekers, Clemens Mellink, Caspar Da Cunha-Bang, Leonie Van Desr Burg, Doreen Te Raa, Fransien de Boer, Jolanda Droogendijk, Cecile Idink, Koen De Heer, Marten Nijziel, Lidwine Tick, Inge Ludwig, Mathijs Silbermann, Aart Beeker, Mar Bellido, Ludo Evers, Gerben Zwezerijnen, Josée Zijlstra, Marcel Kap, Carsten Niemann, Arnon Kater
Publikováno v:
HemaSphere, Vol 7, p e797861a (2023)
Externí odkaz:
https://doaj.org/article/def1784e57be41248dd5770881eba9b2
Autor:
Marten Hansen, Eszter Varga, Tatjana Wüst, Clemens Mellink, Anne-Marie van der Kevie-Kersemaekers, Marieke von Lindern, Emile van den Akker
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 42-45 (2017)
Mobilized peripheral blood (MPB) CD34+ cells were differentiated to CD34+/CD41+ megakaryoblasts. Cells were sorted to obtain a pure megakaryoblast population which was reprogrammed with a hOKSM self-silencing polycistronic lentiviral vector. Resultin
Externí odkaz:
https://doaj.org/article/f717d64c255d4e09b6b8655e1b9d9213
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:
Alexander C. Leeksma, Panagiotis Baliakas, Theodoros Moysiadis, Anna Puiggros, Karla Plevova, Anne-Marie van der Kevie-Kersemaekers, Hidde Posthuma, Ana E. Rodriguez-Vicente, Anh Nhi Tran, Gisela Barbany, Larry Mansouri, Rebeqa Gunnarsson, Helen Parker, Eva van den Berg, Mar Bellido, Zadie Davis, Meaghan Wall, Ilaria Scarpelli, Anders Österborg, Lotta Hansson, Marie Jarosova, Paolo Ghia, Pino Poddighe, Blanca Espinet, Sarka Pospisilova, Constantine Tam, Loïc Ysebaert, Florence Nguyen-Khac, David Oscier, Claudia Haferlach, Jacqueline Schoumans, Marian Stevens-Kroef, Eric Eldering, Kostas Stamatopoulos, Richard Rosenquist, Jonathan C. Strefford, Clemens Mellink, Arnon P. Kater
Publikováno v:
Haematologica, Vol 106, Iss 1 (2020)
Complex karyotype (CK) identified by chromosome-banding analysis (CBA) has shown prognostic value in chronic lymphocytic leukemia (CLL). Genomic arrays offer high-resolution genome-wide detection of copy-number alterations (CNAs) and could therefore
Externí odkaz:
https://doaj.org/article/b0edf60d944d4c6fab629017cf3cd09c
Autor:
Mark-David Levin, Sabina Kersting, Julie M.N. Dubois, Yvette Norden, Johan A Dobber, Yvonne W.S. Jauw, Anne-Marie van der Kevie-Kersemaekers, Clemens Mellink, Koen de Heer, Leonie van der Burg, Doreen Te Raa, Fransien de Boer, Jolanda Droogendijk, Cecile Idink, Marten R. Nijziel, Lidwine W. Tick, Inge Ludwig, Matthijs Silbermann, Aart Beeker, Mar Bellido, Ludo M. Evers, Gerben JC Zwezerijnen, Carsten U Niemann, Arnon P. Kater
Publikováno v:
Blood. 140:4137-4139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed1625ac71a83ac6d32654e613af2049
https://doi.org/10.1182/blood-2022-163209
https://doi.org/10.1182/blood-2022-163209
Autor:
Peter Henneman, Arjan Bouman, Adri Mul, Lia Knegt, Anne-Marie van der Kevie-Kersemaekers, Nitash Zwaveling-Soonawala, Hanne E J Meijers-Heijboer, A S Paul van Trotsenburg, Marcel M Mannens
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0194938 (2018)
Down syndrome (DS) is the most frequent genetic cause of intellectual disability. Despite the fact that more than 50 years have passed since the discovery of its genetic aberrations, the exact pathogenesis of the DS phenotype has remained largely une
Externí odkaz:
https://doaj.org/article/71f8f06ba8d14e2f8486496b239d453c
Autor:
Paul J. Hengeveld, Y. Emre Ertem, Julie M. N. Dubois, Clemens H. M. Mellink, Anne-Marie van der Kevie-Kersemaekers, Ludo M. Evers, Kim Heezen, P. Martijn Kolijn, Olaf R. F. Mook, M. Mahdi Motazacker, Kazem Nasserinejad, S. Kersting, Peter E. Westerweel, Carsten U. Niemann, Arnon P. Kater, Anton W. Langerak, Mark-David Levin
Publikováno v:
Leukemia, 36(7), 1935-1938. Nature Publishing Group
Hengeveld, P J, Ertem, Y E, Dubois, J M N, Mellink, C H M, van der Kevie-Kersemaekers, A-M, Evers, L M, Heezen, K, Kolijn, P M, Mook, O R F, Motazacker, M M, Nasserinejad, K, Kersting, S, Westerweel, P E, Niemann, C U, Kater, A P, Langerak, A W & Levin, M-D 2022, ' Clinicobiological characteristics and treatment efficacy of novel agents in chronic lymphocytic leukemia with IGLV3-21R110 ', Leukemia, vol. 36, no. 7, pp. 1935-1938 . https://doi.org/10.1038/s41375-022-01600-6
Hengeveld, P J, Ertem, Y E, Dubois, J M N, Mellink, C H M, van der Kevie-Kersemaekers, A-M, Evers, L M, Heezen, K, Kolijn, P M, Mook, O R F, Motazacker, M M, Nasserinejad, K, Kersting, S, Westerweel, P E, Niemann, C U, Kater, A P, Langerak, A W & Levin, M-D 2022, ' Clinicobiological characteristics and treatment efficacy of novel agents in chronic lymphocytic leukemia with IGLV3-21R110 ', Leukemia, vol. 36, no. 7, pp. 1935-1938 . https://doi.org/10.1038/s41375-022-01600-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faddf632bed0aa0326c60d56e6fb24a1
https://pure.eur.nl/en/publications/cca58e3c-bfba-46df-b5e8-942d64040987
https://pure.eur.nl/en/publications/cca58e3c-bfba-46df-b5e8-942d64040987
Autor:
Paul J, Hengeveld, Y Emre, Ertem, Julie M N, Dubois, Clemens H M, Mellink, Anne-Marie, van der Kevie-Kersemaekers, Ludo M, Evers, Kim, Heezen, P Martijn, Kolijn, Olaf R F, Mook, M Mahdi, Motazacker, Kazem, Nasserinejad, S, Kersting, Peter E, Westerweel, Carsten U, Niemann, Arnon P, Kater, Anton W, Langerak, Mark-David, Levin
Publikováno v:
Leukemia. 36(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d871805ee1fd3a775813c05e53695dd
https://pubmed.ncbi.nlm.nih.gov/35585140
https://pubmed.ncbi.nlm.nih.gov/35585140
Autor:
Anne-Marie van der Kevie-Kersemaekers, Clemens Mellink, Yanwen Jiang, Michelle Boyer, Arnon P. Kater, Brenda J. Chyla, Marcus Lefebure, John F. Seymour, Julie Dubois, Barbara Eichhorst, Peter Hillmen, Relja Popovic, Jenny Wu, Carolyn Owen, Anton W. Langerak, Rosemary Harrup, Maria Thadani-Mulero, Thomas J. Kipps, Fengjiao Dunbar
Publikováno v:
Blood. 138:1548-1548
Introduction: In the MURANO trial (NCT02005471), fixed-duration VenR (2 yrs Ven + R for the first 6 mo) improved survival and rates of undetectable minimal residual disease (MRD) over bendamustine (Benda)-R in pts with R/R CLL. Novel recurrent mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e12a037a8f3ed3e892d3c4aef6a2aca2
https://doi.org/10.1182/blood-2021-147731
https://doi.org/10.1182/blood-2021-147731
Autor:
Marielle Alders, Arjan Bouman, Roelof-Jan Oostra, Anne-Marie van der Kevie-Kersemaekers, Merel C. van Maarle, Nikki Thuijs, Elisabeth van Leeuwen
Publikováno v:
Bouman, A, Alders, M, Oostra, R J, van Leeuwen, E, Thuijs, N, van der Kevie-Kersemaekers, A-M & van Maarle, M 2017, ' Oral-facial-digital syndrome type 1 in males : Congenital heart defects are included in its phenotypic spectrum ', American Journal of Medical Genetics Part A, vol. 173, no. 5, pp. 1383-1389 . https://doi.org/10.1002/ajmg.a.38179
American journal of medical genetics. Part A, 173(5), 1383-1389. Wiley-Liss Inc.
American Journal of Medical Genetics Part A, 173(5), 1383-1389. Wiley-Liss Inc.
American Journal of Medical Genetics. Part a
American journal of medical genetics. Part A, 173(5), 1383-1389. Wiley-Liss Inc.
American Journal of Medical Genetics Part A, 173(5), 1383-1389. Wiley-Liss Inc.
American Journal of Medical Genetics. Part a
Oral-facial-digital syndrome type 1 (OFD1; OMIM# 311200) is an X-linked dominant ciliopathy caused by mutations in the OFD1 gene. This condition is characterized by facial anomalies and abnormalities of oral tissues, digits, brain, and kidneys. Almos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e76aab185a95c90295ef582759aeee7
https://doi.org/10.1002/ajmg.a.38179
https://doi.org/10.1002/ajmg.a.38179