Zobrazeno 1 - 10
of 239
pro vyhledávání: '"Stavast, A."'
Autor:
de Groot, Fleur A., Dekker, Tim J.A., Doorduijn, Jeanette K., Böhringer, Stefan, Brink, Mirian, de Groen, Ruben A.L., de Haan, Lorraine M., Woei-A-Jin, F.J. Sherida H., Noordenbos, Troy, Sijs-Szabo, Aniko, Oudshoorn, Mirjam A., Lam, King H., Diepstra, Arjan, te Boome, Liane C.J., Terpstra, Valeska, Bohmer, Lara H., Nicolae, Alina, Posthuma, Eduardus F.M., Koens, Lianne, Durian, Marc F., Stavast, Jeroen, van der Poel, Marjolein W.M., Hamid, Myrurgia Abdul, Stevens, Wendy B.C., van Rooij, Sjo L.M., Oostvogels, Rimke S., Mühlebner, Angelika, Neelis, Karen J., van den Brand, Michiel, Tousseyn, Thomas, Dierickx, Daan, de Weerdt, Okke, Beeker, Aart, Jansen, Patty M., Kersten, Marie José, Zijlstra, Josée M., Chamuleau, Martine E.D., Veelken, Hendrik, Bromberg, Jacoline C.E., Nijland, Marcel, Vermaat, Joost S.P.
Publikováno v:
In European Journal of Cancer December 2024 213
Akademický článek
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Publikováno v:
In Cancer Letters 28 July 2018 427:28-37
Autor:
Stefan J. Erkeland, Christiaan J. Stavast, Joyce Schilperoord-Vermeulen, Giada Dal Collo, Harmen J.G. van de Werken, Leticia G. Leon, Antoinette van Hoven-Beijen, Iris van Zuijen, Yvonne M. Mueller, Eric M. Bindels, Dick de Ridder, Mies C. Kappers-Klunne, Kirsten van Lom, Vincent H.J. van der Velden, Anton W. Langerak
Publikováno v:
Haematologica, Vol 107, Iss 1 (2021)
T-cell prolymphocytic leukemia (T-PLL) is mostly characterized by aberrant expansion of small- to medium-sized prolymphocytes with a mature post-thymic phenotype, high aggressiveness of the disease and poor prognosis. However, T-PLL is more heterogen
Externí odkaz:
https://doaj.org/article/c51dcad216b44704bc99e3de44c2cf7a
Publikováno v:
Cells, Vol 11, Iss 5, p 769 (2022)
Mounting data show that MIR139 is commonly silenced in solid cancer and hematological malignancies. MIR139 acts as a critical tumor suppressor by tuning the cellular response to different types of stress, including DNA damage, and by repressing oncog
Externí odkaz:
https://doaj.org/article/656cf7badba14b6b995aeee0a8a57c9d
Autor:
Jorn L. J. C. Assmann, Leticia G. Leon, Christiaan J. Stavast, Sanne E. van den Bogaerdt, Joyce Schilperoord-Vermeulen, Yorick Sandberg, Mar Bellido, Stefan J. Erkeland, David J. Feith, Thomas P. Loughran Jr, Anton W. Langerak
Publikováno v:
Leukemia, 36. Nature Publishing Group
Leukemia, 36(4), 983-993. Nature Publishing Group
Leukemia, 36(4), 983-993. Nature Publishing Group
T-LGL cells arise as a consequence of chronic antigenic stimulation and inflammation and thrive because of constitutive activation of the STAT3 and ERK pathway. Notably, in 40% of patients, constitutive STAT3 activation is due to STAT3 activating mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcbe792e0080c94f752304297c31470b
https://pure.eur.nl/en/publications/5f9453c3-f066-447b-80af-1c45f5f46d92
https://pure.eur.nl/en/publications/5f9453c3-f066-447b-80af-1c45f5f46d92
Autor:
Khalil, Ramzi, Boels, Margien G. S., Bezuijen, A., Boers, J. E., de Bruin, P. C., van Dijk, M. A. A. M., Drillenburg, P., Hamel, A. F., Hazelbag, H. M., Jonges, G. N., Kibbelaar, R. E., Lam, K. H., van der Linden, H., van Marsdijk, J., Meijer, C., Nagtegaal, I. D., Oudejans, J. J., Roelofs, J. J. T. H., Rozendaal, L., Sastrowijoto, S. H., Smits, M. M., Stavast, J., van den Berg, Bernard M., Bruijn, Jan A., Rabelink, Ton J., Hogendoorn, Pancras C. W., Baelde, Hans J.
Publikováno v:
Molecular Genetics and Genomics, 297(2), 397-405. Springer Verlag
Molecular Genetics and Genomics, 297, 397-405. SPRINGER HEIDELBERG
Molecular Genetics and Genomics, 297, 2, pp. 397-405
Molecular genetics and genomics, 297(2), 397-405. Springer Verlag
Molecular Genetics and Genomics, 297, 397-405
PALGA Group 2022, ' Mutations in the heparan sulfate backbone elongating enzymes EXT1 and EXT2 have no major effect on endothelial glycocalyx and the glomerular filtration barrier ', Molecular Genetics and Genomics, vol. 297, no. 2, pp. 397-405 . https://doi.org/10.1007/s00438-022-01854-w
Molecular Genetics and Genomics, 297, 397-405. SPRINGER HEIDELBERG
Molecular Genetics and Genomics, 297, 2, pp. 397-405
Molecular genetics and genomics, 297(2), 397-405. Springer Verlag
Molecular Genetics and Genomics, 297, 397-405
PALGA Group 2022, ' Mutations in the heparan sulfate backbone elongating enzymes EXT1 and EXT2 have no major effect on endothelial glycocalyx and the glomerular filtration barrier ', Molecular Genetics and Genomics, vol. 297, no. 2, pp. 397-405 . https://doi.org/10.1007/s00438-022-01854-w
In this study, the effect of heterozygous germline mutations in the heparan sulfate (HS) glycosaminoglycan chain co-polymerases EXT1 and EXT2 on glomerular barrier function and the endothelial glycocalyx in humans is investigated. Heparan sulfate (HS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::700e116cf9b9787512352b8734dc7158
https://doi.org/10.1007/s00438-022-01854-w
https://doi.org/10.1007/s00438-022-01854-w
Publikováno v:
Cells, Vol 8, Iss 11, p 1465 (2019)
MicroRNAs (miRNAs) are critical regulators of gene expression. As miRNAs are frequently deregulated in many human diseases, including cancer and immunological disorders, it is important to understand their biological functions. Typically, miRNA-encod
Externí odkaz:
https://doaj.org/article/af2196bd956c4634a3a51f48865b053c
Autor:
Magda Mulder, Mariette Swart, Gregory Ralph Weir, Susan Thiart, Hiske Smart, Anita Stavast, Zhavandre Van der Merwe, Febe A Bruwer, Geertien C Boersema, Johanna E Sander, Maria Gattorno Giaquinto-Cilliers, Patricia J Idensohn
Publikováno v:
Advances in Skin & Wound Care. 34:11-22
To synthesize the evidence regarding nonhealable and maintenance wound management and propose an interprofessional referral pathway for wound management.This continuing education activity is intended for physicians, physician assistants, nurse practi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d8fba9fb464fae38f651bb036a3ec35
https://doi.org/10.1097/01.asw.0000722740.93179.9f
https://doi.org/10.1097/01.asw.0000722740.93179.9f
Autor:
Vincent H.J. van der Velden, Kirsten van Lom, Stefan J. Erkeland, Joyce Schilperoord-Vermeulen, Harmen J.G. van de Werken, Eric M.J. Bindels, Anton W. Langerak, Antoinette van Hoven-Beijen, Giada Dal Collo, Mies C. Kappers-Klunne, Leticia G. Leon, Dick de Ridder, Yvonne M. Mueller, Christiaan J. Stavast, Iris van Zuijen
Publikováno v:
Haematologica 107 (2022) 1
Haematologica
Haematologica, 107(1), 143-153. Ferrata Storti Foundation
Haematologica, 107(1), 143-153
Haematologica
Haematologica, 107(1), 143-153. Ferrata Storti Foundation
Haematologica, 107(1), 143-153
T-cell prolymphocytic leukemia (T-PLL) is mostly characterized by aberrant expansion of small- to medium-sized prolymphocytes with a mature post-thymic phenotype, high aggressiveness of the disease and poor prognosis. However, T-PLL is more heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a49bf6663df046ef631dd27b68efa01
