Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marijke Valk"'
Autor:
Emma Lång, Anna Połeć, Anna Lång, Marijke Valk, Pernille Blicher, Alexander D. Rowe, Kim A. Tønseth, Catherine J. Jackson, Tor P. Utheim, Liesbeth M. C. Janssen, Jens Eriksson, Stig Ove Bøe
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-15 (2018)
Epithelial sheet migration requires polarized and coordinated cell movement. Here, the authors demonstrate serum-activated collective migration followed by polarized asymmetric cell divisions in otherwise quiescent human keratinocyte monolayers in th
Externí odkaz:
https://doaj.org/article/56730725888641c7b0f946697f96d47e
Autor:
Kim Alexander Tønseth, Jens Eriksson, Alexander D. Rowe, Liesbeth M. C. Janssen, Catherine Jackson, Anna Połeć, Tor Paaske Utheim, Pernille Blicher, Stig Ove Bøe, Anna Ulrika Lång, Marijke Valk, Emma Lång
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-15 (2018)
Nature Communications, 9(1):3665. Nature Publishing Group
Nature Communications
Nature Communications, 9(1):3665. Nature Publishing Group
Nature Communications
Epithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective
Publikováno v:
Haematologica, Vol 98, Iss 5 (2013)
Externí odkaz:
https://doaj.org/article/0f638a0d22ec484ba6ec8a0e076ff0b7
Autor:
Judith H. E. Verhagen-Oldenampsen, Jurgen R. Haanstra, Paulina M. H. van Strien, Marijke Valkhof, Ivo P. Touw, Marieke von Lindern
Publikováno v:
Anemia, Vol 2012 (2012)
The endonuclease complex Ercc1/Xpf is involved in interstrand crosslink repair and functions downstream of the Fanconi pathway. Loss of Ercc1 causes hematopoietic defects similar to those seen in Fanconi Anemia. Ercc1−/− mice die 3-4 weeks after
Externí odkaz:
https://doaj.org/article/e097eb68b92c4f35aff5534b3d7bd528
Autor:
Renée Beekman, Marijke Valkhof, Stefan J Erkeland, Erdogan Taskesen, Veronika Rockova, Justine K Peeters, Peter J M Valk, Bob Löwenberg, Ivo P Touw
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26537 (2011)
Acute myeloid leukemia (AML) results from multiple genetic and epigenetic aberrations, many of which remain unidentified. Frequent loss of large chromosomal regions marks haplo-insufficiency as one of the major mechanisms contributing to leukemogenes
Externí odkaz:
https://doaj.org/article/964aa76b293d4d1f93e7d2fe879265e4