Zobrazeno 1 - 2
of 2
pro vyhledávání: '"M L, Kuijjer"'
Autor:
P J, de Vos van Steenwijk, T H, Ramwadhdoebe, R, Goedemans, E M, Doorduijn, J J, van Ham, A, Gorter, T, van Hall, M L, Kuijjer, M I E, van Poelgeest, S H, van der Burg, E S, Jordanova
Publikováno v:
International journal of cancer. 133(12)
One of the hallmarks of cancer is the influx of myeloid cells. In our study, we investigated the constitution of tumor-infiltrating myeloid cells and their relationship to other tumor-infiltrating immune cells, tumor characteristics and the disease-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a392d9d3c27ebf270c6e3e37387d5c77
https://pubmed.ncbi.nlm.nih.gov/23740735
https://pubmed.ncbi.nlm.nih.gov/23740735
Autor:
Luca Sangiorgi, Ronald van Eijk, Catherine Godfraind, Judith V.M.G. Bovée, Jolieke G. van Oosterwijk, Sofie L. J. Verbeke, Maayke A. J. H. van Ruler, Pio D'Adamo, Danielle Meijer, Bernadette Liegl-Atzwanger, Karolin Hansén Nord, Lars-Gunnar Kindblom, Raf Sciot, Kyle C. Kurek, Miikka Vikkula, Mikel San-Julian, Anne-Marie Cleton-Jansen, Jan Oosting, Nisha Limaye, Laurence M. Boon, Karoly Szuhai, Tom van Wezel, Berkin Toker, Soeren Daugaard, Marieke L. Kuijjer, Twinkal C. Pansuriya, Pim J. French
Publikováno v:
Nature Genetics, 43(12), 1256-U124. Nature Publishing Group
Nature genetics
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
Nature Genetics, 43(12), 1256-U124
Nature genetics
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
Nature Genetics, 43(12), 1256-U124
Ollier disease and Maffucci syndrome are non-hereditary skeletal disorders characterized by multiple enchondromas (Ollier disease) combined with spindle cell hemangiomas (Maffucci syndrome). We report somatic heterozygous mutations in IDH1 (c.394C>T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::813422f5c3e79f2b2db5a122df98d7bb
https://hdl.handle.net/10171/36487
https://hdl.handle.net/10171/36487
