Opening the archives for state of the art tumour genetic research: sample processing for array-CGH using decalcified, formalin-fixed, paraffin-embedded tissue-derived DNA samples

por de Jong, Danielle, Verbeke, Sofie LJ, Meijer, Danielle, Hogendoorn, Pancras CW, Bovee, Judith VMG, Szuhai, Károly
Publicado 2011

Expression of aromatase and estrogen receptor alpha in chondrosarcoma, but no beneficial effect of inhibiting estrogen signaling both in vitro and in vivo

por Meijer, Danielle, Gelderblom, Hans, Karperien, Marcel, Cleton-Jansen, Anne-Marie, Hogendoorn, Pancras CW, Bovée, Judith VMG
Publicado 2011

Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases

por Valke, Lars L. F. G., Rijpma, Sanna, Meijer, Danielle, Schols, Saskia E. M., van Heerde, Waander L.
Publicado 2022

A critical assessment of SELDI-TOF-MS for biomarker discovery in serum and tissue of patients with an ovarian mass

por Wegdam, Wouter, Moerland, Perry D, Meijer, Danielle, de Jong, Shreyas M, Hoefsloot, Huub C J, Kenter, Gemma G, Buist, Marrije R, Aerts, Johannes MF G
Publicado 2012

Label-Free LC-MS(e) in Tissue and Serum Reveals Protein Networks Underlying Differences between Benign and Malignant Serous Ovarian Tumors

por Wegdam, Wouter, Argmann, Carmen A., Kramer, Gertjan, Vissers, Johannes P., Buist, Marrije R., Kenter, Gemma G., Aerts, Johannes M. F. G., Meijer, Danielle, Moerland, Perry D.
Publicado 2014

Fibrinolytic assays in bleeding of unknown cause: Improvement in diagnostic yield

por Valke, Lars L. F. G., Meijer, Danielle, Nieuwenhuizen, Laurens, Laros‐van Gorkom, Britta A. P., Blijlevens, Nicole M. A., van Heerde, Waander L., Schols, Saskia E. M.
Publicado 2022

ChAdOx1 vaccination, blood coagulation, and inflammation: No effect on coagulation but increased interleukin‐6

por Willems, Loes H., Nagy, Magdolna, Ten Cate, Hugo, Spronk, Henri M. H., Jacobs, Lotte M. C., Kranendonk, Josephine, van Leeuwen, Maaike, Meijer, Danielle, Middeldorp, Saskia, Groh, Laszlo A., Warlé, Michiel C.
Publicado 2021

Von Willebrand disease type 2M: Correlation between genotype and phenotype

por Maas, Dominique P. M. S. M., Atiq, Ferdows, Blijlevens, Nicole M. A., Brons, Paul P. T., Krouwel, Sandy, Laros‐van Gorkom, Britta A. P., Leebeek, Frank W. G., Nieuwenhuizen, Laurens, Schoormans, Selene C. M., Simons, Annet, Meijer, Daniëlle, van Heerde, Waander L., Schols, Saskia E. M.
Publicado 2021

In patients with hemophilia, a decreased thrombin generation profile is associated with a severe bleeding phenotype

por Verhagen, Marieke J.A., van Heerde, Waander L., van der Bom, Johanna G., Beckers, Erik A.M., Blijlevens, Nicole M.A., Coppens, Michiel, Gouw, Samantha C., Jansen, Joop H., Leebeek, Frank W.G., van Vulpen, Lize F.D., Meijer, Daniëlle, Schols, Saskia E.M.
Publicado 2023

Somatic mosaic IDH1 or IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

por Pansuriya, Twinkal C., van Eijk, Ronald, Adamo, Pio d', van Ruler, Maayke A.J.H., Kuijjer, Marieke L., Oosting, Jan, Cleton-Jansen, Anne-Marie, van Oosterwijk, Jolieke G., Verbeke, Sofie L.J., Meijer, Daniëlle, van Wezel, Tom, Nord, Karolin H., Sangiorgi, Luca, Toker, Berkin, Liegl-Atzwanger, Bernadette, San-Julian, Mikel, Sciot, Raf, Limaye, Nisha, Kindblom, Lars-Gunnar, Daugaard, Soeren, Godfraind, Catherine, Boon, Laurence M., Vikkula, Miikka, Kurek, Kyle C., Szuhai, Karoly, French, Pim J., Bovée, Judith V.M.G.
Publicado 2011