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A common single-nucleotide variant in T is strongly associated with chordoma Pillay, Nischalan; Plagnol, Vincent; Tarpey, Patrick S.; Lobo, Samira B.; Presneau, Nadege; Szuhai, Karoly; Halai, Dina; Berisha, Fitim; Cannon, Stephen R.; Mead, Simon; Kasperaviciute, Dalia; Palmen, Jutta; Talmud, Philippa J.; Kindblom, Lars-Gunnar; Amary, M. Fernanda; Tirabosco, Roberto; Flanagan, Adrienne M. 分享 收藏
Expression of 11β-hydroxysteroid dehydrogenase enzymes in human osteosarcoma: potential role in pathogenesis and as targets for treatments Patel, Pushpa; Hardy, Rowan; Sumathi, Vaiyapuri; Bartle, Gillian; Kindblom, Lars-Gunnar; Grimer, Robert; Bujalska, Iwona; Stewart, Paul M.; Rabbitt, Elizabeth; Gittoes, Neil J. L.; Cooper, Mark S. 分享 收藏
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Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome Pansuriya, Twinkal C.; van Eijk, Ronald; d'Adamo, Pio; van Ruler, Maayke A. J. H.; Kuijjer, Marieke L.; Oosting, Jan; Cleton-Jansen, Anne-Marie; van Oosterwijk, Jolieke G.; Verbeke, Sofie L. J.; Meijer, Danielle; 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.; Bovee, Judith V. M. G. 分享 收藏
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The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target Shalaby, Asem; Presneau, Nadege; Ye, Hongtao; Halai, Dina; Berisha, Fitim; Idowu, Bernadine; Leithner, Andreas; Liegl, Bernadette; Briggs, Timothy R. W.; Bacsi, Krisztian; Kindblom, Lars-Gunnar; Athanasou, Nicholas; Amary, Maria Fernanda; Hogendoorn, Pancras C. W.; Tirabosco, Roberto; Flanagan, Adrienne M. 分享 收藏
Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study Presneau, Nadege; Shalaby, Asem; Ye, Hongtao; Pillay, Nischalan; Halai, Dina; Idowu, Bernadine; Tirabosco, Roberto; Whitwell, Duncan; Jacques, Thomas S.; Kindblom, Lars-Gunnar; Bruederlein, Silke; Moeller, Peter; Leithner, Andreas; Liegl, Bernadette; Amary, Fernanda M.; Athanasou, Nicholas N.; Hogendoorn, Pancras C. W.; Mertens, Fredrik; Szuhai, Karoly; Flanagan, Adrienne M. 分享 收藏
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Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions Hallor, Karolin H.; Sciot, Raf; Staaf, Johan; Heidenblad, Markus; Rydholm, Anders; Bauer, Henrik C. F.; Astrom, Kristina; Domanski, Henryk A.; Meis, Jeanne M.; Kindblom, Lars-Gunnar; Panagopoulos, Ioannis; Mandahl, Nils; Mertens, Fredrik 分享 收藏
Prognostic value of KIT Exon 11 deletions in GISTs -: Reply Kindblom, Lars-Gunnar; Meis-Kindblom, Jeanne M.; Andersson, Johanna; Bumming, Per; Sihto, Harri; Nupponen, Nina; Joensuu, Heikki; Oden, Anders; Gustavsson, Bengt; Nilsson, Bengt 分享 收藏
Gastrointestinal stromal tumors with KIT Exon 11 deletions are associated with poor prognosis Andersson, Johanna; Bumming, Per; Meis-Kindblom, Jeanne M.; Sihto, Harri; Nupponen, Nina; Joensuu, Heikki; Oden, Anders; Gustavsson, Bengt; Kindblom, Lars-Gunnar; Nilsson, Bengt 分享 收藏
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A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer Einbeigi, Z; Bergman, A; Kindblom, LG; Martinsson, T; Meis-Kindblom, JM; Nordling, M; Suurküla, M; Wahlström, J; Wallgren, A; Karlsson, P 分享 收藏
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