検索結果 - Lars‐Gunnar Kindblom
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The Complexity of KIT Gene Mutations and Chromosome Rearrangements and Their Clinical Correlation in Gastrointestinal Stromal (Pacemaker Cell) Tumors 著者: Johanna C. Andersson‐Assarsson, Helene Sjögren, Jeanne M. Meis‐Kindblom, Göran Stenman, Pierre Åman, Lars‐Gunnar Kindblom
出版事項 2002Artigo -
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GFAP-Deficient Astrocytes Are Capable of Stellationin VitroWhen Cocultured with Neurons and Exhibit a Reduced Amount of Intermediate Filaments and an Increased Cell Saturation Dens... 著者: Milos Pekny, Camilla Eliasson, C. L. Chien, Lars Gunnar Kindblom, Ronald K.H. Liem, Anders Hamberger, Christer Betsholtz
出版事項 1998Artigo -
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Gastrointestinal stromal tumors: The incidence, prevalence, clinical course, and prognostication in the preimatinib mesylate era 著者: Bengt Nilsson, Per Bümming, Jeanne M. Meis‐Kindblom, Anders Odén, Aydin Dortok, Bengt Gustavsson, Katarzyna Sablinska, Lars‐Gunnar Kindblom
出版事項 2005Artigo -
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Studies on the Molecular Pathogenesis of Extraskeletal Myxoid Chondrosarcoma—Cytogenetic, Molecular Genetic, and cDNA Microarray Analyses 著者: Helene Sjögren, Jeanne M. Meis‐Kindblom, Charlotte Örndal, Peter Bergh, Konrad Ptaszyński, Pierre Åman, Lars‐Gunnar Kindblom, Göran Stenman
出版事項 2003Artigo -
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Synovial sarcoma 著者: Peter Bergh, Jeanne M. Meis‐Kindblom, F. Gherlinzoni, �rjan Berlin, Patrizia Bacchini, Franco Bertoni, B Gunterberg, Lars‐Gunnar Kindblom
出版事項 1999Artigo -
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Concomitant deletions of tumor suppressor genes <i>MEN1</i> and <i>AIP</i> are essential for the pathogenesis of the brown fat tumor hibernoma 著者: Karolin H. Nord, Linda Magnusson, Margareth Isaksson, Jenny Nilsson, Henrik Lilljebjörn, Henryk A. Domanski, Lars‐Gunnar Kindblom, Nils Mandahl, Fredrik Mertens
出版事項 2010Artigo -
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Gastrointestinal Stromal Tumors With KIT Exon 11 Deletions Are Associated With Poor Prognosis 著者: Johanna C. Andersson‐Assarsson, Per Bümming, Jeanne M. Meis‐Kindblom, Harri Sihto, Nina N. Nupponen, Heikki Joensuu, Anders Odén, Bengt Gustavsson, Lars‐Gunnar Kindblom, Bengt Nilsson
出版事項 2006Artigo -
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Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome 著者: Twinkal C. Pansuriya, Ronald van Eijk, Pio D’Adamo, Maayke A.J.H. van Ruler, Marieke L. Kuijjer, Jan Oosting, Anne‐Marie Cleton‐Jansen, Jolieke G. van Oosterwijk, Sofie Verbeke, Daniëlle Meijer, Tom van Wezel, Karolin H. Nord, Luca Sangiorgi, Berkin Toker, Bernadette Liegl‐Atzwanger, Mikel San-Julián, Raf Sciot, Nisha Limaye, Lars‐Gunnar Kindblom, Soeren Daugaard, Catherine Godfraind, Laurence M. Boon, Miikka Vikkula, Kyle C. Kurek, Károly Szuhai, Pim J. French, Judith V.M.G. Bovée
出版事項 2011Artigo
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