Division of Clinical Genetics

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  1. SYT-SSX is critical for cyclin D1 expression in synovial sarcoma cells: A gain of function of the t(X;18)(p11.2;q11.2) translocation

    Xie, YT., Skytting, B., Nilsson, G., Gasbarri, A., Haslam, K., Bartolazzi, A., Brodin, B., Nils Mandahl & Larsson, O., 2002, In : Cancer Research. 62, 13, p. 3861-3867

    Research output: Contribution to journalArticle

  2. Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas

    Yang, K., Lui, WO., Xie, YT., Zhang, AJ., Skytting, B., Nils Mandahl, Larsson, C. & Larsson, O., 2002, In : Oncogene. 21, 26, p. 4181-4190

    Research output: Contribution to journalArticle

  3. Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

    Minjun Yang, Vesterlund, M., Siavelis, I., Moura-Castro, L. H., Anders Castor, Thoas Fioretos, Jafari, R., Henrik Lilljebjörn, Odom, D. T., Linda Olsson, Naveen Ravi, Eleanor L. Woodward, Harewood, L., Lehtiö, J. & Kajsa Paulsson, 2019 Apr 3, In : Nature Communications. 10, 1, 1519.

    Research output: Contribution to journalArticle

  4. CCL2 secreted from cancer-associated mesothelial cells promotes peritoneal metastasis of ovarian cancer cells through the P38-MAPK pathway

    Hiroaki Yasui, Kajiyama, H., Tamauchi, S., Suzuki, S., Peng, Y., Yoshikawa, N., Sugiyama, M., Nakamura, K. & Kikkawa, F., 2019 Sep 21, In : Clinical and Experimental Metastasis.

    Research output: Contribution to journalArticle

  5. Genetic Abnormalities of the Transcription Factor T (Brachyury) in Sporadic Chordomas

    Ye, H., Shalaby, A., Presneau, N., Pillay, N., Idowu, B., Halai, D., Tirabosco, R., Jacques, T., Fredrik Mertens, Szuhai, K., Kindblom, L., Hogendoom, P. & Flanagan, A. M., 2010, In : The Journal Of Molecular Diagnostics. 12, 6, p. 906-906

    Research output: Contribution to journalPublished meeting abstract

  6. Friedreich ataxia in patients with FXN p.R165P point mutation.

    Ygland, E., Taroni, F., Gellera, C., Dunø, M., Johnels, P., Soller, M. & Andreas Puschmann, 2012, In : European Journal of Neurology. 19, suppl1, p. 727-727

    Research output: Contribution to journalPublished meeting abstract

  7. Friedreich's ataxia in patients with FXN p.R165P point mutation

    E. Ygland, Taroni, F., Gellera, C., Duno, M., Johnels, P., Soller, M. & A. Puschmann, 2012 Sep 1, In : European Journal of Neurology. 19, Suppl 1, p. 727 1 p.

    Research output: Contribution to journalPublished meeting abstract

  8. Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.

    EMIL YGLAND, Taroni, F., Gellera, C., Caldarazzo, S., Duno, M., Soller, M. & Andreas Puschmann, 2014, In : Parkinsonism & Related Disorders. 20, 8, p. 919-923

    Research output: Contribution to journalArticle

  9. Expression of Epstein-Barr Virus-Encoded LMP1 and hTERT Extends the Life Span and Immortalizes Primary Cultures of Nasopharyngeal Epithelial Cells

    Yip, Y-L., Tsang, C-M., Deng, W., Cheung, P-Y., Jin, Y., Cheung, A. L-M., Lung, M. L. & Tsao, S-W., 2010, In : Journal of Medical Virology. 82, 10, p. 1711-1723

    Research output: Contribution to journalArticle

  10. Efficient Immortalization of Primary Nasopharyngeal Epithelial Cells for EBV Infection Study

    Yip, Y. L., Pang, P. S., Deng, W., Tsang, C. M., Zeng, M., Hau, P. M., Man, C., Jin, Y., Yuen, A. P. W. & Tsao, S. W., 2013, In : PLoS ONE. 8, 10, e78395.

    Research output: Contribution to journalArticle