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Nature Genetics|August 1, 1993
EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft partsJ Zucman, O Delattre, C Desmaze, et al.
European Journal of Haematology|March 1, 1997
Amplification of multiple regions of chromosome 12, including 12q13-15, in chronic lymphocytic leukaemiaM Merup, G Juliusson, X Wu, et al.
The Journal of Pathology. Clinical Research|November 23, 2022
Deep learning-based image analysis reveals significant differences in the number and distribution of mucosal CD3 and γδ T cells between Crohn's disease and ulcerative colitisElin Synnøve Røyset, Henrik P Sahlin Pettersen, Weili Xu, et al.
The American Journal of Pathology|February 13, 2001
A transplantable human carcinoid as model for somatostatin receptor-mediated and amine transporter-mediated radionuclide uptakeL Kölby, P Bernhardt, H Ahlman, et al.
Human Molecular Genetics|December 1, 1995
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocationY Labelle, J Zucman, G Stenman, et al.
Scientific Reports|January 30, 2025
Tofacitinib and budesonide treatment affect stemness and chemokine release in IBD patient-derived colonoidsArun Sridhar, Ingunn Bakke, Shreya Gopalakrishnan, et al.
Cancer Genetics and Cytogenetics|January 1, 1996
Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12S Wanschura, G Belge, G Stenman, et al.
Cancer Genetics and Cytogenetics|April 1, 1994
Distinct Xp11.2 breakpoint regions in synovial sarcoma revealed by metaphase and interphase FISH: relationship to histologic subtypesB de Leeuw, R F Suijkerbuijk, D Olde Weghuis, et al.
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