نتایج جستجو برای: q35

تعداد نتایج: 269  

Journal: :Frontiers in bioscience 2015
Irina Bonzheim Julia Steinhilber Falko Fend Laurence Lamant Leticia Quintanilla-Martinez

The current classification of lymphoid neoplasms is based on the integrated utilisation of morphological, immunohistochemical, genetic and clinical criteria to define disease entities. Anaplastic large cell lymphoma is a paradigm for the identification of a disease entity based on morphological observations and immunophenotype, which paved the way for the subsequent discovery of the characteris...

2016
Ahmad Monabati Akbar Safaei Sadat Nouri Moeinadin Safavi Freidoon Solhjoo

Mixed phenotype acute leukemia (MPAL) is a rare neoplasm which accounts for 2-5% of all leukemias and it is classified under heading of acute leukemia of ambiguous lineage in 2008 WHO classification. This patient was a 61-year-old man who presented with malaise and weakness. In physical examination there was cervical and axillary lymphadenopathy. Paraclinical evaluation revealed anemia (Hb = 10...

Journal: :Blood 2003
Momoko Nishikori Yoshitomo Maesako Chiyoko Ueda Masayuki Kurata Takashi Uchiyama Hitoshi Ohno

Anaplastic large cell lymphoma (ALCL) with t(2;5)(p23;q35) and Hodgkin disease (HD) share many cellular features, including expression of CD30. We compared gene expression profiles of 4 ALCL (Karpas 299, SU-DHL-1, DEL, SR-786) and 3 HD cell lines and found that BCL3, which encodes a nuclear protein belonging to the I kappa B family of inhibitors of nuclear factor-kappa B (NF-kappa B) transcript...

2014
Y Nakamura Y Ito N Wakimoto E Kakegawa Y Uchida M Bessho

Hematological malignancies with FGFR1 abnormality (8p11 myeloproliferative syndrome; EMS) are rare atypical stem cell disorders characterized by eosinophilia, T-cell proliferation and progression to acute myeloid leukemia. In EMS, fibroblast growth factor receptor 1 (FGFR1) gene at 8p11 is disrupted by chromosomal translocation, resulting in the formation of chimeric products with various partn...

Journal: :Cytogenetics and cell genetics 2001
M A Lee-Kirsch K Engel E Paditz A Rösen-Wolff Y A Lee M Gahr

The homeobox 11L2 gene (HOX11L2, TLX-3, Rnx) encodes a transcription factor and constitutes together with the HOX11 (TLX) and HOX11L1 (TLX-1, Enx) genes a distinct family of orphan homeobox genes (Kennedy et al., 1991; Roberts et al., 1994; Shirasawa et al., 1997, 2000). In the chick and mouse embryo HOX11L2 is expressed within cranial sensory ganglia, neural crest-derived dorsal root and sympa...

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