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MeSH Review

Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

 
 
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Disease relevance of Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

 

High impact information on Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

 

Chemical compound and disease context of Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

 

Biological context of Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

 

Anatomical context of Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

  • Human T cell leukemia/lymphoma virus I infection and subsequent cloning of normal human B cells. Direct responsiveness of cloned cells to recombinant interleukin 2 by differentiation in the absence of enhanced proliferation [21].
  • HTLV antigens were present on endothelial syncytia passaged in culture for greater than 3 months as detected by an anti-p19 monoclonal antibody, which detects a core protein of HTLV-I, and by ATLL sera [22].
  • Sera and peripheral blood cells of an adult T-cell leukemia patient and several clinically normal members of his family from the northwest coast of Japan were examined for evidence of infection with human T-cell leukemia (lymphoma) virus (HTLV) [23].
  • A multilobulated nuclear appearance is an important diagnostic marker of ATLL, and we have now identified that the molecular mechanisms underlying these formations occur through microtubule rearrangement via phosphatidylinositol 3-kinase (PI3-kinase) activation by AILIM/ICOS signaling [24].
  • Seroreactivity to an envelope protein of human T-cell leukemia/lymphoma virus in patients with CD3- (natural killer) lymphoproliferative disease of granular lymphocytes [25].
 

Gene context of Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

 

Analytical, diagnostic and therapeutic context of Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated

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