[Immunophenotype analysis on neoplastic cells in bone marrow and peripheral blood of angioimmunoblastic T-cell lymphoma]. 2009

Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang

UI MeSH Term Description Entries
D007119 Immunoblastic Lymphadenopathy A disorder characterized by proliferation of arborizing small vessels, prominent immunoblastic proliferations and amorphous acidophilic interstitial material. Clinical manifestations include fever, sweats, weight loss, generalized lymphadenopathy and frequently hepatosplenomegaly. Angioimmunoblastic Lymphadenopathy,Lymphadenopathy, Immunoblastic,Angioimmunoblastic Lymphadenopathies,Immunoblastic Lymphadenopathies,Lymphadenopathies, Angioimmunoblastic,Lymphadenopathies, Immunoblastic,Lymphadenopathy, Angioimmunoblastic
D001854 Bone Marrow Cells Cells contained in the bone marrow including fat cells (see ADIPOCYTES); STROMAL CELLS; MEGAKARYOCYTES; and the immediate precursors of most blood cells. Bone Marrow Cell,Cell, Bone Marrow,Cells, Bone Marrow,Marrow Cell, Bone,Marrow Cells, Bone
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D015260 Neprilysin Enzyme that is a major constituent of kidney brush-border membranes and is also present to a lesser degree in the brain and other tissues. It preferentially catalyzes cleavage at the amino group of hydrophobic residues of the B-chain of insulin as well as opioid peptides and other biologically active peptides. The enzyme is inhibited primarily by EDTA, phosphoramidon, and thiorphan and is reactivated by zinc. Neprilysin is identical to common acute lymphoblastic leukemia antigen (CALLA Antigen), an important marker in the diagnosis of human acute lymphocytic leukemia. There is no relationship with CALLA PLANT. Antigens, CD10,Antigens, Leukemia, Common Acute Lymphoblastic,CALLA Antigen,CD10 Antigens,Common Acute Lymphoblastic Leukemia Antigens,Endopeptidase-24.11,Enkephalin Dipeptidyl Carboxypeptidase,Enkephalinase,Kidney-Brush-Border Neutral Proteinase,Membrane Metallo-Endopeptidase,Atriopeptidase,CD10 Antigen,Enkephalinase-24.11,Neutral Endopeptidase,Neutral Endopeptidase 24.11,Thermolysin-Like Metalloendopeptidase,YGG-Forming Enzyme,Antigen, CD10,Carboxypeptidase, Enkephalin Dipeptidyl,Dipeptidyl Carboxypeptidase, Enkephalin,Endopeptidase 24.11,Endopeptidase 24.11, Neutral,Endopeptidase, Neutral,Enkephalinase 24.11,Enzyme, YGG-Forming,Kidney Brush Border Neutral Proteinase,Membrane Metallo Endopeptidase,Metallo-Endopeptidase, Membrane,Metalloendopeptidase, Thermolysin-Like,Neutral Proteinase, Kidney-Brush-Border,Thermolysin Like Metalloendopeptidase,YGG Forming Enzyme
D015496 CD4-Positive T-Lymphocytes A critical subpopulation of T-lymphocytes involved in the induction of most immunological functions. The HIV virus has selective tropism for the T4 cell which expresses the CD4 phenotypic marker, a receptor for HIV. In fact, the key element in the profound immunosuppression seen in HIV infection is the depletion of this subset of T-lymphocytes. T4 Cells,T4 Lymphocytes,CD4-Positive Lymphocytes,CD4 Positive T Lymphocytes,CD4-Positive Lymphocyte,CD4-Positive T-Lymphocyte,Lymphocyte, CD4-Positive,Lymphocytes, CD4-Positive,T-Lymphocyte, CD4-Positive,T-Lymphocytes, CD4-Positive,T4 Cell,T4 Lymphocyte
D015704 CD4 Antigens 55-kDa antigens found on HELPER-INDUCER T-LYMPHOCYTES and on a variety of other immune cell types. They are members of the immunoglobulin supergene family and are implicated as associative recognition elements in MAJOR HISTOCOMPATIBILITY COMPLEX class II-restricted immune responses. On T-lymphocytes they define the helper/inducer subset. T4 antigens also serve as INTERLEUKIN-15 receptors and bind to the HIV receptors, binding directly to the HIV ENVELOPE PROTEIN GP120. Antigens, CD4,CD4 Molecule,CD4 Receptor,CD4 Receptors,Receptors, CD4,T4 Antigens, T-Cell,CD4 Antigen,Receptors, Surface CD4,Surface CD4 Receptor,Antigen, CD4,Antigens, T-Cell T4,CD4 Receptor, Surface,CD4 Receptors, Surface,Receptor, CD4,Surface CD4 Receptors,T-Cell T4 Antigens,T4 Antigens, T Cell
D016130 Immunophenotyping Process of classifying cells of the immune system based on structural and functional differences. The process is commonly used to analyze and sort T-lymphocytes into subsets based on CD antigens by the technique of flow cytometry. Lymphocyte Immunophenotyping,Lymphocyte Subtyping,Immunologic Subtyping,Immunologic Subtypings,Lymphocyte Phenotyping,Subtyping, Immunologic,Subtypings, Immunologic,Immunophenotyping, Lymphocyte,Immunophenotypings,Immunophenotypings, Lymphocyte,Lymphocyte Immunophenotypings,Lymphocyte Phenotypings,Lymphocyte Subtypings,Phenotyping, Lymphocyte,Phenotypings, Lymphocyte,Subtyping, Lymphocyte,Subtypings, Lymphocyte
D016399 Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. T-Cell Lymphoma,Lymphoma, T Cell,Lymphomas, T-Cell,T Cell Lymphoma,T-Cell Lymphomas
D017464 Receptors, Complement 3d Molecular sites on or in B-lymphocytes, follicular dendritic cells, lymphoid cells, and epithelial cells that recognize and combine with COMPLEMENT C3D. Human complement receptor 2 (CR2) serves as a receptor for both C3dg and the gp350/220 glycoprotein of HERPESVIRUS 4, HUMAN, and binds the monoclonal antibody OKB7, which blocks binding of both ligands to the receptor. Antigens, CD21,C3d Receptors,CD21 Antigens,CR2 Receptors,Complement 3d Receptors,Complement Receptors 2,Epstein-Barr Virus Receptors,Receptors, C3d,Receptors, CR2,CD 21 Antigens,CD21 Antigen,Complement 3d Receptor,Complement Receptor 2,Epstein-Barr Virus Receptor,Herpesvirus 4 Receptors, Human,Receptors, Epstein-Barr Virus,Antigen, CD21,Antigens, CD 21,Epstein Barr Virus Receptor,Epstein Barr Virus Receptors,Receptor 2, Complement,Receptor, Complement 3d,Receptor, Epstein-Barr Virus,Receptors 2, Complement,Receptors, Epstein Barr Virus,Virus Receptor, Epstein-Barr,Virus Receptors, Epstein-Barr
D018106 CD28 Antigens Costimulatory T-LYMPHOCYTE receptors that have specificity for CD80 ANTIGEN and CD86 ANTIGEN. Activation of this receptor results in increased T-cell proliferation, cytokine production and promotion of T-cell survival. Antigens, CD28,CD28 Antigen,T-Cell-Specific Surface Glycoprotein CD28,TP44 Receptor,Antigen, CD28,Receptor, TP44,T Cell Specific Surface Glycoprotein CD28

Related Publications

Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
August 2006, British journal of haematology,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
January 2007, Acta haematologica,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
January 2002, Blood,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
March 2007, Histopathology,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
July 2011, [Rinsho ketsueki] The Japanese journal of clinical hematology,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
January 2007, Internal medicine (Tokyo, Japan),
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
April 2015, Leukemia & lymphoma,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
April 2024, Indian journal of pathology & microbiology,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
January 2010, Human pathology,
Li-xin Zhang, and Jun Ye, and Tao-hong Lu, and Gai-nü Jiang, and Wei Xiao, and Xue-jun Zhu, and Ya-bao Chen, and Tong-jing Xing, and Zheng-dong Wu, and Jun-xing Huang
May 2009, American journal of clinical pathology,
Copied contents to your clipboard!