These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

71 related articles for article (PubMed ID: 3493909)

  • 21. Patterns of B-lymphocyte gene expression elicited by lipopolysaccharide mitogen.
    Janossy G; Snajdr J; Simak-Ellis M
    Immunology; 1976 Jun; 30(6):799-810. PubMed ID: 1088414
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Requirement for macrophages or for macrophage- or T cell-derived factors in the mitogenic stimulation of murine B lymphocytes by lipopolysaccharides.
    Corbel C; Melchers F
    Eur J Immunol; 1983 Jul; 13(7):528-33. PubMed ID: 6603363
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Status of T- and B-lymphocytes in long living CBA--F1 (CBA X C57BL/6) chimeras].
    Cherniakhovskaia IIu; Nesterenko VG; Filitis LN; Fontalin LN; Novikova TK
    Biull Eksp Biol Med; 1978 Aug; 86(8):197-200. PubMed ID: 28802
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Reduced responsiveness of immature B cells to the B cell mitogen, lipoprotein.
    Phillips RA; Melchers F
    J Immunol; 1979 Apr; 122(4):1473-5. PubMed ID: 376719
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The decline in murine splenic PHA and LPS responsiveness with age is primarily due to an intrinsic mechanism.
    Averill LE; Wolf NS
    J Immunol; 1985 Jun; 134(6):3859-63. PubMed ID: 3872904
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MALA-1: a surface antigen expressed on activated murine T and B lymphocytes.
    Takei F
    J Immunol; 1984 Jul; 133(1):345-50. PubMed ID: 6609986
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Altered production and renewal of natural killer cells in B-lymphocyte-deficient CBA/N mice.
    Miller SC; Christopher FL
    Nat Immun Cell Growth Regul; 1989; 8(5):245-54. PubMed ID: 2594018
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Long-lived lymphocytes include lipopolysaccharide-reactive B cells.
    Levy M
    Cell Immunol; 1985 Dec; 96(2):290-300. PubMed ID: 2874893
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clonal persistence of B lymphocytes in normal mice is determined by variable region-dependent selection.
    Thomas-Vaslin V; Andrade L; Freitas A; Coutinho A
    Eur J Immunol; 1991 Sep; 21(9):2239-46. PubMed ID: 1909646
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Induction or suppression of B cell proliferation and differentiation by phytohemagglutinin or concanavalin A in mouse spleen cell cultures.
    Piguet PF; Dewey HK; Vassalli P
    J Immunol; 1976 Nov; 117(5 Pt.2):1817-23. PubMed ID: 1086865
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Heterogeneity of mouse B lymphocytes: studies using in vitro response to lipopolysaccharide.
    Lamelin JP; Vassalli P
    Ann Immunol (Paris); 1975; 126(5-6):523-39. PubMed ID: 132134
    [TBL] [Abstract][Full Text] [Related]  

  • 32. LPS regulation of the immune response: Bacteroides endotoxin induces mitogenic, polyclonal, and antibody responses in classical LPS responsive but not C3H/HeJ mice.
    Wannemuehler MJ; Michalek SM; Jirillo E; Williamson SI; Hirasawa M; McGhee JR
    J Immunol; 1984 Jul; 133(1):299-305. PubMed ID: 6202784
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Frequencies of mitogen-reactive B cells in the mouse. Lipopolysaccharide-, lipoprotein- and Nocardia mitogen-reactive B cells in CBA/N mice.
    Huber B; Melchers F
    Eur J Immunol; 1979 Oct; 9(10):827-9. PubMed ID: 316394
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Difference in B cell mitogen responsiveness between closely related strains of mice.
    Rosenstreich DL; Glode LM
    J Immunol; 1975 Sep; 115(3):777-80. PubMed ID: 239063
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Nuclear morphology and morphometry of B-lymphocyte transformation. Implications for follicular center cell lymphomas.
    Dardick I; Sinnott NM; Hall R; Bajenko-Carr TA; Setterfield G
    Am J Pathol; 1983 Apr; 111(1):35-49. PubMed ID: 6340518
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Induction of differentiation in a B lymphoma X B lymphocyte hybrid line. II. Intraclonal heterogeneity in growth, secretion of IgM, and cytokine production in response to lipopolysaccharide.
    Little J; Alling DW; Asofsky R
    J Immunol; 1993 Mar; 150(6):2129-38. PubMed ID: 8450206
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Immunoglobulin C-gene expression. III. Possible induction of specific genetic events in activated B lymphocytes by the polyclonal stimuli driving clonal expansion.
    Martinez-Alonso C; Coutinho A
    Eur J Immunol; 1982 Jun; 12(6):502-6. PubMed ID: 6214408
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Effects of tobacco glycoprotein (TGP) on the immune system. I. TGP is a T-independent B cell mitogen for murine lymphoid cells.
    Choy JW; Becker CG; Siskind GW; Francus T
    J Immunol; 1985 May; 134(5):3193-8. PubMed ID: 3872329
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The graft-versus-host reaction and immune function. IV. B cell functional defect associated with a depletion of splenic colony-forming units in marrow of graft-versus-host-reactive mice.
    Seddik M; Seemayer TA; Lapp WS
    Transplantation; 1986 Feb; 41(2):242-7. PubMed ID: 3511585
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Aging increases expression of LPS-induced autoantibody-secreting B cells.
    Meredith PJ; Kristie JA; Walford RL
    J Immunol; 1979 Jul; 123(1):87-91. PubMed ID: 312885
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.