118 related articles for article (PubMed ID: 9519858)
1. Phenotypic convergence and divergence of surface immunoglobulin and CD40 signals.
Axcrona K; Akerblad P; Leanderson T
Scand J Immunol; 1998 Mar; 47(3):210-7. PubMed ID: 9519858
[TBL] [Abstract][Full Text] [Related]
2. Inhibitory coreceptors activated by antigens but not by anti-Ig heavy chain antibodies install requirement of costimulation through CD40 for survival and proliferation of B cells.
Hokazono Y; Adachi T; Wabl M; Tada N; Amagasa T; Tsubata T
J Immunol; 2003 Aug; 171(4):1835-43. PubMed ID: 12902484
[TBL] [Abstract][Full Text] [Related]
3. Activation mediated by RP105 but not CD40 makes normal B cells susceptible to anti-IgM-induced apoptosis: a role for Fc receptor coligation.
Yamashita Y; Miyake K; Miura Y; Kaneko Y; Yagita H; Suda T; Nagata S; Nomura J; Sakaguchi N; Kimoto M
J Exp Med; 1996 Jul; 184(1):113-20. PubMed ID: 8691124
[TBL] [Abstract][Full Text] [Related]
4. Cognate T cell help for CD40-deficient B cells induces c-myc RNA expression, but DNA synthesis requires an additional signal through surface Ig.
Schrader CE; Stavnezer J; Kikutani H; Parker DC
J Immunol; 1997 Jan; 158(1):153-62. PubMed ID: 8977186
[TBL] [Abstract][Full Text] [Related]
5. Activated T cells induce expression of B7/BB1 on normal or leukemic B cells through a CD40-dependent signal.
Ranheim EA; Kipps TJ
J Exp Med; 1993 Apr; 177(4):925-35. PubMed ID: 7681471
[TBL] [Abstract][Full Text] [Related]
6. Distinct activation signals determine whether IL-21 induces B cell costimulation, growth arrest, or Bim-dependent apoptosis.
Jin H; Carrio R; Yu A; Malek TR
J Immunol; 2004 Jul; 173(1):657-65. PubMed ID: 15210829
[TBL] [Abstract][Full Text] [Related]
7. Regulation of B cell growth and differentiation via CD21 and CD40.
Axcrona K; Gray D; Leanderson T
Eur J Immunol; 1996 Sep; 26(9):2203-7. PubMed ID: 8814268
[TBL] [Abstract][Full Text] [Related]
8. Impairment of B-lymphocyte differentiation induced by dual triggering of the B-cell antigen receptor and CD40 in advanced HIV-1-disease.
Conge AM; Tarte K; Reynes J; Segondy M; Gerfaux J; Zembala M; Vendrell JP
AIDS; 1998 Aug; 12(12):1437-49. PubMed ID: 9727564
[TBL] [Abstract][Full Text] [Related]
9. B cells lacking RelB are defective in proliferative responses, but undergo normal B cell maturation to Ig secretion and Ig class switching.
Snapper CM; Rosas FR; Zelazowski P; Moorman MA; Kehry MR; Bravo R; Weih F
J Exp Med; 1996 Oct; 184(4):1537-41. PubMed ID: 8879226
[TBL] [Abstract][Full Text] [Related]
10. Role of CD40 in a T cell-mediated negative regulation of Ig production.
Majlessi L; Bordenave G
J Immunol; 2001 Jan; 166(2):841-7. PubMed ID: 11145658
[TBL] [Abstract][Full Text] [Related]
11. IL-10 inhibits lipopolysaccharide-induced murine B cell proliferation and cross-linking of surface antigen receptors or ligation of CD40 restores the response.
Marcelletti JF
J Immunol; 1996 Oct; 157(8):3323-33. PubMed ID: 8871628
[TBL] [Abstract][Full Text] [Related]
12. Cutting edge: CD40 engagement eliminates the need for Bruton's tyrosine kinase in B cell receptor signaling for NF-kappa B.
Mizuno T; Rothstein TL
J Immunol; 2003 Mar; 170(6):2806-10. PubMed ID: 12626529
[TBL] [Abstract][Full Text] [Related]
13. Induction of IL-5 receptors on normal B cells by cross-linking surface Ig with anti-Ig-dextran.
Allison KC; Strober W; Harriman GR
J Immunol; 1991 Jun; 146(12):4197-203. PubMed ID: 1710244
[TBL] [Abstract][Full Text] [Related]
14. Anti-CD40 monoclonal antibody induces the proliferation of murine B cells as a B-cell mitogen through a distinct pathway from receptors for antigens or lipopolysaccharide.
Nomura J; Inui S; Yamasaki T; Kataoka S; Maeda K; Nakanishi K; Sakaguchi N
Immunol Lett; 1995 Mar; 45(3):195-203. PubMed ID: 7558174
[TBL] [Abstract][Full Text] [Related]
15. B cells activated by lipopolysaccharide, but not by anti-Ig and anti-CD40 antibody, induce anergy in CD8+ T cells: role of TGF-beta 1.
Parekh VV; Prasad DV; Banerjee PP; Joshi BN; Kumar A; Mishra GC
J Immunol; 2003 Jun; 170(12):5897-911. PubMed ID: 12794116
[TBL] [Abstract][Full Text] [Related]
16. Ligation of CD40 with soluble CD40 ligand reverses anti-immunoglobulin-mediated negative signalling in murine B lymphoma cell lines but not in immature B cells from neonatal mice.
Marshall-Clarke S; Owen G; Tasker L
Immunology; 1996 Apr; 87(4):624-32. PubMed ID: 8675219
[TBL] [Abstract][Full Text] [Related]
17. Mechanisms regulating IgA class-specific immunoglobulin production in murine gut-associated lymphoid tissues. I. T cells derived from Peyer's patches that switch sIgM B cells to sIgA B cells in vitro.
Kawanishi H; Saltzman LE; Strober W
J Exp Med; 1983 Feb; 157(2):433-50. PubMed ID: 6185611
[TBL] [Abstract][Full Text] [Related]
18. B cell receptor-induced apoptosis in primary transitional murine B cells: signaling requirements and modulation by T cell help.
Sater RA; Sandel PC; Monroe JG
Int Immunol; 1998 Nov; 10(11):1673-82. PubMed ID: 9846696
[TBL] [Abstract][Full Text] [Related]
19. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) elevates basal B-cell intracellular calcium concentration and suppresses surface Ig- but not CD40-induced antibody secretion.
Karras JG; Morris DL; Matulka RA; Kramer CM; Holsapple MP
Toxicol Appl Pharmacol; 1996 Apr; 137(2):275-84. PubMed ID: 8661353
[TBL] [Abstract][Full Text] [Related]
20. Regulation of mucosal IgA production in vitro by autoreactive immunoregulatory T cells from murine Peyer's patches.
Kawanishi H; Mirabella S
Cell Immunol; 1988 Jul; 114(2):324-35. PubMed ID: 2898979
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]