BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 16845395)

  • 1. Signaling protein SWAP-70 is required for efficient B cell homing to lymphoid organs.
    Pearce G; Angeli V; Randolph GJ; Junt T; von Andrian U; Schnittler HJ; Jessberger R
    Nat Immunol; 2006 Aug; 7(8):827-34. PubMed ID: 16845395
    [TBL] [Abstract][Full Text] [Related]  

  • 2. SWAP-70 controls formation of the splenic marginal zone through regulating T1B-cell differentiation.
    Chopin M; Quemeneur L; Ripich T; Jessberger R
    Eur J Immunol; 2010 Dec; 40(12):3544-56. PubMed ID: 21108474
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SWAP-70 deficiency causes high-affinity plasma cell generation despite impaired germinal center formation.
    Quemeneur L; Angeli V; Chopin M; Jessberger R
    Blood; 2008 Mar; 111(5):2714-24. PubMed ID: 18094331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SYK regulates B-cell migration by phosphorylation of the F-actin interacting protein SWAP-70.
    Pearce G; Audzevich T; Jessberger R
    Blood; 2011 Feb; 117(5):1574-84. PubMed ID: 21123826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differences in the migration of B and T lymphocytes: organ-selective localization in vivo and the role of lymphocyte-endothelial cell recognition.
    Stevens SK; Weissman IL; Butcher EC
    J Immunol; 1982 Feb; 128(2):844-51. PubMed ID: 6976385
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Myo1g is required for efficient adhesion and migration of activated B lymphocytes to inguinal lymph nodes.
    Cruz-Zárate D; López-Ortega O; Girón-Pérez DA; Gonzalez-Suarez AM; García-Cordero JL; Schnoor M; Santos-Argumedo L
    Sci Rep; 2021 Mar; 11(1):7197. PubMed ID: 33785780
    [TBL] [Abstract][Full Text] [Related]  

  • 7. VCAM-1 is not involved in LPAM-1 (alpha 4 beta p/alpha 4 beta 7) mediated binding of lymphoma cells to high endothelial venules of mucosa-associated lymph nodes.
    Hahne M; Lenter M; Jäger U; Isenmann S; Vestweber D
    Eur J Cell Biol; 1993 Aug; 61(2):290-8. PubMed ID: 7693472
    [TBL] [Abstract][Full Text] [Related]  

  • 8. HEVs, lymphatics and homeostatic immune cell trafficking in lymph nodes.
    Girard JP; Moussion C; Förster R
    Nat Rev Immunol; 2012 Nov; 12(11):762-73. PubMed ID: 23018291
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fine tuning of IRF-4 expression by SWAP-70 controls the initiation of plasma cell development.
    Chopin M; Chacón-Martínez CA; Jessberger R
    Eur J Immunol; 2011 Oct; 41(10):3063-74. PubMed ID: 21728176
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Distribution and phenotype of rotavirus-specific B cells induced during the antigen-driven primary response to 2/6 virus-like particles administered by the intrarectal and the intranasal routes.
    Di Martino C; Basset C; Ogier A; Charpilienne A; Poncet D; Kohli E
    J Leukoc Biol; 2007 Oct; 82(4):821-8. PubMed ID: 17652448
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression of switch-associated protein 70 is associated with lymphocyte activation and reduced disability in multiple sclerosis.
    Türkoğlu R; Özyurt S; Ulusoy C; Erdağ E; Tüzün E
    Immunol Lett; 2016 Sep; 177():75-7. PubMed ID: 27495372
    [No Abstract]   [Full Text] [Related]  

  • 12. Regulation of systemic autoimmunity and CD11c
    Manni M; Ricker E; Pernis AB
    Cell Immunol; 2017 Nov; 321():46-51. PubMed ID: 28780965
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extrafollicular activation of lymph node B cells by antigen-bearing dendritic cells.
    Qi H; Egen JG; Huang AY; Germain RN
    Science; 2006 Jun; 312(5780):1672-6. PubMed ID: 16778060
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differential expression of homing receptors and vascular addressins in tonsils and draining lymph nodes: Effect of Brucella infection in sheep.
    Suraud V; Olivier M; Bodier CC; Guilloteau LA
    Vet Immunol Immunopathol; 2007 Feb; 115(3-4):239-50. PubMed ID: 17161868
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of SWAP-70 with the B cell antigen receptor complex.
    Masat L; Caldwell J; Armstrong R; Khoshnevisan H; Jessberger R; Herndier B; Wabl M; Ferrick D
    Proc Natl Acad Sci U S A; 2000 Feb; 97(5):2180-4. PubMed ID: 10681448
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Talin1 is required for integrin-dependent B lymphocyte homing to lymph nodes and the bone marrow but not for follicular B-cell maturation in the spleen.
    Manevich-Mendelson E; Grabovsky V; Feigelson SW; Cinamon G; Gore Y; Goverse G; Monkley SJ; Margalit R; Melamed D; Mebius RE; Critchley DR; Shachar I; Alon R
    Blood; 2010 Dec; 116(26):5907-18. PubMed ID: 20923969
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CXCL12 mediates CCR7-independent homing of central memory cells, but not naive T cells, in peripheral lymph nodes.
    Scimone ML; Felbinger TW; Mazo IB; Stein JV; Von Andrian UH; Weninger W
    J Exp Med; 2004 Apr; 199(8):1113-20. PubMed ID: 15096537
    [TBL] [Abstract][Full Text] [Related]  

  • 18. B and T lymphocyte subsets enter peripheral lymph nodes and Peyer's patches without preference in vivo: no correlation occurs between their localization in different types of high endothelial venules and the expression of CD44, VLA-4, LFA-1, ICAM-1, CD2 or L-selectin.
    Westermann J; Nagahori Y; Walter S; Heerwagen C; Miyasaka M; Pabst R
    Eur J Immunol; 1994 Oct; 24(10):2312-6. PubMed ID: 7523135
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SWAP-70 is required for oncogenic transformation by v-Src in mouse embryo fibroblasts.
    Fukui Y; Tanaka T; Tachikawa H; Ihara S
    Biochem Biophys Res Commun; 2007 May; 356(2):512-6. PubMed ID: 17367752
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The interaction of high endothelial venules with T and B cells in peripheral lymph nodes after antigenic stimulation.
    Kraal G; Twisk A
    Eur J Immunol; 1984 Jun; 14(6):586-8. PubMed ID: 6610559
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.