BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 12217406)

  • 1. Synaptotagmin II negatively regulates MHC class II presentation by mast cells.
    Baram D; Peng Z; Medalia O; Mekori YA; Sagi-Eisenberg R
    Mol Immunol; 2002 Sep; 38(16-18):1347-52. PubMed ID: 12217406
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synaptotagmin regulates mast cell functions.
    Baram D; Mekori YA; Sagi-Eisenberg R
    Immunol Rev; 2001 Feb; 179():25-34. PubMed ID: 11292024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synaptotagmin II negatively regulates Ca2+-triggered exocytosis of lysosomes in mast cells.
    Baram D; Adachi R; Medalia O; Tuvim M; Dickey BF; Mekori YA; Sagi-Eisenberg R
    J Exp Med; 1999 May; 189(10):1649-58. PubMed ID: 10330444
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ca2+-dependent exocytosis in mast cells is stimulated by the Ca2+ sensor, synaptotagmin I.
    Baram D; Linial M; Mekori YA; Sagi-Eisenberg R
    J Immunol; 1998 Nov; 161(10):5120-3. PubMed ID: 9820478
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Suppression of Synaptotagmin II restrains phorbolester-induced downregulation of protein kinase Calpha by diverting the kinase from a degradative pathway to the recycling endocytic compartment.
    Peng Z; Grimberg E; Sagi-Eisenberg R
    J Cell Sci; 2002 Aug; 115(Pt 15):3083-92. PubMed ID: 12118064
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synaptotagmin III is a critical factor for the formation of the perinuclear endocytic recycling compartment and determination of secretory granules size.
    Grimberg E; Peng Z; Hammel I; Sagi-Eisenberg R
    J Cell Sci; 2003 Jan; 116(Pt 1):145-54. PubMed ID: 12456724
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The mast cell: where endocytosis and regulated exocytosis meet.
    Sagi-Eisenberg R
    Immunol Rev; 2007 Jun; 217():292-303. PubMed ID: 17498067
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synaptotagmin IX, a possible linker between the perinuclear endocytic recycling compartment and the microtubules.
    Haberman Y; Grimberg E; Fukuda M; Sagi-Eisenberg R
    J Cell Sci; 2003 Nov; 116(Pt 21):4307-18. PubMed ID: 12966166
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The distribution of synaptotagmin II in RBL-2H3 and its regulation on exocytosis of lysosomes in RBL-2H3.
    Zhang J; Wu J; Pan S; Lv W
    Cell Mol Immunol; 2005 Jun; 2(3):205-9. PubMed ID: 16212888
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Secretory granules of mast cells accumulate mature and immature MHC class II molecules.
    Vincent-Schneider H; Théry C; Mazzeo D; Tenza D; Raposo G; Bonnerot C
    J Cell Sci; 2001 Jan; 114(Pt 2):323-34. PubMed ID: 11148134
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Anti-sense RNA inhibits the expression of synaptotagmin II in RBL-2H3 and enhances the exocytosis of lysosomes in RBL-2H3.
    Zhang J; Lu W; Li Y; Wu J; Zhang C
    J Huazhong Univ Sci Technolog Med Sci; 2005; 25(2):117-20. PubMed ID: 16116949
    [TBL] [Abstract][Full Text] [Related]  

  • 12. O-glycosylation is essential for intracellular targeting of synaptotagmins I and II in non-neuronal specialized secretory cells.
    Atiya-Nasagi Y; Cohen H; Medalia O; Fukudan M; Sagi-Eisenberg R
    J Cell Sci; 2005 Apr; 118(Pt 7):1363-72. PubMed ID: 15755799
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synaptotagmin (Syt) IX is an essential determinant for protein sorting to secretory granules in mast cells.
    Haberman Y; Ziv I; Gorzalczany Y; Hirschberg K; Mittleman L; Fukuda M; Sagi-Eisenberg R
    Blood; 2007 Apr; 109(8):3385-92. PubMed ID: 17164344
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Antigen-dependent stimulation by bone marrow-derived mast cells of MHC class II-restricted T cell hybridoma.
    Frandji P; Oskéritzian C; Cacaraci F; Lapeyre J; Peronet R; David B; Guillet JG; Mécheri S
    J Immunol; 1993 Dec; 151(11):6318-28. PubMed ID: 8245470
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The antigen presentation function of bone marrow-derived mast cells is spatiotemporally restricted to a subset expressing high levels of cell surface FcepsilonRI and MHC II.
    Gong J; Yang NS; Croft M; Weng IC; Sun L; Liu FT; Chen SS
    BMC Immunol; 2010 Jun; 11():34. PubMed ID: 20591187
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distribution of the presynaptic calcium sensors, synaptotagmin I/II and synaptotagmin III, in the goldfish and rodent retinas.
    Berntson AK; Morgans CW
    J Vis; 2003; 3(4):274-80. PubMed ID: 12803536
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Differential role of the Ca(2+) sensor synaptotagmin VII in macrophages and dendritic cells.
    Becker SM; Delamarre L; Mellman I; Andrews NW
    Immunobiology; 2009; 214(7):495-505. PubMed ID: 19157638
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synaptotagmin V and IX isoforms control Ca2+ -dependent insulin exocytosis.
    Iezzi M; Kouri G; Fukuda M; Wollheim CB
    J Cell Sci; 2004 Jul; 117(Pt 15):3119-27. PubMed ID: 15190121
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNA interference-mediated silencing of synaptotagmin IX, but not synaptotagmin I, inhibits dense-core vesicle exocytosis in PC12 cells.
    Fukuda M
    Biochem J; 2004 Jun; 380(Pt 3):875-9. PubMed ID: 15015935
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Accumulation of major histocompatibility complex class II molecules in mast cell secretory granules and their release upon degranulation.
    Raposo G; Tenza D; Mecheri S; Peronet R; Bonnerot C; Desaymard C
    Mol Biol Cell; 1997 Dec; 8(12):2631-45. PubMed ID: 9398681
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.