BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 24910990)

  • 21. Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal disease.
    Kögl T; Müller J; Jessen B; Schmitt-Graeff A; Janka G; Ehl S; zur Stadt U; Aichele P
    Blood; 2013 Jan; 121(4):604-13. PubMed ID: 23190531
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Munc18c interaction with syntaxin 4 monomers and SNARE complex intermediates in GLUT4 vesicle trafficking.
    D'Andrea-Merrins M; Chang L; Lam AD; Ernst SA; Stuenkel EL
    J Biol Chem; 2007 Jun; 282(22):16553-66. PubMed ID: 17412693
    [TBL] [Abstract][Full Text] [Related]  

  • 23. An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2.
    Müller ML; Chiang SC; Meeths M; Tesi B; Entesarian M; Nilsson D; Wood SM; Nordenskjöld M; Henter JI; Naqvi A; Bryceson YT
    Front Immunol; 2014 Jan; 4():515. PubMed ID: 24459464
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cutting edge: syntaxin 11 regulates lymphocyte-mediated secretion and cytotoxicity.
    Arneson LN; Brickshawana A; Segovis CM; Schoon RA; Dick CJ; Leibson PJ
    J Immunol; 2007 Sep; 179(6):3397-401. PubMed ID: 17785771
    [TBL] [Abstract][Full Text] [Related]  

  • 25. STX11 mutations and clinical phenotypes of familial hemophagocytic lymphohistiocytosis in North America.
    Marsh RA; Satake N; Biroschak J; Jacobs T; Johnson J; Jordan MB; Bleesing JJ; Filipovich AH; Zhang K
    Pediatr Blood Cancer; 2010 Jul; 55(1):134-40. PubMed ID: 20486178
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Expression and subcellular localization of syntaxin 11 in human neutrophils.
    Xie LX; de la Iglesia-Vicente J; Fang YX; Mollinedo F
    Inflamm Res; 2009 Jul; 58(7):407-12. PubMed ID: 19259622
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.
    Rohr J; Beutel K; Maul-Pavicic A; Vraetz T; Thiel J; Warnatz K; Bondzio I; Gross-Wieltsch U; Schündeln M; Schütz B; Woessmann W; Groll AH; Strahm B; Pagel J; Speckmann C; Janka G; Griffiths G; Schwarz K; zur Stadt U; Ehl S
    Haematologica; 2010 Dec; 95(12):2080-7. PubMed ID: 20823128
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.
    Rudd E; Göransdotter Ericson K; Zheng C; Uysal Z; Ozkan A; Gürgey A; Fadeel B; Nordenskjöld M; Henter JI
    J Med Genet; 2006 Apr; 43(4):e14. PubMed ID: 16582076
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Evidence for a conserved inhibitory binding mode between the membrane fusion assembly factors Munc18 and syntaxin in animals.
    Morey C; Kienle CN; Klöpper TH; Burkhardt P; Fasshauer D
    J Biol Chem; 2017 Dec; 292(50):20449-20460. PubMed ID: 29046354
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production.
    Chiang SC; Theorell J; Entesarian M; Meeths M; Mastafa M; Al-Herz W; Frisk P; Gilmour KC; Ifversen M; Langenskiöld C; Machaczka M; Naqvi A; Payne J; Perez-Martinez A; Sabel M; Unal E; Unal S; Winiarski J; Nordenskjöld M; Ljunggren HG; Henter JI; Bryceson YT
    Blood; 2013 Feb; 121(8):1345-56. PubMed ID: 23287865
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel STXBP2 mutation causing familial hemophagocytic lymphohistiocytosis.
    Jain R; Puliyel M; Moses PD; Sieni E
    Indian Pediatr; 2012 Jun; 49(6):488-90. PubMed ID: 22796692
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A CD57
    Hori M; Yasumi T; Shimodera S; Shibata H; Hiejima E; Oda H; Izawa K; Kawai T; Ishimura M; Nakano N; Shirakawa R; Nishikomori R; Takada H; Morita S; Horiuchi H; Ohara O; Ishii E; Heike T
    J Clin Immunol; 2017 Jan; 37(1):92-99. PubMed ID: 27896523
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rescue of Munc18-1 and -2 double knockdown reveals the essential functions of interaction between Munc18 and closed syntaxin in PC12 cells.
    Han L; Jiang T; Han GA; Malintan NT; Xie L; Wang L; Tse FW; Gaisano HY; Collins BM; Meunier FA; Sugita S
    Mol Biol Cell; 2009 Dec; 20(23):4962-75. PubMed ID: 19812250
    [TBL] [Abstract][Full Text] [Related]  

  • 34. VAMP3, syntaxin-13 and SNAP23 are involved in secretion of matrix metalloproteinases, degradation of the extracellular matrix and cell invasion.
    Kean MJ; Williams KC; Skalski M; Myers D; Burtnik A; Foster D; Coppolino MG
    J Cell Sci; 2009 Nov; 122(Pt 22):4089-98. PubMed ID: 19910495
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling.
    Kostova EB; Beuger BM; Veldthuis M; van der Werff Ten Bosch J; Kühnle I; van den Akker E; van den Berg TK; van Zwieten R; van Bruggen R
    Exp Hematol; 2015 Dec; 43(12):1072-1076.e2. PubMed ID: 26320718
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
    Zur Stadt U; Beutel K; Kolberg S; Schneppenheim R; Kabisch H; Janka G; Hennies HC
    Hum Mutat; 2006 Jan; 27(1):62-8. PubMed ID: 16278825
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Sec1/Munc18 protein stabilizes fusion-competent syntaxin for membrane fusion in Arabidopsis cytokinesis.
    Park M; Touihri S; Müller I; Mayer U; Jürgens G
    Dev Cell; 2012 May; 22(5):989-1000. PubMed ID: 22595672
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease.
    Marcenaro S; Gallo F; Martini S; Santoro A; Griffiths GM; Aricó M; Moretta L; Pende D
    Blood; 2006 Oct; 108(7):2316-23. PubMed ID: 16778144
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Defects in neutrophil granule mobilization and bactericidal activity in familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) syndrome caused by STXBP2/Munc18-2 mutations.
    Zhao XW; Gazendam RP; Drewniak A; van Houdt M; Tool AT; van Hamme JL; Kustiawan I; Meijer AB; Janssen H; Russell DG; van de Corput L; Tesselaar K; Boelens JJ; Kuhnle I; Van Der Werff Ten Bosch J; Kuijpers TW; van den Berg TK
    Blood; 2013 Jul; 122(1):109-11. PubMed ID: 23687090
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Syntaxin-11, but not syntaxin-2 or syntaxin-4, is required for platelet secretion.
    Ye S; Karim ZA; Al Hawas R; Pessin JE; Filipovich AH; Whiteheart SW
    Blood; 2012 Sep; 120(12):2484-92. PubMed ID: 22767500
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.