BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 15661029)

  • 1. Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis.
    Ménasché G; Feldmann J; Fischer A; de Saint Basile G
    Immunol Rev; 2005 Feb; 203():165-79. PubMed ID: 15661029
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defective cytotoxic granule-mediated cell death pathway impairs T lymphocyte homeostasis.
    de Saint Basile G; Fischer A
    Curr Opin Rheumatol; 2003 Jul; 15(4):436-45. PubMed ID: 12819472
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Defect in lytic granule exocytosis: several causes, a same effect].
    Ménasché G; Ménager M; Le Deist F; Fischer A; de Saint Basile G
    Med Sci (Paris); 2006; 22(8-9):733-8. PubMed ID: 16962048
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Perforin gene defects in familial hemophagocytic lymphohistiocytosis.
    Stepp SE; Dufourcq-Lagelouse R; Le Deist F; Bhawan S; Certain S; Mathew PA; Henter JI; Bennett M; Fischer A; de Saint Basile G; Kumar V
    Science; 1999 Dec; 286(5446):1957-9. PubMed ID: 10583959
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene.
    Voskoboinik I; Thia MC; De Bono A; Browne K; Cretney E; Jackson JT; Darcy PK; Jane SM; Smyth MJ; Trapani JA
    J Exp Med; 2004 Sep; 200(6):811-6. PubMed ID: 15365097
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pathogenesis of hemophagocytic syndrome (HPS).
    Larroche C; Mouthon L
    Autoimmun Rev; 2004 Feb; 3(2):69-75. PubMed ID: 15003190
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions.
    Ishii E; Ueda I; Shirakawa R; Yamamoto K; Horiuchi H; Ohga S; Furuno K; Morimoto A; Imayoshi M; Ogata Y; Zaitsu M; Sako M; Koike K; Sakata A; Takada H; Hara T; Imashuku S; Sasazuki T; Yasukawa M
    Blood; 2005 May; 105(9):3442-8. PubMed ID: 15632205
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Delivering the kiss of death.
    Trambas CM; Griffiths GM
    Nat Immunol; 2003 May; 4(5):399-403. PubMed ID: 12719728
    [TBL] [Abstract][Full Text] [Related]  

  • 9. On the pathogenesis of perforin defects and related immunodeficiencies.
    Moretta L; Moretta A; Hengartner H; Zinkernagel RM
    Immunol Today; 2000 Nov; 21(11):593-4. PubMed ID: 11221685
    [No Abstract]   [Full Text] [Related]  

  • 10. Familial hemophagocytic lymphohistiocytosis: too little cell death can seriously damage your health.
    Fadeel B; Orrenius S; Henter JI
    Leuk Lymphoma; 2001 Jun; 42(1-2):13-20. PubMed ID: 11699200
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biology and treatment of familial hemophagocytic lymphohistiocytosis: importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis.
    Henter JI
    Med Pediatr Oncol; 2002 May; 38(5):305-9. PubMed ID: 11979453
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Perforin deficiency: fighting unarmed?
    Arnaout RA
    Immunol Today; 2000 Nov; 21(11):592; author reply 593-4. PubMed ID: 11221684
    [No Abstract]   [Full Text] [Related]  

  • 13. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
    Göransdotter Ericson K; Fadeel B; Nilsson-Ardnor S; Söderhäll C; Samuelsson A; Janka G; Schneider M; Gürgey A; Yalman N; Révész T; Egeler R; Jahnukainen K; Storm-Mathiesen I; Haraldsson A; Poole J; de Saint Basile G; Nordenskjöld M; Henter J
    Am J Hum Genet; 2001 Mar; 68(3):590-7. PubMed ID: 11179007
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences.
    Ishii E; Ohga S; Imashuku S; Kimura N; Ueda I; Morimoto A; Yamamoto K; Yasukawa M
    Crit Rev Oncol Hematol; 2005 Mar; 53(3):209-23. PubMed ID: 15718147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Linking albinism and immunity: the secrets of secretory lysosomes.
    Stinchcombe J; Bossi G; Griffiths GM
    Science; 2004 Jul; 305(5680):55-9. PubMed ID: 15232098
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Perforin and lymphohistiocytic proliferative disorders.
    Katano H; Cohen JI
    Br J Haematol; 2005 Mar; 128(6):739-50. PubMed ID: 15755277
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited defects in lymphocyte cytotoxic activity.
    Pachlopnik Schmid J; Côte M; Ménager MM; Burgess A; Nehme N; Ménasché G; Fischer A; de Saint Basile G
    Immunol Rev; 2010 May; 235(1):10-23. PubMed ID: 20536552
    [TBL] [Abstract][Full Text] [Related]  

  • 18. No mutations of SAP/SH2D1A/DSHP and perforin genes in patients with Epstein-Barr virus-associated hemophagocytic syndrome in Japan.
    Ma X; Okamura A; Yosioka M; Ishiguro N; Kikuta H; Kobayashi K
    J Med Virol; 2001 Oct; 65(2):358-61. PubMed ID: 11536244
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Perforin deficiency and familial hemophagocytic lymphohistiocytosis.
    Zipursky A
    Pediatr Res; 2001 Jan; 49(1):3. PubMed ID: 11134481
    [No Abstract]   [Full Text] [Related]  

  • 20. Gene abnormalities in patients with hemophagocytic lymphohistiocytosis.
    Grunebaum E; Roifman CM
    Isr Med Assoc J; 2002 May; 4(5):366-9. PubMed ID: 12040827
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.