169 related articles for article (PubMed ID: 15661029)
21. [Familial hemophagocytic lymphohistiocytosis(FHL)].
Kawa K
Ryoikibetsu Shokogun Shirizu; 2000; (32):553-6. PubMed ID: 11212803
[No Abstract] [Full Text] [Related]
22. Development of hemophagocytic lymphohistiocytosis in triplets infected with HHV-8.
Grossman WJ; Radhi M; Schauer D; Gerday E; Grose C; Goldman FD
Blood; 2005 Aug; 106(4):1203-6. PubMed ID: 15840696
[TBL] [Abstract][Full Text] [Related]
23. Polygenic mutations in the cytotoxicity pathway increase susceptibility to develop HLH immunopathology in mice.
Sepulveda FE; Garrigue A; Maschalidi S; Garfa-Traore M; Ménasché G; Fischer A; de Saint Basile G
Blood; 2016 Apr; 127(17):2113-21. PubMed ID: 26864340
[TBL] [Abstract][Full Text] [Related]
24. An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.
Muralitharan S; Al Lamki Z; Dennison D; Christie BS; Wali YA; Zachariah M; Romana M; Bayoumi R; Krishnamoorthy R
Am J Hematol; 2005 Jan; 78(1):59-63. PubMed ID: 15609274
[TBL] [Abstract][Full Text] [Related]
25. Perforin-mediated target-cell death and immune homeostasis.
Voskoboinik I; Smyth MJ; Trapani JA
Nat Rev Immunol; 2006 Dec; 6(12):940-52. PubMed ID: 17124515
[TBL] [Abstract][Full Text] [Related]
26. Functional significance of the perforin/granzyme cell death pathway.
Trapani JA; Smyth MJ
Nat Rev Immunol; 2002 Oct; 2(10):735-47. PubMed ID: 12360212
[TBL] [Abstract][Full Text] [Related]
27. The defect of the perforin granule system in cytotoxic T lymphocytes of atopic patients--are perforin reduction and hyperreleasability of clinical relevance?
Ambach A; Bonnekoh B; Gollnick H
J Dtsch Dermatol Ges; 2003 Dec; 1(12):938-44. PubMed ID: 16285645
[TBL] [Abstract][Full Text] [Related]
28. Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.
Ericson KG; Fadeel B; Andersson M; Gudmundsson GH; Gürgey A; Yalman N; Janka G; Nordenskjöld M; Henter JI
Hum Genet; 2003 Jan; 112(1):98-9. PubMed ID: 12483306
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH).
zur Stadt U; Pruggmayer M; Jung H; Henter JI; Schneider M; Kabisch H; Janka G
Prenat Diagn; 2002 Jan; 22(1):80-1. PubMed ID: 11810660
[No Abstract] [Full Text] [Related]
31. Cellular and molecular mechanisms of activation of MHC nonrestricted cytotoxic cells by IL-12.
Cesano A; Visonneau S; Clark SC; Santoli D
J Immunol; 1993 Sep; 151(6):2943-57. PubMed ID: 8104216
[TBL] [Abstract][Full Text] [Related]
32. Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.
Feldmann J; Le Deist F; Ouachée-Chardin M; Certain S; Alexander S; Quartier P; Haddad E; Wulffraat N; Casanova JL; Blanche S; Fischer A; de Saint Basile G
Br J Haematol; 2002 Jun; 117(4):965-72. PubMed ID: 12060139
[TBL] [Abstract][Full Text] [Related]
33. Serial killing by cytotoxic T lymphocytes: T cell receptor triggers degranulation, re-filling of the lytic granules and secretion of lytic proteins via a non-granule pathway.
Isaaz S; Baetz K; Olsen K; Podack E; Griffiths GM
Eur J Immunol; 1995 Apr; 25(4):1071-9. PubMed ID: 7737276
[TBL] [Abstract][Full Text] [Related]
34. Unlocking the secrets of cytotoxic granule proteins.
Smyth MJ; Kelly JM; Sutton VR; Davis JE; Browne KA; Sayers TJ; Trapani JA
J Leukoc Biol; 2001 Jul; 70(1):18-29. PubMed ID: 11435481
[TBL] [Abstract][Full Text] [Related]
35. Involvement of granule proteins in T-cell-mediated cytolysis.
Krähenbühl O; Tschopp J
Nat Immun Cell Growth Regul; 1990; 9(4):274-82. PubMed ID: 2215515
[TBL] [Abstract][Full Text] [Related]
36. Identification of a population of CD4+ CTL that utilizes a perforin- rather than a Fas ligand-dependent cytotoxic mechanism.
Williams NS; Engelhard VH
J Immunol; 1996 Jan; 156(1):153-9. PubMed ID: 8598456
[TBL] [Abstract][Full Text] [Related]
37. Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations.
Clementi R; Emmi L; Maccario R; Liotta F; Moretta L; Danesino C; Aricó M
Blood; 2002 Sep; 100(6):2266-7. PubMed ID: 12229880
[No Abstract] [Full Text] [Related]
38. Natural killer cell dysfunction in patients with systemic-onset juvenile rheumatoid arthritis and macrophage activation syndrome.
Grom AA; Villanueva J; Lee S; Goldmuntz EA; Passo MH; Filipovich A
J Pediatr; 2003 Mar; 142(3):292-6. PubMed ID: 12640378
[TBL] [Abstract][Full Text] [Related]
39. MRL/lpr CD4- CD8- and CD8+ T cells, respectively, mediate Fas-dependent and perforin cytotoxic pathways.
Benihoud K; Bonardelle D; Bobé P; Kiger N
Eur J Immunol; 1997 Feb; 27(2):415-20. PubMed ID: 9045912
[TBL] [Abstract][Full Text] [Related]
40. Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity.
Feldmann J; Ménasché G; Callebaut I; Minard-Colin V; Bader-Meunier B; Le Clainche L; Fischer A; Le Deist F; Tardieu M; de Saint Basile G
Blood; 2005 Apr; 105(7):2658-63. PubMed ID: 15598808
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]