BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 15755897)

  • 41. Heterozygosity for the common perforin mutation, p.A91V, impairs the cytotoxicity of primary natural killer cells from healthy individuals.
    House IG; Thia K; Brennan AJ; Tothill R; Dobrovic A; Yeh WZ; Saffery R; Chatterton Z; Trapani JA; Voskoboinik I
    Immunol Cell Biol; 2015 Jul; 93(6):575-80. PubMed ID: 25776844
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Variations of the perforin gene in patients with type 1 diabetes.
    Orilieri E; Cappellano G; Clementi R; Cometa A; Ferretti M; Cerutti E; Cadario F; Martinetti M; Larizza D; Calcaterra V; D'Annunzio G; Lorini R; Cerutti F; Bruno G; Chiocchetti A; Dianzani U
    Diabetes; 2008 Apr; 57(4):1078-83. PubMed ID: 18198357
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mutations in the perforin gene in children with hemophagocytic lymphohistiocytosis.
    Lu G; Xie ZD; Shen KL; Ye LJ; Wu RH; Liu CY; Jin YK; Yang S
    Chin Med J (Engl); 2009 Dec; 122(23):2851-5. PubMed ID: 20092789
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Familial hemophagocytic lymphohistiocytosis(FHL)].
    Kawa K
    Ryoikibetsu Shokogun Shirizu; 2000; (32):553-6. PubMed ID: 11212803
    [No Abstract]   [Full Text] [Related]  

  • 45. Mutations of perforin and Munc13-4 do not mark HLH by NK defects.
    Schneider EM
    Pediatr Blood Cancer; 2006 Apr; 46(4):409-11. PubMed ID: 16365870
    [No Abstract]   [Full Text] [Related]  

  • 46. A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain.
    Turtzo LC; Lin DD; Hartung H; Barker PB; Arceci R; Yohay K
    J Child Neurol; 2007 Jul; 22(7):863-8. PubMed ID: 17715280
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Patients of African ancestry with hemophagocytic lymphohistiocytosis share a common haplotype of PRF1 with a 50delT mutation.
    Lee SM; Sumegi J; Villanueva J; Tabata Y; Zhang K; Chakraborty R; Sheng X; Clementi R; de Saint Basile G; Filipovich AH
    J Pediatr; 2006 Jul; 149(1):134-7. PubMed ID: 16860143
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis.
    Karandikar NJ; Kroft SH; Yegappan S; Rogers BB; Aquino VM; Lee KM; Kumar V; Guenaga FJ; Jaffe ES; Douek DC; McKenna RW
    Blood; 2004 Oct; 104(7):2007-9. PubMed ID: 15205266
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients.
    An O; Gursoy A; Gurgey A; Keskin O
    Protein Sci; 2013 Jun; 22(6):823-39. PubMed ID: 23592409
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Perforin activity and immune homeostasis: the common A91V polymorphism in perforin results in both presynaptic and postsynaptic defects in function.
    Voskoboinik I; Sutton VR; Ciccone A; House CM; Chia J; Darcy PK; Yagita H; Trapani JA
    Blood; 2007 Aug; 110(4):1184-90. PubMed ID: 17475905
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Primary hemophagocytic lymphohistiocytosis in Turkish children.
    Gürgey A; Göğüş S; Ozyürek E; Aslan D; Gümrük F; Cetin M; Yüce A; Ceyhan M; Seçmeer G; Yetgin S; Hiçsönmez G
    Pediatr Hematol Oncol; 2003; 20(5):367-71. PubMed ID: 12775534
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Characterisation of diverse PRF1 mutations leading to decreased natural killer cell activity in North American families with haemophagocytic lymphohistiocytosis.
    Molleran Lee S; Villanueva J; Sumegi J; Zhang K; Kogawa K; Davis J; Filipovich AH
    J Med Genet; 2004 Feb; 41(2):137-44. PubMed ID: 14757862
    [No Abstract]   [Full Text] [Related]  

  • 53. Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis type-2.
    Mhatre S; Madkaikar M; Jijina F; Ghosh K
    J Pediatr Hematol Oncol; 2014 Nov; 36(8):e524-7. PubMed ID: 24390453
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. 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]  

  • 56. A novel perforin gene mutation in a Japanese family with hemophagocytic lymphohistiocytosis.
    Ueda I; Kohdera U; Hibi S; Inaba T; Yamamoto K; Sugimoto T; Morimoto A; Ishii E; Imashuku S
    Int J Hematol; 2006 Jan; 83(1):51-4. PubMed ID: 16443553
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A proportion of patients with lymphoma may harbor mutations of the perforin gene.
    Clementi R; Locatelli F; Dupré L; Garaventa A; Emmi L; Bregni M; Cefalo G; Moretta A; Danesino C; Comis M; Pession A; Ramenghi U; Maccario R; Aricò M; Roncarolo MG
    Blood; 2005 Jun; 105(11):4424-8. PubMed ID: 15728124
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Late Onset of Primary Hemophagocytic Lymphohistiocytosis (HLH) with a Novel Constellation of Compound Heterozygosity Involving Two Missense Variants in the
    Stadermann A; Haar M; Riecke A; Mayer T; Neumann C; Bauer A; Schulz A; Nagarathinam K; Gebauer N; Böhm S; Groß M; Grunert M; Müller M; Witte H
    Int J Mol Sci; 2024 Feb; 25(5):. PubMed ID: 38474010
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Fatal hemophagocytic lymphohistiocytosis in X-linked chronic granulomatous disease associated with a perforin gene variant.
    van Montfrans JM; Rudd E; van de Corput L; Henter JI; Nikkels P; Wulffraat N; Boelens JJ
    Pediatr Blood Cancer; 2009 Apr; 52(4):527-9. PubMed ID: 19058215
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Molecular study of the perforin gene in familial hematological malignancies.
    El Abed R; Bourdon V; Voskoboinik I; Omri H; Youssef YB; Laatiri MA; Huiart L; Eisinger F; Rabayrol L; Frenay M; Gesta P; Demange L; Dreyfus H; Bonadona V; Dugast C; Zattara H; Faivre L; Zaier M; Jemni SY; Noguchi T; Sobol H; Soua Z
    Hered Cancer Clin Pract; 2011 Sep; 9(1):9. PubMed ID: 21936944
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.