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Journal Abstract Search

65 related items for PubMed ID: 18661484

  • 1. Screening, identification, and functional analysis of three novel missense mutations in the TRADD gene in children with ALL and ALPS.
    Dechant MJ, Scheuerpflug CG, Pauly E, van der Werff Ten Bosch J, Debatin KM, Fellenberg J.
    Pediatr Blood Cancer; 2008 Nov; 51(5):616-20. PubMed ID: 18661484
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  • 2. Tumor necrosis factor receptor-1-induced neuronal death by TRADD contributes to the pathogenesis of Japanese encephalitis.
    Swarup V, Das S, Ghosh S, Basu A.
    J Neurochem; 2007 Oct; 103(2):771-83. PubMed ID: 17666051
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  • 10. MEN1 missense mutations impair sensitization to apoptosis induced by wild-type menin in endocrine pancreatic tumor cells.
    Bazzi W, Renon M, Vercherat C, Hamze Z, Lacheretz-Bernigaud A, Wang H, Blanc M, Roche C, Calender A, Chayvialle JA, Scoazec JY, Cordier-Bussat M.
    Gastroenterology; 2008 Nov; 135(5):1698-1709.e2. PubMed ID: 18775714
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  • 11. Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.
    Hellberg A, Schmidt-Melbye AC, Reid ME, Olsson ML.
    Transfusion; 2008 Mar; 48(3):479-87. PubMed ID: 18067504
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  • 12. Human T-cell leukemia virus type I infects human lung epithelial cells and induces gene expression of cytokines, chemokines and cell adhesion molecules.
    Teruya H, Tomita M, Senba M, Ishikawa C, Tamayose M, Miyazato A, Yara S, Tanaka Y, Iwakura Y, Fujita J, Mori N.
    Retrovirology; 2008 Sep 22; 5():86. PubMed ID: 18808681
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  • 13. Autoimmune lymphoproliferative syndrome: a cause of chronic splenomegaly, lymphadenopathy, and cytopenias in children-report on diagnosis and management of five patients.
    Alvarado CS, Straus SE, Li S, Dale JK, Mann K, Le A, Lauer SJ.
    Pediatr Blood Cancer; 2004 Aug 22; 43(2):164-9. PubMed ID: 15236285
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  • 14. Identification of variations in the human phosphoinositide 3-kinase p110delta gene in children with primary B-cell immunodeficiency of unknown aetiology.
    Jou ST, Chien YH, Yang YH, Wang TC, Shyur SD, Chou CC, Chang ML, Lin DT, Lin KH, Chiang BL.
    Int J Immunogenet; 2006 Oct 22; 33(5):361-9. PubMed ID: 16984281
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  • 18. Autoimmune lymphoproliferative syndrome in a patient with a new minimal deletion in the death domain of the FAS gene.
    Gualco G, van den Berg A, Koopmans S, Bacchi LM, Carneiro SS, Ruiz E, Vecchi AP, Chan JK.
    Hum Pathol; 2008 Jan 22; 39(1):137-41. PubMed ID: 18070632
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  • 19. Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype.
    Worth A, Thrasher AJ, Gaspar HB.
    Br J Haematol; 2006 Apr 22; 133(2):124-40. PubMed ID: 16611303
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  • 20. Impact of genotype on survival of children with T-cell acute lymphoblastic leukemia treated according to the French protocol FRALLE-93: the effect of TLX3/HOX11L2 gene expression on outcome.
    Ballerini P, Landman-Parker J, Cayuela JM, Asnafi V, Labopin M, Gandemer V, Perel Y, Michel G, Leblanc T, Schmitt C, Fasola S, Hagemejier A, Sigaux F, Auclerc MF, Douay L, Leverger G, Baruchel A.
    Haematologica; 2008 Nov 22; 93(11):1658-65. PubMed ID: 18835836
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