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Journal Abstract Search


150 related items for PubMed ID: 12483306

  • 21. Healthy lifestyles are associated with higher levels of perforin, granulysin and granzymes A/B-expressing cells in peripheral blood lymphocytes.
    Li Q, Morimoto K, Nakadai A, Qu T, Matsushima H, Katsumata M, Shimizu T, Inagaki H, Hirata Y, Hirata K, Kawada T, Lu Y, Nakayama K, Krensky AM.
    Prev Med; 2007 Feb; 44(2):117-23. PubMed ID: 17030356
    [Abstract] [Full Text] [Related]

  • 22. 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 01; 105(7):2658-63. PubMed ID: 15598808
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  • 23. [Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation--the first diagnosed case in the Czech Republic].
    Spísek R, Mejstríková E, Formánková R, Zizková H, Vávra V, Hrusák O, Sedivá A, Sedlácek P, Starý J.
    Cas Lek Cesk; 2006 Apr 01; 145(1):50-4. PubMed ID: 16468242
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  • 24. Perforin deficiency and familial hemophagocytic lymphohistiocytosis.
    Zipursky A.
    Pediatr Res; 2001 Jan 01; 49(1):3. PubMed ID: 11134481
    [No Abstract] [Full Text] [Related]

  • 25. Perforin and granzyme B of cytotoxic T lymphocyte mediate apoptosis irrespective of Helicobacter pylori infection: possible act as a trigger of peptic ulcer formation.
    Ohara T, Morishita T, Suzuki H, Masaoka T, Ishii H.
    Hepatogastroenterology; 2003 Jan 01; 50(54):1774-9. PubMed ID: 14696402
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  • 26. Familial hemophagocytic lymphohistiocytosis: too little cell death can seriously damage your health.
    Fadeel B, Orrenius S, Henter JI.
    Leuk Lymphoma; 2001 Jun 01; 42(1-2):13-20. PubMed ID: 11699200
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  • 27. Mechanisms of lysis by activated cytotoxic cells expressing perforin and granzyme-B genes and the protein TIA-1 in muscle biopsies of myositis.
    Cherin P, Herson S, Crevon MC, Hauw JJ, Cervera P, Galanaud P, Emilie D.
    J Rheumatol; 1996 Jul 01; 23(7):1135-42. PubMed ID: 8823683
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  • 28. Perforin defects of primary haemophagocytic lymphohistiocytosis in Japan.
    Suga N, Takada H, Nomura A, Ohga S, Ishii E, Ihara K, Ohshima K, Hara T.
    Br J Haematol; 2002 Feb 01; 116(2):346-9. PubMed ID: 11841437
    [Abstract] [Full Text] [Related]

  • 29. Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis.
    Del Giudice E, Savoldi G, Notarangelo LD, Di Benedetto L, Manganelli F, Bruzzese E, Romano A, Santoro L.
    Acta Paediatr; 2003 Feb 01; 92(3):398-401. PubMed ID: 12725560
    [Abstract] [Full Text] [Related]

  • 30. Stably transfected antisense granzyme B and perforin constructs inhibit human granule-mediated lytic ability.
    Bochan MR, Goebel WS, Brahmi Z.
    Cell Immunol; 1995 Sep 01; 164(2):234-9. PubMed ID: 7656332
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  • 32. [The effect of immunosuppression on the expression of perforin and granzyme B mRNA in hamster to rat liver transplantation].
    Zhang S, Wu M, Yao H.
    Zhonghua Yi Xue Za Zhi; 1998 Nov 01; 78(11):859-61. PubMed ID: 11038783
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  • 35. Modulation of perforin and granzyme messenger RNA expression in human natural killer cells.
    Salcedo TW, Azzoni L, Wolf SF, Perussia B.
    J Immunol; 1993 Sep 01; 151(5):2511-20. PubMed ID: 8103068
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  • 36. 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 01; 52(4):527-9. PubMed ID: 19058215
    [Abstract] [Full Text] [Related]

  • 37. Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.
    Zhang K, Johnson JA, Biroschak J, Villanueva J, Lee SM, Bleesing JJ, Risma KA, Wenstrup RJ, Filipovich AH.
    Int J Immunogenet; 2007 Aug 01; 34(4):231-3. PubMed ID: 17627755
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