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325 related items for PubMed ID: 11102984

  • 21. Molecular genetic analysis of X-linked hypogammaglobulinemia and isolated growth hormone deficiency.
    Stewart DM, Notarangelo LD, Kurman CC, Staudt LM, Nelson DL.
    J Immunol; 1995 Sep 01; 155(5):2770-4. PubMed ID: 7650402
    [Abstract] [Full Text] [Related]

  • 22. Genotype/phenotype correlations in X-linked agammaglobulinemia.
    Broides A, Yang W, Conley ME.
    Clin Immunol; 2006 Sep 01; 118(2-3):195-200. PubMed ID: 16297664
    [Abstract] [Full Text] [Related]

  • 23. Early arrest in B cell development in transgenic mice that express the E41K Bruton's tyrosine kinase mutant under the control of the CD19 promoter region.
    Maas A, Dingjan GM, Grosveld F, Hendriks RW.
    J Immunol; 1999 Jun 01; 162(11):6526-33. PubMed ID: 10352268
    [Abstract] [Full Text] [Related]

  • 24. Prevalence of BTK mutations in male Algerian patterns with agammaglobulinemia and severe B cell lymphopenia.
    Boushaki S, Tahiat A, Meddour Y, Chan KW, Chaib S, Benhalla N, Smati L, Bensenouci A, Lau YL, Magdinier F, Djidjik R.
    Clin Immunol; 2015 Dec 01; 161(2):286-90. PubMed ID: 26387629
    [Abstract] [Full Text] [Related]

  • 25. Identification of nine novel mutations in the Bruton's tyrosine kinase gene in X-linked agammaglobulinaemia patients.
    Orlandi P, Ritis K, Moschese V, Angelini F, Arvanitidis K, Speletas M, Sideras P, Plebani A, Rossi P.
    Hum Mutat; 2000 Jan 01; 15(1):117. PubMed ID: 10612838
    [Abstract] [Full Text] [Related]

  • 26. Identification of Bruton's tyrosine kinase (Btk) gene mutations and characterization of the derived proteins in 35 X-linked agammaglobulinemia families: a nationwide study of Btk deficiency in Japan.
    Hashimoto S, Tsukada S, Matsushita M, Miyawaki T, Niida Y, Yachie A, Kobayashi S, Iwata T, Hayakawa H, Matsuoka H, Tsuge I, Yamadori T, Kunikata T, Arai S, Yoshizaki K, Taniguchi N, Kishimoto T.
    Blood; 1996 Jul 15; 88(2):561-73. PubMed ID: 8695804
    [Abstract] [Full Text] [Related]

  • 27. Bruton's tyrosine kinase is not essential for LPS-induced activation of human monocytes.
    Pérez de Diego R, López-Granados E, Pozo M, Rodríguez C, Sabina P, Ferreira A, Fontan G, García-Rodríguez MC, Alemany S.
    J Allergy Clin Immunol; 2006 Jun 15; 117(6):1462-9. PubMed ID: 16751014
    [Abstract] [Full Text] [Related]

  • 28. Genotype-phenotype correlation in Bruton's tyrosine kinase deficiency.
    Teimourian S, Nasseri S, Pouladi N, Yeganeh M, Aghamohammadi A.
    J Pediatr Hematol Oncol; 2008 Sep 15; 30(9):679-83. PubMed ID: 18776760
    [Abstract] [Full Text] [Related]

  • 29. Atypical X-linked agammaglobulinemia diagnosed in three adults.
    Hashimoto S, Miyawaki T, Futatani T, Kanegane H, Usui K, Nukiwa T, Namiuchi S, Matsushita M, Yamadori T, Suemura M, Kishimoto T, Tsukada S.
    Intern Med; 1999 Sep 15; 38(9):722-5. PubMed ID: 10480303
    [Abstract] [Full Text] [Related]

  • 30. Molecular analysis of Bruton's tyrosine kinase gene in Spain.
    Rodríguez MC, Granados EL, Cerdán AF, Casariego GF.
    Hum Mutat; 2001 Sep 15; 18(1):84. PubMed ID: 11438999
    [Abstract] [Full Text] [Related]

  • 31. Bruton's tyrosine kinase controls a sustained calcium signal essential for B lineage development and function.
    Rawlings DJ.
    Clin Immunol; 1999 Jun 15; 91(3):243-53. PubMed ID: 10370369
    [Abstract] [Full Text] [Related]

  • 32. Characterization of germline mutations of the gene encoding Bruton's tyrosine kinase in families with X-linked agammaglobulinemia.
    Hagemann TL, Rosen FS, Kwan SP.
    Hum Mutat; 1995 Jun 15; 5(4):296-302. PubMed ID: 7627183
    [Abstract] [Full Text] [Related]

  • 33. De novo mutation in the BTK gene of atypical X-linked agammaglobulinemia in a patient with recurrent pyoderma.
    Lin MT, Chien YH, Shyur SD, Huang LH, Chiang YC, Wen DC, Liang PH, Yang HC.
    Ann Allergy Asthma Immunol; 2006 May 15; 96(5):744-8. PubMed ID: 16729790
    [Abstract] [Full Text] [Related]

  • 34. Mutation analysis of the gene encoding Bruton's tyrosine kinase in a family with a sporadic case of X-linked agammaglobulinemia reveals three female carriers.
    Hagemann TL, Assa'ad AH, Kwan SP.
    Am J Med Genet; 1995 Nov 06; 59(2):188-92. PubMed ID: 8588584
    [Abstract] [Full Text] [Related]

  • 35. X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group.
    Moschese V, Orlandi P, Plebani A, Arvanitidis K, Fiorini M, Speletas M, Mella P, Ritis K, Sideras P, Finocchi A, Livadiotti S, Rossi P.
    Mol Med; 2000 Feb 06; 6(2):104-13. PubMed ID: 10859027
    [Abstract] [Full Text] [Related]

  • 36. Novel insertions of Bruton tyrosine kinase in patients with X-linked agammaglobulinemia.
    Okoh MP, Kainulainen L, Heiskanen K, Isa MN, Varming K, Ruuskanen O, Vihinen M.
    Hum Mutat; 2002 Dec 06; 20(6):480-1. PubMed ID: 12442285
    [Abstract] [Full Text] [Related]

  • 37. Characterization of novel Bruton's tyrosine kinase gene mutations in Central European patients with agammaglobulinemia.
    Kristufek D, Aspalter RM, Eibl MM, Wolf HM.
    Mol Immunol; 2007 Mar 06; 44(7):1639-43. PubMed ID: 17045652
    [Abstract] [Full Text] [Related]

  • 38. A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia.
    López-Granados E, Pérez de Diego R, Ferreira Cerdán A, Fontán Casariego G, García Rodríguez MC.
    J Allergy Clin Immunol; 2005 Sep 06; 116(3):690-7. PubMed ID: 16159644
    [Abstract] [Full Text] [Related]

  • 39. Expression of the X-linked agammaglobulinemia gene, btk in B-cell acute lymphoblastic leukemia.
    Katz FE, Lovering RC, Bradley LA, Rigley KP, Brown D, Cotter F, Chessells JM, Levinsky RJ, Kinnon C.
    Leukemia; 1994 Apr 06; 8(4):574-7. PubMed ID: 8152253
    [Abstract] [Full Text] [Related]

  • 40. Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling.
    Lindvall JM, Blomberg KE, Väliaho J, Vargas L, Heinonen JE, Berglöf A, Mohamed AJ, Nore BF, Vihinen M, Smith CI.
    Immunol Rev; 2005 Feb 06; 203():200-15. PubMed ID: 15661031
    [Abstract] [Full Text] [Related]

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