BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 9449702)

  • 1. Molecular basis of selective IgG2 deficiency. The mutated membrane-bound form of gamma2 heavy chain caused complete IGG2 deficiency in two Japanese siblings.
    Tashita H; Fukao T; Kaneko H; Teramoto T; Inoue R; Kasahara K; Kondo N
    J Clin Invest; 1998 Feb; 101(3):677-81. PubMed ID: 9449702
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fate of the mutated IgG2 heavy chain: lack of expression of mutated membrane-bound IgG2 on the B cell surface in selective IgG2 deficiency.
    Terada T; Kaneko H; Fukao T; Tashita H; Li AL; Takemura M; Kondo N
    Int Immunol; 2001 Feb; 13(2):249-56. PubMed ID: 11157858
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Selective IgG2 deficiency due to a point mutation causing abnormal splicing of the Cgamma2 gene.
    Zhao Y; Pan-Hammarström Q; Zhao Z; Wen S; Hammarström L
    Int Immunol; 2005 Jan; 17(1):95-101. PubMed ID: 15569770
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gamma 3 gene-disrupted mice selectively deficient in the dominant IgG subclass made to bacterial polysaccharides undergo normal isotype switching after immunization with polysaccharide-protein conjugate vaccines.
    Shapiro DA; Threadgill DS; Copfer MJ; Corey DA; McCool TL; McCormick LL; Magnuson TR; Greenspan NS; Schreiber JR
    J Immunol; 1998 Oct; 161(7):3393-9. PubMed ID: 9759856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two siblings with deficiency of IgA1, IgG2, IgG4 and IgE due to deletion of immunoglobulin heavy chain constant region genes.
    Plebani A; Carbonara AO; Bottaro A; Gallina R; Boccazzi C; Crispino P; Ruggeri L; Soresina A; Meini A; Duina M
    Year Immunol; 1993; 7():231-5. PubMed ID: 8372508
    [No Abstract]   [Full Text] [Related]  

  • 6. CD40 ligand exerts differential effects on the expression of I gamma transcripts in subclones of an IgM+ human B cell lymphoma line.
    Ford GS; Yin CH; Barnhart B; Sztam K; Covey LR
    J Immunol; 1998 Jan; 160(2):595-605. PubMed ID: 9551893
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Structural analysis of human gamma 3 intervening regions and switch regions: implication for the low frequency of switching in IgG3-deficient patients.
    Pan Q; Lindersson Y; Sideras P; Hammarström L
    Eur J Immunol; 1997 Nov; 27(11):2920-6. PubMed ID: 9394819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Baboon immunoglobulin constant region heavy chains: identification of four IGHG genes.
    Attanasio R; Jayashankar L; Engleman CN; Scinicariello F
    Immunogenetics; 2002 Nov; 54(8):556-61. PubMed ID: 12439618
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transfer by BMT of IgG2 deficiency involving an immunoglobulin heavy chain constant region deletion and a silent IgG2 gene.
    Olsson PG; Gustafson R; Hammarström V; Lönnqvist B; Smith CI; Hammarström L
    Bone Marrow Transplant; 1993 May; 11(5):409-14. PubMed ID: 8504277
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gamma heavy chain disease in man: independent structural abnormalities and reduced transcription of a functionally rearranged lambda L-chain gene result in the absence of L-chains.
    Teng MH; Rosen S; Gorny MK; Alexander A; Buxbaum J
    Blood Cells Mol Dis; 2000 Jun; 26(3):177-85. PubMed ID: 10950937
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The evolutionarily conserved sequence upstream of the human Ig heavy chain S gamma 3 region is an inducible promoter: synergistic activation by CD40 ligand and IL-4 via cooperative NF-kappa B and STAT-6 binding sites.
    Schaffer A; Cerutti A; Shah S; Zan H; Casali P
    J Immunol; 1999 May; 162(9):5327-36. PubMed ID: 10228008
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Restricted immunoglobulin constant heavy G chain genes in primary immunodeficiencies.
    Oxelius VA; Ochs HD; Hammarström L
    Clin Immunol; 2008 Aug; 128(2):190-8. PubMed ID: 18502179
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues.
    Pepe CM; Saraco NI; Baquedano MS; Guercio G; Vaiani E; Marino R; Pandey AV; Flück CE; Rivarola MA; Belgorosky A
    Clin Endocrinol (Oxf); 2007 Nov; 67(5):698-705. PubMed ID: 17608756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency.
    Kutukculer N; Karaca NE; Demircioglu O; Aksu G
    Pediatr Allergy Immunol; 2007 Mar; 18(2):167-73. PubMed ID: 17338791
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Germ line transcription in mice bearing neor gene downstream of Igamma3 exon in the Ig heavy chain locus.
    Samara M; Oruc Z; Dougier HL; Essawi T; Cogné M; Khamlichi AA
    Int Immunol; 2006 Apr; 18(4):581-9. PubMed ID: 16507599
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genomic organization and structure of the 5'-flanking region of the TEX101 gene: alternative promoter usage and splicing generate transcript variants with distinct 5'-untranslated region.
    Tsukamoto H; Takizawa T; Takamori K; Ogawa H; Araki Y
    Mol Reprod Dev; 2007 Feb; 74(2):154-62. PubMed ID: 16941676
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex.
    Tsuruta M; Mitsubuchi H; Mardy S; Miura Y; Hayashida Y; Kinugasa A; Ishitsu T; Matsuda I; Indo Y
    J Hum Genet; 1998; 43(2):91-100. PubMed ID: 9621512
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of protein Salpha gene mutations including four novel mutations in eight unrelated patients with protein S deficiency.
    Okada H; Takagi A; Murate T; Adachi T; Yamamoto K; Matsushita T; Takamatsu J; Sugita K; Sugimoto M; Yoshioka A; Yamazaki T; Saito H; Kojima T
    Br J Haematol; 2004 Jul; 126(2):219-25. PubMed ID: 15238143
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Failure of IgG production due to a defect in the opening of the chromatin structure of I gamma 1 region in a patient with IgG and IgA deficiency.
    Kondo N; Inoue R; Kasahara K; Kaneko H; Kameyama T; Orii T
    Clin Exp Immunol; 1995 Jan; 99(1):21-8. PubMed ID: 7813107
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.