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PUBMED FOR HANDHELDS

Journal Abstract Search


254 related items for PubMed ID: 3366897

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  • 3. Identification of a deletion in the adenosine deaminase gene in a child with severe combined immunodeficiency.
    Markert ML, Hershfield MS, Wiginton DA, States JC, Ward FE, Bigner SH, Buckley RH, Kaufman RE, Hutton JJ.
    J Immunol; 1987 May 15; 138(10):3203-6. PubMed ID: 3571974
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  • 4. Severe combined immune deficiency due to a homozygous 3.2-kb deletion spanning the promoter and first exon of the adenosine deaminase gene.
    Berkvens TM, Gerritsen EJ, Oldenburg M, Breukel C, Wijnen JT, van Ormondt H, Vossen JM, van der Eb AJ, Meera Khan P.
    Nucleic Acids Res; 1987 Nov 25; 15(22):9365-78. PubMed ID: 3684597
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  • 5. Adenosine deaminase (ADA) deficiency in cells derived from humans with severe combined immunodeficiency is due to an aberration of the ADA protein.
    Valerio D, Duyvesteyn MG, van Ormondt H, Meera Khan P, van der Eb AJ.
    Nucleic Acids Res; 1984 Jan 25; 12(2):1015-24. PubMed ID: 6198631
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  • 6. Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency.
    Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JM, Lechler RI, Webster AD, Sun XM, Webb JC, Soutar AK.
    J Immunol; 1994 Sep 01; 153(5):2331-9. PubMed ID: 8051429
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  • 9. Linkage disequilibrium analysis of the human adenosine deaminase (ada) gene provides evidence for a lack of correlation between hot spots of equal and unequal homologous recombination.
    Cruciani F, Bernardini L, Santolamazza P, Modiano D, Torroni A, Scozzari R.
    Genomics; 2003 Jul 01; 82(1):20-33. PubMed ID: 12809673
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  • 11. Novel deletion and a new missense mutation (Glu 217 Lys) at the catalytic site in two adenosine deaminase alleles of a patient with neonatal onset adenosine deaminase- severe combined immunodeficiency.
    Hirschhorn R, Nicknam MN, Eng F, Yang DR, Borkowsky W.
    J Immunol; 1992 Nov 01; 149(9):3107-12. PubMed ID: 1401934
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  • 14. Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency.
    Hirschhorn R, Tzall S, Ellenbogen A, Orkin SH.
    J Clin Invest; 1989 Feb 01; 83(2):497-501. PubMed ID: 2783588
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  • 15. Paradoxical expression of adenosine deaminase in T cells cultured from a patient with adenosine deaminase deficiency and combine immunodeficiency.
    Arredondo-Vega FX, Kurtzberg J, Chaffee S, Santisteban I, Reisner E, Povey MS, Hershfield MS.
    J Clin Invest; 1990 Aug 01; 86(2):444-52. PubMed ID: 1974554
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  • 17. Hot spot mutations in adenosine deaminase deficiency.
    Hirschhorn R, Tzall S, Ellenbogen A.
    Proc Natl Acad Sci U S A; 1990 Aug 01; 87(16):6171-5. PubMed ID: 2166947
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