These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

160 related items for PubMed ID: 11807006

  • 21. Establishment and characterization of adenosine deaminase-deficient human T cell lines.
    Kohn DB, Mitsuya H, Ballow M, Selegue JE, Barankiewicz J, Cohen A, Gelfand E, Anderson WF, Blaese RM.
    J Immunol; 1989 Jun 01; 142(11):3971-7. PubMed ID: 2497184
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. [Genetic analysis of two patients with adenosine deaminase (ADA)-deficiency: detection of three novel mutations and characterization of two paradoxical carriers].
    Oda N, Ariga T, Ono S, Kobayashi I, Kawamura N, Okano M, Kobayashi Y, Taniuchi S, Terada K, Kataoka N, Sakiyama Y.
    Arerugi; 2000 Dec 01; 49(12):1173-80. PubMed ID: 11197883
    [Abstract] [Full Text] [Related]

  • 25. Normal and mutant human adenosine deaminase genes.
    Akeson AL, Wiginton DA, Hutton JJ.
    J Cell Biochem; 1989 Mar 01; 39(3):217-28. PubMed ID: 2651461
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Molecular basis of adenosine deaminase deficiency.
    Markert ML.
    Immunodeficiency; 1994 Mar 01; 5(2):141-57. PubMed ID: 8032366
    [Abstract] [Full Text] [Related]

  • 29. A homozygous 5 base-pair deletion in exon 10 of the adenosine deaminase (ADA) gene in a child with severe combined immunodeficiency and very low levels of ADA mRNA and protein.
    Gossage DL, Norby-Slycord CJ, Hershfield MS, Markert ML.
    Hum Mol Genet; 1993 Sep 01; 2(9):1493-4. PubMed ID: 8242080
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Severe combined immune deficiency in an adenosine deaminase-deficient patient.
    Ozdemir O.
    Allergy Asthma Proc; 2006 Sep 01; 27(2):172-4. PubMed ID: 16724639
    [Abstract] [Full Text] [Related]

  • 32. Long-term efficacy of enzyme replacement therapy for adenosine deaminase (ADA)-deficient severe combined immunodeficiency (SCID).
    Chan B, Wara D, Bastian J, Hershfield MS, Bohnsack J, Azen CG, Parkman R, Weinberg K, Kohn DB.
    Clin Immunol; 2005 Nov 01; 117(2):133-43. PubMed ID: 16112907
    [Abstract] [Full Text] [Related]

  • 33. The binding site of human adenosine deaminase for CD26/Dipeptidyl peptidase IV: the Arg142Gln mutation impairs binding to cd26 but does not cause immune deficiency.
    Richard E, Arredondo-Vega FX, Santisteban I, Kelly SJ, Patel DD, Hershfield MS.
    J Exp Med; 2000 Nov 06; 192(9):1223-36. PubMed ID: 11067872
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry.
    Sanchez JJ, Monaghan G, Børsting C, Norbury G, Morling N, Gaspar HB.
    Ann Hum Genet; 2007 May 06; 71(Pt 3):336-47. PubMed ID: 17181544
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 8.