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Journal Abstract Search

174 related items for PubMed ID: 138091

  • 1. Linkage between the gene (or genes) controlling synthesis of the fourth component of complement and the major histocompatibility complex.
    Ochs HD, Rosenfeld SI, Thomas ED, Giblett ER, Alper CA, Dupont B, Schaller JG, Gilliland BC, Hansen JA, Wedgwood RJ.
    N Engl J Med; 1977 Mar 03; 296(9):470-5. PubMed ID: 138091
    [Abstract] [Full Text] [Related]

  • 2. The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement.
    Raum D, Glass D, Carpenter CB, Alper CA, Schur PH.
    J Clin Invest; 1976 Nov 03; 58(5):1240-8. PubMed ID: 993342
    [Abstract] [Full Text] [Related]

  • 3. Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.
    Welch TR, Beischel LS, Choi E, Balakrishnan K, Bishof NA.
    J Clin Invest; 1990 Aug 03; 86(2):675-8. PubMed ID: 2384609
    [Abstract] [Full Text] [Related]

  • 4. Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens.
    Muir WA, Hedrick S, Alper CA, Ratnoff OD, Schacter B, Wisnieski JJ.
    J Clin Invest; 1984 Oct 03; 74(4):1509-14. PubMed ID: 6480834
    [Abstract] [Full Text] [Related]

  • 5. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, de Waall LP, Bos JD, Asghar SS.
    Exp Clin Immunogenet; 1996 Oct 03; 13(2):104-11. PubMed ID: 9063702
    [Abstract] [Full Text] [Related]

  • 6. Complement genes on chromosome 6.
    Bruns GA.
    N Engl J Med; 1977 Mar 03; 296(9):510-11. PubMed ID: 834229
    [No Abstract] [Full Text] [Related]

  • 7. Hereditary C2 deficiency: diagnosis and HLA gene complex associations.
    Gibson DJ, Glass D, Carpenter CB, Schur PH.
    J Immunol; 1976 Apr 03; 116(4):1065-70. PubMed ID: 1082903
    [Abstract] [Full Text] [Related]

  • 8. Hereditary C4 deficiency--genetic studies and linkage to HLA.
    Ballow M, McLean RH, Einarson M, Martin S, Yunis EJ, Dupont B, O'Neill GJ.
    Transplant Proc; 1979 Dec 03; 11(4):1710-2. PubMed ID: 531924
    [No Abstract] [Full Text] [Related]

  • 9. Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA).
    Merritt AD, Petersen BH, Biegel AA, Meyers DA, Brooks GF, Hodes ME.
    Birth Defects Orig Artic Ser; 1976 Dec 03; 12(7):331-4. PubMed ID: 1024635
    [No Abstract] [Full Text] [Related]

  • 10. [Genetic study of C4 deficiency: relation to major histocompatibility complex].
    Hauptmann G, Grosshans E, Tongio MM, Mayer S, Grosse-Wilde H, Rittner C.
    Ann Dermatol Syphiligr (Paris); 1976 Dec 03; 103(3):304-6. PubMed ID: 1008524
    [No Abstract] [Full Text] [Related]

  • 11. The locus for glyoxalase I (GLO) is between HLA-A and PGM3 on chromosome 6 of man.
    Meera Khan P, Volkers WS, Doppert BA, Bijnen AB, Schreuder I, Van Rood JJ.
    Birth Defects Orig Artic Ser; 1976 Dec 03; 12(7):328-30. PubMed ID: 1024634
    [No Abstract] [Full Text] [Related]

  • 12. Hereditary C2 deficiency: Genetic studies and association with the HL-A system.
    Day NK, L'Esperance R, Good RA, Michael AF, Hansen JA, Dupont B, Jersild C.
    J Exp Med; 1975 Jun 01; 141(6):1464-9. PubMed ID: 1127385
    [Abstract] [Full Text] [Related]

  • 13. Familial systemic lupus erythematosus and C4 deficiency.
    Berliner S, Weinberger A, Zamir R, Salomon F, Joshua H, Pinkhas J.
    Scand J Rheumatol; 1981 Jun 01; 10(4):280-2. PubMed ID: 7323783
    [Abstract] [Full Text] [Related]

  • 14. Severe systemic lupus erythematosus with nephritis in a boy with deficiency of the fourth component of complement.
    Schaller JG, Gilliland BG, Ochs HD, Leddy JP, Agodoa LC, Rosenfeld SI.
    Arthritis Rheum; 1977 Jun 01; 20(8):1519-25. PubMed ID: 921824
    [Abstract] [Full Text] [Related]

  • 15. Which complement assays and typings are necessary for the diagnosis of complement deficiency in patients with lupus erythematosus? A study of 25 patients.
    Boeckler P, Meyer A, Uring-Lambert B, Goetz J, Cribier B, Hauptmann G, Lipsker D.
    Clin Immunol; 2006 Nov 01; 121(2):198-202. PubMed ID: 16987709
    [Abstract] [Full Text] [Related]

  • 16. Polymorphism of factor B of the properdin system (C3PA, GBG, and Bf) and histocompatibility-complement linkage.
    Hauptmann G, Tongio MM, Mayer S.
    Rev Fr Transfus Immunohematol; 1976 Sep 01; 19(3):471-86. PubMed ID: 1006055
    [Abstract] [Full Text] [Related]

  • 17. DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex.
    Whitehead AS, Woods DE, Fleischnick E, Chin JE, Yunis EJ, Katz AJ, Gerald PS, Alper CA, Colten HR.
    N Engl J Med; 1984 Jan 12; 310(2):88-91. PubMed ID: 6581384
    [Abstract] [Full Text] [Related]

  • 18. Investigations of red cell glyoxalase in recombinant families.
    Pretorius AM, Scholz S, Kuntz B, Albert ED.
    Eur J Immunol; 1976 Oct 12; 6(10):759-61. PubMed ID: 1015713
    [Abstract] [Full Text] [Related]

  • 19. Association of systemic lupus erythematosus and SLE-like syndromes with hereditary and acquired complement deficiency states.
    Agnello V.
    Arthritis Rheum; 1978 Jun 12; 21(5 Suppl):S146-52. PubMed ID: 666879
    [Abstract] [Full Text] [Related]

  • 20. Polymorphism of the complement components in human pathology.
    Brai M, Accardo P, Bellavia D.
    Ann Ital Med Int; 1994 Jun 12; 9(3):167-72. PubMed ID: 7946894
    [Abstract] [Full Text] [Related]

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