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Journal Abstract Search

203 related items for PubMed ID: 124762

  • 1. Mixed lymphocyte culture determinants and C2 deficiency: LD-7a associated with C2 deficiency in four families.
    Fu SM, Stern R, Kunkel HG, Dupont B, Hansen JA, Day NK, Good RA, Jersild C, Fotino M.
    J Exp Med; 1975 Aug 01; 142(2):495-506. PubMed ID: 124762
    [Abstract] [Full Text] [Related]

  • 2. Linkage of gene for C2 deficiency and the major histocompatibility complex MHC in man. Family study of a further case.
    Day NK, Rubinstein P, Case D, Hansen JA, Good RA, Walker ME, Tulchin N, Dupont B, Jersild C.
    Vox Sang; 1976 Aug 01; 31(2):96-102. PubMed ID: 133535
    [Abstract] [Full Text] [Related]

  • 3. Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement.
    Fu SM, Kunkel HG, Brusman HP, Allen FH, Fotino M.
    J Exp Med; 1974 Oct 01; 140(4):1108-11. PubMed ID: 4427089
    [Abstract] [Full Text] [Related]

  • 4. HLA antigen studies in a family with C2 deficiency.
    Opelz G, Glovsky MM.
    J Immunogenet; 1976 Oct 01; 3(5):303-6. PubMed ID: 137935
    [Abstract] [Full Text] [Related]

  • 5. Hereditary C2 deficiency: association with skin lesions resembling the discoid lesion of systemic lupus erythematosus.
    Stern R, Fu SM, Fotino M, Agnello V, Kunkel HG.
    Arthritis Rheum; 1976 Oct 01; 19(3):517-22. PubMed ID: 132935
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Genetic linkage between the HL-A system and a deficit of the second component (C2) of complement.
    Wolski KP, Schmid FR, Mittal KK.
    Science; 1975 Jun 06; 188(4192):1020-2. PubMed ID: 1145185
    [Abstract] [Full Text] [Related]

  • 8. Association of C2 deficiency and the HL-A haplotype 10, W18.
    Fu SM, Kunkel HG.
    Transplantation; 1975 Aug 06; 20(2):179-80. PubMed ID: 1179476
    [No Abstract] [Full Text] [Related]

  • 9. 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 06; 19(3):471-86. PubMed ID: 1006055
    [Abstract] [Full Text] [Related]

  • 10. Hereditary C2 deficiency: diagnosis and HLA gene complex associations.
    Gibson DJ, Glass D, Carpenter CB, Schur PH.
    J Immunol; 1976 Apr 06; 116(4):1065-70. PubMed ID: 1082903
    [Abstract] [Full Text] [Related]

  • 11. 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 06; 58(5):1240-8. PubMed ID: 993342
    [Abstract] [Full Text] [Related]

  • 12. Linkage relationship of C2 deficiency, HLA and glyoxalase I loci.
    Mahowald ML, Dalmasso AP, Petzel RA, Yunis EJ.
    Vox Sang; 1979 Nov 06; 37(6):321-8. PubMed ID: 161677
    [Abstract] [Full Text] [Related]

  • 13. Genetic linkage between the HL-A system and a deficit of the second component (C2) of complement in four generations of a family.
    Wolski KP, Schmid FR, Mittal KK.
    Tissue Antigens; 1976 Jan 06; 7(1):35-8. PubMed ID: 1251436
    [No Abstract] [Full Text] [Related]

  • 14. Identification of five lymphocyte activating determinants in man.
    Thorsby E, Helgesen A, Rankin B, Möller E, Kaakinen A.
    Tissue Antigens; 1975 Sep 06; 6(3):147-60. PubMed ID: 52910
    [Abstract] [Full Text] [Related]

  • 15. C2 Hypocomplementaemia in multiple sclerosis.
    Bertrams J, Opferkuch W, Grosse-Wilde H, Luboldt W, Schuppien W, Kuwert E.
    Lancet; 1976 Dec 18; 2(7999):1358-9. PubMed ID: 63832
    [No Abstract] [Full Text] [Related]

  • 16. LD homozygous cells in the Warao population: a possible new allele at the LD1 locus within the main histocompatibility region in man.
    Layrisse Z, de Rodríguez MP, Heinen HD, Layrisse M.
    Tissue Antigens; 1975 Nov 18; 6(5):326-34. PubMed ID: 129884
    [Abstract] [Full Text] [Related]

  • 17. Hypocomplementaemic multiple sclerosis: heterozygous C2 deficiency linked to HLA A10, B18.
    Trouillas P, Berthoux F, Betuel H, Boisson D, Aimard G, Devic M.
    Lancet; 1976 Nov 06; 2(7993):1023. PubMed ID: 62239
    [No Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. An estimation of the recombination fraction between the MLC locus and the FOUR locus.
    Keuning JJ, van den Tweel JG, Gabb BW, Termijtelen A, Goulmy E, Blokland E, Elferink BG, van Rood JJ.
    Tissue Antigens; 1975 Sep 03; 6(3):107-15. PubMed ID: 52907
    [Abstract] [Full Text] [Related]

  • 20. Studies on the C2-deficiency gene in man.
    Mortensen JP, Buskjaer L, Lamm LU.
    Immunology; 1980 Apr 03; 39(4):541-9. PubMed ID: 7380478
    [Abstract] [Full Text] [Related]

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