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Journal Abstract Search

118 related items for PubMed ID: 133535

  • 1. 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; 31(2):96-102. PubMed ID: 133535
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. 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
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  • 9. 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
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  • 10. 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]

  • 11. 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]

  • 12. 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]

  • 13. Familial discoid lupus erythematosus associated with heterozygote C2 deficiency.
    Belin DC, Bordwell BJ, Einarson ME, McLean RH, Weinstein A, Yunis EJ, Rothfield NF.
    Arthritis Rheum; 1980 Aug 06; 23(8):898-903. PubMed ID: 6902670
    [Abstract] [Full Text] [Related]

  • 14. Complement genes of the major histocompatibility complex (complotypes), extended haplotypes and disease markers.
    Alper CA, Awdeh Z, Raum D, Yunis EJ.
    Biochem Soc Symp; 1986 Aug 06; 51():19-28. PubMed ID: 3493006
    [Abstract] [Full Text] [Related]

  • 15. Hereditary C2 deficiency associated with immune complex disease.
    McPherson AJ, McKenzie I, Castaldi PA, Stewart GJ.
    Aust J Exp Biol Med Sci; 1978 Feb 06; 56(1):81-98. PubMed ID: 149533
    [Abstract] [Full Text] [Related]

  • 16. The HLA system and inherited deficiencies of the complement system.
    Jersild C, Rubinstein P, Day NK.
    Transplant Rev; 1976 Feb 06; 32():43-71. PubMed ID: 790689
    [No Abstract] [Full Text] [Related]

  • 17. 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 Feb 06; 19(3):517-22. PubMed ID: 132935
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 Nov 06; 13(2):104-11. PubMed ID: 9063702
    [Abstract] [Full Text] [Related]

  • 20. Studies on the C2-deficiency gene in man.
    Mortensen JP, Buskjaer L, Lamm LU.
    Immunology; 1980 Apr 06; 39(4):541-9. PubMed ID: 7380478
    [Abstract] [Full Text] [Related]

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