BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 6950690)

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

  • 22. 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; 2(7993):1023. PubMed ID: 62239
    [No Abstract]   [Full Text] [Related]  

  • 23. [Familial glomerulonephritis and hereditary deficiency of C2].
    Genin C; Freycon MT; Berthoux FC; Lepetit JC; Bétuel H; Freidel C; Freycon F
    Arch Fr Pediatr; 1978 Dec; 35(10):1085-95. PubMed ID: 107905
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetics of complement deficiencies associated with lupus-like syndromes.
    Schur PH
    Arthritis Rheum; 1978 Jun; 21(5 Suppl):S153-60. PubMed ID: 96843
    [TBL] [Abstract][Full Text] [Related]  

  • 25. HLA genotypes in a family with a case of homozygous C2 deficiency and discoid lupus erythematosus.
    Braathen LR; Bratlie A; Teisberg P
    Acta Derm Venereol; 1986; 66(5):419-22. PubMed ID: 2431580
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family.
    Delâge JM; Lehner-Netsch G; Lafleur R; Simard J; Brun G; Prochazka E
    Immunology; 1979 Jun; 37(2):419-28. PubMed ID: 468307
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Lupus erythematosus and hereditary lack of complement. Review of about one case of C2 deficit (author's transl)].
    Morel P; Sohier J; Peltier AP; Cottenot F; Civatte J
    Ann Dermatol Venereol; 1977 Dec; 104(12):831-9. PubMed ID: 613949
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Complement factor 2 deficiency: a clinical and serological family study.
    D'Cruz D; Taylor J; Ahmed T; Asherson R; Khamashta M; Hughes GR
    Ann Rheum Dis; 1992 Nov; 51(11):1254-6. PubMed ID: 1361318
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency.
    Alper CA; Xu J; Cosmopoulos K; Dolinski B; Stein R; Uko G; Larsen CE; Dubey DP; Densen P; Truedsson L; Sturfelt G; Sjöholm AG
    J Clin Immunol; 2003 Jul; 23(4):297-305. PubMed ID: 12959222
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Complete deficiency in the C2 fraction of complement associated with a glomerular nephropathy: apropos of 2 cases].
    Ayed K; Bardi R; Sassi F; Gorgi Y; Ben Maiz H; Haddad S; Ben Ayed H
    Nephrologie; 1988; 9(5):239-44. PubMed ID: 3216945
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Subacute cutaneous lupus erythematosus in multiple members of a family with C2 deficiency.
    Callen JP; Hodge SJ; Kulick KB; Stelzer G; Buchino JJ
    Arch Dermatol; 1987 Jan; 123(1):66-70. PubMed ID: 3467658
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular heterogeneity of second and fourth components of complement and their genes in systemic sclerosis and association of HLA alleles A1, B8 and DR3 with limited and DR5 with diffuse systemic sclerosis.
    Venneker GT; van den Hoogen FH; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; Boerbooms AM; de Waal LP; Bos JD; Asghar SS
    Exp Clin Immunogenet; 1998; 15(2):90-9. PubMed ID: 9691203
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polymorphism of the second component of human complement (C2). Observation of the rare phenotype (C2 2 (= C2 B) and data on the localization of the C2 locus in the HLA region.
    Dewald G; Rittner C
    Vox Sang; 1979; 37(1):47-54. PubMed ID: 40340
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Recurrent pyogenic infections in individuals with absence of the second component of complement.
    Sampson HA; Walchner AM; Baker PJ
    J Clin Immunol; 1982 Jan; 2(1):39-45. PubMed ID: 6980226
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Association of low C2 and C4 serum levels with the HLA-DW2 allele in healthy individuals.
    Nerl C; Grosse-Wilde H; Valet G
    J Exp Med; 1978 Sep; 148(3):704-13. PubMed ID: 702053
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prevalence of the type I complement C2 deficiency gene in Swedish systemic lupus erythematosus patients.
    Truedsson L; Sturfelt G; Nived O
    Lupus; 1993 Oct; 2(5):325-7. PubMed ID: 8305927
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Inherited deficiency of the second component of complement. Rheumatic disease associations.
    Glass D; Raum D; Gibson D; Stillman JS; Schur PH
    J Clin Invest; 1976 Oct; 58(4):853-61. PubMed ID: 965492
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Heterozygous C2-deficiency and myasthenia gravis.
    Riggs JE; Griggs RC; Rosenfeld SI; May AG; Penn AS
    Neurology; 1980 Aug; 30(8):871-3. PubMed ID: 7191069
    [TBL] [Abstract][Full Text] [Related]  

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

  • 40. Ordering of genes for HLA antigens and complement components on the human 6th chromosome.
    Carpenter CB; Raum D; Glass D; Schur PH
    Prog Clin Biol Res; 1977; 16():9-20. PubMed ID: 302950
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.