BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 1469300)

  • 1. Molecular heterogeneity of the fourth component of complement (C4) and its genes in vitiligo.
    Venneker GT; Westerhof W; de Vries IJ; Drayer NM; Wolthers BG; de Waal LP; Bos JD; Asghar SS
    J Invest Dermatol; 1992 Dec; 99(6):853-8. PubMed ID: 1469300
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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; 13(2):104-11. PubMed ID: 9063702
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosus.
    Goldstein R; Arnett FC; McLean RH; Bias WB; Duvic M
    Arthritis Rheum; 1988 Jun; 31(6):736-44. PubMed ID: 3260100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4.
    Hartmann D; Fremeaux-Bacchi V; Weiss L; Meyer A; Blouin J; Hauptmann G; Kazatchkine M; Uring-Lambert B
    J Clin Immunol; 1997 Mar; 17(2):176-84. PubMed ID: 9083894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Class III alleles and high-risk MHC haplotypes in type I diabetes mellitus, Graves' disease and Hashimoto's thyroiditis.
    Skanes VM; Barnard J; Farid N; Marshall WH; Murphy L; Rideout D; Taylor R; Xidos G; Larsen B
    Mol Biol Med; 1986 Apr; 3(2):143-57. PubMed ID: 3461234
    [TBL] [Abstract][Full Text] [Related]  

  • 7. C4 complement allotypes in juvenile dermatomyositis.
    Robb SA; Fielder AH; Saunders CE; Davey NJ; Burley MW; Lord DH; Batchelor JR; Dubowitz V
    Hum Immunol; 1988 May; 22(1):31-8. PubMed ID: 3260584
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human C4 polymorphism: pedigree analysis of qualitative, quantitative, and functional parameters as a basis for phenotype interpretations.
    Mauff G; Bender K; Giles CM; Goldmann S; Opferkuch W; Wachauf B
    Hum Genet; 1984; 65(4):362-72. PubMed ID: 6420328
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysis.
    Uring-Lambert B; Vegnaduzzi N; Carroll MC; Tongio MM; Goetz J; Hauptmann G
    FEBS Lett; 1987 Jun; 217(1):65-8. PubMed ID: 2885219
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular basis of complete C4 deficiency. A study of three patients.
    Uring-Lambert B; Mascart-Lemone F; Tongio MM; Goetz J; Hauptmann G
    Hum Immunol; 1989 Feb; 24(2):125-32. PubMed ID: 2784426
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.
    Schneider PM; Carroll MC; Alper CA; Rittner C; Whitehead AS; Yunis EJ; Colten HR
    J Clin Invest; 1986 Sep; 78(3):650-7. PubMed ID: 3018042
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inherited deficiency of the fourth component of human complement.
    Hauptmann G; Tappeiner G; Schifferli JA
    Immunodefic Rev; 1988; 1(1):3-22. PubMed ID: 3078708
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
    Donohoue PA; van Dop C; McLean RH; White PC; Jospe N; Migeon CJ
    J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.
    Fasano MB; Winkelstein JA; LaRosa T; Bias WB; McLean RH
    J Clin Invest; 1992 Oct; 90(4):1180-4. PubMed ID: 1401055
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from southern Brazil: the Kaingang and the Guarani.
    Weg-Remers S; Brenden M; Schwarz E; Witzel K; Schneider PM; Guerra LK; Rehfeldt IR; Lima MT; Hartmann D; Petzl-Erler ML; de Messias IJ; Mauff G
    Hum Genet; 1997 Oct; 100(5-6):548-56. PubMed ID: 9341869
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.
    White PC; Grossberger D; Onufer BJ; Chaplin DD; New MI; Dupont B; Strominger JL
    Proc Natl Acad Sci U S A; 1985 Feb; 82(4):1089-93. PubMed ID: 2983330
    [TBL] [Abstract][Full Text] [Related]  

  • 17. C4A gene deletion: association with Graves' disease.
    Ratanachaiyavong S; Lloyd L; McGregor AM
    J Mol Endocrinol; 1989 Sep; 3(2):145-53. PubMed ID: 2570594
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.
    Fielder AH; Walport MJ; Batchelor JR; Rynes RI; Black CM; Dodi IA; Hughes GR
    Br Med J (Clin Res Ed); 1983 Feb; 286(6363):425-8. PubMed ID: 6401549
    [TBL] [Abstract][Full Text] [Related]  

  • 19. C4 null alleles in childhood onset systemic lupus erythematosus. Is there any relationship with renal disease?
    Clemenceau S; Castellano F; Montes de Oca M; Kaplan C; Danon F; Levy M
    Pediatr Nephrol; 1990 May; 4(3):207-12. PubMed ID: 2400645
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family.
    Fremeaux-Bacchi V; Uring-Lambert B; Weiss L; Brun P; Blouin J; Hartmann D; Loirat C; Hauptmann G; Kazatchkine MD
    J Clin Immunol; 1994 Sep; 14(5):273-9. PubMed ID: 7814456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.