BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

312 related articles for article (PubMed ID: 3036685)

  • 1. Gene organization of haplotypes expressing two different C4A allotypes.
    Palsdottir A; Arnason A; Fossdal R; Jensson O
    Hum Genet; 1987 Jul; 76(3):220-4. PubMed ID: 3036685
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA polymorphism of human HLA-linked complement C4 allotypes, including C4 null alleles, in the Finnish population.
    Partanen J; Peltonen L; Koskimies S; Carroll MC
    Hum Hered; 1987; 37(4):241-9. PubMed ID: 2888726
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.
    Carroll MC; Palsdottir A; Belt KT; Porter RR
    EMBO J; 1985 Oct; 4(10):2547-52. PubMed ID: 2996881
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus.
    Braun L; Schneider PM; Giles CM; Bertrams J; Rittner C
    J Exp Med; 1990 Jan; 171(1):129-40. PubMed ID: 2295875
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes.
    Palsdottir A; Fossdal R; Arnason A; Edwards JH; Jensson O
    Immunogenetics; 1987; 25(5):299-304. PubMed ID: 2883116
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Restriction fragment analysis of duplication of the fourth component of complement (C4A).
    McLean RH; Donohoue PA; Jospe N; Bias WB; Van Dop C; Migeon CJ
    Genomics; 1988 Jan; 2(1):76-85. PubMed ID: 2838414
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Definitive RFLPs to distinguish between the human complement C4A/C4B isotypes and the major Rodgers/Chido determinants: application to the study of C4 null alleles.
    Yu CY; Campbell RD
    Immunogenetics; 1987; 25(6):383-90. PubMed ID: 2439447
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Human C4 haplotypes with duplicated C4A or C4B.
    Raum D; Awdeh Z; Anderson J; Strong L; Granados J; Teran L; Giblett E; Yunis EJ; Alper CA
    Am J Hum Genet; 1984 Jan; 36(1):72-9. PubMed ID: 6607672
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Molecular characterisation of C4 null alleles found in Felty's syndrome.
    Hillarby MC; Strachan T; Grennan DM
    Ann Rheum Dis; 1990 Oct; 49(10):763-7. PubMed ID: 1978638
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.
    Blanchong CA; Chung EK; Rupert KL; Yang Y; Yang Z; Zhou B; Moulds JM; Yu CY
    Int Immunopharmacol; 2001 Mar; 1(3):365-92. PubMed ID: 11367523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Complement component C4 deficiencies and gene alterations in patients with systemic lupus erythematosus.
    Fan Q; Uring-Lambert B; Weill B; Gautreau C; Menkes CJ; Delpech M
    Eur J Immunogenet; 1993 Feb; 20(1):11-21. PubMed ID: 8095158
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of two hybrid C4 allotypes (C4A*12 and C4B*3) by electrophoretic, serological and restriction fragment length polymorphism analyses.
    McLean RH; Bias WB; Giles C; Yu CY; Campbell RD
    Tissue Antigens; 1990 Feb; 35(2):75-81. PubMed ID: 1693017
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Neonatal lupus erythematosus syndrome: analysis of C4 allotypes and C4 genes in 18 families.
    Watson RM; Scheel JN; Petri M; Lee LA; Bias WB; McLean RH
    Medicine (Baltimore); 1992 Mar; 71(2):84-95. PubMed ID: 1545698
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.