These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 2221823)

  • 1. Use of DNA amplification (PCR) and direct DNA sequencing in the characterization of C4 alleles.
    Berg ES; Markussen G; Teisberg P; Olaisen B
    Ann Hum Genet; 1990 Jul; 54(3):183-9. PubMed ID: 2221823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haplotype study on C4 polymorphism in Japanese. Associations with MHC alleles, complotypes, and HLA-complement haplotypes.
    Tokunaga K; Omoto K; Akaza T; Akiyama N; Amemiya H; Naito S; Sasazuki T; Satoh H; Juji T
    Immunogenetics; 1985; 22(4):359-65. PubMed ID: 3850846
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic analysis of C4 polymorphism by use of DNA amplification (PCR), allele-specific oligonucleotide probes and allele-specific restriction enzymes.
    Berg ES; Teisberg P; Olaisen B
    Ann Hum Genet; 1989 Jul; 53(3):221-7. PubMed ID: 2556959
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA sequence analysis of the C4 antigen WH: evidence for two mechanisms of expression.
    Moulds JM; Roberts SL; Wells TD
    Immunogenetics; 1996; 44(2):104-7. PubMed ID: 8662071
    [TBL] [Abstract][Full Text] [Related]  

  • 5. C4d DNA sequences of two infrequent human allotypes (C4A13 and C4B12) and the presence of signal sequences enhancing recombination.
    Martínez-Quiles N; Paz-Artal E; Moreno-Pelayo MA; Longás J; Ferre-López S; Rosal M; Arnaiz-Villena A
    J Immunol; 1998 Oct; 161(7):3438-43. PubMed ID: 9759862
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.
    Witzel K; Chu X; Rittner C; Schneider PM
    Hum Immunol; 1995 Jul; 43(3):165-73. PubMed ID: 7558933
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect.
    Anderson MJ; Milner CM; Cotton RG; Campbell RD
    J Immunol; 1992 May; 148(9):2795-802. PubMed ID: 1573268
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Complete sequence of the complement C4 gene from the HLA-A1, B8, C4AQ0, C4B1, DR3 haplotype.
    Ulgiati D; Townend DC; Christiansen FT; Dawkins RL; Abraham LJ
    Immunogenetics; 1996; 43(4):250-2. PubMed ID: 8575831
    [No Abstract]   [Full Text] [Related]  

  • 10. Serum concentrations of C4 isotypes and factor B in type I C2 deficiency suggest haplotype-dependent quantitative expression of MHC class III complement genes.
    Truedsson L; Gullstrand B; Jönsson T; Klint C
    Exp Clin Immunogenet; 1995; 12(2):66-73. PubMed ID: 7576717
    [TBL] [Abstract][Full Text] [Related]  

  • 11. C4d DNA sequence of complement C4B93 and recombination mechanisms for its generation.
    López-Goyanes A; Moreno MA; Ferre S; Paz-Artal E
    Tissue Antigens; 2004 Mar; 63(3):260-2. PubMed ID: 14989716
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter study.
    Hartung K; Baur MP; Coldewey R; Fricke M; Kalden JR; Lakomek HJ; Peter HH; Schendel D; Schneider PM; Seuchter SA
    J Clin Invest; 1992 Oct; 90(4):1346-51. PubMed ID: 1401069
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of two new C4 alleles by DNA sequencing and evidence for a historical recombination of serologically defined C4A and C4B alleles.
    Hui J; Oka A; Tomizawa M; Tay GK; Kulski JK; Penhale WJ; Iaschi SP; Makino S; Tamiya G; Inoko H
    Tissue Antigens; 2004 Mar; 63(3):263-9. PubMed ID: 14989717
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Use of allele-specific sequencing primers is an efficient alternative to PCR subcloning of low-copy nuclear genes.
    Scheen AC; Pfeil BE; Petri A; Heidari N; Nylinder S; Oxelman B
    Mol Ecol Resour; 2012 Jan; 12(1):128-35. PubMed ID: 21943046
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes.
    Wu YL; Savelli SL; Yang Y; Zhou B; Rovin BH; Birmingham DJ; Nagaraja HN; Hebert LA; Yu CY
    J Immunol; 2007 Sep; 179(5):3012-25. PubMed ID: 17709516
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reference typing report for complement component C4.
    Mauff G; Luther B; Schneider PM; Rittner C; Stradmann-Bellinghausen B; Dawkins R; Moulds JM
    Exp Clin Immunogenet; 1998; 15(4):249-60. PubMed ID: 10072635
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The structural basis of the multiple forms of human complement component C4.
    Belt KT; Carroll MC; Porter RR
    Cell; 1984 Apr; 36(4):907-14. PubMed ID: 6546707
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus.
    Gyllensten UB; Erlich HA
    Proc Natl Acad Sci U S A; 1988 Oct; 85(20):7652-6. PubMed ID: 3174659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of DRB alleles in rhesus monkeys using polymerase chain reaction-sequence-specific primers (PCR-SSP) amplification.
    Lobashevsky A; Smith JP; Kasten-Jolly J; Horton H; Knapp L; Bontrop RE; Watkins D; Thomas J
    Tissue Antigens; 1999 Sep; 54(3):254-63. PubMed ID: 10519362
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DNA analysis in a MHC heterozygous patient with complete C4 deficiency--homozygosity for C4 gene deletion and C4 pseudogene.
    Nordin Fredrikson G; Truedsson L; Sjöholm AG; Kjellman M
    Exp Clin Immunogenet; 1991; 8(1):29-37. PubMed ID: 1910860
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.