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 *

155 related articles for article (PubMed ID: 2551816)

  • 21. Direct observation of the gene organization of the complement C4 and 21-hydroxylase loci by pulsed field gel electrophoresis.
    Dunham I; Sargent CA; Dawkins RL; Campbell RD
    J Exp Med; 1989 May; 169(5):1803-18. PubMed ID: 2565949
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.
    Carroll MC; Campbell RD; Porter RR
    Proc Natl Acad Sci U S A; 1985 Jan; 82(2):521-5. PubMed ID: 3871526
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.
    Rumsby G; Carroll MC; Porter RR; Grant DB; Hjelm M
    J Med Genet; 1986 Jun; 23(3):204-9. PubMed ID: 3487654
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype.
    Chu X; Braun-Heimer L; Rittner C; Schneider PM
    Exp Clin Immunogenet; 1992; 9(2):80-5. PubMed ID: 1489553
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.
    Ghanem N; Lobaccaro JM; Buresi C; Abbal M; Halaby G; Sultan C; Lefranc G
    Hum Genet; 1990 Dec; 86(2):117-25. PubMed ID: 1979956
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [Mutations in 21-hydroxylase gene caused by gene conversion-like events].
    Urabe K
    Fukuoka Igaku Zasshi; 1990 Feb; 81(2):77-87. PubMed ID: 2328938
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Lack of deletion of complement C4 and steroid 21-hydroxylase genes in Japanese patients with primary Sjögren's syndrome.
    Moriuchi J; Ichikawa Y; Takaya M; Shimizu H; Uchiyama M; Inoko H; Tsuji K; Arimori S
    J Rheumatol; 1992 May; 19(5):700-3. PubMed ID: 1351942
    [TBL] [Abstract][Full Text] [Related]  

  • 33. C4B gene polymorphism detected in a human cosmid clone.
    Prentice HL; Schneider PM; Strominger JL
    Immunogenetics; 1986; 23(4):274-6. PubMed ID: 3009318
    [No Abstract]   [Full Text] [Related]  

  • 34. Lethal deletion of the complement component C4 and steroid 21-hydroxylase genes in the mouse H-2 class III region, caused by meiotic recombination.
    Shiroishi T; Sagai T; Natsuume-Sakai S; Moriwaki K
    Proc Natl Acad Sci U S A; 1987 May; 84(9):2819-23. PubMed ID: 3495003
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Frequent deletion and duplication of the steroid 21-hydroxylase genes.
    Werkmeister JW; New MI; Dupont B; White PC
    Am J Hum Genet; 1986 Oct; 39(4):461-9. PubMed ID: 3490178
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.
    Saxena K; Kitzmiller KJ; Wu YL; Zhou B; Esack N; Hiremath L; Chung EK; Yang Y; Yu CY
    Mol Immunol; 2009 Apr; 46(7):1289-303. PubMed ID: 19135723
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Steroid 21-hydroxylase deficiency and the major histocompatibility complex.
    White PC; Werkmeister J; New MI; Dupont B
    Hum Immunol; 1986 Apr; 15(4):404-15. PubMed ID: 3009365
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase.
    Carroll MC; Belt KT; Palsdottir A; Yu Y
    Immunol Rev; 1985 Oct; 87():39-60. PubMed ID: 2997023
    [No Abstract]   [Full Text] [Related]  

  • 39. The genomic structure of two ancestral haplotypes carrying C4A duplications.
    Tokunaga K; Zhang WJ; Christiansen FT; Dawkins RL
    Immunogenetics; 1991; 34(4):247-51. PubMed ID: 1680806
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families.
    Sinnott PJ; Costigan C; Dyer PA; Harris R; Strachan T
    Hum Genet; 1991 Jul; 87(3):361-6. PubMed ID: 1677925
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.