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 *

120 related articles for article (PubMed ID: 8582328)

  • 1. Constitutive human steroid 21-hydroxylase promoter gene and pseudogene activity in steroidogenic and nonsteroidogenic cells with the luciferase gene as a reporter.
    Kyllo JH; Collins MM; Donohoue PA
    Endocr Res; 1995 Nov; 21(4):777-91. PubMed ID: 8582328
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The -104G nucleotide of the human CYP21 gene is important for CYP21 transcription activity and protein interaction.
    Chin KK; Chang SF
    Nucleic Acids Res; 1998 Apr; 26(8):1959-64. PubMed ID: 9518489
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The chimeric CYP21P/CYP21 gene and 21-hydroxylase deficiency.
    Lee HH
    J Hum Genet; 2004; 49(2):65-72. PubMed ID: 14730433
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CYP21 and CYP21P variability in steroid 21-hydroxylase deficiency patients and in the general population in the Netherlands.
    Koppens PF; Hoogenboezem T; Degenhart HJ
    Eur J Hum Genet; 2000 Nov; 8(11):827-36. PubMed ID: 11093272
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The suppression effect of DNA sequences within the C4A region on the transcription activity of human CYP21.
    Chang SF; Cheng CL
    Endocr Res; 1998; 24(3-4):625-30. PubMed ID: 9888550
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Structural analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency.
    Lee HH; Niu DM; Lin RW; Chan P; Lin CY
    J Hum Genet; 2002; 47(10):517-22. PubMed ID: 12376740
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in steroid 21-hydroxylase (CYP21).
    White PC; Tusie-Luna MT; New MI; Speiser PW
    Hum Mutat; 1994; 3(4):373-8. PubMed ID: 8081391
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module.
    Lee HH
    Mol Genet Metab; 2005 Jan; 84(1):4-8. PubMed ID: 15639189
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms.
    Tusié-Luna MT; White PC
    Proc Natl Acad Sci U S A; 1995 Nov; 92(23):10796-800. PubMed ID: 7479886
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Single-nucleotide polymorphisms in intron 2 of CYP21P: evidence for a higher rate of mutation at CpG dinucleotides in the functional steroid 21-hydroxylase gene and application to segregation analysis in congenital adrenal hyperplasia.
    Jiddou RR; Wei WL; Sane KS; Killeen AA
    Clin Chem; 1999 May; 45(5):625-9. PubMed ID: 10222348
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Expression of green fluorescent protein vector by promoter sequence of CYP21 gene and CYP21P gene].
    Han B; Wang XM; Zhang YF; Gu XF
    Yi Chuan Xue Bao; 2002 May; 29(5):396-401. PubMed ID: 12043565
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency.
    Lee HH; Chang SF; Lo FS; Chao HT; Lin CY
    Mol Genet Metab; 2003 Jul; 79(3):214-20. PubMed ID: 12855227
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional analysis of four CYP21 mutations from spanish patients with congenital adrenal hyperplasia.
    Nunez BS; Lobato MN; White PC; Meseguer A
    Biochem Biophys Res Commun; 1999 Sep; 262(3):635-7. PubMed ID: 10471376
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CYP21 pseudogene transcripts are much less abundant than those from the active gene in normal human adrenocortical cells under various conditions in culture.
    Endoh A; Yang L; Hornsby PJ
    Mol Cell Endocrinol; 1998 Feb; 137(1):13-9. PubMed ID: 9607724
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.
    Lee HH; Chang SF; Tsai FJ; Tsai LP; Lin CY
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2726-9. PubMed ID: 12788880
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CYP21 mutations and congenital adrenal hyperplasia.
    Lee HH
    Clin Genet; 2001 May; 59(5):293-301. PubMed ID: 11359457
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diversity of the CYP21P-like gene in CYP21 deficiency.
    Lee HH
    DNA Cell Biol; 2005 Jan; 24(1):1-9. PubMed ID: 15684714
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Salt-wasting congenital adrenal hyperplasia: detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction.
    Owerbach D; Ballard AL; Draznin MB
    J Clin Endocrinol Metab; 1992 Mar; 74(3):553-8. PubMed ID: 1740489
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency.
    Lee HH; Chang JG; Tsai CH; Tsai FJ; Chao HT; Chung B
    Clin Chem; 2000 May; 46(5):606-11. PubMed ID: 10794740
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The human complement C4B/steroid 21-hydroxylase (CYP21) and complement C4A/21-hydroxylase pseudogene (CYP21P) intergenic sequences: comparison and identification of possible regulatory elements.
    Donohoue PA; Collins MM
    Biochem Biophys Res Commun; 1992 Jul; 186(1):256-62. PubMed ID: 1385946
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.