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.
110 related articles for article (PubMed ID: 9888550)
1. 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]
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. 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]
4. 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]
5. Organization of C4 and CYP21 loci in gorilla and orangutan. Kawaguchi H; Klein J Hum Immunol; 1992 Mar; 33(3):153-62. PubMed ID: 1618655 [TBL] [Abstract][Full Text] [Related]
6. Sequences promoting the transcription of the human XA gene overlapping P450c21A correctly predict the presence of a novel, adrenal-specific, truncated form of tenascin-X. Tee MK; Thomson AA; Bristow J; Miller WL Genomics; 1995 Jul; 28(2):171-8. PubMed ID: 8530023 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Transcriptional regulatory elements of the human gene for cytochrome P450c21 (steroid 21-hydroxylase) lie within intron 35 of the linked C4B gene. Wijesuriya SD; Zhang G; Dardis A; Miller WL J Biol Chem; 1999 Dec; 274(53):38097-106. PubMed ID: 10608879 [TBL] [Abstract][Full Text] [Related]
10. A promoter within intron 35 of the human C4A gene initiates abundant adrenal-specific transcription of a 1 kb RNA: location of a cryptic CYP21 promoter element? Tee MK; Babalola GO; Aza-Blanc P; Speek M; Gitelman SE; Miller WL Hum Mol Genet; 1995 Nov; 4(11):2109-16. PubMed ID: 8589688 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in The Netherlands. Koppens PF; Hoogenboezem T; Halley DJ; Barendse CA; Oostenbrink AJ; Degenhart HJ Eur J Pediatr; 1992 Dec; 151(12):885-92. PubMed ID: 1473541 [TBL] [Abstract][Full Text] [Related]
17. Organization of the chimpanzee C4-CYP21 region: implications for the evolution of human genes. Kawaguchi H; Golubic M; Figueroa F; Klein J Eur J Immunol; 1990 Apr; 20(4):739-45. PubMed ID: 2347361 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region. Donohoue PA; Guethlein L; Collins MM; Van Dop C; Migeon CJ; Bias WB; Schmeckpeper BJ Tissue Antigens; 1995 Sep; 46(3 ( Pt 1)):163-72. PubMed ID: 8525475 [TBL] [Abstract][Full Text] [Related]
20. Identification of promoter elements in the mouse 21-hydroxylase (Cyp21) gene that require a functional cyclic adenosine 3',5'-monophosphate-dependent protein kinase. Parissenti AM; Parker KL; Schimmer BP Mol Endocrinol; 1993 Feb; 7(2):283-90. PubMed ID: 8385740 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]