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 *

112 related articles for article (PubMed ID: 7925109)

  • 41. Structure of human steroid 21-hydroxylase genes.
    White PC; New MI; Dupont B
    Proc Natl Acad Sci U S A; 1986 Jul; 83(14):5111-5. PubMed ID: 3487786
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region.
    Boehm BO; Rosak C; Boehm TL; Kuehnl P; White PC; Schöffling K
    Mol Biol Med; 1986 Oct; 3(5):437-48. PubMed ID: 2882404
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Nucleotide sequence analysis of murine 21-hydroxylase genes: mutations affecting gene expression.
    Chaplin DD; Galbraith LJ; Seidman JG; White PC; Parker KL
    Proc Natl Acad Sci U S A; 1986 Dec; 83(24):9601-5. PubMed ID: 3491986
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia.
    Jospe N; Donohoue PA; Van Dop C; McLean RH; Bias WB; Migeon CJ
    Biochem Biophys Res Commun; 1987 Feb; 142(3):798-804. PubMed ID: 3030300
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Different isozymes of mouse 11 beta-hydroxylase produce mineralocorticoids and glucocorticoids.
    Domalik LJ; Chaplin DD; Kirkman MS; Wu RC; Liu WW; Howard TA; Seldin MF; Parker KL
    Mol Endocrinol; 1991 Dec; 5(12):1853-61. PubMed ID: 1686470
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Molecular analysis of 21-hydroxylase gene expression in mouse adrenal cells.
    Parker KL; Chaplin DD; Wong M; Seidman JG; Schimmer BP
    Endocr Res; 1986; 12(4):409-27. PubMed ID: 2435543
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Expression of murine 21-hydroxylase in mouse adrenal glands and in transfected Y1 adrenocortical tumor cells.
    Parker KL; Chaplin DD; Wong M; Seidman JG; Smith JA; Schimmer BP
    Proc Natl Acad Sci U S A; 1985 Dec; 82(23):7860-4. PubMed ID: 2999780
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S; Lin-Su K; New MI
    Pediatr Clin North Am; 2011 Oct; 58(5):1281-300, xii. PubMed ID: 21981961
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Nonisotopic detection of point mutations in CYP21B gene in steroid 21-hydroxylase deficiency.
    Ezquieta B; Varela JM; Jariego C; Oliver A; Gracia R
    Clin Chem; 1996 Jul; 42(7):1108-10. PubMed ID: 8674198
    [No Abstract]   [Full Text] [Related]  

  • 50. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Speiser PW; White PC
    Clin Endocrinol (Oxf); 1998 Oct; 49(4):411-7. PubMed ID: 9876336
    [No Abstract]   [Full Text] [Related]  

  • 51. [Molecular basis of steroid 21-hydroxylase deficiency].
    Kupczyk P; Sawiński P; Trzeciak WH
    Postepy Biochem; 1995; 41(1):38-47. PubMed ID: 7777432
    [No Abstract]   [Full Text] [Related]  

  • 52. Adrenocortical-specific transgene expression directed by steroid hydroxylase gene promoters.
    Morley SD; Viard I; Parker KL; Mullins JJ
    Endocr Res; 1996 Nov; 22(4):631-9. PubMed ID: 8969922
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Amplification refractory mutation system analysis of point mutations by capillary electrophoresis.
    Carrera P; Righetti PG; Gelfi C; Ferrari M
    Methods Mol Biol; 2001; 163():95-108. PubMed ID: 11242967
    [No Abstract]   [Full Text] [Related]  

  • 54. An AAVrh10-CAG-CYP21-HA vector allows persistent correction of 21-hydroxylase deficiency in a Cyp21
    Perdomini M; Dos Santos C; Goumeaux C; Blouin V; Bougnères P
    Gene Ther; 2017 May; 24(5):275-281. PubMed ID: 28165447
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.
    Morel Y; Bristow J; Gitelman SE; Miller WL
    Proc Natl Acad Sci U S A; 1989 Sep; 86(17):6582-6. PubMed ID: 2475872
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Management considerations for the adult with congenital adrenal hyperplasia.
    Auchus RJ
    Mol Cell Endocrinol; 2015 Jun; 408():190-7. PubMed ID: 25643980
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A case of first trimester prenatal diagnosis of 21-hydroxylase deficiency with human complement C4 cDNA probe.
    Nakura J; Miki T; Nishikawa K; Takemoto Y; Kamino K; Takai S; Hayashi K; Ogihara T
    Endocrinol Jpn; 1990 Oct; 37(5):615-8. PubMed ID: 1982260
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.
    Lin D; Harikrishna JA; Moore CC; Jones KL; Miller WL
    J Biol Chem; 1991 Aug; 266(24):15992-8. PubMed ID: 1714904
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency--the adult woman.
    Hagenfeldt KB
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S67-71. PubMed ID: 15135781
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Deletion pattern in the 21-hydroxylase gene detected by polymerase chain reaction.
    Kinoshita E; Matsumoto T; Kondoh T; Yoshimoto M; Niikawa N; Tsuji Y
    Acta Paediatr Jpn; 1991 Feb; 33(1):1-5. PubMed ID: 1853706
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.