BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 2913051)

  • 1. Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.
    Morel Y; André J; Uring-Lambert B; Hauptmann G; Bétuel H; Tossi M; Forest MG; David M; Bertrand J; Miller WL
    J Clin Invest; 1989 Feb; 83(2):527-36. PubMed ID: 2913051
    [TBL] [Abstract][Full Text] [Related]  

  • 2. P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.
    Matteson KJ; Phillips JA; Miller WL; Chung BC; Orlando PJ; Frisch H; Ferrandez A; Burr IM
    Proc Natl Acad Sci U S A; 1987 Aug; 84(16):5858-62. PubMed ID: 3497399
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA types.
    Morel Y; David M; Forest MG; Betuel H; Hauptman G; Andre J; Bertrand J; Miller WL
    J Clin Endocrinol Metab; 1989 Mar; 68(3):592-9. PubMed ID: 2783935
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.
    White PC; Vitek A; Dupont B; New MI
    Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4436-40. PubMed ID: 3260033
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
    White PC; New MI; Dupont B
    Proc Natl Acad Sci U S A; 1984 Dec; 81(23):7505-9. PubMed ID: 6334310
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of the duplicated human C4/P450c21/X gene cluster.
    Miller WL; Gitelman SE; Bristow J; Morel Y
    J Steroid Biochem Mol Biol; 1992 Dec; 43(8):961-71. PubMed ID: 22217841
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular and endocrine characterization of a mutation involving a recombination between the steroid 21-hydroxylase functional gene and pseudogene.
    Killeen AA; Sane KS; Orr HT
    J Steroid Biochem Mol Biol; 1991 Jun; 38(6):677-86. PubMed ID: 1905948
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 families.
    Strumberg D; Hauffa BP; Horsthemke B; Grosse-Wilde H
    Eur J Pediatr; 1992 Nov; 151(11):821-6. PubMed ID: 1361434
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Gene heterogeneity in adrenal 21-hydroxylase].
    Morel Y
    Presse Med; 1991 May; 20(20):945-9. PubMed ID: 1829200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exon 7 Ncol restriction site within CYP21B (steroid 21-hydroxylase) is a normal polymorphism.
    Donohoue PA; Sandrini Neto R; Collins MM; Migeon CJ
    Mol Endocrinol; 1990 Sep; 4(9):1354-62. PubMed ID: 1978247
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan.
    Lee JS; Tsai HM; Shieh RP; Chen SH; Tsai WY; Chung BC
    J Formos Med Assoc; 1990 Jul; 89(7):534-40. PubMed ID: 1979594
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiency.
    Einaudi S; Borelli I; Lala R; Praticŏ L; Curtoni ES; De Sanctis C
    J Pediatr Endocrinol; 1994; 7(4):349-55. PubMed ID: 7735374
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to 21-hydroxylase enzyme deficiency].
    Dardis A; Marino R; Bergadá I; Escobar ME; Gryngarten M; Rivarola MA; Belgorosky A
    Medicina (B Aires); 2001; 61(1):28-34. PubMed ID: 11265620
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Detection of steroid 21-hydroxylase gene variation among normal Chinese and patients with congenital adrenal hyperplasia].
    Pan X
    Zhonghua Yi Xue Za Zhi; 1991 Jun; 71(6):318-20, 24. PubMed ID: 1667494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Molecular characterization of 21-hydroxylase deficiency in 70 Italian families.
    Carrera P; Ferrari M; Beccaro F; Spiga I; Zanussi M; Rigon F; Braggion F; Zacchello F; Greggio N
    Hum Hered; 1993; 43(3):190-6. PubMed ID: 8330883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular genetics of 21-hydroxylase deficiency in congenital adrenal hyperplasia].
    Lobaccaro JM; Ghanem N; Lefranc G; Sultan C
    C R Seances Soc Biol Fil; 1990; 184(1):75-86. PubMed ID: 1964845
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited congenital adrenal hyperplasia in the rabbit is caused by a deletion in the gene encoding cytochrome P450 cholesterol side-chain cleavage enzyme.
    Yang X; Iwamoto K; Wang M; Artwohl J; Mason JI; Pang S
    Endocrinology; 1993 May; 132(5):1977-82. PubMed ID: 7682938
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.