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 *

190 related articles for article (PubMed ID: 14730433)

  • 21. 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]  

  • 22. Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease associations.
    Yang Z; Mendoza AR; Welch TR; Zipf WB; Yu CY
    J Biol Chem; 1999 Apr; 274(17):12147-56. PubMed ID: 10207042
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.
    Donohoue PA; Jospe N; Migeon CJ; Van Dop C
    Genomics; 1989 Oct; 5(3):397-406. PubMed ID: 2613228
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia.
    Wedell A
    Clin Lab Med; 1996 Mar; 16(1):125-37. PubMed ID: 8867587
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of 21-hydroxylase deficiency caused by gene conversion and rearrangements: pitfalls and molecular diagnostic solutions.
    Mao R; Nelson L; Kates R; Miller CE; Donaldson DL; Tang W; Ward K
    Prenat Diagn; 2002 Dec; 22(13):1171-6. PubMed ID: 12478627
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.
    Collier S; Sinnott PJ; Dyer PA; Price DA; Harris R; Strachan T
    EMBO J; 1989 May; 8(5):1393-402. PubMed ID: 2788573
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles.
    Levo A; Partanen J
    Hum Genet; 1997 Apr; 99(4):488-97. PubMed ID: 9099839
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. Online.
    Krone N; Braun A; Roscher AA; Schwarz HP
    Hum Mutat; 1999; 14(1):90-1. PubMed ID: 10447270
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.
    Blanchong CA; Zhou B; Rupert KL; Chung EK; Jones KN; Sotos JF; Zipf WB; Rennebohm RM; Yung Yu C
    J Exp Med; 2000 Jun; 191(12):2183-96. PubMed ID: 10859342
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles.
    Killeen AA; Jiddou RR; Sane KS
    Clin Chem; 1998 Dec; 44(12):2410-5. PubMed ID: 9836705
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.
    Partanen J; Koskimies S; Sipilä I; Lipsanen V
    Am J Hum Genet; 1989 May; 44(5):660-70. PubMed ID: 2565078
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency.
    Tukel T; Uyguner O; Wei JQ; Yuksel-Apak M; Saka N; Song DX; Kayserili H; Bas F; Gunoz H; Wilson RC; New MI; Wollnik B
    J Clin Endocrinol Metab; 2003 Dec; 88(12):5893-7. PubMed ID: 14671187
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese.
    Lee HH; Chao HT; Lee YJ; Shu SG; Chao MC; Kuo JM; Chung BC
    Hum Genet; 1998 Sep; 103(3):304-10. PubMed ID: 9799085
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Coeli-Lacchini FB; Turatti W; Elias PC; Elias LL; Martinelli CE; Moreira AC; Antonini SR; de Castro M
    Gene; 2013 Sep; 526(2):239-45. PubMed ID: 23570880
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.