Literature DB >> 3010994

Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes.

P A Donohoue, N Jospe, C J Migeon, R H McLean, W B Bias, P C White, C Van Dop.   

Abstract

Restriction maps were constructed for the two human 21-hydroxylase genes (21-OHA and 21-OHB) by using DNA from subjects homozygous for a deletion of each gene. Comparing the patterns of these two genes, a KpnI restriction site occurred in the 21-OHA gene in place of a TaqI site in the 21-OHB gene about 1-kb from the 5' end of the gene, and an extra EcoRI site was located 500 bp 5' to the common EcoRI site. The DNA of fourteen unrelated normal subjects was digested with nine restriction endonucleases (AccI, BamHI, BgIII, EcoRI, HindIII, KpnI, MspI, SacI and TaqI). Restriction fragment length polymorphisms were found with EcoRI, HindIII and AccI that resulted from polymorphic endonuclease sites outside the genes.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3010994     DOI: 10.1016/0006-291x(86)90499-7

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  10 in total

1.  Highly polymorphic XbaI RFLPs of the human 21-hydroxylase genes among Chinese.

Authors:  L Chen; X Pan; Y Shen; Z Chen; Y Zhang; R Chen
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

Authors:  M A Levine; T G Ahn; S F Klupt; K D Kaufman; P M Smallwood; H R Bourne; K A Sullivan; C Van Dop
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

3.  Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency.

Authors:  T Matsumoto; T Kondoh; T Kamei; M Yoshimoto; Y Tsuji; K Suzumori; R Izumi; N Iwatani; N Niikawa
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

4.  Class III gene rearrangements in Thai/Chinese supratypes containing null or defective C4 alleles.

Authors:  P H Kay; E Martin; R L Dawkins; P Charoenwong
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

5.  Extensive genomic polymorphism in mouse 21-hydroxylase region.

Authors:  D Gillet; E Mornet; A Rocca; L Degos; D Cohen; M Pla
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

6.  The modification and expression of 21-hydroxylase gene in normal human adrenal gland and adrenal cancer.

Authors:  A Ogo; M Haji; T Yanase; K Kato; H Nawata
Journal:  J Endocrinol Invest       Date:  1991-11       Impact factor: 4.256

7.  Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

Authors:  P C White; A Vitek; B Dupont; M I New
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

8.  Frequent deletion and duplication of the steroid 21-hydroxylase genes.

Authors:  J W Werkmeister; M I New; B Dupont; P C White
Journal:  Am J Hum Genet       Date:  1986-10       Impact factor: 11.025

9.  P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.

Authors:  K J Matteson; J A Phillips; W L Miller; B C Chung; P J Orlando; H Frisch; A Ferrandez; I M Burr
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

10.  Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 families.

Authors:  D Strumberg; B P Hauffa; B Horsthemke; H Grosse-Wilde
Journal:  Eur J Pediatr       Date:  1992-11       Impact factor: 3.183

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.