Literature DB >> 8004113

Steroid 11 beta-hydroxylase deficiency caused by a five base pair duplication in the CYP11B1 gene.

C A Skinner1, G Rumsby.   

Abstract

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Year:  1994        PMID: 8004113     DOI: 10.1093/hmg/3.2.377

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


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  6 in total

1.  Whether, when, and why Skinner published on biological participation in behavior.

Authors:  Edward K Morris; Junelyn F Lazo; Nathaniel G Smith
Journal:  Behav Anal       Date:  2004

2.  Bibliographic processes and products, and a bibliography of the published primary-source works of B. F. Skinner.

Authors:  Edward K Morris; Nathaniel G Smith
Journal:  Behav Anal       Date:  2003

Review 3.  Progress in molecular-genetic studies on congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.

Authors:  Li-Qiang Zhao; Su Han; Hao-Ming Tian
Journal:  World J Pediatr       Date:  2008-05       Impact factor: 2.764

Review 4.  The next 150 years of congenital adrenal hyperplasia.

Authors:  Adina F Turcu; Richard J Auchus
Journal:  J Steroid Biochem Mol Biol       Date:  2015-06-03       Impact factor: 4.292

Review 5.  11 Beta-hydroxylase deficiency.

Authors:  F Mantero; G Opocher; D Armanini; S Filipponi
Journal:  J Endocrinol Invest       Date:  1995 Jul-Aug       Impact factor: 4.256

6.  Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiency.

Authors:  Silvia Parajes; Lourdes Loidi; Nicole Reisch; Vivek Dhir; Ian T Rose; Rainer Hampel; Marcus Quinkler; Gerard S Conway; Lidia Castro-Feijóo; David Araujo-Vilar; Manuel Pombo; Fernando Dominguez; Emma L Williams; Trevor R Cole; Jeremy M Kirk; Elke Kaminsky; Gill Rumsby; Wiebke Arlt; Nils Krone
Journal:  J Clin Endocrinol Metab       Date:  2010-01-20       Impact factor: 5.958

  6 in total

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