Restoration of adrenal steroidogenesis by adenovirus-mediated transfer of human cytochromeP450 21-hydroxylase into the adrenal gland of21-hydroxylase-deficient mice-Reference-Cited by-同舟云学术

Restoration of adrenal steroidogenesis by adenovirus-mediated transfer of human cytochromeP450 21-hydroxylase into the adrenal gland of21-hydroxylase-deficient mice

Published:1999-11 Issue:11 Volume:6 Page:1898-1903
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Tajima T,Okada T,Ma X-M,Ramsey W J,Bornstein S R,Aguilera G

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3301018.pdf

Reference28 articles.

1. New MI . Diagnosis and management of congenital adrenal hyperplasia Annu Rev Med 1998 49: 311–328

2. Pang S . Congenital adrenal hyperplasia Endocrinol Metab Clin N Am 1997 26: 853–889

3. Cutler GB Jr, Laue L . Congenital adrenal hyperplasia due to 21-hydroxylase deficiency New Engl J Med 1990 223: 1806–1813

4. Cutler GB Jr . Treatment of congenital adrenal hyperplasia: the case for new medical approaches J Clin Endocrinol Metab 1996 81: 3185–3186

5. Migeon CJ . Can the long range results of the treatment of congenital adrenal hyperplasia be improved? J Clin Endocr Metab 1996 81: 3187–3189

Cited by 66 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Approach to the Child and Adolescent With Adrenal Insufficiency;The Journal of Clinical Endocrinology & Metabolism;2024-08-18

2. Genome editing in the adrenal gland: a novel strategy for treating congenital adrenal hyperplasia;Exploration of Endocrine and Metabolic Diseases;2024-07-09

3. AAV-delivered hepato-adrenal cooperativity in steroidogenesis: Implications for gene therapy for congenital adrenal hyperplasia;Molecular Therapy - Methods & Clinical Development;2024-06

4. Congenital Adrenal Hyperplasia – A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India;Indian Journal of Endocrinology and Metabolism;2024-03

5. Cost-effective genotyping for classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) in resource-poor settings: multiplex ligation probe amplification (MLPA) with/without sequential next-generation sequencing (NGS);Hormones;2023-03-23