Mixed-model QSAR at the human mineralocorticoid receptor: Predicting binding mode and affinity of anabolic steroids-Reference-Cited by-同舟云学术

Mixed-model QSAR at the human mineralocorticoid receptor: Predicting binding mode and affinity of anabolic steroids

Published:2009-09 Issue:3 Volume:189 Page:219-224
ISSN:0378-4274
Container-title:Toxicology Letters
language:en
Short-container-title:Toxicology Letters

Author:

Peristera Ourania,Spreafico Morena,Smiesko Martin,Ernst Beat,Vedani Angelo

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference27 articles.

1. Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor;Arriza;Science,1987

2. A ligand-mediated hydrogen bond network required for the activation of the mineralocorticoid receptor;Bledsoe;J. Biol. Chem.,2005

3. Damstra, T., Barlow, S., Bergman, A., Kavlock, R., Van der Kraak, G., 2002. Global assessment of the state-of-the-science of endocrine disruptors. International Program on Chemical Safety, WHO, pp. 1–133.

4. The steroid and thyroid hormone receptor superfamily;Evans;Science,1998

5. The mineralocorticoid receptor and oxidative stress;Fiebeler;Heart Fail. Rev.,2005

Cited by 10 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. A battery of in silico models application for pesticides exerting reproductive health effects: Assessment of performance and prioritization of mechanistic studies;Toxicology in Vitro;2023-12

2. The History and Development of Quantitative Structure-Activity Relationships (QSARs);Oncology;2017

3. An Introduction to the Basic Concepts in QSAR-Aided Drug Design;Oncology;2017

4. An Introduction to the Basic Concepts in QSAR-Aided Drug Design;Quantitative Structure-Activity Relationships in Drug Design, Predictive Toxicology, and Risk Assessment;2015

5. Computational Toxicology in Drug Discovery: Opportunities and Limitations;Challenges and Advances in Computational Chemistry and Physics;2014