نتایج جستجو برای: 5α reductase

تعداد نتایج: 44837  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Kai-Hsiung Chang Rui Li Mahboubeh Papari-Zareei Lori Watumull Yan Daniel Zhao Richard J Auchus Nima Sharifi

In the majority of cases, advanced prostate cancer responds initially to androgen deprivation therapy by depletion of gonadal testosterone. The response is usually transient, and metastatic tumors almost invariably eventually progress as castration-resistant prostate cancer (CRPC). The development of CRPC is dependent upon the intratumoral generation of the potent androgen, dihydrotestosterone ...

Journal: :Asian journal of andrology 2011
Huan-Tao Zong Xiao-Xia Peng Chen-Chen Yang Yong Zhang

5α-reductase inhibitors (5α-RIs), including finasteride and dutasteride, are commonly used medical therapies for benign prostatic hyperplasia (BPH). Many studies reported that preoperative 5α-RI had impact on intraoperative haemorrhage during surgery for BPH, but it was still in controversial. So, we conducted a systematic review of the effects and mechanisms of 5α-RIs on intraoperative bleedin...

Journal: :JAMA 2012
Shalender Bhasin Thomas G Travison Thomas W Storer Kishore Lakshman Manas Kaushik Norman A Mazer Ahn-Hoa Ngyuen Maithili N Davda Hernan Jara Adam Aakil Stephan Anderson Philip E Knapp Samson Hanka Nurahmed Mohammed Pierre Daou Renee Miciek Jagadish Ulloor Anqi Zhang Brad Brooks Katie Orwoll Leife Hede-Brierley Richard Eder Ayan Elmi Geeta Bhasin Lauren Collins Ravinder Singh Shehzad Basaria

CONTEXT Steroid 5α-reductase inhibitors are used to treat benign prostatic hyperplasia and androgenic alopecia, but the role of 5α-dihydrotestosterone (DHT) in mediating testosterone's effects on muscle, sexual function, erythropoiesis, and other androgen-dependent processes remains poorly understood. OBJECTIVE To determine whether testosterone's effects on muscle mass, strength, sexual funct...

Journal: :Journal of Enzyme Inhibition and Medicinal Chemistry 2011

2018
Michael V. Fiandalo John J. Stocking Elena A. Pop John H. Wilton Krystin M. Mantione Yun Li Kristopher M. Attwood Gissou Azabdaftari Yue Wu David S. Watt Elizabeth M. Wilson James L. Mohler

Androgen deprivation therapy (ADT) is palliative and prostate cancer (CaP) recurs as lethal castration-recurrent/resistant CaP (CRPC). One mechanism that provides CaP resistance to ADT is primary backdoor androgen metabolism, which uses up to four 3α-oxidoreductases to convert 5α-androstane-3α,17β-diol (DIOL) to dihydrotestosterone (DHT). The goal was to determine whether inhibition of 3α-oxido...

Journal: :Prostate Cancer and Prostatic Diseases 2012

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