نتایج جستجو برای: 17α

تعداد نتایج: 979  

2016
Sankar N. Maity Mark A. Titus Revekka Gyftaki Guanglin Wu Jing-Fang Lu S. Ramachandran Elsa M. Li-Ning-Tapia Christopher J. Logothetis John C. Araujo Eleni Efstathiou

Cytochrome P450 17α-hydroxylase/17,20-lyase (CYP17A1) is a validated treatment target for the treatment of metastatic castration-resistant prostate cancer (CRPC). Abiraterone acetate (AA) inhibits both 17α-hydroxylase (hydroxylase) and 17,20-lyase (lyase) reactions catalyzed by CYP17A1 and thus depletes androgen biosynthesis. However, coadministration of prednisone is required to suppress the m...

2012
Jae-Hong Kim Sung Yul Lee Hae-Jin Lee Na-Young Yoon Won-Soo Lee

BACKGROUND There are several commercially available agents to treat female pattern hair loss (FPHL), including minoxidil solution, anti-androgen agents and mineral supplements. However, these treatments are not always satisfactory. We report the results of a clinical trial of 17α-estradiol (Ell-Cranell® alpha 0.025%) solution to Korean female patients with FPHL. OBJECTIVE This study was desig...

2013
Saifullah Saifullah Khan Azizuddin Sobia Ahsan Halim Muhammad Kashif Almas Jabeen Muhmammad Asif Muhammad Ahmed Mesaik Zaheer Ul-Haq Ahsana Dar Muhammad Iqbal Choudhary

BACKGROUND Plant Biotransformation is one of the tools for structural modifications of the organic substrate of low, moderate or high biological value utilizing plant cultured cells, these modifications of organic structures may lead to biologically augmented products and which may be ultimately substantial in cure or improvement of various morbidities and diseases. RESULTS Azadirachta indica...

Journal: :Acta biochimica Polonica 2018
Rafał Podgórski David Aebisher Monika Stompor Dominika Podgórska Artur Mazur

The aim of this paper is a straightforward presentation of the steroidogenesis process and the most common type of congenital adrenal hyperplasia (CAH) - 21-hydroxylase deficiency - as well as the analytical diagnostic methods that are used to recognize this disease. CAH is a family of common autosomal recessive disorders characterized by impaired adrenal cortisol biosynthesis with associated a...

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