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Research 30 of 629
- The steroidogenic inhibitor finasteride reverses pramipexole-induced alterations in probability discounting
- Sex steroid synthesis in human skin in situ: The roles of aromatase and steroidogenic acute regulatory protein in the homeostasis of human skin
- Steroidogenic enzymes in skin.
- The 5α-reductase inhibitor finasteride reduces opioid self-administration
- Social isolation alters GABAA receptors plasticity and function: effect of voluntary consumption of ethanol
- Repurposing steroidogenesis inhibitors for the therapy of neuropsychiatric disorders: Promises and caveats
- Search for New antineoplastic agents based on structural modifications of steroidal 5α-reductase, 17β-hydroxysteroid dehydrogenase, and 17α-hydroxylase/17,20-lyase inhibitors
- New Nonsteroidal Molecules as Blockers of the Steroidogenic Pathway
- Disruption of androgen metabolism, regulation and effects : involvement of steroidogenic enzymes
- Increase in formalin-induced tonic pain by 5alpha-reductase and aromatase inhibition in female rats
- Involvement of neurosteroids in the anxiolytic-like effects of AC-5216 in mice
- Palmitoylethanolamide Stimulation Induces Allopregnanolone Synthesis in C6 Cells and Primary Astrocytes: Involvement of Peroxisome-Proliferator Activated Receptor-α
- Alleviation of Mechanical Allodynia by 14,15-Epoxyeicosatrienoic Acid in a Central Poststroke Pain Model: Possible Role of Allopregnanolone and δ-Subunit-Containing Gamma-Aminobutyric Acid A Receptors
- Overexpression of the 18 kDa translocator protein (TSPO) in the hippocampal dentate gyrus produced anxiolytic and antidepressant-like behavioural effects
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- Sulfatase inhibitors: a patent review
- Steroidogenic Isoenzymes in Human Hair and Their Potential Role in Androgenetic Alopecia
- The Dark Side of 5α-Reductase Inhibitors' Therapy: Sexual Dysfunction, High Gleason Grade Prostate Cancer and Depression
- Novel type 1 5a-reductase Inhibitors with Antiproliferative Potential on LNCaP cells
- Evaluation of 5α-reductase inhibitory activity of certain herbs useful as antiandrogens
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Hydroxysteroid Dehydrogenase (17β -HSD3, 17β-HSD5, and 3α-HSD3) Inhibitors:Extragonadal Regulation of Intracellular Sex Steroid Hormone Levels
- 11α-Hydroxyprogesterone, a potent 11β-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5α-reductase and cytochrome P450 17α-hydroxylase/17,20-lyase to produce C11α-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro
- Targets to treat androgen excess in polycystic ovary syndrome
- The Mechanisms of Anabolic Steroids, Selective Androgen Receptor Modulators and Myostatin Inhibitors
- Early embryonic exposure of freshwater gastropods to pharmaceutical 5-alpha-reductase inhibitors results in a surprising open-coiled “banana-shaped” shell
- Proteasome Inhibitors: An Expanding Army Attacking a Unique Target
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Is dehydroepiandrosterone a hormone?
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors