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1 lowed by 17,20 lyase activity needed for sex steroid synthesis.
2 ct on adrenocorticotropic hormone-stimulated steroid synthesis.
3 and SF-1-dependent Cyp11a1 transcription for steroid synthesis.
4 at can further suppress de novo intratumoral steroid synthesis.
5  support region-specific regulation of brain steroid synthesis.
6 nd the 17,20 lyase activity required for sex steroid synthesis.
7 adrenocortical disease (PPNAD) and increased steroid synthesis.
8 ds 4-6, respectively, were prepared by total steroid synthesis.
9 stablished, other than as precursors for sex steroid synthesis.
10  noninvasive measure of adrenal function and steroid synthesis.
11  delivering sterols to the mitochondrion for steroid synthesis.
12 ch drives P450scc expression and neuroactive steroid synthesis.
13  can affect behavior, changes in local brain steroid synthesis also can modulate behavior.
14  of four sex steroids, and inhibitors of sex steroid synthesis (aminoglutethimide, ketoconazole, and
15 tors, cholesterol, and a substrate for rapid steroid synthesis, an essential requirement for mammalia
16 0c17-knockout mice would have disordered sex steroid synthesis and disordered brain DHEA production a
17                       Chemical inhibition of steroid synthesis and mechanical removal of follicle cel
18 terol metabolism and bile-acid biosynthesis; steroid synthesis and metabolism; vitamin D(3) synthesis
19 ficking from PMs to mitochondria for adrenal steroid synthesis and underscore the importance of vesic
20 F-1-induced leptin expression, modulates sex steroid synthesis by acting directly on steroidogenic ge
21 d in adrenal and gonadal tissues to initiate steroid synthesis by catalyzing the conversion of pregne
22  the availability of adrenal cholesterol for steroid synthesis by decreasing the expression of choles
23                               We showed that steroid synthesis could also be activated in mouse stero
24 nges in the expression of hormone receptors, steroid synthesis enzymes, and BMPs and their receptors.
25 ignaling and blocked by inhibitors of Delta5 steroid synthesis enzymes.
26                    Peripheral intracrine sex steroid synthesis from adrenal precursors dehydroepiandr
27 ms leading to adrenal cortex development and steroid synthesis in humans remain poorly understood due
28 eroids in the impeded pathways and excessive steroid synthesis in other adrenal biosynthetic pathways
29 d identify potential sites of active de novo steroid synthesis in the brain.
30 (LH), a pituitary hormone that regulates sex steroid synthesis in the testes.
31 he role of CYP17, a key enzyme mediating sex steroid synthesis, in Xenopus ovarian androgen productio
32 -2, animals received no further treatment; a steroid synthesis inhibitor, trilostane (TRL); TRL + R50
33 be classified into pituitary-directed drugs, steroid synthesis inhibitors, and glucocorticoid recepto
34 ats, the stress effect is blocked by adrenal steroid synthesis inhibitors, and mimicked by daily inje
35  genes associated with cancer, inflammation, steroid-synthesis, insulin-synthesis, neurotransmitter p
36                                     In mice, steroid synthesis is activated in steroidogenic cells by
37 ed by NOTCH, ACTIVIN, and WNT signaling, and steroid synthesis is amplified by ACTH/PKA signaling and
38 ways that regulate cytoskeletal dynamics and steroid synthesis/lipid metabolism.
39 und reduced expression of key enzymes in the steroid synthesis pathway and reduced serum progesterone
40 se endocrine disruption via perturbations in steroid synthesis (steroidogenesis) has become increasin
41 eceptor (LXR) ligands on StAR expression and steroid synthesis, suggesting HSL-mediated steroidogenes
42                          Genes involved with steroid synthesis, tissue remodeling, and apoptosis, in
43 t, all of the genes required for de novo sex steroid synthesis would be expressed in regions that wou