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1 designer drugs (DREADDs) specifically in the adrenal cortex.
2  of the bovine adrenodoxin (Adx) gene in the adrenal cortex.
3  system, which results in hyperplasia of the adrenal cortex.
4 immunohistochemistry to the liver and to the adrenal cortex.
5  pathway different from that existing in the adrenal cortex.
6 nce of optimal steroidogenic capacity in the adrenal cortex.
7 -induced release of corticosteroids from the adrenal cortex.
8 deglycosylation of DLIF isolated from bovine adrenal cortex.
9 5 may have tumor suppressor functions in the adrenal cortex.
10  zone-specific steroid production within the adrenal cortex.
11 n or by autonomous cortisol release from the adrenal cortex.
12 me is caused by tumors or hyperplasia of the adrenal cortex.
13 n that leads to release of cortisol from the adrenal cortex.
14 dogenic cells in the zona fasciculata of the adrenal cortex.
15 alamic control of the anterior pituitary and adrenal cortex.
16 a is an aggressive, lethal malignancy of the adrenal cortex.
17 ple organs, including the testis, ovary, and adrenal cortex.
18 chain fatty acids, particularly in brain and adrenal cortex.
19 GP prior to the separation between gonad and adrenal cortex.
20 g in the release of glucocorticoids from the adrenal cortex.
21 timulation of aldosterone secretion from the adrenal cortex.
22 roidogenic tissues, including the gonads and adrenal cortex.
23  of several steroidogenic genes in the human adrenal cortex.
24 ase that is upregulated during growth of the adrenal cortex.
25 el to investigate androgen signalling in the adrenal cortex.
26 marily expressed in the liver, intestine and adrenal cortex.
27 ly modified and was similar to normal bovine adrenal cortex.
28                           Development of the adrenal cortex, a vital endocrine organ, originates in t
29 elevated glucocorticoid concentrations after adrenal cortex activation; and e) release of bacterial p
30 lished the anti-apoptotic action of serum in adrenal cortex adenocarcinoma (SW13) cells.
31                                 In the human adrenal cortex, adrenocorticotropin (ACTH) activates CYP
32                        It is produced by the adrenal cortex after angiotensin II activation of angiot
33                                       In the adrenal cortex, an emblematic endocrine organ that media
34 that PKA 1) induces metabolic changes in the adrenal cortex and 2) phosphorylates CtBP proteins, part
35 g in increased steroidogenic activity in the adrenal cortex and an elevation of cortisol levels in th
36 udes the release of glucocorticoids from the adrenal cortex and catecholamines from the adrenal medul
37      It has been proposed that the mammalian adrenal cortex and gonad are derived from the same primo
38 uclear receptor selectively expressed in the adrenal cortex and gonads, where it mediates the hormona
39 mice exhibited highly reduced Tspo levels in adrenal cortex and gonads.
40 athway--in both embryonic development of the adrenal cortex and in maintenance of the adult organ.
41 pituitary-adrenal (LHPA) axis, with enlarged adrenal cortex and increased glucocorticoid levels.
42 rect Sf1 expression exclusively in the fetal adrenal cortex and is bound by both Sf1 and Dax1.
43  a dual-specificity PDE that is expressed in adrenal cortex and is partially inhibited by tadalafil a
44  the expression of CYP2D16 in the guinea pig adrenal cortex and its relationship to adrenal xenobioti
45 orticoid/catecholamine) interactions in both adrenal cortex and medulla is much greater in fetal shee
46 rticosterone content and hyperplasia of both adrenal cortex and medulla.
47 ter usage of IL-18 gene and suggest that the adrenal cortex and not immune cells may be the source of
48 e adrenal gland, some of which traversed the adrenal cortex and reached the adrenal medulla.
49 ituitary, with consequent stimulation of the adrenal cortex and release of glucocorticoids critical f
50 t levels in the inner zone of the guinea pig adrenal cortex and suggest a major role for this isozyme
51 n the human stomach and, very weakly, in the adrenal cortex and the brain.
52 und, type II PtdIns 4-kinase activity of the adrenal cortex and the type III enzyme of bovine brain.
53 that depends in part on the integrity of the adrenal cortex and vagus.
54 lt adrenocortical steroidogenic cells (fetal adrenal cortex and/or the adrenal capsule).
55 otein specific to the inner zones of the rat adrenal cortex, and called inner zone antigen (IZAg), wa
56 ency that impairs cortisol production by the adrenal cortex, and can lead to sexual ambiguity in both
57 , which ultimately gives rise to the kidney, adrenal cortex, and gonad.
58 ing hsp70 (the liver, pancreas, heart, lung, adrenal cortex, and intestine).
59 67 that is produced in human islets, testis, adrenal cortex, and perhaps other endocrine tissues, but
60 ng pancreatic islets, parathyroids, thyroid, adrenal cortex, and pituitary are seen by 16 months.
61 ogenic tissues, including the testis, ovary, adrenal cortex, and placenta.
62 ally drives glucocorticoid production in the adrenal cortex, and the sympathetic-adrenal-medullary ax
63 arious oronasal regions), bone, spinal cord, adrenal cortex, and the uro-anogenital region in the neo
64  in the locus coeruleus, inferior olive, and adrenal cortex; and decreased AT(2) receptor binding in
65 adrenal capsular cells to the differentiated adrenal cortex are not fully understood.
66 roxylase, an intracellular key enzyme of the adrenal cortex, are found in >90% of patients, but these
67 e III PI 4-kinases were isolated from bovine adrenal cortex as [3H]WT-labeled 110- and 210-kDa protei
68 nco-developmental genes present in the fetal adrenal cortex, as well as local adrenal paracrine and a
69 PHA revealed diffuse binding patterns in the adrenal cortex, avid binding in some adenomas, and "hot
70 al alterations in the hypothalamic-pituitary-adrenal cortex axis and the sympathetic nervous system,
71 i) theca interna cells in the ovary; and (j) adrenal cortex (but not adrenal medulla).
72 y in the zona fasciculata/reticularis of the adrenal cortex, but also in the Leydig cell, kidney and
73 pha is involved in similar regulation in the adrenal cortex, but it also substantially modulates gluc
74  thus of angiotensin, and (3) stimulation of adrenal cortex by angiotensin is consistent with all the
75 ation of SF-1-dependent transcription in the adrenal cortex by signaling molecules such as protein ki
76              Aldosterone, synthesized in the adrenal cortex by the enzyme CYP11B2, induces positive s
77 A), the predominant androgen secreted by the adrenal cortex, can be converted to both potent androgen
78 tervention and induction of immunity against adrenal cortex cancer.
79                                              Adrenal Cortex Carcinoma (ACC) is an aggressive tumour w
80 iency of 21-hydroxylase is a disorder of the adrenal cortex characterised by cortisol deficiency, wit
81 l development and homeostatic renewal of the adrenal cortex depend on capsular stem cells and cortica
82 of EG-VEGF in a responsive cell type, bovine adrenal cortex-derived endothelial (ACE) cells.
83 gene transcription, and cell cycle arrest in adrenal cortex-derived Y1 cells.
84                    The mechanisms leading to adrenal cortex development and steroid synthesis in huma
85 evated circulating corticosterone and severe adrenal cortex disruption.
86 high levels in peripheral tissues, including adrenal cortex (E16-E21) and cochlear ganglia (E19-P3),
87 Here we report that VEGF treatment of bovine adrenal cortex endothelial cells resulted in a 5-fold in
88                                       Bovine adrenal cortex endothelial cells were incubated with 200
89                        Finally, treatment of adrenal cortex endothelial cells with VEGF or phorbol es
90 nchiolar epithelium of the lung, myocardium, adrenal cortex, epithelium of the seminal vesicles, prox
91 in, is synthesized in mammalian placenta and adrenal cortex from cholesterol through the novel acidic
92 hways involved in the differentiation of the adrenal cortex from the adrenogonadal primordium (AGP) h
93 ed2 is required for the specification of the adrenal cortex from the AGP.
94 sis, were identified that distinguish normal adrenal cortex from tumor.
95 noninvasive method for the evaluation of the adrenal cortex function in pediatric asthmatic patients.
96 atients with bronchial asthma, a decrease in adrenal cortex function occurs.
97                                           In adrenal cortex, GNA11/Q mutations appear clinically sile
98            The tissue distribution of DAX-1 (adrenal cortex, gonads, hypothalamus, and pituitary) is
99  placenta, brain, testis, ovary, spleen, and adrenal cortex have the highest levels of expression of
100 amplified from RNA of interrenal tissue (the adrenal cortex homolog) from the southern stingray (Dasy
101 y-adrenal (HPA) axis, resulting in increased adrenal cortex hyperplasia and corticosterone production
102  20alpha-DHOPA paralleled the development of adrenal cortex hyperplasia, hypercortisolism, and spleen
103 tary and counterregulative adaptation of the adrenal cortex in abused women without major depressive
104 ignificant structural disorganization of the adrenal cortex in both sexes, with increased adrenal cor
105                    Cortisol, secreted in the adrenal cortex in response to stress, is an informative
106 promoting effect of high levels of LH on the adrenal cortex in the absence of ovarian tumors.
107              Inactivation of Lgr4 within the adrenal cortex in the mouse model caused decreased WNT s
108 , theca cells of the ovary, and cells of the adrenal cortex in transgenic animals.
109 timulated SAPK activity 3-4-fold both in the adrenal cortex in vivo and in the Y1 adrenocortical cell
110 K by ACTH, ERK activity was inhibited in the adrenal cortex in vivo and in Y1 adrenal cells.
111 ybridization showed that, in contrast to the adrenal cortex, in spleen and duodenum IL-18 is primaril
112 secretion, adrenal hypertrophy, and a larger adrenal cortex indicating chronic activation of the hypo
113 egulation of these synthetic pathways in the adrenal cortex inner zone during acute inflammation.
114 logical control of cortisol synthesis in the adrenal cortex involves stimulation of adrenocorticotrop
115             Glucocorticoid production in the adrenal cortex is activated in response to an increase i
116 goxin-like immunoreactive factor (DLIF) from adrenal cortex is an endogenous molecule with structural
117          Steroid hormone biosynthesis in the adrenal cortex is controlled by adrenocorticotropin (ACT
118         Thus, homeostatic maintenance of the adrenal cortex is dependent on varying levels of Wnt/bet
119 nduced and maintained and how renewal of the adrenal cortex is ensured remain a mystery.
120                                          The adrenal cortex is the major site of production of steroi
121 ike states to ultimately generate fetal zone adrenal-cortex-like cells (FZLCs), as evidenced by histo
122 al medullae denervation, suggesting that the adrenal cortex mediates this effect.
123 ttes that provide a structural framework for adrenal cortex morphogenesis and plasticity.
124 ontrary, FADS2 expression is elevated in the adrenal cortex of obese mice, and plasma corticosterone
125                          Histologically, the adrenal cortex of StAR knockout mice contained florid li
126    Here we report that the patches in mosaic adrenal cortex of the mouse and rat are also fractal and
127 gh levels of glucocorticoids produced by the adrenal cortex of the stressed subject reduce neurogenes
128  we show zona glomerulosa cells in the adult adrenal cortex organize into rosettes through adherens j
129                                              Adrenal cortex physiology relies on functional zonation,
130                         As distinct from the adrenal cortex, production of A, B, Aldo, 18OHdeoxycorti
131 ortical blunting resides at the level of the adrenal cortex rather than higher up the axis.
132  effects of stress and with mediation by the adrenal cortex, restraint stress evoked repeated transie
133 adrenal cortex in both sexes, with increased adrenal cortex size in female mice and increased cell pr
134  impact of LGR4 inactivation was analyzed by adrenal cortex-specific ablation of Lgr4, using Lgr4fl/f
135 lysis showed that IGIF is synthesized in the adrenal cortex, specifically in the zona reticularis and
136          Herein, we recapitulate human fetal adrenal cortex specification processes through stepwise
137 pha contributes to the maintenance of normal adrenal cortex structure and cell proliferation, by modu
138 rom the inner zone (zona reticularis) of the adrenal cortex than from the outer zones, coinciding wit
139 a Wnt/beta-catenin signaling gradient in the adrenal cortex that is disrupted upon loss of ZNRF3.
140 osolic PtdIns 4-kinase (cPI4K) in the bovine adrenal cortex that is distinguished from previously kno
141 n a sea of the other cell type, while in the adrenal cortex the pattern is one of alternating cords o
142                                 In the human adrenal cortex, the peptide hormone adrenocorticotropin
143  that during organogenesis in both liver and adrenal cortex, the same basic mechanism is directed to
144     It is expressed exclusively in the outer adrenal cortex, the site of cell proliferation, and in t
145 athology, and to disorders that affected the adrenal cortex, the spinal cord, the cerebellum and the
146  of anti-inflammatory glucocorticoids by the adrenal cortex, thereby representing an endogenous feedb
147                                 In the human adrenal cortex this process may be a precursor of adrena
148  that PKA acts as a tumour suppressor in the adrenal cortex, through repression of WNT signalling.
149  steroidogenic capacity is maintained in the adrenal cortex throughout life.
150 apidly secrete catecholamines (CAs), and the adrenal cortex to release progesterone (PROG), which may
151 e from the pituitary, which then acts on the adrenal cortex to stimulate the secretion of corticoster
152 lls with nuclear p21 and p53 appeared in the adrenal cortex together with DNA damage detected by in s
153  investigate the role of beta-catenin in the adrenal cortex, we used two Sf1/Cre transgenes to inacti
154  reticularis and the zona fasciculata of the adrenal cortex, where its levels are elevated by acute s
155     Finally, mice deficient for SR-BI in the adrenal cortex, where the receptor provides lipoprotein-
156                                Tumors of the adrenal cortex, whether benign or malignant, are often a
157          To investigate this, we studied the adrenal cortex, which is composed of functionally distin
158 from resistance to the action of ACTH on the adrenal cortex, which stimulates glucocorticoid producti
159 pecific ablation of androgen receptor in the adrenal cortex with or without reduction of circulating
160 , we compared the expression of IL-18 in the adrenal cortex with that of spleen and duodenum, two oth
161     Abnormal lipid storage is evident in the adrenal cortex, with characteristic lamellar-lipid inclu
162 ptor (AR) is widely expressed throughout the adrenal cortex, yet the wider role for androgen signalli

 
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