コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 onal-like exocytosis (testes, pituitary, and adrenal gland).
2 etagamma signaling in both the heart and the adrenal gland.
3 gnals that could affect transcription in the adrenal gland.
4 B) were seen in the lung, liver, kidney, and adrenal gland.
5 including the peripheral nervous system and adrenal gland.
6 cyclic GMP production in the kidney and the adrenal gland.
7 are controlled by CREM/ICER in the liver and adrenal gland.
8 d on 10 ACC, 6 benign adenomas, and 1 normal adrenal gland.
9 ucing cells of the testis, the ovary and the adrenal gland.
10 ts, 90% of neuroblastomas are located in the adrenal gland.
11 n of the synthetic enzymes for PGE(2) in the adrenal gland.
12 tissue-specific manner, most commonly in the adrenal gland.
13 nism by which SF-1 exerts its actions in the adrenal gland.
14 ation to kidney but not to BAT, hindlimb, or adrenal gland.
15 inimally invasive approach to removal of the adrenal gland.
16 hetic nerve activity to kidney, hindlimb, or adrenal gland.
17 stion from the adrenal medulla of the bovine adrenal gland.
18 n C, such as the hippocampal neurons and the adrenal gland.
19 ifically for HHV-6A), testis, esophagus, and adrenal gland.
20 f pseudorabies virus (PRV) injected into the adrenal gland.
21 ndly perturbs cholesterol homeostasis in the adrenal gland.
22 rtant role in the functional zonation of the adrenal gland.
23 ntrast, decreased MIF protein content in the adrenal gland.
24 , liver, small intestine, kidney, ovary, and adrenal gland.
25 inant (PRV-BaBlu) was injected into the left adrenal gland.
26 functioning and nonfunctioning tumors of the adrenal gland.
27 ne silencing in lung, muscle, fat, heart and adrenal gland.
28 t subsequently metastasized to the liver and adrenal gland.
29 ably enterocytes), the pancreas and also the adrenal gland.
30 through a mechanism affecting primarily the adrenal gland.
31 brane in the liver, blood-brain barrier, and adrenal gland.
32 n human serum and epidermis, and the porcine adrenal gland.
33 pinal mediastinum, retroperitoneum, neck and adrenal gland.
34 the 61 observed SFCs (82%) found in the left adrenal gland.
35 tal secretory events from thin slices of the adrenal gland.
36 essed genes in zona glomerulosa of the human adrenal gland.
37 atterns in different functional zones of the adrenal gland.
38 ction of corticotropin in these hyperplastic adrenal glands.
39 med for reasons other than the evaluation of adrenal glands.
40 ive steroid hormones, mainly produced by the adrenal glands.
41 er food restriction were dependent on intact adrenal glands.
42 y have a role in ROS detoxification in human adrenal glands.
43 oxoglutarate receptor 1 (OXGR1) expressed in adrenal glands.
44 ng in the release of corticosterone from the adrenal glands.
45 and human brain and in the bovine liver and adrenal glands.
46 between adrenal glands with PHEO and normal adrenal glands.
47 omas, and one undetermined) and seven normal adrenal glands.
48 multiple brain regions, skeletal muscle, and adrenal glands.
49 lowed by focal hemorrhaging of the ileum and adrenal glands.
50 rs agreed on visualization of 27 of 40 (68%) adrenal glands.
51 the HPA stress response in the pituitary or adrenal glands.
52 well as studies on metastatic disease to the adrenal glands.
53 induced the production of dopamine from the adrenal glands.
54 s, indicating release of these steroids from adrenal glands.
55 ons including the central nervous system and adrenal glands.
56 ting glucocorticoid hormone synthesis in the adrenal glands.
57 art, lungs, spleen, bone marrow, thyroid and adrenal glands.
58 enzymes, were severely reduced in postnatal adrenal glands.
59 nucleus of the amygdala, independent of the adrenal glands.
60 ects are dependent on both the pituitary and adrenal glands.
61 ates the production of catecholamines in the adrenal glands.
62 lipids in the different functional zones of adrenal glands.
64 omocytoma and paraganglioma than for healthy adrenal glands (11.9 +/- 2.0 vs. 9.9 +/- 1.5 vs. 3.7 +/-
66 697 (42.9%) in the liver, 138 (8.5%) in the adrenal glands, 38 (2.3%) in the pancreas, 109 (6.7%) in
70 FCs in the left adrenal gland than the right adrenal gland and 50 of the 61 observed SFCs (82%) found
72 -derived secosteroids in the skin, serum and adrenal gland and based on their concentrations and biol
75 holamines are produced in the medulla of the adrenal gland and may participate in the intraglandular
76 was imaged at 150-200 mum resolution in rat adrenal gland and mouse brain sections and confirmed wit
77 NB) is a childhood cancer that arises in the adrenal gland and often shows differentiated neuronal an
79 nance imaging excluded common lesions of the adrenal gland and showed lymphadenopathy around the majo
81 shed beta4, alpha3, and alpha5 expression in adrenal gland and to a lesser extent in the superior cer
82 g 2DG; 70.3% +/- 1.8% of SPN innervating the adrenal glands and 37.4% +/- 3% of SPN innervating celia
84 in the paraventricular nucleus, hypoplastic adrenal glands and decreased stress-induced corticostero
86 In summary, GX sPLA(2) is expressed in mouse adrenal glands and functions to negatively regulate cort
88 ous system accounts for (a) primary sites in adrenal glands and in paraspinal locations from neck to
89 astatic spread of the tumor to the liver and adrenal glands and increased the median survival time of
90 oping genitourinary tract, heart, spleen and adrenal glands and is crucial for their development, how
91 curs in spontaneously hypertensive rat (SHR) adrenal glands and plasma, but central expression is une
92 253 (64%), 70 (18%), and 71 (18%) of the 394 adrenal glands and reader 2 classified 258 (65%), 45 (11
93 lungs, hypoplastic/ectopic kidneys, aplastic adrenal glands and spleen, as well as atretic trachea an
94 e role of the brain, neuroendocrine factors (adrenal gland) and gastrointestinal systems (colon) in p
95 l erythropoiesis (which notably included the adrenal gland), and integration with mouse developmental
96 crease in aldosterone synthase expression in adrenal gland, and a two-fold decrease in renin expressi
97 f corticosterone, as well as similar thymus, adrenal gland, and body weights, suggesting that variabl
99 in selected tissues, such as lens, brain and adrenal gland, and its degradation products can inflict
102 isseminated form usually involves the liver, adrenal gland, and lung, and resembles the clinical pict
103 Together, these data suggest that the liver, adrenal gland, and lymphatic organs are important sites
104 brain (33.6% v 23.0%; P =.004), bone marrow, adrenal gland, and pericardium (24.7% v 15.9%; P =.004).
106 e exception of low concentrations in rectum, adrenal gland, and thymus from a single patient with vCJ
111 cidates how host responses within the liver, adrenal glands, and lymphoid tissues contribute to EBOV
112 understanding of tissue injury in the liver, adrenal glands, and lymphoid tissues remains limited.
113 e the transcriptomes of human embryos, fetal adrenal glands, and neuroblastoma at single-cell level a
114 ncers and hypervascular tumors of the brain, adrenal glands, and pancreas as well as erythrocytosis.
116 It is expressed in the hypothalamus, the adrenal glands, and the testis, but sequences determinin
121 producing zona glomerulosa (zG) cells of the adrenal gland arrange in distinct multi-cellular rosette
122 of Gbetagamma signaling in the heart and the adrenal gland as a novel therapeutic approach for heart
123 t viability and function, and we explore the adrenal gland as an alternative transplantation site for
124 classified the morphologic features of each adrenal gland as normal, smoothly enlarged, or nodular a
125 cer, smooth enlargement or nodularity of the adrenal glands at baseline CT is not associated with inc
126 ial for cholinergic synaptic transmission in adrenal gland, autonomic ganglia, pineal gland, and seve
127 d high expression in the locus coeruleus and adrenal gland, but also in sympathetically innervated or
129 l root ganglion cells, sciatic nerve, and in adrenal glands, but its expression is greatly decreased
130 ctable in adult mouse atria, ventricles, and adrenal glands, but Kcne3(-/-) mice exhibited 2.3-fold e
131 tachycardia was evoked after removal of both adrenal glands, but was absent after beta-adrenergic rec
133 pression was detected in spleen, thymus, and adrenal gland by ribonuclease protection assay, and disc
134 ng accumulation of free cholesterol in mouse adrenal glands by controlling expression of genes involv
135 was to distinguish between PPGLs and normal adrenal glands by evaluating semiquantitative (123)I-MIB
136 ogenous lipids on tissue sections of porcine adrenal glands by MALDI-Fourier-transform ion cyclotron
137 d catecholamine production in isolated mouse adrenal glands by restoring adrenal alpha2-AR feedback i
143 ents with carcinomas of the salivary glands, adrenal gland, colon, parotid gland, kidney, thyroid gla
146 thyroid, parathyroids, pituitary, gonad, and adrenal glands, constitute a major health problem in all
147 in several subcortical regions; however, the adrenal glands contribute to 3alpha,5alpha-THP elevation
149 loss could sensitise PC cells and tumours to adrenal gland-derived androgens, which persist even afte
151 er featuring cardiac arrhythmias, autism and adrenal gland dysfunction that originates from a de novo
153 ral nervous system (CNS), kidneys, pancreas, adrenal glands, epididymis, broad ligament, and the endo
155 In comparison with rat forebrain extracts, adrenal gland extracts exhibited TH hyperphosphorylation
157 e first undertook transcriptome profiling on adrenal glands from blood pressure extreme mouse strains
158 11B2) expression was evaluated in 127 normal adrenal glands from deceased kidney donors (age, 9 month
160 al in fetal development, T-cell function and adrenal gland growth homeostasis, and that the functions
162 erum corticosterone levels were measured and adrenal glands harvested for histologic evaluation of he
164 g puberty, the synthesis of androgens by the adrenal gland has been considered of little physiologic
165 However, the function and structure of the adrenal glands have not been examined in inflammatory bo
171 ing pituitary, testis, pancreas, kidney, and adrenal gland, hyperproliferative phenotypes associated
172 ed with controls, aged HCM females exhibited adrenal gland hypertrophy, reduced volume in mood-relate
173 the presence or absence of metastases to the adrenal glands (ie, any new focal adrenal mass) at final
178 ns (SFCs) (</=5 mm) were seen in one or both adrenal glands in 19 of the 38 patients with fCCM (50%),
179 the female, the testis in the male, and the adrenal glands in all pigs contain greater concentration
180 The mechanisms behind destruction of the adrenal glands in autoimmune Addison's disease remain un
182 steroid hormone cortisol is released by the adrenal glands in response to stress and serves as a mes
183 tially important novel target of SF-1 in the adrenal gland, indicating that regulation of angiogenesi
184 control the steroid hormone biosynthesis in adrenal glands, indicating their important roles in endo
185 (MyD88) in systemic and local activation of adrenal gland inflammation and glucocorticoid production
186 high-thoracic level (Th1) SCI disconnecting adrenal gland innervation, compared with low-thoracic le
192 c assistance, particularly in patients whose adrenal gland is located well superior to the 12th rib,
194 the AT(1b) angiotensin receptor gene in the adrenal gland is upregulated by the first week of life r
195 identification of mediastinal structures and adrenal glands is still much lower than that in standard
197 ent lipid classes that play in the mammalian adrenal glands, it is necessary to comprehensively deter
198 no restoration was achieved in adult liver, adrenal gland, kidney medulla, spleen, peritoneal cavity
199 the treatment of solitary metastases to the adrenal gland, laparoscopic adrenalectomy provides equiv
201 s in significant damage to the liver and the adrenal glands, little is known about the molecular sign
202 evealed lesions in several tissues including adrenal glands, lymphoid organs, bone, bone marrow, gast
204 l suggests that ischemia and necrosis of the adrenal glands may be responsible for the adrenal insuff
207 mutant embryos exhibit complete agenesis of adrenal glands, metanephric kidneys, gonads, and defects
211 to assess for associations between baseline adrenal gland morphologic features and subsequent develo
212 no significant association between baseline adrenal gland morphologic features and subsequent develo
215 mistry confirmed that within adult and fetal adrenal gland NGFIB expression paralleled expression of
220 oduction, was approximately 2-fold higher in adrenal glands of GX KO mice compared with WT mice, wher
222 osterone and ACTH levels than males, whereas adrenal glands of MS animals weighed less than those of
224 ative trait locus (eQTL and pQTL) mapping in adrenal glands of the HXB/BXH recombinant inbred (RI) st
226 patients with lymphoma with normal-appearing adrenal glands on prior CT examination (less than a 5% p
228 that expressed PPE mRNA and projected to the adrenal glands or celiac ganglia were activated, suggest
230 ours of the central nervous system, kidneys, adrenal glands, pancreas, and reproductive adnexal organ
231 an +/- SD], 42.9 +/- 13.3 y) with unilateral adrenal gland PHEO and in 13 control subjects (5 men and
232 eting, resulting in effective imaging of the adrenal glands, pituitary gland, lymph nodes, pancreas,
233 etyrapone may produce effects outside of the adrenal gland, presumably in the central nervous system,
240 e 28 tumors were located in the liver, lung, adrenal gland, retroperitoneum, gluteal muscle, inguinal
243 st to the testis and ovary, the mutant adult adrenal gland showed a lack of Sf1-deleted cells and our
245 However, with scheme B, no overlap in the adrenal gland SI-to-liver SI ratio between adenomas and
246 Because of the limited availability of human adrenal glands, sources of xenogeneic chromaffin cells w
249 KV RNA in the brain, thymus, lungs, kidneys, adrenal glands, spleen, liver, and small intestine.
250 were made in functionally different targets: adrenal gland, stellate ganglion which regulates the hea
251 f familial cases and the involvement of both adrenal glands suggest a genetic origin of this conditio
252 ne case, SKNBE(2)C iCSCs metastasized to the adrenal gland, suggesting their increased metastatic pot
253 observation of low S6K2 levels in the human adrenal gland supports the development of S6K1 inhibitor
255 the mouse Acsvl3 mRNA is highly expressed in adrenal gland, testis, and ovary, with lower expression
257 of 19 patients having more SFCs in the left adrenal gland than the right adrenal gland and 50 of the
259 ing adenomas (APAs) are benign tumors of the adrenal gland that constitutively produce the salt-retai
260 holamine biosynthesis and secretion from the adrenal gland that results in early embryonic lethality.
261 acrophages, the glucocorticoid production in adrenal glands, the leukocyte recruitment to peritoneum
262 ation of fresh frozen mouse liver and rabbit adrenal gland tissue sections with a range of higher spa
263 d in neuroblastoma cells compared to healthy adrenal gland tissue, consistent with a posttranscriptio
265 mized mice were transplanted with denervated adrenal glands to restore physiologic glucocorticoid lev
267 is substantial alpha2AR dysregulation in the adrenal gland, triggered by increased expression and act
269 zation with trans-synaptic labeling from the adrenal gland using pseudorabies virus identified presym
270 l progenitor cells from digestions of murine adrenal glands utilizing hydrodynamic inertial lift forc
271 of 2 readers, and uptake of (18)F-FDG in the adrenal gland was compared with liver activity and score
273 Ability to confirm visualization of the adrenal glands was determined for (18)F-FDG PET alone an
274 ino acid sequence of the peptide from bovine adrenal glands was HSSYEDELSEVL EKPNDQAE PKEVTEEVSSKDAAE
275 y delete GRK2 in the chromaffin cells of the adrenal gland, we crossed PNMTCre mice, expressing Cre r
276 nit of PP2A is expressed in brain but not in adrenal glands, we tested the hypothesis that PP2A/B'bet
279 between adrenal glands with PHEO and normal adrenal glands were 7.3 (100% sensitivity) and 10.1 (100
281 killed 6 hours after the injection, and the adrenal glands were collected for measurement of steroid
282 n CRPC, and indicated that steroids from the adrenal glands were contributing to this AR activity.
283 d beta-catenin and elevated Igf2 expression, adrenal glands were larger, displayed earlier onset of h
284 transcriptomes of 19 ACC tumors and 4 normal adrenal glands were profiled on Affymetrix U133 Plus2 ex
285 netic resonance (MR) imaging findings in the adrenal glands were reviewed retrospectively in 12 patie
286 evels as a basal protective mechanism in the adrenal gland, where cholesterol is under constant flux.
287 l motor nerve to the vicinity of the forming adrenal gland, where they detach from the nerve and form
288 nduces a strong inflammatory response in the adrenal glands, which is accompanied by cell death and h
289 ed XPLAC is expressed mostly in placenta and adrenal gland while XTES is exclusively expressed in pri
292 The 2 readers agreed on visualization of the adrenal glands with PET alone for 2 of 40 (5%) glands.
294 (18)F-FDA accumulation was observed in all adrenal glands with PHEO and in 6 of 13 control adrenal
296 F-FDA PET facilitate the distinction between adrenal glands with PHEO and normal adrenal glands.
297 d uptake values (SUVs) were compared between adrenal glands with PHEO and normal left adrenal glands
299 induced a local inflammatory response in the adrenal gland within 4 hours of administration, coupled
300 1.0 mg/kg per day) inhibits AT(1) binding in adrenal gland zona glomerulosa and kidney glomeruli.