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1 and for persistent infection in the salivary gland.
2 bserved SFCs (82%) found in the left adrenal gland.
3 oreactive T and B cells within the pituitary gland.
4 ttern of melatonin secretion from the pineal gland.
5 helial cells in epithelial patterning of the gland.
6 ancreas, kidneys, liver, heart, and salivary gland.
7 g development and postnatally in the mammary gland.
8 operative multiparametric MR imaging and the gland.
9 ke in kidneys, urinary bladder, and lacrimal gland.
10 co analysis of the developing mouse salivary gland.
11 li vaccine-induced protection of the mammary gland.
12 ion that might cause a bulge in the prostate gland.
13 action on critical targets like the mammary gland.
14 specialisation in the different parts of the gland.
15 serum and epidermis, and the porcine adrenal gland.
16 phocytes undergo activation in the pituitary gland.
17 -Tyr is localized in the nematode esophageal gland.
18 ent KRT5(+) epithelial cells in the lacrimal gland.
19 al with several different cancerous foci per gland.
20 nd CD4(+) IFN-gamma(+) cells in the lacrimal gland.
21 tion of T and B lymphocytes in the pituitary gland.
22 diastinum, retroperitoneum, neck and adrenal gland.
23 ary for long-term maintenance of the mammary gland.
24 to mononuclear infiltrations in the salivary gland.
25 regulatory expression evolution in the venom gland.
26 ing the postnatal development of the mammary gland.
27 ing, and application of fluids from exocrine glands.
28 livary glands and potentially other exocrine glands.
29 ollagen type IIIalpha1 and NF-kB in lacrimal glands.
30 of inflammatory/immune cells in the lacrimal glands.
31 ake in both mouse thyroid and mouse salivary glands.
32 large vacuoles, or in small and ill-defined glands.
33 , accelerating the pathology in the salivary glands.
34 cular clock gene expression in mouse mammary glands.
35 of the small-molecule agents in the salivary glands.
36 r T cell accumulation in uninfected salivary glands.
37 ation (UR) phenomenon in Drosophila salivary glands.
38 ipoatrophy and complete absence of sebaceous glands.
39 acinar cells in submandibular and sublingual glands.
40 neonatal FOXA2-deleted mice lacking uterine glands.
41 ate glands were divergent from fiber-forming glands.
42 was abundant in keratinocytes and sebaceous glands.
43 rine glands, specifically the major salivary glands.
44 pressing mouse tissues, thyroid and salivary glands.
45 serous, and mucous acinar cells of salivary glands.
46 5 revealed mean doses of 2.3 Sv for salivary glands, 0.7 Sv for kidneys, and 0.05 Sv for red marrow t
47 wth of parathyroid tissue either as a single gland (80% of cases) or as a multiple gland disorder (15
48 cluded gross enlargement of the left parotid gland, a focal lesion in the right parotid gland, and ce
52 he left adrenal gland than the right adrenal gland and 50 of the 61 observed SFCs (82%) found in the
56 pyrene (BaP) metabolism in the mouse mammary gland and develop a circadian in vitro model for investi
57 sed macrophage recruitment to the developing gland and increased density of the ductal epithelial net
59 by lymphocytic infiltration of the salivary gland and loss of saliva secretion, predominantly in wom
62 MV), a herpesvirus that infects the salivary gland and promotes the accumulation of salivary gland ti
63 rmone concentrations that may affect mammary gland and pubertal development.We evaluated the relation
64 re x Tph1 (FL/FL) dams had decreased mammary gland and serum serotonin concentrations compared to con
65 aging excluded common lesions of the adrenal gland and showed lymphadenopathy around the major vessel
66 wever, the functions of GLIS3 in the thyroid gland and the mechanism by which GLIS3 dysfunction cause
67 rare inflammatory condition of the pituitary gland and usually affects women of childbearing age.
68 e influences BaP metabolism in mouse mammary glands and describe an in vitro model that can be used t
73 of self-assembly is conserved across spider glands and species is currently unknown because quantita
74 o midgut, female ovaries, and male accessory glands and spreads rapidly throughout mosquito populatio
75 y and provide original evidence that uterine glands and, by inference, their secretions play importan
76 genitors specialise into distal (tips of the gland) and proximal (the stalk region) identities that p
80 e present in normal and diseased parathyroid glands, and if so, whether they had any functional effec
82 threshold for all lesions and the pituitary gland; and for (18)F-FDG (C)-RD of SUVs of the whole bra
83 rymna scolopes, have an accessory nidamental gland (ANG) housing a bacterial consortium that is hypot
84 oxc1 was specifically ablated in skin, sweat glands appeared mature, but the mice were severely hypoh
86 results of our study indicate that lacrimal glands are capable of tissue repair after duct ligation-
87 alize to the parotid, salivary, and lacrimal glands as well as to the kidney, leading to dose-limitin
90 t were transitioning into SPEM cells only in gland bases, rather than the proliferative stem cell zon
91 e pars tuberalis (PT) of the fetal pituitary gland, before the fetal circadian system and autonomous
92 t difference in the ADC value of the thyroid gland between patients and the control group (P=0.001).
95 te T cell recruitment to uninfected salivary glands but that redundant mechanisms mediate T cell recr
96 hism in cellular infiltrates of the salivary glands by using functional single-cell microengraving an
97 We concluded that ADC values of the thyroid gland can be used to differentiate Graves' disease from
100 tear volume, anterior blepharitis, meibomian gland capping) and tear inflammatory cytokine levels.
101 It is significantly more common in lacrimal gland carcinoma compared with dacryoadenitis and in mali
102 116 patients was reviewed: 39 with lacrimal gland carcinoma, 37 with lymphoma, and 40 with dacryoade
103 The "wedge sign" is most common in lacrimal gland carcinoma, but can occur in patients with severe f
104 etal sheep induced by removal of the thyroid gland caused asymmetric organ growth, increased pancreat
106 rabbit conjunctival epithelium and lacrimal gland cell spheroids, and recapitulates the aqueous and
109 in the shape of the prostate and the central gland (combined central and transitional zones) between
110 luding cuticular hydrocarbons and mandibular gland components that act as H. saltator pheromones, and
112 by LIF and was maintained to term in uterine gland-containing adult FOXA2-deleted mice, pregnancy fai
114 T cell recruitment to uninfected salivary glands depended on chemokines and the integrin alpha4 Se
115 this technique is able to detect parathyroid gland devascularization before it is visually apparent t
116 effects include persistent delays in mammary gland development (perfluorooctanoic acid; PFOA) and sup
117 role for the major CLP gene Irf6 in salivary gland development and a significant role in regulating o
118 ealed its specific roles in pubertal mammary gland development and potential contributions to breast
120 s showed that it is not required for mammary gland development during puberty, it is not clear whethe
122 onmental chemical exposure on normal mammary gland development in rats to motivate and evaluate the p
123 our data reveal crucial features of lacrimal gland development that have broad implications for under
124 to study the hormonal regulation of mammary gland development, and to test newly synthesized chemica
125 the arrest in tooth, thymus, and parathyroid gland development, suggesting that the relationship of P
132 uses, and ocular surface impact of meibomian gland disease (MGD), as well as its relationship to dry
135 tion as the best model describing follicular gland diversification, and revealed high rates of dispar
136 We found that MUC5B emerged from submucosal gland ducts in the form of strands composed of multiple
139 n = 32) and compromised (n = 27) parathyroid glands during thyroid surgery with an accuracy of 91.5%.
140 nimal or less effect on normal human mammary gland epithelial cells (HMECs) and estrogen receptor-pos
141 of accessible chromatin in the mouse mammary gland epithelial EpH4 cell line and its Ras-transformed
146 spidroin, a spidroin expressed only in venom glands, evolutionary mechanisms for spidroin diversifica
147 ma(-/-), NOD.H-2(h4) mouse model of salivary gland exocrinopathy ameliorated salivary gland inflammat
148 orial chronic disorder in which the lacrimal glands fail to produce enough tears to maintain a health
149 ld-type stroma, fully repopulate the mammary gland fat pad, undergo unperturbed ductal outgrowth and
150 sts were elevated in cGVHD-affected lacrimal gland fibroblasts and (2) that they could be reduced by
154 pression was evaluated in 127 normal adrenal glands from deceased kidney donors (age, 9 months to 68
155 We profiled microRNA (miRNA) in parathyroid glands from experimental hyperparathyroidism models and
156 suggest that careful evaluation of salivary gland function and the implementation of early oral heal
159 e points (30 min to 2 h), irradiated parotid glands had significantly decreased levels of the histone
161 ically, anti-inflammatory therapy, meibomian gland heating and expression, and scleral contact lenses
163 al levels of autophagy in the normal mammary gland, highlighting the potential of vitamin D as a canc
164 MT-associated genes in normal murine mammary gland homeostasis and human breast cancer still remains
168 controls, aged HCM females exhibited adrenal gland hypertrophy, reduced volume in mood-related brain
169 d localized a specific area of the pituitary gland (i.e., adenohypophysis) known to secrete neuropept
173 The agrp2 gene was expressed in the pineal gland in a previously uncharacterized subgroup of cells.
175 we compared T cell migration to the salivary gland in mice that were infected or not with murine CMV
180 cy of FCH PET/MR imaging for localization of glands in patients with four-gland hyperplasia remains t
181 observed that autonomic innervation of sweat glands in the footpads was significantly reduced in db/d
182 antle, instead of the specialised hypodermal glands in the second antennular segment as reported in t
183 (-) cells that are able to repopulate entire glands, including the base, upon depletion of the Lgr5(+
185 Fgf20 deficiency does not impede mammary gland induction, but compromises mammary bud growth, as
186 ary gland exocrinopathy ameliorated salivary gland inflammation and enhanced carbachol-induced saliva
190 oracic level (Th1) SCI disconnecting adrenal gland innervation, compared with low-thoracic level (Th9
191 originates from secretion from the pituitary gland into the circulation and from absorption of OT in
192 mosquito infection by 50%, impedes salivary gland invasion 10-fold, and causes a complete absence of
193 by dynamic tissue remodeling in the mammary gland involving ductal elongation, resolution into the m
197 ysis of the function of TAp63 in the mammary gland is critical for improved diagnosis and patient car
199 models, PELP1 overexpression in the mammary gland leads to premalignant lesions and eventually mamma
200 To describe the involvement of the lacrimal gland (LG) in blepharophimosis-ptosis-epicanthus inversu
202 tem (GI), followed by the bronchi, endocrine glands-like C cells of the thyroid (medullary carcinoma)
204 produced by the clustered temporary adhesive glands located within the mantle, instead of the special
206 ized by lymphocytic infiltration of exocrine glands, mainly salivary and lacrimal, resulting in oral
207 that bacteria dwelling in an animal's scent glands metabolize the glands' primary products into odor
210 variables across tumor and non-tumor mammary gland microvasculature with and without application of R
211 ogenitor cell subpopulations driving mammary gland morphogenesis and homoeostasis are poorly understo
214 mice, in the thyroid, stomach, and salivary gland, NIS is absent, and hence there is no active accum
216 native silk, obtained directly from the silk gland of Bombyx mori silkworms, into micron-scale capsul
219 al chemokines were expressed in the salivary glands of infected and uninfected mice, and many of thes
222 in NTDs originating from the major ampullate glands of the spider species Euprosthenops australis, Ne
224 ription factor expressed specifically in the glands of the uterus and is a critical regulator of post
229 stromal and systemic roles in murine mammary gland organogenesis, yet specific functions remain undef
233 rmal mice showed uptake in thyroid, salivary glands (percentage injected dose/g at 30 min, 563 +/- 14
236 g in an animal's scent glands metabolize the glands' primary products into odorous compounds used by
239 more, lineage tracing in postnatal and adult glands provides the first direct evidence of unipotent K
240 athologies can disrupt function of meibomian glands, ranging from congenital to acquired causes.
241 y due to downregulation of expression in the gland rather than gene death through coding sequence deg
242 nvestigating evolutionary diversification of glands responsible for the production of chemical signal
243 exogenous endothelial cells to reconstituted glands restored epithelial patterning, as did supplement
244 SC-loaded native de-cellularized rat parotid gland scaffolds into the renal capsule of nude mice led
245 circuit by which a single compound, exocrine gland-secreted peptide-1 (ESP1), enhances reproductive b
247 ooth muscle contraction, airway and exocrine gland secretion, and rhythmic movements of the gastroint
248 pounds present in 'pure' versus 'mixed' anal-gland secretions ('paste') of adult meerkats (Suricata s
249 pathogen must traverse the mosquito salivary gland (SG) for transmission to a new host, making the SG
251 significantly reduced hamster ear sebaceous gland size, indicating that this pro-drug approach was c
252 lts show that in primary mouse submandibular gland (SMG) epithelial cells, P2X7R activation also indu
254 1007 in muscle, submandibular and sublingual gland, spleen, pancreas, liver, and gallbladder was obse
255 sults provide further insights into lacrimal gland stem/progenitor cell physiology and their potentia
258 ween the developing mouse and human lacrimal gland, supporting the use of mice to understand human de
259 f the epithelial invaginations on the cement glands supports the involvement of exocytosis in the sec
262 atients having more SFCs in the left adrenal gland than the right adrenal gland and 50 of the 61 obse
263 he Drosophila hematopoietic organ, the lymph gland, the posterior signaling center (PSC) acts as a ni
265 these studies indicate that damaged salivary gland tissue can grow and differentiate when treated wit
266 p53-/- breast tumor tissue or normal mammary gland tissue with methyl-tert-butyl ether (MTBE) results
270 s cortical F-actin dismantling, enabling the glands to stretch as they accumulate secreted products i
272 nteractions between CSCs and CAFs in mammary gland tumors driven by combined activation of Wnt/beta-c
275 tion of spidroin expression in distinct silk gland types indicates that glands can express multiple s
276 ng that shifts in gene expression among silk gland types were not necessarily coupled with gene dupli
278 volume (PFV) with normalisation to prostate gland volume on pelvic magnetic resonance imaging (MRI)
279 usion coefficient (ADC) value of the thyroid gland was calculated and correlated with Tc-99m uptake a
281 upporting T cell recruitment to the salivary gland, we compared T cell migration to the salivary glan
282 of the developing human and murine salivary gland, we demonstrate an unexpected role for SOX2 and pa
286 le in bone metabolism, we hypothesized these glands were the sites of a functional interaction betwee
287 s lymphocytic infiltration into the salivary glands when used with small doses of the steroid, dexame
288 ped an ex vivo culture method of the mammary gland where the direct action of estrogens can be tested
289 nerve to the vicinity of the forming adrenal gland, where they detach from the nerve and form postsyn
290 ce were morphologically normal and contained glands, whereas the uteri of neonatal FOXA2-deleted mice
291 NH is emitted from exocrine opisthonotal oil glands, which are potent organs for chemical defense in
292 ption of blood supply to healthy parathyroid glands, which are responsible for regulating calcium.
295 he crown squamate ancestor lacked follicular glands, which therefore originated and diversified subse
296 alence of pathogenic effector T cells in the glands with a sexually dimorphic selection bias of TCR r
297 hole-exome radiogenomic analysis of prostate glands with adenocarcinoma shows a continuum of mutation
299 d to be in well-to-moderately differentiated glands with nuclear polarization, but exclusive sTRA sta
300 ized by malformations of the teeth, hair and glands, with milder deficiencies affecting only the teet
301 P) in their developing epidermis and mammary glands] with those from wild type, we show that transgen
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