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 hormone and monoamine storage and regulated secretion.
2 knockdown abolished glucose-induced insulin secretion.
3 ion and gasdermin D-dependent interleukin-18 secretion.
4 meostasis resulting from an enhanced insulin secretion.
5 trol the viral infection involving IFN-gamma secretion.
6 istently inhibits insulin concentrations and secretion.
7 yRa x fasting insulin) x first-phase insulin secretion.
8 ase-containing exosomes and stimulates their secretion.
9 te and alterations in adiponectin and leptin secretion.
10 el, leading to reduced airway surface liquid secretion.
11 1 mRNA levels, but BBS4 also modulates FSTL1 secretion.
12 of muscarinic M3 receptor-stimulated insulin secretion.
13 echanism of P-CAB inhibition of gastric acid secretion.
14 ked glucose intolerance with reduced insulin secretion.
15 irulent M. marinum strain with reduced ESX-1 secretion.
16 ects in both insulin sensitivity and insulin secretion.
17 at PFAS alter glucose metabolism and insulin secretion.
18 beta-cell apoptosis and insufficient insulin secretion.
19 onsible for the galectin-3-mediated cytokine secretion.
20 potently silence gene expression and protein secretion.
21 n B resulted in decreased OA uptake and VLDL secretion.
22 roducing cells known to impair gonadotrophin secretion.
23 eptor site on SecA are essential for protein secretion.
24 ent and increased glucose-stimulated insulin secretion.
25 creatic beta-cells that impair fetal insulin secretion.
26 hibited GHRH-, but not ghrelin-stimulated GH-secretion.
27 due to defects in glucose-stimulated insulin secretion.
28 well as SNAP-23 and SNAP-29 completes cargo secretion.
29 in increased Th17 polarization and cytokine secretion.
30 EMO expression, NFkappaB activation, and IL6 secretion.
31 pected to produce adverse effects on insulin secretion.
32 interferon genes (STING)-dependent cytokine secretion.
33 d active gamma-glutamyltranspeptidase enzyme secretion.
34 nergetics control glucose-stimulated insulin secretion.
35 , where it mediates phosphatidylcholine (PC) secretion.
36 e of IGSF1 as regulator of pituitary hormone secretion.
37 NLRP3-mediated interleukin-1beta (IL-1beta) secretion.
38 e is an O-acyltransferase that regulates Wnt secretion.
39 creased insulin content and impaired insulin secretion.
40 LRP3 inflammasome-mediated interleukin-1beta secretion.
41 ciated with gonadotropin biosynthesis and/or secretion.
42 use parietal cells induced constitutive acid secretion.
43 ion of the substrates of this machine before secretion.
44 had detectable ZIKV RNA in saliva or vaginal secretions.
45 t least one oral pathogen in their prostatic secretions.
46 espectively; P = 0.9) or first-phase insulin secretion (-21 +/- 212 compared with 24 +/- 184 mU/L, re
47 e major protein-biogenic pathway for protein secretion across the cytoplasmic membrane or insertion o
50 mponent of the T1SS system abrogated type VI secretion activity under nutrient-limited conditions, in
54 tors, SAR405 and VPS34-IN1, induced abnormal secretion and affected thrombus growth at arterial shear
56 , the NLRC3 CARD alone could dampen IL-1beta secretion and ASC speck formation induced by NALP3 mutan
58 alpha that are critical for assembly-induced secretion and biological activity of IL-12 versus misfol
59 creases basal and glucose-stimulated insulin secretion and Ca(2+) uptake in the presence of glibencla
61 isrupt the Golgi apparatus, interfering with secretion and compromising intestinal antimicrobial defe
62 neous injection of HC-HA/PTX3 preserved tear secretion and conjunctival goblet cell density and mitig
65 osolic Ca(2+) negatively regulates adipokine secretion and have uncovered an evolutionarily conserved
66 ted the importance of apolipoproteins in HCV secretion and infectivity, leading to the notion that HC
67 entially create an imbalance between insulin secretion and insulin-stimulated glucose utilization in
68 pendent increases of alpha and dense-granule secretion and integrin alphaIIbbeta3 activation, and agg
70 ucose-stimulated Ca(2+) dynamics and insulin secretion and recapitulated the pattern of improved proi
71 e of similar bacterial DNA in both prostatic secretion and subgingival dental plaque from the same in
74 entrations have been attributed to increased secretion and/or decreased insulin clearance by liver or
75 d high levels of bacterial shedding in nasal secretions and was temporally correlated with, and depen
79 mpaired glucose tolerance, defective insulin secretion, and increased apoptosis when a combined high-
80 il recruitment, interleukin-1beta [IL-1beta] secretion, and lactate dehydrogenase release) compared t
82 used to evaluate barrier function, cytokine secretion, and protein expression under basal conditions
83 inhibited T cell proliferation, blocked IL-2 secretion, and rendered T cells unresponsive to further
84 uscle contraction, airway and exocrine gland secretion, and rhythmic movements of the gastrointestina
85 se a reduction of insulin sensitivity and/or secretion (anti-incretin effect) to defend against hyper
87 ng regulators of glucose sensing and hormone secretion, are differentially expressed in these cell ty
88 cA-RH7777 cells resulted in an increased TAG secretion as compared with cells co-expressing cathepsin
92 ly associated with lower first-phase insulin secretion but has no evidence for an effect on type 2 di
93 s by GDH in the L cell may explain why GLP-1 secretion, but not that of insulin, is activated by thes
95 though glucose is known to stimulate insulin secretion by beta cells, whether it directly engages nut
96 ets, since Ex-4 treatment stimulated insulin secretion by both juvenile and adult human beta cells.
98 s a hub molecule during collagen folding and secretion by directing other molecules to reach their ta
103 thermore, we show that BM components require secretion by migrating macrophages (hemocytes) during th
104 of rapamycin's inhibitory effect on IL-1beta secretion by the IL-1 receptor antagonist anakinra in ph
105 ence of native AVR3a is cleaved off prior to secretion by the pathogen and the N terminus of the matu
108 ferential effects of male and female gonadal secretions (commonly referred to as sex hormones), which
109 slow gastric emptying and alter gut hormone secretion compared with a control but have no suppressiv
112 rapamycin (mTOR) kinase, promotes glutamate secretion, cystine uptake, and incorporation into glutat
114 al activity, 24-h glycemia, and 24-h insulin secretion did not differ between intervention days.
115 ase (PD) and include disruption of melatonin secretion, disturbances of glucose, insulin resistance a
116 ded head-of-bed elevation, use of subglottic secretion drainage endotracheal tubes, oral care, chlorh
117 mportance of PKR, TRIF, and TBK1 in cytokine secretion during L. pneumophila infection of macrophages
120 um liver tests, bile flow, biliary bile salt secretion, fecal bile salt loss, and expression of major
121 of Vascular Endothelial Growth Factor (VEGF) secretion for this pathway of hypoxia-mediated self-rene
122 Silencing of Rab5 shifts receptor-triggered secretion from a compound to a full exocytosis mode, in
125 rthermore, the TsSP-induced reduction of TNF secretion from DCs is reversed by receptor antagonists f
127 825 did not affect pro-inflammatory cytokine secretion from other ROCK-positive cell types, corrobora
129 nflammatory mechanism demonstrated that IL-6 secretion from synovial fibroblasts was induced by chond
130 re of cultured neurons to fetal plasma or to secretions from the placenta or from model trophoblast b
131 biosynthesis and glucose-stimulated insulin secretion (GSIS) in a PKA-dependent manner and prevented
132 ghrelin inhibits glucose-stimulated insulin secretion (GSIS), the effect of obestatin on GSIS is unc
138 doses of BPA significantly impaired insulin secretion in male but not female F1 and F2 offspring.
141 l pathway as an important mechanism for mHtt secretion in mouse neuroblastoma and striatal cell lines
144 retion components and mechanisms of type VII secretion in pathogenic and environmental bacteria.
145 in human diarrheas, (R)-BPO-27 blocked fluid secretion in primary cultures of enteroids from human sm
146 ma, p < 0.05) and reduced leukocyte cytokine secretion in response to lipopolysaccharide stimulation.
148 novel signaling pathway contributing to IL-8 secretion in the CF bronchial epithelium with KL functio
149 crystallin in astrocytes to decrease exosome secretion in the HD brains, contributing to non-cell-aut
150 cient to depolarize the cell and evoke GLP-1 secretion in the model, suggesting a crucial role for SG
152 y, let-7 and miR-148 antagonism modified PTH secretion in vivo and in vitro, implying roles for these
154 NEMO-mediated regulation of NFkappaB and IL6 secretion, increased phosphorylation of STAT3 on Ser727,
155 stance, synergistically with lowered insulin secretion, increases serum glucose levels, which stimula
156 beta-cell function measured with the insulin secretion/insulin sensitivity (disposition) index increa
162 onstrate that increased EGFL7 expression and secretion is an autocrine mechanism supporting growth of
165 that minimizing the driving force for Cl(-) secretion is the main requirement for secreting 140 mm H
178 ation of this effector, termed Tne2 (Type VI secretion NADase effector family 2), demonstrates that i
180 In alphaRaptorKO mice, impaired glucagon secretion occurred in response to different secretagogue
183 henomena are due, in part, to the deployment/secretion of a "decoy flare," for example, anomalous can
184 We further show that 4-PBA triggers the secretion of a KDEL-tagged luminal resident, implying th
185 lar replicative cycle of T. gondii including secretion of adhesins, motility, invasion, and egress.
186 mpounds that prime microbial pattern-induced secretion of antimicrobial furanocoumarins (phytoalexins
188 dings imply a role for the RxLR motif in the secretion of AVR3a by the pathogen, rather than a direct
190 th in vivo and in vitro, as characterized by secretion of both proinflammatory and anti-inflammatory
191 urb protein folding, assembly or polarity of secretion of C1QTNF5 and, importantly, all appear to des
192 g by MSC was found to be mediated in part by secretion of cathelicidin and was significantly increase
193 The altered bile salt pool stimulated robust secretion of cholesterol into the intestinal lumen via t
194 als are a major endocrine site of production/secretion of constitutive pepcan-12, as shown by its mar
195 pathway that can be targeted to inhibit the secretion of cytokines by modulating either CXCR4 or CXC
197 riptomic signature suggesting expression and secretion of extracellular proteins, while mature RRCs e
200 phase of TLR signaling and the TLR-dependent secretion of IL-10 (controlled by IRAKs 1 and 2) was onl
201 n armored CAR T cell capable of constitutive secretion of IL-12, and delineate the mechanisms via whi
202 rm cytotrophoblast cells, with a predominant secretion of IL-1beta and IL-6, a result confirmed in hu
205 of Vgamma9/Vdelta2 T cells promoted mucosal secretion of IL-22 and ICOSL/TNF-alpha-dependent release
207 immune system to maintain homeostasis is the secretion of immunoglobulins (Igs) across epithelial bar
208 rd an inflammatory phenotype, with increased secretion of inflammatory cytokines as well as chemokine
209 y HOCl treatment was demonstrated by reduced secretion of inflammatory cytokines in affected skin tis
210 ereas knockdown of Irf5 blunted CB1R-induced secretion of inflammatory cytokines without affecting CC
214 ed epidermal structure, ascribed to aberrant secretion of lamellar bodies, which are essential for ep
217 f pathogenic lymphocyte infiltration and the secretion of pro-inflammatory cytokines are involved in
219 ive pathway prevents the correct folding and secretion of proteins that are known to form non-native
220 raves' disease, but not control sera, led to secretion of TG with an increased intrinsic ability to f
221 minent example of bacterial cooperation, the secretion of the peptide siderophore pyoverdine by Pseud
222 mutants promote longevity through increased secretion of the polysaccharide colanic acid (CA), which
223 inflammasome results in caspase-1-dependent secretion of the proinflammatory cytokines IL-1beta and
224 A2 activity in these splenic macrophages and secretion of the resistance-inducing lipid mediator, lys
225 osa as a model system, the authors show that secretion of the siderophore pyoverdine only incurs a fi
229 s of new protein, is not caused by decreased secretion of TSP-4, and is mediated by activation of SMA
230 y, leading to the notion that HCV coopts the secretion of very-low-density lipoprotein (VLDL) for its
236 present in 'pure' versus 'mixed' anal-gland secretions ('paste') of adult meerkats (Suricata suricat
237 us intermedius mediate cell contact- and Esx secretion pathway-dependent growth inhibition of diverse
241 that uterine glands and, by inference, their secretions play important roles in blastocyst implantati
242 analog on KATP channel activity and insulin secretion point to participation of the cGMP/PKG and cAM
243 reases NALP3-induced IL-1beta maturation and secretion, pro-caspase-1 cleavage, and speck formation b
245 uding regulation of insulin biosynthesis and secretion, promotion of satiety, and preservation of bet
246 hydrpxnonenal both assayed by ELISA, insulin secretion quantified using ELISA or radioimmunoassay, an
247 n of TLR4 or SPAK normalizes hyperactive CSF secretion rates and reduces PHH symptoms, as does treatm
249 characterized by airway inflammation, mucus secretion, remodeling and hyperresponsiveness (AHR).
251 se homeostasis, insulin sensitivity, insulin secretion, steatosis, metabolic inflammation, pancreatic
252 flammasome activation, cell death, and IL-18 secretion, suggesting that restoring mitophagy and inhib
253 ter species produce both a functional type I secretion system (T1SS) and a contact-dependent inhibiti
255 enic Gram-negative bacteria use the type III secretion system (T3SS) to deliver effector proteins int
257 genetic architectures (GA1-3) of the type VI secretion system (T6SS), an effector delivery pathway th
259 ia an unknown mechanism by bacterial type VI secretion system 5 (T6SS-5), which is an essential virul
262 el apparatus, a widespread exopolysaccharide secretion system found in environmental and pathogenic b
264 V tag, which can pass through the type three secretion system, allowed visualization and quantificati
265 omplex, IcmSW, for translocation through the secretion system, but its role in pathogenicity has rema
270 d homologs of this toxin are associated with secretion systems in many Gram-negative and Gram-positiv
272 the Liberibacter virulence traits, including secretion systems, putative effectors, and lipopolysacch
275 Tsc1 deletion results in an increase in CTGF secretion that non-cell autonomously stunts oligodendroc
276 uring pancreatitis maintains VAMP8-dependent secretion, thereby preventing accumulation of activated
278 osmolarity stimulate thirst and vasopressin secretion through a central osmoreceptor; however, centr
279 ion with sIL-6R promoted VEGF expression and secretion through a transcriptional mechanism involving
280 ype 1 (AT1R), stimulates acute catecholamine secretion through coupling with the transient receptor p
281 oteins and inducing proinflammatory cytokine secretion through protease-activated receptor 2 (PAR2).
282 cardiomyocytes decreased VEGF expression and secretion to levels sufficient to blunt in vitro tube fo
284 riggering cellular cytotoxicity and cytokine secretion upon high-affinity interaction with the cognat
285 ncreases in KL, TGF-beta also increased IL-8 secretion via activation of FGFR1 and Smad 3 signaling.
286 s reveals that Drp1 does not control insulin secretion via its effect on proton leak but instead via
287 progesterone inhibits LH surge and pulsatile secretion via its receptor in the ARC and/or AVPV nuclei
288 O2 consumption, and ATP production), insulin secretion was almost completely restored at elevated glu
289 tic properties in vitro cBiTE expression and secretion was detected in supernatants from ICOVIR-15K-c
293 50s genes involved in the biosynthesis of MG secretions, we analyzed by means of qPCR, the expression
294 conceptus aromatase expression and estrogen secretion were decreased, indicating that IL1B2 may be i
296 ven by increased tumor necrosis factor (TNF) secretion, which leads to activation in turn of c-Jun N-
297 human macrophages exposed to HCV induce CCL5 secretion, which plays a significant role in hepatic inf
298 mportant in ensuring that excessive chloride secretion, with the accompanying loss of fluid, is not n
300 th necessary and sufficient to cause exosome secretion without affecting the endoplasmic reticulum/Go
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。