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1 ormally present in wounds, wound healing was impaired.
2 bone morphogenetic protein (BMP) signals are impaired.
3 dour-induced attractive social responses are impaired.
4 apoA-IV gene expression and food intake are impaired.
5 resence is attenuated and mating behavior is impaired.
8 Deficits in the salience network suggest an impaired ability to process physiologically salient even
9 I (Gly119Arg and Leu131Arg) variants have an impaired ability to regulate complement activation and m
12 molecules, disrupted glutamate homoeostasis, impaired action of antipsychotics, and development of an
13 w enhancers in embryonic stem cells leads to impaired activation of HoxA genes upon differentiation,
15 NADH production rate remained significantly impaired after 10 min of reperfusion after global ischem
16 These aspects of daily life are known to be impaired after extended wake, yet, the underlying neuron
20 nificant difference was observed between the impaired and nonimpaired groups in the association of fr
22 tion of sorted LPS-stimulated MZ B cells was impaired, and aged bumble mice were unable to respond to
24 nsmission in medial prefrontal cortex (mPFC) impaired appetitive trace conditioning at a 2 s trace in
25 h genetic and physiologic evidence points to impaired arousal responses to hypercarbia and hypoxia, w
26 Moreover, whether such dynamic coupling is impaired as a consequence of brain aging in later life,
28 ce, activation of PI3 kinase-mTOR signaling, impaired autophagy, mitochondrial dysfunction, stem cell
29 found increased anxiety-related behavior and impaired aversive learning as well as markedly affected
30 alization of these proinflammatory cytokines impaired bacterial clearance and eliminated host protect
32 stasis, including lack of recovery sleep and impaired behavioral adjustment to a novel task after sle
34 d S1450F in rodents, respectively) displayed impaired binding to membrane-associated guanylate kinase
36 levated blood viscosity, which contribute to impaired blood flow and other pathophysiological aspects
37 e with knockout of SREBP2 in astrocytes have impaired brain development and behavioral and motor defe
38 WM development are a major factor underlying impaired brain growth and microcephaly in the disorder.
39 eir ligands Fgfs Deleting Fgfr1/2/3 not only impaired bSC dendritogenesis but also abolished glutamat
41 e inhibitor, restored performance in animals impaired by continuous stimulation but did not improve p
42 the catalytic activity of the enzyme was not impaired by exposure to radiation during the pulse radio
43 ing was increased by Gab2 overexpression and impaired by Gab2 deletion via regulation of Jak2 and sig
44 o to investigate single molecule dynamics is impaired by the absence of an efficient way to chemicall
47 d a mechanism-based SCF partial agonist that impaired c-Kit dimerization, truncating downstream signa
49 ay of symptomatic characteristics, including impaired Ca(2+) transients, upregulation of Na(+)/Ca(2+)
50 yed diacylglycerol clearance from the PM and impaired Ca(2+)-triggered phosphatidylserine scrambling.
53 larization toward a regulatory phenotype and impaired CD8(+) T cell allo-reactive responses, includin
57 C4 synthase-deficient eosinophils exhibited impaired chemotaxis to CCL19 that was restored by exogen
58 tic mechanisms involved in CF, which include impaired chloride permeability and persistent lung infla
62 children <5 y of age and is associated with impaired cognitive and motor development and increased m
67 of reduced CXCL12 scavenging by mutants with impaired CXCL12 affinity required drastically reduced re
68 ive neural tube defects (NTDs) indicate that impaired de novo thymidylate (dTMP) synthesis through ch
74 M) is a rare cardiomyopathy characterized by impaired diastolic ventricular function resulting in a p
75 Surprisingly, reduced GATA1 expression and impaired differentiation were limited to megakaryocytes,
77 e imaging (MRI) is hypothesized to represent impaired drainage of interstitial fluid from the brain a
78 erimental data suggest that efferocytosis is impaired during atherogenesis caused by dysregulation of
79 62+/-11 years; 16% (n=237) were cognitively impaired during hospitalization, and 11% (n=174) were im
81 , ECD mRNA levels were increased, suggesting impaired ECD translation as the mechanism for reduced pr
82 ed in a halt of cell proliferation, severely impaired EGFR signaling and the onset of cellular senesc
84 al compartments, respectively, supporting an impaired endocytic lipid antigen presentation for T cell
85 anoparticle-positive areas further exhibited impaired endothelial barrier function as illuminated by
86 results in decreased glycolysis, leading to impaired endothelial cell proliferation and migration.
87 reased local TNF-alpha levels, might lead to impaired eosinophil resolution and could contribute to t
88 Both patients and murine models revealed an impaired epidermal structure, ascribed to aberrant secre
89 Furthermore, we found that a PKA inhibitor impaired ES cell proliferation, tumor growth and metasta
91 ot affect synapse numbers but differentially impaired excitatory or inhibitory synaptic functions in
94 ategorically specific, as inactivation of ML impaired face detection while sparing body and object de
95 fulfilled the inclusion criteria (NAFLD with impaired fasting glucose or impaired glucose tolerance)
96 y of elderly women in Denmark, we found that impaired fasting plasma glucose concentration was associ
98 sion of meristem/tissue identity markers are impaired from the "symmetry-breaking" periclinal cell di
100 thromboxane A2 production may contribute to impaired functional dilator and hyperaemic responses at
102 CHK2 activation in response to irradiation, impaired G2 checkpoint proficiency and radiosensitizatio
104 by fungal and bacterial infections caused by impaired generation of TH17 cells; meanwhile, some patie
106 In conclusion, SGLT2-I treatment improves impaired glucose effectiveness in the liver and insulin
109 sformed and categorized into quartiles) with impaired glucose tolerance (IGT) and gestational diabete
112 th control littermates, knockout mice showed impaired glucose tolerance and circulating leptin, GLP-1
113 edentary dams produced female offspring with impaired glucose tolerance compared with offspring of ch
114 ese patients with coronary heart disease and impaired glucose tolerance were randomly assigned (1:1),
115 , HbA1c [-10 g/L (95% CI: -12.90, -7.10 g/L; impaired glucose tolerance) and -6 g/L (95% CI: -8.47, -
116 eria (NAFLD with impaired fasting glucose or impaired glucose tolerance) and were randomly assigned i
117 ese patients with coronary heart disease and impaired glucose tolerance, acarbose did not reduce the
118 mice, resulted in decreased beta cell mass, impaired glucose tolerance, defective insulin secretion,
120 selective deletion of StarD10 in mice led to impaired glucose-stimulated Ca(2+) dynamics and insulin
121 (-/-) mice, oxidative stress associated with impaired glutathione synthesis and nuclear factor erythr
122 he context of neuronal diseases caused by an impaired glyoxalase system and elevated levels of dicarb
125 Overexpressing PEX1 in wild-type plants impaired growth, suggesting that excessive PEX1 can be d
132 PD-1 identifies "exhausted" CD8 T cells with impaired HIV-specific effector functions, but its role o
135 factors, environmental toxins and stressors, impaired immune responses, mitochondrial dysfunction, an
136 regs in vivo at the start or stop of therapy impaired immune tolerance, highlighting the dependence o
138 associated RH domain-interacting protein was impaired in a male fetus with IP, leading to defective l
140 nity between Sesn2 and AMPK upstream LKB1 is impaired in aged hearts during ischemia (P < 0.05 vs. yo
142 on fork stalling, as replication-restart was impaired in both SMI#9-pretreated and RAD6B-silenced cel
143 binding of the UBXD1 adaptor protein that is impaired in disease; this underlies the potential for re
144 formation of NEMO-containing structures was impaired in fibroblasts from patients with IP carrying t
145 berculosis-specific CD4 T cells was markedly impaired in HIV-infected individuals, compared with HIV-
147 ils and inflammatory cytokine production are impaired in M-ILK-deficient mice, and activation of epit
148 cose uptake and hypertrophic growth were not impaired in muscle-specific GLUT4 knockout mice, demonst
151 evelopmental plasticity and connectivity are impaired in sensory systems in DS model mice, that such
152 o the CD4(+)CD8(-) single-positive stage are impaired in Themis(-/-) mice, suggesting that Themis mig
154 pro-apoptotic mediators CamkII and Stat1 was impaired in Trpc3-deficient M1 cells, gathering insight
159 rosclerotic lesion that displays features of impaired inflammation resolution, notably a necrotic cor
160 er-associated rare variant (M2145T) in TGEF2 impaired inhibition by the TGEF2 pleckstrin-homology dom
162 se the possibility that septic patients have impaired insulin clearance, which could increase their s
164 ucible ablation of LDB1 in mature beta cells impaired insulin secretion and glucose homeostasis.
166 by trapping it in the endosomes, leading to impaired insulin signaling and insulin-stimulated mitoch
170 s from MetSyn or LPS-injected rats exhibited impaired intrinsic contractile activity and associated i
171 t is similar to wild-type aged hearts (i.e., impaired ischemic AMPK activation and higher sensitivity
175 its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles,
176 ed that recycling of the TCR-CD3 complex was impaired, leading to increased lysosomal targeting and r
177 related behavior, hyperhedonia, hyperphagia, impaired learning and memory and exaggerated startle res
181 y (LAD) syndrome in humans, characterized by impaired leukocyte recruitment and recurrent infections.
182 n ZFP36L1-deficient mice were accompanied by impaired lipid absorption that was consistent with alter
183 gatroban is contraindicated in patients with impaired liver function, and activated partial thrombopl
187 restricted trafficking of CAR T cells to and impaired long-term persistence at the tumor site, as wel
188 nfants are predisposed to illness because of impaired lung function or whether respiratory illness re
194 est that ribosomal deficiency contributes to impaired megakaryopoiesis in myeloproliferative neoplasm
198 nts with sporadic late-onset AD suggest that impaired mitophagy contributes to synaptic dysfunction a
200 ith excessive manganese accumulation was the impaired motor function observed in the Zip14 KO mice.
201 : +44%) shortly after exposure (30 min), and impaired motor functions (falls: +83%; time top: -43%; t
205 allergy development, possibly indicating an impaired mucosal barrier function in allergic children.
207 genetic variants act through a mechanism of impaired muscle cell differentiation and tissue formatio
208 rmal spectra of basic behavioral activities, impaired muscle grip strength, and defects in motor coor
209 tion with Cobra Venom Factor (CVF) result in impaired muscle regeneration following cardiotoxin-induc
212 m levels in HFpEF are neither a result of an impaired Na(+) gradient nor expression changes in key io
213 ses a spectrum of brain malformations due to impaired neuronal migration in the developing cerebral c
214 subjects, causing hemolytic anemia linked to impaired nicotinamide adenine dinucleotide phosphate (NA
217 mitant with reduced NMDA-evoked currents and impaired NMDAR-dependent insertion of GluA1 at stimulate
218 OS dysfunction, as indicated by the level of impaired O2 extraction from arterial blood during peak e
220 ary cells revealed one substitution severely impaired OGFOD1-dependent hydroxylation of a neighboring
221 rated that senescent-cell conditioned medium impaired osteoblast mineralization and enhanced osteocla
222 rovascular obstruction during a VOC leads to impaired oxygen supply to the periphery and ischemia rep
224 earch has linked age-related hearing loss to impaired performance across cognitive domains and increa
226 by the Confocal Leak Score (CLS; range: 0=no impaired permeability to 100=complete loss of barrier fu
227 2-expressing macrophages were accompanied by impaired phosphorylation of IL-1R-associated kinase 1 (I
228 aves of polyprenol-deficient plants revealed impaired photosystem II operating efficiency, and their
229 r people face a high risk of muscle loss and impaired physical function, which may contribute to sarc
231 naling or cathepsin B function significantly impaired PNI in vivo Correlative studies in human specim
234 " crossed the fixed threshold from intact to impaired pressure reactivity (pressure reactivity index
236 The presence of Retro94 results in severely impaired production of infectious virions, with a decrea
237 icating a possible mechanism contributing to impaired proliferative capacity of M. tuberculosis-speci
242 We have investigated the pathogenesis of impaired RDD in diabetic rodents exhibiting features of
244 pro-inflammatory activation of macrophages, impaired recruitment and activation of peritoneal fibrob
245 inment in MARCO(-/-) mice was accompanied by impaired recruitment of Ly6C(high) monocytes and monocyt
246 d that the phosphorylation of PTPN12 by CDK2 impaired recruitment of the serine/threonine-protein kin
249 tive efferocytosis and its possible links to impaired resolution in atherosclerosis are incompletely
251 with unrestrained fibroblast proliferation, impaired scar remodeling, reduced fibroblast-derived col
253 paired spatial tuning of neural activity and impaired sparse coding of information, and deficits in t
254 lope of the "inverted-U" input-output curve, impaired spatial tuning of neural activity and impaired
255 assium chloride cotransporter expression and impaired spinal gamma-aminobutyric acid type A receptor
257 to the DeltaICP0 HSV-1 is in part due to an impaired STING pathway.IMPORTANCE The DNA sensor STING p
261 elated and non-combat related mental stress, impaired sympathetic and cardiovagal baroreflex sensitiv
262 atric disorders including cognitive decline, impaired synaptic plasticity, reduced sociability, hyper
263 ficiency (SCID) is characterized by severely impaired T-cell development and is fatal without treatme
264 rneurons, even transiently during the delay, impaired task performance, primarily by increasing inapp
266 the organ of Corti and the vestibular organ, impaired terminal differentiation manifests as immature
270 ir spatial learning or retrieval per se, but impaired the ability to follow changing spatial rules.
271 Gi-DREADDs in the basolateral amygdala (BLA) impaired the acquisition of both conditioned fear extinc
272 Conditional deletion of T-bet from B cells impaired the formation of germinal centers and mitigated
273 The absence of functional PNPLA1 in mice impaired the formation of omega-O-acylceramides and led
274 Mutations in ARTEMIS-deficient patients impaired the interaction with the C terminus and also af
275 Hyperglycemia and hyperinsulinemia also impaired the PI3K/Akt while enhancing the ERK/p38MAPK/JN
276 netic ablation of sensors of apoptotic cells impaired the proliferation of tissue-resident macrophage
278 However, despite conscious access being impaired, the ability to decode the presence of integrat
279 xtensive long-term culture-induced MSC aging impaired their osteogenic ability and subsequent bony ca
283 atures between patients in XP subgroups with impaired transcription coupled nucleotide excision repai
287 sm in ECs did not cause energy distress, but impaired tricarboxylic acid (TCA) cycle anaplerosis, mac
288 n, increased SOCS-1 expression, and severely impaired tTreg cell development in embryos, adults, and
290 , activation of AMPK signaling in muscle was impaired under starved conditions, while mTORC1 signalin
292 unx3 deficiency limited clonal expansion and impaired upregulation of cytotoxic molecules in TEFF cel
300 sed gene expression, and both mechanisms are impaired when TET2 and nuclear factor kappaB are downreg
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