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1 erms and tended to be retained in evolution (stasis).
2 s- or aberrant signaling-induced senescence (stasis).
3 (P<0.043) reduced LA velocities and elevated stasis.
4 es with WFI is associated with a low rate of stasis.
5  fibril growth are interrupted by periods of stasis.
6 biology, would evidence extreme evolutionary stasis.
7  ascending slopes and hence, escape adaptive stasis.
8 n in critical illness due in part to gastric stasis.
9  though unmodified oxyhemoglobin exacerbated stasis.
10 osts and was not maintained in environmental stasis.
11 ies of steps followed by periods of relative stasis.
12 te, and the eukaryote, is often symbiosis or stasis.
13 o hypoxia, inflammation, and lymphatic fluid stasis.
14 urst of diversification followed by extended stasis.
15 ures (e.g. ribosomal dimers) upon entry into stasis.
16 icularly when characterized by morphological stasis.
17 ignore the growth arrest signals produced by stasis.
18 ventually leading to a paucity of genes, and stasis.
19  suggesting a persistence mechanism via cell stasis.
20 hich has been shown to mediate microvascular stasis.
21 er time to cause morphological evolution and stasis.
22 amma-mediated activation of p21-induced cell stasis.
23 nd anorexia associated with gastrointestinal stasis.
24 cence-associated beta-galactosidase-positive stasis.
25 f both pathways is required to achieve tumor stasis.
26 indicate a remarkable degree of evolutionary stasis.
27  mechanisms proposed to explain evolutionary stasis.
28 ided nearly equally between random walks and stasis.
29 models: directional change, random walk, and stasis.
30  less likely than shape traits to experience stasis.
31  TAE and TRIP MR imaging were repeated until stasis.
32 zed form of cell cycle arrest termed S-phase stasis.
33 pansions interspersed among periods of range stasis.
34 may improve bile flow and reduce gallbladder stasis.
35 ion in different cell types does not promote stasis.
36 , recurrent UTI, hypercalciuria, and urinary stasis.
37 are advantageous in periods of environmental stasis.
38 ludge-filled gallbladder, suggestive of bile stasis.
39               Bacterial ribosomes never left stasis.
40 er the first week of treatment before tumour stasis.
41 mammals is a classic example of evolutionary stasis.
42 contribute to the occurrence of evolutionary stasis.
43 duce thrombosis risk because of reduced flow stasis.
44 lution with niche conservatism and long-term stasis?
45 /kg QD is well tolerated and results in near stasis (92% TGI) in an HCT116 mouse xenograft model.
46 eding head injury is associated with gastric stasis, a symptom of collapse of autonomic control of th
47                                       Venous stasis activated fibrinolysis, measured by D-dimer level
48         We conclude that experimental venous stasis activates the fibrinolytic system to block the de
49                         The ribosome entered stasis after LUCA and remained in that state for billion
50                                     Cellular stasis, also known as telomere-independent senescence, p
51 flow in the normal range: 25%/68% for LA/LAA stasis and 38%/60% for LA/LAA peak velocities.
52 ing to ASL dehydration, which promotes mucus stasis and a failure of mucus clearance, leaving smokers
53 itrergic pyloric inhibition leads to gastric stasis and bezoars.
54 protein-folding reservoir might promote both stasis and change.
55                             HMEC that escape stasis and continue to proliferate become genomically un
56  to maintain their organization and to avoid stasis and death.
57  prothrombotic milieu characterized by blood stasis and endothelial dysfunction.
58  the range edge, from rapid spread to border stasis and even retraction, highlight future opportuniti
59 ting TLR4 dependency, UP-LPS-induced gastric stasis and ileus of TLR4(WT) mice were absent in mutant
60 in causing functional UP-LPS-induced gastric stasis and ileus.
61 by approximately 2 and 5 logs, compared with stasis and in the vehicle-treated control, respectively.
62 node (RPLN) metastases that may cause venous stasis and increase the risk of VTE development.
63 ng lymphatic network expansion reduces lymph stasis and increases clearance of fluid and cells, inclu
64 volume, which is predicted to initiate mucus stasis and infection.
65                            Relative arterial stasis and near abolition of t-PA release will strongly
66 oduct carbon monoxide or biliverdin inhibits stasis and NF-kappaB, VCAM-1, and ICAM-1 expression.
67                                     Relative stasis and occasional rapid subclone growth may characte
68  to interact with RAS causes long-term tumor stasis and partial regression.
69 ht be a useful strategy for inducing S-phase stasis and promoting the radiosensitization of checkpoin
70 2 ligand), which increases PMo mass, reduced stasis and SCD associated organ damage.
71            Inhibition of CFTR leads to mucus stasis and severe airway disease.
72  involution occurred in the presence of milk stasis and STAT3 activation, indicating that neither is
73 s in Townes sickle mice exacerbated vascular stasis and tissue damage, whereas treatment with muramyl
74                  Anatomic maps of LA and LAA stasis and velocity were calculated to quantify atrial p
75 ly lead to replication fork collapse, growth stasis and/or cell death.
76             These effects lead to tumor cell stasis and/or death.
77 ns that deplete ASL volume and produce mucus stasis, and (b) potential shear stress-dependent therapi
78            Opiliones epitomize morphological stasis, and all known fossils have been placed within th
79 nd decreases NF-kB activation, microvascular stasis, and mortality in transgenic sickle mouse models.
80 g, respectively, compared with the number at stasis, and only reduced CFUs by approximately 1 log and
81 tial compression devices to minimizes venous stasis, and optimize intravascular volume to minimize th
82 A methylation step coincides with overcoming stasis, and results in few to hundreds of changes, depen
83 abetes, hypertension, hyperlipidemia, venous stasis, and sleep apnea.
84  lipids in M. tuberculosis during growth and stasis, and speculate about how this regulation might af
85  Virchow's triad: hypercoagulability, venous stasis, and vascular damage; together these factors lead
86                                The subgenome stasis, apart from the single-chromosome translocation,
87  the underlying causes of niche lability vs. stasis are poorly understood.
88   We also interpret Stemonitis morphological stasis as evidence of strong environmental selection fav
89 ring a stress-associated senescence barrier (stasis) associated with elevated levels of cyclin-depend
90 d regarding the link between venous valvular stasis-associated hypoxia and thrombosis.
91 R2 ADCs in Founder 5 was observed with tumor stasis at 0.5-1 mg/kg, 1 mg/kg, and 3-6 mg/kg for 6, 8,
92                                        Tumor stasis at 2 mg/kg was observed for anti-CD22 6 in WSU-DL
93 how a remarkably high degree of evolutionary stasis at the levels of nucleotide sequence, gene synten
94 ological staining of CD31 confirmed vascular stasis at various time points post-PDT (post photodynami
95                             The evolutionary stasis between influenza virus and its natural host may
96 n last years, may account for the phenotypic stasis between living Stemonitis species and this fossil
97 ycER via 4-OHT deprivation resulted in tumor stasis but only partial regression.
98 mic intervals are not periods of hemodynamic stasis but, rather, phases with dynamic changes in intra
99 regained aggressive growth after a period of stasis, but interestingly, without re-expression of Delt
100 of these afferents presumably causes gastric stasis by activating downstream NST neurons that, in tur
101 data suggest that S. aureus likely undergoes stasis by protecting selective mRNA with RNA-binding pro
102                            Ependymal ciliary stasis by purified pneumolysin was also blocked by the a
103                      These results show that stasis can be achieved without good levels of adaptation
104 n here allows recognition that morphological stasis can be the dominant evolutionary pattern within s
105 ons in red cell flux, as opposed to vascular stasis, can cause temporal variations in pO2 that extend
106 mpair airway hydration, leading to the mucus stasis characteristic of both cystic fibrosis and CB.
107 r in the microcirculation, it is likely that stasis contributes to thrombotic risk, due in large part
108              Only erythrocyte aggregation at stasis correlated significantly with current CD4+ T-lymp
109 h Red-Queen type of continuous evolution and stasis could result from a model with biotically driven
110                                        Early stasis (defined as slowed antegrade flow, before total v
111                                              Stasis dermatitis (SD) is a common disease in the elderl
112 asia and GERD groups suggesting that luminal stasis does increase biomarker levels for any of the cyt
113 equential CRVO presumably advanced by venous stasis due to decrease in arterial inflow.
114 , coupled with a tendency toward gallbladder stasis (due to the absence of CCK-induced contraction),
115 lies most models for both anomalous climatic stasis during the mid-Proterozoic and extreme climate pe
116                The compounds produced tumour stasis during the treatment period and upon cessation of
117 f viral evolution, with periods of antigenic stasis during which genetic diversity grows, and with ep
118 d, Xenopus laevis tadpoles enter a period of stasis during which neural progenitor proliferation is d
119                                              Stasis DVT demonstrated that the highest FDG signal occu
120 ar veins and also a novel model of recurrent stasis DVT in mice.
121 rwent ligation of the jugular vein to induce stasis DVT.
122 d pathways, and reformulation of the radical-stasis equations.
123        Archaeal ribosomes have remained near stasis, except for the superphylum Asgard, which has acc
124         We examined the relationship between stasis, fibrinolysis, and the development of experimenta
125  provide evidence of over 3,000 y of dietary stasis followed by a decline of ca. 1.8 per thousand in
126 ng with the predominant mode of evolutionary stasis for courtship behavior and morphology.
127 ition of a sophisticated behavioral suite in stasis for over 110 million years and an ancient plant-i
128 s, provide a remarkable case of evolutionary stasis for since the chimpanzee-human split c.8 Ma among
129 sceptibility is commonly ascribed to urinary stasis from elevated residual urine volumes.
130 ing Ulp1 and subsequently affect sumoylation stasis, growth, and DNA repair.
131 rowth of genomically stable multilineage pre-stasis HMEC populations can greatly enhance experimentat
132  the properties of growing and senescent pre-stasis HMEC with growing and senescent post-selection HM
133              Thus, the effects of blood flow stasis, hypercoagulability of blood, and the characteris
134  divergences consistent with the morphologic stasis hypothesis than for a more recent radiation.
135      Analogue 10 demonstrated complete tumor stasis in a Met-dependent GTL-16 human gastric carcinoma
136  deep veins of the lower limb and preventing stasis in a variety of subject groups.
137 an volume, 0.25 mL +/- 0.09) led to complete stasis in all kidneys.
138 es of the initial lead compound led to tumor stasis in an activated B-cell-like (ABC) diffuse large B
139 been associated with increases, decreases or stasis in body size in different populations.
140  Improved understanding of the role of mucus stasis in causing bacterial colonization has led to incr
141 nce and exit limbs into the hernia (n = 17), stasis in clustered bowel (n = 16), densely matted bowel
142  was not generally accompanied by decline or stasis in cropland area at a national scale during this
143       Pronounced organism-wide morphological stasis in evolution has resulted in taxa with unusually
144                      This finding of extreme stasis in genome architecture, also reported previously
145 n morphological evolution is associated with stasis in genome evolution.
146       Many putative examples of evolutionary stasis in influenza A virus appear to be due to laborato
147 bility may paradoxically create evolutionary stasis in long-term host relationships.
148 nt is not the primary cause of morphological stasis in Malpighiaceae.
149              A recent hypothesis posits that stasis in mammalian presacral count is due to stabilizin
150 changes in presacral vertebral number led to stasis in mammals that rely on dorsomobility of the spin
151 ortant general question is whether long-term stasis in morphological evolution is associated with sta
152 cantly attenuates heme-induced microvascular stasis in mouse models of VOC.
153          This negative-feedback loop imposes stasis in neuroectoderm and mesendoderm differentiation,
154 d by PRL in mammosphere cultures and by milk stasis in nursing dams, suggesting that the gene is cont
155 ion can produce broad spectrum tumour growth stasis in ovarian cancer xenograft models during continu
156 istaltic contractions resulted in esophageal stasis in patients with GERD or SERD.
157     This exposure does not achieve bacterial stasis in pneumonia models.
158          In addition, TSA prevented vascular stasis in sickle mice, it exhibited activity as an iron
159 -kB activation and H/R-induced microvascular stasis in sickle mice.
160 e (CO) or biliverdin, inhibits microvascular stasis in sickle mice.
161  in all nonhematopoietic cells, also reduces stasis in sickle mice.
162 inhibition by tin protoporphyrin exacerbates stasis in sickle mice.
163 and adhesion molecules that promote vascular stasis in sickle, but not in normal, mice in response to
164 dhesion molecules and promotes microvascular stasis in sickle, but not normal, mice in response to hy
165      Abnormal changes in flow are evident by stasis in the left atrium, and seen as spontaneous echoc
166 evelopment of the upright posture and venous stasis in the lower extremities.
167 t harvestmen implies extensive morphological stasis in the order.
168                                     Apparent stasis in the size of a sexually selected trait thus mas
169 1 and inhibits hypoxia/reoxygenation-induced stasis in the skin of sickle mice.
170 ambrian Stages 3-5 - revealing morphological stasis in the wake of the Cambrian explosion.
171 The multipeak landscape imposes evolutionary stasis, in which control systems resist invasion by incr
172                                   Effects of stasis-induced deep vein thrombosis and fibrinolysis on
173                             We established a stasis-induced DVT model in murine jugular veins and als
174                                In a model of stasis-induced thrombosis created by ligation of the inf
175 brinolysis by alpha2AP appears essential for stasis-induced thrombus development, which suggests that
176  that it is punctuated, with long periods of stasis interspersed by sudden gains or losses of multipl
177         As in previous studies, we find that stasis is common in the fossil record, as is a strict ve
178 variation in microsporogenesis, and that the stasis is likely to be due principally to selective pres
179  account for radiation despite morphological stasis is that although selection on pollinator efficien
180            One possible explanation for this stasis is that there are genetic or developmental constr
181                           The first barrier, stasis, is mediated by the retinoblastoma protein and ca
182 by cultured HMEC in which the first barrier, stasis, is retinoblastoma-mediated and independent of te
183                                         Flow stasis leads to acute endothelial dysfunction and apopto
184 n and inhibits hypoxia/reoxygenation-induced stasis, leukocyte-endothelium interactions, and NF-kappa
185             Historically attributed to blood stasis, little is known about the adverse effects of ele
186                         Despite the apparent stasis, mass was associated with weather across the prev
187                     Fossil data suggest that stasis may be a common mode of evolution, while modern d
188 ctive programs, and that this consequence of stasis may be a target for pharmacological modulation.
189                   Nevertheless, evolutionary stasis may occur for traits involved in social interacti
190 y and hydraulic traits, despite evolutionary stasis, may have enabled adaptation to a wide range of e
191                                      Using a stasis model of DVT in the mouse, we investigated the ro
192                                    Using the stasis model of venous thrombosis and resolution in mice
193                                Using a mouse stasis model of VT, we found that gal3bp and gal3 were l
194                 No phenotype in the complete stasis model was observed.
195 ncreased thrombus formation in a mouse blood stasis model.
196  (n = 2), recurrent UTI (n = 2), and urinary stasis (n = 2).
197  of digestion manifested as gastrointestinal stasis, nausea, and emesis associated with illness.
198 ogical patterns, including the prevalence of stasis, need not be inconsistent with adaptive evolution
199 ional relationship between melanocyte growth stasis, nevus biology, and fibrogenic signaling was furt
200   We test whether the long-term evolutionary stasis observed for pollen morphogenesis (microsporogene
201 l artery of the right kidney until capillary stasis occurred.
202 slowed antegrade flow, before total vascular stasis) occurred in 12 of 154 (7.8%) radioembolization p
203         In the absence of TGR5, intrahepatic stasis of abnormally hydrophobic bile and excessive infl
204             Loss of contractility leading to stasis of blood flow following left atrial appendage ele
205 nct gills and a stalk, suggests evolutionary stasis of body form for approximately 99 Myr and highlig
206                               The subsequent stasis of ingested food not only leads to symptoms of dy
207  VWAK and FYAK after onset of disease led to stasis of its progression and suppression of histopathol
208 n, may have contributed to the ~700,000 year stasis of the Oldowan technocomplex, and (ii) teaching o
209                                              Stasis of venous blood triggers deep vein thrombosis by
210 enced early increases followed by periods of stasis often lasting tens of millions of years.
211 (2) ascertaining if the consequences of cold stasis on the hepatic endothelium can be pharmacological
212 g a stable toxin protein that can cause cell stasis or death, another encoding a labile antitoxin pro
213  contrast, venous thrombosis is dominated by stasis or depressed flows, endothelial inflammation, whi
214 spheres thus may be more suitable when early stasis or reflux is a concern, in the setting of hepatoc
215 zed with anti-VEGFA treatment to cause tumor stasis or regression.
216 alpha inhibition resulted in transient tumor stasis or tumor regression, and inhibiting HIF-1alpha in
217 otected from thrombosis induced by complete (stasis) or partial (stenosis) flow restriction in the IV
218 s where they reside under conditions of near stasis, or to quickly rise towards the surface and erupt
219 shoe crabs, noted for relative morphological stasis over geological time, suggests that genomic diver
220  pheromone delivery system show evolutionary stasis over millions of years.
221 individual gene segments, suggesting genetic stasis over recent years.
222 ified each other, producing a net outcome of stasis over time.
223 trols: increased erythrocyte aggregation, at stasis (P < 0.001) and low shear stress (P < 0.001), inc
224              While the causes underlying the stasis paradox are hotly debated, comprehensive attempts
225                              This so-called "stasis paradox" highlights our inability to predict evol
226                                 Cultured pre-stasis populations contained cells expressing markers as
227 s is steady, or whether there are periods of stasis punctuated by occasional large changes.
228 ith 4D flow-based LA velocities (r=0.41) and stasis (r=-0.39).
229 cused overwhelmingly on three simple models: stasis, random walks, and directional evolution.
230 ggested that the toxin MazF(Sa) induced cell stasis rather than cell death.
231 allows for assays of agents that induce cell stasis rather than death.
232 ugs which are anticipated to result in tumor stasis rather than regression.
233 ased intraabdominal pressure enhances venous stasis, reduces intraoperative portal venous blood flow,
234  dual specificity, LinDYRK1, which acts as a stasis regulator in other organisms.
235 conditions lead to continual evolution or to stasis remains a major challenge.
236 involves inflammation, coagulation, vascular stasis, reperfusion injury, iron-based oxidative biochem
237                                              Stasis represents the consequences of growth conditions
238       The former hypothesis of morphological stasis requires most living platyrrhine genera to have d
239      Congenital IHBDD predisposes to biliary stasis, resulting in intrahepatic lithiasis, septic comp
240 thelial ion transport likely initiates mucus stasis, resulting in persistent airway infections and ch
241 lymphedema specimens, we show that lymphatic stasis results in a CD4 T-cell inflammation and T-helper
242 l neovascular membrane (CNVM; 10,15), venous stasis retinopathy (VSR; 10,2), choroidal infarction (0,
243       All eyes had varying degrees of venous stasis retinopathy and intraretinal edema overlying the
244      We present an impressive case of venous stasis retinopathy in a 10-year-old boy with ocular hype
245                               By now, venous stasis retinopathy in children due to Valsalva maneuver
246 ein, wich are subsumed under the term venous stasis retinopathy, may occur as transient blurred visio
247 alsalva maneuver is a risk factor for venous stasis retinopathy.
248  wild vertebrate populations, and phenotypic stasis seems to be the norm.
249 er gallbladder volumes (predisposing to bile stasis), significant retardation of small-intestinal tra
250 on secondary to gradients of lymphatic fluid stasis stabilizes HIF-1alpha thereafter (3-6 wk).
251 , prolonging survival concomitant with tumor stasis (stable disease).
252  exogenous acute and chronic stress signals (STASIS: stress or aberrant signaling-induced senescence)
253  to genome-wide admixture, mitochondrial DNA stasis supports that this introgression was male-driven,
254                                      Urinary stasis, surgical disruption of urogenital tissues, and a
255 ditions for intraspecific dominance, whereas stasis tends to homogenize the system.
256 oblasts showed greater similarity to HMEC at stasis than at telomere dysfunction, although their gene
257 on directly contributes to the microvascular stasis that causes VOC.
258 the fossil record, as is a strict version of stasis that entails no real evolutionary changes.
259 d by remarkable ecological and morphological stasis that persists to the present day.
260 ly reduced GI motility, culminating in frank stasis that was primarily responsible for decreasing lon
261 A 4-m.y. period of climatic and evolutionary stasis then ensued.
262 P4OX) had little to no effect on H/R-induced stasis, though unmodified oxyhemoglobin exacerbated stas
263 3.1 human prostate xenograft model, inducing stasis throughout the approximately 30-day dosing.
264 years), followed by broad-scale evolutionary stasis throughout the remainder of the Cambrian.
265 irectional change, unbiased random walk, and stasis to a dataset of 635 traits across 153 species lin
266 r view of this period from one of biological stasis to a time of continued high activity levels.
267  elements that reduce shear stress and avoid stasis to reduce the frequent adverse events of bleeding
268 cal interactions, whereas both Red-Queen and stasis type of evolution may result if the ecological in
269 f P multocida via his cat licking the venous stasis ulcers on his legs.
270 ea, obesity hypoventilation syndrome, venous stasis ulcers, intestinal leak, small bowel obstruction,
271 ch clots triggered by inflammation and blood stasis, underlie devastating, and sometimes fatal, occlu
272 of 22 faunas spanning the Holocene documents stasis up to the middle Holocene in all traits studied (
273 ify atrial peak velocity, mean velocity, and stasis (velocities <0.1 m/s).
274 ignificantly between HMEC populations at the stasis versus telomere dysfunction senescence barriers.
275                                Evaluation of stasis via imaging and biomarkers associated with thromb
276 s grown in a serum-free medium that overcame stasis via silencing of p16 expression and that display
277  tail lymphedema model where sustained fluid stasis was generated on disruption of lymphatic flow, re
278 tently lower (by 21%/12%; P<0.001) while LAA stasis was higher (by 58%; P<0.001) compared with the LA
279 f evolutionary processes, we found that this stasis was mostly attributable to a decrease in the fide
280                                     Vascular stasis was not seen in these experiments.
281                                     Complete stasis was observed at 40 mg/kg in the BXPC3 human pancr
282 few to hundreds of changes, depending on how stasis was overcome.
283 r to determine whether other factors promote stasis, we compared the fitness trajectories of populati
284 Examining T-cell recruitment in human venous stasis, we show that superficial varicose veins preferen
285 te of mycobacterial ribosomes during hypoxic stasis, we show that the dormancy regulator DosR is requ
286 ion Bowel abnormalities and gallbladder bile stasis were common findings on abdominal images of patie
287 ntrast, lower LAA velocity and increased LAA stasis were only found in a fraction (38 of 60) of AF pa
288 , mucin hypersecretion likely produces mucus stasis, which contributes to key infectious and inflamma
289 ecretion; reduction of bile flow and biliary stasis, which leads to the development of cholestasis; a
290 l lines, supporting a role of this kinase in stasis, while in stationary growth phase, LinDYRK1(-/-)
291 model, such analytically derived conditions: Stasis will predominantly emerge whenever the ecological
292 hypoxia or nitric oxide results in bacterial stasis with concomitant induction of a 47-gene regulon c
293 bition of PABP1 and SMB methylation and cell stasis with IC50 values in the nanomolar range.
294 icroembolization of atherothrombotic debris, stasis with intravascular cell aggregates, and finally,
295 ns of GS contraction, expansion and relative stasis, with annual diploid species evolving smaller GS
296 desert-soil microbial communities enter into stasis, with limited species turnover, and reactivate ra
297 re required for preservation of regenerative stasis within diverse epithelial tissues.
298 t forward as an explanation for evolutionary stasis within lineages and niche conservatism within cla
299  relative frequency of gradual change versus stasis within lineages.
300  antioxidant treatment blocked heme-mediated stasis, WPB degranulation, and oxidant production.

 
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