ライフサイエンスコーパス: outflow

1 to increase aqueous humor drainage (increase outflow).

2 ts are an alternative way to drive molecular outflows).

3 e anterior segments, whereas genipin reduced outflow.

4 e regions critical for maintaining autonomic outflow.

5 n adaptive level of baseline parasympathetic outflow.

6 modulating sympathetic nervous system (SNS) outflow.

7 is indistinguishable from the thoracolumbar outflow.

8 penditure, glucose homeostasis and autonomic outflow.

9 eletal remodeling regulates TM stiffness and outflow.

10 ed with increased muscle tone and thus motor outflow.

11 infrared galaxy hosting a powerful molecular outflow.

12 weak magnetic fields, driving accretion and outflow.

13 tion via the sympathetic and parasympathetic outflow.

14 hrough softening of the meshwork to increase outflow.

15 spaces between cells, allowing greater fluid outflow.

16 changes in its expression alter sympathetic outflow.

17 to increases in ventilation and sympathetic outflow.

18 with strong radiative feedback and powerful outflows.

19 n to produce relatively low-velocity bipolar outflows.

20 sensitivity, bone metabolism and sympathetic outflow; all of these have been implicated in mood disor

21 tricular nucleus (PVN) regulates sympathetic outflow and blood pressure.

22 esponse to manoeuvres increasing sympathetic outflow and by measuring activity-dependent slowing at 2

23 nvestigated and that atrial volume, pulmonic outflow and interventricular septal motion may provide v

24 ecular meshwork is the primary impediment to outflow and its ablation benefits those eyes relatively

25 plays a key role in promoting aqueous humor outflow and maintenance of normal intraocular pressure.

26 this setting should provide adequate venous outflow and minimize the risk of thrombosis and subseque

27 offer the potential to improve aqueous humor outflow and protect RGCs simultaneously, and present new

28 he first evidence for heightened sympathetic outflow and reduced cBRS in RA that can be independent o

29 deep convection also reduces the convective outflow and the anvil cloud fraction.

30 iative feedback; or by the interplay between outflows and inflows.

31 the brain to regulate food intake, autonomic outflow, and endocrine function to maintain energy balan

32 The absorption features produced by these outflows are variable, but no clear link has been found

33 of speed and energy) of these-the ultrafast outflows-are the subset of X-ray-detected outflows with

34 mically rich molecular gas in the form of an outflow, as well as dust.

35 sympathetic nerve activity and noradrenaline outflow associated with hypertension may be primary cont

36 eveal star formation occurring in a galactic outflow at a redshift of 0.0448.

37 ents without obstruction to left ventricular outflow at rest and/or under physiological exercise and

38 r and the angle between the left ventricular outflow axis and aortic root (left ventricle/aorta angle

39 The extent of outflow beds accessed was measured with canalograms.

40 data suggest that episodic, accretion-driven outflow begins in the earliest phase of protostellar evo

41 tion may also be occurring in other galactic outflows, but may have been missed by previous observati

42 rs leads to increases of cardiac sympathetic outflow, cardiac arrhythmogenesis and impairment in card

43 Along the outflow channel, AsSum increased from 5.45 to 13.86 mumo

44 and sediment samples along the hot spring's outflow channel.

45 the sympathetic nervous system into discrete outflow channels that project to well-defined target tis

46 uminous channels, the southern circum-Chryse outflow channels.

47 patic inflow (portal venous blood [PVB]) and outflow compartment (hepatic venous blood [HVB]) of a tr

48 0.08 MPa) pressures and for water inflow and outflow conditions.

49 s asymmetric central influences on autonomic outflow, contributing to cardiac arrhythmia.

50 This outflow could be the high-velocity tail of the neutron-r

51 ld via greater increases in skin sympathetic outflow coupled with an increased reliance on non-adrene

52 ess elicits greater increases in sympathetic outflow directed to the cutaneous vasculature and, corre

53 he protostar reveals 22 distinct features of outflow ejecta, the most recent having the highest veloc

54 t obstruction, unequivocal patterns of focal outflow enhancement by TMB were seen in this training mo

55 We assessed outflow enhancement by trabecular micro-bypass (TMB) imp

56 IOP, consistent with an 2-fold increase in outflow facilities.

57 An increase in outflow facility (decrease in IOP) is demonstrated in a

58 , AAV-mediated expression of MMP-3 increased outflow facility and decreased IOP, and controlled expre

59 TRPV4 inhibition enhanced the outflow facility and lowered perfusate pressure in biomi

60 Nitric oxide signaling alterations in outflow facility and retinal blood flow autoregulation a

61 Outflow facility for phosphate-buffered saline (0.0027 +

62 NAs targeting ZO-1 and tricellulin increased outflow facility significantly.

63 t the stiffer the ECM, the lower the aqueous outflow facility through the TM.

64 antly reduced IOP and improved aqueous humor outflow facility, which was sustained for at least 9 wk.

65 Fbeta2 on transcellular pressure changes and outflow facility.

66 nt, and correlated with reduced conventional outflow facility.

67 Here we report that an outflow from a young, class 0 protostar, at the hub of t

68 We previously demonstrated the SNS outflow from brain to BAT using the retrograde SNS-speci

69 ubglacial systems, and (iii) that predicting outflow from climate models alone, without recognition o

70 C) provide the bulk of resistance to aqueous outflow from the anterior chamber.

71 e communication pathways involve sympathetic outflow from the brain to the peripheral immune system t

72 phic settings, with sites closer to riverine outflow from the east and south of Moreton Bay having hi

73 how that the initial ascent of the meltwater outflow from the ice shelf cavity triggers a centrifugal

74 uscle-rich tissue structure that distributes outflow from the ventricle-prevents epicardial regenerat

75 ionic neurons of the cranial parasympathetic outflow from those of the thoracolumbar sympathetic outf

76 of the turbulent properties of the meltwater outflows from beneath a rapidly melting Antarctic ice sh

77 mmer monsoon of one hemisphere is linked via outflows from the winter monsoon of the opposing hemisph

78 al chemistry associated with Asian pollution outflow, from airborne observations made over the Malays

79 hifted absorption lines must occur in a fast-outflowing gas, whereas the emission lines originate in

80 ear); and 3) post-pump via thrombosis of the outflow graft or stenosis of the anastomosis to the aort

81 the absence of an impaired sinusoidal blood outflow has been so far of unclear significance.

82 es (MMPs) contribute to conventional aqueous outflow homeostasis in their capacity to remodel extrace

83 groundwater budget based on normalized human outflow (hout) and inflow (hin).

84 mm, 95% CI: 1.02-1.18, P=0.015), false lumen outflow (HR 0.999 per mL/min, 95% CI: 0.998-1.000; P=0.0

85 r export of N and P, we monitored stormwater outflow in a residential watershed in Saint Paul, Minnes

86 thalamus is involved in elevated sympathetic outflow in hypertension.

87 from those of the thoracolumbar sympathetic outflow in mice.

88 IOP) via microbead occlusion of ocular fluid outflow in mice.

89 accumulated and thereby curtailed glycolytic outflow in nitrogen-limited yeast.

90 rise of the level of maximum meridional mass outflow in the upper troposphere (200-100 hPa) of the de

91 is enhanced stability reduces the convective outflow in the upper troposphere and decreases the anvil

92 The inferred sBC* shows that Asian outflows in spring bring much more BC aerosols to the mi

93 Recent observations of large-scale molecular outflows in ultraluminous infrared galaxies support this

94 Gas outflows (in the form of disk winds) release huge quanti

95 TMB resulted in an insignificant (p > 0.05) outflow increase of 13 +/- 5%, 14 +/- 8%, 9 +/- 3%, and

96 Increased sympathetic outflow is a major contributor to the progression of chr

97 d other laboratories of PAG control of motor outflow is also discussed.

98 Tonic hyper-activation of sympathetic neural outflow is commonly observed in patients with CHF.

99 By every single one, the sacral outflow is indistinguishable from the thoracolumbar outf

100 The inferred star-formation rate in the outflow is larger than 15 solar masses per year.

101 s with large accretion disks imply that this outflow is probably a fundamental ingredient in regulati

102 energetics of these two types of wide-angle outflows is consistent with the energy-conserving mechan

103 for star formation occurring within galactic outflows is still missing.

104 can be caused by increased resistance to AH outflow, is a major risk factor for open-angle glaucoma.

105 work (TM) plays an important role in aqueous outflow, its anatomy in relation to at-risk populations

106 utflows may ignite star formation within the outflow itself.

107 lack holes of stellar mass launch collimated outflows (jets) of ionized matter that approach the spee

108 nergy detectors, suggesting a single ionized outflow, linking the low- and high-energy absorption lin

109 eductions calculated by comparing inflow and outflow loads may not be relevant at watershed scales.

110 The combined effects of the inflow and outflow maintains a chemical microenvironment, where the

111 eral recent models predict that such massive outflows may ignite star formation within the outflow it

112 We hypothesized that our ex vivo outflow model is sensitive enough to allow computing ind

113 xistence of a mildly relativistic wide-angle outflow moving towards us.

114 s III/IV symptoms than the 324 patients with outflow obstruction (1.6%/year vs. 7.4%/year rest obstru

115 Arterial hypoperfusion secondary to outflow obstruction from a central retinal vein obstruct

116 Stent placement for iliofemoral venous outflow obstruction results in high technical success an

117 ventricular septal defect, left ventricular outflow obstruction, surgery early in the Mustard and Se

118 asculature without evidence of thrombosis or outflow obstruction.

119 patency in patients with iliofemoral venous outflow obstruction.

120 olic displacement into the outflow tract and outflow obstruction.

121 m and ram2 suggested that FatM increases the outflow of 16:0 fatty acids from the plastid, for subseq

122 The outflow of a cytosolic enzyme, lactate dehydrogenase, wa

123 irds, Ipc axons control the ascending tectal outflow of retinal signals through direct synaptic conta

124 final inhibitory control over the integrated outflow of the cerebellar cortex.

125 e OOC surface, and the release of GGT to the outflow of the OOC were evaluated with the fluorescence

126 ant contamination of surface waters from the outflow of water treatment facilities is an issue of gro

127 eveal feedback in the form of galactic-scale outflows of gas in galaxies with high rates of star form

128 glaucoma surgeries that enhance conventional outflow offer a favorable risk profile over traditional

129 shows them as solar wind composition plasma outflowing on open magnetic field lines.

130 nal evidence for star formation triggered by outflows or jets into their host galaxy, as a consequenc

131 Sudden removal of gas through outflows or stripping is one of the mechanisms often pro

132 Theoretical models suggest that these outflows originate as energy-conserving flows driven by

133 uum and the velocity or optical depth of the outflows, owing to the long timescales of quasar variabi

134 potential IOP sensor within the conventional outflow pathway and a novel target for treating ocular h

135 stance-generating region of the conventional outflow pathway and locally liberates a controlled dose

136 ance to its outflow through the conventional outflow pathway comprising the trabecular meshwork (TM)

137 ing that excess NO partially compensates for outflow pathway dysfunction.

138 ed RhoA GTPase activity in the trabecular AH outflow pathway increases intraocular pressure in a Rho

139 terations in morphology of the aqueous humor outflow pathway were observed after treatment with the m

140 argets within the conventional aqueous humor outflow pathway, which is thought to be regulated/dysreg

141 PT ligands in the development of the aqueous outflow pathway.

142 tive gauge of patency through the trabecular outflow pathway.

143 AIT achieved extensive access to outflow pathways beyond the surgical site itself.

144 ming system may have several parallel neural outflow pathways that provide a road map for understandi

145 e (IOP); however, its therapeutic effects on outflow physiology are location- and dose-dependent.

146 -B (Lat-B)-induced actin depolymerization on outflow physiology in live mice.

147 These outflows power prompt, brief and intense flashes of gamm

148 However, the mass outflow rates are found to be insufficient to balance th

149 Treatment with BAPN increased outflow rates in perfused human and porcine anterior seg

150 hase of protostellar evolution, and that the outflow remains intact in a very clustered environment,

151 matrix cross-linking has profound effects on outflow resistance and ECM composition and are consisten

152 respectively, to investigate the effects on outflow resistance and ECM remodeling.

153 trices, which has a direct impact on aqueous outflow resistance and IOP.

154 Outflow resistance changed in graded fashion, decreasing

155 Outflow resistance in the aqueous drainage tract distal

156 meshwork (TM) provides most of aqueous humor outflow resistance in the eye, an in vitro bioengineered

157 Actomyosin contractility modulates outflow resistance of the aqueous drainage tissues and i

158 Resulting outflow resistance was about 10 times lower with 10 muM

159 elivering drugs and simultaneously analyzing outflow resistance was tested in live C57BL/6 mice.

160 C endothelium is an important determinant of outflow resistance, and suggest that SC endothelial TJs

161 chanisms are important to modulating aqueous outflow resistance, mirroring mechanisms in primates.

162 Purpose To investigate whether sinovenous outflow restriction (SOR) is more strongly associated wi

163 dulatory effects of EA on spinal sympathetic outflow result in improved organ perfusion with reduced

164 efects in the anterior chamber aqueous humor outflow structures of the eye result in elevated intraoc

165 by developmental defects in 2 aqueous humor outflow structures, Schlemm's canal (SC) and the trabecu

166 thological processes that affect ventricular outflow, subarachnoid space function, or cerebral venous

167 s did not correlate well with improvement in outflow, suggesting instead that about 30 eyes are neede

168 of aqueous movement through the conventional outflow system.

169 ons have revealed massive galactic molecular outflows that may have the physical conditions (high gas

170 If the gas flow is identified as a genuine outflow then it is in the fastest five per cent of such

171 processes and hydrodynamic resistance to its outflow through the conventional outflow pathway compris

172 cellular bases of increased resistance to AH outflow through the trabecular meshwork in ocular hypert

173 uence of this climate shift, new deep waters outflowing through Gibraltar will impact the North Atlan

174 velopment nor adult form of the conventional outflow tissues according to rigorous quantitative ultra

175 rimentally elevated, cells of the Cav-1(-/-) outflow tissues are more susceptible to plasma membrane

176 ivation increases sympathetic nervous system outflow to skeletal muscle.

177 tral nervous system by dampening sympathetic outflow to the adipose tissue.

178 (SSNA), transduction of this efferent neural outflow to the cutaneous vasculature, and peripheral vas

179 EF rats exacerbated increases in sympathetic outflow to the heart (229.6 +/- 43.2% vs. 296.0 +/- 43.9

180 tworks, influencing in turn sympatho-humoral outflows to the circulation.

181 lmonary left ventricle, and left ventricular outflow tract (LVOT) conduit dysfunction has not been st

182 Cardiac left ventricular outflow tract (LVOT) defects represent a common but hete

183 e mitral valve could reduce left ventricular outflow tract (LVOT) obstruction and associated mitral r

184 (VAs) originating from the left ventricular outflow tract (LVOT) sometimes require catheter ablation

185 (VAs) originating from the left ventricular outflow tract (LVOT) sometimes require catheter ablation

186 (VAs) originating from the left ventricular outflow tract (LVOT), an alternative approach from the a

187 play key roles in development of the cardiac outflow tract (OFT) for establishment of completely sepa

188 Outflow tract (OFT) malformation accounts for approximat

189 ecades, the mechanisms underlying RA-induced outflow tract (OFT) malformations are not understood.

190 In mammals, the outflow tract (OFT) of the developing heart septates int

191 mouse identifies common progenitors for the outflow tract (OFT), LV, atrium and SV but not the right

192 ve rise to the right ventricle and primitive outflow tract (OFT).

193 ght ventricle (P=0.037) and left ventricular outflow tract (P<0.001) and higher in left ventricle-rig

194 act compared with the right-left ventricular outflow tract (P=0.75) pairs.

195 ignaling is required for EMT in the proximal outflow tract (pOFT) but not atrioventricular canal (AVC

196 placed epicardially on the right ventricular outflow tract (RVOT) before video-assisted thoracoscopic

197 atients with postoperative right ventricular outflow tract (RVOT) obstruction or pulmonary regurgitat

198 imings across the right ventricle (RV) body, outflow tract (RVOT), and left ventricle were calculated

199 maximal Doppler velocity in left ventricular outflow tract (VmaxAo) measured using either approach, a

200 ryological context for understanding cardiac outflow tract alignment and membranous ventricular septa

201 lesion, supporting the idea that AHF-derived outflow tract alignment defects may constitute an embryo

202 function in the AHF results in a spectrum of outflow tract alignment defects ranging from overriding

203 Moreover, we found a range of outflow tract alignment defects resulting from a single

204 myocardial movements that are essential for outflow tract and atrioventricular septation.

205 erning of structures formed from NCC such as outflow tract and cranial nerves.

206 acity, regulated by the neighbouring cardiac outflow tract and Hh signalling.

207 preventing MV systolic displacement into the outflow tract and outflow obstruction.

208 second heart field (AHF), gives rise to the outflow tract and the majority of the right ventricle an

209 regulates the signaling processes leading to outflow tract and valve morphogenesis and ventricular tr

210 Thirty-two patients with idiopathic RV outflow tract arrhythmias and 32 control subjects, match

211 nts with ARVC compared with patients with RV outflow tract arrhythmias and controls.

212 arteriosus in basal actinopterygians, to an outflow tract commanded by the non-valved, elastic, bulb

213 o difference in E12 in the right ventricular outflow tract compared with the right-left ventricular o

214 median age, 19 years) with right ventricular outflow tract conduit obstruction or regurgitation.

215 apy for dysfunctional right ventricular (RV) outflow tract conduits.

216 Surgical right ventricular outflow tract cryoablation was performed in 22 patients

217 TOF in 22q11.2DS and may function in cardiac outflow tract development.

218 a mean (SD) follow-up of 6.4 (2.5) years, RV outflow tract dimension increased from 35 mm (interquart

219 The RV size was determined by RV outflow tract dimension, and RV and left ventricular (LV

220 ution involves the transition from a cardiac outflow tract dominated by a multi-valved conus arterios

221 disease patient with right ventricular (RV) outflow tract dysfunction.

222 lation without wall motion abnormalities; RV outflow tract ectopy; and exercise-induced T-wave pseudo

223 inding EGF-like growth factor to Jag1-mutant outflow tract explant cultures rescued the hyperprolifer

224 RV T1 correlated inversely with RV outflow tract gradient (r=-0.28, P=0.02).

225 IVSd was not related to left ventricular outflow tract gradient reduction at rest (P=0.883) or du

226 estent and lower discharge right ventricular outflow tract gradient were associated with longer freed

227 zation data in 162 consecutive patients with outflow tract gradients (median [interquartile range], 9

228 ASA had equal effects on left ventricular outflow tract gradients and symptoms throughout the spec

229 Left ventricular outflow tract gradients are absent in an important propo

230 the anterior subepicardial right ventricular outflow tract in 11 patients (group B).

231 the derived, monovalvar, bulbar state of the outflow tract in modern actinopterygians.

232 As a result, full blood momentum in the outflow tract is used to facilitate early ejection.

233 associated with ascending aortic dilatation, outflow tract malrotation, overriding aorta, double outl

234 activity in the epicardial right ventricular outflow tract may be beneficial in patients with Brugada

235 However, left ventricular outflow tract obstruction (LVOTO) has been traditionally

236 ntly accompanied by dynamic left ventricular outflow tract obstruction and symptoms of dyspnea, angin

237 sk of Ebstein's anomaly (a right ventricular outflow tract obstruction defect) in infants and overall

238 The prevalence of right ventricular outflow tract obstruction defects was 0.60% among lithiu

239 Patients with severe left ventricular outflow tract obstruction had a bisferiens pressure wave

240 tral valve was discovered as the cause of LV outflow tract obstruction in the M-mode echocardiography

241 whereas proximally, severe left ventricular outflow tract obstruction is associated with an addition

242 Left ventricular outflow tract obstruction is present at rest in about on

243 ern was evident, which is associated with LV outflow tract obstruction loss and right ventricle systo

244 ands were younger with less left ventricular outflow tract obstruction than G- probands, however, had

245 ntry, including 249 in whom left ventricular outflow tract obstruction was absent both at rest and fo

246 95% CI 3.60-25.91%), while left ventricular outflow tract obstruction/mid-ventricular obstruction (L

247 ization are present in the right ventricular outflow tract of BrS patients.

248 d connect the dorsal head vasculature to the outflow tract of the heart.

249 In patients referred for left ventricle outflow tract premature ventricular contraction ablation

250 ght consecutive patients with left ventricle outflow tract premature ventricular contraction were inc

251 n evaluated in response to right ventricular outflow tract PVCs with fixed short, fixed long, and var

252 ects in children requiring right ventricular outflow tract reconstruction typically involves multiple

253 conduction slowing in the right ventricular outflow tract region.

254 rs), 32 patients underwent right ventricular outflow tract reintervention for obstruction (n=27, with

255 ntractions originating in the left ventricle outflow tract represent a significant subgroup of patien

256 an isolated subepicardial right ventricular outflow tract scar serving as a substrate for fast VT in

257 Larger preoperative RV outflow tract scar was associated with a smaller improve

258 diac phenotype (119-113 Ma) and suggest that outflow tract simplification in actinopterygians is comp

259 or early primary repair by right ventricular outflow tract stenting (stent).

260 Right ventricular outflow tract stenting of symptomatic tetralogy of Fallo

261 were placed into the right ventricular apex/outflow tract through a subclavian vein puncture with a

262 ng the left ventricle is reversed toward the outflow tract through rotating reversal flow around the

263 la: LVEI=indexed LV end-systolic diameter/LV outflow tract time-velocity integral.

264 irect transcriptional target of MEF2C in the outflow tract via an AHF-restricted Tdgf1 enhancer.

265 00 ventricular extrasystoles (or >500 non-RV outflow tract) per 24 h; and symptoms, ventricular tachy

266 ns (3087 [50%] ventricular bodies, 756 [12%] outflow tract, and 162 [3%] epicardial).

267 y run in parallel along the left ventricular outflow tract, but in the Nkx2-5(+/-)/Sspn(KO) mutant th

268 terior right free wall and right ventricular outflow tract, which increased after flecainide from 17.

269 ection flow velocity in the left ventricular outflow tract, with consequent loss of flow momentum.

270 delay in the anterolateral right ventricular outflow tract.

271 displacement into the left ventricular (LV) outflow tract.

272 al arches and the septation of the heart and outflow tract.

273 locity-time integral of the left ventricular outflow tract.

274 tracellular matrix homeostasis in HDAC3-null outflow tracts and semilunar valves, and pharmacological

275 hose that affect the proper alignment of the outflow tracts and septation of the ventricles are a hig

276 lve replacement in dilated right ventricular outflow tracts, permitting lower risk, nonsurgical pulmo

277 tern blot, and qRT-PCR were performed on the outflow vein at 7 and 21 days after AVF creation.

278 ich were injected into the adventitia of the outflow vein at the time of AVF creation in the MSC grou

279 nd CorMatrix scaffold was wrapped around the outflow vein compared to control mice that received no s

280 termine whether CorMatrix wrapped around the outflow vein of arteriovenous fistula (AVF) at the time

281 Venous neointimal hyperplasia (VNH) at the outflow vein of hemodialysis AVF is a major factor contr

282 ion in cell density and proliferation in the outflow veins treated with CorMatrix compared to control

283 In conclusion, outflow veins treated with CorMatrix have reduced VNH.

284 In outflow veins treated with CorMatrix, there was an incre

285 urce is surrounded by powerful winds with an outflow velocity of about 0.2 times that of light, as pr

286 Results Sinovenous outflow was significantly more restrictive (lower median

287 in the stormwater runoff to 40% in the pond outflow water and DON was less aromatic and had lower ov

288 on of DON in the urban stormwater runoff and outflow water from an urban stormwater retention pond.

289 d lower overall molecular weight in the pond outflow water than in the stormwater runoff.

290 FT-ICR-MS in the stormwater runoff and pond outflow water, which were only 13% different in runoff a

291 which were only 13% different in runoff and outflow water.

292 ins, and tannins in DON from runoff and pond outflow water.

293 pressure, vagal tone and muscle sympathetic outflow were comparable during spontaneous and controlle

294 rganic N (DIN) mass reductions (inflow minus outflow) were greater in the Dry Basin than in the Wet B

295 In particular, black-hole transients have outflows whose properties are strongly coupled to those

296 We find that the outflowing wind is neutral, has a large covering factor,

297 1 increases in a dose-dependent manner urine outflow with concomitant reduction of urine osmolality,

298 re disrupts normal regulation of sympathetic outflow with effects on cardiovascular parameters.

299 approximately 0.03 solar masses) wind-driven outflow with moderate electron fraction (Ye approximatel

300 st outflows-are the subset of X-ray-detected outflows with velocities higher than 10,000 kilometres p