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1 terature received the moniker "The Forgotten Ventricle".
2 The Impella unloads the left ventricle.
3 tal heart tissue with an underdeveloped left ventricle.
4 KE was quantified in the left and right ventricle.
5 he anterior SHF results in hypoplastic right ventricle.
6 the left ventricle (LV) becomes the systemic ventricle.
7 saligned, resulting in a double outlet right ventricle.
8 lumes of elevated velocity (EVV) in the left ventricle.
9 ocytin injections at the floor of the fourth ventricle.
10 revealed thrombus within the left atrium and ventricle.
11 y arteries to guide their expansion down the ventricle.
12 ac lymphatic vessels fail to expand onto the ventricle.
13 s adjacent to the anterior wall of the third ventricle.
14 e processes from a distant part of the third ventricle.
15 -reservoirs to the frontal horn of a lateral ventricle.
16 (ER) stress, and apoptosis in diabetic left ventricle.
17 ing a standard, 17-segment model of the left ventricle.
18 pendyma of the adjacent surface of the third ventricle.
19 ems from the anterolateral part of the third ventricle.
20 oding the 3-dimensional geometry of the left ventricle.
21 ed cardiomyocyte nuclear density in the left ventricle.
22 LV fibroblasts nor cardiomyocytes of either ventricle.
23 art Association 17-segment model of the left ventricle.
24 dicating the systolic force generated by the ventricle.
25 he bottom and the lateral walls of the third ventricle.
26 ss well understood in patients with a single ventricle.
27 chromatin interaction data from LA and left ventricle.
28 C-PBR28 SUVR calculated using the WB without ventricles.
29 e atrioventricular node and the fascicles or ventricles.
30 ted markers, in the developing mouse cardiac ventricles.
31 mpairment, thin corpus callosum and enlarged ventricles.
32 1 positive microglia surrounding the lateral ventricles.
33 cast that showed the shape and extent of the ventricles.
34 rves do not converge on the lateral or third ventricles.
35 affects synchronized contraction of the two ventricles.
36 ed studies of the skull, brain, and cerebral ventricles.
37 the surface of the inflow tract to reach the ventricles.
38 f the cerebrospinal fluid (CSF)-filled brain ventricles.
39 cilia beat in multiciliated cells from brain ventricles.
40 ers and ~5000 enhancers active in human left ventricles.
41 y promoter and enhancer regions used in left ventricles.
42 cipital cortex, and whole brain (WB) without ventricles.
43 white matter (26 mL; P < .001), mean lateral ventricles (2.2 mL; P < .001), and mean summated brain a
44 - 1.06 vs 15.88 +/- 0.81; p < 0.05) and left ventricles (20.14 +/- 1.40 vs 14.17 +/- 1.53; p < 0.05).
45 queductal, 32.7% periependymal along lateral ventricles, 3.4% large hemispheric, 6.0% diencephalic, 4
48 A specialized neurogenic niche along the ventricles accumulates millions of progenitor cells in t
49 d the implantation of eMSCs into the lateral ventricle activated relevant pathways associated with th
51 s physiological mechanism protects the right ventricle against acute changes in preload, and its impa
58 derlie hypokalemia-induced arrhythmia in the ventricle and atrium but also vary between atrial myocyt
59 xpressed in the cardiac outflow tract, right ventricle and atrium, pharyngeal mesoderm, peripheral ne
60 tion cohort, cardiac MRI mPAP model 1 (right ventricle and black blood) was defined as follows: -179
62 function has lagged behind that of the left ventricle and historically, the RV has even been referre
63 been viewed as less important than the left ventricle and in contemporary literature received the mo
64 e between occipital horn of the left lateral ventricle and internal surface of the cranium and third
66 natomical analysis suggested greater lateral ventricle and putamen volume in duplication carriers.
67 contact the cerebrospinal fluid in the third ventricle and send processes into the hypothalamic paren
69 ght atrium (synchrony), or for 2 weeks right ventricle and then 2 weeks normal sinus (resynchronizati
70 SHR capillary density is increased in both ventricles and at all ages, including before the onset o
72 inal fluid (CSF) is produced in the cerebral ventricles and circulates within the subarachnoid space
73 progressive enlargement of lateral and third ventricles and deceleration of ciliary beating on ependy
74 ent animals, and new PVS connections between ventricles and different parts of the brain parenchyma w
77 tionship between K(+) channel mRNA levels in ventricles and peripheral blood mononuclear cells and th
78 and brain tissue (P = 0.004) to the lateral ventricles and significantly lower (11)C-PiB signal clea
79 the subventricular zone (SVZ) of the lateral ventricles and striatum of mice with genetic deletion (D
81 tical thickness and 34 surface area, lateral ventricles and total intracranial volume measures separa
83 hypoplasia of the corpus callosum, enlarged ventricles, and decreased thickness of the somatosensory
86 fied the choroid plexus of the mouse lateral ventricle as the major source of miR-204 that is release
87 revealed suggesting a possible role for the ventricles as a source or sink for solutes in the brain.
89 the pulmonary vascular system and the right ventricle, as well as their coupling, as important conce
91 glucose transporter 4 expression in the left ventricle at 8 d after TAC, indicating altered glucose m
92 brain and hippocampal volume, and sulcal and ventricle atrophy using nested multivariate regression a
94 By 24 hpf, embryos expressed ttpa in brain ventricle borders, which showed abnormal closure in E- e
95 ed fractions from syndecan-4(-/-) mouse left ventricles but increased nuclear MLP when syndecan-4 was
96 induce locomotion when injected in the brain ventricles but to inhibit fictive locomotion when bath-a
97 ft ventricular cavity, myocardium, and right ventricle by processing an incoming time series of perfu
100 xosome treatment significantly improved left ventricle cardiac function, inhibited cell apoptosis, re
101 function in myocardial repair, improved left ventricle cardiac function, reduced MI scar size, and en
102 us, and amygdala volumes and greater lateral ventricle, caudate, and accumbens volumes (Cohen's d val
103 interrogate these functions in adult lateral ventricle ChP in whole-mount explants and in awake mice.
107 circulation in neonatal patients with single ventricle congenital heart defects, but this complex pro
108 innate abnormalities associated with single-ventricle congenital heart disease exposes these patient
109 on; isolated lung, upper torso, direct right ventricle contrast injection, and whole body with partia
110 ablation and 5 with structurally normal left ventricles (controls) undergoing premature ventricular c
111 ograft (right and left atria, right and left ventricles, coronary arteries) compared to the native re
112 conduction delay in RVOT, but not RV or left ventricle, correlated to the degree of J-ST point elevat
113 f encapsulated MSCs (eMSCs) into the lateral ventricle counteracted depressive-like behavior and enha
114 shown that CSF flow within and across brain ventricles depends on cilia motility of the ependymal ce
115 e (SV) at 12 weeks of age and decreased left ventricle diastolic volume with subsequent reduced SV co
117 al valve disease and may develop as the left ventricle dilates or remodels or as a result of leaflet
120 sence of periependymal lesions along lateral ventricles discriminated neuromyelitis optica patients i
121 SCPC was performed for palliation of single ventricle disease who underwent chest MRI between July 2
122 ior horn width of the right and left lateral ventricle, distance between occipital horn of the left l
124 , and maximum rate of pressure change in the ventricle (dP/dt(max) ), as well as energy utilization a
127 ion, followed by 4 weeks pacing at the right ventricle (dyssynchrony), right atrium (synchrony), or f
129 there was a significant improvement in left ventricle ejection fraction from 30+/-11% to 42+/-15%.
130 y disease, a reduction in the estimated left ventricle epicardial volume correlated with a loss of pu
131 in the critical tasks of segmenting the left ventricle, estimating ejection fraction and assessing ca
132 t the implantation of eMSCs into the lateral ventricle exerted antidepressant effects likely acting v
133 ients had significant enlargement of lateral ventricles (F(1,59) = 48.89; p < 0.001) and reduction of
134 infused in vivo into the CSF-filled lateral ventricle followed by ex vivo high-resolution MR imaging
138 active, or anatomical properties of the left ventricle for reproducing measured patient phenotypes.
139 ction of right ventricular diameter as right ventricle free wall thickness was increased and an incre
141 ing cells to ependymal regions bordering the ventricles from the forebrain to the hindbrain, and obse
142 istomicrograph of transverse sections of the ventricles from the Mb group did not show abnormalities.
143 cardiac fibrosis response and preserves left ventricle function as compared to control-exosome admini
144 t disease are more likely to experience left ventricle function recovery with successful AF ablation.
146 centric myocardial hypertrophy, altered left ventricle geometry, perturbed systolic and diastolic fun
148 turbances, thin corpus callosum, and widened ventricles); global delay with significant alteration of
149 siological properties in failing human heart ventricles have not been examined for a circadian expres
150 fects [ASD], aortic arch defects, and single-ventricle heart) and subgroups of specific heart defects
151 counts, pulmonary vessel density, and right ventricle hypertrophy (RVH).Measurements and Main Result
152 e stress allowed myocardial energetics, left ventricle hypertrophy, and diastolic dysfunction to reco
154 reduced inflammatory parameters in the left ventricle (IFN-gamma, IL-6, and IL-1beta), as well as in
156 wed a hypodense area in the apex of the left ventricle in a 57-year-old man with a history of anterio
157 n (EF), were measured for the left and right ventricle in both end-expiration and end-inspiration.
161 crest contribution to cardiomyocytes of the ventricles in Gallus gallus, supported by Wnt1-Cre linea
162 Infusion of neurotensin into the fourth ventricle induced NREM sleep-like cortical activity, whe
166 r cell, which strongly correlated to that in ventricles, inversely associated to CRP and IL (interleu
167 farction border zone and in the hypertrophic ventricle, involving regulatory sequences proximal to Np
168 at irregular deposition of Sspo within brain ventricles is associated with idiopathic-like scoliosis
170 brillation(AF) while amyloid deposits in the ventricles is increasingly being diagnosed in patients w
171 phalus (CH), characterized by enlarged brain ventricles, is considered a disease of excessive cerebro
172 ved in fibrosis and adhesion, whereas in the ventricles, it controlled inflammation and endocytosis.
173 on the body surface, coronary sinus and left ventricle leads, requires a delivered charge of 0.04+/-0
174 em cell-derived SAN-like pacemaker cells and ventricle-like cells and identified thousands of putativ
175 ned for the investigated organs (brain, left ventricle, liver, and muscle) due to different animal ha
176 men including, at least partly, cardiac left ventricle, liver, spleen, and kidney (n = 2) or three 10
177 mal, parotid, and submandibular glands; left ventricle; liver; spleen; kidneys; bowel; urinary bladde
181 usion alone, mechanically unloading the left ventricle (LV) before reperfusion reduces infarct size a
182 When remodeling and enlargement of the left ventricle (LV) cause annular dilatation and tethering of
184 palmitate can, at least in part, offset left ventricle (LV) dysfunction in hearts from diabetic mice,
185 c MRI data included segmentation of the left ventricle (LV) in cardiac MRI perfusion and cardiac MRI
192 entricle (RV) does not respond like the left ventricle (LV) to guideline-directed medical therapy of
194 he transcriptional profile of the human left ventricle (LV, n=4) and right ventricle (RV, n=4) after
196 ation did not increase cAMP in USP20-KO left ventricles (LVs), whereas NKH477-induced adenylyl cyclas
197 s bind differently to syndecan-4 in the left ventricle lysate from aortic-banded heart failure (ABHF)
198 on of the immune cell population in the left ventricle manifested by lowered abundance of proinflamma
200 Lower MFR was associated with higher left ventricle mass index and higher left ventricle volumes b
201 (mean % change +/- SE = 13.3 +/- 1.9), third ventricle (mean % change +/- SE = 10.4 +/- 1.1), and the
202 torial ventricular structures, i.e., lateral ventricle (mean % change +/- SE = 13.3 +/- 1.9), third v
203 +/- SE = 7.7 +/- 1.6; P = 0.0009), the third ventricle (mean % change +/- SE = 4.7 +/- 1.3; P = 0.006
204 residual increases in volume for the lateral ventricle (mean % change +/- SE = 7.7 +/- 1.6; P = 0.000
205 .001) and ratio of scar volume to total left ventricle myocardial volume (%LGE) (r = 0.91, P < .001).
207 cribing myocyte orientations) of healthy rat ventricles-obtained using diffusion tensor imaging at 10
209 serelaxin's antifibrotic actions in the left ventricle of mice with cardiomyopathy, indicating that c
210 ression was significantly suppressed in left ventricle of mice with transverse aortic constriction-in
211 CaM-M37Q, into the anterior wall of the left ventricle of RyR2 wild type or mutant mouse hearts.
212 Fibroblasts were isolated from the left ventricle of the explanted hearts of transplant recipien
213 xenon dissolved in the blood inside the left ventricle of the heart, it is possible to directly measu
215 RT2104) is injected into the mPFC or lateral ventricle of wild-type mice, it reverses chronic unpredi
216 implanted epicardially on the right and left ventricles of a porcine model and were inductively power
217 itude of (11)C-PiB PET signal in the lateral ventricles of an independent group of Alzheimer and mild
219 s show a circadian expression pattern in the ventricles of failing human hearts, which may underlie a
220 s the distribution of CM size throughout the ventricles of intact mouse heart, in which cells in the
222 e alpha(1C) I-II loop, which is increased in ventricles of patients with end-stage heart failure, inc
223 cells divide in the ventricular zone at the ventricles of the embryonic brain, self-renew and genera
227 adaptive atlas algorithm to segment the left ventricle on CAC-CT, extracting 107 radiomics features f
230 y and late remodelling of the left and right ventricle over the course of monocrotaline-induced PAH t
231 11)C-PiB signal clearance out of the lateral ventricles (P = 0.002) in Alzheimer subjects than in hea
232 ation in stellate ganglia (p = 0.02) but not ventricles (p = 0.2) of PVC-CM and recovered animals ver
233 ay severe OFT and RV hypoplasia and a single ventricle phenotype due to decreased proliferation of Se
236 ior horn width of the right and left lateral ventricle, posterior horn width of the right and left la
237 tance 1.5[2.2, 0.9] WU, and transmural right ventricle pressure 10[15, 6] mmHg during exhalation.
238 P(PL) demonstrated unchanged transmural left ventricle pressure and systemic blood pressure after LRM
239 ds and Results We used a mouse model of left ventricle pressure overload coupled to in vitro studies
241 econd model, cardiac MRI mPAP model 2 (right ventricle pulmonary artery), which excludes the black bl
245 ofiles are associated with aorta dilatation, ventricle remodeling, aneurysms, and development of athe
247 ol, 14.6 ng) ouabain into each lateral brain ventricle results in increased locomotor activity, stere
249 e and function in children with single right ventricle (RV) anomalies may be influenced by shunt type
252 rioration, specifically a reduction in right ventricle (RV) ejection fraction and stroke volume (SV)
253 orated into a patient-specific silicon right ventricle (RV) emulating severe FTR, on which Kay repair
255 recognition of the crucial role of the right ventricle (RV) in determining functional status and prog
257 as those with tetralogy of Fallot, the right ventricle (RV) is subject to pressure overload stress, l
258 ionale: Remodeling and fibrosis of the right ventricle (RV) may cause RV dysfunction and poor surviva
259 o confirm HB capture/exclude that only right ventricle (RV) myocardial septal pacing is present.
260 unction and structure were assessed in right ventricle (RV) myocardium collected from patients with R
263 odelling of the pulmonary arteries and right ventricle (RV), which leads to functional decline of car
265 the human left ventricle (LV, n=4) and right ventricle (RV, n=4) after 0, 4, and 8 hours of cold stor
266 Patients with systemic morphological right ventricles (RVs), including congenitally corrected trans
268 ook transcriptome analysis of human DMD left ventricle samples and found that DMD hiPSC-derived cardi
270 caques had persistent enlargement of lateral ventricles, smaller volumes and altered functional conne
271 HD were categorized into those with a single ventricle (SV) or two ventricles (TVs) and those with ao
273 oblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal musc
274 te administration of liraglutide into fourth ventricle, the area with easy access to the AP and NTS,
275 and cell contractility specific to the right ventricle; these changes could explain the lower cardiac
276 d we also find that LBBB will cause the left ventricle to contract later than the right ventricle, wh
277 oxygenated blood is delivered from the left ventricle to end organs with each cardiac cycle (200 mil
278 to those with a single ventricle (SV) or two ventricles (TVs) and those with aortic obstruction (AO)
279 we compared well and poorly healing cardiac ventricles using a transgenic fish model that exhibits h
280 e close relationship between the RV and left ventricle (ventricular interdependence) and its coupling
281 y matter and amygdala volume, larger lateral ventricle volume, and lower structural connectivity in p
282 er left ventricle mass index and higher left ventricle volumes but not with ejection fraction or dias
284 aller hearts compared to males, with thinner ventricle walls and more mononucleated cardiomyocytes.
287 magnitude of (11)C-PiB signal in the lateral ventricles was calculated as area under the curve from 3
290 is greater than 25% of the perimeter of the ventricle, when the width is approximately half that of
291 t ventricle to contract later than the right ventricle, which in turn affects synchronized contractio
292 d-contacting DA nuclei surrounding the 3(rd) ventricle, which lack distal projections outside of the
293 lly and functionally different from the left ventricle, which precludes direct extrapolation of our k
294 lity of the ependymal cells lining the brain ventricles, which play a crucial role to maintain patenc
295 nd internal surface of the cranium and third ventricle width depending on the severity of leukoaraios
296 deos, our model accurately segments the left ventricle with a Dice similarity coefficient of 0.92, pr
299 animals developed dilated and hypertrophied ventricles with preserved systolic functions due to comp
300 and nodoventricular AP appear to connect the ventricles with the CS musculature in the region of the