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1 intraaortic balloon pump to unload the left ventricle).
2 us, pallidum, putamen, thalamus, and lateral ventricle).
3 cutive patients with VA origins in the right ventricle.
4 of ectopic atrial gene expression within the ventricle.
5 ding along the ventral third into the fourth ventricle.
6 eload, and progressive dilation of the right ventricle.
7 en located in pons and/or adjacent to fourth ventricle.
8 +/-12 ms; P=0.0005) compared with RV or left ventricle.
9 ervals prolongation in the RVOT, RV, or left ventricle.
10 n of ciliated ependymal cells in the lateral ventricle.
11 band is one of the muscle bands in the right ventricle.
12 benefit lung vessels and the remodeled right ventricle.
13 from human donor and heart failure (HF) left ventricle.
14 excitation-contraction coupling in the heart ventricle.
15 n the brainstem, olfactory bulb, and lateral ventricle.
16 otch signaling, resulting in nontrabeculated ventricle.
17 ummation over all slices covering the entire ventricle.
18 ng the structural integrity of the infarcted ventricle.
19 2 (81%) had no antegrade flow from the right ventricle.
20 vement at the inferolateral wall of the left ventricle.
21 posteromedial papillary muscles of the left ventricle.
22 ulti-scale computational models of the human ventricle.
23 erm ventriculus terminalis (VT) or the fifth ventricle.
24 l heterogeneity of AP repolarisations in the ventricle.
25 action potential repolarization in the human ventricle.
26 localization within the mouse brain-lateral ventricle.
27 ng the aorta, aortic valve annulus, and left ventricle.
28 losum, and enlargement of the third cerebral ventricle.
29 the surface of the inflow tract to reach the ventricles.
30 the subventricular zone (SVZ) of the lateral ventricles.
31 were unremarkable except for mildly enlarged ventricles.
32 expressed in the atria as compared with the ventricles.
33 measured 1-5 mm and 6-10 mm from the lateral ventricles.
34 ients with variable initiation sites in both ventricles.
35 in the CaMKIIdeltac-Tg compared with the WT ventricles.
36 the ependymal cells surrounding the lateral ventricles.
37 eltac-overexpressing (CaMKIIdeltac-Tg) mouse ventricles.
38 chain 7 mRNA expression is detected in left ventricles.
39 ransfer ratio-increases close to the lateral ventricles.
40 ore penetrating more readily into atria than ventricles.
41 terval, -0.58 to -0.31); double-outlet right ventricle, -0.48 (95% confidence interval, -0.87 to -0.1
42 n was highest in complex CHD, such as single ventricle (22.8%) and d-transposition of the great arter
45 CSF) continuously flows through the cerebral ventricles, a process essential for brain homeostasis.
46 ved from neonatal mouse heart left and right ventricles, a total of 45 167 unique transcripts were id
47 ty in 74% of left ventricle and 84% of right ventricle acquisitions and performs better than SSFP in
50 matter junctions, and structures lining the ventricles; all cases of acute blast exposure showed ear
53 ade, as the majority of patients with single ventricle anatomy who have undergone the Fontan operatio
54 MI than placebo-control animals (15.7 g left ventricle and 12.0 g left ventricle versus 22.8 g left v
55 elds good to moderate quality in 74% of left ventricle and 84% of right ventricle acquisitions and pe
56 safe and improved contractility of the left ventricle and atrium in a large animal model of nonische
57 5001 for the Prevention of Remodeling of the Ventricle and Congestive Heart Failure After Acute Myoca
58 from overriding aorta to double-outlet right ventricle and dextro-transposition of the great arteries
59 -differentiating cells that form the initial ventricle and in late-differentiating cells that append
60 ncreased in the infarcted region of the left ventricle and in the circulation of wild-type mice after
61 1 lesion adjacent to the body of the lateral ventricle and in the inferior temporal lobe; or (2) the
62 lobe cortical thickness and greater lateral ventricle and inferior lateral ventricle volumes were se
63 ube (HT), with the FHF contributing the left ventricle and part of the atria, and the SHF the rest of
66 nsmural electrophysiological gradient in the ventricle and provides compelling evidence that genetic
67 dent effects of circulating histones on left ventricle and right ventricle function at clinically rel
72 d ependymal (E1) cells line the walls of the ventricles and contribute importantly to CSF flow throug
73 n transfer ratio was highest adjacent to the ventricles and decreased with distance from them; in opt
74 three types of ependymal cilia in the brain ventricles and demonstrate the involvement of ethanol as
76 al metastatic tumors in the third and fourth ventricles and in the suprasellar region remained stable
78 Phosphorylation of Hsp20 occurs largely in ventricles and is vital for the cardioprotective effects
79 ise primarily to cardiovascular cells of the ventricles and only to few atrial cells (<5%) of the dif
80 protrude into the central canal of the brain ventricles and spinal cord to circulate the cerebral spi
81 euroblasts as they transit along the lateral ventricles and then through the anterior forebrain to th
82 nearly normal electrical activation of both ventricles and thereby avoids ventricular dyssynchrony.
83 s were made at 222 sites (excluding the left ventricle) and compared with measurements from intracard
84 n ischemic pathogenesis, a more dilated left ventricle, and a detectable hs-troponin had lower odds o
85 e commonly present in patients with a single ventricle, and detection of these lesions increases as c
86 iate analysis, weight <4 kg, having a single ventricle, and emergency status were significantly assoc
87 ion of the great arteries, subpulmonary left ventricle, and left ventricular outflow tract (LVOT) con
88 L KCNQ1 mutation and pro-arrhythmia in human ventricles, and establishes partial inhibition of IKs as
89 ntation of global gray matter, white matter, ventricles, and hippocampi was performed by using softwa
91 cular haemorrhage obstructing the 3rd or 4th ventricles, and no underlying pathology were adaptively
94 of the Pnmt(+) cells in the left atrium and ventricle appeared to be working cardiomyocytes based on
97 the pulmonary vascular system and the right ventricle, as well as their coupling, as important conce
98 d in acute stages of inflammation after left ventricle assisted device (LVAD) implantation for patien
99 action coupling is strikingly different from ventricle because atrial myocytes lack a transverse tubu
100 anging from 0 (uptake less than that in left ventricle blood pool) to 4 (diffuse uptake greater than
101 of action potential repolarization in human ventricle can be captured by data from single myocytes w
103 led leftward asymmetry for thalamus, lateral ventricle, caudate and putamen volumes, and rightward as
105 s differed in underlying anatomy (expected 2-ventricle circulation in 60% of PDA stents versus 45% of
106 Multivariable analysis indicated that <2-ventricle circulation status was associated with </=mild
110 -fold more highly expressed in the male left ventricle compared with females in young adult C57BL/6 m
112 at 0.3 nmol perfused into the contralateral ventricle, considerably suppressed the magnitude of CSD
113 conduction delay in RVOT, but not RV or left ventricle, correlated to the degree of J-ST point elevat
114 0.148; P=4.27 x 10(-3)) and enlarged lateral ventricles (d=-0.260; P=3.93 x 10(-5)) in patients.
115 void lesions adjacent to the body of lateral ventricles, Dawson's fingers, T1 hypointense lesions (mu
116 Gene expression studies in Notch-activated ventricles demonstrate upregulation of Purkinje-enriched
117 logical studies on cardiomyocytes from right ventricle demonstrated a shorter action potential durati
118 n parallel, the radial glia that contact the ventricle develop distinct gene expression profile and "
121 hy were able to detect a difference in right ventricle diameter of approximately 10 mm with a sensiti
122 thm analysis during resuscitation, the right ventricle diameter was 32 mm (95% CI, 29-35) in the hypo
125 ession, direct targets of FXR1 in human left ventricle dilated cardiomyopathy (DCM) biopsy samples an
126 uring induction of cardiac arrest, the right ventricle dilated in all groups (p < 0.01 for all).
128 cephalus (PHH), an expansion of the cerebral ventricles due to CSF accumulation following intraventri
130 ally mediated by diseases affecting the left ventricle during follow-up (myocardial infarction [MI],
131 cur in the heart and in particular the right ventricle during WLS, and give an indication of the limi
132 tudies have mostly focused on modeling right ventricle dysfunction or failure and pulmonary artery hy
134 e tracing, we show that the third and fourth ventricle E2 and E3 epithelia originate from the anterio
135 function of the proximal aorta and the left ventricle (eg, aortic arch pulse wave velocity and diste
138 (mean difference: 43+/-22.5 mL), higher left ventricle end-systolic volume (mean difference: 34+/-20.
139 ates the pressure exerted by the contracting ventricle (end systolic pressure) to its volume (end sys
140 g a 64-electrode basket catheter on the left ventricle endocardium and 54 6-electrode plunge needles
142 ndrome, AES is commonly located in the right ventricle epicardium and ajmaline exposes its extent and
143 tensive areas of AES were found in the right ventricle epicardium, which were wider in group 1 (P=0.0
144 e hippocampus or infusion of noggin into the ventricles exerted antidepressant and anxiolytic activit
148 d to quantify the edema-based AAR (% of left ventricle) following ischemic preconditioning (IPC) or c
149 e plane (VP) during segmentation of the left ventricle for SPECT myocardial perfusion imaging (MPI) q
150 tration methods to segment the motion of the ventricle from high resolution 4-D light sheet image dat
153 ulating histones on left ventricle and right ventricle function at clinically relevant concentrations
156 r pacemaker placement included systemic left ventricle (hazard ratio [HR], 2.2; P=0.006) and lateral
160 d: 1) scars involving the subtricuspid right ventricle in 46 patients (group A); and 2) scars restric
161 t IUGR also leads to impairment of the right ventricle in addition to the left ventricle classically
164 etermine whether the absence of subpulmonary ventricle in the Fontan circulation would make patients
166 ltaex13/Deltaex13 mice show enlarged lateral ventricles in the brain as well as impaired working memo
169 on transfer ratio was lowest adjacent to the ventricles, increased over the first 5 mm, and then para
170 duction during development, and in the adult ventricle, injury-induced Notch reactivation initiates g
173 dy was to test the hypothesis that the right ventricle is more dilated during resuscitation from card
174 monary hypertension, the status of the right ventricle is one of the most important predictors of bot
177 ved in fibrosis and adhesion, whereas in the ventricles, it controlled inflammation and endocytosis.
179 prospectively evaluate the accuracy of left ventricle (LV) analysis with a two-dimensional real-time
180 nitor populations that give rise to the left ventricle (LV) and sinus venosus (SV) are still ambiguou
181 hough contributors to remodeling of the left ventricle (LV) have been well studied in general populat
184 ), overactive inflammation remodels the left ventricle (LV) leading to heart failure coinciding with
186 Purpose To determine if excess greater left ventricle (LV) trabeculation is associated with decrease
187 ventricular hypertrophy, a thick-walled left ventricle (LV) ultimately transitions to a dilated cardi
188 Ventricle stenosis and fusion of the lateral ventricle (LV) walls is associated with a massive declin
189 ortic constriction activated FYN in the left ventricle (LV), and FYN-deficient mice displayed exacerb
191 g did not reduce final infarct size (9% left ventricle [LV]; interquartile range [IQR]: 3% to 18% vs.
193 was then implemented in a 3-dimensional left ventricle model, demonstrating that such early afterdepo
194 ted arrhythmia dynamics in multi-scale human ventricle models associated with the SQT2-related V307L
197 MIB2, have been found in patients with left ventricle non-compaction (LVNC), we investigated members
203 s were implanted with a cannula in the third ventricle of the brain through which an inhibitor of pho
204 days after in utero electroporation into the ventricle of the developing brain, a dramatically lower
205 sion of 100 ng of HIV-1 Tat into the lateral ventricle of yellow fluorescent protein-expressing trans
209 SOD1 was injected into the cerebral lateral ventricles of neonatal SOD1(G93A) mice, and impact on di
210 ently up-regulated in the atria and the left ventricles of RacET mice on mRNA and protein levels.
211 show that choroid plexus, within the lateral ventricles of the adult brain, secretes signals that reg
212 icroglia, and the ependymal cells lining the ventricles of the brain expressed all three proteins.
213 ronine (T3) in coconut oil into the midbrain ventricle or into the eye, selectively increased tectal
214 urs until clot clearance of third and fourth ventricles) or a combined treatment approach of IVF and-
216 Twenty-eight consecutive patients with left ventricle outflow tract premature ventricular contractio
218 ricular contractions originating in the left ventricle outflow tract represent a significant subgroup
219 entricle, E12 values were lower in the right ventricle (P=0.037) and left ventricular outflow tract (
220 (P<0.001) and higher in left ventricle-right ventricle pairs (P=0.021) and left ventricular epicardiu
227 Newborns with prenatal diagnosis of single ventricle physiology and transposition of the great arte
229 though structural abnormalities of the right ventricle predominate, it is well recognized that left v
231 previous intracardiac repair, systemic right ventricle, pulmonary hypertension, pulmonary regurgitati
232 er to predict lesion depth in right and left ventricle (r=0.47; P<0.0001; multiple regression P=0.002
234 Analysis showed that the volume of the left ventricle receiving 5 Gy (LV-V5) was the most important
235 ood Institute Pediatric Heart Network Single Ventricle Reconstruction Trial public data set was used.
236 rs (losartan) microinjected into the lateral ventricle reduced BP level of HS, but not of Cont group.
241 e IVH with tamponade of the third and fourth ventricles requiring placement of external ventricular d
243 preferentially dysregulated in the atria and ventricles revealed distinct MEF2A-dependent cellular pr
244 r outflow tract (P<0.001) and higher in left ventricle-right ventricle pairs (P=0.021) and left ventr
245 s characterized by echocardiography and left ventricle/right ventricle catheter-derived variables.
247 vals and activation timings across the right ventricle (RV) body, outflow tract (RVOT), and left vent
249 been identified at early stages in the right ventricle (RV) of infants with HLHS, although the molecu
251 (P < .001), larger left (P = .023) and right ventricles (RV; P = .002), and worse RV function (P < .0
252 te matter, callosal volume, and/or increased ventricle size was associated with decreased full-scale
256 "reactive" ependymal cells in aging-related ventricle stenosis; moreover, they also contribute to th
257 formance of Electrodes implanted in the Left Ventricle) study is a prospective multicenter non-random
258 and-upon clot clearance of third and fourth ventricles-subsequent placement of an LD for drainage of
261 compared to our previous report of the left ventricle, suggesting there is likely to be a component
263 ial strain gradient was observed in the left ventricle that showed universal increment from the epica
264 ection from the base to the apex of the left ventricle, there was a trend of decreasing peak systolic
266 f LGE localized at the junction of the right ventricle to the septum was respectively observed in 11
268 in left ventricular (LV) function, the left ventricle undergoes structural remodelling under the inf
269 imaging of tissue taken from the sheep left ventricle using serial block face scanning electron micr
270 we compared well and poorly healing cardiac ventricles using a transgenic fish model that exhibits h
271 imals (15.7 g left ventricle and 12.0 g left ventricle versus 22.8 g left ventricle, respectively).
273 eater lateral ventricle and inferior lateral ventricle volumes were seen in the AC+ participants rela
274 emporal cortex, thalamus, putamen, and third ventricle volumes, consistent with biological heterogene
279 oups at the third rhythm analysis, the right ventricle was larger for hypovolemia than for primary ar
283 hamber sections that covered the entire left ventricle were acquired by using simultaneous multisecti
284 , circumferential, longitudinal) of the left ventricle were analyzed using DRA on steady-state free p
285 le (RV) body, outflow tract (RVOT), and left ventricle were calculated and analyzed at baseline and w
286 ons of interest for TA encompassing the left ventricle were drawn by two blinded, independent readers
288 n the ventral wall of the hypothalamic third ventricle, which is formed by specialized ependymal cell
289 lectrophysiological features of native human ventricle, which, along with specific selection criteria
290 ed subepicardially into the anterobasal left ventricle with 40 to 75 rhythmically contracting embryoi
293 of VA from the papillary muscles of the left ventricle with either cryoenergy or radiofrequency.
294 Three-dimensional tractograms of the left ventricle with no SMS and rate 2 and rate 3 SMS excitati
295 ed by secondary causes and a nondilated left ventricle with preserved or increased ejection fraction.
297 her demonstrated how EF can be maintained in ventricles with increased wall thickness or reduced diam
299 ed hydrocephalus and grossly dilated lateral ventricles, with accumulation of 2-hydroxyglutarate and
300 versus subendocardium in both left and right ventricles, with lower levels in Hey2(+/-) mice compared
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