ライフサイエンスコーパス: atrium

1 ed (mean, 2.3+/-0.9 per patient; 72% in left atrium).

2 lation in types III versus I (P=0.02 in left atrium).

3 ctric remodeling in the intact, fibrillating atrium.

4 emodeling in the left ventricle and the left atrium.

5 n vein puncture with a redundant loop in the atrium.

6 ia activation in the previously ablated left atrium.

7 V), which is no longer committed to the left atrium.

8 the sole measure specifically evaluating the atrium.

9 d T-tubules and topography than in the right atrium.

10 obstructed pulmonary venous drainage to left atrium.

11 acing lead positioned in the posterior right atrium.

12 40.2 (n=12) expression ratio of SAN to right atrium.

13 al conduction patterns of the right and left atrium.

14 active gene transcription in the human right atrium.

15 69% reentries and 71% foci were in the left atrium.

16 erformed, which revealed two lesions in left atrium.

17 stabilize the intercalated disc in postnatal atrium.

18 with limited linear ablation within the left atrium.

19 n the dorsal surface of the embryonic common atrium.

20 e DE was detected at the left posterior left atrium.

21 within the ventricle and do not populate the atrium.

22 into the hepatic vein, right atrium or left atrium.

23 nalis/pectinate muscle, pulmonary veins/left atrium.

24 ical impedance of blood in-vivo in the right atrium.

25 to a complete and transmural ablation in the atrium.

26 ions that are selective for the fibrillating atrium.

27 ires simultaneous global mapping of the left atrium.

28 the right coronary artery through the right atrium.

29 ucible boundary between the LAA and the left atrium.

30 ed in the left atrium and 52.2% in the right atrium.

31 homeostasis and electrical stability in the atrium.

32 sets, including 86 axial LGE CMR planes per atrium.

33 hat produce the distinct architecture of the atrium.

34 7 in the right atrium versus 12 in the left atrium; 15 extrapulmonary).

35 ffective refractory period (ERP) in the left atrium (251 +/- 25 ms vs. 233 +/- 32 ms, p = 0.04), and

36 centers (age 63 +/- 10 years; 33 women; left atrium 38 +/- 7 mm; left ventricular ejection fraction 6

37 prolonged electrogram duration in the right atrium (39.7+/-4.2 to 42.3+/-4.3 ms; P=0.01) and right v

38 entricle (127+/-28 vs 83+/-14 mL/m(2)), left atrium (65+/-16 vs 41+/-9 mL/m(2)), and right atrium (78

39 trium (65+/-16 vs 41+/-9 mL/m(2)), and right atrium (78+/-17 vs 56+/-17 mL/m(2); P<0.01 for all).

40 3 pacing stimuli enabled consistent RA-left atrium activation until sinus rhythm was restored.

41 ry veins do not connect normally to the left atrium, allowing mixing of pulmonary and systemic blood.

42 n atrioventricular septal defect or a common atrium along with postaxial polydactyly.

43 The left atrium anatomy (volume, AP diameter), anatomy of the pul

44 ctric rotors, 47.8% were located in the left atrium and 52.2% in the right atrium.

45 ained before venous cannulation of the right atrium and after myocardial reperfusion.

46 atrial fibrillation with methylation in PBL, atrium and artery.

47 significantly higher expressed in the right atrium and atrioventricular node compared with left vent

48 ntials were more often observed at the right atrium and Bachmann's bundle (P<0.001).

49 e cardio-phrenic space, compressing the left atrium and causing medium lobe atelectasis; bilateral pl

50 iesterase (PDE), PDE4, is expressed in human atrium and contributes to the control of electrical stab

51 ctrogram-based catheter ablation in the left atrium and coronary sinus after pulmonary vein isolation

52 rial fibrillation patients with dilated left atrium and hypertension or failed prior atrial fibrillat

53 morpholino injection causes dilation of the atrium and inflow tract and compromised blood circulatio

54 g a highly reproducible boundary between the atrium and LAA needed to obtain LAA metrics useful for p

55 We examined the reference values of left atrium and left ventricle (LV) structure in a large ethn

56 normal position and normal size of the left atrium and left ventricle with a normal ejection fractio

57 ral annulus disjunction (MAD), a larger left atrium and left ventricular end-systolic diameter, and T

58 re and volume, and shortened ERP in the left atrium and PV are potential factors facilitating and per

59 e mapping (EnSite Precision, Abbott) of left atrium and PVs were performed using a conventional circu

60 nd in the nearest atrium (rho=0.96 for right atrium and rho=0.92 for left atrium) and the DF gradient

61 The mean LGE burden for left atrium and right atrium was 23.9+/-1.6% and 15.9+/-1.8%,

62 Left pSHF moves to dorsal left atrium and superior AVC, whereas right pSHF contributes

63 strictly delimited cluster between the right atrium and superior vena cava.

64 progenitors for the outflow tract (OFT), LV, atrium and SV but not the right ventricle (RV).

65 tional and structural parameters of the left atrium and the left atrial appendage which have been sho

66 uced RV function (manifest as a larger right atrium and ventricle and lower RV stroke work index), an

67 kably, many of the Pnmt(+) cells in the left atrium and ventricle appeared to be working cardiomyocyt

68 cardiogram revealed thrombus within the left atrium and ventricle.

69 l input functions were derived from the left atrium and, in the case of (62)Cu-ETS, corrected for par

70 epigenetics in hard-to-access tissues (e.g. atrium) and might enable non-invasive disease screening

71 =0.96 for right atrium and rho=0.92 for left atrium) and the DF gradient between them (rho=0.93).

72 Blood samples were taken from the LA, right atrium, and femoral vein at baseline and at 15 min in al

73 ious H(2)R mutants, at the isolated gp right atrium, and in GTPase assays for activity on recombinant

74 HF contributes to right atrium, ventral left atrium, and inferior AVC.

75 ameter at annulus, right AVV overriding left atrium, and LV width.

76 In guinea-pig left ventricle, left atrium, and right atrium, carbenoxolone increased R(j) b

77 equire careful navigation of the aorta, left atrium, and right heart, including detailed understandin

78 ung, an 18F sheath was delivered to the left atrium, and the left atrial port was closed using an off

79 ery prediction; from 0.39 to 0.95 for PBL-to-atrium; and from 0.81 to 0.98 for lymphoblastoid cell li

80 y the most efficacious, followed by the left atrium-aorta system and the left ventricle-aorta system

81 e, under ventricular fibrillation, the right atrium-aorta system was significantly the most efficacio

82 n arterial pressure comparable with the left atrium-aorta system.

83 ory support systems were compared: (1) right atrium-aorta, extracorporeal membrane oxygenation (n=4);

84 rporeal membrane oxygenation (n=4); (2) left atrium-aorta, TandemHeart system (n=4); (3) left ventric

85 age, sex, type of atrial fibrillation, left atrium area, hypertension, structural heart disease, pre

86 ime to reappraise the concept of the failing atrium as a primary cause or aggravating factor of the s

87 retic peptides stored in them identified the atrium as an endocrine organ.

88 Standard leads were placed in the right atrium, at the right ventricular apex, and in a coronary

89 l myocardial structural changes in the right atrium, atrial fibrillation (AF) is a disease of variabl

90 s) underwent epicardial mapping of the right atrium, Bachmann bundle, and left atrium during sinus rh

91 (interelectrode distances 2 mm) of the right atrium, Bachmann's bundle, the left atrioventricular gro

92 emia-induced arrhythmia in the ventricle and atrium but also vary between atrial myocytes depending o

93 merous ablation lesions in the low-flow left atrium, but cerebral embolic risk in ventricular ablatio

94 PITX2 is expressed in the adult left atrium, but much less so in other heart chambers.

95 od viscosity continuously in the human right atrium by a dedicated central venous catheter equipped w

96 isolating the pulmonary veins from the left atrium by catheter ablation is superior to antiarrhythmi

97 oxygenation return blood flow upon the right atrium by considering the physiologic effects during int

98 a-pig left ventricle, left atrium, and right atrium, carbenoxolone increased R(j) by 28+/-9%, 26+/-16

99 the inferior vena cava and pulmonary venous atrium (cavoatrial overlap).

100 8.9 vs 7.5; image quality, 438 vs 91), left atrium (CNR, 8.0 vs 5.3; image quality, 1006 vs 29), RV

101 ll P < .05) greater in systole for the right atrium (CNR, 8.9 vs 7.5; image quality, 438 vs 91), left

102 Islet-1(+) cells in the right atrium coexpressed the sinoatrial node pacemaker cell ma

103 as lower for tachycardias involving the left atrium compared with right atrial tachycardias.

104 seven patients (11%), no coronary sinus-left atrium connection was seen; however, all showed a corona

105 h, number, and extent of coronary sinus-left atrium connections were recorded.

106 In contrast, the right posterior left atrium contained predominantly patchy DE.

107 ex myocyte arrangement in the posterior left atrium contributes to activation time dispersion adjacen

108 We hypothesized that the left atrium could be accessed directly through the posterior

109 , while contrast leakage and air in the left atrium could be excluded.

110 tolic pressure gradient between RV and right atrium (DeltaPRV-RA), tricuspid regurgitation velocity-t

111 sident hCPCs, we isolated and expanded right atrium-derived CPCs from all patients (n=103) across all

112 (2) a reduction in cardiac fibrosis and left atrium diameter (marker of end-diastolic pressure), sugg

113 9% women; mean age, 63+/-10 years, mean left atrium diameter, 45+/-6 mm) with a history of paroxysmal

114 nding persistent AF (age, 68+/-7 years; left atrium diameter, 46+/-3 mm; and AF duration, 25+/-15 mon

115 whereas the transmural pressure of the right atrium did not change.

116 ntricular dimension, deceleration time, left atrium dimension, E/e', and pro B-type natriuretic pepti

117 prevents upregulation of miR-1 in the right atrium during coronary artery bypass graft.

118 us mating plug and transferred to the female atrium during mating.

119 the right atrium, Bachmann bundle, and left atrium during sinus rhythm.

120 cular injury in the superior vena cava-right atrium during transvenous lead extraction is more likely

121 g of the mitral valve leaflets into the left atrium during ventricular systole.

122 vs 19.0 +/- 7.8, P = .002) and lower LA left atrium ejection fraction (45.9 +/- 10.7 vs 51.3 +/- 8.7,

123 8 versus 28.6+/-4.3 cm(2); P=0.02), and left atrium (end-diastolic volume, 65+/-19 versus 72+/-19; P=

124 ventricular dysfunction (LVEF<50%) and left atrium enlargement were independently associated with lo

125 rk Heart Association III to IV classes, left atrium enlargement, and improvement/normality of LVEF at

126 (ANP) is not amidated, Pam expression in the atrium exceeds levels in any other tissue.

127 iomyocytes were isolated from right and left atrium, followed by electrophysiological and molecular c

128 monly used on the posterior wall of the left atrium for atrial fibrillation ablation to prevent esoph

129 eterization of the inferior vena cava, right atrium, foramen ovale, and left atrium with a guidewire

130 itates careful distinction of far-field left atrium from the local coronary sinus electrograms beside

131 phase has been proposed as a measure of left atrium function in a range of cardiac conditions, with t

132 delta-cells, vascular smooth muscle, cardiac atrium, gastric antrum/pylorus, enteric neurones, and va

133 LATER score (Male, Bundle brunch block, Left atrium >/=47 mm, Type of AF [paroxysmal, persistent or l

134 A bigger proportion of myocytes in the left atrium had organized T-tubules and topography than in th

135 ation of ganglionated plexi (GP) in the left atrium has been proposed in different subgroup of patien

136 blood temperature (T) as obtained from right atrium impedance measurements: Viscosity(imp)=(-15.574+1

137 ulature-associated genes that may render the atrium impenetrable to additional mates.

138 FIRM analysis revealed sources in the right atrium in 85% of patients (1.8 +/- 1.3) and in the left

139 5% of patients (1.8 +/- 1.3) and in the left atrium in 90% of patients (2.0 +/- 1.3).

140 ptor (TGF-beta-RII-DN) in the posterior left atrium in a canine heart failure model will sufficiently

141 oved contractility of the left ventricle and atrium in a large animal model of nonischemic HF.

142 in the remainder of the morphological right atrium in all but 1 patient.

143 ICE probe was positioned in the right atrium in all patients, in the pulmonary artery in 64 of

144 placed on the epicardial surface of the left atrium in dogs.

145 f individual embryonic cardiomyocytes to the atrium in zebrafish by multicolor fate-mapping and we co

146 ery) and pressure (pulmonary artery and left atrium) in 18 healthy minipigs under acute haemodynamic

147 ed foci originating from pulmonary vein-left atrium interfaces.

148 stium atrial timing during low lateral right atrium IP at cycle length of 600 ms through 300 ms was c

149 The posterior left atrium is an arrhythmogenic substrate that contributes t

150 Amyloid infiltration of the atrium is described in patients with valvular heart dise

151 the inferior vena cava and pulmonary venous atrium is feasible.

152 whereas the transmural pressure of the right atrium is not changed.

153 the nerve-rich fat in the HF posterior left atrium is positively correlated with AF EGM entropy.

154 al adipose tissue mass posterior to the left atrium is related to AF independent of demographical and

155 lthough Pitx2 is expressed in postnatal left atrium, it is unknown whether Pitx2 has distinct postnat

156 luate the impact of an incision in the right atrium joining the lateral tunnel suture line and the tr

157 recorded biatrially at baseline, in the left atrium (LA) after PVI and linear lesions (roof and mitra

158 ngenital P-MAIVF communicating with the left atrium (LA) and an aberrant right subclavian artery, mis

159 suggests a link between fibrosis in the left atrium (LA) and atrial fibrillation (AF), the most commo

160 blation demonstrates the anatomy of the left atrium (LA) and pulmonary veins with significant differe

161 The size and function of the left atrium (LA) and right atrium (RA) are related closely wi

162 ng modalities are able to visualize the left atrium (LA) and, therefore, allow for quantification of

163 ength (CL) gradient between PVs and the left atrium (LA) in an attempt to identify the subset of pati

164 fibrillation (AF) by fast rotors in the left atrium (LA) or at the pulmonary veins (PVs) is not fully

165 Pulmonary veins (PVs) and left atrium (LA) play a critical role in the pathophysiology

166 trical and structural remodeling in the left atrium (LA) that begets atrial myopathy and arrhythmias.

167 ion of the pulmonary veins (PV) and the left atrium (LA) using computed tomography.

168 activity in the right atrium (RA), the left atrium (LA), and both atria, respectively, were analyzed

169 ore (Age, Persistent AF, imPaired eGFR, Left atrium (LA), EF) was calculated at baseline, while MB-LA

170 erall increase in mean z scores for LV, left atrium (LA), RV, interventricular septum, and LV posteri

171 risk of thromboembolic stroke from the left atrium (LA), the exact mechanisms remain poorly understo

172 um likely affects its coupling with the left atrium (LA), this issue has not been investigated in hum

173 ased on low-voltage areas (LVAs) in the left atrium (LA).

174 of the mediastinum and drained into the left atrium (LA).

175 on and electrical function of the adult left atrium (LA).

176 Bmp9 in the germ line and Bmp10 in the right atrium led to dramatic changes in vascular tone and dimi

177 ft ventricular cavity >54 mm, 87% had a left atrium </=40, and 100% had an E/E' <12.

178 e inferior vena cava to the pulmonary venous atrium may be an effective route for access in these pat

179 ental pacing (IP) from the low lateral right atrium may distinguish slow conduction from complete CTI

180 ramen ovale, increased pressure in the right atrium may result in widening of the foramen and consequ

181 locity and image intensity ratio in the left atrium (mean +/- SD) were 0.98 +/- 0.46 and 0.95 +/- 0.2

182 Coronary sinus-left atrium muscle connections were seen in 58 of the 65 pati

183 onary sinus function and coronary sinus-left atrium muscle connections.

184 ystole, indicating that coronary sinus-right atrium muscle continuity is likely the primary cause for

185 Coronary sinus-right atrium muscle continuity was indirectly evaluated by mea

186 EBW mostly occurred at right atrium (N=105, 48%) and left atrioventricular groove (N=

187 d were more commonly identified in the right atrium (n=25) than in the right ventricle (n=5).

188 del approximating the esophagus to the right atrium (n=4) and by direct ablation within its lumen (n=

189 vascular access, navigation within the left atrium, occlusion, snaring, and 3-dimensional relational

190 hox were significantly increased in the left atrium of goats after 2 weeks of AF and in patients who

191 ection+electroporation in the posterior left atrium of plasmid expressing a dominant-negative TGF-bet

192 ogen synthase kinase-3beta (GSK3beta) in the atrium of the Akita mouse results in decreased SREBP-1,

193 8 and caspase 9 in the basal and post-CP/Rep atrium of uncontrolled type 2 diabetic group compared wi

194 hrough drainage into the hepatic vein, right atrium or left atrium.

195 Linear ablation within the left atrium (OR, 0.22; 95% CI, 0.10-0.49; P<0.001), but not c

196 ns, specifically in the inferoposterior left atrium (p < 0.01), superior right atrium (p < 0.05), and

197 erior left atrium (p < 0.01), superior right atrium (p < 0.05), and inferior right atrium (p < 0.05).

198 right atrium (p < 0.05), and inferior right atrium (p < 0.05).

199 grades that did not differ from surrounding atrium (P=NS).

200 The association between LA left atrium parameters and myocardial fibrosis was evaluated

201 e cardiac outflow tract, right ventricle and atrium, pharyngeal mesoderm, peripheral neurons, and hin

202 ower and target LSI for ablation on the left atrium posterior wall (20 W/LSI 4, 20 W/LSI 5, 40 W/LSI

203 All 4 pulmonary veins and the left atrium posterior wall were found isolated in 69% and 23%

204 n change the electric conduction of the left atrium, potentially leading to atrial fibrillation (AF).

205 (63%), the coated aorta (40%), and the right atrium pseudo-tumoral infiltration (36%).

206 An 8F AcuNav probe was introduced into right atrium, pulmonary artery, and coronary sinus.

207 ed cardiac output and pressures in the right atrium, pulmonary artery, and pulmonary capillary wedge

208 Pressure measurements from the right atrium, pulmonary artery, and pulmonary capillary wedge

209 Thermodynamics in the left atrium-pulmonary vein (PV) junction, phrenic nerve, and

210 ooling spread radially from the balloon-left atrium-PV contact point.

211 placed on the epicardial surface of the left atrium-PV junction, as well as on the phrenic nerve and

212 d function of the left atrium (LA) and right atrium (RA) are related closely with the prognosis of ca

213 nsvenous leads were implanted into the right atrium (RA), coronary sinus, and left pulmonary artery o

214 eflect well electrical activity in the right atrium (RA), the left atrium (LA), and both atria, respe

215 had complex ATs involving the lateral right atrium (RA).

216 of GP in the posterior surface of the right atrium (RA).

217 the inferior and medial aspect of the right atrium (RA).

218 gher in SAN than in atria, with SAN to right atrium ratios of 6.1+/-0.9 and 4.6+/-0.6 (n=12), respect

219 (PV) isolation is associated with PV to left atrium reconduction.

220 sequently, high rates of pulmonary vein-left atrium reconnections are consistently seen in clinical s

221 terizing ILA in the superior vena cava-right atrium region.

222 Reduced LA left atrium regional and global function are related to both

223 We used higher I(to,fast) density in atrium, removed I(to,slow), and included an atrial-speci

224 rms and detecting their transcripts in human atrium, reported here are their functional effects on hu

225 ement of corresponding currents in the right atrium resulted in shortened action potential duration a

226 Histological evaluation of the left atrium revealed that percent fibrosis was significantly

227 nt correlation with DFs found in the nearest atrium (rho=0.96 for right atrium and rho=0.92 for left

228 for all stable VTs and with pacing from the atrium, right ventricular apex, and an left ventricular

229 luded 14 mitral (4 RF/2 RF+PF/8 PF), 34 left atrium roof (12 RF/22 PF), and 44 cavotricuspid isthmus

230 e delivered initially from the lateral right atrium, scanning diastole with a 10-ms decrement until A

231 mount and distribution of fibrosis in the HF atrium seems to contribute to slowing and increased orga

232 de (selective INa blocker) produced enhanced atrium-selective effects on maximal phase 0 upstroke and

233 at adding K(+)-channel blockade improves the atrium-selective electrophysiological profile and anti-A

234 Enhancement of atrium-selective K(2P)3.1 currents contributes to APD sh

235 with IKr block increased rate-dependent and atrium-selective peak INa reduction, increased AF select

236 infarction and implantation of an LV-to-left atrium shunt to create standardized moderate volume over

237 personalized computational model of the left atrium simulated AF induction via rapid pacing.

238 ent of the pulmonary vein ostia and the left atrium size in computed tomography presents a good inter

239 CONVERGE permitted left atrium size up to 6 cm and imposed no limits on AF durat

240 The variability of the left atrium size was 21% for the diameter and 35% for the vol

241 s; body mass index, 31.7+/-6.0 kg/m(2); left atrium size, 54+/-10 mm, with persistent/long-standing p

242 Modulation of atrium-specific Kir3.x channels, which generate a consti

243 Atrium-specific Kir3.x controls the induction, dynamics,

244 ythmias and identifies Kir3.x as a promising atrium-specific target for antiarrhythmic strategies.

245 vs 51.3 +/- 8.7, P < .001), maximal LA left atrium strain ( Smax maximum LA strain ) (25.4 +/- 10.7

246 30.6 +/- 10.6, P < .001) and maximum LA left atrium strain rate ( SRmax maximum LA strain rate ) (1.0

247 .42 vs -1.01 +/- 0.48, P < .001) and LA left atrium strain rate at atrial contraction peak ( SRA LA s

248 0.51, P < .001), and lower absolute LA left atrium strain rate at early diastolic peak ( SRE LA stra

249 at the right ventricle (dyssynchrony), right atrium (synchrony), or for 2 weeks right ventricle and t

250 ogeneously distributed in the posterior left atrium than in the left atrial appendage.

251 y and AmpII protein levels were lower in the atrium than in the ventricle.

252 DF/FI/Shannon entropy in the posterior left atrium than left atrial appendage, with the decrease in

253 unced reverse remodeling effects on the left atrium that independently correlate with improved clinic

254 From the right atrium, the whole LAA cavity could not be seen in any pa

255 s: the junction between vena cavae and right atrium; the tricuspid annulus; or between TV leaflets, i

256 s and high autonomic nerve density in the HF atrium, these findings may help enhance the precision an

257 BMP10 expression is restricted to the right atrium, though ventricular hypertrophy is accompanied by

258 -7 versus 19.4+/-4.3 minutes; P<0.001), left atrium time (104+/-25 versus 92+/-23 minutes; P<0.01), a

259 ft ventricle to aortic pressure, in the left atrium to left atrial pressure, and in all heart chamber

260 Blood was withdrawn from the right atrium to measure pH.

261 coronary sinus diverticulum and one a right atrium to right ventricle diverticulum.

262 t, ranging from the upper border of the left atrium to the bottom of the heart, for a total of 23 683

263 tution characteristics of the posterior left atrium, translating into a decrease in AF and increased

264 hat can facilitate the repolarization of the atrium under conditions of excessive mechanical stress.

265 homeostasis and electrical stability in the atrium under physiological and stress conditions, mice w

266 ation lesions with a gap were created in the atrium using fluoroscopy and an electroanatomic system i

267 individual lesions were created in the right atrium using radiofrequency energy (30 W/48 degrees C/17

268 AVC, whereas right pSHF contributes to right atrium, ventral left atrium, and inferior AVC.

269 At 110-120 hpf, distinct AV valve, atrium, ventricle, and bulbus arteriosus form, accompani

270 ients (1.8+/-1.1 per patient; 7 in the right atrium versus 12 in the left atrium; 15 extrapulmonary).

271 originate from the differential response of atrium versus ventricle to pathological insult.

272 secutive days, were delivered into the right atrium via a multiport pulmonary artery catheter during

273 In a multivariable-adjusted estimates, left atrium volume >165 mL, absent normal sinus rhythm at adm

274 rsistent AF patients had larger indexed left atrium volume (55 +/- 18 ml vs. 41 +/- 12 ml and 47 +/-

275 0; 95% CI, 1.09-1.33; P<0.001), maximum left atrium volume before mitral valve opening (HR, 1.02; 95%

276 gitudinal systolic function and maximum left atrium volume before mitral valve opening, and as such c

277 oup had significantly higher minimum LA left atrium volume than the control group (mean, 22.0 +/- 10.

278 LA left atrium volume, strain, and strain rate were analyzed by

279 nd measured global longitudinal strain, left atrium volumes, and PALS within 48 hours of admission.

280 apping of endo- and epicardial lateral right atrium wall was performed in patients with persistent AF

281 he mean LGE burden for left atrium and right atrium was 23.9+/-1.6% and 15.9+/-1.8%, respectively.

282 were ablated for the first time (71%); left atrium was 43+/-6 mm; and left ventricular function was

283 Access to the left atrium was achieved in all 5 animals and all survived.

284 that active BMP10 secreted from mouse right atrium was in the prodomain-bound form.

285 Access to the pulmonary venous atrium was necessary in 33 procedures, via fenestration

286 A simulated trajectory to the left atrium was present in all of 10 human cardiac computed t

287 asma and BMP10 secreted from the mouse right atrium were fully active.

288 Catheter/sheath manipulations in left atrium were performed in 25 of 27 pigs outfitted with mi

289 ophysiological mapping of the anterior right atrium were utilized to quantify EpAT volumes and to ass

290 annels, KCNE4L protein was detected in human atrium, where it co-localized with Kv4.3.

291 nce after secretion from the liver and right atrium, whereas a direct role in the regulation of VSMCs

292 s to structural and neural remodeling in the atrium, which enhances AF complexity and perpetuation.

293 itionally inactivated Pitx2 in the postnatal atrium while leaving its developmental function intact.

294 cava, right atrium, foramen ovale, and left atrium with a guidewire and 1.8F to 2.6F tapered cathete

295 on of the pulmonary veins and posterior left atrium with a single ring of radiofrequency lesions (sin

296 dy, favorable reverse remodeling of the left atrium with CRT-D therapy was associated with a signific

297 sinus via femoral sheaths and into the right atrium with fluoroscopic guidance.

298 the atrial DFs and the identification of the atrium with the highest frequency, opening the possibili

299 of TGF-beta signaling in the posterior left atrium-with resulting decrease in replacement fibrosis-l

300 ght interatrial shunt to decompress the left atrium (without compromising left ventricular filling or