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

3 al conduction patterns of the right and left atrium.

4 active gene transcription in the human right atrium.

5 69% reentries and 71% foci were in the left atrium.

6 erformed, which revealed two lesions in left atrium.

7 stabilize the intercalated disc in postnatal atrium.

8 with limited linear ablation within the left atrium.

9 n the dorsal surface of the embryonic common atrium.

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

11 within the ventricle and do not populate the atrium.

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

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

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

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

16 to a complete and transmural ablation in the atrium.

17 ions that are selective for the fibrillating atrium.

18 ires simultaneous global mapping of the left atrium.

19 the right coronary artery through the right atrium.

20 homeostasis and electrical stability in the atrium.

21 trical and anatomical remodeling of the left atrium.

22 (hCDCs) grown from neonatal and infant right atrium.

23 , and the conduction pathways into the right atrium.

24 tive curvature being concave toward the left atrium.

25 its the SAN-specific genetic program in left atrium.

26 pholamban protein ratio in SAN than in right atrium.

27 ansferase, is expressed only in the neonatal atrium.

28 tructure was functionally insulated from the atrium.

29 nction of TREK-1 and TREK-2 in the embryonic atrium.

30 rdium and is the dominant SUR isoform in the atrium.

31 ts two major chambers, the ventricle and the atrium.

32 icle, and a bipolar pacing wire in the right atrium.

33 5 located in right atrium and 10 in the left atrium.

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

35 hat produce the distinct architecture of the atrium.

36 emodeling in the left ventricle and the left atrium.

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

38 ia activation in the previously ablated left atrium.

39 the sole measure specifically evaluating the atrium.

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

41 acing lead positioned in the posterior right atrium.

42 7 in the right atrium versus 12 in the left atrium; 15 extrapulmonary).

43 inferior SAN (138+/-24 ms; P=0.01) or right atrium (164+/-33 ms; P=0.001) and was associated with a

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

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

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

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

48 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).

49 We address this challenge with ATRIUM, a method for case-control association testing wi

50 3 pacing stimuli enabled consistent RA-left atrium activation until sinus rhythm was restored.

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

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

53 e 22 patients, including 15 located in right atrium and 10 in the left atrium.

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

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

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

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

58 s to 2 microg of ET-1 injected into the left atrium and attenuated the ischaemia-related increase in

59 to 5 microg of U46619 injected into the left atrium and attenuated the ischaemia-related increase in

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

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

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

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

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

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

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

67 dysfunction of melanocyte-like cells in the atrium and pulmonary veins may contribute to atrial arrh

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

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

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

71 eutic hypothermia system placed in the right atrium and set at a target of 32 degrees C.

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

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

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

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

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

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

78 Thus, the regulated (between atrium and ventricle) and aberrant (knockout in the neon

79 specifically expressed in the heart in both atrium and ventricle.

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

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

82 estone that allows for the heart to receive (atrium) and pump (ventricle) blood throughout a closed c

83 =0.96 for right atrium and rho=0.92 for left atrium) and the DF gradient between them (rho=0.93).

84 were manually segmented to isolate the left atrium, and custom software was implemented to quantify

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

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

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

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

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

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

91 es in flow are evident by stasis in the left atrium, and seen as spontaneous echocontrast.

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

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

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

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

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

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

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

99 capacity was also greatest in neonatal right atrium as evidenced by c-kit(+), NKX2-5(+), NOTCH1(+), a

100 After baseline recording, we paced the left atrium at 20 Hz for 1 week and then monitored left stell

101 ips, with the belly being convex to the left atrium at midsystole and concave at maximal valve openin

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

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

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

105 F underwent 3-dimensional DE-MRI of the left atrium before the ablation.

106 highly and almost equally expressed in ED11 atrium but much less expressed in ED11 ventricle.

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

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

109 c beats arising from the pulmonary veins and atrium, but the source and mechanism of these beats rema

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

111 tructure was functionally insulated from the atrium by connective tissue, fat, and coronary arteries,

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

113 e perturb the routing of the gut to the left atrium by laser ablation and pharmacology to show that t

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

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

116 8.9 vs 7.5; image quality, 438 vs 91), left atrium (CNR, 8.0 vs 5.3; image quality, 1006 vs 29), RV

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

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

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

120 in the left ventricle as well as in the left atrium confirmed the presence of cavity obliteration in

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

122 rillation group showed a coronary sinus-left atrium connection, which was single in five patients and

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

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

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

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

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

128 The difference in left atrium (Delta LA) volume index was significant (P=0.002)

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

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

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

132 9% women; mean age, 63+/-10 years, mean left atrium diameter, 45+/-6 mm) with a history of paroxysmal

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

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

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

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

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

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

139 8 versus 28.6+/-4.3 cm(2); P=0.02), and left atrium (end-diastolic volume, 65+/-19 versus 72+/-19; P=

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

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

142 icle) and aberrant (knockout in the neonatal atrium) expression of a single glycogene was sufficient

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

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

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

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

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

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

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

150 Catheters were targeted to the right atrium, His bundle, and right ventricle of 10 mongrel do

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

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

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

154 5% of patients (1.8 +/- 1.3) and in the left atrium in 90% of patients (2.0 +/- 1.3).

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

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

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

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

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

160 esponsive to the Hh ligand migrated into the atrium in normal numbers but populated the atrial free w

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

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

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

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

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

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

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

168 We demonstrate that ATRIUM is robust in that it maintains the nominal type I

169 ion between the left ventricle and the right atrium, is presented.

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

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

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

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

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

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

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

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

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

179 in 1 (ET-1, 1, 2 and 4 microg) into the left atrium (LA) stimulated seven ischaemically sensitive car

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

181 A(2) mimetic, U46619, injected into the left atrium (LA), stimulated seven ischaemically sensitive ca

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 ene expression, including Shox2, in the left atrium of embryos and young adults.

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

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

202 i.EF1alpha-eGFP was transferred to the right atrium of Spague-Dawley (SD) rats and acetylcholine (ACh

203 TREK-1 is highly expressed in the atrium of the adult heart.

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

205 8 and caspase 9 in the basal and post-CP/Rep atrium of uncontrolled type 2 diabetic group compared wi

206 n = 50) or to ablation of CFAEs in the left atrium or coronary sinus for up to 2 additional hours of

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

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

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

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

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

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

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

214 ents, was patent at the entry into the right atrium (PFO) in 62 patients (61.4% of patients with flap

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

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

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

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

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

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

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

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

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

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

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

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

227 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

248 30.6 +/- 10.6, P < .001) and maximum LA left atrium strain rate ( SRmax maximum LA strain rate ) (1.0

249 .42 vs -1.01 +/- 0.48, P < .001) and LA left atrium strain rate at atrial contraction peak ( SRA LA s

250 0.51, P < .001), and lower absolute LA left atrium strain rate at early diastolic peak ( SRE LA stra

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

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

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

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

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

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

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

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

259 -7 versus 19.4+/-4.3 minutes; P<0.001), left atrium time (104+/-25 versus 92+/-23 minutes; P<0.01), a

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

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

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

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 ATRIUM uses LD information from an external reference pa

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

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

269 mbrane potential in 25 isolated canine right atrium, using previously described criteria of the timin

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

271 Tbx5 is expressed in the developing atrium, ventricle and in pectoral fin fields, but its ge

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

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

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

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

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

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

278 0; 95% CI, 1.09-1.33; P<0.001), maximum left atrium volume before mitral valve opening (HR, 1.02; 95%

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

280 Left atrium volume index increased during CNI (46.73+/-16.3 5

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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