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1 selective preservation of embryonic vessels (aortic arches).
2 layer of the wall of the ascending aorta and aortic arch.
3 N accumulation in atheroprone regions of the aortic arch.
4 es in NHPs displaying the typical two-artery aortic arch.
5 nfirm the number of arterial branches in the aortic arch.
6 oam cells, in atherosclerotic lesions in the aortic arch.
7 y clipping the arteries originating from the aortic arch.
8 ring repairs of the ascending and transverse aortic arch.
9 994 repairs of the ascending and transverse aortic arch.
10 1107 repairs of the ascending and transverse aortic arch.
11 ring repairs of the ascending and transverse aortic arch.
12 ous system, skin, craniofacial skeleton, and aortic arch.
13 m, resulting in randomized laterality of the aortic arch.
14 terpart underlie left-sided formation of the aortic arch.
15 patterning of the cardiac outflow tract and aortic arch.
16 atherosclerosis at both the aortic root and aortic arch.
17 rtery is a rare congenital anomaly involving aortic arch.
18 , interrupted aortic arches, and right-sided aortic arches.
19 e cardiac outflow tract and the formation of aortic arches.
21 mation and initial sprouting are normal, but aortic arches 5 and 6 fail to form a lumenized connectio
24 investigate this process, we focused on the aortic arch (AA) blood vessels, which are known to remod
25 AP2B was detected in vivo in mouse and swine aortic arch (AA) endothelia exposed to chronic disturbed
26 1 null mice show defects such as interrupted aortic arch, aberrant subclavian artery and Tetralogy of
27 nal Kv7 channels in the baroreceptors of the aortic arch adjust the sensitivity of the mechanosensiti
30 osclerotic plaques in carotid artery, heart, aortic arch and aorta in acute and chronic atheroscleros
31 e had smaller atherosclerotic plaques in the aortic arch and aortic roots, but showed little differen
33 of endothelium located in athero-susceptible aortic arch and athero-protected descending thoracic aor
34 The overlapping QTLs for curvature of the aortic arch and atherosclerosis support that the ontogen
37 ocardiofacial syndrome phenotypes, including aortic arch and cardiac outflow tract abnormalities.
38 netic element of Gbx2, which is required for aortic arch and cardiac outflow tract development, and i
41 stretch of baroreceptors in the wall of the aortic arch and carotid sinus initiates autonomic reflex
42 , reflexogenic areas of the carotid sinuses, aortic arch and coronary arteries and the pulmonary arte
44 define age-related geometric changes of the aortic arch and determine their relationship to central
45 study tested the applicability of published aortic arch and ductal Z scores (measured just before th
46 face immunohistochemical examination of rat aortic arch and experimentally stenosed abdominal aorta
47 ation contributed to 75% of all strokes; for aortic arch and extracranial carotid artery calcificatio
48 ng cells to finely control patterning of the aortic arch and great arteries specifically during the p
50 MO4, which showed higher expression in mouse aortic arch and in human coronary endothelium in an asym
51 ion line length, thoracic cage ratio at both aortic arch and inferior pulmonary vein level, thoracic
52 ed to specific focal localization within the aortic arch and its branches, as detected by fluorescenc
53 scular wall assembly, were restricted to the aortic arch and its branches, compromising the brachioce
55 C57Bl/6 mice were subjected to 5 minutes of aortic arch and left subclavian occlusion with subsequen
59 w tract (OFT) into the functionally separate aortic arch and pulmonary trunk is dependent upon the dy
63 ith larger calcification volumes in both the aortic arch and the carotid arteries but attenuated afte
64 redisposition with both calcification in the aortic arch and the carotid arteries, providing novel in
65 aneurysms involving both the ascending aorta/aortic arch and the descending thoracic or thoracoabdomi
67 ry effects of LA were more pronounced in the aortic arch and the thoracic aorta than in the aortic si
68 ngitudinal and transversal remodeling of the aortic arch and their relationship with LV mass and remo
69 mouse models by approximately 20% and in the aortic arch and thoracic aorta of apoE-/- and apoE/low-d
70 tail in endothelium of the atherosusceptible aortic arch and was found to be partially activated.
71 e had ~2-fold greater atherosclerosis in the aortic arch and ~2-8-fold greater atherosclerosis in the
72 ave been shown to interact in patterning the aortic arch, and both genes are required in formation an
74 measured on a parasagittal GRE image of the aortic arch, and Deltat was extracted from ascending and
75 osis, enhanced macrophage recruitment to the aortic arch, and more abundant mRNA for monocyte chemota
76 ted previously in the carotid labyrinth, the aortic arch, and the pulmocutaneous artery of frogs.
80 scle differentiation resulted in interrupted aortic arch, aneurysms and failure to assemble extracell
81 nsions, distensibility, pulse wave velocity, aortic arch angle, left ventricular (LV) mass, LV systol
84 second of two parts, describes the repair of aortic arch anomalies, left-to-right shunts, valvular di
85 Nissl staining showed that in NHPs with the aortic arch anomaly clipping only two of three arterial
86 extra arterial aortic branch recognizes this aortic arch anomaly in Rhesus macaques that warrants a c
87 der to reveal the pathological effect of the aortic arch anomaly, we compared the hippocampal cell lo
91 t myeloid cells present in the intima of the aortic arch are not DCs but instead specialized aortic i
92 n, and dissection of the ascending aorta and aortic arch are often associated conditions that complic
93 ich is crucial for normal development of the aortic arch arteries and cranial vasculature during embr
94 ifferentiation into smooth muscle within the aortic arch arteries and impaired cardiac outflow tract
95 neural crest results in misalignment of the aortic arch arteries and outflow tract, contributing to
96 evelopmental defects affecting the heart and aortic arch arteries are a significant phenotype observe
97 formations that affect the outflow tract and aortic arch arteries with failure of the 3rd and 4th pha
98 5-11.0 had well-developed pharyngeal arches, aortic arch arteries, and no signs of cardiac failure.
99 sel malformations, hypoplastic pulmonary and aortic arch arteries, cardiac malformations, micrognathi
100 ands, craniofacial skeleton, cranial nerves, aortic arch arteries, cardiac outflow tract and cephalic
107 ized by the NC mediated morphogenesis of the aortic arch artery and differentiation of NC cells into
109 hogenesis of PAAs and their derivatives, the aortic arch artery and its major branches; however, thei
113 ion assays and is sufficient to recapitulate aortic arch artery expression of Jagged1 in transgenic m
114 s showed that signaling by the ECM regulates aortic arch artery morphogenesis at multiple steps: (1)
116 nd endocardial precursors does not result in aortic arch artery patterning defects or embryonic death
119 t and subsequent embolization of debris from aortic arch atheroma or from the calcified valve itself
120 l atrial fibrillation, patent foramen ovale, aortic arch atherosclerosis, atrial cardiopathy, and sub
123 ections with intimal flap extension into the aortic arch between the innominate and left subclavian a
125 rom 2-dimensional regions of interest in the aortic arch blood pool and in the right lobe of the live
126 ncy of IL-17A/IL-17RA preferentially reduced aortic arch, but not thoracoabdominal aortic T cell, neu
127 Deficiency of IL-17A or IL-17RA reduced aortic arch, but not thoracoabdominal aortic TNFalpha an
128 Most prominent associations were found for aortic arch calcification and cardiovascular mortality (
130 measured manually at 3 predetermined levels (aortic arch, carina, and bronchus intermedius) to confir
132 ponse to stimulation of baroreceptors in the aortic arch, carotid sinuses and coronary arteries, stim
141 offspring of normal weight mothers, PRRs of aortic arch defects and transposition of the great arter
143 great arteries, atrial septal defects [ASD], aortic arch defects, and single-ventricle heart) and sub
144 erase chain reaction analysis of lesion-rich aortic arches demonstrated a marked reduction in mRNA fo
145 ntified at the level of the ascending aorta, aortic arch, descending thoracic aorta, and coronary art
146 bserved at the level of the ascending aorta, aortic arch, descending thoracic aorta, and the coronary
147 ular smooth muscle cells (SMCs) around those aortic arches destined for survival and reorganization,
149 ve angiogenesis defects depicted by abnormal aortic arch development, hyperactive ectopic blood vesse
150 NCCs resulted in defects in craniofacial and aortic arch development, the latter with variable penetr
151 nsight into the factors that guide branchial aortic arch development, we examined the process by whic
152 ere isolated from the inner curvature of the aortic arch (DF; athero-susceptible) and a nearby UF reg
153 relation between wall shear stress (WSS) and aortic arch diameter in the developing embryo, and obser
155 es such as cardiac thrombi, cardiac tumours, aortic arch disease and other rare cardiac anomalies.
157 he outcome of endovascular repair of chronic aortic arch dissecting aneurysms with a custom-made bran
163 otic calcification in the coronary arteries, aortic arch, extracranial, and intracranial internal car
165 rosclerosis support that the ontogeny of the aortic arch formation is a potential risk factor for ath
166 sclerosis regression in which plaque-bearing aortic arches from apolipoprotein E-deficient (apoE(-/-)
167 r CCR7-dependent regression, we transplanted aortic arches from atherosclerotic Apoe-/- mice, or from
168 rosclerosis, P2X7 expression was analyzed in aortic arches from low density lipoprotein receptor(-/-)
169 h, diameters, height, width, and curvature), aortic arch function (local aortic distensibility and ar
170 sing magnetic resonance imaging to determine aortic arch geometry (length, diameters, height, width,
171 us work, we examined hemodynamic loading and aortic arch growth in the chick embryo at Hamburger-Hami
172 tellation of congenital malformations of the aortic arch, heart, thymus, and parathyroid glands descr
174 s, including interrupted aortic arch type B, aortic arch hypoplasia, double-outlet right ventricle, a
176 ent truncus arteriosus (PTA) and interrupted aortic arch (IAA), which are associated with the faulty
177 as high across all territories imaged except aortic arch (ICC values from 0.90 to 0.97, arch 0.71).
178 achieved superior hemodynamic and integrated aortic arch imaging outcomes compared with BA patients.
180 lesser curvature and branching point of the aortic arch in mice as well as human pulmonary artery br
181 report for the first time an anomaly of the aortic arch in some Rhesus macaques that appears as a ke
188 ed that the extent of atherosclerosis in the aortic arch is significantly correlated in males, but no
189 5 and alphav integrins developed interrupted aortic arches, large brachiocephalic/carotid artery aneu
190 LR -/- mice, compound 13 showed reduction of aortic arch lesion progression and no plasma or hepatic
191 analysis identified 2 significant peaks for aortic arch lesion size on chromosome 1 (105 Mb, LOD=5.0
192 er, overall area and cellular composition of aortic arch lesions did not differ significantly among g
194 ate and subclavian arteries arising from the aortic arch, macroscopic visualization of these two arte
197 phologies of vagal afferent terminals in the aortic arch may serve as substrates for the future inves
200 indow of increased vulnerability to aberrant aortic arch morphogenesis with the potential for profoun
204 (n=7), coarctation of the aorta/hypoplastic aortic arch (n=5), tetralogy of Fallot (n=1), hypoplasti
206 f the inner, but not the outer, curvature of aortic arch, nor the straight segment of thoracic aorta
207 have undergone balloon aortoplasty (BD) for aortic arch obstruction (COA) after the Norwood procedur
210 ion of lesions was observed in the aorta and aortic arch of anti-OX40L-treated mice compared with con
211 sham: 0.97+/-0.05 s(-1); P=0.068) and in the aortic arch of ApoE(-/-) mice compared with WT mice (Apo
212 Notably, the extent of lesion size in the aortic arch of Senp2(+/-)/Ldlr(-/-) mice was much larger
215 ed with genes progressively regulated in the aortic arches of 2 mouse models of atherosclerosis durin
217 e injections revealed that the transition in aortic arch pattern is not a uniform process and multipl
218 xhibited cardiovascular anomalies, including aortic arch patterning defects, pulmonary artery stenosi
219 fluorescent dye microinjections to identify aortic arch patterns and measured diameters using both i
220 ed that these two stages contained different aortic arch patterns with no inter-embryo variation.
224 eurons, immunohistochemistry and an isolated aortic arch preparation were used to demonstrate the pre
225 e proximal aorta and the left ventricle (eg, aortic arch pulse wave velocity and distensibility) as w
226 The authors estimated that a 1% increase in aortic arch PWV (in meters per second) is related to a 0
227 d ascending aortic distensibility, increased aortic arch PWV (p < 0.001), and increased central blood
231 l predictive model of subsequent WMH burden, aortic arch PWV provides a distinct contribution along w
234 lume adjusted for sex and ethnicity included aortic arch PWV, age, systolic blood pressure, hypertens
235 ants undergoing biventricular repair without aortic arch reconstruction, 89 (86%) returned for neurod
236 root replacement in 21 (38), with ascending aortic/arch reconstruction in 13 (23) and mitral valve s
238 sm that impacts the timing of events such as aortic arch regression and generation, leading to the va
239 e factors associated with increased risk for aortic arch reintervention in patients who have undergon
241 was to evaluate the outcome of endovascular aortic arch repair for chronic dissection with a custom-
243 ement, 5 valve surgery, 2 septal myectomy, 1 aortic arch replacement, 1 myocardial bridge unroofing,
244 oss-sectional measurements were taken of the aortic arch, right ventricular (RV) outflow tract (RVOT)
245 wed decreased atherosclerotic lesions in the aortic arch, root (57%, P<0.001), and the entire aorta (
246 eptor did not develop smaller lesions in the aortic arch, root, and thoracoabdominal aorta compared w
247 ty of abdominal aortic aneurysms, and caused aortic arch ruptures and dissections, indicating that al
250 hemodynamic waves to quantify the effect of aortic arch stiffening on transmitted pulsatility to cer
251 reduced suprarenal aortic diameter, reduced aortic arch Sudan IV staining, higher serum HDL levels,
253 the current techniques and results of hybrid aortic arch surgery centered around a new classification
254 arrest (DHCA; n = 53) in children undergoing aortic arch surgery during a period from January 2008 to
255 perimental, totally endoscopic approaches to aortic arch surgery have been performed successfully.
260 o HLHS had retrograde flow in the transverse aortic arch (TAA), 88% had left-to-right flow across the
262 a large-diameter, highly compliant, elastic aortic arch that allows the aorta to accommodate blood e
264 inal organs and dissection or rupture of the aortic arch, the prognosis of focal single-organ vasculi
269 ion from the bilaterally symmetric embryonic aortic arches to the mature great vessels is a complex m
270 ascular abnormalities, including interrupted aortic arch type B, aortic arch hypoplasia, double-outle
271 h arteries can result in interruption of the aortic arch type B, typically found in DiGeorge syndrome
272 ontralateral internal carotid artery, and an aortic arch type II, with a trend for aortic arch type I
273 ion, lesion length, lesion eccentricity, and aortic arch type III were significantly associated with
275 contralateral carotid stenosis, and complex aortic arch type were predictive for bilateral ischemic
276 Age, hypertension, lesion morphology, and aortic arch type were predictive for procedural-related
278 lengthening, and decreased curvature of the aortic arch (unfolding) were all significantly associate
279 have measured regional stiffness within the aortic arch using pulse wave velocity (PWV) and have fou
282 ressed during morphogenesis of the heart and aortic arch vessels and at early stages of cartilage dev
283 ) locus cause a pronounced dilatation of the aortic arch vessels as well as aberrant patterning of th
289 (-/-) mice, the (64)Cu-GPVI-Fc uptake in the aortic arch was significantly higher compared with WT mi
290 oracic cross-sectional area/[height]2 at the aortic arch were found to have good correlation with spi
292 ificantly increased incidence of interrupted aortic arch when compared with Tbx1 heterozygous mice.
293 AA) is a rare congenital malformation of the aortic arch, which might be accompanied with other coexi
294 etected 3 arterial branches arising from the aortic arch, which prompted us to subsequently search fo
297 Developmental anomalies of the carotid and aortic arch with intracranial bleeding is a rare occurre
299 or reconstruction of the ascending aorta or aortic arch) with intraoperative bleeding (blood volume
300 gy have facilitated methods of replacing the aortic arch without deep hypothermic circulatory arrest