ライフサイエンスコーパス: arch

1 context of age-related clonal hematopoiesis (ARCH).

2 n the past age-related clonal hematopoiesis (ARCH).

3 , such as the proton pump archaerhodopsin-3 (Arch).

4 ve preservation of embryonic vessels (aortic arches).

5 al-aboral axis in mouse embryonic mandibular arch.

6 ffness relationship of the transverse tarsal arch.

7 celerated epigenetic age in individuals with ARCH.

8 mportant for morphogenesis of the mandibular arch.

9 per contralateral quadrants within the same arch.

10 sclerosis at both the aortic root and aortic arch.

11 regulating cartilaginous joints in the hyoid arch.

12 s always preserved by a complete deep palmar arch.

13 th Tfb3 binding on two opposite faces of the Arch.

14 the maxillary process of the first branchial arch.

15 that dictates the energy-saving role of the arch.

16 suggestive of a reduced medial longitudinal arch.

17 y during development of the first pharyngeal arch.

18 ess and hypoplasia of clavicle and zygomatic arch.

19 fore include at least the vertebral body and arch.

20 y preventing it to fully fuse with posterior arches.

21 long the dorsoventral axis of the developing arches.

22 ired for vagus innervation of the pharyngeal arches.

23 genes in distinct regions of the pharyngeal arches.

24 d with blood vessels in anamniote pharyngeal arches.

25 riginally evolved via transformation of gill arches.

26 vatives from the first and second pharyngeal arches.

27 ertebral body (or centrum) and the vertebral arches.

28 rs, which contribute to posterior pharyngeal arches.

29 d in the second and more posterior branchial arches.

30 The mandibular portion of pharyngeal arch 1 is patterned dorsally by Jagged-Notch signaling a

31 stered in the mesodermal cores of pharyngeal arch 2 (PA2), where they downregulate nkx2.5 expression.

32 hydroboration of the alkenylboronate to give ArCH(2)CH(BCy(2))Bpin, again leading to catalyst inhibit

33 ulation of SHF-derived ECs in the pharyngeal arches, (2) remodeling of the EC plexus in the fourth ar

34 Right side aortic arch (23.91%) was the most common associated abnormality

35 se debates centre on the medial longitudinal arch(5,6) and have not considered whether stiffness is a

36 with increasing differences from the aortic arch (8 HU) to the iliac arteries (95 HU).

37 ing of Meis, Pbx, and Hoxa2 in the branchial arches, a series of segments in the developing vertebrat

38 Here we show that the transverse tarsal arch, acting through the inter-metatarsal tissues, is re

39 ARCH also confers an increased risk for non-haematologic

40 derived from the first and second branchial arches also share a clonal relationship with different S

41 g the stability of the interface between the Arch and 4FeS domains in XPD.

42 ansient opening of the interface between the Arch and 4FeS domains, allowing access to a second bindi

43 tic plaques in carotid artery, heart, aortic arch and aorta in acute and chronic atherosclerosis indu

44 h of baroreceptors in the wall of the aortic arch and carotid sinus initiates autonomic reflexes to c

45 ding aorta and underestimation (<12%) in the arch and descending aorta.

46 the pressure-derived function of the palmar arch and forearm arterial collateral circulation during

47 nvasive hemodynamic assessment of the palmar arch and forearm arterial function reveals collateral su

48 Palmar arch and forearm collateral function was determined usin

49 e invasive CFI measurements, arterial palmar arch and forearm function was tested noninvasively by th

50 e length, thoracic cage ratio at both aortic arch and inferior pulmonary vein level, thoracic cross-s

51 pecific focal localization within the aortic arch and its branches, as detected by fluorescence molec

52 s had equal atherosclerosis burden in aortic arch and root.

53 (-/-) Tlr7 (-/-) mice showed reduced aortic arch and sinus lesion areas.

54 he oral-aboral axis of the distal mandibular arch and subsequently duplication of dentary bone in the

55 Major aortic branches of the arch and visceral segment add additional technical compl

56 distribute to the thoracic wall, pharyngeal arches and heart.

57 rated structures that segment the pharyngeal arches and help pattern the vertebrate face.

58 enes, is expressed throughout the pharyngeal arches and is considered a key gene, when mutated, for t

59 We propose that gill arches and paired fins are serially homologous as deriva

60 developmental progression of the pharyngeal arches and show that experimentally altering the timing

61 ed on a parasagittal GRE image of the aortic arch, and Deltat was extracted from ascending and descen

62 s, including the postzygopophysis, vertebral arch, and spinous process, which causes biomechanical al

63 This was broadly observed in aortic root, arch, and total aorta of male mice, whereas the effect w

64 are broadly expressed across mouse branchial arches, and HOXA2, which is expressed in the second and

65 evolutionary relationship between centra and arches, and their varying modes of skeletal mineralizati

66 All auxiliary proteins are in the "arch-and-heel" region and connected to the core through

67 the developing gill arches establishes gill arch anteroposterior polarity and maintains the prolifer

68 However, aortic arch apoptosis ((99m)Tc-rhAnnexin V-128) increased signi

69 id cells present in the intima of the aortic arch are not DCs but instead specialized aortic intima r

70 ectoral fin skeleton from mesoderm, the gill arches are of dual origin, receiving contributions from

71 OFT, instead contributing to the pharyngeal arch arteries (PAAs), and second, a loss of first heart

72 ental defects affecting the heart and aortic arch arteries are a significant phenotype observed in in

73 e that the generation of proper OFT size and arch arteries requires Pbx-dependent stratification of u

74 s with failure of the 3rd and 4th pharyngeal arch arteries to form correctly.

75 ons that affect the outflow tract and aortic arch arteries with failure of the 3rd and 4th pharyngeal

76 the NC mediated morphogenesis of the aortic arch artery and differentiation of NC cells into vascula

77 d the remodeling of the PAAs into the aortic arch artery and its major branches.

78 is of PAAs and their derivatives, the aortic arch artery and its major branches; however, their speci

79 considered a key gene, when mutated, for the arch artery defects.

80 d that signaling by the ECM regulates aortic arch artery morphogenesis at multiple steps: (1) accumul

81 integrin alpha5beta1 and Fn1 regulate aortic arch artery morphogenesis.

82 uring normal morphogenesis of the pharyngeal arch artery system.

83 ll mean irregularity index in the mandibular arch at baseline was 8.5 +/- 3.8 mm (95% CI, 7.6 to 9.3)

84 associations for microinfarction were: TAVI (arch atheroma grade: r=0.46; P=0.0001) and SAVR (concomi

85 l fibrillation, patent foramen ovale, aortic arch atherosclerosis, atrial cardiopathy, and substenoti

86 ered maternal care, represented by decreased arched-back nursing and increased frequency of exits fro

87 This indicates the important role of aortic arch biomechanics on heart-brain coupling.

88 resulted in enlarged, hemorrhaging branchial arch blood vessels and hydrocephalus.

89 c cells associated with zebrafish pharyngeal arch blood vessels, and propose a new model for amniote

90 vascular regions with disturbed blood flow (arches, branches, and bifurcations).

91 veloped a neck fold from the hyoid branchial arch by preventing it to fully fuse with posterior arche

92 Arch calcification trended to progress more in those wit

93 d manually at 3 predetermined levels (aortic arch, carina, and bronchus intermedius) to confirm ECAC

94 Calcification of the ascending aorta, arch, carotid, and coronary arteries was quantified.

95 ate is the anti-Markovnikov addition product ArCH = CHBCy(2).

96 Endovascular treatment of aortic arch chronic dissections with a branched endograft is as

97 by Tugal-Tutkin and Urgancioglu in (Graefes Arch Clin Exp Ophthalmol 244:742-6, 2006).

98 ients (Tugal-Tutkun and Urgancioglu, Graefes Arch Clin Exp Ophthalmol 244:742-6, 2006; Tugal-Tutkun e

99 genes with regional expression in zebrafish arch CNCCs reveals complex regulation by Edn1 and points

100 antly smaller lesion surface areas on aortic arches compared to the PBS control.

101 Restricting arch compression had no effect on the cost of walking or

102 Restricting arch compression near maximally (~80%) during moderate-s

103 del data confirm that it is the end-range of arch compression that dictates the energy-saving role of

104 tudy provides the first direct evidence that arch compression/recoil during locomotion contributes to

105 Yet, both proteins adopt highly similar beta-arch conformations within the N-terminal ~21 residues.

106 Aortic arches containing plaques developed in Ldlr(-/-) mice we

107 The present simulations suggest that aortic arch curvature is an important risk factor for embolic s

108 s), in the pharynx, the feeding organ [where Arch(D95N) showed approximately 128% DeltaF/F increase p

109 We systematically assessed Arch(D95N), Archon, QuasAr, and the eFRET sensors MacQ-m

110 ing of normal weight mothers, PRRs of aortic arch defects and transposition of the great arteries wer

111 PRRs of aortic arch defects increased with maternal obesity severity.

112 rteries, atrial septal defects [ASD], aortic arch defects, and single-ventricle heart) and subgroups

113 ffness contribution of the transverse tarsal arch, demonstrate its predictive power using mechanical

114 e (tooth-bounded versus terminal position in arch), dental arch (mandibular or maxillary), arch locat

115 g external ear anomalies, abnormal branchial arch derivatives, heart malformations, diaphragmatic her

116 f the second heart field (SHF) and branchial arch-derived head muscles.

117 bi- or unilateral OME, the fourth pharyngeal arch-derived levator veli palatini muscles were hypoplas

118 ooth muscle cells (SMCs) around those aortic arches destined for survival and reorganization, and ide

119 e transcription factor SIX1 regulates dorsal arch development not only by inducing dorsal Jag1 expres

120 nderlying evolutionary changes in pharyngeal arch development, here we investigate embryos and larvae

121 ogenesis defects depicted by abnormal aortic arch development, hyperactive ectopic blood vessel sprou

122 NCCs, resulting in abnormal chick pharyngeal arch development.

123 ate that there are some variations in dental arch dimensions among ethnic groups and between genders.

124 as cardiac thrombi, cardiac tumours, aortic arch disease and other rare cardiac anomalies.

125 the prevalence of occlusive tibial and pedal arch disease is very high.

126 crest-derived cells (NCCs) of the pharyngeal arches display a malformed stapes.

127 ome of endovascular repair of chronic aortic arch dissecting aneurysms with a custom-made branched en

128 Medical, Bloomington, IN) for chronic aortic arch dissection.

129 ocalize the Tfb3-binding surface on the Rad3 Arch domain.

130 ; pelvic girdle extremely small and strongly arched; dorsal and caudal fins absent; tail stings and c

131 astic energy-saving role of the longitudinal arch during running, and suggest that arch supports used

132 Vertebral arch elements were present in early stem vertebrates, wh

133 Swine aortic arch endothelia exhibited elevated ROS, NOX4, HIF-1alpha

134 E7.5 in the SHF and contribute to pharyngeal arch endothelium between E7.5 and E9.5.

135 Emergence of this Pou3f3 arch enhancer >430 Mya and subsequent modifications may

136 We identify a deeply conserved Pou3f3 arch enhancer present in humans through sharks but undet

137 m a signalling centre in the developing gill arches establishes gill arch anteroposterior polarity an

138 one and athero-resistant areas of the aortic arch even in wild-type mice.

139 rgent patterns correlate with the pharyngeal arch expression of Pou3f3 orthologs.

140 cers account for their restricted versus pan-arch expression patterns.

141 proach based on a pyrene platform with polar arches extending from aryl substituents.

142 lcification in the coronary arteries, aortic arch, extracranial, and intracranial internal carotid ar

143 features including telecanthus, epicanthus, arched eyebrows, and low-set ears.

144 consisting of macrocephaly, prominent eyes, arched eyebrows, hypertelorism, a glabellar nevus flamme

145 The over-arching finding was that, for most configurations, perfo

146 presence of an energy-saving longitudinally arched foot in H. erectus.

147 ebral body for 18 of 57 patients, the neural arch for 21 of 57 patients, and the articular process fo

148 sequently, SHF-derived ECs in the pharyngeal arches form a plexus of small blood vessels, which remod

149 In most vertebrates, pharyngeal arches form in a stereotypic anterior-to-posterior progr

150 h protofilament consists of an extended beta arch formed by residues 106 to 145 of the prion protein,

151 otch2 signaling in patterning the pharyngeal arches from fish to mouse to man, despite the very diffe

152 osis, P2X7 expression was analyzed in aortic arches from low density lipoprotein receptor(-/-) mice c

153 Patients with full-arch grafting reconstructions lost significantly more im

154 in neonatal mice expressing archaerhopsin-3 (Arch), halorhodopsin (eNpHR), or channelrhodopsin-2 (ChR

155 e energy-sparing spring theory of the foot's arch has become central to interpretations of the foot's

156 bryonic structures, including the pharyngeal arches, heart, and anterior somites.

157 ng the craniofacial skeleton, ear, branchial arches, heart, lungs, diaphragm, gut, kidneys, and gonad

158 otonation of E-/Z-2-halogeno-2-CF3 styrenes [ArCH horizontal lineC(X)CF3, X = F, Cl, Br] in superacid

159 The presence of coarctation shelf and aortic arch hypoplasia were more common in fetuses with CoA tha

160 he anatomical foundation of Gegenbaur's gill arch hypothesis.

161 is the central mediator of dorsal mandibular arch identity, thus ensuring separation of bone developm

162 Hoxa2, which specifies second arch (IIBA) identity, recognizes a subset of Meis prebou

163 to define the width and length of the dental arch in 12-year-old Vietnamese children, and to elucidat

164 ion tree for the diagnosis and follow-up for ARCH in a research setting.

165 the lumbar cord in mice expressing eNpHR or Arch in ChAT(+) or Isl1(+) neurons, depressed motoneuron

166 oline acetyltransferase neurons (ChAT(+)) or Arch in LIM-homeodomain transcription factor Isl1(+) neu

167 curvature and branching point of the aortic arch in mice as well as human pulmonary artery branches.

168 5' ends are accommodated by a small, mobile arch in the active site that binds recessed ends at its

169 eting of vagus motor axons to the pharyngeal arches in zebrafish.

170 Age-related clonal haemopoiesis (ARCH) in healthy individuals was initially observed thro

171 .g., larger limb joints, spring-like plantar arch) in Homo was somewhat mosaic, with the full enduran

172 n cause of age-related clonal hematopoiesis (ARCH) in older individuals, and are among the most commo

173 The rate of palmar arch incompleteness and the clinical consequences after

174 etero-hexameric, membrane-attached, retromer arches indicates that VARP will prefer binding to assemb

175 Aortic arch inflammation ((18)F-FDG uptake) did not differ over

176 Aortic arch inflammation ((18)F-FDG) and apoptosis ((99m)Tc-rhA

177 2) remodeling of the EC plexus in the fourth arches into the PAAs, and (3) differentiation of neural

178 Although it remains unclear whether ARCH is a marker of aging or plays an active role in the

179 ARCH is associated not just with chronological aging but

180 ARCH is associated with an increased risk for haematolog

181 The FSE-arch is conserved in the related MERS-CoV and is under p

182 ARCH is defined as the gradual, clonal expansion of HSPC

183 More recently, several groups reported that ARCH is driven by somatic mutations [2], with the most p

184 shows that the metabolic energy saved by the arch is largely explained by the passive-elastic work it

185 Whether ARCH is linked to accelerated ageing has remained unexpl

186 dages that project laterally from their gill arches, known as branchial rays.

187 grasped branches in favor of a longitudinal arch (LA) that stiffens the foot and aids bipedal gait.

188 lphav integrins developed interrupted aortic arches, large brachiocephalic/carotid artery aneurysms a

189 neath the orogen, the Moho beneath Qilian is arch-like, shallower beneath the center and deepens by u

190 rch), dental arch (mandibular or maxillary), arch location (anterior or posterior), smoking status, t

191 ciated with self-reported pain measures, the arch location (mandible), and number of treated sites (>

192 eveloped model, incorporating flat upper and arched lower fiber layers connected by ground substance,

193 ed versus terminal position in arch), dental arch (mandibular or maxillary), arch location (anterior

194 gested here that treating or even preventing ARCH may prove to be beneficial for human health.

195 Proliferation was reduced in the branchial arch mesenchyme of Yap and Taz CNC conditional knockout

196 c progenitors present in anterior pharyngeal arch mesoderm at mid-gestation.

197 r source of myocardium and of the pharyngeal arch mesoderm that gives rise to skeletal muscles.

198 The wavelike silicon dioxide arch microstructure exhibits Young modulus and fracture

199 mon carotid artery using an idealized aortic arch model.

200 The uniquely arched morphology of the human midfoot is thought to sti

201 boxyl side chain of Glu89 (located along the arch motif in hExo1) flips frequently from the reactant

202 ormational entropy is catalyzed, in part, by arch motions and transient binding interactions between

203 Coupling of substrate-dependent arch motions to transition-state stabilization suppresse

204 matic mutations [2], with the most prevalent ARCH mutations being in the DNMT3A and TET2 genes, previ

205 y extracted human teeth of each type on each arch ( n = 80 teeth) were inspected for enamel crack pat

206 coarctation of the aorta/hypoplastic aortic arch (n=5), tetralogy of Fallot (n=1), hypoplastic right

207 for sex, syndrome, tricuspid regurgitation, arch obstruction, and shunt type.

208 is affected by the second, transverse tarsal arch of the human foot(16).

209 navicular joint and flattening of the medial arch of the left foot.

210 ations are essential to shape the mandibular arch of the mouse embryo.

211 gets the Gly(312)-Pro(313)-Gly(314)-Arg(315) arch of the third hypervariable (V3) loop of the HIV-1 s

212 uced glucose uptake in the spleen and aortic arch of these mice.

213 together, the representative sizes of dental arches of 12-year-old Vietnamese children have been defi

214 bones derived from the equivalent pharyngeal arches of mammals.

215 no dissection occurs in the thoracic aortic arches of the mice with TAD model.

216 osin in the small muscles joining the neural arches of the spine suggesting that loss of myosin funct

217 ements derived from the first two pharyngeal arches of zebrafish.

218 on assists the departure, through the mobile arch, of the nucleotide monophosphate product from the c

219 approach could be relevant for patients with ARCH or AML caused by loss-of-function DNMT3A mutations.

220 AoD originated in the distal arch or descending aorta in 71%; 52% of affected patient

221 with the removal protocol, age, sex, dental arch or tooth type (p > 0.05/Cox), but was nearly 5-time

222 regulated release of protons through either Arch or voltage-gated proton channel Hv1 activated neigh

223 the two layers separate to form a pronounced arch over the remaining BM width.

224 r efficiently (straight towards an object or arched over an obstacle) or inefficiently (straight towa

225 inefficiently (straight towards obstacle or arched over empty space).

226 Medial motor area fibers (M2/M3/M4) arched over the caudate and lateral motor area fibers (M

227 ith incompleteness of the superficial palmar arch ( P=0.13).

228 l PFP was associated with PLC (P < .001) and arch (P = .006) injuries but not with body (P = .056), l

229 les that are derived from the 4th pharyngeal arch (PA); however, the tensor veli palatini, derived fr

230 grate from the neural tube to the pharyngeal arches (PAs) of the developing embryo and, subsequently,

231 fy the prevalence of tibial artery and pedal arch patency by angiography in these patients.

232 Selective Aortic Arch Perfusion (SAAP) combines thoracic aortic balloon h

233 ts gill cover formation, whereas ectopic pan-arch Pou3f3b expression generates ectopic skeletal eleme

234 ht-activated proton pump, Archaerhodopsin-3 (Arch), proton transients induced ASIC currents in both n

235 mal aorta and the left ventricle (eg, aortic arch pulse wave velocity and distensibility) as well as

236 However, effects of aortic arch PWV on the transmission of harmful excessive pulsat

237 g gingival phenotype (e.g., age, sex, dental arch, race, crown forms, etc.)?

238 topic expression of Sema3c in the pharyngeal arch region.

239 However, why some aortic arches regress while others are incorporated into the ma

240 evaluate the outcome of endovascular aortic arch repair for chronic dissection with a custom-made br

241 Rates of hemiarch, and total arch repair were similar between the sexes; however, wom

242 ally tuned and electrostatically driven MEMS arch resonator operated in air.

243 bdominal aortic aneurysms, and caused aortic arch ruptures and dissections, indicating that alpha2(V)

244 the unique acceleration of the entire hyoid arch segment, with earlier and orchestrated development

245 ur proposed that paired fins evolved as gill arch serial homologues, but this hypothesis is now widel

246 The palmar arches serve as the most important conduits for digital

247 wafer with a deliberate curvature to form an arch shape.

248 ves the CS and binds to streptomycin and the Arch-shape structure is disassembled.

249 ty of aptamer toward its target, property of Arch-shape structure of Apt-CS conjugate to act as a gat

250 xo I), complimentary strand of aptamer (CS), Arch-shape structure of aptamer (Apt)-CS conjugate and g

251 The ELL2 domain has the same arch-shaped fold as the tight junction protein occludin.

252 The arch-shaped Z944 molecule reclines in the central cavity

253 rior grafted sites, 19 anterior, and 17 full-arch sites.

254 We find that while the jaw and hyoid arch skeleton derive from neural crest, and the pectoral

255 TLR7 deficiency also reduced aortic arch SMC loss and lesion intima and media cell apoptosis

256 neural crest (NC, ascending aorta/transverse arch) SMC lineages to model MFS aortic pathology.

257 Incompleteness of the superficial palmar arch (SPA) was present in 46%, the deep palmar arch was

258 f elastic recoil (P < .001), as was cephalic arch stenosis in fistulas (P = .047) and autogenous fist

259 namic waves to quantify the effect of aortic arch stiffening on transmitted pulsatility to cerebral v

260 plasma etching can be used to fabricate the arched stripe arrays.

261 This approach of fabricating a wavelike arch structure may become a promising route to produce a

262 R acts as sacrificial layer to form wavelike arched structures.

263 udinal arch during running, and suggest that arch supports used in some footwear and orthotics may in

264 rfusion (SACP) in children undergoing aortic arch surgery are unclear.

265 (DHCA; n = 53) in children undergoing aortic arch surgery during a period from January 2008 to Decemb

266 t-term outcomes in children receiving aortic arch surgery under CPB.

267 and its large branches, resulting in aortic arch syndrome, blindness, and stroke.

268 inhibitor show lower SMC loss in the aortic arch than controls.

269 e-diameter, highly compliant, elastic aortic arch that allows the aorta to accommodate blood ejected

270 on in vivo, and drive preservation of aortic arches that ought to regress.

271 ed a long-range RNA-RNA interaction, the FSE-arch, that encircles the programmed ribosomal frameshift

272 ontribution of SHF-derived ECs to pharyngeal arches, the remodeling of endothelial plexus into the PA

273 icted compression of the foot's longitudinal arch, this study provides the first direct evidence that

274 ion in the pharyngeal endoderm of the dorsal arch, thus preventing dorsal EDNRA signaling.

275 l crest-derived structures, including aortic arch, thymus, and cranial nerves.

276 h human fetal ear and mouse second branchial arch tissue confirmed that genes located among associate

277 fferent nerve endings innervating the aortic arch to function as a baroreceptor.

278 TKE values were integrated over the aortic arch to obtain peak TKE.

279 ght trajectories upwards to avoid obstacles, arched trajectories downward towards goals).

280 Inspiratory-phase photoinhibition in Arch-transfected mice during inspiration increased tidal

281 odes of vibrations of slightly curved beams (arches): two-one internal resonance, three-one internal

282 easured regional stiffness within the aortic arch using pulse wave velocity (PWV) and have found a st

283 In thoracoabdominal NRP opening the aortic arch vessels to atmosphere allows collateral flow to be

284 ude the descending aorta and open the aortic arch vessels to atmosphere.

285 minins and show that a human-like transverse arch was a key step in the evolution of human bipedalism

286 The pedal arch was absent or incomplete in 86 of 103 (83.5%) limbs

287 Atherosclerotic burden in aortic arch was assessed by haematoxilin & eosin immunohistoche

288 ch (SPA) was present in 46%, the deep palmar arch was complete in all patients.

289 lectrical activity under conditions in which Arch was inefficient.

290 ated inhibitory proton pump Archaerhodopsin (Arch) was expressed under control of the sensory neuron-

291 cross-sectional area/[height]2 at the aortic arch were found to have good correlation with spirometry

292 ly increased incidence of interrupted aortic arch when compared with Tbx1 heterozygous mice.

293 yonic neural folds and migrate to pharyngeal arches, which give rise to most mid-facial structures.

294 initial alignment (0.018-in. nickel-titanium arch wire), and final alignment (0.019 x 0.025-in. stain

295 tart: placement of 0.014-in. nickel-titanium arch wire), initial alignment (0.018-in. nickel-titanium

296 alignment (0.019 x 0.025-in. stainless steel arch wire).

297 We report a case of the right-sided aortic arch with aplasia of the left brachiocephalic trunk in a

298 isual field in the right eye showed inferior arch with fixation sparing and supero-temporal central s

299 The right aortic arch with mirror-image of branching arteries without coe

300 onstruction of the ascending aorta or aortic arch) with intraoperative bleeding (blood volume between