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1 n the past age-related clonal hematopoiesis (ARCH).
2 , such as the proton pump archaerhodopsin-3 (Arch).
3 ve preservation of embryonic vessels (aortic arches).
4 th Tfb3 binding on two opposite faces of the Arch.
5 the maxillary process of the first branchial arch.
6 that dictates the energy-saving role of the arch.
7 suggestive of a reduced medial longitudinal arch.
8 y during development of the first pharyngeal arch.
9 ess and hypoplasia of clavicle and zygomatic arch.
10 s a rare congenital anomaly involving aortic arch.
11 ells derived from mouse embryonic pharyngeal arch.
12 rentiate into cardiac cells as they exit the arch.
13 ry NC population allocated to the mandibular arch.
14 sclerosis at both the aortic root and aortic arch.
15 regulating cartilaginous joints in the hyoid arch.
16 s always preserved by a complete deep palmar arch.
17 mportant for morphogenesis of the mandibular arch.
18 vatives from the first and second pharyngeal arches.
19 ertebral body (or centrum) and the vertebral arches.
20 l active in the oral epithelium or branchial arches.
21 failed to condense correctly into pharyngeal arches.
22 argely similar in Hox-positive and -negative arches.
23 s apoptosis of neural crest in the branchial arches.
24 somites, ventral blood island and branchial arches.
25 doubling time after populating the branchial arches.
26 roliferation within the posterior pharyngeal arches.
27 long the dorsoventral axis of the developing arches.
28 genes in distinct regions of the pharyngeal arches.
29 d with blood vessels in anamniote pharyngeal arches.
30 riginally evolved via transformation of gill arches.
33 stered in the mesodermal cores of pharyngeal arch 2 (PA2), where they downregulate nkx2.5 expression.
34 ing of Meis, Pbx, and Hoxa2 in the branchial arches, a series of segments in the developing vertebrat
35 s detected in vivo in mouse and swine aortic arch (AA) endothelia exposed to chronic disturbed flow,
36 asured the cardiorespiratory consequences of Arch activation (10 s) in conscious rats during normoxia
37 derived from the first and second branchial arches also share a clonal relationship with different S
40 ansient opening of the interface between the Arch and 4FeS domains, allowing access to a second bindi
41 tic plaques in carotid artery, heart, aortic arch and aorta in acute and chronic atherosclerosis indu
44 lement of Gbx2, which is required for aortic arch and cardiac outflow tract development, and is a kno
45 ontributed to 75% of all strokes; for aortic arch and extracranial carotid artery calcification this
46 pecific focal localization within the aortic arch and its branches, as detected by fluorescence molec
55 to control the remodelling of the pharyngeal arches and the septation of the heart and outflow tract.
56 his Introduction highlights some of the over-arching and intersecting priorities for addressing cause
58 This was broadly observed in aortic root, arch, and total aorta of male mice, whereas the effect w
59 are able to migrate, populate the branchial arches, and display some elements of correct proximo-dis
62 evolutionary relationship between centra and arches, and their varying modes of skeletal mineralizati
65 the developing gill arches establishes gill arch anteroposterior polarity and maintains the prolifer
70 OFT, instead contributing to the pharyngeal arch arteries (PAAs), and second, a loss of first heart
71 crucial for normal development of the aortic arch arteries and cranial vasculature during embryonic d
74 the NC mediated morphogenesis of the aortic arch artery and differentiation of NC cells into vascula
76 matically improve the absolute brightness of Arch, as confirmed biochemically and with live-cell imag
77 to investigate the patency of the ulnopalmar arches, as well as handgrip strength tests to examine th
78 ll mean irregularity index in the mandibular arch at baseline was 8.5 +/- 3.8 mm (95% CI, 7.6 to 9.3)
79 associations for microinfarction were: TAVI (arch atheroma grade: r=0.46; P=0.0001) and SAVR (concomi
80 l fibrillation, patent foramen ovale, aortic arch atherosclerosis, atrial cardiopathy, and substenoti
81 that both CRF-R1 and CRF-R2 agonists reduced arched back nursing (ABN) rapidly and after a delay, res
82 As a proof-of-concept for the application of Arch-based sensors in vivo, we show fluorescence voltage
84 with intimal flap extension into the aortic arch between the innominate and left subclavian arteries
86 c cells associated with zebrafish pharyngeal arch blood vessels, and propose a new model for amniote
88 aintained by the dominant CDC31-16 showed an arched bridge, indicating Kar1's function in tethering S
89 prominent associations were found for aortic arch calcification and cardiovascular mortality (age- an
92 d manually at 3 predetermined levels (aortic arch, carina, and bronchus intermedius) to confirm ECAC
94 a non-cell-autonomous increase in pharyngeal arch cell death accompanied by alterations in Fgf8 and S
95 for the expression of Lhx8 in the maxillary arch cells and that Lhx8_enh1 was a direct target of the
97 nvolves failure in neural tube and vertebral arch closure at early gestational ages, followed by subs
98 genes with regional expression in zebrafish arch CNCCs reveals complex regulation by Edn1 and points
101 del data confirm that it is the end-range of arch compression that dictates the energy-saving role of
102 tudy provides the first direct evidence that arch compression/recoil during locomotion contributes to
105 The present simulations suggest that aortic arch curvature is an important risk factor for embolic s
108 g external ear anomalies, abnormal branchial arch derivatives, heart malformations, diaphragmatic her
110 are not viable and display severe branchial arch-derived facial skeleton defects, including absence
112 bi- or unilateral OME, the fourth pharyngeal arch-derived levator veli palatini muscles were hypoplas
113 at the level of the ascending aorta, aortic arch, descending thoracic aorta, and coronary arteries b
114 at the level of the ascending aorta, aortic arch, descending thoracic aorta, and the coronary arteri
115 ooth muscle cells (SMCs) around those aortic arches destined for survival and reorganization, and ide
116 embryos, mutation of Prdm1 affects branchial arch development and leads to persistent truncus arterio
117 e transcription factor SIX1 regulates dorsal arch development not only by inducing dorsal Jag1 expres
126 y among many radiologists to categorize such arch dissections as type A lesions, thus making them an
128 Previous work indicated that deletion of the arch domain has minimal effect on Mtr4 unwinding activit
129 lates helicase activity and suggest that the arch domain plays a previously unrecognized role in unwi
132 astic energy-saving role of the longitudinal arch during running, and suggest that arch supports used
133 h a delay in expression of Fgf8 in branchial arch ectoderm and a failure of neural crest cells in the
134 brafish foxi1 is also expressed in branchial arch ectoderm and endoderm, and morpholino knock-down of
135 t likely perturb the patterning of branchial arches, either through excessive activity (under a reces
136 ASAP1 and a previously described citrine-Arch electrochromic Forster resonance energy transfer se
140 m a signalling centre in the developing gill arches establishes gill arch anteroposterior polarity an
141 early gnathostomes, and theories about gill arch evolution were driven by information gleaned mostly
142 indicate that the extreme distal pharyngeal arch expression domain of Hand1 defines a novel bHLH-dep
144 lcification in the coronary arteries, aortic arch, extracranial, and intracranial internal carotid ar
145 consisting of macrocephaly, prominent eyes, arched eyebrows, hypertelorism, a glabellar nevus flamme
146 ndings thus reinterpret the polarity of some arch features of the crown jawed vertebrates and invert
150 ebral body for 18 of 57 patients, the neural arch for 21 of 57 patients, and the articular process fo
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 02), and Norwood discharge peak echo-Doppler arch gradient (hazard ratio, 1.07 per 1 mm Hg; P<0.01).
155 in neonatal mice expressing archaerhopsin-3 (Arch), halorhodopsin (eNpHR), or channelrhodopsin-2 (ChR
156 e energy-sparing spring theory of the foot's arch has become central to interpretations of the foot's
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 trifluorobut-3-en-2-ols [CF3-allyl alcohols, ArCH horizontal lineCHCH(OH)CF3] with arenes under activ
160 The presence of coarctation shelf and aortic arch hypoplasia were more common in fetuses with CoA tha
162 is the central mediator of dorsal mandibular arch identity, thus ensuring separation of bone developm
166 the lumbar cord in mice expressing eNpHR or Arch in ChAT(+) or Isl1(+) neurons, depressed motoneuron
167 oline acetyltransferase neurons (ChAT(+)) or Arch in LIM-homeodomain transcription factor Isl1(+) neu
168 curvature and branching point of the aortic arch in mice as well as human pulmonary artery branches.
169 5' ends are accommodated by a small, mobile arch in the active site that binds recessed ends at its
170 r, until now little was known about visceral arches in early gnathostomes, and theories about gill ar
171 .g., larger limb joints, spring-like plantar arch) in Homo was somewhat mosaic, with the full enduran
172 euroepithelium, the mandibular and maxillary arches, including both their mesenchymal and ectodermal
177 ecting the stepwise transformation of a gill arch into a jaw) or developmental genetic data (for exam
181 shows that the metabolic energy saved by the arch is largely explained by the passive-elastic work it
183 lphav integrins developed interrupted aortic arches, large brachiocephalic/carotid artery aneurysms a
184 Specifically, FAP251-null cilia lack an arch-like density at the RS3 base, whereas FAP61-null ci
185 neath the orogen, the Moho beneath Qilian is arch-like, shallower beneath the center and deepens by u
186 eveloped model, incorporating flat upper and arched lower fiber layers connected by ground substance,
188 Proliferation was reduced in the branchial arch mesenchyme of Yap and Taz CNC conditional knockout
192 ormational entropy is catalyzed, in part, by arch motions and transient binding interactions between
194 y extracted human teeth of each type on each arch ( n = 80 teeth) were inspected for enamel crack pat
198 coarctation of the aorta/hypoplastic aortic arch (n=5), tetralogy of Fallot (n=1), hypoplastic right
202 .97+/-0.05 s(-1); P=0.068) and in the aortic arch of ApoE(-/-) mice compared with WT mice (ApoE(-/-):
205 gets the Gly(312)-Pro(313)-Gly(314)-Arg(315) arch of the third hypervariable (V3) loop of the HIV-1 s
208 osin in the small muscles joining the neural arches of the spine suggesting that loss of myosin funct
210 r of this protein family, Archaerhodopsin-3 (Arch) of halobacterium Halorubrum sodomense, was recentl
211 ArSR, ArSAr'), selenides (ArSePh), alcohols [ArCH(OH)R], amino derivatives [ArCH(NHSO2Ar')R), and 1,2
212 gene profiling of microdissected pharyngeal arch one (PA1) from Tbx1(+/+) and Tbx1(-/-) embryos at s
214 regulated release of protons through either Arch or voltage-gated proton channel Hv1 activated neigh
218 l PFP was associated with PLC (P < .001) and arch (P = .006) injuries but not with body (P = .056), l
219 les that are derived from the 4th pharyngeal arch (PA); however, the tensor veli palatini, derived fr
220 ike (Nbl) depletes CPCs in second pharyngeal arches (PA2s) and is associated with an atrophic heart.
221 grate from the neural tube to the pharyngeal arches (PAs) of the developing embryo and, subsequently,
224 and emx2 expression in the second pharyngeal arch, presaging the differentiation of the reduced dorsa
225 ap of candidate enhancers from the maxillary arch (primordium for the upper jaw) of mouse embryos.
226 ht-activated proton pump, Archaerhodopsin-3 (Arch), proton transients induced ASIC currents in both n
227 ly transduced RTN and nearby C1 neurons with Arch (PRSx8-ArchT-EYFP-LVV) and measured the cardiorespi
228 mal aorta and the left ventricle (eg, aortic arch pulse wave velocity and distensibility) as well as
232 extend the primary surgery to aortic root or arch repair leads to a highly complex clinical course.
233 for complicated distal dissection and distal arch repair, and has recently been discussed as a pre-em
235 5 valve surgery, 2 septal myectomy, 1 aortic arch replacement, 1 myocardial bridge unroofing, and 1 m
237 e-sparing aortic root replacement; 12% total arch replacement; 3% in-hospital mortality) at 2 tertiar
238 nternal to the gills--the visceral branchial arches--represents one of the key events in early jawed
240 bdominal aortic aneurysms, and caused aortic arch ruptures and dissections, indicating that alpha2(V)
241 Gegenbaur's classical hypothesis of jaw-gill arch serial homology is widely cited, but remains unsupp
245 ty of aptamer toward its target, property of Arch-shape structure of Apt-CS conjugate to act as a gat
246 xo I), complimentary strand of aptamer (CS), Arch-shape structure of aptamer (Apt)-CS conjugate and g
250 differentiation of the reduced dorsal hyoid arch skeletal element typical of modern anamniote tetrap
252 Incompleteness of the superficial palmar arch (SPA) was present in 46%, the deep palmar arch was
253 f elastic recoil (P < .001), as was cephalic arch stenosis in fistulas (P = .047) and autogenous fist
255 This approach of fabricating a wavelike arch structure may become a promising route to produce a
258 udinal arch during running, and suggest that arch supports used in some footwear and orthotics may in
261 r rates of dental anomalies in the maxillary arch than did controls for primary (21% vs. 4%, P = 3 x
262 e develop from transient embryonic branchial arches that are populated by cranial neural crest cells.
263 shment of signaling centers in the branchial arches that are required for neural crest survival, patt
265 icted compression of the foot's longitudinal arch, this study provides the first direct evidence that
268 at heat shock induction of fgf3 in zebrafish arch tissue can rescue cell death in foxi1 morphants.
269 h human fetal ear and mouse second branchial arch tissue confirmed that genes located among associate
274 odes of vibrations of slightly curved beams (arches): two-one internal resonance, three-one internal
275 nly (type 1) or involving the entire AAo and arch (type 3) was found in the majority of RN-BAV patien
283 ice, the (64)Cu-GPVI-Fc uptake in the aortic arch was significantly higher compared with WT mice (Apo
284 ty during NC cell migration to the branchial arches was altered when premigratory cells were reduced
285 ated inhibitory proton pump Archaerhodopsin (Arch) was expressed under control of the sensory neuron-
287 teries, distal plantar arteries, and plantar arch were scored as fair to good; and for presence of co
289 hannelrhodopsin-2 (ChR2) or Archaerhodopsin (Arch) were expressed in glycinergic preBotC neurons of g
290 yonic neural folds and migrate to pharyngeal arches, which give rise to most mid-facial structures.
291 initial alignment (0.018-in. nickel-titanium arch wire), and final alignment (0.019 x 0.025-in. stain
292 tart: placement of 0.014-in. nickel-titanium arch wire), initial alignment (0.018-in. nickel-titanium
294 We report a case of the right-sided aortic arch with aplasia of the left brachiocephalic trunk in a
295 isual field in the right eye showed inferior arch with fixation sparing and supero-temporal central s
296 opmental anomalies of the carotid and aortic arch with intracranial bleeding is a rare occurrence and
298 onstruction of the ascending aorta or aortic arch) with intraoperative bleeding (blood volume between
299 death of mesenchymal cells in the mandibular arch without affecting epithelial proliferation and surv
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