ライフサイエンスコーパス: appendage

1 ctivation during pacing from the left atrial appendage.

2 wing each arm to be elaborated into a unique appendage.

3 sis and repair of a fast-turnover ectodermal appendage.

4 disruption, and exclusion of the left atrial appendage.

5 serted into the incision in the right atrial appendage.

6 apons, such as the mantis shrimp's raptorial appendage.

7 exocuticle of an impact-resistant crustacean appendage.

8 l bags (6) and 1 thrombus in the left atrial appendage.

9 bifurcation and thrombus in the left atrial appendage.

10 oth reflexive and flexible movements of this appendage.

11 or neurons, the first such collection for an appendage.

12 tissues, including the gonad, intestine and appendages.

13 ed for the morphogenesis of other Drosophila appendages.

14 t of the hemichordates and a pair of feeding appendages.

15 tion, known as gliding, involves no external appendages.

16 hypotheses on the origin of jaws and paired appendages.

17 from the periphery toward the root of distal appendages.

18 nts, leading to regeneration of miniaturized appendages.

19 obopodians, worm-like animals with annulated appendages.

20 cilia depends on a set of centriole's distal appendages.

21 ntennae and epipodite-bearing biramous trunk appendages.

22 Galalpha(1,4)-GlcNAc and Manbeta(1,4)-GlcNAc appendages.

23 nces in the number of the respiratory dorsal appendages.

24 nsferases is expressed specifically in adult appendages.

25 sidue peptides that are used as the antibody appendages.

26 hout using flagella, pili, or other external appendages.

27 ionship between muscles and their associated appendages.

28 Feeding stages show regressed locomotor appendages.

29 during development for the formation of skin appendages.

30 pecialization in both abdominal and thoracic appendages.

31 and a chelate limb followed by two biramous appendages.

32 e to the plasma membrane via mother-specific appendages.

33 , and Hippo molecules localize to BBs and BB-appendages.

34 ites often branched extensively and had long appendages.

35 tes that maintain the capacity to regenerate appendages.

36 well as radiodont-like raptorial frontalmost appendages.

37 aps are present corresponding to the sensory appendages.

38 e crucial insights into the origin of paired appendages [2].

39 ancestral pair of pre-ocular (protocerebral) appendages [3-5].

40 in AI: diverticula (30), accessory auricular appendages (5), septal aneurysms (8), septal bags (6) an

41 s bound to an affinity-generating lipophilic appendage, a polyethylene glycol-based linker and the NT

42 eostatic conditions and after exfoliation or appendage amputation.

43 l and lateral regions of the developing wing appendage and reduced levels of Dpp affects similarly th

44 Here we analyse details of appendage and soft-tissue preservation in Yunnanolimulus

45 oskeleton is well documented by fossils, but appendage and soft-tissue preservation is extremely rare

46 , and mechanical properties of the raptorial appendage and the carapace under long-term ocean acidifi

47 l protein 83 (CEP83) eliminates these distal appendages and disrupts the anchorage of the centrosome

48 pulation through the movement of the feeding appendages and egestion work in concert, splitting large

49 constitutively expressed in ectoderm-derived appendages and in palmar/plantar epidermis and is robust

50 features plesiomorphic raptorial frontalmost appendages and includes Kylinxia, megacheirans, pancheli

51 vasoactive peptides with synthetic chemical appendages and protein blocking domains.

52 helicerata originated from megacheiran great appendages and that the sensorial antennae in Mandibulat

53 the tip touching the duodenum, the rectum or appendages, and a long appendix located in the scrotum a

54 transformations and disparity of frontalmost appendages, and the origin of crucial evolutionary innov

55 IDDosome component PIDD1 to centriole distal appendages, and this interaction is required for PIDDoso

56 at the radiodont and megacheiran frontalmost appendages are homologous, that the chelicerae of Chelic

57 Lobular appendages are present in mutant mice lacking BCs, imply

58 The skin epidermis and its appendages are subjected to daily assaults from the exte

59 Their most prominent head appendages are the two pairs of very long biramous anten

60 bunit, one on the hinge and the other on the appendage, are necessary and sufficient for functional c

61 he traditional portrayal of mammalian distal appendage as a pinwheel-like structure that is maintaine

62 me-wide screen, we identify centriole distal appendages as critical for PIDDosome activation in cells

63 s early during the development of ectodermal appendages-as early as the embryonic placode stage-and p

64 high resolution, the initial steps of distal appendage assembly.

65 n tomography we reveal that mammalian distal appendages associate with two centriole microtubule trip

66 veral analogues substituted with aminopropyl appendages at C5 displayed dominant TLR8-agonistic activ

67 Monogenean parasites have attachment appendages at their haptoral regions that help them to m

68 ysed oxidation to characterize their n-alkyl appendages attached to aromatic cores.

69 For instance, voluntarily releasing appendages (autotomy) to escape potential predators.

70 specialized body region composed of multiple appendage-bearing segments and whose complex evolution h

71 Reconstructing appendage-bearing skin in cultures and in bioengineered

72 s-sectional study and collected right atrial appendage biopsies.

73 inxia, megacheirans, panchelicerates, 'great-appendage' bivalved euarthropods and isoxyids.

74 alize and quantify how incorporation into an appendage blastema broadens the progeny contributions of

75 ds may also possess similarly differentiated appendages, but these details are obstructed by the limi

76 tions in patterning surface ectoderm and its appendages by controlling division orientation.

77 iquids or crawl on surfaces by rotating long appendages called flagella.

78 specialized class of mineralizing epithelial appendages called odontodes.

79 Ubiquitous microbial appendages called pili are involved in sensing surfaces

80 ia are decorated with long, exquisitely thin appendages called type IV pili (T4P), dynamic filaments

81 The morphology and range of motion of appendages can be revealed in fossils; however, biologic

82 Furthermore, human skin and its appendages can be used as highly accessible and clinical

83 orin protein core, uncovered in human atrial appendages, can regulate the local bioavailability of an

84 ene for the development of epidermis and its appendages, can respond to skin morphogenetic signals.

85 using multiple Type IV Pili (TFP), motorized appendages capable of force generation via linear extens

86 ta on the safety and efficacy of left atrial appendage closure (LAAC) for stroke prevention in patien

87 Percutaneous left atrial appendage closure (LAAC) is noninferior to vitamin K ant

88 gulation system activation after left atrial appendage closure (LAAC) remains unknown.

89 Left atrial appendage closure (LAAC) was approved by the U.S. Food a

90 llation) trial demonstrated that left atrial appendage closure (LAAC) with the Watchman device (Bosto

91 The implantation of left atrial appendage closure device (WATCHMAN, Boston Scientific, N

92 verview of current transcatheter left atrial appendage closure devices and review the results associa

93 er the past decade, percutaneous left atrial appendage closure has emerged as a valid alternative to

94 patients receiving the WATCHMAN left atrial appendage closure technology was designed to collect pro

95 Patients Receiving the WATCHMAN Left Atrial Appendage Closure Technology, patients with a WATCHMAN l

96 (Left Atrial Appendage Closure vs. Novel Anticoagulation Agents in At

97 Left Atrial Appendage Closure vs. Novel Anticoagulation Agents in At

98 ient's self-management [PSM] and left atrial appendage closure) are based on the concept of combining

99 tral and tricuspid valve repair, left atrial appendage closure, and paravalvular leak closure).

100 view the results associated with left atrial appendage closure, focusing on procedural and late outco

101 During left atrial appendage closure, the estimated dose absorbed by partic

102 In the study, we performed left atrial appendage closure.

103 Type IV pili (T4P) are bacterial appendages composed of protein subunits, called pilins,

104 These appendages consist of long tubular structures that protr

105 PS-NPs significantly decreased the appendage curling and heartbeat rate in F0 and reduced r

106 ent 2, the plastic leachate also reduced the appendage curling rate but increased growth and reproduc

107 nts that are observed proximal to the distal appendages (DAPs) in vertebrates.

108 itched gears" multiple times from the distal appendages (DAPs) to the ciliary compartment (CC), movin

109 Distal appendages (DAs) of the mother centriole are essential f

110 The hair-like cell appendages denoted as type IV pili are crucial for biofi

111 parallel activation of a genetic program for appendage development that was present in the bilaterian

112 components of the EDA pathway disrupt normal appendage development, leading to the human disorder hyp

113 that these transcription factors play during appendage development, their target genes and the mechan

114 l to investigate the molecular basis of skin appendage differences.

115 minates the early evolution of pancrustacean appendage differentiation and represents the oldest uneq

116 histopathologic changes in the right atrial appendage do not predict POAF.

117 Jointed exoskeletons permit rapid appendage-driven locomotion but retain the soft-bodied,

118 associated muscles (e.g., apical muscle) and appendages (e.g., tube feet and papulae).

119 o stasis of blood flow following left atrial appendage electrical isolation (LAAEI) could lead to thr

120 n relation to the centriole microtubules and appendage electron densities.

121 tachycardia ablation and Lariat left atrial appendage exclusion.

122 trated the mode of interaction with analogue appendages extending toward the PARP-1 adenosine-binding

123 mordia contribute to both ventral and dorsal appendage fates.

124 ys a pretelsonic segment bearing non-walking appendages, features as-yet known in all vicissicaudatan

125 , jet propulsion, undulatory locomotion, and appendages for movement.

126 , demonstrating the specificity of subdistal appendages for these events.

127 The appendages form an interlocked assembly attaching the ta

128 cial role the epidermis plays in barrier and appendage formation.

129 agellum are related pathogenicity-associated appendages found at the surface of many disease-causing

130 Type IV pili (T4P) are filamentous appendages found on many Bacteria and Archaea.

131 intracardiac echocardiography imaging of the appendage from the right ventricular outflow.

132 METHODS AND Human CPCs from the right atrial appendages from children of different ages undergoing ca

133 Human CPCs from the right atrial appendages from children of different ages undergoing ca

134 In contrast, atrial appendages from patients in persistent atrial fibrillati

135 a cleavage site that was not found in atrial appendages from patients in sinus rhythm.

136 and glutathione were also present in atrial appendages from surgical patients >=75 years as compared

137 ins were identified in left and right atrial appendages from the same patients.

138 onic placode stage-and plays a role in adult appendage function.

139 These appendages generate a feeding current to enhance the enc

140 for dissecting the regulatory mechanisms of appendage generation and reveals a range of requirements

141 a mechanism by which the Sp factors control appendage growth through the Notch signaling.

142 The predatory appendage had significantly higher % Mg under ocean acid

143 The diversification of paired appendages has been a major factor in the evolutionary r

144 zodiazepines bearing easily functionalizable appendages has been developed by ring-opening of activat

145 ce, an understanding of the origin of paired appendages has remained elusive.

146 NDISA)-PDA, offer a perfect platform for the appendage/immobilization of small nanocrystals inside re

147 e evolution of the digestive system, cranial appendages, immune system, metabolism, body size, cursor

148 intracardiac echocardiography imaging of the appendage in DOAC compliant patients.

149 hol intake, and occlusion of the left atrial appendage in patients with atrial fibrillation and perma

150 precise measurement of the positions of each appendage in three-dimensional (3D) space.

151 eliminated or converted into functional skin appendages in a niche-dependent manner.

152 We amputated appendages in a variety of cave-adapted and surface-dwel

153 remnant of the evolutionary history of this appendage, in which cells of the subcoxa of the leg coal

154 bstituted oxazole products bearing different appendages including different heterocyclic moieties wer

155 nd, is essential for the development of skin appendages including the breast.

156 Consequently, the carbohydrate appendage influences both the assembly behavior and the

157 5 (Tbx5), a gene indispensable for pectoral appendage initiation and development.

158 is shown that the nature of the carbohydrate appendage is crucial for the supramolecular (co)polymeri

159 , grooming of the antennae and other sensory appendages is an important strategy to enhance sensory a

160 Incessant FAT originating in the atrial appendages is more likely to respond to ivabradine than

161 and lateral diffusion and exchange with skin appendages is presented.

162 CEP164-dependent TTBK2 recruitment to distal appendages is required for subsequent CEP83 phosphorylat

163 to undergo empirical electrical left atrial appendage isolation along with extensive ablation (group

164 (Effect of Empirical Left Atrial Appendage Isolation on Long-term Procedure Outcome in Pa

165 Randomized trials of left atrial appendage (LAA) closure with the Watchman device have sh

166 ical electrical isolation of the left atrial appendage (LAA) could improve success at follow-up.

167 Left atrial appendage (LAA) electric isolation is reported to improv

168 dy was to evaluate the impact of left atrial appendage (LAA) exclusion on short-term outcomes in pati

169 rization of left atrial (LA) and left atrial appendage (LAA) flow dynamics in patients with atrial fi

170 nus rhythm at 6 months to assess left atrial appendage (LAA) function were included in this analysis.

171 Prophylactic exclusion of the left atrial appendage (LAA) is often performed during cardiac surger

172 Electric left atrial appendage (LAA) isolation (LAAI) may occur during cathet

173 duce 4-dimensional images of the left atrial appendage (LAA).

174 on of a pyrazolo[1,5-a]pyridine heterocyclic appendage led to a series of high-affinity dopamine rece

175 tachycardia ablation and Lariat left atrial appendage ligation that involve the epicardial space are

176 basal bodies, each extending a basal foot-an appendage linking motile cilia together to ensure coordi

177 orming a ring pattern consistent with distal appendage localisation.

178 hich also triggers the acquisition of distal appendage markers on daughter centrioles and the loss of

179 usive feeding programs with distinct sensory appendages, meal sizes, digestive tract targets, and met

180 the core BB structure and to the base of BB-appendage microtubules and striated fiber.

181 s of attachment ranging from aerial roots to appendages modified into hooks and tendrils on the leave

182 g molecular and cellular events that precede appendage morphogenesis has been challenging due to the

183 raphy [24] to reveal the three-dimensionally appendage morphology of the Chengjiang bivalved euarthro

184 e the ability to produce both unusually fast appendage movement and limb force needed for locomotion.

185 s tissue regeneration evidenced by epidermal appendage neogenesis and lack of scarring.

186 -immunoreactive (TH-ir) arborizations in the appendage neuromeres, as well as three prominent plurise

187 red to project to the brain and decorate the appendage neuromeres.

188 CCV in patients with endocardial left atrial appendage occlusion (LAAO) devices.

189 atients with stroke, 84 received left atrial appendage occlusion (LAAO) devices.

190 Left atrial appendage occlusion (LAAO) to prevent stroke in patients

191 consecutive patients undergoing left atrial appendage occlusion at Aarhus University Hospital, Denma

192 nology, patients with a WATCHMAN left atrial appendage occlusion device had consistently low rates of

193 ite-specific therapy directed at left atrial appendage occlusion has been now studied for stroke prev

194 are addressing the usefulness of left atrial appendage occlusion in both primary and secondary stroke

195 Left atrial appendage occlusion indication was based on the European

196 lated thrombosis (DRT) following left atrial appendage occlusion is a rare but feared complication.

197 Left atrial appendage occlusion with WATCHMAN has emerged as viable

198 ercutaneous therapies, including left atrial appendage occlusion, for stroke prevention have emerged,

199 prevention strategies, including left atrial appendage occlusion, in patients with atrial fibrillatio

200 In this study, we demonstrate that appendage of a single asparagusic acid residue (AspA tag

201 e organization of the ciliary basal foot, an appendage of basal bodies whose main role is to provide

202 ological investigations by imaging a walking appendage of Euperipatoides rowelli, a representative of

203 ning the RNA-dependent RNA polymerase and an appendage of globular domains containing an mRNA capping

204 The highly mobile chin appendage of Gnathonemus petersii, the Schnauzenorgan, i

205 The appendages of arthropods and vertebrates are not homolog

206 The reduced labrum and deutocerebral great appendages of L. illecebrosa also strengthen the affinit

207 of the labrum relative to the pre-oral great appendages of L. illecebrosa indicates that these limbs

208 in arterioles isolated from the right atrial appendages of patients with HFpEF.

209 chanism, whereby gauche interactions between appendages of the approaching maltol-derived ylides are

210 phenotype of cardiomyocytes from the atrial appendages of the heart led to the discovery that these

211 AKNA localizes at the subdistal appendages of the mother centriole in specific subtypes

212 ily focused on the sulfonamide and benzamide appendages of the scaffold.

213 paralogues of Hox genes are revealed in the appendages of two species of horseshoe crabs.

214 luding type IV pili, bacterial extracellular appendages often essential for attachment to host cells.

215 ous aromatic rings and to chiral amino ester appendages on the other side.

216 up to all euarthropods that have frontalmost appendages on the second head segment (Deuteropoda)(5-9)

217 luding the chelicerae, five pairs of walking appendages, opisthosomal appendages with book gills, mus

218 izing secondary axial structures such as the appendages, or during homeostasis in postnatal stages an

219 The star consists of 22 fleshy appendages, or rays, that are covered in Eimer's organs.

220 therefore serially homologous with the first appendage pair of extant euarthropods [1, 2, 4, 6, 8].

221 Vertebrate appendage patterning is programmed by Hox-TALE factor-bo

222 es, or gnathostomes, have two sets of paired appendages, pectoral and pelvic fins in fishes and fore-

223 pili are prototypical bacterial cell-surface appendages playing essential roles in mediating adhesion

224 Here we show that expression of a sensory appendage protein (SAP2), which is enriched in the legs,

225 he majority of cenexin, the mother centriole appendage protein and PLK1 binding partner, resides.

226 Here we characterize a novel distal appendage protein ANKRD26 and detail, in high resolution

227 The distal appendage protein ANKRD26 is found to interact with and

228 The distal appendage protein Cep164 appears to be a key actor invol

229 trast, the essential mother centriole distal appendage protein CEP164 did not play a role in either p

230 TBK2 is recruited to the centriole by distal appendage protein CEP164, little is known about TTBK2 su

231 Sclt1 gene, which encodes a centriole distal appendage protein important for ciliogenesis.

232 , we identified a mother centriole subdistal appendage protein, cenexin, as a critical player in symm

233 rate that TRAPPC14 interacts with the distal appendage proteins Fas-binding factor 1 (FBF1) and centr

234 croscopy to precisely determine where distal appendage proteins localize in relation to the centriole

235 and disrupts the localization of the distal appendage proteins SCLT1 and FBF1 and components of the

236 ration studies revealed that the hydrophobic appendages provide hyperstable collagen triple helices (

237 rovide support for a common origin of paired appendage regeneration in Osteichthyes (bony vertebrates

238 support a deep evolutionary origin of paired appendage regeneration in Osteichthyes and provide an ev

239 Understanding how to promote organ and appendage regeneration is a key goal of regenerative med

240 Vertebrate appendage regeneration requires precisely coordinated re

241 fferentiation reveals common gene groups for appendage regeneration with potential implications in re

242 (lobe-finned vertebrates) capable of paired appendage regeneration, regardless of the amputation lev

243 ramework for studies on the genetic basis of appendage regeneration.

244 consistent with a shared genetic program of appendage regeneration.

245 nctional studies of positional memory during appendage regeneration.

246 erful model system for the study of limb and appendage regeneration.

247 deficient, restricting our understanding of appendage regeneration.

248 as the % Ca and mechanical properties of the appendage remained unchanged.

249 However, its effectiveness on skin appendages remains to be confirmed in vivo.

250 at these excitatory synapses are formed onto appendages resembling dendritic spines, spines have not

251 y heal with scar, as characterized by dermal appendage restoration and organized collagen architectur

252 Right atrial appendage samples were prospectively collected during ca

253 e highly correlated in 233 human left atrial appendage samples.

254 Here, by characterizing centriole subdistal appendages (sDAP) in cells exclusively growing submerged

255 Subdistal appendages (sDAPs) are centriolar elements that are obse

256 Centrioles acquire subdistal appendages (sDAPs) during primary cilium formation.

257 distribution of core components of subdistal appendages (SDAs) and of recycling endosomes, which may

258 tion of the missing structure is recalled by appendage stump cells has puzzled researchers for centur

259 e from cells with proximal identities in the appendage stump.

260 mal hyperkeratosis, or abnormalities in skin appendages, such as nail plate dystrophy and structural

261 cal trials, PROTECT-AF (Watchman Left Atrial Appendage System for Embolic PROTECTion in Patients With

262 The PROTECT AF (WATCHMAN Left Atrial Appendage System for Embolic Protection in Patients With

263 of ASP are torsion of the testis (TT) or its appendages (TA) and epidymo-orchitis (EO).

264 ram-positive bacteria, extracellular protein appendages termed pili are necessary for adherence under

265 It is a late-evolving epidermal appendage that has the primary function of providing nut

266 The primary cilium, a sensory appendage that is present in most mammalian cells, plays

267 The mother centriole in RGPs develops distal appendages that anchor it to the apical membrane.

268 apparatus consisting of sensor-studded mouth appendages that are in constant motion.

269 d by having a robust first pair of raptorial appendages that bear well-developed ventral-facing spine

270 a new class of sensors bearing antenna-like appendages that can extend the wavelength of the chiropt

271 ironment, jawed vertebrates evolved skeletal appendages that drive oxygenated water unidirectionally

272 Fimbriae (also known as pili) are appendages that extend up to 2 mum beyond the cell surfa

273 Many motility organelles are complex surface appendages that have evolved a tight, hierarchical regul

274 bserve a highly periodic motion of the mouth appendages that is mirrored in oscillations of nearby tr

275 Conjugative pili are widespread bacterial appendages that play important roles in horizontal gene

276 ates, rays and holocephalans) possess paired appendages that project laterally from their gill arches

277 Fimbriae are protein-based filamentous appendages that protrude from the bacterial cell surface

278 f S. enterica depends on flagella, which are appendages that the bacteria use to move through the env

279 skin is a multilayered organ, equipped with appendages (that is, follicles and glands), that is crit

280 investigated the syringe-like blood-feeding appendage, the stylet, and discovered that sexually dimo

281 lasma is fully equipped with cirri (thoracic appendages), these are no longer used for filter feeding

282 termination, noninducibility or left atrial appendage thrombus.

283 To address this subject, human left atrial appendage tissues were obtained from 10 patients who und

284 ~80 degrees C, exposing these extracellular appendages to a very harsh environment.

285 Pilomatricoma, a benign skin appendage tumor, also known as calcifying epithelioma, c

286 We further show that distal appendages undergo a dramatic ultra-structural reorganiz

287 te their presynaptic structures, the lobular appendages, until BCs differentiate about a week after R

288 strates can be sensitive to small changes in appendage use.

289 along the posterior base of the left atrial appendage visualized by selective angiography.

290 FAT originating in the atrial appendages was a predictor of ivabradine response compar

291 Optimization of the core and aryl appendages was performed by scanning and matrix librarie

292 Excised right atrial appendages were analyzed histologically to characterize

293 eters of the left atrium and the left atrial appendage which have been shown to be associated with is

294 a loss of mitochondria inside their lobular appendages, which may indicate an energetic failure; and

295 , combination of the pyrazolo[1,5-a]pyridine appendage with a 5-hydroxy-N-propyl-2-aminotetraline uni

296 ed with dorsal outgrowths to evolve a dorsal appendage with motor control.

297 ve pairs of walking appendages, opisthosomal appendages with book gills, muscles, and fine setae perm

298 p characterized by enlarged raptorial "great appendages" with a central role in competing hypotheses

299 intracardiac echocardiography imaging of the appendage; with low risk of complications.

300 ), organs (Xenopus gills and mouse skin) and appendages (Xenopus tail), and provide recommendations o