ライフサイエンスコーパス: claw

1 rojecting from the pRNA ring resemble an RNA claw.

2 ripheral neurons in the transplanted feeding claw.

3 f transverse skin folds just proximal to the claw.

4 , isolated on the basis of homology to CRABS CLAW.

5 The second digit supports a massive, hooked claw.

6 various keratinized organs such as nails or claws.

7 es PIASx knockdown-induced loss of dendritic claws.

8 etarsus, which is characterized by a pair of claws.

9 osts in place of nonfeeding, nonchemosensory claws.

10 ng, those of calcified salmon teeth and crab claws.

11 ir large size and powerfully built teeth and claws.

12 s, swelling, en passant boutons, boutons, or claws.

13 anosaurus is known for its excessively large claws.

14 latively tighter grip strength in the manual claws.

15 body, which receive input on large dendritic claws.

16 was identified recently by homology to CRABS CLAW, a gene involved in carpel and nectary development

17 he hind foot that terminates in a sicklelike claw, a unique characteristic of the theropod groups Tro

18 static pressure and the force exerted during claw adduction and observed a strong correlation between

19 rganisms such as zebrafish (Danio rerio) and clawed African frog (Xenopus laevis).

20 ad subfamily with highest homology scored to clawed African frog and human Smad2.

21 Percepta (PTI-00703 cat's claw and a specific oolong tea extract) was determined t

22 curred nearly instantly when PTI-00703 cat's claw and Abeta fibrils were mixed together as shown by a

23 Spt4/5 binds in the middle of RNA polymerase claw and encloses the DNA, reminiscent of the DNA polyme

24 Samples of claw and leg meat of 185 red king crabs (Paralithodes ca

25 ic analysis suggests that the enlarged thumb claw and robust forelimb evolved during the Jurassic, be

26 ngate, slender legs with pectinate pretarsal claws and lacking trumpet-shaped empodia.

27 red significantly from muscle (white meat in claws and legs).

28 Here, by taking inspiration from claws and scales found in nature, we show that buckling

29 he jaw, and traditional morphometrics of the claws and skull are compared between bohaiornithids and

30 tannin fractions of Uncaria tomentosa (Cat's Claw) and Malus domestica (apple).

31 monomer has four domains: N-terminal, body, claw, and C-terminal.

32 e teeth, a rostral rhamphotheca, long manual claws, and a wide, opisthopubic pelvis.

33 flippers with little digit mobility, reduced claws, and hydrodynamic characteristics comparable to th

34 capsular support had posterior chamber iris-claw aphakic IOL implantation between 2007 and 2012.

35 red molecular claw." The key residues of the claw are not conserved in two C7 family members that do

36 attachment and the low, flat-bottomed pedal claws are consistent with aquatic foot-propelled locomot

37 orest plant (i.e. Uncaria tomentosa or cat's claw) as both a potent "plaque and tangle" inhibitor and

38 long setae, legs with only one single tarsal claw associated with two additional long setae, etc.

39 was also identified as the most potent cat's claw bark powder (Uncaria tomentosa) to reduce and inhib

40 (greater than 400 ng 20 E/ml) than pretarsal claws, bristles, and other joints (greater than 40 ng 20

41 l, monocot and eudicot species, we show that CLAW can rapidly produce chloroplast genome assemblies w

42 relative to normal force is required because claws can find more usable surface, but this trend rever

43 Remarkably, parrotlet claws can undergo superfast movements, within 1-2 ms, on

44 laeobiology of Megaraptora, a group of large-clawed carnivorous theropod dinosaurs known from Cretace

45 Here, we present CLAW (Chloroplast Long-read Assembly Workflow), an easy

46 ts lowermost third receives the axons of the clawed class II Kenyon cells, which are the first to dif

47 . pungens was a relatively large (~ 1.3 kg), claw-climbing arborealist capable of frequent clinging o

48 or experimental work and is applied here for claw closure at realistic conditions.

49 Simulations show that during claw closure, a high velocity jet forms, inducing vortex

50 echanisms of cavitation formation during the claw closure.

51 We report here that the maize CRABS CLAW co-orthologs drooping leaf1 (drl1) and drl2 are req

52 The paralogous loci encode maize CRABS CLAW co-orthologs in the YABBY family of transcriptional

53 ets, which resemble crabs with four distinct claws, convert reactants in solution into products and t

54 dentify PHABULOSA (PHB), REVOLUTA, and CRABS CLAW (CRC) as potential downstream targets of SEUSS (SEU

55 ms in eudicot angiosperm species using CRABS CLAW (CRC), a gene required for nectaries in Arabidopsis

56 cers of the mutant floral phenotype of crabs claw (crc), a gene that specifies abaxial identity in ca

57 Other YABBY proteins (e.g. CRABS CLAW [CRC] and YABBY3 [YAB3]) can substitute for INO in

58 that the major components of PTI-00703 cat's claw crossed the blood-brain-barrier and entered the bra

59 a soft mud-silt substrate, projecting their claws deeply to register their traces on an underlying s

60 PTI-00703 cat's claw demonstrated both the ability to prevent formation/

61 To investigate the action of Fzd6 in claw development at the molecular level, we compared gen

62 The molecular mechanism of nail (and claw) development is largely unknown, but we have recent

63 ule neuron dendrites with impaired dendritic claw differentiation in the cerebellar cortex.

64 knockdown suppresses PIASx-induced dendritic claw differentiation, and expression of sumoylated MEF2A

65 ne-403, which led to inhibition of dendritic claw differentiation.

66 sumoylated at lysine-403 promoted dendritic claw differentiation.

67 l domain is freed to bind integrins, and the claw domain rotates to expose and project its membrane i

68 Cat's claw (Doxantha unguis-cati L.) vine accumulates nearly 8

69 dinosaurs that includes birds and the sickle-clawed Dromaeosauridae, has hitherto been largely restri

70 pidermis, alopecia, hair follicle dystrophy, claw dystrophy, and abnormal pigmentation.

71 and inspired by the tardigrade's mechanical claw engagement, coupled to an RBC membrane coating, to

72 diated by a positively charged pocket in the Claw, enhanced by p62 phosphorylation, mutually exclusiv

73 e predicted amino acid sequence of the cat's claw enzyme with that of the castor Delta9-18:0-ACP desa

74 ro-regional specificities (scales, feathers, claws, etc.) established by typical enhancers control fi

75 When chemically stimulated, the transplanted claws evoke feeding behavior not observed in normal male

76 ns the PCNA ring through a large-scale 'crab-claw' expansion of both RFC and PCNA that explains how R

77 in successfully transplanted female feeding claws express the enhanced sensitivity to chemical cues

78 omparison to 17 other manufacturers of cat's claw extracts tested.

79 omparison to 17 other manufacturers of cat's claw extracts.

80 d involucrin in the epidermal portion of the claw field in the knockout embryos.

81 lities that typically develop a high-arched "claw foot" appearance later in life.

82 eric globular domain that we designated the "Claw" for its shape.

83 f another YABBY protein coding region (CRABS CLAW) for INO overcomes this negative regulation, indica

84 puncture tools, such as fangs, stingers, and claws, for prey capture, defense, and other critical bio

85 the overall differentiation process of nail/claw formation.

86 ted in the brain of adult zebrafish, African claw frog, and mouse in a comparative manner.

87 Mangold Organizer (SMO) in the South African Clawed Frog (X. laevis), a popular model of development,

88 gments between the violet pigment of African clawed frog (Xenopus laevis) and its ancestral UV pigmen

89 es from 16-cell embryos of the South African clawed frog (Xenopus laevis) and microextraction of thei

90 We address this question using the African clawed frog (Xenopus laevis) as a model.

91 vealed that expressing HvSWEET11b in African clawed frog (Xenopus laevis) oocytes facilitated the bid

92 Here, we show that AID from African clawed frog (Xenopus laevis), but not pufferfish (Takifu

93 the bull frog (Rana catesbeiana) and in the clawed frog (Xenopus laevis), which demonstrates that th

94 dothelin signaling components in the African clawed frog (Xenopus laevis).

95 a full-size Tg coding sequence from western clawed frog (Xenopus tropicalis) and zebrafish (Danio re

96 Here we show, by using a clawed frog (Xenopus tropicalis), that GRP is not a mamm

97 hepcidins (tHEP1 and tHEP2) from the Western clawed frog (Xenopus tropicalis).

98 vertebrates, such as mouse, chicken, western clawed frog and zebrafish, are widely used in toxicity t

99 ith their human, mouse, chicken, and western clawed frog orthologs, resulting in 366 alignments.

100 ass II beta chains, more similar to HLA-DRB, clawed frog Xela-F3, and nurse shark Gici-B.

101 ight into embryonic nutrition in the African clawed frog Xenopus laevis by studying YPs.

102 We have determined that the clawed frog Xenopus laevis contains twice the number of

103 The African clawed frog Xenopus laevis has been instrumental to inve

104 The African clawed frog Xenopus laevis is an important model organis

105 ral tube closure in mouse and in the African Clawed Frog Xenopus laevis to elucidate the etiology of

106 bines experimental advantages of the African clawed frog Xenopus laevis with more tractable genetics.

107 amphibian epidermis derived from the African clawed frog Xenopus laevis, and imaged calcium activity

108 In the clawed frog Xenopus laevis, neural crest induction depen

109 clamp recordings on oocytes from the African clawed frog Xenopus laevis, which endogenously express T

110 recent work on vocalizations of the African clawed frog Xenopus laevis.

111 nous ALF and TFIIA activities in the African clawed frog Xenopus laevis.

112 in the retinal photoreceptors of the African clawed frog Xenopus laevis.

113 ix separating these epithelia in the African clawed frog Xenopus laevis.

114 method using oocytes from the South African clawed frog Xenopus laevis.

115 The western clawed frog Xenopus tropicalis is an important model for

116 ions in the germline and soma of the African clawed frog Xenopus tropicalis.

117 erio (zebrafish) and Xenopus laevis (African clawed frog) embryos, zygotic irf6 transcripts are prese

118 6-, 32-, and 50-cell Xenopus laevis (African clawed frog) embryos.

119 tudy gastrulation in Xenopus laevis (African clawed frog) embryos.

120 s and to classic model organisms (zebrafish, clawed frog) in one- and two-protein imaging experiments

121 Larvae of Silurana tropicalis (Western clawed frog) were exposed to DY7-contaminated water (0 t

122 ammalian tetrapods (anole lizard and African clawed frog).

123 d consequences of tetraploidy in the African clawed frog, we sequenced the Xenopus laevis genome and

124 We show here that the South African clawed frog, Xenopus laevis, is a suitable model for inv

125 or: the courtship songs of the South African clawed frog, Xenopus laevis.

126 roles in vocal communication in the African clawed frog, Xenopus laevis.

127 ty reference genome sequence for the western clawed frog, Xenopus tropicalis, along with draft chromo

128 The African clawed frog, Xenopus, is a widely used comparative model

129 Vocal behaviors of African clawed frogs (Xenopus laevis) are produced by a single p

130 Male and female African clawed frogs (Xenopus laevis) produce rhythmic, sexually

131 Male and female African clawed frogs (Xenopus laevis) produce sexually dimorphic

132 affect the development of testes in African clawed frogs (Xenopus laevis), but little is known about

133 ular basis of temporal complexity of African clawed frogs (Xenopus laevis).

134 of atrazine on sexual development in African clawed frogs (Xenopus laevis).

135 istence of Dracunculus infections in African clawed frogs (Xenopus laevis).

136 MicroRNAs from the testes of clawed frogs (Xenopus) were extracted and the expression

137 rt1-paralogue (dm-w) of female-heterogametic clawed frogs (Xenopus; ZW /ZZ ), is known across >8740 s

138 viposition is imminent, female South African clawed frogs swim to an advertising male and produce an

139 . medinensis L3s were recovered from African clawed frogs tissues up to 58 days post-infection, and D

140 ds isolated from cane toads Bufo marinus and clawed frogs Xenopus laevis.

141 hich occurs naturally on the skin of African clawed frogs--was immobilized on gold microelectrodes vi

142 us laevis) and Western (Silurana tropicalis) clawed frogs.

143 A swimming microrobot design with clawed geometry, a red blood cell (RBC) membrane-camoufl

144 d jumping fleas, violent spider jaws, shrimp claw hammers, and squirting beetles and cucumbers.

145 cases because of slippage of one of the iris-claw haptics and spontaneous complete posterior dislocat

146 Percepta's main ingredient, PTI-00703 cat's claw, has previously been shown to reduce brain amyloid

147 have been conducted seeking evidence for the CLAW hypothesis.

148 sults indicate that it is time to retire the CLAW hypothesis.

149 ecific polyphenol content in PTI-00703 cat's claw (i.e. polyphenols and proanthocyanidins) as we have

150 mmalian poxviruses use a conserved molecular claw in a C7-like protein to target SAMD9 and overcome h

151 uctural analysis reveals a tripartite lysine claw in NPP1 that stabilizes the terminal phosphate of A

152 that also contained polyphenols and/or cat's claw in their product demonstrated some AB fibril and ta

153 ion of postsynaptic granule neuron dendritic claws in the cerebellar cortex.

154 differentiation of granule neuron dendritic claws in the cerebellar cortex.

155 sis of postsynaptic granule neuron dendritic claws in the cerebellar cortex.

156 there were agenesis and hyperpigmentation of claws, interdigital webbing, reduced footpads, and trans

157 ropupillary implantation of the Artisan iris-claw intraocular lens (RPICIOL) in several aphakic condi

158 formation on the centration and tilt of iris-claw intraocular lenses (IC-IOLs) is limited.

159 change by retropupillary fixation of an iris claw IOL (n = 50).

160 ange with retropupillary fixation of an iris-claw IOL (n = 50).

161 atic dislocation of a posterior aphakic iris-claw IOL in 1 eye.

162 The following data were obtained: Iris-claw IOL model, Iridal or retroiridal enclavation, A-con

163 erior implantation technique of aphakic iris-claw IOL provided good visual outcomes with a favorable

164 (ACIOL), iris-claw IOL, retropupillary iris-claw IOL, 10-0 polypropylene iris-sutured posterior cham

165 OL) and the re-emergence of the iris-fixated claw IOL, ACIOL implantation for aphakia has regained po

166 valuated: anterior chamber IOL (ACIOL), iris-claw IOL, retropupillary iris-claw IOL, 10-0 polypropyle

167 and formula for aphakia correction with iris-claw IOLs to achieve the best refractive status in cases

168 ased on recent findings that PTI-00703 cat's claw is a specific and potent inhibitor/reducer of all t

169 The claw is affiliated with dense medial and lateral beds of

170 While CRABS CLAW is essential for nectary gland formation, its ectop

171 ndritic morphologies reminiscent of class II clawed Kenyon cells that supply the gamma lobes in other

172 d by a special class of intrinsic neuron-the clawed Kenyon cells-that are the first to differentiate

173 osophila melanogaster, Class II (also called clawed) Kenyon cells are well known for their extensive

174 rch diameter and texture, but foot, toe, and claw kinematics become surface-specific upon touchdown.

175 4) or IOL exchange with a retropupillar iris-claw lens (n = 50).

176 ange with retropupillary fixation of an iris-claw lens (n=51).

177 f inflammation due to a secondary implant of claw lenses, angle-supported IOLs, and scleral-fixated I

178 s, iris- or scleral-sutured lenses, and iris-claw lenses.

179 ance of short branches that gave a striking, claw-like appearance to many of the distal dendrites.

180 The non-virion RNAP has a crab-claw-like architecture.

181 Stem-I and the Stem-II S-turn assemble a claw-like decoding module, while the antiterminator, Ste

182 characterized by missing central digits and claw-like distal extremities.

183 ate, with the clamp loader opening in a crab-claw-like fashion upon ATP-binding.

184 ivates the complex are subtle, and that crab-claw-like movements are not a significant component of t

185 were characterized by several dendrites with claw-like terminals that received synaptic contacts from

186 st naturally-occurring virus reported in any clawed lobster species.

187 rus clarkii and Orconectes rusticus, and the clawed lobster, Homarus americanus.

188 ventrosum is closer to that of Nephropidae (clawed lobsters) than Astacidae (freshwater crayfish), t

189 PTI-00703 cat's claw (main ingredient in percepta) was also identified a

190 d 4 nmi north and south, and their brown and claw meat were analyzed separately.

191 mples were mussel tissue, squid muscle, crab claw meat, whale meat, cod muscle, Greenland halibut mus

192 Such differences were not found for claw meat.

193 RFC) revealed that it functions using a crab-claw mechanism, where clamp opening is coupled to a mass

194 ers a large NKR-P1 surface area via a "polar claw" mechanism.

195 ometry of the claw used here is a simplified claw model, based on prior experimental work.

196 ism that orchestrates postsynaptic dendritic claw morphogenesis in the cerebellar cortex and suggest

197 epression of gnathal fate, and Antp dictates claw morphology.

198 um Model (HEM), are employed to describe the claw motion and cavitating flow field respectively.

199 li clamp loader opens the clamp using a crab-claw motion at a single pivot point, whereas the eukaryo

200 CLAW-MRM employs trimmed mean of m-value (TMM) normaliza

201 To improve usability, CLAW-MRM incorporates a natural language interface power

202 Enhancing biological relevance, CLAW-MRM integrates LIGER (lipidome gene enrichment reac

203 and integrating AI-assisted bioinformatics, CLAW-MRM provides an end-to-end workflow from data acqui

204 To evaluate CLAW-MRM's performance, we analyzed lipid profiles in li

205 d workflow for multiple reaction monitoring (CLAW-MRM), a platform designed to automate lipid annotat

206 Through CLAW-MRM-based LIGER, we identified metabolic pathways e

207 n poly(A)+ mRNAs from epidermis, limb bud or claw muscle and in total RNAs from ovary and gill, and t

208 Both lipid and aqueous extracts of raw claw muscle were analyzed by (1)H NMR spectroscopy and M

209 of the exoskeleton, epidermis, limb buds and claw muscle were probed with a monoclonal Ab against chi

210 of transformation was obtained with a CRABS-CLAW mutant that maintains an open gynoecium.

211 hen output to newly identified noncircadian "claw" neurons (CLs).

212 human hand (social condition) and mechanical claw (non-social condition) constructing a three-block t

213 aracterized by an extensive size range, with clawed NWMs (subfamily Callitrichinae, or callitrichines

214 sibility seems plausible: the three pairs of claw octopamine neurosecretory cells show immunostaining

215 The programmable actuator can mimic the claw of a hawk to grab a block, crawl like an inchworm,

216 are characteristic of the terminal dendritic claw of granule cells.

217 ing the mandibles of the dracula ant and the claw of the pistol shrimp.

218 ear-old male who presented with weakness and clawing of the medial digits of the right hand (main-en-

219 hat equivalent elements make up the jaws and claws of extant Onychophora.

220 cavitation-shooting weapons found in the big claws of male and female snapping shrimp, we test whethe

221 ues seen in female, but not male, neurons in claws of normal animals.

222 e describe a complex feature in the terminal claws of the mid-Cambrian lobopodian Hallucigenia sparsa

223 Limb proportions and retention of claws on all digits indicate that the new bat may have b

224 The digits form extra hyperpigmented claws on the lateral sides.

225 The unguis (hoof, claw, or nail) of the first digit (D1, also known as the

226 Schmorl nodes were associated with claw (P <.001) but not traction (P =.72) osteophytes.

227 throughout the peripheral nervous system of claw paw (clp) mutant mice suggest that the clp gene pro

228 ormation in the hypomyelinating mouse mutant claw paw (clp).

229 pou3f1 appears to require the claw paw gene product for activation of at least some of

230 mice exhibited a more severe phenotype than claw paw mice and had gliogenic defects in sensory, symp

231 as the mutated gene in spontaneously arising claw paw mutant mice), but Lgi4 is not known to play any

232 ice showed a subtly but appreciably modified claw phenotype.

233 SENTATION: Two patients with a previous iris-claw PIOL implantation were enrolled.

234 matter and teas from 11 samples of the cat's claw plant.

235 on expression in Escherichia coli, the cat's claw polypeptide functioned as a Delta9 acyl-ACP desatur

236 nerate shock waves by closing their snapping claws rapidly enough to form cavitation bubbles that rel

237 Rather, CRABS CLAW regulates transcription spatially, whereas GYMNOS r

238 specific constituents within PTI-00703 cat's claw responsible for both the observed "plaque" and "tan

239 Successfully transplanted claws retain donor morphologies and contain chemosensory

240 Imaging odor responses of these dendritic claws revealed that input channels with distinct odor tu

241 rvations validate that both of the RNAP crab claw's pincers are mobile, as both beta and beta' have s

242 aturases were isolated from developing cat's claw seeds.

243 and foot scales, hinging of foot joints and claw shape and size all inform the grasping ability, cur

244 Pedal claw shape and size are quantitatively analysed using tr

245 quaticus core RNA polymerase reveals a "crab claw"-shaped molecule with a 27 A wide internal channel.

246 's C-terminal domain (CTD) assumes a lobster claw-shaped form, the minor prong of which adheres to a

247 Hemigrapsus takanoi, the Japanese brush-clawed shore crab, is a highly successful invader in Eur

248 The claw snaps closed extremely rapidly, averaging 93 us, 17

249 typified by a crescent-shaped ssDNA binding claw that is flexibly appended to an APE2 endonuclease/e

250 years, and a large hand with long, trenchant claws that firmly establishes the loss of obligatory qua

251 Mutations in CRABS CLAW, the founding family member, display ectopic format

252 In this hypothesis--referred to as CLAW--the increase in cloud condensation nuclei led to a

253 r forming a unique "three-fingered molecular claw." The key residues of the claw are not conserved in

254 e nucleotide state of RagA while the Raptor "claw" threads between the GTPase domains to detect that

255 d therefore, they act redundantly with CRABS CLAW to establish polarity.

256 Snapping shrimps use a special shaped claw to generate a cavitating high speed water jet.

257 terisation, allowing individuals to optimise CLAW to their specific use cases.

258 rs, supporting the hook-and-pull function of claws to bring vegetation to its mouth.

259 explain scaling in organs from fiddler crab claws to human brains.

260 human (Homo sapiens), murine (Mus musculus), clawed toad (Xenopus laevis) and the yeasts Schizosaccha

261 (Ambystoma mexicanum), and the South African clawed toad (Xenopus laevis), we traced the origins of f

262 hanol and a salinity of 5); (ii) the African clawed toad Xenopus laevis (stages 24, 32 and 34 exposed

263 yte nuclear envelopes (NEs) from the African clawed toad Xenopus laevis, immunogold labeling of compo

264 gs and sperm chromatin, respectively, of the clawed toad Xenopus laevis.

265 a simple vertebrate model, the embryo of the clawed toad, Xenopus laevis, in which a known GABAergic

266 of the jelly coating from the South African clawed toad, Xenopus laevis.

267 six patients and no controls (P = 0.01), and claw toes were present in 12 patients and four controls

268 tern characterized by forelimb hyperflexure, clawed toes of all limbs, and a kinked tail.

269 cterized by the preservation of only the pes claw traces, that we interpret as having been left by wa

270 ) fastening ear loops behind the head with a claw-type hair clip, (4) enhancing the mask/face seal wi

271 PTI-00703 cat's claw (Uncaria tomentosa from a specific Peruvian source)

272 0703 cat's claw was the most effective cat's claw (Uncaria tomentosa) ingredient for reducing /disagg

273 ionally, 18 different manufacturers of cat's claw (Uncaria tomentosa) were directly compared for thei

274 The geometry of the claw used here is a simplified claw model, based on prio

275 occurring paralogs, such as that from cat's claw vine (Doxantha unguis-cati).

276 CLAW was designed such that users have complete control

277 d specific polyphenol within PTI-00703 cat's claw was epicatechin-4beta-8-epicatechin (i.e. an epicat

278 In addition, PTI-00703 cat's claw was the most effective cat's claw (Uncaria tomentos

279 Joints, bristles, and claws were dependent on 20E for differentiation between

280 Female and male chemosensory feeding claws were transplanted onto male hosts in place of nonf

281 most joints, the bristles, and the pretarsal claws, were examined to investigate how 20E controls the

282 Males use their enlarged major claw, which can exceed 30% of body mass, to snap a 1 mm-

283 ction with probabilistic friction from their claws, which they drag to find surface asperities-draggi

284 lls produce fixed distributions of dendritic claws while presynaptic processes are plastic.

285 We expect that CLAW will provide researchers (with varying levels of bi

286 multiple times, specifically, the gain of D1 claws with subterranean habits and the loss of D1 ungues