ライフサイエンスコーパス: claw

1 ripheral neurons in the transplanted feeding claw.

2 f transverse skin folds just proximal to the claw.

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

4 The second digit supports a massive, hooked claw.

5 rojecting from the pRNA ring resemble an RNA claw.

6 es PIASx knockdown-induced loss of dendritic claws.

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

8 osts in place of nonfeeding, nonchemosensory claws.

9 anosaurus is known for its excessively large claws.

10 body, which receive input on large dendritic claws.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 echanisms of cavitation formation during the claw closure.

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

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

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

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

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

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

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

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

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

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

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

42 sumoylated at lysine-403 promoted dendritic claw differentiation.

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

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

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

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

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

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

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

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

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

52 the overall differentiation process of nail/claw formation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 6-, 32-, and 50-cell Xenopus laevis (African clawed frog) embryos.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 have been conducted seeking evidence for the CLAW hypothesis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 Such differences were not found for claw meat.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 ice showed a subtly but appreciably modified claw phenotype.

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

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

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

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

161 Successfully transplanted claws retain donor morphologies and contain chemosensory

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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