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1  nonhistaminergic pruritogens (e.g., cowhage spicules).
2 urchin embryo forms an endoskeletal calcitic spicule.
3 onstitute the protein matrix of the skeletal spicule.
4 port via the primary mesenchyme cells to the spicule.
5 thus increasing the overall strength of each spicule.
6 tment, where they integrate into the growing spicule.
7 o mineralogically distinct layers within the spicules.
8 ower shocks that drive upward flows and form spicules.
9 rved occurrence and properties of individual spicules.
10 retory system, hermaphrodite vulva, and male spicules.
11 perimental manipulation of isolated skeletal spicules.
12 rant migrations and morphologically abnormal spicules.
13 ype male tail, including those that form the spicules.
14 from the endoderm and is concentrated in the spicules.
15 a-generated acanthocytes were imprinted with spicules.
16 ls (PMCs), which form the embryonic skeleton spicules.
17 e an endoskeleton consisting of two calcitic spicules.
18  deposition and integration into the forming spicules.
19 this taxon possessed a skeleton comprised of spicules.
20 t linear, "h"- and "H"-shaped, or triradiate spicules.
21 letal elements of the siliceous sponges, the spicules.
22 develop a structural mechanics model for the spicules.
23 together by organic matrix to form laminated spicules.
24  silicateins in silicification of the sponge spicule and offer the prospect of a new synthetic route
25 nd modern heteroscleromorphs, with hexactine spicules and a globose body form inherited from reticulo
26 re presented: (1) the formation of siliceous spicules and frustules in sponges and diatoms, respectiv
27       Studies of mineralization of embryonic spicules and of the sea urchin genome have identified se
28  lineage, the lineage that gives rise to the spicules and other male copulatory structures.
29 nd fine-scale surface features consisting of spicules and spines that scatter light into intense stra
30  larval eyes or ocelli, epidermal calcareous spicules, and a collection of serially reiterated epider
31 s to calcite (CaCO3) formation in sea urchin spicules, and not proto-aragonite or poorly crystalline
32 d morphogenesis of the posterior hypodermis, spicules, and proctodeum.
33 ct SM30 proteins are identified in embryonic spicules, and they have apparent molecular masses of app
34 tial filopodial cables within which skeletal spicules are deposited.
35                                              Spicules are dynamic jets propelled upwards (at speeds o
36 his observation, we found that lin-29 mutant spicules are on average 43% shorter than wild-type spicu
37                                              Spicules are shown to occur when magnetic tension is amp
38                                     PMCs and spicules are therefore directly exposed to strong change
39  materials (namely mollusk shells and sponge spicules) are discussed here.
40              The skeletal elements, known as spicules, are millimeter-long, axisymmetric, silica rods
41 , e.g., teeth, bones, shells, carapaces, and spicules, are of considerable interest to chemists and m
42 anics calculations and information about the spicules' arrangement within the sponge to develop a str
43 ir-2.1(0) males, the hypercontraction of the spicule-associated muscles pinch the vas deferens openin
44                 We show that the SPV and SPD spicule-associated sensory neurons and the spicule socke
45 pressed in the protractor muscles and in the spicule-associated SPC and PCB cholinergic neurons.
46 nstruct an elaborate calcareous endoskeletal spicule beginning at gastrulation.
47 , containing the three molluscan groups with spicules but without true shells, and they support the m
48 50, SM30, and PM27, in the three-dimensional spicule by studying changes in protein localization duri
49 l slit to widen, so that the male copulatory spicules can easily insert.
50                                          The spicules can function as single-mode, few-mode, or multi
51 evelopment goes awry after the generation of spicule cells, when spicule morphogenesis occurs in wild
52 eticulate, tufted skeleton of minute monaxon spicules, characteristic of the fossil demosponge family
53     A minority of these aggregates had short spicule-coated membranes, which resembled the beginnings
54 e aggregates finally are introduced into the spicule compartment, where they integrate into the growi
55 , while SM30 may play a role in secretion of spicule components.
56  respectively; (2) the structure of skeletal spicules composed of amorphous calcium carbonate in some
57                            The difference in spicule composition of the classes is interpreted throug
58                                       Silica spicules constitute 75% of the dry weight of the sponge
59                                         Each spicule contains a central protein filament, shown by x-
60  triggered rapid erythrocyte conversion into spicule-covered echinocytes, followed by MP shedding.
61 cowhage, the nonhistaminergic itch-producing spicules covering the pod of the legume Mucuna pruriens.
62 longation: elongated spicules with defective spicule cuticle can be formed.
63 for both spicule elongation and formation of spicule cuticle.
64 nly necessary but also sufficient to produce spicule cuticle.
65 NA-mediated interference results in the same spicule defect as caused by overexpression of POP-1, a T
66  cues secreted by other cells in the embryo, spicules deposited in PMC culture lack the complex branc
67 in defining the extracellular space in which spicule deposition occurs, while SM30 may play a role in
68                           In lin-29 mutants, spicule development goes awry after the generation of sp
69        A TGFbeta-like signal is required for spicule development in Caenorhabditis elegans males.
70 show that during Caenorhabditis elegans male spicule development, the specification of a glial versus
71 body size, but functional in sensory ray and spicule development.
72           LEV-11 (tropomyosin) regulates the spicules directly by controlling the male sex muscles an
73 etinal degeneration and the presence of bone spicules distributed throughout the retina at younger ag
74 eir role in the continued elaboration of the spicule during later stages of embryogenesis.
75  spicule socket cells are essential for both spicule elongation and formation of spicule cuticle.
76 beta signaling pathways might be involved in spicule elongation.
77 y separable from their function in mediating spicule elongation: elongated spicules with defective sp
78  the defecation cycle in hermaphrodites, and spicule eversion during mating in the male.
79 uncated PDGF receptor-beta inhibited gut and spicule formation and differentiation along the oral-abo
80 e role of proteases in these early events of spicule formation and their role in the continued elabor
81 lation (which has been considered before for spicule formation) and by p-modes (which are solar globa
82 ody size, male tail sensory ray identity and spicule formation.
83 chymal cells (PMCs) that are responsible for spicule formation.
84 d study of the optical properties of basalia spicules from the glass sponge Euplectella aspergillum a
85             Because cutaneous application of spicules from the plant Mucuna pruriens (cowhage) has be
86 on itch produced by intradermal insertion of spicules from the pods of a cowhage plant (Mucuna prurie
87 s elegans males to protract their copulatory spicules from their tail and insert them into the hermap
88 ons and sheath cells, although important for spicule function, are dispensable for spicule morphology
89 ate that unc-103 controls various aspects of spicule function.
90 emoval of the inhibitor allows resumption of spicule growth.
91 bonate and matrix proteins to the site(s) of spicule growth.
92 rs close to observational limits (< 500 km), spicules have been largely unexplained since their disco
93 rents to different chemical stimuli (cowhage spicules, histamine, capsaicin).
94 ponge monophyly and demosponge-hexactinellid spicule homology, and supports the primitive, stem-silic
95                 Continued elaboration of the spicule, however, is completely stopped; addition of the
96 dylcholine into irregular, curved and knobby spicules; i.e., echinocytosis became acanthocytosis.
97 ubunits comprising the axial cores of silica spicules in a marine sponge chemically and spatially dir
98              We present a case of follicular spicules in a patient with MM, which is very reminiscent
99                     The arrangement of these spicules in Eiffelia is shown to be precisely equivalent
100 n microscopy (PEEM), here we examine forming spicules in embryos of Strongylocentrotus purpuratus sea
101                                   Follicular spicules in MM are probably not caused by the trichodysp
102                      The cause of follicular spicules in multiple myeloma (MM) is not known.
103 e chromosphere is permeated by jets known as spicules, in which plasma is propelled at speeds of 50 t
104 ore, urea converted the axisymmetric conical spicules induced by lysophosphatidylcholine into irregul
105 the subsequent steps of vulva attachment via spicule insertion and sperm transfer.
106  response, backing, turning, vulva location, spicule insertion and sperm transfer.
107          Here, we report that confinement of spicule insertion attempts to the vulva is facilitated b
108 ndependent spicule protraction show abnormal spicule insertion behavior during sex.
109 phrodites, backing, turning, vulva location, spicule insertion, and sperm transfer, culminating in cr
110  response, backing, turning, vulva location, spicule insertion, and sperm transfer.
111 rs undergo prolonged contraction to keep the spicules inside the hermaphrodite until sperm transfer i
112 how the presence of diagnostic hexactinellid spicules integrated into the skeletal mesh.
113                        The assembly of these spicules into bundles, effected by the laminated silica-
114 muscle contractions to insert his copulatory spicules into his mate.
115 mating, the insertion of the male copulatory spicules into its mate, requires UNC-103 ERG (ether-a-go
116 ng behavior, the male inserts his copulatory spicules into the hermaphrodite by regulating periodic a
117 f the Caenorhabditis elegans male copulatory spicules into the hermaphrodite during mating.
118               The erythrocytes have numerous spicules irregularly distributed over the cell surface.
119                                         Each spicule is covered with recurved barbs and has an intern
120 chromospheric plasma in fountainlike jets or spicules is accelerated upward into the corona, with muc
121                            The origin of the spicules is poorly understood, although they are expecte
122  spicule traces, in which the cuticle of the spicules is secreted.
123 , as well as other proteins found within the spicule, is central to understanding their function, we
124 he midperipheral retina, accompanied by bone spicule-like pigmentary deposits and a reduced or absent
125          Dilated funduscopy also showed bone spicule-like pigmented deposits, typical for retinitis p
126  apparatus consisting of thousands of anchor spicules (long, hair-like glassy fibers).
127 rize the proteins that comprise the integral spicule matrix of the Strongylocentrotus purpuratus embr
128 blotting analysis indicates that SM50 is the spicule matrix protein with the most alkaline isoelectri
129                Comparisons between embryonic spicule matrix proteins and adult spine integral matrix
130 eals that there are 12 strongly radiolabeled spicule matrix proteins and approximately three dozen le
131 ular matrix proteins, cell surface proteins, spicule matrix proteins and transcription factors.
132  we undertook to develop methods to localize spicule matrix proteins in intact spicules, using immuno
133 ctrophoresis of [35S]methionine radiolabeled spicule matrix proteins reveals that there are 12 strong
134 oelectric points; however, there are several spicule matrix proteins that have more alkaline isoelect
135 t prevent the continued synthesis of several spicule matrix proteins.
136 ately three dozen less strongly radiolabeled spicule matrix proteins.
137 of a gene, SM50, encoding a component of the spicule matrix, which plays an integral role in the form
138  position; small fossils containing putative spicules may specifically record the presence of sponges
139  after the generation of spicule cells, when spicule morphogenesis occurs in wild-type males.
140                  Caenorhabditis elegans male spicule morphogenesis requires the coordinated cellular
141                                       During spicule morphogenesis, the expression of an egl-17::GFP
142 lt of failure of socket cell movement during spicule morphogenesis.
143 Cs), are important both for PMC guidance and spicule morphogenesis.
144                               Similarly, the spicule morphology clearly differed between both treatme
145 in-31 result in identical cell migration and spicule morphology defects.
146                          Calcification rate, spicule morphology, major biochemical constituents (prot
147 nt for spicule function, are dispensable for spicule morphology.
148                             These repetitive spicule movements continue until the male shifts off the
149 is required for the male to sustain rhythmic spicule muscle contractions during attempts to breach th
150 hrodite by regulating periodic and prolonged spicule muscle contractions.
151 NAD(+) salvage pathway, cannot mate due to a spicule muscle defect.
152 nt ACh receptors and calcium channels in the spicule muscles to mediate these contractile behaviors.
153 opodia that elongates anteriorly towards the spicule muscles.
154 R-3(mAChR)/G alpha(q) pathway sensitizes the spicule neurons and muscles before and during mating so
155                            We found that the spicule neurons and sheath cells, although important for
156 tocoelic cavity, as well as abnormalities in spicule number and shape.
157 scan shells; (4) the development of skeletal spicules of sea urchin embryos; and (5) the formation of
158 hat silicatein-a protein found in the silica spicules of the sponge Tethya aurantia--can hydrolyse an
159 organisms, including the primitive skeleton (spicule) of the sea urchin embryo, the structural and fu
160 rganic core of the glassy skeletal elements (spicules) of a marine sponge, has led to the development
161  monkey after topical application of cowhage spicules or intradermal injection of histamine and capsa
162 of eight shell plates (valves) surrounded by spicules or scales, and fossil evidence suggests that th
163                 On the other hand, epidermal spicules originate from both pretrochal and postrochal c
164 nts of these parameters in the native sponge spicules, our modeling results correlate remarkably well
165 ive in TGF-beta signaling display a crumpled spicules phenotype as a result of failure of socket cell
166 ) amplitudes, cataract, and funduscopic bone spicule pigmentation.
167 thy volunteers with heat-inactivated cowhage spicules previously soaked in the peptide.
168 ro, also using XANES-PEEM, assay to identify spicule proteins that may play a role in stabilizing var
169 itability levels that regulate the timing of spicule protraction and the success of male mating behav
170                              unc-103-induced spicule protraction can be suppressed by killing the SPC
171                Additionally, unc-103-induced spicule protraction can be suppressed by reducing a phar
172         UNC-103 also regulates the timing of spicule protraction during mating behavior.
173 males that do not display mating-independent spicule protraction show abnormal spicule insertion beha
174 holinergic transmission reduces drug-induced spicule protraction, suggesting that drug-stimulated neu
175 elated gene/UNC-103 K(+) channels to control spicule protraction.
176  we show that specific slo-1 isoforms affect spicule protraction.
177 rg1); unc-103(lf) males restores spontaneous spicule protraction.
178 lopment is critical for function of the male spicule protractor muscles during adulthood, but these m
179  ACh (acetylcholine) activates nAChRs on the spicule protractor muscles to induce the attached spicul
180                                      Cowhage spicules provide an important model for histamine-indepe
181 te gonad and for the development of the male spicule, rays and gonad.
182  uniform silicon structures, the anisotropic spicule requires greater force for detachment from colla
183 aics, that the formation of wild-type-length spicules requires lin-29(+) in the AB.p lineage, the lin
184 ca cylinder progressively decreases from the spicule's core to its periphery, which we hypothesize is
185 nes serving as illumination points along the spicule shaft.
186 tor, induces spiculogenesis and controls the spicule shape in PMC culture.
187  same length and volume, we predict that the spicules' shape enhances this critical load by up to 30%
188                        We also find that the spicules' shape is close to the shape of the column that
189 chanics model along with measurements of the spicules' shape to estimate the load they can transmit b
190 one of the matrix proteins of the sea urchin spicule, SM 30, has been shown to contain a carbohydrate
191 nt occluded matrix protein in the sea urchin spicules, SM50, stabilizes ACC . H(2)O in vitro.
192 an egl-17::GFP reporter gene is found in the spicule socket cells and its expression appears to be re
193                             In contrast, the spicule socket cells are essential for both spicule elon
194 D spicule-associated sensory neurons and the spicule socket neuronal support cells function with intr
195 03(lf) alleles cause males to protract their spicules spontaneously in the absence of mating cues.
196 nhibitor during the active elongation of the spicule stops further elongation immediately.
197 ted from California purple sea urchin larval spicules, Strongylocentrotus purpuratus) ACC were studie
198    To evaluate this hypothesis, we created a spicule structural mechanics model, in which we fixed th
199 e two antigens are widely distributed in the spicule, suggest that this technique should be applicabl
200 tein could not be detected on the surface of spicules that had been isolated from embryo homogenates
201 ptic sex muscles execute rhythmic copulatory spicule thrusts.
202 ment through cellular endings exposed at the spicule tips and regulate both sperm release into the he
203                                     When the spicule tips penetrate the vulva, the protractors underg
204 ules to extend from the male tail before the spicule tips penetrate the vulva.
205 xperiments emphasize the similarity of these spicules to commercial optical fibers, the absence of an
206 e premature prolonged contractions cause the spicules to extend from the male tail before the spicule
207 le protractor muscles to induce the attached spicules to extend from the tail.
208 s undergo periodic contractions to allow the spicules to reattempt insertion if a previous thrust fai
209 tal materials (bone, shark cartilage, sponge spicules) to attachment devices (mussel byssal threads),
210 ions of these cells form cellular molds, the spicule traces, in which the cuticle of the spicules is
211                   We find, however, that the spicules use a completely new strategy.
212 o localize spicule matrix proteins in intact spicules, using immunogold techniques and scanning elect
213                       However, when isolated spicules were etched for 2 min with dilute acetic acid (
214 isolated from the skin lesions; however, the spicules were positive for Merkel cell carcinoma virus,
215  the constraints imposed by neighboring bone spicules, which limit the amount of interstitium from wh
216 es are on average 43% shorter than wild-type spicules while other male mating structures appear unalt
217  tear and treated retinoblastoma scar), bone spicules, white without pressure, and peripheral drusen,
218  that results in oriented single-crystalline spicules with a complex branching shape and smoothly cur
219 n in mediating spicule elongation: elongated spicules with defective spicule cuticle can be formed.
220 e compare magnetohydrodynamic simulations of spicules with observations from the Interface Region Ima
221 -selective, producing mesostructured silicon spicules with skeletonlike morphology, 3D tectonic motif

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