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1 story entitled 'The Curious Case of Benjamin Button'.
2  for the standardized manufacture of 'double-buttons'.
3 ing from 67,000 to 128,000 cells per corneal button).
4 ingle limbs (i.e., a single finger pushing a button).
5 ts indicated stimulus identity by pressing a button.
6 sin-related proteins clustered at a terminal button.
7 remove the corneal epithelial cells from the button.
8 larging at the distal end to form a terminal button.
9 states, 1-stream and 2-stream, by pressing a button.
10 ithout disturbing the radiolabeled leukocyte button.
11  properly the supernatant from the leukocyte button.
12 USTALW) can be performed with the click of a button.
13 te publication-ready plots at the click of a button.
14 ck was thermally uncomfortable by pressing a button.
15 phatics at E16.5 were joined by zippers, not buttons.
16 s for further refinement via convenient push buttons.
17 e consistently detected in all three corneal buttons.
18 rophages were observed in one of the corneal buttons.
19 nd have them press "shoot" and "don't shoot" buttons.
20 ng due to retrieval suppression and pressing buttons.
21 ing the molecular identity and regulation of buttons.
22 ted with the touch of a finger to one of its buttons.
23 ers of hydrophobic residues forming "leucine buttons."
24 on) so that there were two radiopaque spring buttons 4 mm apart on the button loop attached to the oc
25  250 mum in thickness) and a small posterior button (5 to 6 mm in diameter).
26                                Three corneal buttons (6-mm diameter) were obtained from each cornea o
27                          By clicking the SCP button, a patient-tailored SCP was generated.
28 ded with rechargeable "cig-a-like" or larger button-activated e-cigarettes, to use ad-libitum in two
29 ide are controlled by individual buttons and buttons also control the visibility of different ribosom
30 hemical analyses were performed on a corneal button and corneal pannus from 2 EEC patients.
31                  In the present study, White Button and Honey Brown (both Agaricus bisporus), Shiitak
32 l features: whether a girl pushes a boy or a button and whether we see it in real-time or in a single
33 fied nucleotide are controlled by individual buttons and buttons also control the visibility of diffe
34 rial quantification was performed on corneal buttons and GFP-expressing Staphylococcus aureus was use
35 onor corneas include pre-formed biosynthetic buttons and in situ-forming matrices that strive to achi
36                                      Corneal buttons and peripheral blood leukocytes were obtained at
37  selected industries (e.g., military uniform buttons and piano keys) and handicraft applications, lit
38                                All 4 corneal buttons and the GAN fascicle remained positive for B-III
39                                However, both buttons and zippers were composed of vascular endothelia
40 onizing 18 silicone gastrostomy devices (12 "buttons" and six tubes converted to skin level devices)
41 of removing the coronary arteries as limited buttons, and anastomosis of the pulmonary artery using o
42 tics decreased rapidly just before birth, as buttons appeared.
43 sting that combinations of elements within a button are required for pairing.
44                                Additionally, buttons are enriched for insulator protein clusters.
45                               In this model, buttons are nonuniformly distributed, such that alignmen
46 ts had zippers, not buttons, suggesting that buttons are specialized junctions rather than immature o
47                                              Buttons are thought to act as primary valves for fluid a
48 initiated voluntary acts, such as pressing a button, are preceded by a surface-negative electrical br
49 xed by a lower proportion of touches for the button associated with the social reward image.
50       For the motor task, subjects pressed a button at a comfortable pace, and activation was compare
51 they were visually cued to press one of four buttons at a time.
52 imilar expression patterns at the click of a button; back-end refactoring from an object oriented to
53 ational modeling to evaluate an alternative "button barcode" model, in which there is only one type o
54  button distributions, many highly effective button barcodes can be easily found, some of which achie
55 tive biophysical model to demonstrate that a button-based mechanism can lead to chromosome-wide pairi
56               Our results strongly support a button-based mechanism of somatic homolog pairing in Dro
57                                              Button batteries (BBs) are commonly found in many househ
58 d does not require starting, stopping, reset buttons, batteries, or maintenance; the timer simply sta
59  be powered and run several times by a small button battery suggesting that it could be integrated to
60 bjects performed bilateral finger tapping on button boxes with a 3-Hz audio cue and a reversing check
61 gically associating domain (TAD) function as buttons, but not all buttons contain TADs.
62 ratocytes were isolated from central corneal buttons by collagenase digestion for 16 hours, seeded on
63 ratocytes were isolated from central corneal buttons by digestion in 1 mg/mL of collagenase A in DMEM
64 hod enables a comprehensive, 20-minute, push-button cardiac MRI examination without ECG gating or bre
65 erformance from five different types of PCFC button cells without degradation after 1400 hours.
66 ned by random pressing, and that certain two-button concept combinations appear more often than expec
67 omain (TAD) function as buttons, but not all buttons contain TADs.
68 led the rapid formation of micrometer-sized "buttons" containing oligomerized viral Gag protein.
69 cantly higher in Royal Trumpet than in White Button, Cremini, and Portobello, while no difference was
70  this presentation is to document results of buttoned device (BD) occlusion of patent ductus arterios
71 the feasibility, safety and effectiveness of buttoned device closure of PDAs.
72 of the multi-institutional U.S. trial of the buttoned device for transcatheter closure of atrial sept
73 y and effectiveness of the fourth generation buttoned device in dosing atrial septal defects (ASDs) a
74 hese data suggest that the fourth generation buttoned device is as effective as earlier generation de
75         In up to 5.5 years of follow-up, the buttoned device provided effective closure in 98% of pat
76 FO closure with the Clamshell, CardioSEAL or Buttoned Devices at two institutions.
77 .2%) with first, second and third generation buttoned devices, the device was modified (fourth genera
78 rdiac defects can be closed with umbrella or buttoned devices.
79  By simulating randomly generated nonuniform button distributions, many highly effective button barco
80                                 Fragments of buttons do not pair, suggesting that combinations of ele
81 ese findings indicate that simply pressing a button does not induce forgetting, on its own, without c
82          Studies have shown that a histidine button engineered into cTnI (cTnI A164H) specifically en
83                 This pH-sensitive 'histidine button' engineered in TnI produces a titratable molecula
84        In this issue of Cell Host & Microbe, Button et al.
85                                        Here, Button et al. develop a phylogenetic network approach to
86 listened to a stream of sounds and pressed a button every time they heard a central target tone, whil
87 E::K-5) was used for transduction of corneal buttons ex vivo.
88    Participants were instructed to release a button following a green LED flash on the device.
89 bitrary rules such as 'for coffee, press red button' following their first-time instruction.
90 /no-go task requires participants to press a button for go stimuli, while inhibiting the response to
91 lly matched healthy control subjects pressed buttons for color of drug-related versus neutral words.
92                        To learn when and how buttons form during development and whether they change
93 g development and inflammation and show that button formation can be promoted by glucocorticoid recep
94                  Dexamethasone also promoted button formation during early postnatal development thro
95                                      Corneal buttons from BALB/c (syngeneic) or C57BL/6 (fully mismat
96 amage in CNTF-modulated explants and corneal buttons from explants was quantified by analysis of pano
97                        Twelve normal corneal buttons from healthy donors were used as controls.
98                          Fresh corneoscleral buttons from human donors (n = 19) and organ-cultured co
99 ated and simple "scripting at the click of a button" functionality that enables researchers to perfor
100 icroscopic examination of an excised corneal button, genomewide linkage analysis, fine mapping linkag
101                                      Corneal buttons harvested from C57BL/6 mice were used in three e
102 point eliminates the need for a back-mounted button in animals already receiving neural implants, the
103 al control adults participated and pressed a button in response to all female faces.
104 ges that can be reached by use of navigation buttons in a frame at the top of the screen.
105 d and preparation of the lamellar transplant buttons in a national cornea bank could improve the cost
106            In inflammation, zippers replaced buttons in airway lymphatics at 14 and 28 days after Myc
107 he posterior margin of the corneas and DSAEK buttons in all cases.
108 ge in disease, we examined the appearance of buttons in mouse embryos and their plasticity in sustain
109 ors (two subtypes) and one single pedicellar button (in L. pygmaea) are located on antennal pedicel.
110                            The proportion of buttons increased from only 6% at E17.5 and 12% at E18.5
111                            Here, we identify buttons interspersed across the fly genome that pair wit
112  mechanically deform in order to bring their buttons into mutual register.
113 ed by the microbiological community to a hot-button issue gaining staunch supporters (on particular p
114  were anchored on the sides by discontinuous button-like junctions (buttons) that differed from conve
115 lls of initial lymphatics have discontinuous button-like junctions (buttons), unlike continuous zippe
116 residue 685 and the concomitant formation of button-like junctions in initial lymphatics.
117 lymphatics transform from a zipper-like to a button-like pattern during collecting vessel development
118  radiopaque spring buttons 4 mm apart on the button loop attached to the occluder.
119       Incorporation of folding plug over the button loop in 10 additional patients produced immediate
120       Incorporation of folding plug over the button loop produces complete PDA occlusion at the time
121                   Of the four mat types, the button mats contained the highest diversity of Cyanobact
122 nities referred to as black, beige, pink and button mats on the surfaces of the thrombolites.
123                 Eight human eye bank corneal buttons (mean age, 73.6 years) were included.
124 g CBs, our studies suggest that the distinct buttoning mechanism we propose for DV closure is elabora
125 102) using our previously described ischemic button model.
126                                         The "button" model of pairing proposes that specific regions
127 gicola is a pathogen of the commercial white button mushroom (Agaricus bisporus) and is the causal ag
128 strate for mushroom cultivation by the white button mushroom (Agaricus bisporus) fruit body was inves
129 over 200 y and worldwide cultivation of the "button mushroom" forms a multibillion dollar industry.
130                                        White button mushrooms (Agaricus bisporous) are a potential br
131 0, 100, and 1000 uM retarded cap browning of button mushrooms (Agaricus bisporus) by 78.35, 31.40, 30
132 rst time, identified and quantified in white button mushrooms (Agaricus bisporus) following treatment
133                                              Button mushrooms are widely produced edible basidiomycet
134  Pseudomonas tolaasii severely damages white button mushrooms by secretion of the pore-forming toxin
135  dried mushrooms, the level of vitamin D2 in button mushrooms was found to be 6.90 mug/g dw, which is
136 idated and applied to commercially available button mushrooms.
137 rs (n = 19) and organ-cultured corneoscleral buttons (n = 10) obtained after Descemet's membrane endo
138 transverse shear properties of 6 mm diameter buttons of matched human cadaver cornea pairs.
139 the coronary arteries are removed as limited buttons of sinus tissue, leaving the transected edge of
140                               Full-thickness buttons of the central macula and the periphery of human
141 , the corneas were prepared to split corneal buttons on day 0 and cultivated for 15 days.
142 sample and reagents is activated by pressing buttons on the cartridge and sustained by exploiting cap
143 e range, temperature control and simple push-button operation.
144               Responses were given as simple button or key presses, which are quick to make and easy
145 , as 391 (23.7%) isolates lacked the typical button or mucoid colony appearance of S. pneumoniae.
146  tactile stimuli and action choices (press a button or not).
147                           Wholemount corneal buttons or cells from enzyme-digested corneas were analy
148      If subtle growth (i.e., granular, small button, or "starry" growth) was considered positive, err
149                                        Thus, buttons pair homologous chromosomes to facilitate cell-t
150 oints along the A-P axis of the embryo in a "buttoning" pattern, divergent from the zippering mechani
151  contain a shared sequence motif, the "pause button" (PB): KCGRWCG.
152 c yellow-fluorescent protein zFP538 from the button polyp Zoanthus sp. and a green-emitting mutant (K
153 nly one type of recognition site or adhesion button, present in many copies in the genome, each of wh
154 and they did so with either a speeded manual button press (humans) or a speeded saccadic eye movement
155  are able to report the sound as a target by button press after approximately 300-500 ms.
156 mp) component that peaked 200 msec after the button press and reversed polarity near the central sulc
157 nd spontaneous trial-to-trial variability in button press force.
158                                         Each button press initiated 30 s of -20 degrees C fluid perfu
159 rticipants were instructed to respond with a button press only to presented stimuli for a particular
160 sponses were invariant to motor output (i.e. button press or not), and to different ways of defining
161 earance of a peripheral target with either a button press or saccade.
162 erception of contingency existed between the button press response and the outcome.
163 ollowing an anticipatory cue, or following a button press response.
164 sented singly and each requiring a different button press response.
165            Training consisted of a two-phase button press task.
166 peak in the mean response time locked to the button press to be principally composed of triphasic, pr
167 g VEP assessments, subjects responded with a button press to infrequent (10%) target stimuli.
168                                            A button press was required in response to soft speech sou
169 ream of visual stimuli and to respond with a button press when a particular target appeared.
170 bjects, the rules were reversed to require a button press whenever an object, but not a circle, appea
171 n each trial, with the patient indicating by button press whether he saw an object on the left, the r
172 which subjects indicated with a differential button press whether the probe was contained in the stud
173 involving very simple motor responses (e.g., button press), errors concern inappropriate action-selec
174 on was reported by pressing or withholding a button press).
175 ponent during the final choice (indicated by button press).
176 a stimulus, indicated their prediction via a button press, and then received feedback.
177 s input (visual, auditory), response output (button press, speech), stimulus category (words, picture
178        During this task, subjects report, by button press, the number of words (1-4) that appear on a
179 nd multisensory (audiovisual) stimuli with a button press, while electrocorticography was recorded ov
180 eding but only partially phase-locked to the button press, with larger complexes preceding quicker mo
181 ditory (button press-tone) and motor-visual (button press-Gabor patch) events.
182 r temporal recalibration for motor-auditory (button press-tone) and motor-visual (button press-Gabor
183 gnaled the time of recognition (T(R)) with a button press.
184 ning a subset of them as targets requiring a button press.
185 n association between presented images and a button press.
186 ore registering their motion decision with a button press.
187 ed subjects to discriminate their emotion by button press.
188 re instructed to respond to the stimuli by a button press.
189 ge, and subjects responded to the target via button press.
190                                    Moreover, button-press forgetting partially reflects output-interf
191   In a subsequent test phase, left and right button-press generated either the same audio-visual stim
192                       VRT was recorded via a button-press response to the sudden appearance of a stim
193 ring the counting Stroop, subjects report by button-press the number of words (one to four) appearing
194 articipants learned two 12-item sequences of button presses (A and B).
195 in which they could choose between making 20 button presses for $1 or 100 button presses for higher a
196 tween making 20 button presses for $1 or 100 button presses for higher amounts (varying from $3 to $7
197  covertly attended location, quicker speeded button presses immediately followed a larger positive (P
198 aried in coherence and responded with either button presses or saccadic eye movements.
199                 However, the nature of pets' button presses remains an open question: are presses del
200                    Split-brain patients made button presses that were less synchronous than either no
201                                 The order of button presses was determined by a complex sequence that
202 s, P < 0.01), while the number of cumulative button presses was greater from 40-60 min in HS for HIGH
203          Considering that these actions were button presses with trivial motor demands, the idiosyncr
204 for both overt behavioral reports (immediate button presses) and silent counting of the perceptual ev
205 n, during the task, responses (left or right button presses) were either directly instructed (forced
206 experiment consisting of periods of rest and button presses, leading to local field potential recordi
207 ty of the hallucinations produced, utilising button presses, retrospective drawing, interviews, and q
208 ry tasks, where participants indicate, using button presses, the timing of encoding and recall of cue
209 itivity to body sensations and more frequent button presses.
210 receiving cooling (TT(cool) ) and cumulative button presses.
211 articipants learned that right and left hand button-presses each produced a specific audio-visual sti
212 ice's actions are implemented via strings of button-presses.
213 he objective contingency between the rate of button pressing and the amount of money they earned.
214  behaving monkey during a simple, sequential button pressing task.
215 t the hypothesis that introduction of double button reduces unbuttoning rate without reducing effecti
216  participations were instructed to abort the button release on these trials.
217                                  The corneal buttons retrieved during keratoplasty were processed for
218         Ex vivo studies with excised corneal buttons revealed that uninfected IL-6(-/-) corneas injec
219     Panoramic images of explants and corneal buttons revealed that VIP treatment reduced CE damage to
220 g tips of lymphatic sprouts had zippers, not buttons, suggesting that buttons are specialized junctio
221 ar switch, most readily described as a "push-button" switch, whereby two discrete and fully occupied
222  and r = -0.45 for Sharp's score), the timed button test (r = -0.62 for NDJ, and r = -0.57 for Sharp'
223 ; grip strength; walking velocity; and timed button test.
224 ; grip strength; walking velocity; the timed-button test; pain; and joint tenderness, swelling, and d
225 is patterned to create touch pads of arrayed buttons that are sensitive to contact with both bare and
226 d with AIC devices comprising soundboards of buttons that can be pressed to produce prerecorded human
227 ides by discontinuous button-like junctions (buttons) that differed from conventional, continuous, zi
228 ing three main ultrastructures: the terminal button, the electrodense core, and the wheel complex.
229                             Click the Cancel button to access the source code without authenticating.
230 ortant features of H4K16: 1) it is the first button to anchor the H4 tail on the adjacent nucleosome;
231                        The subject pressed a button to answer a ring tone, and then covertly answered
232 ther half of the blocks) in order to press a button to any deviant sound at that location.
233 ease over time, they decided when to press a button to bank their winnings, knowing that if they did
234 netic resonance imaging while they pressed a button to earn money as the response-reward relationship
235 ts played a game where they tried to press a button to earn points in a challenge with a brain-comput
236 t a time at fixation, and subjects pressed a button to every target.
237        Participants were required to press a button to indicate whether a briefly presented tone was
238 tation of each face pair, subjects pressed a button to indicate whether a subsequent asterisk appeare
239 ions (180 degrees ) while subjects pressed a button to occasional targets at one attended location.
240 ation experiment, participants could press a button to receive intravenous alcohol using the Computer
241  support in favor of inteins acting as pause buttons to arrest protein function until needed; then, a
242 latively close proximity of these L2 density buttons to one another raised the possibility of homotyp
243 unidimensional strategy: pressing one of two buttons to rotate a visual grating that stimulates a mod
244 ome-shaped tumors in 79% of patients, collar-button tumors in 17% of patients, irregular tumor in 1 p
245                                  The corneal buttons underwent histopathologic and immunofluorescence
246 cs have discontinuous button-like junctions (buttons), unlike continuous zipper-like junctions (zippe
247  procedure or cut from a whole corneal graft button unsuitable for keratoplasty.
248         Complex manual tasks-everything from buttoning up a shirt to playing the piano-fundamentally
249 nd then form intermediate closure points to "button-up" the folds.
250                      Affected larvae display buttoned-up, the ETH-null phenotype characterized by dou
251 havioral sequence, and exhibit the phenotype buttoned-up, which is characterized by incomplete ecdysi
252 ld consciously based his character, Benjamin Button, upon individuals with HGPS.
253 was performed on ex vivo human corneoscleral buttons using a depth-sensing needle, based on optical c
254                     Although vascular access buttons (VABs) offer significant advantages, their wides
255 eter mechanical scrape injury was made, each button was cultured for 24, 48, or 72 hours in serum-fre
256                        In a PKP, the corneal button was initially secured with 8 or 16 sutures and th
257  ("the coffee is ready about 3 min after the button was pressed").
258                               The white cell button was then resuspended in 4 ml of platelet-poor pla
259 e anterior stromal surface of bovine corneal buttons was measured after the epithelium was scraped aw
260 ying there's a chance that when we push that button, we destroy the world?" The physicist says, "The
261 red by a conserved salt-bridge, the "charged button." We also modeled structures for three other C. e
262 puter (iPad), where two differently coloured buttons were associated with a social and a nonsocial re
263                                      Corneal buttons were collected from patients with keratoconus, h
264                                      Corneal buttons were collected from patients with keratoconus, n
265 -versus-volume curves of all corneal-scleral buttons were concave-up asymptotes, demonstrating elasti
266 EC-DM) complexes from normal and FED corneal buttons were dissected from the epithelium/stroma.
267                               Thirty corneal buttons were examined, 18 of which were from patients af
268                A total of 1748 corneoscleral buttons were harvested from 10,265 deceased persons (17%
269                                      Corneal buttons were harvested from C57BL/6 mice and decellulari
270                  The dissected corneoscleral buttons were immersed in OCT media and frozen in liquid
271                     To study cell migration, buttons were nested within acellular uncompressed outer
272                                 FECD corneal buttons were obtained from transplantations and normal h
273        Electron microscopy showed that these buttons were packed with budding viral crescents.
274                                      Corneal buttons were placed in culture and immunocytochemistry a
275             Thirteen bisected Fuchs' corneal buttons were processed at the time of corneal transplant
276                                  The corneal buttons were processed for light, transmission, and scan
277 eudophakic bullous keratopathy (PBK) corneal buttons were removed during transplantation, and normal
278           Passenger leukocyte numbers in the buttons were significantly reduced by all three treatmen
279                                              Buttons were single and double labeled using phalloidin
280           Organ cultured human corneoscleral buttons were studied.
281                                  The corneal buttons were then evaluated by hematoxylin-eosin stainin
282                      Six-millimeter-diameter buttons were then incubated in media supplemented with 1
283                                  The corneal buttons were transplanted after overnight incubation in
284   Two-millimeter-diameter guinea pig corneal buttons were transplanted into 1.5-mm-diameter graft bed
285 antic category as the first two, and another button when it belonged to a different category.
286           Participants were asked to press a button when the third picture of a triplet belonged to t
287 ate a central target and to press a response button when they saw a stimulus that was randomly presen
288                           Subjects pressed a button whenever a rare target appeared.
289 were required to count mentally or to push a button whenever a target appeared.
290 ing an auditory discrimination task (press a button whenever an auditory pattern changes).
291 t or right finger stimulation and to press a button whenever they perceived a target pulse embedded i
292 (AX-CPT), which required subjects to press a button whenever they saw a letter A followed by a letter
293 hout initial lymphatics via openings between buttons, which open and close without disrupting junctio
294 h HLA-DM and may function as a pH-sensitive "button," which is closed at pH 7.0 but opens below pH 6.
295 ovements in a virtual environment to touch a button whose shape varied randomly from trial to trial-b
296  or pseudowords (experiment 2) by pressing a button with their right or left hand, while transitionin
297 perceiving a change in velocity by pushing a button with their thumb.
298 ion time task, subjects pressed each of four buttons with a different finger of the right hand in res
299 05-in Nitinol wires in the shape of two flat buttons with a short connecting waist with a diameter co
300 dependent cytotoxicity (CDC) by treating the buttons with anti-CD45 mAb plus complement.
301 quence of pushing five spatially distributed buttons without visual guidance.

 
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