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1 aspects of human embryonic development 'in a dish'.
2 d (from the time of plating cells on imaging dishes).
3  systems (CS) (a bioreactor system and petri dishes).
4 and wakefulness can now be investigated in a dish.
5 er epithelium attached to the tissue culture dish.
6 ion such as tapping on the side of the Petri dish.
7  years old, she ate enokitake with a hot-pot dish.
8  the points where the cell touches the Petri dish.
9 ite (17%), probable (26%), or possible (31%) DISH.
10 ls are prevented from adherence to a culture dish.
11 ng fibroblast cells when coated on a culture dish.
12 s are allowed to form a monolayer in plastic dish.
13  cells cultured on hard gel or rigid plastic dish.
14 nded up and detached from the tissue culture dish.
15 lagen matrix that is attached to the culture dish.
16 by scraping nongoblet cells from the culture dish.
17 ls enables us to assay cardiac activity in a dish.
18 cronutrients (FSM) in a traditional Tunisian dish.
19 r hPSC-based neuronal control of organs in a dish.
20 lasm that died and detached from the culture dish.
21 losely resembling ankylosing spondylitis and DISH.
22 ulating the in vivo situation in the culture dish.
23 gen bed (-astrocyte) within the same culture dish.
24 ds of different materials were agitated on a dish.
25 que features of human brain development in a dish.
26 tion them in a single layer on a polystyrene dish.
27 ered when consumed as a traditional prepared dish.
28 or neurons in the spinal cord and in culture dishes.
29 trees were accompanied by unmanipulated side dishes.
30 affect the consumption of the vegetable side dishes.
31 ormed in the lids of 38 mm polystyrene Petri dishes.
32 grown on standard, very stiff tissue culture dishes.
33 h VEGF and plated on type IV collagen-coated dishes.
34 c-Fos-expressing OCPs in the lower Transwell dishes.
35 val on poly-hydroxyethyl methacrylate-coated dishes.
36 grown monoxenically on bicompartmental petri dishes.
37 vity with B16-F10 cells using peptide-coated dishes.
38  and by crystal violet staining of confluent dishes.
39 d out using cells on the surfaces of culture dishes.
40 pattern following culture on polyHEMA-coated dishes.
41 e gels of various compositions cast in Petri dishes.
42 hydroxyethyl-methacrylate) (polyHEMA)-coated dishes.
43  two hundred seventy-one 384-well microtiter dishes.
44 by anti-CD3/anti-CD28 immobilized on plastic dishes.
45 ined by measuring DNA content of the culture dishes.
46 hesized FN was released and deposited on the dishes.
47  until the 5th day after seeding the culture dishes.
48 tate tissues and cultured on collagen-coated dishes.
49 rophages during 7 days of culture in plastic dishes.
50 pan-cadherin antibody immobilized on plastic dishes.
51 onjugated Sepharose beads and peptide-coated dishes.
52 ated by binding cells onto Ab-coated plastic dishes.
53 onectin fragments coated onto tissue culture dishes.
54 mounts of sodium coming from meats and mixed dishes.
55 in and monomeric CD48 immobilized on plastic dishes.
56  test molecules were placed in 35 mm culture dishes.
57 nd most abundantly to gelatin-coated culture dishes.
58 lected with paper points and plated in Petri dishes.
59 the cultures on commercial polystyrene Petri dishes.
60 ulture systems such as well plates and Petri dishes.
61 eneration of yield factors for South African dishes.
62 dients and nutrients of Cameroon traditional dishes.
63 y in nutrient values has been reported among dishes.
64  differentiated in vitro on uncoated culture dishes (2D) or encapsulated in self-assembling, RADA-16
65 baby foods (8.8%), soups (6.1%), pasta mixed dishes (4.0%), and human milk (3.9%).
66 %), soups (5.4%), cheese (5.2%), pasta mixed dishes (5.1%), and frankfurters and sausages (4.6%).
67                 Fish sauce imparted to Roman dishes a moderately salty, slightly fishy taste that com
68 nergy compulsory (consumption required) side dishes accompanied each meal.
69 different ratios and placing them in a Petri dish after which they are recorded using a camera and th
70                           The concurrence of DISH and chondrocalcinosis suggests a shared pathogenic
71                                  Concomitant DISH and chondrocalcinosis was diagnosed in 12 patients.
72 capitulate RBM20 familial DCM phenotype in a dish and establish a tool to dissect disease-relevant de
73 modeling human musculoskeletal diseases in a dish and for rapid drug screening.
74 al endothelial cells attached to the culture dish and grew to fill the flask.
75  lens capsular bags were pinned to a culture dish and grown in the presence or absence of the SFK inh
76 rgen dispersal over 20 minutes using a petri dish and immunochromatographic test.
77 ns of SM imaging techniques beyond the petri dish and opens the possibility to explore the molecular
78 ion of the cells by removal from the culture dish and replating had substantial positive effects on t
79 ng the amount of salt in the recipe for each dish and the amount of each dish eaten by respondents.
80 ed with enamel matrix derivative in a dampen dish and then added to the EMD-treated defects.
81 l for modeling intercellular physiology in a dish and to further translational studies, but it has pr
82  and a second group received it in a serving dish and took the amount they desired on their plates.
83 ethod for generating cerebral organoids in a dish and use it to model microcephaly.
84 oximately 2 h for preparation of the culture dishes and a further 3-4 h for isolation and plating out
85 essed VHL gene, suppressed growth on plastic dishes and anchorage-independent colony formation in sof
86 ependent adhesion of B16 cells to Gg3-coated dishes and associated signaling were not reduced or abol
87 roximately 100 mg/mL), or on collagen-coated dishes and cultured for up to 7 days in serum-free media
88   Subsequent exposure of these "clean" Petri dishes and foil squares to indoor air in two different r
89 e of HSCs isolated from rat liver on plastic dishes and HSC-T6 on a basement membrane-like matrix wer
90 crobial peptides in keratinocytes on plastic dishes and in composite grafts.
91 ane (CAM) of quail embryos cultured in petri dishes and incubated for an additional 24 or 48 hours un
92 se rat hepatocytes plated on collagen-coated dishes and maintained in dimethyl sulfoxide (DMSO)-suppl
93 ers' demand in having access to more healthy dishes and peculiar sensory attributes.
94  Entrees were served with unmanipulated side dishes and snacks, and children were instructed to eat a
95  cells displayed reduced adhesion to culture dishes and were found to secrete an extracellular matrix
96 own to confluence on 35 x 10 mm cell culture dishes and were used from passages 10-14.
97 th diffuse idiopathic skeletal hyperostosis (DISH) and/or chondrocalcinosis, were identified on the i
98 de new colours, textures and vibrancy to any dish, and apart from the "glam" factor, they can constit
99 inent nucleoli, attach poorly to the culture dish, and are sensitive to apoptosis but have increased
100 g was dissected free, pinned flat on a petri dish, and incubated in Eagle's minimal essential medium
101 ines are applied onto the surface of a Petri dish, and then immersed under culture medium in which ce
102  expression after cell detached from culture dish, and this finding highlights the importance of incr
103 ifferentiated from PSCs remain immature in a dish, and thus there are serious caveats to their use in
104 ultivation with seedlings in bipartite Petri dishes, and (35)S was assimilated from the bacterial VOC
105 by pork and chicken dim sum foods and noodle dishes, and a "vegetable-fruit-soy" pattern characterize
106 ng factor and IL-1 on bone slices or plastic dishes, and assessed osteoclast and resorption pit forma
107 MEDSAH coating on tissue culture polystyrene dishes, and for the feeder-free culture of hES cells on
108 s, in cells attached to poly-d-lysine-coated dishes, and in attached cells pretreated with the RGD-co
109  type A or O viruses, immobilized on plastic dishes, and significantly inhibited viral replication, a
110 e the epitope tag, immobilized on microtiter dishes, and tested for their ability to bind purified so
111 nd the nature of ingredients in the analyzed dishes, and thus defined different daily nutrient intake
112 structure of islets from bioreactor, but not dish, appeared healthy and closely resembled fresh islet
113  thinning rate measured at the center of the dish appears as a robust observable to quantify the role
114 te the current limitations, the disease-in-a-dish approach allows for progressive time course analyse
115 tiation induction subtraction hybridization (DISH) approach.
116            Compared with traditional culture dish approaches, this pipeline enhances experimental pre
117                Unlike MuSCs on rigid plastic dishes (approximately 10(6) kilopascals), MuSCs cultured
118 DNA samples could be collected from the same dish as the metabolites; and (4) cell lines that grew in
119                               The microtiter dish assay is a more expedient method for measuring tran
120  that altered biofilm formation in a 96-well dish assay originally defined this locus, which is compr
121 here the development of a 96-well microtiter dish assay.
122 in B. cereus UW85 using a 96-well microtiter dish assay.
123 ages of pregnancy using a static-based Petri dish assay.
124 cations for drug screening and 'disease in a dish' assay capabilities.
125                                  Smart Petri dish based on this technology can significantly streamli
126 sed by using a validated, self-administered, dish-based, semiquantitative food-frequency questionnair
127 setup suggested uses opaque masks in a Petri dish bathed in ultraviolet radiation, but is based on th
128 reated with RANKL in vitro in tissue culture dishes, bone slices, and a co-culture system containing
129  with fibronectin, the cells attached to the dish but grew slowly.
130 levated in cells grown on fibronectin-coated dishes but is decreased on laminin and poly-d-lysine, a
131 ne macroscopic fluorescent plaque in a Petri dish by plating it in a host bacterial medium.
132  endothelial differentiation on CHL-modified dishes by >50%.
133 own on glass slides and in polystyrene petri dishes by using light microscopy and scanning and transm
134 HEF1 in cells attached to fibronectin-coated dishes, calcitonin failed to stimulate the phosphorylati
135                   Products in the meat mixed dishes category had the highest mean and median sodium c
136                Using this approach with 1000 DISH cDNA clones (approximately 10% of the DISH library)
137 l cells (Caco-2) were grown on 35-mm culture dishes, chamber slides, or in a bicameral culture system
138 was constructed and differentially expressed DISH clones were isolated and evaluated using a high thr
139 tween household cleaning activities (washing dishes/clothes, mopping, toilet cleaning, and washing wi
140 s also promoted endothelial cell adhesion to dishes coated with 0.1 microg of peptide and inhibited a
141 dependent conditions by transferring them to dishes coated with agar to prevent attachment to underly
142              Schwann cells adhered poorly to dishes coated with alpha4(V)-NTD that lacked the heparin
143 site inhibited spreading of Schwann cells on dishes coated with alpha4(V)-NTD.
144 9,000) was enhanced in the fraction bound to dishes coated with asialo-GM2 (Gg3) or with anti-GM3 mon
145 d size on the micrometer scale or on plastic dishes coated with defined ECM molecular coating densiti
146 SCs were induced to differentiate in culture dishes coated with poly-l-lysine and mouse laminin in th
147 helial cells were plated onto tissue culture dishes coated with purified fibronectin or a matrix elab
148  a chondrocyte-specific phenotype on plastic dishes coated with the hydrogel poly(2-hydroxyethyl meth
149  because rat fibroblasts failed to adhere to dishes coated with this polypeptide.
150 is of Schwann cell adhesion and spreading on dishes coated with various type V collagen domains revea
151  two compartments (BI Petri dish); two Petri dishes connected with tubing; and a microtiter-based ass
152  made it the basic condiment for traditional dishes consumed in many Southeast Asian countries.
153 es, but not those attached to tissue culture dishes, contained approximately 10-15% of ACAT on the ce
154 idopsis or tobacco plant seedlings): a Petri dish containing two compartments (BI Petri dish); two Pe
155             HTM cells were plated in culture dishes containing a polymerized deformable silicone subs
156            The coverslips were then moved to dishes containing either confluent RMG monolayers or no
157 rages contributed less, whereas cereal-based dishes contributed more in 2012 than in 1995.
158 ts functioned better compared with fresh and dish-cultured islets on day 30 postgrafting.
159 titration studies revealed that 250 fresh or dish-cultured, but only 30 to 120 bioreactor-cultured, i
160 ed particle beam in conjunction with a strip dish design, we show here that the cyclooxygenase-2 (COX
161 field attraction (deflection angle and Petri-dish displacement methods), heating (infrared thermometr
162 correlated with Abeta reduction following in-dish dosing of this radioligand or a non-radioactive gam
163  recipe for each dish and the amount of each dish eaten by respondents.
164 lating Swiss 3T3 cells on fibronectin-coated dishes elicited a transient inhibition of Rho, followed
165 ese explants were transferred to new culture dishes every week for 9 weeks.
166 mmobilized on the surface of plastic culture dishes failed to induce resistance and resulted in high
167 opic cell culture in traditional polystyrene dishes, flasks or well-plates.
168 ssays in 96-well plates, compared with 30-mm dishes for (125)I binding assays to whole cells.
169      Such devices might be 'electronic Petri dishes' for the direct stimulation of, and measurement f
170 ple analysis of APR activity in a microtiter dish format.
171 data are presented for 117 commonly consumed dishes from three eco-regions.
172 ozen and heat-treated ready meals (only main dishes) from the continental European market were analys
173   MT has also proven to be a fertile culture dish--full of direction- and disparity-selective neurons
174  of regulation and the expression pattern of DISH genes were also evaluated by microchip cDNA array s
175                               Even in single dishes, GFP-transfected cells in contact with other neur
176 led morphology, are less adherent to culture dishes, grow to a higher saturation density, and can for
177 evels were obtained in bioreactor-grown than dish-grown 1-month constructs).
178 cells were obtained in bioreactor-grown than dish-grown 3-day constructs) and subsequently affected c
179 tion of cells to extracellular matrix-coated dishes has enabled rapid and consistent injection of mac
180 n a lawn of bacteria on an agar-filled Petri dish; however, this rate-limiting step requires up to 12
181                                   On plastic dishes, human, bovine, and rabbit keratocytes lose their
182 ls in soft-agar or plated on polyHEMA-coated dishes; (iii) CRBP inhibited protein kinase B/Akt activa
183 ulture, and fibroblasts overgrow the culture dish in 1 or 2 weeks.
184 nses and were trained to approach their food dish in response to a specific acoustic stimulus.
185 perimental and one control groups (6-8 Petri dishes in each group).
186 ewborn mice were grown on collagen IV coated dishes in murine fibroblast conditioned medium with 0.06
187 ly extended bacterial populations in a Petri dish is presented on the basis of an exact formula obtai
188 and 129 traditional/common Serbian composite dishes is a prerequisite for nutritional research in Ser
189 d medicine and modeling cardiac disease in a dish, it is important to standardize the protocol to imp
190 trates including polydimethylsiloxane, Petri dishes, Kapton tapes, thermal release tapes, and many ty
191 of p16(INK4A) during cell culture on plastic dishes leads to a state of permanent replicative arrest
192 dom clones were isolated from the subtracted DISH library and analyzed by reverse Northern and Northe
193 0 DISH cDNA clones (approximately 10% of the DISH library) has resulted in the identification and clo
194                                           In dishes maintained in a vertical orientation, wild-type h
195 generating therapeutic human T cells 'in the dish' may be useful for cancer immunotherapy and other m
196  cultures were maintained on multi-electrode dishes (MED) with an 8x8 array of electrodes and examine
197     Herein, a novel transwell insert culture dish method is used to show that X-irradiation induces m
198 A and protein synthesis), and tissue culture dishes (migration).
199 current study has furthered the disease in a dish model of HD by generating new non-integrating HD an
200  and stiff stripes improves current NMJ-in-a-dish models by inducing both mouse and human myoblast du
201                                     NMJ-in-a-dish models have been developed to examine human MN-asso
202  fibre degradation processes in disease-in-a-dish-models.
203                          Thus, pathogen-free dishes must be made available.
204 ltrathin films that relies on no more than a dish of fluid and a low-magnification microscope.
205            Modeling human embryogenesis in a dish opens up new possibilities for the study of early d
206 several foods and ingredients, but no single dish or ingredient explained a substantial number of cas
207 oled-CCD camera either directly from culture dishes or by implanting them into mice.
208 beled cells were washed, seeded into culture dishes or glass slides, covered with photographic emulsi
209 her poly(2-hydroxyethyl methacrylate)-coated dishes or in the presence of GRGDTP and formed cell clus
210 ells cultured in either two-dimensional flat dishes or in three-dimensional Matrigel conditions.
211 oic acid, by fibroblasts cultured on plastic dishes or in type I collagen gels, was examined.
212 slets or mouse islets cultured in stationary dishes or microgravity bioreactors were transplanted to
213  cell removal after day 21 on tissue culture dishes or on BM.
214 t S. mutans biofilms grown on either plastic dishes or on collagen membrane and assayed by CFU, live-
215                          Heating glass Petri dishes or squares of aluminum foil to about 350-400 degr
216                       D407 cells cultured in dishes or Transwell inserts were treated with cobalt chl
217 lated at low density (1 x 10(3) cells/1.5-cm dish) or at high density in the presence of an anti-HB-E
218 , culturing cells on type II collagen-coated dishes, or overexpression of full-length annexin V) resu
219 red into standard 96-/384-well plates, Petri dishes, or vials for cloning, PCR, and other single-cell
220                              Both allogeneic dish- or bioreactor-cultured islets survived more than 1
221 enable development of so-called disease-in-a-dish personalised models to study disease mechanisms and
222 served on interior surfaces, including dust, dish plates, windows, mirrors, fabric cloth, and wood.
223  technology can be used to build smart Petri dish platforms, termed ePetri, for cell culture experime
224    Koose, a West African delicacy, is a side dish prepared by deep frying thick cowpea paste.
225 d the antioxidant properties of some popular dishes prepared in a dedicated lab-kitchen: spaghetti al
226 and transfection of cells in a single 100-mm dish produces 10(7) individual clones so that a repertoi
227 nded Swiss 3T3 cells onto fibronectin-coated dishes promoted phosphorylation of endogenous focal adhe
228 ed to recapitulate the ARVC phenotype in the dish, provide mechanistic insights into early disease pa
229 n for 6 wk, a vitamin A-fortified rice curry dish providing 850 microg retinal activity equivalents/d
230 he presence of bacteria or on tissue culture dishes rather than in suspension culture.
231       Allergen levels in extracts from Petri dish samples, which had been kept frozen, dropped about
232                                          The DISH scheme and the genes presently identified using thi
233 tiation induction subtraction hybridization (DISH) scheme is being used.
234 cked conditions used for cooking of mushroom dishes, since only a narrow group of mushrooms can be ea
235  acid (18) content (HPLC/fluorescence) in 16 dishes specifically conceived for phenylketonuric patien
236 evel lost their ability to adhere to culture dishes, suggesting a role for Porimin in cell adhesion.
237 ients could be easily transferred to a petri dish surface by stamping.
238  transduced with Ad.hTid-1 detached from the dish surface.
239     The optimized procedure for the BI Petri dish system is described in this protocol and can be wid
240 V time-lapse fluorescence self-imaging Petri dish system, termed the Talbot Fluorescence ePetri, whic
241  bursts have been detected with large single-dish telescopes with arcminute localizations, and attemp
242 times more infectious virus per cell culture dish than the much more labor-intensive organotypic cult
243 n the Western hemisphere, characterized many dishes that ancient Romans consumed >2000 y ago.
244 symmetric adhesive islands on tissue culture dishes that rectify the random movement of cells and dir
245                                      The new dishes that result engage our senses in unexpected ways.
246 ration of tumor cells grown in mCLCA1-coated dishes, the ability to form tumor cell colonies on CLCA-
247 printed in seconds on plastic or glass Petri dishes; then, interfacial forces pin liquids to substrat
248 vitro viability and proliferation in plastic dishes, there was a marked difference in a more relevant
249 minishes binding in vitro to selectin-coated dishes, thrombin-activated platelets, and tumor necrosis
250 ailed to regrow were transferred to adherent dishes to evaluate clonogenicity; growth-controlled sphe
251 (2-hydroxyethyl methacrylate)-coated plastic dishes to prevent the loss of cartilage-specific phenoty
252 e phenotype and drug response in the culture dish, to provide novel insights into disease and drug th
253 on six-well tissue culture plates or imaging dishes, treatment with CuFL, stimulation of NO synthases
254  Conventionally, they are performed in Petri dishes, tubes, or well plates, using milliliters of reag
255 i dish containing two compartments (BI Petri dish); two Petri dishes connected with tubing; and a mic
256 s were formed on the bottom of a polystyrene dish under water-saturated heptane.
257 ies were harvested directly from the culture dishes under a fluorescence microscope, and total DNA wa
258 -transformed fibroblasts adherent to culture dishes under normoxic conditions, the growth of these ad
259 by counting of cells attached to the culture dish using image analysis.
260                                          The dish was filled almost completely with beads, such that
261              The previously occupied culture dish was stained for lacZ to detect transduced epithelia
262 y of single CFU-GEMM colonies into 2 degrees dishes was >96% and yielded 2 degrees colonies of CFU-GM
263 at spreading of Mac-1-null PMNs to IC-coated dishes was equivalent to that of wild-type PMNs at 5-12
264 59 on attachment and spreading on CAP-coated dishes was examined.
265       Homemade turshi, a fermented vegetable dish, was the likely cause.
266 ration, post-meal cleaning activities (e.g., dish-washing), clothing maintenance (e.g., laundry), and
267 ial cells (bPAECs) to the surface of a Petri dish were investigated.
268                                   Microtiter dishes were coated with anti-EGFR monoclonal antibodies
269                          When tissue culture dishes were coated with fibronectin, the cells attached
270 63%) and S. aureus (55%) outbreaks, and rice dishes were commonly implicated in B. cereus outbreaks (
271                              Meat or poultry dishes were commonly implicated in C. perfringens (63%)
272  alimentary tracts, and excreta on the petri dishes were cultured for H. pylori, whose identity was c
273 nd percentages of nutrient intake from mixed dishes were independently and consistently associated wi
274 iferation and adhesion to fibronectin-coated dishes were inhibited by knockdown of beta1-integrin usi
275                          After 48 hours, the dishes were placed on an inverted microscope and treated
276 cal and histological analysis, and the petri dishes were replaced with fresh sterile plates with fres
277                                        Petri dishes were used to collect airborne dust samples during
278 cuisine for many centuries by Romans in many dishes, where it has now been replaced by celery.
279    HPTFs were grown in microgrooved silicone dishes, where they became elongated in shape and aligned
280 s produce more functionally active NMJs-in-a-dish, which could be used to elucidate disease pathology
281 a glance, we can perceive whether a stack of dishes will topple, a branch will support a child's weig
282 ll immobilization included coating the Petri dish with 100 microg/mL fibronectin, a seeding cell dens
283  for dispersions of PPL and mPPL in a Teflon dish with a stirred subphase to minimize diffusion resis
284 g bacterial colonies directly from the Petri dish with absolutely no sample preparation needed.
285 issected and sealed on a custom-made acrylic dish with an O-ring.
286 LTC(4)) was measured in a 96-well microtiter dish with rapid filtration onto a Perkin Elmer unifilter
287  of LPA as well as in vivo, adherence to the dish with scattered shape, and enhanced phosphorylation
288 etching was then applied to silicone culture dishes with a 4% or 8% stretch at a stretching frequency
289 e frequency of anodal turning was greater on dishes with a net positive charge (Plastek C) than on th
290                                         Some dishes with confluent RMG cells were exposed to D,L-thre
291 ylysine by growing neurons on tissue culture dishes with different net surface charges.
292  human neutrophils adherent to plastic petri dishes with the purified chemotactic factors C5a and kal
293 ice and paratha) and low consumption of meat dishes; with vegetable curries contributing most towards
294 ive microbial colonies directly from a Petri dish without any sample preparation.
295 der to recapitulate reprogramming in a Petri dish without the use of oocytes.
296 olonies grown on soft nutrient agar in Petri-dishes without any sample pretreatment.
297 sion-deficient (sad) mutants grew in plastic dishes without attaching to the substrate.
298 tured by transferring spheres to new culture dishes without employing enzymatic dissociation.
299     When plated at high density onto plastic dishes without FCS, WT and NRKvector formed few attachme
300 rom living bacterial colonies grown in Petri dishes, without any sample pretreatment.

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