ライフサイエンスコーパス: -attached

1 ed 26S proteasomes with unnatural amino-acid-attached fluorophores in a series of FRET- and anisotrop

2 enoic acids and keto-eicosatetraenoic acids--attached to either phosphatidylethanolamine or phosphati

3 hat generates force by cycling between actin-attached (strong binding: ADP or rigor) and actin-detach

4 n contrast to the detached partners of actin-attached heads.

5 Here the number of actin-attached motors per half-myosin filament (n) during V0 s

6 Here, the number of actin-attached motors per half-thick filament during V0 shorte

7 ht in some way to swing axially on the actin-attached motor domain, thus propelling the actin filamen

8 ilt of the lever arm domain during the actin-attached working stroke.

9 ng between the two lobes of the RLC to actin-attached myosin heads in muscle fibers, and suggest that

10 The Ala-attached support has been used to synthesize tri- to oct

11 latory process in which a subset of alveolus-attached AMs intercommunicates immunosuppressive signals

12 recording of triaxial acceleration by animal-attached devices has been proposed as a way forward for

13 movement displacements recorded from animal-attached electronic tags to show that diverse marine pre

14 The auxiliary-attached cyclobutanecarboxamides 15a, 15g, and 15h, prep

15 Baboon-attached motion/GPS tracking collars showed that raiding

16 enzyme still contained normal levels of BclA-attached oligosaccharides.

17 th of a 2D view into the amount of a 3D bone-attached root surface area (BA-RSA) by using a dental la

18 Osteomyelitis pathogens are bone-attached biofilms, making antibiotic delivery challengin

19 e animals, its occurrence in sessile (bottom-attached) species is limited to members of the ancient p

20 ding strain 14DCB1, the most positive carbon-attached H atom discriminates active from nonactive chlo

21 Fragmentation of lithium cation-attached alpha- and beta-O-methyl-glucopyranoside precur

22 Cell-attached and whole-cell recordings revealed that excitat

23 Cell-attached capacitance measurements indicated that inhibit

24 Cell-attached patch clamp recordings confirmed that perisomat

25 Cell-attached patch recording on the hair-cell apical membran

26 Cell-attached patch recordings of unitary LTCC currents confi

27 Cell-attached patch recordings were performed in transfected

28 Cell-attached patch-clamp analysis of cultured astrocytes rev

29 Cell-attached patches and whole-cell currents from this mutan

30 Cell-attached recording is extensively used to study the firi

31 Cell-attached recordings reveal a highly reliable and precise

32 Cell-attached semaphorins interact in trans with plexins on o

33 ng experiments show that establishing a cell-attached recording can result in an increased somatic Ca

34 uorescence microscopy, amperometry, and cell-attached capacitance measurements.

35 ic nucleus (SCN), using patch clamp and cell-attached electrophysiological recordings, RT-PCR, immuno

36 unitary currents in the inside-out and cell-attached modes of the patch-clamp technique.

37 terized by carbon fiber amperometry and cell-attached patch capacitance measurements.

38 tigated by carbon fiber amperometry and cell-attached patch capacitance measurements.

39 ta-cell were examined by whole-cell and cell-attached patch clamp capacitance measurements in INS 832

40 (GFP) tag and performed whole-cell and cell-attached patch clamp recordings.

41 ents were observed using whole-cell and cell-attached patch configurations.

42 sted in voltage-clamped whole cells and cell-attached patches by bath flow and patch pressure, respec

43 Nucleated and cell-attached patches revealed that VGSC density at the soma

44 Whole-cell current-clamp and cell-attached recordings from labeled RMTg neurons were perfo

45 Using simultaneous calcium imaging and cell-attached recordings from three genetically labeled DSGC

46 al-590, combined two-photon imaging and cell-attached recordings revealed that, despite the relativel

47 ision of firing in perforated-patch and cell-attached recordings.

48 Cx43 hemichannels were detected in both cell-attached and inside-out patch recordings in C6 cells exp

49 8 CFTR channel activity evident in both cell-attached membrane patches and planar phospholipid bilaye

50 In this study, by cell-attached recordings in the developing optic tectum of ze

51 Single-channel cell-attached analysis demonstrated that PS primarily affecte

52 recordings in all four configurations (cell-attached, inside-out, outside-out, and whole-cell).

53 conductance microscopy and conventional cell-attached patch clamp with a software modification that a

54 ent protein (RFP) and targeted them for cell-attached electrophysiological recordings.

55 yocytes) and sealed to the membrane for cell-attached recording of ion channels.

56 we recorded steady-state currents from cell-attached and outside-out patches.

57 channel activity could be recorded from cell-attached patches of acutely dissociated neurons bathed i

58 Single-channel recordings from cell-attached patches revealed that basal and evoked IK(ATP)

59 ) single-channel openings recorded from cell-attached patches, an effect that was blocked by the PKG-

60 In the majority of recordings from cell-attached patches, MS channels have a conductance of appr

61 e recorded single-channel currents from cell-attached patches.

62 Here, we used a classifier derived from cell-attached recordings to separate putative pyramidal cells

63 this, we used in vivo two-photon guided cell-attached recording in conjunction with spatially restric

64 e established two-photon imaging guided cell-attached recordings from genetically labeled inhibitory

65 Here, cell-attached capacitance recording was used to study single

66 Here, cell-attached recordings in rat primary auditory cortex revea

67 cordings, we performed calcium imaging, cell-attached, and whole-cell recordings of PC and PV cells w

68 These Cl(-) channels were observed in cell-attached apical patches of principal cells after stimula

69 f membrane excitability, we recorded in cell-attached configuration spontaneous action currents from

70 find that this rate depends on time in cell-attached mode, on pipette potential, and on pipette ioni

71 and microvesicle fusion was enhanced in cell-attached patches and dense-core vesicle fusion pores had

72 ibited currents of similar magnitude in cell-attached patches as in inside-out patches exposed to 10

73 otoxin- or PEG-CAT-sensitive fashion in cell-attached patches but had little effect on channel openin

74 In cell-attached patches from cardiac myocytes and Na(V)1.5-expr

75 e activity of single K(ATP) channels in cell-attached patches of granule cells in the mouse dentate g

76 In cell-attached patches of mesenteric arterial smooth muscle ce

77 t recombinant GluN1/GluN2B receptors in cell-attached patches of transiently transfected HEK293 cells

78 we now investigate TRPM8 inhibition in cell-attached patches using HEK293 cells expressing TRPM8 alo

79 for activation of the 20 pS channel in cell-attached patches was approximately 200 nm.

80 In cell-attached patches with 140 mM KCl and 1 mM Mg2+ in the ba

81 At pH 7.9 in cell-attached patches, ifenprodil increased the occupancy of

82 In cell-attached patches, number of open channels x open probabi

83 s and mechanosensitivity was studied in cell-attached patches.

84 gly, increased cytoskeletal rigidity in cell-attached patches.

85 e rise to very small inward currents in cell-attached patches.

86 In cell-attached recordings of Kir6.1/SUR2B single channel activ

87 In cell-attached recordings, mitral cells responded to high freq

88 Here, we employed minimally invasive cell-attached patch-clamping, single-cell qPCR and specific s

89 ivated ion channels in arterial myocyte cell-attached patches that were inhibited by TMEM16A antibodi

90 ranule cells as measured by noninvasive cell-attached recordings.

91 tion locally to the external surface of cell-attached patches through the recording pipette.

92 e determined by a race between entry of cell-attached virions and competing inactivation processes, w

93 experimental conditions are optimized, cell-attached recordings in small neurons may report erroneou

94 Using 2P-guided whole-cell or cell-attached recordings in positive neurons expressing any o

95 Here we perform cell-attached recording of molecular layer interneurons in ce

96 By performing cell-attached current and capacitance recordings predominantl

97 CR-induced TRPC3c channel opening rate (cell-attached patch) matched the maximum activation achieved

98 -seal whole-cell somatic and loose-seal cell-attached axonal/dendritic patch-clamp recordings and com

99 Simultaneous cell-attached loose-patch recordings of Na(+) currents on eac

100 In brain slices, cell-attached recordings of membrane potential show that CO2/

101 archical cellular structure by stacking cell-attached microplate structures with specific configurati

102 We used in vivo two-photon targeted cell-attached recording to compare the response properties of

103 electrophysiological recordings in the cell-attached configuration demonstrated that activated alpha

104 In the cell-attached configuration, H(2)O(2) significantly increased

105 f the outer and inner monolayers in the cell-attached configuration, whereas a substantial difference

106 This implies that the magnitude of the cell-attached current is regulated not only by intracellular

107 d positive pressures >=5 mmHg under the cell-attached mode, activated piezo2 currents in MCC-13 and h

108 rrent amplitude to that measured in the cell-attached mode.

109 We find that of the cell-attached particles, between 20 and 50% ultimately penetr

110 ted nucleus accumbens neurons using the cell-attached patch clamp configuration.

111 Using the cell-attached patch clamp technique, we investigated the hypo

112 rom single TRPV1 ion channels using the cell-attached patch clamp technique.

113 s for recording LTCC currents using the cell-attached patch-clamp technique.

114 6 activations were only observed in the cell-attached patches but not in the inside-out patches.

115 Unexpectedly, these cell-attached currents are significantly smaller (by approxim

116 ce or physiological distinction through cell-attached recordings.

117 Application of negative pressure to cell-attached patches (-20 mmHg) caused a 19-fold increase in

118 fluorometry is superior to traditional cell-attached MA for measuring the intrinsic mechanical prope

119 Here, we used cell-attached and whole-cell recordings in vitro to study act

120 Direct measurement of I(KA) using cell-attached patch-clamp recordings revealed that there was

121 selected independent of spiking, using cell-attached recordings and two-photon calcium imaging, in t

122 Using cell-attached recordings in vivo, we demonstrate that electri

123 of GABA transmission was analyzed using cell-attached recordings.

124 Using cell-attached unitary current recordings from GluN1-2a/GluN2A

125 Here we use in vivo cell-attached and whole-cell voltage-clamp recordings to reve

126 In vivo cell-attached recordings revealed differences between the sou

127 Visualized in vivo cell-attached recordings show that division by PV neurons alt

128 vesicles in mouse chromaffin cells with cell-attached capacitance measurements that offer millisecond

129 r membrane neck (the fission-pore) with cell-attached capacitance measurements to detect CME of singl

130 educed ATP-sensitivity display non-zero cell-attached currents.

131 We show that the stability of chromosome-attached kinetochore-MTs (K-MTs) is important for bipola

132 and 11-times higher than those of covalently-attached GOx (CA) on acid-treated CNTs and simply-adsorb

133 We utilized suction cup-attached biologging tags equipped with stereo hydrophone

134 on between the membrane and the cytoskeleton-attached protein anchors embedded in the membrane matrix

135 Erk signaling also regulates PDH flux in ECM-attached cells.

136 -overexpressing cells when compared with ECM-attached cells.

137 f the folding thermodynamics of an electrode-attached, redox-reporter-modified protein.

138 egatively-charged AuNC@BSA electrostatically-attached onto MSN-NH3(+), affording highly loaded pH-res

139 End-attached filaments transiently paused but resumed growth

140 Aggrecan was chemically end-attached onto gold-coated planar silicon substrates and

141 Thus, the mechanisms that remove endothelial-attached sickle RBCs from the microvasculature are expec

142 C uptake by PMos was specific to endothelial-attached sickle, but not control, RBCs and occurred most

143 val, and larger adult size relative to fruit-attached individuals.

144 V pressures are precisely matched in the GUV-attached configuration, breaking the patch membrane also

145 In hindlimb-attached semi-isolated preparations, passive flexion-ext

146 rization and depolymerization at kinetochore-attached microtubule ends.

147 ce and also by destabilizing the kinetochore-attached microtubule tip.

148 These kinetochore-attached K-fibres generate pushing and pulling forces, w

149 rinsic-switching time of the two kinetochore-attached microtubule fibres, with the centromeric spring

150 (cFLIP) and TNFalpha stimulation of laminin-attached cells in which cFLIP had been downregulated res

151 he first total synthesis of the amino linker-attached, conjugation-ready tetrasaccharide of O-PS of Y

152 the total synthesis of an aminopropyl linker-attached trisaccharide repeating unit of Staphylococcus

153 ctivity relationships of bivalent and linker-attached compounds in mAChRs.

154 ns to access the structurally complex linker-attached trisaccharide repeating units, which are valuab

155 reactivity-based one-pot assembly of linker-attached Lc(4) and IV(2)Fuc-Lc(4), which are components

156 , FHL-1, CFHR1, and plasminogen, and the Lpd-attached regulators are relevant for innate immune escap

157 ues when they were incubated with lymphocyte-attached HIV-1.

158 re PI3K/mTOR signalling is decreased, matrix-attached human mammary epithelial cells upregulate and i

159 responses to PI3K/mTOR inhibition in matrix-attached cells resemble well-conserved stress responses

160 of mRNA fluctuations among individual matrix-attached epithelial cells, we found that a subset of FOX

161 apoptosis of matrix-detached, but not matrix-attached cancer cells, suggesting that matrix-attached c

162 We stochastically profiled matrix-attached human epithelial cells in a three-dimensional c

163 ttached cancer cells, suggesting that matrix-attached cells use alternate mechanisms to maintain nutr

164 inner matrix-deprived cells, whereas matrix-attached cells are resistant.

165 pinning, and filament bending of a membrane-attached cytoskeletal filament can be sufficient to pres

166 suggests that Twinkle is part of a membrane-attached replication platform.

167 We report that the extracellular membrane-attached protein nyctalopin is required for the normal e

168 and that ZipA-stabilized FtsZ forms membrane-attached spiral-like structures in the bacterial cytopla

169 tion of VPS29s in hetero-hexameric, membrane-attached, retromer arches indicates that VARP will prefe

170 tes, we detect and image individual membrane-attached actin filaments diffusing within the acto-myosi

171 relative disposition of their inner membrane-attached export platform, C-ring/pods and ATPase complex

172 cally analogous to an intracellular membrane-attached contractile phage tail.

173 Full-length Efa6 is membrane-attached, hence primarily blocks MTs in the periphery of

174 rate that hSnf7 proteins form novel membrane-attached filaments that can promote or stabilize negativ

175 lized protein machinery composed of membrane-attached (t-SNARE) and vesicle-attached (v-SNARE) protei

176 s evolutionarily conserved class of membrane-attached proteins regulates key aspects of APP-dependent

177 Instead, the plasma-membrane-attached PLDgamma1 protein colocalized and associated wi

178 Our data indicate that membrane-attached vesicles comprise the readily releasable pool o

179 In green sulfur bacteria, the membrane-attached Fenna-Matthews-Olson (FMO) antenna protein func

180 ently labeled CaM or CaBP1 with the membrane-attached proximal C terminus (pCT) and the N terminus (N

181 somes, it is twice as stiff, due to membrane-attached protein components.

182 The transition from soluble to membrane-attached ribosomes occurs shortly after the first transm

183 porting checkpoint proteins from microtubule-attached kinetochores to spindle poles.

184 mediated removal of Spindly from microtubule-attached kinetochores, rather than poleward transport pe

185 methods, we solved structures of microtubule-attached, dimeric kinesin bound to an ATP analog.

186 ly motif mutants are retained on microtubule-attached kinetochores along with checkpoint proteins, re

187 cleotide states encompassing the microtubule-attached kinetic cycle of a kinesin motor.

188 Incubation of human tissue with monocyte-attached HIV resulted in productive tissue infection.

189 n, with greater SWV values within the muscle-attached region than those outside of the muscle-attache

190 ched region than those outside of the muscle-attached region.

191 sociation with NEMO leads to removal of NEMO-attached linear polyubiquitin chains and subsequent inhi

192 These ECS cells grow as non-attached spheroids, and display enhanced migration and i

193 tric epithelium and a larger subgroup of non-attached bacteria that are freely swimming.

194 K) creates a permanent flap that remains non-attached to the underlying laser-modified stroma.

195 Many NP-attached ligands, however, are difficult to ionize by LD

196 and uses it as a substratum to deliver ParB-attached cargo DNA, and ParB drives ParA dynamics, allow

197 nd size-fractions associated with a particle-attached or free-swimming lifestyle could reflect adapta

198 ysiological characteristics between particle-attached and free-living MGIIs.

199 of living organisms and settling of particle-attached organisms lead to uneven distributions of biota

200 that primary successions may shape particle-attached bacterial communities in the ocean and that rap

201 rine particles and demonstrate that particle-attached communities undergo rapid, reproducible success

202 Like ZA itself, the PGN-attached drug (PGN-ZA) binds specifically to viral neura

203 iferative effect on cells growing as plastic-attached monolayer cultures (i.e. standard tissue cultur

204 ng causes shortening and bending of platelet-attached fibers, resulting in formation of fiber kinks.

205 so released horseradish peroxidase (HRP) pre-attached to the amplification probes, and the resultant

206 olymer monomer with ssDNA probe sequence pre-attached.

207 holes to form fiber networks that were "pre-attached" to the substrate and other fibers.

208 its heparin ligand, as induced by a protein-attached lanthanide spin label, provided structural rest

209 ns are introduced nonuniformly along protein-attached HS polysaccharide chains by specific enzymes.

210 ed and so the graft was flipped, centred, re-attached and finally stabilized by an intracameral gas b

211 The detached retina was successfully re-attached surgically and the subretinal fluid was gradual

212 Thus, the contribution of receptor-attached phosphates to arrestin binding varies depending

213 favorable for its interaction with receptor-attached phosphates.

214 The interaction of rhodopsin-attached phosphates with Lys-14 and Lys-15 in beta-stran

215 ich are then replaced by more distant ribbon-attached vesicles, creating opportunities for new vesicl

216 Factor assists in the maturation of ribosome-attached nascent chains by acting as both a holdase and

217 wobble, and Fourier analysis of moving, ring-attached beads corroborates this prediction.

218 wing 2 major wave events as compared to rock-attached kelp.

219 compartments: surface biological crust, root-attached, and the broader rhizosphere.

220 europathic rat dorsal horn, with dorsal root-attached preparations, soluble FKN (sFKN) contents are i

221 In "semi-attached OCCM," the Mcm3 and Mcm7 WHDs latch onto ORC-Cd

222 . (2019) used long-term monitoring of a site-attached temperate reef fish, the purple wrasse (Notolab

223 correlated with mechanical states of spindle-attached kinetochores, provided a nanometer-scale map of

224 e resistance to many DUBs of long, substrate-attached Lys(48)-linked chains helps ensure that protein

225 separate two distinct areas on the substrate-attached cell surface from each other: an external area

226 not plectin, colocalize along the substratum-attached surface.

227 Surface-attached bacterial communities called biofilms display a

228 nts to the geometrical features of a surface-attached biomolecule.

229 bility of this DNA to hybridize to a surface-attached complementary strand.

230 te the assembly and utilization of a surface-attached double-stranded DNA catenane composed of two in

231 uitment to an abiotic surface allows surface-attached bacteria time to grow and form aggregates that

232 Although surface-attached bacteria often experience strong chemical gradi

233 g evaluations on both planktonic and surface-attached bacteria provided new insights on these distinc

234 tches between free-living motile and surface-attached sessile lifestyles.

235 Biofilms are surface-attached agglomerations of microorganisms embedded in an

236 on, bacteria form biofilms which are surface-attached communities of enriched populations containing

237 ng planktonic bacteria, biofilms are surface-attached communities of slow- or non-replicating bacteri

238 distinguishable whether proteins are surface-attached or free in bulk solution.

239 Pili are surface-attached, fibrous virulence factors that play key roles

240 be the surprising reactivity between surface-attached (a) 0.9, 1.6, and 4.1 nm diameter weakly stabil

241 cies.Most bacteria live in biofilms, surface-attached communities encased in an extracellular matrix.

242 Biofilms, surface-attached communities of bacteria encased in an extracell

243 ural systems, bacteria form complex, surface-attached communities known as biofilms.

244 Microbes commonly live in dense surface-attached communities where cells layer on top of one ano

245 ently calculated in two-dimensional, surface-attached populations.

246 ting relevance of this mechanism for surface-attached platelets under physiological flow.

247 the environment, most bacteria form surface-attached cell communities called biofilms.

248 Many species of bacteria form surface-attached communities known as biofilms.

249 Bacteria form surface-attached communities, known as biofilms, which are centr

250 marine environments, where it forms surface-attached communities commonly described as biofilms.

251 omastigote morphology but also forms surface-attached haptomonads and amastigotes.

252 hedding of extracellular matrix from surface-attached biofilms generates a sieve-like network that ca

253 For the heterogeneous, surface-attached material generated from [Cp*Ir(H(2)O)(3)](2+),

254 s to the formation of hyperbiofilms, surface-attached communities reaching high density.

255 Microbes are predominantly found in surface-attached and spatially structured polymicrobial communit

256 Many bacteria on earth exist in surface-attached communities known as biofilms.

257 ression in suspended cultures and in surface-attached microcolonies revealed that QS onset in both sy

258 n nature, bacteria primarily live in surface-attached, multicellular communities, termed biofilms (1-

259 However, how individual surface-attached bacteria self-organize into microcolonies, the

260 force-free association of individual surface-attached fibrinogen and alphaIIbbeta3 molecules and forc

261 ordinates subunit self-assembly into surface-attached fibers.

262 cellular state and the multicellular surface-attached community state (biofilm) by a range of mechani

263 ufficient to induce virulence in non-surface-attached cells, suggesting that PilY1 mediates surface m

264 n method, single cells that were not surface-attached were isolated with a 100 +/- 0% efficiency and

265 rength and probability of binding of surface-attached antibodies with oligomeric PF4 to simulate inte

266 We discovered that accumulation of surface-attached biofilm has little effect on flow through such

267 The crowding of surface-attached biomolecules may thus be a richer, more complex

268 iofilms are microbial communities of surface-attached cells embedded in a self-produced extracellular

269 f biofilms--organized communities of surface-attached cells--but physiologically and genetically defi

270 nt planktonic cells or as members of surface-attached communities called biofilms.

271 Biofilms are composed of surface-attached microbial communities.

272 te thermodynamic and kinetic data on surface-attached antibodies with their respective antigens.

273 Like all sessile organisms, surface-attached communities of bacteria known as biofilms must

274 n which surface shear stress orients surface-attached P. aeruginosa cells along the flow direction, c

275 ents that cannot be reached by other surface-attached bacteria.

276 ngth and head number (N) moving over surface-attached F-actin in vitro.

277 cleotide conjugates with the silicon surface-attached complementary sequence.

278 owding on the stability of a simple, surface-attached DNA stem-loop.

279 simulate the growth of a two-species surface-attached community where food (resource) is traded for d

280 ctin glycoprotein ligand 1), and the surface-attached chemokine fractalkine, all implicated in leukoc

281 dominant life stage is formed by the surface-attached colony that shows many complex features: coloni

282 surfaces and hybridization with the surface-attached DNA, new methodologies have been developed.

283 PS), while the binding of cocaine to surface-attached MN4 was evaluated using the electromagnetic pie

284 bacteria from single motile cells to surface-attached multicellular communities.

285 the AFM probe, from its complex with surface-attached C3b.

286 ending downward and interacting with surface-attached C4b, which further interacts with the adjacent

287 repeatedly brought into contact with surface-attached purified alphaIIbbeta3.

288 ia, including persister cells within surface-attached biofilms and slow-growing pathogens lead to chr

289 Pneumococci were present within surface-attached biofilms in coinfected animals, and a greater p

290 responsible for transferring the N-terminus-attached catalytic domain across the endosomal membrane

291 air through well-defined interactions of tip-attached 2D crystal nanomesas with 2D crystal and SiO(x)

292 Turf-attached kelp allocated a significantly greater percenta

293 Turf-attached kelp required significantly (2 to 4 times) less

294 d of membrane-attached (t-SNARE) and vesicle-attached (v-SNARE) proteins that zipper together to form

295 glycosylated mucin-like domain of the virion-attached glycoprotein (GP).

296 V entry requires the interplay of the virion-attached hemagglutinin-esterase and fusion glycoproteins

297 ors a large family of more than 20 cell wall-attached epithelial adhesins (Epas).

298 Rib domains within these bacterial cell wall-attached proteins has been suggested as a mechanism of i

299 sive matrix molecules), in which a cell wall-attached stalk enables long range interactions via its a

300 5 months of follow-up, with a clear and well-attached graft.