ライフサイエンスコーパス: nanodomain

1 channels, enabling near-field imaging of the nanodomain.

2 0.81 ( 220 mAh g(-1)) were identified in the nanodomain.

3 ric fields and depletion of local sodium ion nanodomains.

4 zation rotation is an abundance of sub-50 nm nanodomains.

5 ated with the promoted formation of gephyrin nanodomains.

6 ion of the size of these highly concentrated nanodomains.

7 ese findings for theoretical descriptions of nanodomains.

8 in small ( approximately 80 nm in diameter) nanodomains.

9 anometers for highly ordered, single-polymer nanodomains.

10 bility, consistent with their confinement in nanodomains.

11 and mutant integrin partitioning into lipid nanodomains.

12 eceptors was interrupted by dwellings within nanodomains.

13 ed signalling components within dedicated PM nanodomains.

14 daries between randomly oriented crystalline nanodomains.

15 m regulating the dynamic and organization of nanodomains.

16 CD22 to be highly mobile and organized into nanodomains.

17 AMPAR nanodomains segregated away from NMDAR nanodomains.

18 taxin-1A in and out of partially overlapping nanodomains.

19 as LRRTM2 is organized in compact and stable nanodomains.

20 maR2 is confined by sphingolipid/cholesterol nanodomains.

21 morphous Si (a-Si) band, embedded with dh-Si nanodomains.

22 IgG and poly(N-isopropylacrylamide) (PNIPAM) nanodomains.

23 he results were interpreted in terms of RTIL nanodomains.

24 the fragmentation of gephyrin in subsynaptic nanodomains.

25 l with alternately segregated donor/acceptor nanodomains.

26 DGs and the formation of perigranular Ca(2+) nanodomains.

27 ten relies on Ca(2+) computations within the nanodomain-a conceptual region extending tens of nanomet

28 ctor X, which binds directly to the membrane nanodomain adjacent to tissue factor.

29 Normally distributed in linear quadrilateral nanodomains along the flagellum, the complex lacking Cat

30 emonstrate that detergent-resistant membrane nanodomains, also known as lipid rafts, are the primary

31 d that different CTLs rarely occupy the same nanodomain, although they appear colocalized using wide-

32 AMPARs are stabilized reversibly in these nanodomains and diffuse freely outside them.

33 alectins restored lateral diffusion in lipid nanodomains and JAK/STAT signaling in patient cells, whe

34 c receptor interactions with actin and lipid nanodomains and reveal a new function for receptor glyco

35 c field coupling, intercellular cleft sodium nanodomains, and LQT3-associated mutant channels, myocyt

36 h mobility with transient incorporation into nanodomains, and the other pool forms immobile clusters,

37 Previously, a number of Ca(2+) nanodomains approximations have been developed, for inst

38 Nanodomains are dynamic in their shape and position with

39 AMPAR nanodomains are often, but not systematically, colocaliz

40 DC-SIGN and CD206 nanodomains are randomly distributed on the plasma membr

41 Some of these nanodomains are so small (radius <5 nm) that they cannot

42 The nanodomains are speculated to be of a micellar structure

43 ycin, suggesting that critical, local Ca(2+) nanodomains around TPCs stimulate granule exocytosis.

44 rolled whether SK channels were expressed in nanodomains as single entities or as a group of multiple

45 localized with synaptic proteins in specific nanodomains, as determined by super-resolution microscop

46 ur results uncover a striking feature of CaV nanodomains, as diffusion-restricted environments that a

47 found these proteins to localize in membrane nanodomains, as observed by colocalization with the nano

48 w that Gpsm2 defines an approximately 200 nm nanodomain at the tips of stereocilia and this localizat

49 exponentially with the area fraction of the nanodomains at fixed surface pressure over the 0.1- to 1

50 lustering at AZs, which likely alters Ca(2+) nanodomains at release sites and thereby affects release

51 Our results do not support the presence of nanodomains based on lipid-phase separation in the basal

52 ive in activating gene expression via Ca(2+) nanodomains because it participates in a membrane-delimi

53 We propose that Ca(2+)-signaling nanodomains between lysosomes and sarcoplasmic reticulum

54 ransforms to amorphous carbon with graphitic nanodomains by catalytic effect of Fe.

55 observed an unexpected and dramatic boost in nanodomain Ca(2+) amplitude, ten-fold higher than predic

56 is provides an accurate approximation to the nanodomain Ca(2+) and buffer concentrations.

57 proved useful in revealing the dependence of nanodomain Ca(2+) distribution on crucial parameters suc

58 However, direct visualization of nanodomain Ca(2+) far exceeds optical resolution of spat

59 ge-sensitive calcium channels, presumably by nanodomain Ca(2+) near the channels, in response to glut

60 Theory predicts that nanodomain Ca(2+) signals differ vastly from the slow su

61 ed in their voltage-dependent gating and use nanodomain Ca(2+) to drive local CaMKII aggregation and

62 ts suggest a model for fast release in which nanodomain Ca(2+) triggers exocytosis of docked vesicles

63 n frog oocytes requires highly localized, or nanodomain, calcium signaling.

64 anized in a random fashion; evidently, these nanodomains can be clustered into larger microdomains th

65 Crucial questions are whether lipid nanodomains can exist in stable equilibrium in membranes

66 stributed on the plasma membrane, whereas HA nanodomains cluster on length scales up to several micro

67 Second, histone nanodomain clusters decompact into mononucleosome fibers

68 yer best described as highly strained VO2(B) nanodomains combined with an extra (Ti,V)O2 layer on the

69 a differing localization to plasma membrane nanodomains compared with wild-type alpha(q).

70 atching the short-range Taylor series of the nanodomain concentration with the long-range asymptotic

71 The nanodomains consist of 6:1 DPPC:cholesterol "complexes"

72 In the outer leaflet, distinct nanodomains consisting of gangliosides are observed.

73 imate, as a lower limit, that DC-SIGN and HA nanodomains contain on average two tetramers or two trim

74 These data implicate subsynaptic nanodomains containing a major psychiatric risk molecule

75 ation spectroscopy we demonstrate that these nanodomains containing hundreds of lipid molecules are f

76 Double-nanodomain coupling between somatic plasma membrane and

77 Nanodomain coupling has several functional advantages, i

78 (PV)-expressing interneurons is triggered by nanodomain coupling of P/Q-type Ca(2+) channels, whereas

79 ease is triggered by microdomain rather than nanodomain coupling.

80 Stable ferroelectric nanodomains created in SrTiO3 were observed at temperatu

81 statistical model indicated that the coronal nanodomains detected likely result from a segmented, gra

82 terol segregates into 10- to 100-nm-diameter nanodomains dispersed throughout primarily dipalmitoylph

83 tes consist of homogeneously dispersed LixSi nanodomains embedded in a highly crystalline Li2O matrix

84 k of Sph and second, coalescence of existing nanodomains ending in large-scale phase separation.

85 omyelin (SM)- and cholesterol (Chol)- driven nanodomains exist in living cells and in model membranes

86 nm nanoclusters or approximately 300-600 nm nanodomains for potential interaction with IL-22R.

87 ains as small as 50 nm in radius and observe nanodomain formation, destruction, and dynamic coalescen

88 plexes within the context of plasma membrane nanodomains has remained a highly challenging task.

89 The investigation of potential nanodomains, however, requires the use of superresolutio

90 observed sensitive variations in the thermal nanodomain IMT behaviour, this suggests that the IMT is

91 en Ca(2+) influx and exocytosis changes from nanodomain in low-frequency tuned hair cells ( approxima

92 recruitment of Ca(2+)-sensitive enzymes to a nanodomain in the immediate vicinity of the LTCC by an u

93 bservation of ferroelectric and ferroelastic nanodomains in (110)-oriented BiFeO3 (BFO) thin films ep

94 lung surfactant, and can explain the role of nanodomains in its surface activity and inhibition by an

95 ns (MC-FRET) identifies directly 10 nm large nanodomains in liquid-disordered model membranes compose

96 The presence and effect of RTIL nanodomains in molecular solvent/RTIL mixture were inves

97 de strong direct evidence of the presence of nanodomains in molecular solvent/RTIL mixtures.

98 cent dyes or sQDs were diffusing in confined nanodomains in PSDs, which were stable for 15 min or lon

99 finement of VDCC within sarcolemmal membrane nanodomains in response to varying tonus of C. elegans b

100 Hybrid lipids generate nanodomains in some model membranes and are also abundan

101 shes the physiological relevance of membrane nanodomains in the control of transmembrane receptor sig

102 to extend the Pade method to estimate Ca(2+) nanodomains in the presence of cooperative Ca(2+) buffer

103 rated iron-rich, redox-active and preceramic nanodomains in the solid state with applications in nano

104 gs suggest that AMPARs rapidly enter stable 'nanodomains' in PSDs with lifetime >15 min, and do not a

105 +) source describing a single-channel Ca(2+) nanodomain, in the presence of a single mobile buffer wi

106 ease in lambda expected from the line-active nanodomains, in analogy to 3D emulsions.

107 is abolished in the GPMVs, whereas transient nanodomain incorporation of ganglioside lipid GM1 is app

108 Nanodomains inserted within a crystalline matrix can pro

109 ation that AMPARs are highly concentrated in nanodomains, instead of diffusively distributed in the P

110 irregularly shaped 100-200 nm poly(alanine) nanodomains interspersed within the PEG phase.

111 ge-carrier trapping times in sp(2) and sp(3) nanodomains is determined.

112 The key to characterizing nanodomains is to monitor the coincidental secondary ion

113 tage-activated Cav3.2 Ca(2+) channels at the nanodomain level to support a previously undescribed tra

114 These associations within membrane nanodomains likely maximise interactions between pigment

115 They are involved in the formation of nanodomains ("lipid rafts"), which serve as important si

116 3/CPK21 with ABI1, however, prevented proper nanodomain localization of the SLAH3/CPK21 protein compl

117 visualising FLS2 and BRI1 within distinct PM nanodomains marked by specific remorin proteins and diff

118 ains, as observed by colocalization with the nanodomain marker remorin Arabidopsis thaliana remorin 1

119 REMs are the best-characterized nanodomain markers via an uncharacterized moiety called

120 +) tuning by the physical composition of the nanodomain may represent an energy-efficient means of lo

121 eir size, fluidity, order and lifetime these nanodomains may represent a relevant model system for ce

122 cell types, NFAT can be activated by Ca(2+) nanodomains near open store-operated Orai1 and voltage-g

123 cepted model of SiCO which is conceived as a nanodomain network of graphene.

124 In the case study on the PbS-Ag system, Ag nanodomains not only contribute to block phonon propagat

125 that the ER-mitochondrial interface hosts a nanodomain of H2O2, which is induced by cytoplasmic [Ca(

126 ured substrates, such printed patterns yield nanodomains of block-copolymers with well-defined sizes,

127 ocal control of BKCa channels by fluctuating nanodomains of Ca(2+).

128 of the grana thylakoid membrane that reveals nanodomains of colocalized PSII and cytb6f complexes.

129 The thin films have nanodomains of crystallinity with lattice spacing simila

130 le-molecule immunolabeling showed that dense nanodomains of PSD-95 were preferentially enriched in AM

131 Vitrification of aqueous nanodroplets yields nanodomains of pure low-density amorphous ice in coexist

132 Structured nanodomains of the metallic VO2 locally and reversibly t

133 ts gross spatial arrangement within specific nanodomains of these nanoparticles and reveal how compar

134 cally segregates into iodide-rich perovskite nanodomains on a length scale of up to a few hundred nan

135 pendent neuroexocytosis and are organized in nanodomains on the plasma membrane of neurons and neuros

136 were controlled by Ca(2+) acting across two nanodomains, one between plasma membrane P/Q Ca(2+) chan

137 The TCR nanoclusters could array to form nanodomains or microdomains on the membrane of clonally

138 The presence of DAG-generated nanodomains, or of DAG-induced lipid packing defects, is

139 es form membranes containing submicroscopic (nanodomain) ordered lipid domains (rafts).

140 onventional lipid-binding motif that confers nanodomain organization.

141 H2O2 nanodomains originate from the mitochondrial cristae, wh

142 domain structure emerges in which elemental nanodomains, potentially capable of binding viruses, are

143 l decomposition starts by the formation of a nanodomain precursor state with a so-called tweed struct

144 Thus, ER-mitochondrial H2O2 nanodomains represent a component of inter-organelle com

145 ene end blocks phase separate into localized nanodomains, resulting in the formation of an optically

146 ting and depalmitoylating enzymes into AMPAR nanodomains segregated away from NMDAR nanodomains.

147 ordering of ferroelectric 109 degrees stripe nanodomains separated by periodic vertical domain walls

148 PSD95 expression level regulates AMPAR nanodomain size and compactness in parallel to miniature

149 self-quenching assays; and 4), evaluation of nanodomain sizes by time-resolved Forster resonance ener

150 We demonstrate that such synaptic gephyrin nanodomains stabilize the amplitude of inhibitory postsy

151 monstrate that the gephyrin rearrangement in nanodomains stabilizes the amplitude of postsynaptic cur

152 ut-of-plane direction and a peculiar rumpled nanodomain structure with very large variation in c/a ra

153 polarization and appearance of the MPB-like nanodomain structure.

154 oscopy we find that ankyrin-G forms distinct nanodomain structures within the spine head and neck.

155 ut the physical basis of naturally occurring nanodomains such as lipid rafts.

156 scopy also reveal the presence of incoherent nanodomains that lithiate as if they are separate partic

157 Periodic nanodomains that self-organize into so-called 'superdoma

158 omplexes and the chain-restricting ionomeric nanodomains that they form.

159 precursors, contain carbon- and silica-rich nanodomains, the latter with extensive substitution of c

160 Syndapin I-enriched membrane nanodomains thus seem to be important spatial cues and o

161 erminal domain of Orai1 as central to Ca(2+) nanodomain-transcription coupling.

162 ethods are needed to detect and characterize nanodomains under normal membrane conditions.

163 ved the formation of low-polarity, raft-like nanodomains upon cholesterol addition or cholera-toxin t

164 partitioning of Ni(OEPone)(+) into the RTIL nanodomain was observed.

165 Moreover, within each nanodomain we observe extensive long range ordering of A

166 2Vdelta2 T cells bearing TCR nanoclusters or nanodomains were able to rerecognize phosphoantigen and

167 of controllable length with "patchy" coronal nanodomains were accessible.

168 tant diffusion is confined by distinct actin nanodomains where conformational changes required for Ja

169 t cholesterol associates with PtdSer to form nanodomains where the headgroups of PtdSer are maintaine

170 orm aggregates leading to formation of lipid nanodomains, which are enriched in cholesterol, phosphat