ライフサイエンスコーパス: hysteretic

1 This hysteretic activation-deactivation cycle is preserved by

2 Rare hysteretic adsorption/desorption isotherms are reported

3 nsition and the inside-strand separation are hysteretic and have an entropy change of approximately 1

4 Our findings show for the first time both hysteretic and irreversible changes in resistivity as a

5 Herein, NDR is introduced in hysteretic and rectified ion transport through single co

6 distribution of the ionic charges during the hysteretic and rectified transport at asymmetric nanoint

7 Hysteretic and rectified transport properties offer exci

8 -dimensional electron system reveals unusual hysteretic and relaxational transport in the fractional

9 r response to cyclic strain is intermittent, hysteretic, and encodes a memory of the largest applied

10 gnificantly rate-limited and that nonlinear, hysteretic, and irreversible sorption/desorption had min

11 The influence of nonlinear, rate-limited, hysteretic, and irreversible sorption/desorption on tran

12 The DW is signalled by a hysteretic anomaly in the in-plane resistivity accompani

13 ed in iodine solution are more compliant and hysteretic as compared to helices in butanol, which exte

14 biomarker-rate relationships were nonlinear hysteretic because tceA and vcrA acted as homologous gen

15 , this transition is characterized by a near hysteretic behavior and a rapid rise of network firing r

16 anoscale pores displayed a unique long-lived hysteretic behavior caused by their ability to form a me

17 These jumps may also exhibit hysteretic behavior dependent on the direction of drivin

18 ne external aldimine formation, indicating a hysteretic behavior in ALAS.

19 de microscopic electrical information of the hysteretic behavior in strained thin film manganites, su

20 subsequent switching to the OFF state shows hysteretic behavior indicating the retention of some oxy

21 listic parameters, we find that the relevant hysteretic behavior may be observed using current state-

22 The highly reproducible hysteretic behavior of G3T multimers has the potential t

23 The hysteretic behavior of one of their constituent variable

24 of such fields manifests itself through the hysteretic behavior of planar Hall resistance observed f

25 s study investigates the temperature-induced hysteretic behavior of resistivity and magnetoresistance

26 oltage as the dominant effect on the channel hysteretic behavior over emission currents from the char

27 The hysteretic behavior toward guest adsorption and desorpti

28 n bonding among PAA units contributed to the hysteretic behavior was supported by experiments with a

29 I(SHG) = f(T) curve defines an unprecedented hysteretic behavior with a SHG OFF state at low (T < 4 d

30 ng step at low relative humidity and without hysteretic behavior-properties essential for energy-effi

31 heir two-electron oxidized forms, indicating hysteretic behavior.

32 noon, leading to T(can)/T(air) slopes >1 and hysteretic behavior.

33 and stimulus path on nonequilibrium thermal hysteretic behavior.

34 each other) demonstrate highly reproducible hysteretic behavior.

35 ing of CO(2) is responsible for the observed hysteretic behavior.

36 on, we demonstrate that the system undergoes hysteretic behaviour and that two different types of Blo

37 ow that bistable skyrmionic textures undergo hysteretic behaviour between two energetically equivalen

38 he temperature at which it is observed, with hysteretic behaviour exhibited between 300 K and 100 K.

39 e to create a synthetic membrane with stable hysteretic behaviour for molecular transport(7-11).

40 ansport, the representation of nonlinear and hysteretic behaviour in soil-xylem hydraulics and the ne

41 CDW, and that dissipation maxima arise from hysteretic behaviour of the CDW phase as the tip oscilla

42 e crystals), we observe prominent and robust hysteretic behaviour of the graphene resistance with an

43 The device exhibits hysteretic (bistable) current/voltage characteristics.

44 (II)-MOF (1) displays distinctive three-step hysteretic breathing behavior under ethane gas pressure

45 ER (type 2), and high rates (~20 ms/beat) to hysteretic btb-ER under periodic pacing and to a vertica

46 d by sublimation, as evidenced by abrupt and hysteretic changes in the dielectric properties in the t

47 a soft domain-wall displacement exhibits non-hysteretic characteristics.

48 , it is paramount to determine their thermal hysteretic characteristics.

49 butions to nonlinearity (e.g., classical and hysteretic) could be due to physical features (defects)

50 ematic changes in the resonance response and hysteretic current control of the ferromagnetic resonanc

51 foundation for understanding a wide range of hysteretic current-voltage behaviour observed in many na

52 Their biophysical properties lead to pinched hysteretic current-voltage dependence as well a classic

53 All devices exhibited a (noncapacitive) hysteretic current-voltage response that switched the de

54 s ([Formula: see text]) exhibits distinctive hysteretic cycles whose shape and looping direction vary

55 e conformation of the PAA chains exhibited a hysteretic dependence on pH, where different effective p

56 e polarization from triboelectrification and hysteretic dielectric polarization from ferroelectric ma

57 principles or guiding rules for this highly hysteretic, dissipative material.

58 Hysteretic drainage and imbibition Pc-Sw curves were mea

59 model makes several explicit predictions on hysteretic dynamic behaviors, system response to pulsed

60 hifts in aquatic ecosystems that may exhibit hysteretic dynamics and a slow return to the initial sta

61 The observed hysteretic dynamics is well reproduced by numerically so

62 over, we demonstrate activity dependence and hysteretic dynamics over the phase diagram due to the im

63 APs with different APDs, and caused multiple hysteretic dynamics.

64 esults demonstrate a previously unrecognized hysteretic effect in the spatial distribution of biomass

65 ic force is expected, we can infer that this hysteretic effect is not inherent to the pure electrosta

66 nalyzing 7SK RNA by SHAPE and demonstrated a hysteretic effect of magnesium on 7SK folding dynamics i

67 Strong recurrent feedback entailed a hysteretic effect on the network which diminished with t

68 se caused by warming, representing a typical hysteretic effect; this hysteretic pattern required EARL

69 Under nonequilibrium conditions, hysteretic effects were observed when CO(2) was dissolvi

70 ties than the original procapsid, suggesting hysteretic effects.

71 ctures have recently been shown to exhibit a hysteretic electric-field-induced metal-insulator quantu

72 ron-free precursor while gaining recoverable hysteretic energy dissipation and maintaining its origin

73 esults indicate that the 20S proteasome is a hysteretic enzyme and is subject to substrate inhibition

74 base unstacking demonstrate that T4 pol is a hysteretic enzyme and must exist in two DNA bound confor

75 A kinetic model of a hysteretic enzyme is proposed to interpret and predict t

76 xperiments clearly demonstrate that DGD is a hysteretic enzyme whose conformational distribution is c

77 steady state and is thus a new example of a hysteretic enzyme.

78 The study also suggests that hysteretic enzymes may be building blocks of synthetic n

79 ttaining steady-state velocity, a feature of hysteretic enzymes that show slow transitions compared w

80 The hysteretic features are attributed to the dynamics of th

81 4% for the fast form, in agreement with the hysteretic fit to the steady-state data.

82 intermediate {N(iso)} responsible for GFP's hysteretic folding behavior is trapped.

83 g landscape with a dual basin leading to the hysteretic folding behavior observed in experiment.

84 l version of the square twist to demonstrate hysteretic folding dynamics at the sub-millimetre scale.

85 or loosely packed barrel under intermediate (hysteretic) folding conditions.

86 pH-induced hysteretic gating of track-etched polycarbonate membrane

87 The hysteretic gating property of the multilayer-modified TE

88 capacitive memory arises from reversible and hysteretic geometrical changes in a lipid bilayer that m

89 ansient adsorption dynamics reveals that the hysteretic H(2) adsorption is an intrinsic adsorption ch

90 rocess, we demonstrate that the system shows hysteretic H(2) adsorption under changes of external pre

91 Recently, hysteretic H(2) adsorption was observed in several nanop

92 istive behavior, showing noncrossing pinched hysteretic I-V loops.

93 urium to temperature and acid variations was hysteretic, i.e. whether the transcriptional regulation

94 nductance switching in high electric fields, hysteretic in voltage.

95 at the level of the individual residue, the hysteretic intermediate state is further characterized i

96 This hysteretic ion dynamics can be regulated by modifying bi

97 which can be observed experimentally through hysteretic jumps of several orders of magnitude in the n

98 Surprisingly, this tuning is hysteretic, keeping the ear tuned up for the bat's possi

99 rate of ALA release is also controlled by a hysteretic kinetic mechanism (observed as a lag in the A

100 activation by vWbp(1-263) is controlled by a hysteretic kinetic mechanism initiated by substrate bind

101 it activates ProT by a substrate-dependent, hysteretic kinetic mechanism.

102 Following the hysteretic lag, a simple first-order primer terminus uns

103 We find that the phase transition shows a hysteretic loop in Raman spectra, and can be reversed by

104 However, large hysteretic losses (which make magnetic refrigeration les

105 eduction (by more than 90 per cent) of these hysteretic losses by alloying the compound with a small

106 interactions and experiences a discontinuous hysteretic magnetic-field-induced switching along [010]

107 the ascending and descending branches of the hysteretic magnetization curve.

108 isotropic, and hysteretic magnetoresistance, hysteretic magnetization, and the polar Kerr effect, all

109 tic order of the kagome metal and exhibits a hysteretic magnetoresistance in the superconducting stat

110 r is evidenced by negative, anisotropic, and hysteretic magnetoresistance, hysteretic magnetization,

111 ranches of a relaxation-like oscillator in a hysteretic manner enabled by the existence of a singular

112 olarization can be induced and reversed in a hysteretic manner in bilayers made of ultrathin insulato

113 This unique hysteretic memory switch may result in persistent infect

114 showed that this bimodality is mediated by a hysteretic memory-switch that results in the stable co-e

115 ground state, we demonstrate that low-field hysteretic metamagnetic transitions produce states with

116 The hysteretic model is parameterised for three independent

117 tive sources of the resting potential, and a hysteretic model of electroporation.

118 A hysteretic model that assumes two slowly interconverting

119 Moreover, cyclic hysteretic multiphase flow is also studied, which is a r

120 findings provide a new avenue for tuning the hysteretic nature of N-LCE at both macro- and microscopi

121 transport phenomena, such as hysteresis and hysteretic negative differential resistance (NDR).

122 bust electronic ratchet states, which enable hysteretic, non-volatile injection of charge carriers th

123 on of 12 genes and this response was neither hysteretic nor accompanied of increased resistance to in

124 s hitherto been conducted to investigate the hysteretic or flow direction-dependent behavior during d

125 h things as dynamic disorder, heterogeneity, hysteretic or mnemonic enzymes across these different fi

126 ubble returns to its original diameter via a hysteretic pathway where most of the expansion occurs in

127 In particular, a hysteretic pattern associated with distance to a keyston

128 presenting a typical hysteretic effect; this hysteretic pattern required EARLY-FLOWERING 3 (ELF3).

129 , a general argument explaining the observed hysteretic patterns remains elusive.

130 For the hysteretic peeling transition, we determined DeltaS appr

131 NA strands are spatially separated after the hysteretic peeling transition.

132 nvolved in the overstretching process: (i) a hysteretic "peeling" off one strand from its complementa

133 conversion have combined with high cost and hysteretic performance to restrict practical use.

134 Here, by exploiting the hysteretic phase transition of vanadium dioxide, an all-

135 Wetting of actual surfaces involves diverse hysteretic phenomena stemming from ever-present imperfec

136 ce spectroscopy of this material exemplifies hysteretic photochromic switching (HPS) between two conf

137 bsorption and emission spectroscopy reveal a hysteretic piezochromism that was not reported for other

138 10 Debye longitudinal molecular dipoles, and hysteretic polarization reversal with a coercive field ~

139 The emergent ferroelectricity and hysteretic polarization switching in ultrathin ZrO(2), c

140 Here, hysteretic reduced-order battery models and adaptive ext

141 hod captures the superparamagnetic and fully hysteretic regimes and the transition between them.

142 gion between the superparamagnetic and fully hysteretic regimes.

143 y predict and experimentally verify that the hysteretic region can be fine-tuned by controlling the i

144 ve feedback switch can markedly increase the hysteretic region, compared to its single-positive feedb

145 etrics that characterize the anisotropic and hysteretic regional mechanical behavior of the lung.

146 This novel modeling approach also reveals a hysteretic relationship between pesticide degradation ra

147 rameters against each other, many pairs have hysteretic relationships that identify the current locat

148 u = -1 the insulating state exhibits a sharp hysteretic resistance enhancement when a perpendicular m

149 te increases following annealing and shows a hysteretic response around the blocking temperature.

150 t magnetic droplet solitons exhibit a strong hysteretic response in field and current, proving the ex

151 Thus, although a hysteretic response is neither necessary nor sufficient,

152 To examine the robustness of the hysteretic response of CDK activity to total cyclin, we

153 Furthermore, we found a hysteretic response of plant diversity to increases and

154 ENSO hysteresis is mainly attributed to the hysteretic response of the tropical Pacific Intertropica

155 We then show how the hysteretic response of the wild-type system can be conve

156 work collectively to generate a switch-like, hysteretic response.

157 M system control--gene copy number--and of a hysteretic response.

158 lobal teleconnection patterns exhibit strong hysteretic responses to carbon dioxide (CO(2)) reduction

159 nly a small group of these materials display hysteretic responses to stimuli.

160 and mesoscopic disorder and associated local hysteretic responses underpin the unique properties of s

161 enrichment rate can modulate a diversity of hysteretic responses within a single aquatic ecosystem,

162 e across the aperture; the curve resembles a hysteretic sawtooth where each jump corresponds to the c

163 Hysteretic sorption and desorption of water is observed

164 ow carrier densities and appears as a set of hysteretic spikes in the resistance of a sample placed i

165 (dpzca)(2)] shows an abrupt, reversible, and hysteretic spin crossover (T(1/2) downward arrow = 168 K

166 alysis of the observed sub-Kelvin zero-field hysteretic spin dynamics of {Cr(III)Dy(III)6} reveals th

167 The complex exhibits a hysteretic spin transition at 117 K upon cooling and 129

168 -1-yl)isonicotinonitrile) exhibits an abrupt hysteretic spin transition near 240 K, with a shoulder o

169 tage measured by the FM electrode exhibits a hysteretic step-like change when sweeping an in-plane ma

170 d arrests the equilibration, here we examine hysteretic stress-strain characteristics in a series of

171 at a cysteine residue is responsible for the hysteretic substrate activation behavior of yeast pyruva

172 an be coupled to create a strongly bistable, hysteretic switch between normal and toxic states.

173 the network into an essentially irreversible hysteretic switch, thereby explaining the sharp, robust

174 d Cdk's subjugate SG dynamics to a conserved hysteretic switch.

175 d the per operon as the key component of the hysteretic switch.

176 components of this pathway can form a robust hysteretic switch.

177 orms the network into a largely irreversible hysteretic switch; the simulations reported here also de

178 A theoretical model to explain the observed hysteretic switching behavior based on electrochemical n

179 idenced by robust anomalous Hall effect with hysteretic switching behavior.

180 ken-spring depinning, as well as spontaneous hysteretic switching between cellular vortex trajectorie

181 he memory write operation through controlled hysteretic switching between the quantized Hall states,

182 linear elastic regime, the shell undergoes a hysteretic, temperature-dependent buckling transition.

183 pin crossover complex with atypical two-step hysteretic thermal switching at 74 K and 84 K shows rich

184 ydro-1H-3-oxide-1-oxyl) undergoes an unusual hysteretic thermo-induced valence tautomeric transition

185 The hysteretic transcriptional response to heat shock was ac

186 a mobile vortex core exhibiting a reversible hysteretic transformation path.

187 On small domains, we identify a hysteretic transition as well as a transition featuring

188 anized in intricate localized patterns, with hysteretic transitions between multiple metastable state

189 t-order transition with hysteresis, gradual, hysteretic two-step or multistep transitions, and incomp

190 so realized in this work, resulting from the hysteretic type of phase transition in PZN-PT(011) at hi

191 ion, high-pressure H2 adsorption data reveal hysteretic uptake and release, with hysteresis loops of

192 ed robustness by estimating the frequency of hysteretic versus nonhysteretic dynamical mechanisms.

193 ormed hydrogels display an unusual, strongly hysteretic volume-phase transition indicating useful the

194 ical potential; moreover, this transition is hysteretic, which we use to demonstrate non-volatile ele