ライフサイエンスコーパス: low-threshold

1 e Raman gain, high conversion efficiency and low threshold.

2 pecific Genetic Testing Institute-ELISA with low threshold.

3 variation in genome size above a relatively low threshold.

4 nd immunoglobulin G (IgG)-specific CLIA with low threshold.

5 dynamic ranges than channels with relatively low thresholds.

6 tending to approximately 1 mum at strikingly low thresholds.

7 irmed by amplified spontaneous emission with low thresholds.

8 370 nm) SP polariton laser with an extremely low threshold (~3.5 MW cm(-2)).

9 drive that they receive, and the density of low-threshold, 4-aminopyridine-sensitive, transient K+ c

10 l horn, activity is dominated by inputs from low threshold A fibers, whereas nociceptive C-fiber inpu

11 reater prevalence of monosynaptic input from low-threshold A-fibers when preceded by early tissue dam

12 Surprisingly, the firing rates of low-threshold Abeta and D-hair mechanoreceptive fibers w

13 t polysynaptic pathways relaying inputs from low-threshold Abeta mechanoreceptors to lamina I output

14 t, whereas lamina III NK1R+ neurons received low-threshold (Abeta fiber) monosynaptic input.

15 Low-threshold activated T-type calcium channels are pres

16 ce, increased voiding frequency and enhanced low threshold afferent nerve activity was observed, sugg

17 Low threshold afferent responses were attenuated in TRPV

18 er cyclic or tonic electrical stimulation of low-threshold afferent pathways in C8 or L2 dorsal roots

19 his primary afferent depolarization (PAD) of low-threshold afferents is mediated by minimally trisyna

20 nced in high-threshold afferents compared to low-threshold afferents.

21 overcome in order to achieve a SPASER with a low threshold, allowing for a continuous wave (cw) opera

22 The confinement leads to polarized, low-threshold amplified spontaneous emission from the po

23 Their ultra-low thresholds and single-mode, single-exciton emission

24 s used to classify individual afferents into low-threshold and high-threshold fibres.

25 This single-mode perovskite laser reaches a low threshold ( approximately 7.6 microJ cm(-2) ) at roo

26 We report a nano-SPASER with a record low threshold at room temperature, optically pumped by u

27 or TRPV1 in the excitability of particularly low threshold bladder afferents.

28 thalamocortical relay cells, production of a low threshold burst upon release from hyperpolarized pot

29 of the tonic current caused the cessation of low-threshold burst firing and promoted tonic firing.

30 ulation of HCN3 function by PIP(2) augmented low-threshold burst firing and spontaneous oscillations;

31 Subicular pyramidal neurons exhibit low-threshold burst firing driven by a spike afterdepola

32 ved that the two major types of CeA neurons, low-threshold bursting (LTB) neurons and regular spiking

33 known about the subcellular localization of low threshold Ca(2)+ channels (T-channels) in the brain.

34 As a result of the presence of a low threshold Ca(2+) channel, spike output functions are

35 Low-threshold Ca(2+) spikes (LTS) are an indispensible s

36 Low-threshold Ca(2+) spikes (LTS) are critical for impor

37 n, because thalamic T-type channels generate low-threshold Ca(2+) spikes that directly correlate with

38 e potential (-50 mV), which suppressed these low-threshold Ca(2+) spikes, induced no plasticity.

39 stsynaptic dendritic Ca(2+) influx evoked by low-threshold Ca(2+) spikes.

40 o depolarization-induced inactivation of the low-threshold Ca2+ current (IT).

41 activation of mitral/tufted cells produced a low-threshold Ca2+ spike (LTS) throughout the granule ce

42 itic current was essential for generation of low-threshold Ca2+ spikes (LTS), and both enflurane and

43 potentials, and inhibits Ca(v)3.2-dependent low-threshold-Ca2+ spikes as well as burst-firing in ret

44 ecordings from DCK/VLO neurons revealed that low threshold calcium currents, Ih currents, and subthre

45 ck burst discharge typically did not produce low threshold calcium spikes or produced a significantly

46 boosted small synaptic inputs and triggered low threshold calcium spikes, while in tonic mode, sodiu

47 eased membrane input resistance, (2) reduced low-threshold calcium burst responses, and (3) weaker ev

48 esults revealed that drugs that suppress the low-threshold calcium current and the hyperpolarization-

49 nt contributor to normal sleep patterns is a low-threshold calcium current mediated by T-type calcium

50 In addition, the low-threshold calcium spike and the sustained endogenous

51 inct firing pattern of Mthal neurons, called low-threshold calcium spike bursts (LTS bursts), is obse

52 onal hyperpolarization and the initiation of low-threshold calcium spike bursts.

53 blockers of calcium channels that eliminated low-threshold calcium spikes (LTS) in ET cells.

54 ency bursts of action potentials mediated by low-threshold calcium spikes due to T-type Ca(2+) channe

55 Here, we recorded T-currents and underlying low-threshold calcium spikes from neurons of nucleus ret

56 re postinhibitory rebound bursts mediated by low-threshold calcium spikes renders the circuit vulnera

57 inotti") cells that had a propensity to fire low-threshold calcium spikes, whereas X94 GFP+ cells wer

58 hich the calyx axons arise); instead somatic low threshold channels consisted of heteromers containin

59 wo base programs, (c) pTP with high- and (d) low-threshold channels deactivated, and (e) MP with high

60 s deactivated, and (e) MP with high- and (f) low-threshold channels deactivated, were created.

61 Low-threshold channels were selected manually and matche

62 The vagus nerve supplies low-threshold chemo- and mechanosensitive afferents to t

63 Here we demonstrate a low-threshold, compact group IV laser that employs a ger

64 e effectiveness of drug combinations used at low threshold concentrations.

65 Low-threshold corneal cold thermoreceptors that express

66 ration of scalable emission wavelength, very low threshold current densities of 29-33 A/cm(2) are ach

67 such as the presence of a photonic band gap, low threshold current density, unconventional angular em

68 re responsible for two-thirds of presynaptic low threshold current, whilst Kv1.1/Kv1.2 heteromers con

69 ry of ultrafast domain wall motions and very low threshold currents in structures designed to stabili

70 rom which orthodromic APs could be evoked at low threshold currents.

71 rolled by an endogenous clock that activates low threshold D2-like receptors in the day, whereas the

72 hyperpolarization enabled the generation of low-threshold depolarizations that occurred in an all-or

73 including opioid agonists and antagonists); low-threshold detoxification and drug cessation programs

74 y to form on the NdAlO3(001) surface, with a low threshold displacement energy and a low formation en

75 32 patients (94%) had a positive OFC with a low threshold dose which provoked severe symptoms.

76 cquisition of cocaine self-administration at low-threshold doses, consistent with increased sensitivi

77 is inhibition results in allodynia, allowing low-threshold drive onto pain and temperature-sensitive

78 l systems for probing nonlinear phenomena at low thresholds due to their small mode volumes and high

79 loping the 'ultimate' nanolaser: a scalable, low-threshold, efficient source of radiation that operat

80 This low-threshold electrochemical stimulation method is appl

81 herent and nonclassical light with extremely low threshold energy.

82 a unique role of these channels in fast and low-threshold exocytosis in an action potential-independ

83 ar mechanism by which these channels control low-threshold exocytosis.

84 ree functional types of afferent fibres: (1) low-threshold fibres (2) wide dynamic range fibres and (

85 to their rapid infiltration into allografts, low threshold for activation, and ability to produce inf

86 shold input power of less than 1 muW, a very low threshold for any laser using colloidal emitters.

87 A low threshold for CT scanning of patients with mild symp

88 e high information storage density and their low threshold for current-driven motion may enable ultra

89 d contacts of patients with tuberculosis and low threshold for empirical treatment of tuberculous men

90 ttle improvement after reaching a relatively low threshold for endovascular repair.

91 idea that the 933W prophage has a relatively low threshold for induction, which may promote Stx2 prod

92 ally limited to embolic stroke, supporting a low threshold for initiating anticoagulation therapy.

93 Healthcare providers should have a low threshold for initiating doxycycline whenever treati

94 r brain metastases, but rather should have a low threshold for MRI of the brain because of the high i

95 ia be checked monthly, and there should be a low threshold for performing a biopsy to evaluate for al

96 and IAC mandates high index of suspicion and low threshold for referral in high volume institutes.

97 conducting quality improvement should have a low threshold for seeking institutional review board gui

98 gs indicate that the erythroid lineage has a low threshold for the induction of p53, providing a basi

99 g for early signs of renal involvement and a low threshold for the use of hydroxyurea as preventative

100 aining medium-term memories for partners and low thresholds for acceptable cooperation (i.e. forgiven

101 ctive specialized accessory structures, have low thresholds for activation, and adapt rapidly to the

102 red late and spontaneously at the expense of low thresholds for activation-induced cell death.

103 me variables; however, it could be useful in low thresholds for treatment.

104 red bandstructure has emerged as a potential low-threshold gain medium, but there has yet to be a suc

105 We leverage the low-threshold gain of these nanocomposite films to produ

106 Optically pumped green lasing with an ultra low threshold has been achieved using an InGaN/GaN based

107 rons to mechanical stimuli are classified as low threshold, high threshold, and wide dynamic range ne

108 near infrared, thus opening the door to very low-threshold, highly unidirectional microcavity diode l

109 The low threshold, in turn, indicates that adoptive T-cell t

110 We measured a low-threshold, inactivating K+ current, i.e. A-current (

111 These findings show that the low threshold inhibitory pathways mediating SICI are nor

112 , NE levels are only high enough to activate low-threshold inhibitory adrenoreceptors.

113 t is likely to be responsible for separating low threshold input from high threshold output neurons o

114 The cells, which receive direct low threshold input, point to a novel location for circu

115 hanges, in particular the novel polysynaptic low-threshold input onto lamina I NK1R+ neurons, may be

116 uron IMI plus a slowly activating transient, low-threshold inward current (ITrans-LTS) that is voltag

117 -time PCR confirmed a coincident increase in low threshold K(+) channel mRNA.

118 lasing threshold of the emitter, providing a low-threshold laser system with small footprint, low pow

119 dots, their advantages as the gain medium in low-threshold lasers have not been clearly demonstrated.

120 Low-threshold lasers realized within compact, high-quali

121 tter interaction in quantum optical devices, low-threshold lasers with minimal power consumption, and

122 from single-molecule biological labelling to low-threshold lasers.

123 h of cesium lead halide nanowires exhibiting low-threshold lasing and high stability.

124 sion or enhancement of spontaneous emission, low-threshold lasing, and quantum information processing

125 hil MMP-9 appears to evoke also a localized, low threshold level vascular endothelial growth factor (

126 This low-threshold (LT) excitatory pathway is normally under

127 al cavity surface emitting micro-lasers with low threshold (<100 pJ, outperforming organic semiconduc

128 (>/=90 ml/min per 1.73 m(2)) to accept and a low threshold (<60 ml/min per 1.73 m(2)) to decline, wit

129 (75%) gastroduodenal convergent neurons had low-threshold (< or =20 mm Hg) responses to GD, whereas

130 Mice showed normal motor activity and low-threshold mechanical and acute noxious heat response

131 cal pain sensitivity, whereas sensitivity to low-threshold mechanical and thermal stimuli was unchang

132 Low-threshold mechanical sensitivity was preserved in be

133 Low-threshold mechanical stimulation of the skin normall

134 cal allodynia, induced by normally innocuous low-threshold mechanical stimulation, represents a cardi

135 n thresholds for temperature, sharpness, and low-threshold mechanical stimuli (von Frey monofilaments

136 the spinal cord circuitry in such a way that low-threshold mechanical stimuli produced pain behavior.

137 cantly higher proportion of nociceptive than low threshold mechanoreceptive (LTM) neurons showed Nav1

138 nical and thermal stimuli, as a nociceptive, low threshold mechanoreceptive (LTM) or unresponsive uni

139 A statistical model of the excitatory low threshold mechanoreceptive fields of spinocervical,

140 (HTM) units), and non-nociceptive (including low-threshold mechanoreceptive (LTM) and cooling units).

141 neurons including nociceptive and cutaneous low-threshold mechanoreceptive (LTM) neurons, 50 had no

142 thought that, after peripheral injury, some low-threshold mechanoreceptive (LTMR) afferents "sprout"

143 sed in the light of similar studies of other low-threshold mechanoreceptive afferent terminals in the

144 , and tyrosine hydroxylase (Th), specific to low-threshold mechanoreceptive C-fibers, which was shown

145 results reveal eleven types: three distinct low-threshold mechanoreceptive neurons, two propriocepti

146 were smaller in amplitude than responses of low threshold mechanoreceptor neurones.

147 spinal cord region implicated in processing low-threshold mechanoreceptor (LTMR) information.

148 elocity brushing stimuli to identify whether low-threshold mechanoreceptor input to these neurons ari

149 te that C-fibres, but not A-fibres, conveyed low-threshold mechanoreceptor inputs to lamina I project

150 sensory neurons (nonpeptidergic and C-fiber low-threshold mechanoreceptor neurons) resistant to dire

151 sponsible for the mechanosensitivity of most low-threshold mechanoreceptor subtypes involved in innoc

152 oorly understood population of unmyelinated, low threshold mechanoreceptors (C-LTMRs).

153 cinergic inhibition and that A- and C-fibers low threshold mechanoreceptors (LTMRs) terminate in lami

154 and are selectively innervated by cutaneous low threshold mechanoreceptors (LTMs).

155 ouble knockout mice the majority of putative low threshold mechanoreceptors did not exhibit ASIC-like

156 Putative low threshold mechanoreceptors exhibited rapidly adaptin

157 n of touch is initiated when fast conducting low-threshold mechanoreceptors (Abeta-LTMRs) generate im

158 VGLUT3-expressing unmyelinated low-threshold mechanoreceptors (C-LTMRs) are proposed to

159 nations of mechanosensory end organs and the low-threshold mechanoreceptors (LTMRs) that innervate th

160 uctures are formed by unique combinations of low-threshold mechanoreceptors (LTMRs), Abeta RA-LTMRs,

161 cted by distinct populations of neurons, the low-threshold mechanoreceptors (LTMRs), which are classi

162 tivation of cutaneous sensory neurons called low-threshold mechanoreceptors (LTMRs).

163 served by specialized sensory neurons termed low-threshold mechanoreceptors (LTMRs).

164 ral terminals of four slowly adapting type I low-threshold mechanoreceptors (SAIs) that innervated th

165 The information coded by the different low-threshold mechanoreceptors are carried by anatomical

166 The rapidly adapting (RA) low-threshold mechanoreceptors respond to movement of th

167 studies show that the mechanosensitivity of low-threshold mechanoreceptors strongly depends on Piezo

168 o the peripheral endings of a broad range of low-threshold mechanoreceptors that innervate both hairy

169 gs, suggesting that these fibers function as low-threshold mechanoreceptors.

170 vo, after classifying them as nociceptive or low-threshold-mechanoreceptors (LTMs) and as having C-,

171 s of thermosensitive, itch sensitive, type C low-threshold mechanosensitive and nociceptive neurons w

172 of touch." Here, we propose that a class of low-threshold mechanosensitive C fibers that innervate t

173 of Ca channels on identified nociceptors and low-threshold mechanosensors (non-nociceptors) isolated

174 pecific subsets of TrkC-expressing cutaneous low-threshold mechanosensory and proprioceptive mechanos

175 t across the skin, begins with activation of low-threshold mechanosensory neurons (LTMRs) that innerv

176 NK1R+ neurons, believed to contribute to the low-threshold mechanosensory pathway.

177 Cav3.1, Cav3.2, and Cav3.3) are activated by low threshold membrane depolarization and contribute gre

178 fibers selectively degenerate compared with low-threshold MNs innervating fatigue resistant slow mus

179 ry afferent nociceptors and more sparsely by low-threshold myelinated afferents.

180 ne-related peptide (CGRP) are upregulated in low-threshold myelinated primary afferents after certain

181 ent involve preservation of the M-current, a low-threshold noninactivating potassium current, during

182 terials are of great interest for studies of low threshold nonlinear phenomena.

183 Elevations in cTnT, even using a low threshold of 0.01 ng/ml, detected during routine cli

184 uce stable lasers emitting at 550 nm, with a low threshold of 6 microJcm(-2).

185 We propose that the relatively low threshold of activation that is required for CD80 in

186 s high-amplitude depolarizing current with a low threshold of activation, high signal amplification g

187 Nevertheless, the low threshold of dilatation (35 degrees C) indicates a p

188 ding C3b and C9, and promote CDC with a very low threshold of MAC binding, thus providing additional

189 ssential for FG development, but that only a low threshold of signaling activity is required for this

190 In addition, these films exhibit low thresholds of 14 +/- 2 muJ cm(-2) for amplified spon

191 a reactive state, toggling between high and low thresholds of activation.

192 e report plasmonic nanolasers with extremely low thresholds on the order of 10 kW cm(-2) at room temp

193 nt years because of the sub-Mott density and low-threshold operation.

194 These gels exhibit fast, reversible, and low-threshold optic switching under applied electric fie

195 Low-threshold or wide-dynamic range neurons in the cunea

196 tic transmission to test whether more direct low-threshold pathways can produce PAD.

197 se-Einstein condensation in the solid-state, low-threshold polariton lasing and is also useful for te

198 n reflex to a treated hand muscle as well as low threshold polysynaptic spinal reflexes involving aff

199 , and TD sensitivity was reduced by block of low threshold potassium channels.

200 In the auditory system, low threshold potassium currents such as those created b

201 ly invested with ion channels containing the low-threshold potassium channel subunit Kv1.1, which pre

202 Low-threshold potassium currents (IKL) predominate in ma

203 Low-threshold potassium currents in deprived NM neurons

204 e.g. coincidence, depolarisation block, and low-threshold potassium currents.

205 o depolarizing current with a Ca2+-dependent low-threshold potential.

206 verall these results demonstrate that PAD of low-threshold primary afferents can occur by more direct

207 Second, a low-threshold, rapidly activating and inactivating Ca2+

208 Kv1.2 alpha-subunits are components of low-threshold, rapidly activating voltage-gated potassiu

209 the familiar regular spiking relay mode and low threshold rebound bursts which characterize these ce

210 ut to phasic cells originated primarily from low threshold receptors, whereas tonic cells demonstrate

211 Thus, a low threshold response adapted for an early temporal ons

212 ts own, Dpp is not sufficient to mediate the low-threshold responses at the end points of the activit

213 the sst2 KO group it appeared to inhibit the low-threshold responses preferentially and failed to aff

214 Of these, 7 (6%) neurons had low-threshold responses to DD (<or=0.2 ml) and 26 (22%)

215 poral expression, which is characteristic of low-threshold responses, but its specification of ventra

216 nels in MPC 9/3L-AH chromaffin cells induced low-threshold secretion that could be prevented by uncou

217 We propose that larvae use low-threshold sensors in the brain to monitor rapid temp

218 re mediated via P2X3 and P2X2/3 receptors on low threshold sensory fibres, while these receptors on h

219 meable AMPA receptors directly contribute to low-threshold sensory afferent drive into the dorsal hor

220 A low threshold should be used to treat suspicion of even

221 uman orofacial system is richly endowed with low-threshold, slowly adapting mechanoreceptors that res

222 rves a dual function in social songbirds: as low-threshold social reinforcement in males and as ultra

223 rmalism to compute the optimal parameters of low-threshold solar-pumped lasers.

224 on-linear optics, communication, sensing and low-threshold solar-pumped lasers.

225 l neuropeptide Y (NPY) interneurons, plateau low threshold spike (PLTS) and NPY-neurogliaform (NGF) c

226 Further, the model produces the low threshold spike behaviour of the relay cell without

227 rrent) PPN cells and depolarized all type I (low threshold spike-LTS current) and type III (A+LTS cur

228 pendent transient (T-type) calcium currents [low-threshold spike (LTS)].

229 ribed NPY-containing, plateau-depolarization low-threshold spike (NPY-PLTS) interneurons.

230 In either cell type, high-frequency low-threshold spike burst or lower-frequency tonic APs u

231 estigations in vitro, these were not typical low-threshold spike bursts.

232 Low-threshold spike interneurons (LTSIs) are important e

233 rly, spikes in fast spiking interneurons and low-threshold spike interneurons failed to elicit detect

234 These recordings reveal that "tonic"' and low-threshold-spike (LTS) "burst" APs in both cell types

235 neurons permits regenerative propagation of low threshold spikes (LTS) accompanied by global dendrit

236 hat they mediate regenerative propagation of low threshold spikes, typical of, but not exclusive to,

237 Ca2+ channels are responsible for generating low-threshold spikes (LTS) that facilitate burst firing

238 nsients evoked by both action potentials and low-threshold spikes are shaped by Ca(2+) uptake by sarc

239 cium channels are responsible for generating low-threshold spikes that facilitate burst firing and ne

240 and an absence of plateau depolarizations or low-threshold spikes.

241 only "detect" Ca(2+) signals associated with low-threshold spikes.

242 recordings and anatomical reconstructions of low threshold spiking (LTS) interneurones from mouse neo

243 n evoked firing: fast spiking, late spiking, low threshold spiking and regular spiking.

244 cally coupled inhibitory interneurons called low-threshold spiking (LTS) cells can fire synchronously

245 photostimulated FS cells, and a minority of low-threshold spiking (LTS) interneurons responded weakl

246 wo major interneuron populations, persistent low-threshold spiking (PLTS) and fast spiking (FS) inter

247 MSNs evoked by activating single persistent low-threshold spiking (PLTS) interneurons in recorded pa

248 dendritic recordings and Ca(2+) imaging from low-threshold spiking cells in rat brain slices with com

249 ite voltage transfer is highly asymmetric in low-threshold spiking cells, and in the somatofugal dire

250 ecific class of inhibitory interneurons, the low-threshold spiking cells.

251 of knowledge of the dendritic properties of low-threshold spiking cells.

252 in LTS generation, because the properties of low-threshold spiking neuron dendrites are unknown, the

253 s are highly conserved between two prominent low-threshold spiking neurons and that these properties

254 rtant consequences for dendritic function in low-threshold spiking neurons.

255 currents in both fast-spiking and persistent low-threshold spiking type GABA interneurons to increase

256 ivity is present in fast-spiking, but not in low-threshold spiking, interneurons of layer V in neocor

257 erneuron subtypes, the fast-spiking (FS) and low threshold-spiking (LTS) cells in layer V of rodent s

258 intrinsic properties, fast-spiking (FS) and low threshold-spiking (LTS) interneuron subpopulations w

259 tsynaptic currents (IPSCs) in the inhibitory low-threshold-spiking (LTS) cell recorded in deprived ba

260 ly coupled neocortical fast-spiking (FS) and low-threshold-spiking (LTS) interneurons and in a conduc

261 the majority (>60%) of fast-spiking (FS) and low-threshold-spiking (LTS) interneurons in all layers o

262 Low-threshold-spiking (LTS) interneurons were instead st

263 sly reported that fast-spiking (FS), but not low-threshold-spiking (LTS), neocortical interneurons fr

264 eurons (fast-spiking interneurons [FSIs] and low-threshold-spiking interneurons [LTSIs]), we apply a

265 spasms and excessive mono- and polysynaptic low threshold spinal reflexes in rats.

266 The analytic approaches yielded low thresholds (standard uptake value ratiolow = 1.21, d

267 i and can signal pain even when activated by low threshold stimulation.

268 non-nociceptive; rapidly and slowly adapting low-threshold stretch receptors).

269 erpolarization-activated cation currents and low threshold T-type calcium currents, and tonic- or ini

270 y -50 mV, consistent with the involvement of low-threshold T-type Ca2+ channels.

271 stent with other spike-wave models increased low-threshold T-type calcium currents within postsynapti

272 , tetrodotoxin-sensitive Na(+)-currents, and low-threshold T-type, isradipine-sensitive L-type, and o

273 eshold targets, while extending the range of low-threshold targets, thus showing opposite effects to

274 The low-threshold, temporally precise, and spatially specifi

275 his developmental change occurred earlier in low-threshold than high-threshold cold thermosensors.

276 infections were present above a predefined (low) threshold, they would be detected with a known unce

277 ng RW settings, HCT uses an unconventionally low threshold; this keeps the missed-feature detection r

278 old TMNs and increases in a subpopulation of low-threshold TMNs.

279 le screen, several mutant lines conferring a low threshold to ECT minimal clonic seizures were mapped

280 ized O2-sensing cells exhibit a particularly low threshold to regulation by O2 supply and function to

281 ehavioral state instability, with apparently low thresholds to transition between states.

282 f an excitatory polysynaptic pathway linking low threshold touch input to pain projection neurons.

283 In the present study, we identify low-threshold transient (T-type) channels as a further s

284 The low-threshold transient calcium current (I(T)) plays a c

285 In 12% of cells (21/182) a low-threshold, transient Kv current (A-current) was pres

286 d self-help remains a viable, slower-acting, low-threshold treatment alternative compared with CBT fo

287 olarization is caused by the activation of a low-threshold TTX-insensitive cationic current that carr

288 Low threshold unmyelinated mechanoafferents (C tactile,

289 e first reconstitution and activation of the low-threshold V23T mutant of MscL in a DIB as a response

290 ively high mobility, high ON/OFF ratios, and low threshold voltage for device activation.

291 ectroluminescent layer are demonstrated with low threshold voltage, narrow bandwidth and high efficie

292 rons, is regulated via dendrotoxin-sensitive low-threshold voltage-activated (LVA) K(+) channels.

293 resence of inwardly rectifying current I(h), low-threshold voltage-activated calcium current I(t), an

294 .1 microM), implicating slow inactivation of low-threshold voltage-activated K+ channels as its mecha

295 Blockage of low-threshold voltage-gated potassium channels selective

296 ronal tone by suppressing a non-inactivating low-threshold voltage-gated potassium current generated

297 aptic release by suppressing the activity of low-threshold voltage-gated T-type (Ca(V)3.2) Ca(2)(+) c

298 have a reduction or complete absence of the low-threshold, voltage-sensitive calcium conductance tha

299 r mobility as high as 6.7 cm(2) V(-1) s(-1), low threshold voltages of<1 V and low subthreshold swing

300 inantly slowly accommodating (SA), firing at low thresholds with little alteration in accommodation r