ライフサイエンスコーパス: low-threshold

1 hether all preterm neonates benefit from the low threshold.

2 pecific Genetic Testing Institute-ELISA with low threshold.

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

4 dynamic ranges than channels with relatively low thresholds.

5 tending to approximately 1 mum at strikingly low thresholds.

6 irmed by amplified spontaneous emission with low thresholds.

7 370 nm) SP polariton laser with an extremely low threshold (~3.5 MW cm(-2)).

8 nally, amplified spontaneous emission with a low threshold 4.16 uJ cm(-2) is achieved and distributed

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 findings provide evidence for a key role for low-threshold activated voltage gated L-type Ca(2+) chan

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

18 Low threshold afferent responses were attenuated in TRPV

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

20 Stimulation of low threshold afferents in the trigeminal nerve produced

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

22 Electrical stimulation of low-threshold afferents proximal to the axotomized L5 sp

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

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

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

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

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

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

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

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

31 nary tract tissues, where it is required for low-threshold bladder-stretch sensing and urethral mictu

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

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

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

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

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

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

38 e then confirmed the presumed site of AP and low-threshold Ca(2+) spike initiation in the proximal ap

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

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

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

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

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

44 generating full-height APs and short-latency low-threshold Ca(2+) spikes.

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

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

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

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

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

50 (ii) localized pharmacological inhibition of low-threshold calcium channels, implicated as a genetic

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

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

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

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

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

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

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

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

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

60 he proportion of neurons expressing Kv1.1, a low-threshold channel that facilitates phasic firing.

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

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

63 Low-threshold channels were selected manually and matche

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

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

66 Low-threshold corneal cold thermoreceptors that express

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

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

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 Low-threshold cutaneous afferents evoke a GABA(A)-recept

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

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

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

79 This low-threshold electrochemical stimulation method is appl

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

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

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

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

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

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

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

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

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

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

90 tients still require close observation and a low threshold for intervention to avoid permanent ophtha

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

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

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

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

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

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

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

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

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

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

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

102 hreshold group and in 19% (61 of 329) in the low-threshold group (odds ratio, 1.57; 95% confidence in

103 shold group) or 25,000 per cubic millimeter (low-threshold group).

104 ompared with 53% (177 of 331 infants) in the low-threshold group.

105 % in the high-threshold group and 22% in the low-threshold group; odds ratio, 1.14; 95% CI, 0.78 to 1

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 he QD medium, which allows for demonstrating low-threshold lasing even with an ultrathin (about three

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

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

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

127 (>/=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

128 (75%) gastroduodenal convergent neurons had low-threshold (< or =20 mm Hg) responses to GD, whereas

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

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

131 Low-threshold mechanical forces activate corneal recepto

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 To examine the contribution of Piezo2, a low-threshold mechanically activated channel, to acute o

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

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

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

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

142 kinin 2-Cre (Tac2(Cre)) receive direct Abeta low threshold mechanoreceptor (LTMR) input and form mono

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

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

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

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

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

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

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

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

151 g nociceptive/pruritoceptive afferents and C-low threshold mechanoreceptors.

152 work has demonstrated the necessity of Abeta-low-threshold mechanoreceptors (Abeta-LTMRs) for mechani

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

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

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

156 To test the contribution of low-threshold mechanoreceptors (LTMRs) to nerve-injury-i

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

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

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

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

161 in are detected by sensory neurons, known as low-threshold mechanoreceptors (LTMRs).

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

163 d sound by amplifying signal transduction in low-threshold mechanoreceptors (Scholz et al., 2017).

164 oll-like receptor 5-positive (TLR5(+)) Abeta low-threshold mechanoreceptors and is directly innervate

165 Low-threshold mechanoreceptors are classified as slow-ad

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 ar-spiking units consistent with SA1 and SA2 low-threshold mechanoreceptors, but some units, which we

170 L2 neurons showed that L2 neurons are Adelta-low-threshold mechanoreceptors.

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

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

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

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

175 egulation by CIRL exerts opposing effects on low-threshold mechanosensors and high-threshold nocicept

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

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

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

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

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

181 influence of nociceptive afferent inputs on low-threshold motor units.

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

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

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

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

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

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

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

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

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

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

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

193 conditions should be closely monitored and a low threshold of suspicion for IA should be maintained.

194 exhibit single-mode operation with an ultra-low threshold of ~0.6 muW and a large spontaneous emissi

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

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

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

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

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

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

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

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

203 l cell carcinoma (MCC)-13 cells; piezo2 is a low-threshold, positive pressure-specific, curvature-sen

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

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

206 Neuron models that included a low-threshold potassium current present in a subset of C

207 : sodium current with rapid inactivation and low-threshold potassium current, IKLT.

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

209 e that, in fM1, SAI is evoked by activity in low threshold, presumably cutaneous afferents, whereas L

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

211 e strong synaptic inputs from both high- and low-threshold primary mechanosensory neurons.

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

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

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

215 in sufficient synaptic transmission to evoke low-threshold responses during blockade of GluA2-lacking

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

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

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

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

220 ent nerve fibres, in which it functions as a low-threshold sensor for structurally diverse electrophi

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

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

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

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

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

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

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

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

229 One such interneuron type is the low-threshold, somatostatin (SST)-expressing cell, which

230 cortical GABAergic interneurons include the low-threshold, somatostatin (SST)-expressing cells and t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

255 nce highlights the extensive connectivity of low-threshold spiking interneurons (LTSIs) within local

256 reviously known about the behavioral role of low-threshold spiking interneurons in the striatum.

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

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

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

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

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

262 which are the cholinergic, fast-spiking, and low threshold-spiking subtypes.

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

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

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

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

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

268 ns and increased inhibitory input drive from low-threshold-spiking somatostatin interneurons in adult

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

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

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

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

273 We show that the low threshold T cells were also sensitive to topological

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 , and high current on/off ratio over 10(7) , low threshold value (75 mum), and steep switching proper

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

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

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

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

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

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

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

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

299 ecificity and identified severe reactors and low threshold with high specificity and high sensitivity

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