ライフサイエンスコーパス: opening of

1 The ultrafast photoinduced ring-opening of 1,3-cyclohexadiene constitutes a textbook exa

2 via unprecedented Ph(3)P-I(2) mediated ring-opening of 1,3-dihydro-1H-benzimidazol-2-ones with secon

3 A domain opening of 13-14 degrees was seen compared to the struct

4 which is initiated via isobenzofuranone ring opening of 2 in a Michael-type reaction.

5 appears to proceed through concomitant ring opening of 2-aminobenzothiazole and S-arylation to give

6 of Ti imidos with nitriles and alkynes, ring opening of 2-imino-2H-azirines, or direct metalation of

7 An unexpected ring opening of 3-aminobenzofurans promoted by NaO tBu in hot

8 eration of 2-amidoallyl cations through ring-opening of 4-benzylidene-2-oxazolines with Sc(OTf)3.

9 H(2)(18)O to elucidate the mechanism of ring opening of 7(*+) and trapping of the resulting distonic

10 A rhodium(III)-catalyzed redox-neutral ring-opening of 7-azabenzonorbornadienes with aromatic ketoxi

11 at mediate neurotransmitter release requires opening of a 'closed' conformation of UNC-64/syntaxin.

12 report that the mechanically triggered ring-opening of a [4.2.0]bicyclooctene (BCOE) mechanophore se

13 eceptor (IP(3)R) allosterically triggers the opening of a Ca(2+)-conducting pore located ~100 angstro

14 y filter to enhance calcium permeability and opening of a canonical gate at the cytoplasmic end of th

15 TRPV1 channels in sensory neurons results in opening of a cation permeation pathway that triggers the

16 g-lived loop conformation coincides with the opening of a cryptic pocket that accommodates thyroxine

17 derstanding of other processes involving the opening of a cyclopropane ring.

18 ule dissection methods reveal that catalytic opening of a DHT motif harbouring a toehold triggers suc

19 Oxidative ring-opening of a furan unveils an amine-tethered dicarbonyl,

20 The opening of a fusion pore during exocytosis creates the f

21 n potassium channel and A1 receptor-mediated opening of a G-protein-coupled inwardly rectifying potas

22 intervention, such as queen clipping and the opening of a hive, causes strong interferences with impo

23 id inhibitory modulation of swimming via the opening of a K(+) channel.

24 rmeability transition, as the consequence of opening of a mitochondrial permeability transition pore

25 famous Donora Zinc Works yet record both the opening of a nearby coal-fired power plant and amendment

26 e influenced by closing a port city; (2) the opening of a new port city in western China will attract

27 including the closure of a tourism city, the opening of a new port city in western China, and the inc

28 Therefore, opening of a non-selective cation channel causes cell de

29 ermeable to osmolytes, proposedly due to the opening of a non-selective protein channel of unknown mo

30 Brief exposure to ATP induces the opening of a nonselective cation channel; while repeated

31 The opening of a nonspecific channel, known as the permeabil

32 ansition in human mitochondria refers to the opening of a nonspecific channel, known as the permeabil

33 Ring opening of a P-B-containing cyclobutene isostere provide

34 earrangement at the portal site leads to the opening of a pore in the capsid shell.

35 covered electronic stabilization through the opening of a shell-closing gap at the top of the occupie

36 adical generated from Ti (III) mediated ring opening of a terminal epoxy ring tethered to a butenolid

37 of presynaptically released glutamate to the opening of a transmembrane cation channel.

38 ctive desymmetrization catalysts in the ring opening of a variety of cyclic anhydrides.

39 The opening of a Watson-Crick double helix is required for c

40 Emerging methods for enantioselective ring opening of acceptor- or donor-only cyclopropanes are the

41 izable appendages has been developed by ring-opening of activated aziridines with 2-hydroxyphenyl acr

42 doles via Lewis acid-catalyzed SN2-type ring opening of activated aziridines with indoles having subs

43 cellular membrane requires the simultaneous opening of activation and inactivation gates of the K(+)

44 While most microfluidic systems use the opening of additional parts of the channel to allow the

45 pigots of males never had the wide shaft and opening of adult females.

46 (Br-PBTC), which selectively potentiates the opening of alpha4beta2*, alpha2beta2*, alpha2beta4*, and

47 erivatives of Br-PBTC can potentiate channel opening of alpha5-containing nAChRs.

48 lasticity; pubertal hormones may trigger the opening of an adolescent critical period for experience-

49 osphine oxide diastereomers accessed by ring-opening of an amino alcohol-derived cyclic sulfamidate.

50 probe recognized miR-196b as a result of the opening of an electrode hairpin probe on a polydopmine-g

51 and regio- and stereoselective nucleophilic opening of an epoxide were used as the main transformati

52 lly occupied during a time that predates the opening of an ice-free corridor (<=14,800 cal yr B.P.),

53 oincident with oxidative stress, precipitate opening of an inner mitochondrial membrane, high-conduct

54 annel, conduction is believed to result from opening of an intracellular constriction that prevents i

55 ted by ligand binding that lead to the rapid opening of an intrinsic cation-selective channel.

56 ion in the animal nervous system through the opening of an ion pore upon binding of neurotransmitters

57 Results BBB openings of approximately 1 cm(3) in volume were visuali

58 n as an optical reporter, we showed that the opening of astrocyte CRAC channels stimulated vesicular

59 The reactions involve a regiospecific ring opening of aziridines with benzimidazoles to give benzoi

60 we disclose a bioinspired strain-driven ring opening of bicyclic methyleneaziridines to 2-amidopentad

61 Together, these pathways model the opening of both an inner and outer gate within the CLC-2

62 Opening of both cyclopropane rings in 2'-aryl-1,1'-bicyc

63 catalyzed by Yb(OTf)(3) also results in the opening of both cyclopropane rings.

64 The static dimensions of the pore openings of both materials are too small to admit either

65 resolutions: first, an atroposelective ring opening of Bringmann-type lactones produces a product wi

66 ond messenger NAADP and thereby promotes the opening of Ca(2+) -permeable two-pore channels (TPCs).

67 ation prompted an unprecedented delay in the opening of California's Dungeness crab fishery that inad

68 n the contrary, neurogranin synchronizes the opening of calmodulin's two lobes and promotes their act

69 complexes of CCAN and shows how the Y-shaped opening of CCAN accommodates Cenp-A(Nuc) to enable speci

70 oiling tendrils, spasmoneme springs, and the opening of chiral seedpods.

71 Thus, local opening of chromatin by interactions between pioneer fac

72 e binding of transcription factors and local opening of chromatin.

73 (op/op) mice in which a mutation mimics the "opening" of ClC-2 by GlialCAM.

74 romatin accessibility profiling showed quick opening of closed chromatin in naive T cells within 5 h

75 This study shows that opening of connexin 43 (Cx43) hemichannels leading to th

76 , ROS-induced oxidative stress regulates the opening of connexin channels in a system mediated by pho

77 ) that are required for the CO(2) -dependent opening of Cx26 hemichannels.

78 ctive and challenging gold(I)-catalyzed ring-opening of cyclic 1,3-dioxolanes and dioxanes by trimeth

79 butadiene with ethylene, electrocyclic ring-opening of cyclobutene, electrocyclic ring-closing of Z-

80 and-directed beta-C-H arylation and the ring opening of cyclopropanecarboxamides is proposed based on

81 strated through the catalytic oxidative ring-opening of cyclopropanes for the synthesis of 1,3-fluoro

82 ent of enantioselective methods for the ring opening of cyclopropanes.

83 se is dynamically regulated by the transient opening of different types of voltage-gated calcium chan

84 A nucleophilic retro-Claisen ring-opening of donor-acceptor cyclobutenes, formed with high

85 ient low-cost method for regioselective ring-opening of donor-acceptor cyclopropanes with the Zn-AcOH

86 A straightforward method for ring opening of donor-acceptor cyclopropanes with trimethylsi

87 ow oscillations were delivered at the airway opening of each model and distributed through the lungs

88 In teleost fish, gill slits arise through opening of endodermal pouches and connect the pharynx to

89 each component that permits this sequential opening of Env remains unknown.

90 In addition, ring-opening of epoxide by an intermediate comprising multipl

91 As an example, it is applied to the opening of epoxides by titanocene in THF, a catalytic sy

92 The opening of epoxides typically requires electrophilic act

93 Although derived specifically from the opening of epoxides, the prediction capabilities of the

94 has implications for the question of whether opening of FNIII domains contributes to the stretching o

95 e of time, reactive fluid transport, and the opening of fractures as rock is exhumed and transformed

96 in the synthesis include the oxidative ring opening of furan and its use as a four-carbon synthon, S

97 junctional tensions of VECs to result in the opening of gaps before the initiation of leukocyte trans

98 e-electron laser to trace the ultrafast ring opening of gas-phase thiophenone molecules following ult

99 from the sonolysis of water, making the ring-opening of glucose energetically unfavorable and leaving

100 tropic glutamate receptor signaling triggers opening of GluD2.

101 Opening of HCN channels requires membrane hyperpolarizat

102 le germ cells of mice involves the transient opening of heterochromatin at megabase-size differential

103 structural changes occur in the ATP-induced opening of Hsp70 to allow substrate exchange.

104 acking to engender lateral branching and the opening of hydraulic cracks along the weak layers, even

105 behaviour with slow magnetic relaxation and opening of hysteresis loops was observed.

106 ge sensor activation is not required for the opening of I (Ks) channels.

107 activity of transcription factors allows for opening of inaccessible regulatory elements and has been

108 stores via activation of phospholipase C and opening of inositol trisphosphate (InsP3) receptors.

109 ains that sense membrane voltage and control opening of ion-selective pores, a mechanism that is cruc

110 llations could be initiated by the transient opening of IP(3) receptors facing either the cytosol or

111 ulation cascade (SDAC) strategy involving an opening of isatoic anhydride and annulation to benzimida

112 g of the neurotransmitter acetylcholine into opening of its central pore.

113 ble mechanism by which OprM is activated via opening of its periplasmic aperture through a concerted

114 oduction, [ATP](i) decreases to increase the openings of K(ATP) channels, which biases the electrical

115 Opening of Kv2.1 channels causes membrane hyperpolarizat

116 The opening of Kv3.4 channels effectively reduces growth con

117 ancing and uncertainty about the complete re-opening of laboratories and campuses, there is a pressin

118 structures in endothelial cells promote the opening of large-scale apertures, thereby breaching the

119 ted by entry of extracellular calcium due to opening of mechanosensitive ion channels and initiates a

120 rily through poration sites for fast ICWs or opening of mechanosensitive ion channels for slow ICWs,

121 ransfer catalysis: the enantioselective ring-opening of meso-aziridinium and episulfonium cations pro

122 Conversely, opening of mitochondrial high-conductance and long-lasti

123 ochondrial respiration and in preventing the opening of mitochondrial permeability transition pore in

124 emonstrated by mitochondrial depolarization, opening of mitochondrial transition pore, release of cyt

125 e last part of the review describes the ring opening of more reactive three-membered rings substitute

126 lso demonstrated that metformin inhibits the opening of mPTP and induces mitochondrial biogenesis.

127 ) S confers embryonic cardiac protection via opening of myocardial K(ATP) channels and not via increa

128 The S(N)2-type ring-opening of N-activated aziridines by anilines followed b

129 rk data to develop models for predicting the opening of new shipping lines and for forecasting trade

130 compromised host-symbiont state and (ii) the opening of niche space for potential pathogens during th

131 back-propagating action potential due to the opening of NMDA receptors and voltage dependent calcium

132 nt for maintaining the normal probability of opening of NMDARs and for keeping NMDARs localized in sy

133 orous structure rather than by the proactive opening of one type of its guest-hosting pores.

134 bifunctional enzyme that catalyzes the ring opening of oxepin-CoA and converts it to 3-oxo-5,6-dehyd

135 Caspase-mediated opening of pannexin 1 channels at the plasma membrane fa

136 depletion of the endoplasmic reticulum with opening of plasma membrane calcium channels.

137 from the endoplasmic reticulum, followed by opening of plasma-membrane calcium-release activated cal

138 CR9501, and demonstrate that it enhances the opening of prefusion-stabilized RSV F trimers.

139 sults reveal that the rate constant for ring opening of radical cations derived from 1'-methyl-3',4'-

140 In addition to the ATP-dependent opening of SecY, reported previously, we observe a count

141 vely-charged Glu did not induce constitutive opening of Slo2.1 or Slo2.2, suggesting that ion permeat

142 ds to LL HC hyperpolarization because of the opening of small-conductance Ca(2+)-activated potassium

143 increased micropore volume results from the opening of some of the small (sodalite) cages, otherwise

144 the most at risk, and factors including the openings of some schools, are considered.

145 dily synthesized through a nucleophilic ring opening of spiro[cyclopropane-1,3'-oxindoles] with the a

146 Opening of stomata in plants with crassulacean acid meta

147 sis, short-term exposure to UVA inhibits the opening of stomata, and this requires a reduction in the

148 including the activation of Rubisco and the opening of stomata, whereas transitions from high to low

149 Our results show that facilitating opening of syntaxin enhances exocytosis in a wide range

150 -carbon bond dissociation and the structural opening of the 1,3-cyclohexadiene ring by the direct mea

151 f this process involves a base-mediated ring opening of the 3-aroylbenzofurans and subsequent Michael

152 eds via a Lewis acid catalyzed SN2-type ring-opening of the activated aziridine followed by a concomi

153 cillin-binding protein (PBP)2a, resulting in opening of the active site, whereby the beta-lactam anti

154 pocket as well as the shallow cavity at the opening of the active site.

155 A deaminase activity, likely by facilitating opening of the active site.

156 Opening of the anion permeation path in this iChS is con

157 d to their isolation and divergence; (1) the opening of the Atlantic Ocean, (2) the breakup of Gondwa

158 substep, our simulations show no significant opening of the ATP-bound beta subunit; instead, we obser

159 ons are a result of nucleophilic iodide ring opening of the aziridine to generate an iodoamine as the

160 rmation, (2) C-O bond formation, and (3) the opening of the azlactone ring.

161 M treatment benefits can be achieved through opening of the BBB before intraarterial infusion of beva

162 Opening of the BBB during a stroke has a negative impact

163 nt a model that is based on a time-dependent opening of the BBB for nanoparticles, followed by a rapi

164 Following beta-lactamase-mediated opening of the beta-lactam, the pyrroline may interconve

165 ylimidazolium iodide (1a) catalyzes the ring opening of the bicyclic amidine system of DBU (1,8-diaza

166 Transient opening of the blood-brain barrier following injury prov

167 dicate that, upon lipopolysaccharide-induced opening of the blood-brain barrier, SLE anti-BC abs are

168 Construction of the five Cu(I) sites at the opening of the bundle lags behind the main core, and the

169 Once closed, re-opening of the canal occurred in a wave, triggered by te

170 C exporters that only requires the transient opening of the cavity for release of the peptide.

171 chable following the reversible ring closure/opening of the central dithienylethene via irradiation w

172 o the channel periphery and remotely control opening of the central pore, has eluded such analysis.

173 tion of KCNE1 with KCNQ1 dramatically delays opening of the channel but the mechanisms by which this

174 during depolarization, which are coupled to opening of the channel pore.

175 e eag domain and CNBHD, which stabilizes the opening of the channel.

176 ical displacement of the cytoskeleton to the opening of the channel.

177 Activation of the P2X7 receptor leads to opening of the characteristic dye-permeable membrane por

178 Rate-determining opening of the chelate by an ancillary ligand followed b

179 cific genes correlated with ploidy-dependent opening of the chromatin as well as, in a subset of test

180 thyltransferase SETD1 as a key factor in the opening of the chromatin on inflammatory gene promoters

181 f structural changes which terminate with an opening of the complex into two separate domains, one of

182 driven by Arf1 in live cells and found that opening of the complex is prerequisite for oligomerizati

183 ATP-free complex optimally and to facilitate opening of the complex upon ATP binding.

184 al dynamics involving twisting and clamshell opening of the complex, whereas VCBC-CUL5 maintains a mo

185 Implantation of the XEN45 with opening of the conjunctiva is a safe and efficacious pro

186 lidines and oxazolidines via S(N)2-type ring-opening of the corresponding activated aziridines and ep

187 situ ring-expansion (via intramolecular ring-opening of the corresponding aziridinium intermediates w

188 etween imbibition of the mature dry seed and opening of the cotyledons, the final stage of seedling e

189 our model, the former is responsible for the opening of the critical period, while the latter limits

190 cular blood flow after ischaemia, despite re-opening of the culprit artery.

191 lin-4(1H)-one, followed by nucleophilic ring opening of the cyclopropyl ring to form desired tetrahyd

192 Opening of the cytoplasmic channel to cations in GtCCR2

193 We propose that the opening of the D1-D2 interface, which binds the CCA tail

194 uces a closing of the D1-D3 interface and an opening of the D1-D2 interface.

195 ing Death Receptor 5, involves a scissorlike opening of the disulfide-linked transmembrane (TM) dimer

196 Opening of the DNA binding cleft of cellular RNA polymer

197 active sound control system fitted onto the opening of the domestic window that attenuates the incid

198 n by changing climatic conditions and by the opening of the Drake Passage and associated intensificat

199 to sound at very young ages, even before the opening of the ears.

200 Neutrophil extravasation requires opening of the endothelial barrier but does not necessar

201 The first step of the ring opening of the epoxide is the rate-determining step of t

202 MIDA boronate (24) comprise two steps: ring opening of the epoxide to a carbocation intermediate fol

203 ation can be explained by Lewis acid induced opening of the epoxy bridge with transfer of one alkyl g

204 Situated at the C-terminal opening of the EscN pore is one molecule of EscO, with p

205 nt laryngeal nerve following the progressive opening of the esophageal prosthesis.

206 mational shifts in the barrel domain lead to opening of the exit pore and rearrangement at the latera

207 mulations, providing sufficient evidence for opening of the expansion cohort (n=41), which was recrui

208 taneous nerve got injured during the fascial opening of the extensor compartment.

209 t of the chromophores became more polar with opening of the external gates as the protein transitione

210 The guest diffusion occurs by opening of the flexible window formed by four pyrazines.

211 M) biosynthetic pathway, the Baeyer-Villiger opening of the fourth ring of premithramycin B (PMB), cr

212 f conformational changes in the T3SS trigger opening of the gate through interactions between FlhB/Sc

213 pyruvate dehydrogenase (PDH), which mediates opening of the gateway from glycolysis to the tricarboxy

214 This inflammatory caspase triggers the opening of the GSDMD pore in the plasma membrane, result

215 s wider than all other HAs due to a tilt and opening of the HA1 subunits of the head domain.

216 that the dominant and repetitive mode of DNA opening of the helicase can be used to allow efficient D

217 attern at the site of modification, a slight opening of the hm(5)rC-G pair compared to the unmodified

218 30 seconds of reperfusion immediately after opening of the infarct-related artery and before stent i

219 binding rotates cytoplasmic domains to favor opening of the inner helical gate.

220 e often generated from [1.1.1]propellane via opening of the internal C-C bond through the addition of

221 ment of a noncanonical toggle switch and the opening of the intracellular crevice for G protein coupl

222 domain 5 (TM5), TM6 and TM7, propagating to opening of the intracellular G(i)-binding site.

223 Comparison of MD trajectories show that opening of the intracellular gate causes a structural ch

224 Opening of the intracellular gate involves a hinge-like

225 ivation mechanism, which proceeds through an opening of the intracellular region allosterically elici

226 The selective opening of the isopropylidene group of 2 led to compound

227 ne product was nonfluorescent; however, upon opening of the lactone ring by the formation of the ethy

228 Sec63 causes wide opening of the lateral gate of the Sec61 channel, primin

229 um ylide to metal-free azirinium ylide, ring-opening of the latter to give a 1,5-diazahexa-1,3,5-trie

230 rst opens, followed by DNA binding, inducing opening of the loader to release autoinhibition.

231 plasmic domains that subsequently drives the opening of the luminal gate, and thereclosing of luminal

232 opment of the modern industrial port and the opening of the Malamocco-Marghera channel in the late 19

233 sonication leads to the mechanochemical ring opening of the MeO-gDCC and the subsequent elimination o

234 s induces Ca(2+) overload and ultimately the opening of the mitochondrial permeability transition por

235 leading to mitochondrial Ca(2+) overload and opening of the mitochondrial permeability transition por

236 /apoptosis, associated with the pathological opening of the mitochondrial permeability transition por

237 However, the opening of the mitochondrial permeability transition por

238 re rapid Ca(2+) overload, featuring an early opening of the mitochondrial transition pore.

239 Potential evidence for an 'opening of the mouth' procedure was found in a snake, al

240 stically, HETEs activated the Ca(2+)-induced opening of the mPTP in failing human myocardium, and the

241 ed small-molecule inhibitors of CypD prevent opening of the mPTP in hepatocytes and the resulting eff

242 Opening of the mPTP represents a major therapeutic targe

243 in-protein interactions that begins with the opening of the N-terminal domain of cTnC, followed by cT

244 ins that travel from the larger to the small opening of the nanopore than for those that travel in th

245 Ca(2+) binding instigates opening of the neck through allosteric means whereas ina

246 oincide with the continental breakup and the opening of the North Atlantic Ocean over a period from 6

247 were likely integral to the BPIP during the opening of the North Atlantic.

248 sociated with the no-reflow phenomenon after opening of the occluded vessels in patients with coronar

249 for colorimetric sensing of fluoride by ring-opening of the otherwise photochromic benzo-/naphthopyra

250 sformation between these two phases involves opening of the P(3) ring at the base of the P(4)Se(3) mo

251 On oxidation, the opening of the P-cluster substantially increases the den

252 Membrane binding may be accompanied by opening of the P2 beta-barrel structure and ligand excha

253 in the disassembly of adherens junctions and opening of the paracellular pathways.

254 to maintain low matrix [Ca(2+)] and prevent opening of the permeability transition pore and cell dea

255 The opening of the permeability transition pore, a nonspecif

256 age-sensing domains (VSDs) that regulate the opening of the pore domain and ensuing permeation of sod

257 Unlike other channels, opening of the pore is due to the repositioning of tethe

258 The opening of the proton channel involves association of th

259 yo-electron microscopy structures reveal the opening of the RagB lid and thus provide direct evidence

260 e bonded to the 1' carbon, which resulted in opening of the ribose ring.

261 ese results reconcile competing ideas on the opening of the rift system by highlighting differences i

262 Release from chromatin involves opening of the ring at the Smc3-Scc1 interface in a reac

263 the inability for transport arises from slow opening of the SBP or the selectivity provided by the tr

264 lation enables further modification and ring opening of the single-ring aromatics vanillate and 3-O-m

265 e (ATP) analogs, which is expected to induce opening of the sliding clamp.

266 uridine derivatives by a base-mediated ring-opening of the spirocyclopropanol moiety.

267 The alternate opening of the stem-loop structure of H(1) and H(2)-AuNP

268 three cycloadditions and electrocyclic ring opening of the strained Dewar anthracene.

269 ation of azetidines is achieved without ring opening of the strained saturated heterocycle by conduct

270 Here we show that opening of the Strait involved at least two major episod

271 teasome conformational dynamics and affected opening of the substrate entry pore.

272 to the polymer, as well as in the subsequent opening of the sulfamate ring once it has been installed

273 Opening of the supplementary chamber may be constrained

274 tric current to intestinal cells resulted in opening of the tight junctions in vitro and a consequent

275 used by the CH2-localized mutation is due to opening of the two CH domains.

276 Opening of the two channels in the dimer is cooperative.

277 aled through either of two discrete actions: opening of the vaginal plates to allow copulation, or ex

278 ble vesicles can be extended from the apical opening of the ventral tube.

279 them small enough to extravasate through the openings of the bone's sinusoidal capillaries and thus l

280 Thermal ring openings of the cyclobutenes give (Z,Z)-1,3-diene produc

281 Ca(2+) efflux from mitochondria during brief openings of the mitochondrial permeability transition po

282 Ring opening of these intermediates with tetrabutylammonium h

283 Here we show that opening of these promoters from their closed state in pr

284 Ring opening of these ultraphosphates with [TBA][OH] yields p

285 However, with the opening of this new era of treatment, limitations of the

286 The initial opening of this ocean cavity followed a period of strong

287 PTP (permeability transition pore) and that opening of this pore leads to necroptosis, a regulated f

288 While opening of TMEM16A requires binding of intracellular Ca(

289 The opening of TRPML1 is associated with distinct dilations

290 Opening of TRPV1 has been proposed to involve two gates

291 ein 2, triggering the transient and specific opening of tumor tight junctions allowing for infiltrati

292 The sequential opening of two transport channels within the quasi-one-d

293 The tethering-facilitated DNA 'opening' of undamaged sites and the dynamic nature of 'o

294 rst examples of selective and regiodivergent opening of unsymmetrical phenonium ions with chloride io

295 At inhibitory synapses, stochastic openings of VACCs trigger the majority of spontaneous re

296 ility through inhibition of K(ATP) channels, opening of voltage-dependent calcium channels, increased

297 Several studies have suggested that opening of voltage-gated Ca(2+) channels near resting me

298 action potential (AP) waveform controls the opening of voltage-gated calcium channels and contribute

299 The opening of voltage-gated ion channels is initiated by tr

300 osis in alpha-cells is tightly linked to the opening of voltage-gated P/Q-type Ca(2+) channels, the a