ライフサイエンスコーパス: clamp

1 stage hyperinsulinemic euglycemic pancreatic clamp).

2 e and during the hyperinsulinemic-euglycemic clamp.

3 termined using a hyperinsulinemic-euglycemic clamp.

4 onditions with a hyperinsulinemic euglycemic clamp.

5 G-PET/MRI during hyperinsulinemic-euglycemic clamp.

6 ation in human atrial myocytes using dynamic clamp.

7 th through the CMG helicase-Pol epsilon-PCNA clamp.

8 at KGlu effects are not specific to the beta-clamp.

9 uctance via dual whole-cell/perforated patch clamp.

10 diomyocytes under field stimulation or patch clamp.

11 primed DNA, an incoming ddTTP, and the PCNA clamp.

12 WPB exocytosis, indicating that it acts as a clamp.

13 is expected to induce opening of the sliding clamp.

14 s as measured by hyperinsulinemic euglycemic clamps.

15 on the oligomerization properties of sliding clamps.

16 d functional T-type VGCC currents when patch clamped.

17 of ischemic conditioning before and/or after clamping.

18 ally been studied in low throughput by patch clamping.

19 se tolerance test and two-step hyperglycemic clamp (100 and 300 mg/dL) followed by intravenous argini

20 obese groups, received a euglycemic insulin-clamp (40 mU/m(2) . min) and an oral glucose tolerance t

21 vesicle, Synaptotagmin-1 oligomers bind and clamp a limited number of 'central' SNARE complexes via

22 The stability of the Escherichia coli beta-clamp, a homodimer, is particularly remarkable.

23 DNA replication requires the sliding clamp, a ring-shaped protein complex that encircles DNA,

24 s of diverse ABCG2 ligands using the pai-pai clamp along with structural studies created a pharmacoph

25 Results from simulated glucose clamps also agree quantitatively with recent GRI publica

26 Clamps also were performed in ghrelin-KO mice and C57BL/

27 Viable cells suitable for patch-clamp analysis were recovered from transplanted human em

28 By combining whole-cell patch-clamp and 2-photon laser scanning microscopy of basket c

29 ptical glutamate sensors combined with patch-clamp and 3D molecular localization reveal that LTP indu

30 t clear.METHODSA hyperinsulinemic-euglycemic clamp and a 3-hour oral glucose tolerance test were perf

31 Thus, a water-mediated clamp and DNA interface enables the PCNA clamp to "water

32 uring the first postnatal weeks, using patch-clamp and field recordings in mouse brain slices (C57Bl/

33 known about the postrecognition MutS mobile clamp and its interactions with MutL.

34 r antigen (PCNA), a homotrimeric DNA sliding clamp and polymerase processivity factor, is loaded onto

35 We used patch clamp and quantitative polymerase chain reaction to meas

36 ethylnicotine was investigated using voltage-clamp and radioligand binding techniques.

37 ctures reveal that TFEalpha bridges the RNAP clamp and stalk domains to open the DNA binding cleft.

38 Patch clamp and surface biotinylation data show reciprocal dow

39 embled excitable membranes using the dynamic clamp and voltage-gated potassium ionic channels (Kv1.3)

40 urrents were measured using whole-cell patch clamping and a fast perfusion system to assess fast (<2

41 Duplex patch clamping and Angle SICM recordings show that I(Na) and I

42 ive 153 to combined lithotripsyof mechanical clamping and EHL.

43 safety of combined lithotripsy of mechanical clamping and electrohydraulics in fragmentation and remo

44 rs of insulin resistance in vivo (euglycemic clamps and HOMA of insulin resistance), and the presence

45 imultaneous membrane-current (ruptured patch-clamp) and [Ca(2+)](i)-recordings in atrial cardiomyocyt

46 nses in models of both warm ischemia (kidney clamping) and prolonged cold ischemia (syngeneic renal t

47 to prevent un-initiated fusion of vesicles (clamping) and to trigger fusion following Ca(2+)-influx.

48 ical, electrophysiological (whole-cell patch clamp), and behavioral approaches were used to examine t

49 r, L-type Ca(2+) current by whole-cell patch-clamp, and cardiomyocyte shortening and Ca(2+) transient

50 vity from a hyperinsulinemic-euglycemic (EU) clamp, and glucose counterregulatory responses from a su

51 michannels, confirmed by dye transfer, patch clamp, and neurobiotin uptake assays.

52 yzed by a 2-step hyperinsulinemic euglycemic clamp, and postprandial interorgan crosstalk of lipid an

53 Automated patch clamp (APC) instruments enable efficient evaluation of e

54 of mouse heart with a modified tissue freeze-clamp approach.

55 Sliding clamps are oligomeric ring-shaped proteins that increase

56 tive Syt1 oligomers, acting as an exocytosis clamp, are critical for maintaining the balance among th

57 Clamp association is also promoted by glycine betaine, a

58 rement with the plasma glucose concentration clamped at the fasting level; and 3) repeat EGP measurem

59 Secondary outcomes included other clamp-based insulin sensitivity measures, biological med

60 mice undergoing euglycemic-hyperinsulinemic clamps, being highly up-regulated in liver and down-regu

61 res linking allosterically the ATP, DNA, and clamp binding sites: residues distinctive of gamma and o

62 ssociated with the alpha2 C-terminus and the clamp-binding loop.

63 During the EU-HYPO clamp, C-peptide levels were proportionately suppressed

64 gands and antibodies for membrane proteins" (CLAMP), can yield ligands with high potency and specific

65 ore-operated Ca(2+) current I(CRAC) in patch-clamped cells, unlike Ins(1,4,5)P(3) consistent with res

66 nanopores works like a pincer to capture and clamp CO(2) and H(2) O precursors simultaneously, thus l

67 However, a stable hydrophobic clamp composed of residues I127, F310, A311, V380, and I

68 Under glucose clamp conditions (study 2), the change in plasma insulin

69 Under pancreatic clamp conditions (study 3), dapagliflozin produced an in

70 constant intravenous infusion and euglycemic clamp conditions.

71 rties concordant with published manual patch clamp data.

72 For 8 of 9 variants, patch clamping data were consistent with the scores.

73 Insulin sensitivity during hyperglycemic clamp declined by ~30% and ~55% (both P < 0.05), respect

74 Whole-cell patch clamping demonstrates that plumbagin and atovaquone inhi

75 ing morphology was compared against a volume clamp device (CNSystems CNAP 500) (n = 3) resulting in s

76 iversal apparatus and methods with a special clamping device of non-thermal atmospheric plasma (NTAP)

77 iversal apparatus and methods with a special clamping device using gas mixtures are promising for imp

78 mM) in the pipet solution used during patch clamping did not recover NKA activity in the plumbagin o

79 logy including an extra "H" beta-strand and "clamping" disulfide, absent in known IgV-like structures

80 on trimer has three receptor-binding domains clamped down by a segment adjacent to the fusion peptide

81 Suprarenal aortic clamping during abdominal aortic aneurysm (AAA) repair r

82 ction, are severely reduced by the substrate clamping effect.

83 age, Wistar rats underwent suprarenal aortic clamping either alone or in combination with short cycle

84 Here we use patch-clamp electrophysiological recordings from identified MO

85 Patch-clamp electrophysiological studies confirmed that the ob

86 Ex vivo patch clamp electrophysiology and immunohistochemical analysis

87 Patch-clamp electrophysiology experiments show that, when expr

88 Using in vitro patch-clamp electrophysiology in brain slices containing the O

89 We use patch-clamp electrophysiology in combination with mutagenesis

90 Using two-electrode voltage clamp electrophysiology in Xenopus laevis oocytes and ra

91 Patch-clamp electrophysiology revealed an increase in excitabi

92 Whole-cell patch-clamp electrophysiology subsequently revealed that 21a h

93 Patch clamp electrophysiology was used to determine the effect

94 Using whole-cell patch clamp electrophysiology we demonstrate that small LNvs (

95 o transgenic reporter mice, whole-cell patch-clamp electrophysiology, and input-specific optogenetics

96 Using patch-clamp electrophysiology, Ca(2+) imaging, calcitonin gene

97 platform of physiological assays using patch-clamp electrophysiology, calcium imaging, and multielect

98 Using mice, we combined patch clamp electrophysiology, chemogenetics, unsupervised clu

99 examine, using male C57BL6/J mice and patch-clamp electrophysiology, how chronic high-fat high-sugar

100 ng live-cell based techniques, such as patch-clamp electrophysiology, is laborious and time-consuming

101 HEK293T cells and performed whole-cell patch-clamp electrophysiology.

102 ivity, using multielectrode arrays and patch clamp electrophysiology.

103 ssion in CA1 neurons was studied using patch clamp electrophysiology.

104 High-throughput patch clamping enabled reclassification of the majority of tes

105 tivity (MSNA, fibular microneurography) when clamping end-tidal gases at baseline levels.

106 ction methods such as ddPCR, sequencing, and clamped enzymatic amplification.

107 hnical arsenal with an interchangeable patch-clamp/ERG system.

108 Furthermore, whole-cell patch clamp experiments and assessment of membrane potential u

109 Q1 antibodies and performed whole-cell patch clamp experiments as well as single-channel recordings o

110 Single-cell patch-clamp experiments confirmed that the osmotic agents indi

111 Dynamic clamp experiments in rodent cortical neurons confirm tha

112 Furthermore, dynamic-clamp experiments revealed that spike fidelity primarily

113 Dynamic Clamp experiments showed that inner- and outer-zone GCs

114 Dual voltage-clamp experiments substantiate low resistance electrical

115 ts using intact plants, and guard cell patch-clamp experiments were performed.

116 In patch-clamp experiments with outside-out patches, THIK-1 curre

117 combines mathematical modelling with dynamic clamp experiments, suggests the difference is due to the

118 ce energy transfer-based biosensors in patch clamp experiments, we discovered a robust voltage depend

119 In whole-cell patch-clamp experiments, we examined the effects of CLN3 co-ex

120 50) of TETS by ~700-fold in whole-cell patch-clamp experiments.

121 d potassium currents in voltage- and current clamp experiments.

122 s laevis oocytes using two-electrode voltage clamp experiments.

123 d change/induced fit" mechanism in which the clamp first opens, followed by DNA binding, inducing ope

124 Voltage clamp fluorometry revealed that the voltage-sensing doma

125 a combination of electrophysiology, voltage-clamp fluorometry, synthetic BigDyn analogs, and noncano

126 Q1 conductance is demonstrated using voltage-clamp fluorometry.

127 ion channel activity, recorded under voltage clamp, follows KfSLAC1 and KfALMT12 transcript abundance

128 Hepatic vessels were clamped for 1 hour in rats fed a high-fat, high-fructose

129 trap MutS at the mismatch en route to mobile clamp formation and stop movement of the mobile clamp on

130 nking, we find that after the initial mobile clamp formation event, MutS undergoes frequent cycles of

131 on provides the molecular basis for the Syt1 clamping function.

132 Because multiple patch clamp has not been used to study LH connectivity, aside

133 The alpha-clamp-helix interactions exhibit structural plasticity w

134 eripheral (glucose uptake during the insulin clamp), hepatic (basal endogenous glucose production x f

135 llowed by a 60-min +5.5 mmol/L hyperglycemic clamp (HG).

136 monal conditions (studies using a pancreatic clamp), hyperglycemia suppressed EGP by ~50% in both hum

137 on rate/insulin (mg/kg/min) by hyperglycemic clamp in 50 adolescents with T1D (age 16.1 +/- 3.0 years

138 al mapping in atrial preparations, and patch clamping in isolated atrial myocytes.

139 s transported into E-S/E-K compartments are 'clamped' in a sub-compartment created by Scc2's associat

140 olation of atrial myocytes, whole-cell patch clamping, in vitro tachypacing of atrial myocytes, lucig

141 The typical profile of I(SK) during AP clamp included an initial peak (mean 1.6 pA/pF) followed

142 e GIR required by ghrelin-KO mice during the clamps, increased plasma corticosterone and growth hormo

143 In voltage-clamped, intact Casq2-/- cardiomyocytes pretreated with

144 R ligands that mimic key native 'carboxylate clamp' interactions between Hsp90 and its TPR cochaperon

145 issociation equilibrium constant of the beta-clamp is of the order of 10 pM in buffers of moderate io

146 o 425 degrees C) and releasing the substrate clamping is shown to dramatically impact ferroelectric s

147 uppressed Ca(2+) oscillations, and the patch-clamped K(ATP) channel opened more frequently when gluco

148 The UV-vis spectrum of the beta-clamp labeled with tetramethylrhodamine shows the charac

149 a conformation before PCNA opening, with the clamp loader ATPase modules forming an overtwisted spira

150 eds to be opened and installed onto DNA by a clamp loader ATPase of the AAA+ family.

151 cificity, as we illustrate for bacterial DNA clamp loader ATPases.

152 The human clamp loader replication factor C (RFC) and sliding clam

153 rystal structure, suggesting that eukaryotic clamp loaders adopt a similar autoinhibited state early

154 pt a similar autoinhibited state early on in clamp loading.

155 yping, including hyperinsulinemic-euglycemic clamps, magnetic resonance spectroscopy, muscle biopsies

156 We suggest that clamping may be a recurrent feature of cohesin complexes

157 amplifiers, configurable into pseudocurrent-clamp mode (for concurrent current injection and voltage

158 and voltage recording) or into pseudovoltage-clamp mode (for concurrent voltage application and curre

159 We used the array in pseudovoltage-clamp mode to measure the effects of drugs on ion-channe

160 In pseudocurrent-clamp mode, the array intracellularly recorded action po

161 In an experimental murine liver clamping model, we aimed to investigate the efficacy of

162 ation and inactivation in intact loose-patch clamped murine skeletal muscle fibres subject to a doubl

163 pump current, I(p), was measured in voltage-clamped myocytes from noninfarct myocardium.

164 The sliding clamp needs to be opened and installed onto DNA by a cla

165 eparations, site-directed mutagenesis, patch-clamp, nerve recordings and pharmacological inhibition t

166 Using whole-cell voltage clamp of Nav1.6, we show that CaMKII inhibition in ND7/2

167 ohistochemistry, Western blotting, and patch clamping of membrane potentials was performed to evaluat

168 near motif IVa, reminiscent of the "arginine clamp" of RNA helicases.

169 Ca(2+) release sensor and as the inhibitor (clamp) of spontaneous and delayed asynchronous release.

170 currents were recorded in whole-cell voltage-clamped OHCs while electrically stimulating the MOC fibe

171 men underwent a euglycemic-hyperinsulinemic clamp on 2 separate days: one day with prior one-legged

172 mp formation and stop movement of the mobile clamp on DNA.

173 These load ring-shaped sliding clamps onto DNA to keep polymerase attached during repli

174 In voltage-clamp oocyte studies using the ubiquitous amantadine-ins

175 After detachment of NusG and clamp opening, RNA polymerase loses its grip on the RNA:

176 ugh mutagenesis of the PCNA/Pol30 polymerase clamp or deleting specific error-prone polymerases aboli

177 als, membrane ion-currents (perforated patch-clamp), or simultaneous membrane-current (ruptured patch

178 triggered by the Belt and Wedge regions that clamp over the ssRNA.

179 Here we show that the sliding clamp PCNA is important for crossover-biased resolution.

180 Ubiquitylation of the eukaryotic sliding clamp, PCNA, activates a pathway of DNA damage bypass th

181 ucleic Acid (PNA) and Xenonucleic Acid (XNA) clamp PCR, enabling detection of low-frequency (<0.01%)

182 MCR(I) was calculated during the insulin-clamp performed with [3-(3)H]glucose and the OGTT and re

183 Patch-clamp physiology in conditional null mutant hippocampal

184 ust for single cell RNA collected by a patch clamp pipette.

185 ned the effect of dapagliflozin on EGP while clamping plasma glucose, insulin, and glucagon concentra

186 stage hyperinsulinemic-euglycemic pancreatic clamp procedure in conjunction with glucose and palmitat

187 sessed using the hyperinsulinemic-euglycemic clamp procedure in conjunction with glucose tracer infus

188 and a low-dose hyperinsulinemic-hypoglycemic clamp procedure.

189 oader replication factor C (RFC) and sliding clamp proliferating cell nuclear antigen (PCNA) are both

190 PVH neuron responsiveness, achieved through clamping PVH neuron activity at high or low levels, both

191 Using a combination of experimental (patch-clamp recording and Ca(2+) imaging at CA3-CA1 synapses)

192 Finally, ex vivo patch-clamp recording from pairs of neighboring cortical pyram

193 Here we used Patch-seq(8) to combine patch-clamp recording, biocytin staining, and single-cell RNA

194 Using perforated patch-clamp recording, we found that optogenetic stimulation o

195 the electrophysiological technique of patch clamp recording.

196 atory neurons, we performed multi-cell patch clamp recordings and Patch-seq on neurons derived from N

197 Using whole-cell patch-clamp recordings combined with optogenetics in male and

198 Whole-cell patch-clamp recordings demonstrate that loss of SIRT1 decrease

199 Patch clamp recordings demonstrated a reduction of all presyna

200 Patch-clamp recordings from cortical interneurons supported th

201 Our patch-clamp recordings from heterologously expressed GlyRs cha

202 In vitro patch-clamp recordings from L5B pyramidal output neurons showe

203 The first patch-clamp recordings from the dendrites of human neocortical

204 Using ex-vivo patch-clamp recordings from up to 55 SCs per mouse, we found t

205 Patch-clamp recordings in slices and RNAscope showed that oxyt

206 However, in vitro patch-clamp recordings indicate 66% (23 of 35) of OVLT neurons

207 male and female ChAT-EGFP mice, and current-clamp recordings obtained from BFCNs chronically exposed

208 tween rod flash responses and recent voltage-clamp recordings of cone flash responses, using a model

209 test these possibilities, we combined patch-clamp recordings of ependymal cells with immunohistochem

210 Here, using patch-clamp recordings of HEK293 cells heterologously co-expre

211 We performed whole-cell patch-clamp recordings of medium spiny neurons (MSNs) in the N

212 Whole-cell patch-clamp recordings of neurons from male mouse ovBNST in vi

213 behavioural hyperalgesia phenotype, voltage-clamp recordings of small and medium dorsal root ganglio

214 Whole-cell patch-clamp recordings of striatal spiny projection neurons an

215 Additionally, we describe the first patch clamp recordings of VENs from neurosurgically-resected t

216 Patch-clamp recordings of ventral CA1 pyramidal cells 24 h aft

217 Whole-cell patch-clamp recordings reveal that detection inside the RF inc

218 Ex vivo patch-clamp recordings revealed that EGC subthreshold responsi

219 Finally, voltage-clamp recordings showed that FMRP modulated I(h) by regu

220 Patch-clamp recordings showed that riluzole suppressed spontan

221 Here, we used voltage-clamp recordings to evaluate the effects of lacosamide o

222 First, we used whole-cell patch-clamp recordings to measure the physiological changes in

223 We use dendrite-soma dual patch-clamp recordings to show that the strong effect of membr

224 Whole-cell patch-clamp recordings were obtained from Purkinje cells in ce

225 In current-clamp recordings, inhibition of T-type calcium channels

226 Using patch clamp recordings, we found that co-expression of Phactr1

227 By paired patch-clamp recordings, we further demonstrate that acutely in

228 In whole-cell patch clamp recordings, we observed larger macroscopic anion c

229 g rabies tracing, calcium imaging, and patch-clamp recordings, we show that corticofugal neurons proj

230 eep-layer PL-PFC neurons analyzed by current-clamp recordings.

231 esthetic TREK-1 currents in whole-cell patch-clamp recordings.

232 uent cycles of mismatch rebinding and mobile clamp reformation without releasing DNA.

233 This clamping requires monoubiquitination of only the FANCD2

234 ponses from a subsequent hypoglycemic (HYPO) clamp.RESULTSLow and intermediate MMTT C-peptide groups

235 The hyperinsulinemic euglycemic clamp revealed that VDR activation greatly increased the

236 at low cost, to reconfigure a typical patch-clamp rig for ERG recordings.

237 economically configuring a traditional patch-clamp rig for performing high signal-to-noise ex vivo ER

238 w to configure an ERG system without a patch-clamp rig.

239 g existing light pathways in a typical patch-clamp rig.

240 Two-electrode voltage clamp showed dose-dependent block of the AQP1 ion curren

241 es key features of I(SK) recording during AP clamp showing that intrinsic rectification limits I(SK)

242 termined using a hyperinsulinemic-euglycemic clamp (SIClamp, insulin rate:120 mU/m2/min).

243 neurotransmitter release but also serves to clamp spontaneous release.

244 or several practices, including delayed cord clamping, stabilisation with intubation, early enteral f

245 , 3.21 to 10.84) in the surgery group during clamp stage 1, and by 5.39 (95% CI, 2.44 to 8.34) and 5.

246 nute in the two groups, respectively, during clamp stage 2; there were no significant differences bet

247 (disposition) index declined by 60% (second clamp step) and by 62% following arginine (both P < 0.00

248 0 min) and second (90-160 min) hyperglycemic clamp steps increased by 3.8-fold and 1.9-fold, respecti

249 y, during the first and second hyperglycemic clamp steps.

250 Optogenetic studies in vivo and dynamic clamp studies in slice indicated that such brief PC supp

251 Hyperinsulinemic-euglycemic clamp studies show that BAM15 improves insulin sensitivi

252 th the Saccharomyces cerevisiae PCNA sliding clamp, suggesting that KGlu effects are not specific to

253 male rats, we employed the action potential-clamp technique to determine the underlying ionic mechan

254 Intriguingly, by patch-clamp technique, we detected significant NO(3) (-) condu

255 ants on SK2 channel function using the patch-clamp technique.

256 were combined with action potential voltage clamp techniques in a physiologically relevant heart fai

257 Two-electrode voltage clamp (TEVC) of transfected Xenopus oocytes revealed tha

258 ed DNA structures, and becomes a sliding DNA clamp that can coordinate the subsequent repair reaction

259 er, our work suggests that FANCD2-FANCI is a clamp that is locked onto DNA by ubiquitin, with distinc

260 o a hydrolysis-independent, diffusive mobile clamp that no longer recognizes the mismatch.

261 30 minutes of warm in situ ischemia by cross-clamping the renal arteries.

262 IIR was established by clamping the superior mesenteric artery (SMA) for 45 min

263 d that this symmetrical pai-pai interaction "clamps" the ligand into the binding pocket.

264 During the clamp, the groups exhibited similar suppression rates of

265 ted clamp and DNA interface enables the PCNA clamp to "waterskate" along the duplex with minimum drag

266 e-directed mutagenesis and single-cell patch-clamp to analyze the functional effect of the four still

267 We made use of a DNA origami-based force clamp to follow the assembly of human initiation complex

268 hus, ATP hydrolysis licenses the MutS mobile clamp to rebind the mismatch.

269 sing untagged NBCe1-A, injected with bCA and clamped to -40 mV, CO(2) / HCO3- exposures markedly decr

270 End-tidal PCO2 and PO2 were effectively clamped to resting values within each condition.

271 dividual frog hair bundles with displacement clamping to control hair bundle motion and measure force

272 of protein biochemistry and whole-cell patch clamping to determine effects of diet manipulation on gl

273 We used high-throughput automated patch clamping to study the function of the 83 variants, with

274 This SCGT could replace patch clamps to study single cell activity via direct measurem

275 hanism has been well-characterized, how Syt1 clamps transmitter release remains enigmatic.

276 Activation occurs through a clamp-twisting mechanism, in which Dip1 forces two core

277 ) for 1 hour by incremental hyperinsulinemic clamps using baseline and 24 hour samples.

278 lative diffusion coefficients of two sliding clamps using fluorescence correlation spectroscopy.

279 e 'peripheral' SNAREpins to produce a stably clamped vesicle.

280 MCR(I) during the insulin clamp was reduced in obese versus nonobese NGT (0.60 +/-

281 The MCR(I) during the insulin clamp was strongly and inversely correlated with IR (r =

282 oot ganglion (DRG), and the whole cell patch clamp was used to examine the amplitude of P2X currents

283 Patch clamp was used to measure I(Na).

284 Physiological self AP-clamp was used to measure I(NaL) and I(Kr) during the AP

285 Delayed cord clamping was done for most neonates (1493 [91.8%] of 162

286 Using whole-cell voltage clamp, we discovered that enhancing S-palmitoylation wit

287 id's effect on I (Ks) Using whole-cell patch clamp, we show that mefenamic acid enhances I (Ks) activ

288 oral glucose tolerance tests and euglycemic clamps were performed, and histochemical analysis and ge

289 ctors present in the wild-type HLB including CLAMP, which normally binds to GAGA repeats in the H3-H4

290 o a deep amphipathic cleft, called the alpha clamp, which resides at the interface of two PA monomers

291 A hyperinsulinemic-euglycemic clamp with femoral arteriovenous balance and glucose tra

292 steatotic male participants to a pancreatic clamp with somatostatin and evaluated hepatic glucose an

293 20 mU/m(2)/min) hyperinsulinemic-euglycemic clamp with stable isotopes, in 6-week postpartum women w

294 r injection, the hepatoduodenal ligament was clamped with a vessel clip, and released 5 min later.

295 ced Ca(2+) entry when membrane potential was clamped with depolarization, the effect of TSPAN-7 on Ca

296 besity underwent hyperinsulinemic-euglycemic clamping with concomitant adipose tissue (AT) microdialy

297 ion on sensory hair cells, we combined patch clamping with fiber labeling in semi-intact cochlear pre

298 order involving 2-h euglycemic-hyperglycemic clamps with coadministration of: 1) SU (glimepiride 1 mg

299 e center of the 3-nm interior channel of the clamp without directly contacting the protein.

300 ate in WPB formation, only exocyst serves to clamp WPB release.