ライフサイエンスコーパス: clamp

1 ate (measured by hyperinsulinemic-euglycemic clamps).

2 on emission tomography during an isoglycemic clamp.

3 vivo brain slices, using whole-cell voltage clamp.

4 interactions between the peptide and varphi clamp.

5 f a concurrent hyperinsulinaemic-euglycaemic clamp.

6 ion and inhibition to CbN cells with dynamic clamp.

7 clamp loader actively opens the beta-sliding clamp.

8 membrane currents were monitored using patch clamp.

9 a clamp, a phenylalanine clamp, and a charge clamp.

10 on net ionic currents measured under voltage clamp.

11 hobic pore loops and cleft structures called clamps.

12 lamp technique similar to conventional patch-clamping.

13 ediate cord clamping and 784 to delayed cord clamping.

14 type mice during hyperinsulinemic-euglycemic clamping.

15 at 36 weeks of gestation than immediate cord clamping.

16 OL1-dependent currents with whole-cell patch clamping.

17 e types of polypeptide clamp sites: an alpha clamp, a phenylalanine clamp, and a charge clamp.

18 ipants underwent a hypoglycemic (2.8 mmol/L) clamp after performing a bout of HIIT on a cycle ergomet

19 postprandial hyperglycemic-hyperinsulinemic clamp after SGLT2-I treatment, E-Rd increased by normali

20 Whole-GUV patch-clamping allows ion transport and other voltage-dependen

21 We demonstrated previously that CLAMP also promotes the formation of another domain of c

22 Delayed cord clamping also reduced the prevalence of anemia (hemoglob

23 Here we report the operation of doubly-clamped aluminium nanobeams in superfluid (4)He at tempe

24 NQ1 mutants increase current levels in patch clamp analyses and are associated with reduced pituitary

25 Whole-cell voltage-clamp analyses in HEK293 cells demonstrated that FGF13 i

26 al, and directional excitation seen in patch-clamp analyses may be an artifact resulting from incompl

27 Patch-clamp analysis confirmed the neuron-like electrophysiolo

28 s in the CeA and, moreover, whole-cell patch clamp analysis of the basal amygdala to CeA projections

29 Patch-clamp analysis of tubules isolated from knockout (KO) mi

30 VRAC activity was examined by using patch-clamp analysis.

31 ion was quantified by Ussing chamber voltage clamp analysis.

32 We have used high-speed pressure clamp and elastomeric pillar arrays to apply distinct me

33 cs, cell-specific ablation, whole cell patch-clamp and immuno-electron microscopy, we found that NAc

34 le cells while recording in whole-cell patch-clamp and juxtacellular configuration from CA3 pyramidal

35 Patch-clamp and loose-patch recordings revealed severely affec

36 s were recorded by using 2-electrode voltage clamp and single-channel electrophysiology, whereas radi

37 In vitro intracellular current clamp and voltage clamp recordings were performed in mus

38 we propose two variants of GENESCs based on clamped and hybrid preferential attachment schemes, and

39 f these, 782 were assigned to immediate cord clamping and 784 to delayed cord clamping.

40 ulin secretion both in vivo in hyperglycemic clamps and ex vivo in isolated islets from high-fat diet

41 coupling the azobenzene unit with two chiral clamps and with a further azobenzene switching unit.

42 metry), insulin secretion (2-h hyperglycemic clamp), and body composition (dual-energy X-ray absorpti

43 clamp sites: an alpha clamp, a phenylalanine clamp, and a charge clamp.

44 ls expressed in Xenopus oocytes were voltage-clamped, and distinct LRET signals were obtained in the

45 behavioral analysis, calcium imaging, patch clamping, and pharmacological tools, validated by mathem

46 Sliding clamps are ring-shaped oligomeric proteins that encircle

47 e second stage, clamp loaders place the open clamps around DNA so that the clamps encircle DNA.

48 (ptDNA) by clamp loaders that open and close clamps around ptDNA in an ATP-fueled reaction.

49 a hyperinsulinemic (4x basal) hyperglycemic clamp (arterial blood glucose 146 +/- 2 mg/dL) with port

50 Here, we test this voltage-clamp-artifact hypothesis in recordings from 62 ON-OFF D

51 The results suggest that patch clamp-assisted single neuron lipidomics could be broadly

52 otein serving as the synaptic vesicle fusion clamp at Drosophila synapses.

53 ral hydrophobic contacts and a strong charge clamp at the interface between these partners.

54 was similar to IKs measured with [Ca(2+) ]i clamped at 500-600 nm.

55 ated after a total of three unsuccessful EVD clamping attempts or need for CSF drainage longer than 1

56 was measured with a nine-step hyperglycemic clamp before and 48 h and 14 days after the start of emp

57 Therefore, CLAMP binding to GA repeat motifs promotes the formation

58 n: proliferating cell nuclear antigen (PCNA) clamp binding/opening/closure/release, ptDNA binding/rel

59 Under current clamp, block of BKCa current increased depolarizing memb

60 ymerases do not form a stable complex on one clamp but alternate their binding.

61 and high NaCl concentrations destabilize the clamp, but neither facilitates the formation of an open

62 HLB formation in Drosophila In addition, the CLAMP (chromatin-linked adaptor for male-specific lethal

63 arly in the initiation involving a transient clamp closure as a prerequisite for DNA melting.

64 , mice underwent hyperinsulinemic-euglycemic clamps combined with radiolabeled glucose to assess live

65 tigate the effects of delayed umbilical cord clamping, compared with early clamping, on hemoglobin an

66 itates the formation of an open clamp loader-clamp complex in experiments presented here.

67 ural and mutational analyses of the Hda-beta clamp complex indicate that the interaction of the beta

68 In RIDA, the Hda-sliding clamp complex loaded onto DNA directly interacts with ad

69 In the octameric Hda-beta clamp complex, the inability of Hda to interact with Dna

70 rmined the crystal structure of the Hda-beta clamp complex.

71 However, clamp conditions do not adequately mimic postprandial ph

72 ting, 230 mg/dL, and 340 mg/dL hyperglycemia clamp conditions.

73 is context, Drosha functions as an antiviral clamp, conferring steric hindrance on the RNA-dependent

74 allenges for obtaining the "whole-GUV" patch-clamp configuration were identified and resolved.

75 asurements using the Cut-open Oocyte Voltage Clamp (COVC) technique.

76 se assays in rat brain synaptosomes, voltage-clamp current measurements in cells expressing transport

77 The pi-clamp cysteine arylation reaction enthalpy of activation

78 agger)) is significantly lower than a non-pi-clamp cysteine.

79 METHODS AND Manual patch-clamp data assessing drug effects on expressed cardiac i

80 nAChR receptor number, which supports patch clamp data showing an age-related loss in ACh efficacy i

81 Among preterm infants, delayed cord clamping did not result in a lower incidence of the comb

82 DNA binding channel and constrain the beta' clamp domain, but with an orientation that is different

83 centromeric nucleosome complex where CENP-C clamps down a stable nucleosome conformation and CENP-N

84 nterfaces in the closed conformation and how clamp dynamics contribute to formation of the open confo

85 measured the effects of these conditions on clamp dynamics.

86 conventional label-free methods (e.g., patch clamps, electrochemical cellular biosensors, etc.) or mo

87 Whole-cell patch-clamp electrophysiological recording is a powerful techn

88 expression systems using whole-cell voltage-clamp electrophysiology and immunohistochemistry.

89 Here, we used whole-cell patch clamp electrophysiology and neuronal reconstructions of

90 Using perforated patch clamp electrophysiology and rat cerebral arterial myocyt

91 We used a combination of patch-clamp electrophysiology and real-time PCR in MNCs in sha

92 or these large-scale studies; however, patch-clamp electrophysiology in microscopic animals typically

93 We showed here with patch-clamp electrophysiology that Ang II activates TRPC chann

94 d molecular modeling, mutagenesis, and patch clamp electrophysiology to elucidate the molecular mecha

95 Indeed, using patch clamp electrophysiology we find that cocaine place condi

96 plasma membrane, but using whole-cell patch clamp electrophysiology we observed that nmrASIC3 is ins

97 Using whole-cell patch-clamp electrophysiology, activation of mGlu5 in ex vivo

98 rubidium ((86)Rb(+)) efflux assays and patch-clamp electrophysiology.

99 nts performed or myocytes isolated for patch-clamp electrophysiology.

100 place the open clamps around DNA so that the clamps encircle DNA.

101 To overcome these voltage-clamp errors, we developed an approach to provide new, a

102 soforms consistent with results from voltage-clamp experiments (EC50 values for alpha4beta3delta, alp

103 In both AP-clamp experiments and simulations, IKs recorded during a

104 Patch-clamp experiments clearly showed that the inward Ca(2+)

105 In glucose clamp experiments conducted in healthy dogs, as plasma g

106 Current-clamp experiments demonstrate that serotonergic afferent

107 Patch-clamp experiments indicated that the C-terminally cleave

108 Patch clamp experiments on hypothalamic slices showed that the

109 Calcium imaging and patch-clamp experiments show that G2A activation sensitizes th

110 Voltage clamp experiments showed activation of inward current wh

111 Patch clamp experiments showed mechanical activation of NMDAR

112 AP clamp experiments showed that spike broadening results f

113 In patch-clamp experiments using native cerebral arterial myocyte

114 Astrocyte patch-clamp experiments verified that the glutamate receptors

115 In voltage-clamp experiments, 2-AG reduced A-type potassium current

116 d via whole animal and brainstem slice patch clamp experiments.

117 milar channel properties in whole-cell patch clamp experiments.

118 Voltage clamp fluorometry (VCF) allows simultaneous measurement

119 e model ion channel, gramicidin, and voltage-clamp fluorometry measurements were performed with a vol

120 Voltage-clamp fluorometry showed a loss of a fast component of S

121 Here, we use voltage clamp fluorometry to determine how KCNE1 and KCNE3 affec

122 changes in voltage sensing, we used voltage-clamp fluorometry to track conformational changes of the

123 Combining transition metal ion FRET, patch-clamp fluorometry, and incorporation of a fluorescent no

124 logy, site-directed mutagenesis, and voltage-clamp fluorometry.

125 rocessive DNA synthesis, acting as a sliding clamp for polymerases.

126 ction surface, which was dependent on charge-clamp formation.

127 yed-clamping group and 9.0% in the immediate-clamping group (P=0.03 in unadjusted analyses; P=0.39 af

128 The mortality was 6.4% in the delayed-clamping group and 9.0% in the immediate-clamping group

129 0.04-0.5) g/dL higher than in the early cord clamping group and a relative risk for anemia of 0.91 (9

130 r iron deficiency was reduced in the delayed clamping group in 60 (22.2%) vs 103 (38.1%) patients (re

131 rd (</=10 seconds after delivery) or delayed clamping (>/=60 seconds after delivery).

132 In current clamp, GTx (i) had almost no effect on the first action

133 In current clamp, GTx had multiple effects: (i) increasing excitabi

134 utation analysis, infants undergoing delayed clamping had higher levels of hemoglobin (10.4 vs 10.2 g

135 Delayed umbilical cord clamping has been shown to improve iron stores in infant

136 However, delayed cord clamping has not been shown to prevent iron deficiency o

137 em combined with hyperinsulinemic euglycemic clamp (HEC) was used.

138 ft of RNA polymerase surrounded by the beta' clamp helices, the beta protrusion, and the beta lobe do

139 d DNA in the presence of ligands locking the clamp in distinct conformations.

140 Using dynamic clamp in hippocampal CA1 pyramidal neurons in brain slic

141 use of the heterotrimeric nature of the PCNA clamp in some archaea, there is potential to occupy and

142 escription of the operation of a hydrophobic clamp in triosephosphate isomerase.

143 The preferred timing of umbilical-cord clamping in preterm infants is unclear.

144 cemic (5.0 mmol/L)-hypoglycemic (2.6 mmol/L) clamps in 11 healthy participants, 10 patients with type

145 mp loading, clamp loaders bind and stabilize clamps in an open conformation, and in the second stage,

146 concentration curve during the hyperglycemic clamp increased by 22 +/- 4 and 23 +/- 4% after 48 h and

147 ostatic interactions in stabilizing the beta-clamp interface.

148 Here, we reveal that voltage clamp is completely ineffective for most excitatory syna

149 omplex (holoenzyme lacking the beta2 sliding clamp), is rapidly exchanged during processive DNA repli

150 ine and during a hyperinsulinemic-euglycemic clamp), lipid oxidation (indirect calorimetry), insulin

151 ted hepatocytes, hyperinsulinemic-euglycemic clamps, liver triglyceride content, and liver enzyme exp

152 results support a model in which the E. coli clamp loader actively opens the beta-sliding clamp.

153 ar exchange in live cells containing labeled clamp loader and polymerase.

154 A AAA+ ATPase in the clamp loader clade, RarA protein is part of a highly con

155 ganization reminiscent of the DNA polymerase clamp loader complexes.

156 has been suggested that clamp opening by the clamp loader takes advantage of spontaneous opening-clos

157 omyces cerevisiae replication factor C (RFC) clamp loader, respectively, and assessed the impact on m

158 neither facilitates the formation of an open clamp loader-clamp complex in experiments presented here

159 In the first stage of clamp loading, clamp loaders bind and stabilize clamps in an open confo

160 open conformation, and in the second stage, clamp loaders place the open clamps around DNA so that t

161 e loaded onto primer-template DNA (ptDNA) by clamp loaders that open and close clamps around ptDNA in

162 In the first stage of clamp loading, clamp loaders bind and stabilize clamps i

163 for T > 110 K and larger contributions from clamping losses for T < 110 K.

164 on of incorrect polymerases at the fork, the clamp machinery directs quality control on the lagging s

165 Namely, 5RK acts as a fusion clamp, making release dependent on stimulation by Ca(2+)

166 Downstream signaling determined by patch-clamp measurements showed decreased hypoxia-induced cell

167 ort a previously unreported two-state "catch-clamp" mechanism of Fn binding by CshA, in which the dis

168 cidating the molecular factors that drive pi-clamp-mediated arylation.

169 After patch clamp-mediated dialysis of cytosolic DAF, the remaining

170 with electrical field stimulation, the patch-clamp method and knock-out technology, we determined the

171 measured by the hyperinsulinemic-euglycemic clamp method.

172 properties, we discovered a four-residue pi-clamp motif (Phe-Cys-Pro-Phe) for regio- and chemoselect

173 ine single-cell PCR, whole muscle cell patch clamp, motility phenotyping (Worminator), and dsRNA for

174 Clamps must be loaded onto primer-template DNA (ptDNA) b

175 ions between hydrophobic side chains in a pi-clamp mutant and the perfluoroaryl probe.

176 y 2, subjects underwent stepped hypoglycemic clamps (nadir 60 mg/dL) with evaluation of counterregula

177 NA polymerase processivity factor or sliding clamp) obtained during chemical denaturation.

178 Voltage clamp of outside-out patches from L2/3 neurons revealed

179 puter simulation and in vivo dynamic voltage clamp of spinal motor neurons in septic rats were employ

180 lle-targeted Ca(2+) imaging and direct patch-clamping of apical vacuolar membranes revealed that ML1

181 re 30 weeks of gestation to either immediate clamping of the umbilical cord (</=10 seconds after deli

182 rtic clamp, until the time of release of the clamp on the renal artery in the recipient.

183 umbilical cord clamping, compared with early clamping, on hemoglobin and ferritin levels at 8 and 12

184 It has been suggested that clamp opening by the clamp loader takes advantage of spo

185 he RNAP active site cleft suggests that RNAP clamp opening is required for Nun to establish its inter

186 Here, the mechanism of the initial clamp opening stage is investigated.

187 Whole-endolysosome patch clamping presents new opportunities to identify and char

188 ons and during a hyperinsulinemic-euglycemic clamp procedure (HECP), with and without concomitant ing

189 How clamp proteins slide on DNA has remained a mystery.

190 e activity of DnaA involves the Hda and beta clamp proteins, which act together to dramatically stimu

191 d metadata and responses to a set of voltage-clamp protocols, we assigned 2378 models of voltage- and

192 TEFM to the DNA forms a downstream "sliding clamp," providing high processivity to the EC.

193 Isolated patch-clamped rabbit ventricular myocytes loaded with Fluo-4 t

194 ments were performed using Fluo-3 in voltage clamped rat ventricular myocytes.

195 ns conformation prolyl amide bond for the pi-clamp reactivity.

196 ce prevented the suppression of EGP during a clamp, reaffirming that the site of insulin action to co

197 bitory drive to PV+ INs using targeted patch-clamp recording in spinal cord slices from adult transge

198 Targeted patch-clamp recording is a powerful method for characterizing

199 etion to this activation pathway using patch clamp recording, GFP-PLCdelta1-PH imaging and co-localiz

200 Using a combination of patch clamp recording, immunoblotting, confocal imaging and st

201 , a technique that combines whole-cell patch-clamp recording, immunohistochemistry, and single-cell R

202 ght-field microscopy with simultaneous patch-clamp recording, phase contrast microscopy, and traction

203 Using whole-cell current clamp recording, we found that L2/3 pyramidal neurons in

204 pecific retrograde tracing, whole-cell patch-clamp recordings and post hoc cell type identification,

205 Dual soma-axon patch-clamp recordings combined with axonal Na(+) imaging and

206 Cell-attached patch clamp recordings confirmed that perisomatic Ih was incre

207 Analysis of simultaneous multiple patch-clamp recordings from 6068 pairs of rat neurons with val

208 e demonstrate platform validation with patch-clamp recordings from a variety of cells in the mouse ne

209 Patch clamp recordings from auditory brainstem neurons and in

210 ulb of Held was assessed by whole-cell patch clamp recordings from auditory neurons in mature (2-4 mo

211 ight on these mechanisms, we performed patch-clamp recordings from basal amygdala (BA) neurons in bra

212 We performed patch-clamp recordings from GPe neurons and found that bath ap

213 urrent was measured using whole-cell voltage-clamp recordings from KF and locus coeruleus (LC) neuron

214 his issue, we made two-photon targeted patch-clamp recordings from rat TC and TRN neuron dendrites to

215 Consistently, patch-clamp recordings from retrovirally labeled new granule c

216 nction Fbxl3(Afh) mutation and perform patch-clamp recordings from SCN brain slices across the projec

217 Using whole-cell patch-clamp recordings from spinal motoneurons and interneuron

218 Here, we used dual patch-clamp recordings from turtle vestibular hair cells and t

219 Whole-cell patch-clamp recordings in brain slices revealed that intrinsic

220 ation in vivo and conducted whole-cell patch-clamp recordings in brain slices to reveal how nanomolar

221 , normally show strong depression in voltage-clamp recordings in brain slices.

222 role of gap junctions was confirmed in patch-clamp recordings in bulb slices from wild-type and conne

223 Patch clamp recordings in GCs reveal that movement is accompan

224 ike activity patterns using whole-cell patch-clamp recordings in HEK293 cells (Cav1.2 alpha1-subunit,

225 Using whole-cell patch-clamp recordings in posthearing mice, we show that only

226 METHODS AND Patch-clamp recordings of cultured neonatal rat ventricular my

227 tative PCR (q-PCR), immunostaining and patch clamp recordings of membrane current and voltage, we ide

228 We used whole-cell patch-clamp recordings of over 460 neurons to characterize neu

229 erlie these differences using in vitro patch-clamp recordings of synaptic events and multiscale imagi

230 igh-throughput calcium-flux assays and patch clamp recordings of transiently transfected HEK-293 cell

231 Perforated patch clamp recordings showed that noradrenalin changes the ac

232 We used site-directed mutagenesis and patch-clamp recordings to probe the ion channel extracellular

233 Here the authors use patch clamp recordings to show that selective tuning of granul

234 Whole-cell current- and voltage-clamp recordings were made from isolated guinea pig myoc

235 itro intracellular current clamp and voltage clamp recordings were performed in muscle from a mouse m

236 Whole-cell voltage clamp recordings were then made from CA1 pyramidal cells

237 e nucleus accumbens (NAc) by combining patch-clamp recordings with calcium imaging and optogenetics.

238 We used in vitro whole-cell patch-clamp recordings with laser-scanning photostimulation an

239 ping techniques with in vitro targeted patch-clamp recordings, allowed identifying a new type of STN

240 In current clamp recordings, microinjection of cross-linked 300 kDa

241 Here, we use a combination of paired patch-clamp recordings, serial EM, and large-scale multi-elect

242 Using patch-clamp recordings, this study measures dendritic propagat

243 Lastly, using gramicidin-perforated patch clamp recordings, we found that the GluK2-mediated incre

244 Using confocal microscopy and patch clamp recordings, we investigated the relevance of TMEM1

245 Using whole-cell patch-clamp recordings, we observed a K(+) conductance mediate

246 aration of peripheral nerve slices for patch-clamp recordings.

247 Delayed cord clamping reduces anemia at 8 and 12 months of age in a h

248 We show that motility and patch-clamp responses to levamisole and pyrantel, but not mora

249 apses with artificial synapses using dynamic clamp restored the original rhythmic bursting, thereby a

250 Current-clamp revealed GnRH neurons fired more action potentials

251 stimulated conditions (lower postprandial or clamp RQ).

252 ntaneous opening-closing fluctuations at the clamp's interface, but our time-resolved fluorescence an

253 t diabetes underwent paired hyperinsulinemic clamps separated by 4 weeks.

254 We conclude that these clamping side chains minimize the Gibbs free energy for

255 Under local dendritic voltage clamp, single-spine activation produced large spine head

256 nel that contains three types of polypeptide clamp sites: an alpha clamp, a phenylalanine clamp, and

257 NMR studies, has revealed how the human PCNA clamp slides on DNA.

258 from the one observed in the archaeal beta' clamp-Spt4/5 complex.

259 At 12 months, delayed cord clamping still resulted in a hemoglobin level of 0.3 (95

260 Insulin clamp studies have shown that the suppressive actions of

261 Dynamic clamp studies in cerebellar slices from weanling mice de

262 Hyperinsulinemic-euglycemic clamping studies revealed that ECSHIP2(Delta/+) was resi

263 a Xenopus oocyte two-microelectrode voltage clamp system revealed mutations with only loss-of-functi

264 th electrical field stimulation or the patch-clamp technique in beating cardiac myocytes, we identifi

265 s of these neurons by using whole-cell patch-clamp technique in vitro Our results showed that PNE mar

266 proposed method can be useful in the dynamic clamp technique of the electrophysiological experiments,

267 ethod is a visually controlled, direct patch-clamp technique similar to conventional patch-clamping.

268 udy we have used the cut-open oocyte voltage-clamp technique to investigate the relationship of fast

269 erved cellular architecture and used a patch-clamp technique to study AMPA-receptor (AMPAR)-mediated

270 In live cells, the patch-clamp technique was used to measure whole-cell plasma me

271 sma membrane ion channels, such as the patch-clamp technique, are not readily applicable to intracell

272 lternatively used planar endolysosomal patch-clamp technique, this method is a visually controlled, d

273 terized using the two-microelectrode voltage clamp technique.

274 imaging technique with the traditional patch clamp technique.

275 small to be resolved directly with the patch-clamp technique.

276 The development of endolysosomal patch-clamp techniques has made it possible to investigate dir

277 cell-based assays and two-electrode voltage clamp (TEVC) technique on M2 channels, respectively.

278 those of bacteria to those of man, possess a clamp that can open and close, and it has been assumed t

279 A binding, generating a fluctuating "protean clamp" that stably traps the substrate.

280 neighboring ligand binding domain to tightly clamp the two polypeptides together.

281 through the anthrax channel (and the varphi clamp), the initial permeation represents a critical ste

282 y bypass (r=0.30, P=0.007), and aortic cross-clamp times (r=0.32, P=0.004).

283 tudies were conducted using whole cell patch-clamp to explore biophysical properties of wild-type and

284 he biological PD neuron, measured in voltage clamp, to constrain parameter values of a conductance-ba

285 rm activity, we developed a method, activity clamp, to distinguish the effects of CBZ on individual n

286 mechanisms, we developed a method, activity clamp, to distinguish the response of individual neurons

287 , subjects were exposed to a series of error-clamp trials to measure the temporal characteristics of

288 he donor renal artery interruption or aortic clamp, until the time of release of the clamp on the ren

289 Insulin sensitivity during the hyperglycemic clamp was not affected by empagliflozin in either IFG or

290 Whole-cell patch clamp was used to assess silent synapses.

291 The median time between delivery and cord clamping was 5 seconds and 60 seconds in the respective

292 s. 2.9 +/- 0.3 mg kg(-1) min(-1)) during the clamp were markedly greater in dogs receiving GLC compar

293 Hyperinsulinemic euglycemic clamps were performed to determine whole-body insulin se

294 e surfaces of Hda make contact with the beta clamp, which is essential for Hda function in RIDA.

295 By using the patch-clamp whole-cell technique, we examined the voltage- and

296 By combining activity clamp with computer simulations, the present study provi

297 ex indicate that the interaction of the beta clamp with Hda controls the ability of Hda to interact w

298 studies: liver (1) H-MRS; euglycemic insulin clamp with measurement of glucose turnover; oral glucose

299 escent cells, as well as a 2-step pancreatic clamping with a [U-(13)C]palmitate infusion to determine

300 efore and during hyperinsulinemic-euglycemic clamps with isotope dilution.