ライフサイエンスコーパス: glucose sensor

1 , where it functions as the body's principal glucose sensor.

2 se the AMP:ATP ratio, AMPK can also act as a glucose sensor.

3 f a minimally invasive, continuous, reusable glucose sensor.

4 MH may act as a fuel sensor rather than as a glucose sensor.

5 P-dependent protein kinase and a cytoplasmic glucose sensor.

6 d to longer wavelengths for a more practical glucose sensor.

7 new flexible high-performance non-enzymatic glucose sensor.

8 tics of the pancreatic beta-cell glucokinase-glucose sensor.

9 d here to in vitro operation of a continuous glucose sensor.

10 was a key characteristic of the microneedle glucose sensor.

11 ll is designed to function as a battery-less glucose sensor.

12 s highlight its potential as a non-enzymatic glucose sensor.

13 or (OECT) to create a flexible non-enzymatic glucose sensor.

14 which is equivalent to that of a commercial glucose sensor.

15 sugar phosphorylation and acts as a genuine glucose sensor.

16 , suggesting that Hxs1 may not function as a glucose sensor.

17 h opens new directions toward more efficient glucose sensors.

18 ard the realization of long-term implantable glucose sensors.

19 to realize multiplexed DET-type lactate and glucose sensors.

20 e used to examine the functional role of MAN glucose sensors.

21 us include a variety of pumps and pumps with glucose sensors.

22 he polymeric-membrane overcoated implantable glucose sensors.

23 eased 3-fold to approximately 1 mA/cm(2) for glucose sensors.

24 ved for NO donor-modified sol-gel film-based glucose sensors.

25 bind to the C-terminal cytoplasmic domain of glucose sensors.

26 We developed a novel algorithm for OCP-based glucose sensors.

27 hysically with Snf1p and also interacts with glucose sensors.

28 atalysts for use in enzyme-free amperometric glucose sensors.

29 <150-sec 10-90% response time, amperometric glucose sensors.

30 t 20% compared to that of larger fiber-optic glucose sensors.

31 ge owing to the dearth of tissue-transparent glucose sensors.

32 ery methods that integrate insulin pumps and glucose sensors.

33 properties of these materials, as promising glucose sensors.

34 [1 aM-5 mM], surpassing previously reported glucose sensors.

35 mV/decade, outperforming previously reported glucose sensors.

36 ode-enzyme interface of three generations of glucose sensors.

37 inducing endocytosis and degradation of the glucose sensors.

38 the Ycks act upstream or at the level of the glucose sensors.

39 entical dimensions to that of the functional glucose sensors (0.5x0.5x5mm) were coated with the PLGA/

40 t C. albicans senses galactose with its Hgt4 glucose sensor, a capability that is enabled by transcri

41 Thus, signals generated by two different glucose sensors act through Grr1p to determine Rgt1p fun

42 membrane coatings to protect electrochemical glucose sensors against surface biofouling.

43 The MARS glucose sensor also functioned under flow conditions (9

44 ng of a wireless, subcutaneously implantable glucose sensor and a body-worn transmitter is described

45 , comprising an enzymatic glucose fuel cell, glucose sensor and a LED indicator, does not require add

46 human glucokinase (GCK), the body's primary glucose sensor and a major determinant of glucose homeos

47 ADP-dependent glucokinase (ADPGK) as a novel glucose sensor and a potential onco-target in specifical

48 he biosensor seamlessly is integrated with a glucose sensor and a wireless measurement system.

49 1 diabetes rely on an accurate subcutaneous glucose sensor and an infusion cannula that delivers ins

50 e glucose transporter, GLUT2, could act as a glucose sensor and the calcium-sensing receptor, CasR, c

51 ecrease the predictive error of a ConA-based glucose sensor and to give a more accurate demonstration

52 LXRalpha may serve as a glucose sensor and, along with ChREBP, may activate lipo

53 Taste cell-expressed glucose sensors and K(ATP) may serve as mediators of the

54 programmable in vitro diagnostics, including glucose sensors and strain-specific Ebola virus sensors.

55 able dictates the cell surface levels of the glucose sensors and that the regulation of glucose senso

56 by promoting degradation of the cell-surface glucose sensors and thus identify MG as a potential glyc

57 y of glucokinase as the pancreatic beta-cell glucose sensor, and they demonstrate that responsiveness

58 pression; (iii) Yck1 interacts with the Rgt2 glucose sensor; and (iv) attaching the C-terminal cytopl

59 which is the primary component of the islet glucose-sensor apparatus, by an NO-dependent mechanism.

60 he following evidence that suggests that the glucose sensors are coupled to the membrane-associated p

61 The analytical characteristics of the glucose sensors are given and compared to previous appro

62 These results suggest that the glucose sensors are inactivated through ubiquitin-mediat

63 Here we provide evidence that these glucose sensors are primary targets of MG in yeast.

64 provide evidence that cell surface levels of glucose sensors are regulated by ubiquitination and degr

65 The glucose sensors are removed from the plasma membrane thr

66 Because glucose sensors are sterilized and stored in a sealed pa

67 mallest fully integrated planar amperometric glucose sensor area reported to date.

68 nted, user-replaced, miniature, amperometric glucose sensors, assisting in the management of diabetes

69 The saturation of nonenzymatic blood glucose sensors at lower than normal blood glucose level

70 We describe a glucose sensor based on a mutant glucose/galactose bindi

71 we present a highly sensitive and selective glucose sensor based on capacitor circuit that is capabl

72 rod electrode was improved for amperometric glucose sensor based on glucose oxidase (GOx).

73 a real-time, quantitative, and biocompatible glucose sensor based on surface-enhanced Raman scatterin

74 ition and transduction mechanisms in optical glucose sensors based upon Concanavalin A (ConA) has ten

75 This response can be used as a glucose sensor by tracing the released H(2)O(2) after en

76 e glucose sensors and that the regulation of glucose sensors by glucose concentration may enable yeas

77 Here we describe a ratiometric glucose sensor capable of measuring micromolar levels of

78 HEXOKINASE1 (HXK1), a metabolic enzyme and glucose sensor, catalyzes the phosphorylation of hexoses

79 se signaling in which glucose binding to the glucose sensors causes them to activate Yck1 in the cell

80 f anterior pituitary cells might function as glucose sensor cells and that direct fuel regulation of

81 sensor in pancreatic beta-cells and in other glucose sensor cells in the body.

82 upregulation of genes that code for the low-glucose sensor CgSnf3, transcriptional regulators CgMig1

83 The dermal glucose sensor consisted of glucose oxidase, 3,3',5,5'-t

84 The Snf3 and Rgt2 glucose sensors contain unusually long C-terminal tails

85 p with standard insulin therapy and a masked glucose sensor (control) in random order, with a 2-week

86 he thus optimized third-generation OCP-based glucose sensor could be operated continuously for more t

87 r, characterization results for microcapsule glucose sensors demonstrate their suitability for monito

88 PE would pave the way for a better future to glucose sensor development as its fabrication was withou

89 d exceptional performance as a non-enzymatic glucose sensor, displaying a linear range of 0.001-5.50

90 conclude that lumenal glucose is sensed by a glucose sensor, distinct from SGLT1, residing on the ext

91 n, constitutively active, signaling forms of glucose sensors do not undergo endocytosis, whereas sign

92 vivo calibration of intravenously implanted glucose sensors during periods of rapid rise and decline

93 imply a role for enterochromaffin cells as "glucose sensors" during ingestion of a meal.

94 lucose, we fabricated, for the first time, a glucose sensor electrode based on radially oriented NiO

95 cent advances on enzymatic and non-enzymatic glucose sensors evolved in the last four years.

96 The resulting OECT-based non-enzymatic glucose sensor exhibits significantly enhanced sensitivi

97 In addition, this glucose sensor favored a very high selectivity towards g

98 nted in vivo devices, particularly implanted glucose sensors, few studies have attempted to elucidate

99 Gck is known to be the glucose sensor for glucose metabolism in beta cells.

100 and glucagon secretion and that it is a key glucose sensor for hypoglycemic counterregulation.

101 ion of an all-printed temporary tattoo-based glucose sensor for noninvasive glycemic monitoring.

102 racellular glucose levels, appears to be the glucose sensor for the glucose-transport-independent pat

103 silica sol-gel matrix as a potential in vivo glucose sensor for use in patients with diabetes.

104 ucose, suggesting that aldolase may act as a glucose sensor for V-ATPase regulation.

105 ultrasensitive, and reliable electrochemical glucose sensors for the early diagnosis of diabetes.

106 is a critical component of the physiological glucose sensor found in cell types that are responsive t

107 all intestine, and in particular its luminal glucose sensors, from the nutrient stream has been propo

108 firming that G6pc2 opposes the action of the glucose sensor glucokinase by hydrolyzing G6P.

109 tent with increases in the expression of the glucose sensor glucokinase, but decreases in that of two

110 th glucose and lactate, and express both the glucose sensor, glucokinase (GK), and the SUR1 subunit o

111 An oxidase-based glucose sensor has been developed that uses a mercaptosi

112 e mesoporous material modified non-enzymatic glucose sensor has been developed through simple, low co

113 The advancement of flexible, wearable glucose sensors has significantly improved continuous gl

114 Signaling by the conserved glucose sensor HEXOKINASE1 (HXK1) has been shown to exer

115 dvanced enzymes for self-monitoring of blood glucose sensors; however, the achievement of direct elec

116 d-glucose cotransporter hSGLT2 and the human glucose sensor hSGLT3 are also addressed.

117 Despite GLUT1 loss, two-photon glucose sensor imaging reveals that astrocytes maintain

118 The response of enzyme electrode glucose sensors implanted in tissues to physiologic bloo

119 f ventilation, the CB has been proposed as a glucose sensor implicated in the control of energy homeo

120 okinase (GK), allowing its crucial role as a glucose sensor in hepatic and pancreatic cells.

121 transporter 2 (GLUT2) has been proposed as a glucose sensor in pancreatic beta cells.

122 Glucokinase acts as a glucose sensor in pancreatic beta cells.

123 lucose transport protein that is part of the glucose sensor in pancreatic beta-cells and facilitates

124 Glucokinase (GK) serves as glucose sensor in pancreatic beta-cells and in other glu

125 sing but can be accounted for by including a glucose sensor in the array.

126 ot a Na+/glucose cotransporter but instead a glucose sensor in the plasma membrane of cholinergic neu

127 nd on readings of implanted sensors, such as glucose sensors in insulin-dependent diabetic patients.

128 escribe both oxygen-based and peroxide-based glucose sensors in spatially homogeneous medium simulati

129 Our data suggest a role for brain glucose sensors in the regulation of GSIS, particularly

130 onstrated that it is possible to generate a "glucose sensor" in skeletal muscle through coexpression

131 co-transporters (SGLTs) may also function as glucose sensors independent of their roles in transporti

132 The glucose sensor initiates a signalling pathway, involving

133 e detection limit of the new 25 mum diameter glucose sensor is 10.0 muM with a linear range up to 4.0

134 The new glucose sensor is at least 25 times faster and its absol

135 l saliva composed of salts and proteins, the glucose sensor is capable of highly sensitive detection

136 addition, the inhibitory effect of MG on the glucose sensors is greatly enhanced in cells lacking Glo

137 The turnover of the glucose sensors is inhibited in endocytosis defective mu

138 glucose transporter that functions as a high-glucose sensor, is required for conversion of Rgt1p into

139 transporter Snf3p, which appears to be a low-glucose sensor, is required for inhibition of Rgt1p repr

140 ) suggest its potential role as the hepatic "glucose sensor," its impact on the regulation of in vivo

141 ing an embedded photonic crystal, yielding a glucose sensor material with a linear and fast response,

142 the present fructose sensor by an analogous glucose sensor may enable translational development of a

143 dation, suggesting that the stability of the glucose sensors may be associated with their ability to

144 Furthermore, non-enzymatic glucose sensors may pave the way for novel glucometer ma

145 ated by luminal monosaccharides, the luminal glucose sensor mediating this process was unknown.

146 h) durations and remain functional as outer glucose sensor membranes.

147 and PYY secretion by 45%, suggesting another glucose sensor might be involved in modulating peptide s

148 malian cell cultures through the use of FRET glucose sensors; moreover, the protocol can be used for

149 Yck1 fails to restore glucose signaling in a glucose sensor mutant.

150 ammals for the mitochondrial isoform is as a glucose sensor necessary for insulin secretion.

151 A non-enzymatic glucose sensor of multi-walled carbon nanotube-ruthenium

152 iated gene editing of glucokinase (Gck), the glucose sensor of the beta-cells, directly in NSG zygote

153 es cerevisiae deploys two different types of glucose sensors on its cell surface that operate in dist

154 This innovative self-powered glucose sensor opens new doors for implementation of bio

155 lucose sensing mechanisms, evolution of such glucose sensors over time, different versions of wearabl

156 We show, for five sets of glucose sensor pairs, calibrated in vivo by withdrawal o

157 over new analytical concepts of self-powered glucose sensors, paper-based glucose sensing and multipl

158 sts, motivated by the clear tenets of the GK glucose-sensor paradigm, have searched for and have disc

159 The present results show that individual glucose sensors performance of the single-port system is

160 This non-enzymatic glucose sensor presents one of the record electrocatalyt

161 ows analytical characteristics comparable to glucose sensors previously reported using conventional e

162 work documents the development of the first glucose sensor prototype based on glucose binding protei

163 a presented herein also demonstrate that the glucose sensor provides stable SERS spectra for at least

164 long to the same family and are described as glucose sensors rather than glucose transporters.

165 f insulin release and is therefore viewed as glucose sensor; remarkably low activity of lactate dehyd

166 OD 2mg/dL) are covered by the oxygen and the glucose sensor, respectively.

167 Glucose sensor reversibility and reusability is evaluate

168 Indeed, we found that the glucose sensor Rgt2 is phosphorylated on Yck consensus s

169 Of note, the low affinity glucose sensor Rgt2 remains stable only in high glucose

170 The yeast cell-surface glucose sensors Rgt2 and Snf3 function as glucose recept

171 east senses glucose through the cell surface glucose sensors Rgt2 and Snf3, which serve as glucose re

172 w glucose sensor, Snf3p, but not on the high glucose sensor, Rgt2p.

173 Thus the stability of these glucose sensors seems to be critically regulated by intr

174 Under biological conditions, the glucose sensor showed no oxygen dependence with 5 mM glu

175 y, it is unlikely that a hepatic portal vein glucose sensor signaling RYGB-induced increased intestin

176 ing this interaction by knocking out two key glucose sensors significantly changes the cell's growth

177 ose transporter appears to function as a low glucose sensor, since it is required for induction of ex

178 s of the signaling pathway involving the low-glucose sensor Snf1 regulate CCC1 transcription and iron

179 minately regulated by both the high affinity glucose sensor Snf3 and the kinase complex SNF1 via the

180 h glucose grown cells, and the high affinity glucose sensor Snf3 is stable only in cells grown in low

181 share the highest sequence identity with the glucose sensors Snf3 and Rgt2 in S. cerevisiae.

182 ntation defect present in cells lacking both glucose sensors (snf3 rgt2).

183 iae senses glucose through two transmembrane glucose sensors, Snf3 and Rgt2.

184 ed the hydrophilic C-terminal domains of the glucose sensors, Snf3 and Rgt2.

185 nsporter in Saccharomyces cerevisiae, to the glucose sensors Snf3p and Rgt2p has led to the hypothesi

186 ogenic mRNA degradation depends upon the low glucose sensor, Snf3p, but not on the high glucose senso

187 function through a pathway that includes two glucose sensors, Snf3p and Rgt2p, and Grr1p.

188 eractions of imino sugars with a novel human glucose sensor, sodium/glucose cotransporter type 3 (hSG

189 Self-powered glucose sensors (SPGSs) could provide an improvement ove

190 A novel and highly sensitive disposable glucose sensor strip was developed using direct laser en

191 Finally, the SERS glucose sensor successfully partitions glucose even when

192 re fibers provide the demonstrated basis for glucose sensors, supercapacitors, and electrical interco

193 ube sheaths on a rubber core, can be used as glucose sensors, supercapacitors, ultrafast strain senso

194 Conversely, overexpression of a glucose sensor suppresses the signaling defect of a yck

195 The biofuel cell structure-based glucose sensor synergizes the advantages of both the glu

196 esults suggest that LmxGT1 may function as a glucose sensor that allows parasites to enter the statio

197 Glucokinase (GK) is a glucose sensor that couples glucose metabolism to insuli

198 re, we introduce a non-enzymatic metal oxide glucose sensor that functions in neutral fluids by elect

199 Arabidopsis hexokinase1 (HXK1) is a glucose sensor that integrates nutrient and hormone sign

200 ne encoding glucokinase (Gck), the mammalian glucose sensor that is mutated in human maturity onset d

201 ility that Hxk2 constitutes an intracellular glucose sensor that operates by changing its conformatio

202 ive, and biocompatible Ir oxide (IrOx)-based glucose sensor that regenerates solely via IrOx-mediatio

203 yeast Saccharomyces cerevisiae encodes a low glucose sensor that regulates expression of an important

204 nsitivity and increased lifetime compared to glucose sensors that are based on conducting polymer fil

205 Hxt2 glucose transporters converts them into glucose sensors that can generate a signal for glucose-i

206 cose transporter homologs, Snf3 and Rgt2, as glucose sensors that generate a signal for induction of

207 the yeast Saccharomyces cerevisiae serve as glucose sensors that generate an intracellular glucose s

208 ough a signal generated by the Snf3 and Rgt2 glucose sensors that leads to depletion of the transcrip

209 ) sensors, sweat biochemical (pH, uric acid, glucose) sensors, thermal stimulators, and humidity ener

210 enzymatic and non-enzymatic electrochemical glucose sensors, they still suffer from high cost, poor

211 s study was to use a subcutaneous continuous glucose sensor to determine time differences in the dyna

212 synthesis, and in pancreatic beta cells as a glucose sensor to initiate glycolysis and insulin signal

213 Plants use HXK as a glucose sensor to interrelate nutrient, light, and hormo

214 Using the well-known GOx-based amperometric glucose sensor to validate our strategy, we have steepen

215 prime a site on the cytoplasmic tails of the glucose sensors to promote binding of the corepressors.

216 erence, a lung function monitor, and a blood glucose sensor) to receive benefits from 28 functions at

217 s revealed a great potential of the wearable glucose sensor toward the provision of reliable physiolo

218 One pathway requires glucose sensor transcript and the second pathway is inde

219 y had the Ycks functioning downstream of the glucose sensors, transmitting the signal from the sensor

220 nd Std1 bound to the cytoplasmic face of the glucose sensors, triggering their degradation and leadin

221 Current continuous glucose sensors use enzymes with a one-to-two week lifes

222 A premier example is the glucose sensor used by diabetic patients.

223 aptamer, while the amperometric biocatalytic glucose sensor utilizes a second-generation mediator-bas

224 A photoluminescence (PL)-based oxygen and glucose sensor utilizing inorganic or organic light emit

225 The resulting glucose sensor was characterized by a short response tim

226 A stable non-enzymatic glucose sensor was constructed by chemical deposition of

227 An amperometric non-enzymatic glucose sensor was developed based on nitrogen-doped gra

228 study a unique non-enzymatic electrochemical glucose sensor was developed, utilising a gold honeycomb

229 ical conductivity sensor, a pH sensor, and a glucose sensor was fabricated on a flexible polyimide su

230 An enzyme free glucose sensor was prepared by a molecular imprinting me

231 atile workflow, the design of a microfluidic glucose sensor was proposed.

232 To determine the role of the VMH as a glucose sensor, we performed experiments designed to spe

233 cence resonance energy transfer (FRET)-based glucose sensor, we show that a small subset of neurons i

234 ne the role of glucokinase, an important CNS glucose sensor, we studied glucokinase-heterozygous knoc

235 more, using this unique fast-response (~2 s) glucose sensor, we were for the first time able to map t

236 Using optical glucose sensors, we identified a new class of sugar tran

237 re enzyme-based amperometric and coulometric glucose sensors were fabricated and applied to measure t

238 fluorescence resonance energy transfer based glucose sensor, wherein a competitive binding (CB) assay

239 x may represent a component of the beta-cell glucose sensor, which links glycolysis, phospholipid hyd

240 rged as a promising alternative to enzymatic glucose sensors, which dominate current clinical practic

241 In addition, this microneedle glucose sensor with a user-friendly designed home diagno

242 open circuit potential (OCP) principle-based glucose sensor with direct electron transfer FADGDH immo

243 loth, which produces a stable, mediator-free glucose sensor with good selectivity, high-sensitivity (

244 A non-enzymatic electrochemical glucose sensor with high sensitivity and selectivity was

245 FRET glucose sensors with different glucose affinities (K(d))

246 However, the glucose sensors with mutations at their putative ubiquit

247 hypothalamus (VMH) has been proposed to be a glucose sensor within the brain and appears to play a cr

248 exin neurons (HONs) have been proposed to be glucose sensors, yet whether they track glucose concentr