ライフサイエンスコーパス: glucose sensor

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

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

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

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

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

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

7 sugar phosphorylation and acts as a genuine glucose sensor.

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

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

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

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

12 he polymeric-membrane overcoated implantable glucose sensors.

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

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

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

16 hysically with Snf1p and also interacts with glucose sensors.

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

18 <150-sec 10-90% response time, amperometric glucose sensors.

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

20 inducing endocytosis and degradation of the glucose sensors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

47 The glucose sensors are removed from the plasma membrane thr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 The glucose sensor initiates a signalling pathway, involving

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

125 Glucose sensor reversibility and reusability is evaluate

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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