ライフサイエンスコーパス: buffer capacity

1 lowing NaHCO(3)(-) infusion (i.e. changes in buffering capacity).

2 flux, pH is altered in a medium with finite buffer capacity.

3 hat M(2) currents can be limited by external buffer capacity.

4 - 0.97 and 2.24 +/- 0.34 slykes of the total buffer capacity.

5 rient status and variables related to soil K buffer capacity.

6 zation by strain Z6 in media with increasing buffer capacity.

7 ntracellular pH (pH(i) ) and increased pH(i) buffer capacity.

8 gene are weak predictors of the duplicate's buffering capacity.

9 ]SR, not to alterations in SR volume or Ca2+ buffering capacity.

10 governed by the mobile fraction of intrinsic buffering capacity.

11 als, consistent with a decrease in glutamate buffering capacity.

12 chronic hyperglycemia may alter the brain's buffering capacity.

13 and that it increases mitochondrial calcium-buffering capacity.

14 due to blunted endoplasmic reticulum Ca(2+) buffering capacity.

15 o millimolar dithionite did not increase the buffering capacity.

16 y causes an increase in mitochondrial Ca(2+) buffering capacity.

17 otential that related to an improved calcium buffering capacity.

18 of calcium, increasing the lysosomal Ca(2+) buffering capacity.

19 n juxtanuclear ones despite their comparable buffering capacity.

20 portant for matching local energy and Ca(2+) buffering capacity.

21 ow level of atmospheric CO2 and a high ocean buffering capacity.

22 e, limited hydraulic conductivity, and redox buffering capacity.

23 gentler droplet environment, despite its low buffering capacity.

24 a from Wld(S) mice exhibited enhanced Ca(2+) buffering capacity.

25 mitochondria, potentiating a loss of Ca(2+) buffering capacity.

26 roducible LC separation due to an acceptable buffering capacity.

27 xia, resulting in substantial loss of Ca(2+) buffering capacity.

28 thylamine or piperazine groups and potential buffering capacity.

29 ls (CGCs) while varying the extracellular pH buffering capacity.

30 be, including a proposed role of cytoplasmic buffering capacity.

31 ent manner that is correlated with predicted buffering capacity.

32 hosphate precipitation in soils of different buffering capacities.

33 used to obtain estimates of cellular Ca(2+) buffering capacities.

34 ator loading yielded estimates of endogenous buffering capacity (44-80) and peak [Ca(2+)] changes at

35 with a significant decrease in saliva pH and buffering capacity, accompanied by an increase in saliva

36 at the site, and the depletion of Al mineral buffering capacity after approximately 5 years.

37 t to the lung, nor a change in eosinophil pH-buffering capacity, allergen-challenged chimeric mice th

38 The very high buffering capacity allows the Mediterranean Sea waters t

39 t SOD1-mediated loss of mitochondrial Ca(2+) buffering capacity, altered mitochondrial morphology, mo

40 specific set of parameters determines model buffer capacity and buffer function, and individual diff

41 ructure, leading to loss of the interstitial buffer capacity and disproportionate interstitial fluid

42 trongly influenced by the electrolyte pH and buffer capacity and not limited to BDD or formaldehyde,

43 and comprehensiveness: proton (H(+)) efflux, buffer capacity and the contributions of glycolytic (L)

44 carbon dioxide, lowering its alkalinity and buffer capacity and thus leading to sharp declines in pH

45 ondria exhibit reduced mitochondrial calcium buffering capacity and are highly sensitive to mitochond

46 oes not alter cytosolic pH but diminishes pH buffering capacity and causes poor growth at low pH in a

47 Additionally, they have an increased calcium buffering capacity and generate fewer mitochondrial reac

48 n significantly reduced saliva flow rate and buffering capacity and increased mucus acidity.

49 Tris-borate has a high-buffering capacity and is therefore widely used in elect

50 lled chemical weathering, which controls the buffering capacity and mineral content of receiving stre

51 idence that Chop depletion reduces ER Ca(2+) buffering capacity and modulates glucose-induced islet C

52 Proteins differ widely in buffering capacity and pI and therefore the same PTMs ma

53 lusion, our findings propose that the proton buffering capacity and protein loading in PLGA MS can be

54 The buffering capacity and response of 2', 7'-bis(2-carboxye

55 sients because of a higher endogenous Ca(2+)-buffering capacity and significantly higher rates of Ca(

56 ructure with the potential to extend stretch-buffering capacity and support a revised model for the f

57 ished physiological values for intracellular buffering capacity and the permeability ratio of lactic

58 hese regimes, neritic platforms modulate the buffering capacity and the timescales (10(3) to 10(5) ye

59 tablish a close link between nuclear calcium buffering capacity and the transcription of genes that d

60 Measurements of H(+) leak rates, buffer capacities, and estimates of surface areas and vo

61 iation in calcium influx density, endogenous buffer capacity, and calcium extrusion density contribut

62 the micelles mostly maintained their proton buffering capacity, and consequently, prevented or delay

63 ter absorption, nutrient inflow, and luminal buffering capacity, and generates testable predictions o

64 emperature sensitivity of pHi, intracellular buffering capacity, and the activity of sarcolemmal acid

65 inc ions, the thresholds of compromised zinc buffering capacity, and the mechanism of cellular homeos

66 pproximately 15 microM), high cytosolic Ca2+ buffering capacity, and the spatial separation of CRUs h

67 rmined during stimulation from pH and tissue buffer capacity, as well as the oxidative phosphorylatio

68 ntrations, solution conductivity, or anolyte buffer capacity at applied voltages up to 1.1 V, as show

69 ntrations, solution conductivity, or anolyte buffer capacity at applied voltages up to 1.1 V, as show

70 is a commonly used additive, despite its low buffering capacity at pH 7.

71 ) and 2,2,2-trifluoroethylamine (TFEA) offer buffering capacity at physiological pH where AmAc falls

72 malian vertebrates, enrichment of retinal pH buffering capacity attenuates horizontal cell feedback,

73 That is, the conventional buffer capacity-based I(H) estimation must also take int

74 consumption) was used to estimate cytosolic buffer capacity (beta).

75 By assuming accepted values of intracellular buffering capacity (beta(i)), intracellular acidificatio

76 romal compartment are relatively low and the buffering capacity (beta) for protons of the lumen is re

77 We report a dynamic sensing concept for buffer capacity by applying water electrolysis to modula

78 Increasing the cytosolic Ca(2+) buffer capacity by internal perfusion with 1 mM EGTA lim

79 rate, Piermont Marsh is expected to lose its buffering capacity by 2080-2100 but will retain some buf

80 APTA into the red cells increased their Ca2+ buffering capacity by 300-600 mumol (340 g Hb)-1.

81 Moreover, exposure to Fe(II) increased the buffering capacity by 44%, while exposure to millimolar

82 ing CaMBP4 or increasing the nuclear calcium buffering capacity by means of expression of a nuclear t

83 ased sensitivity likely results from reduced buffering capacity by non-DA cells, leading to more PQ(+

84 f RVH rats, and (2) that a blunted ER Ca(2+) buffering capacity contributes to the altered NMDAR-Delt

85 are consistent with the hypothesis that Ca2+ buffering capacity contributes to the control of intrins

86 The authors report marked variation in buffering capacity, correlated with wing size, wing colo

87 of MON and SAL was observed in aerobic, low-buffer capacity culture series as a result of abiotic ac

88 main transformation process in aerobic, high-buffer capacity culture series.

89 plify electrode addressing and to counteract buffering capacity depletion arising from the high elect

90 The cytosolic Ca2+ buffering capacity, determined as the ratio of the expec

91 Drastically increasing the buffer capacity did not stand out as a viable solution f

92 Ryanodine also had little effect on the buffering capacity during 800-1000 ms of the depolarizin

93 that improves exercise performance and blood buffering capacity during strenuous exercise.

94 tly, the evolved strain has no translational buffering capacity, enabling effective translation of ab

95 mps, counter-ion fluxes, membrane potential, buffering capacity, etc.) work together to achieve speci

96 show that external seawater temperature and buffering capacity exert the first-order control on the

97 ewer striatal dopamine terminals and reduced buffering capacity; fluctuations in plasma levodopa conc

98 s also indicated that algae have substantial buffering capacity for free heavy metals in their cytoso

99 ll was dialysed with a solution of increased buffering capacity for protons.

100 nsistent with alkalinization, increasing the buffering capacity from 3 to 24 mm HEPES at pH 7.4 resul

101 tween intermittent contractions and inherent buffering capacity had minimal impact on predicted fatig

102 Acidification of samples at varying buffer capacity has been investigated: the higher the bu

103 Weak carbonate buffering capacity (high Revelle factor, RF) amplifies a

104 tenuation was a function of cytoplasmic Ca2+ buffering capacity; i.e., loading increasing concentrati

105 At applied external voltages >1.1 V, the buffer capacity impacted performance, with current densi

106 At applied external voltages >1.1 V, the buffer capacity impacted performance, with current densi

107 ame modeling approach to examine the marsh's buffering capacity in a changing climate, considering a

108 A decrease in mitochondrial Ca2+ buffering capacity in cells affected by these lysosomal

109 cell patch-clamp dialysis and quantified its buffering capacity in murine hippocampal slices using co

110 m human brain that suggested loss of calcium buffering capacity in neurons correlated with areas of n

111 y potentially underlying a reduced metabolic buffering capacity in nonobese LBW men.

112 ection to achieve balanced diets and provide buffering capacity in the face of variable food quality.

113 The model also predicts that an increase in buffering capacity in the nucleoplasm would cause a peri

114 orce for equalization is a higher Ca(2+)-CaM-buffering capacity in the nucleus compared with the cyto

115 Increasing pH buffering capacity in the pipette solution with 40 mm HE

116 ed, and there was no evidence for reduced pH-buffering capacity in the skeletal muscle.

117 For example, buffering capacity increases to 23% amongst highly expre

118 Thus, we can realize a buffering-capacity independent monitoring of changes in

119 r has proven challenging because of a signal buffering capacity inherent in the functionally relevant

120 Atmospheric multiphase buffering capacity is a crucial physicochemical property

121 ticular, it suggests that the Class 1 Ca(2+) buffering capacity is auto-regulated by the rate at whic

122 l mg(-1) Chl of the total sequestered domain buffering capacity is contributed by lysines with anomol

123 Mitochondria also buffer Ca(2+), and their buffering capacity is dependent on DeltaPsi Here, we cha

124 that increasing neuronal mitochondrial Ca2+-buffering capacity is not beneficial in the R6/2 mouse m

125 However, a reduction in the buffer capacity leads to large deviations from the expec

126 activation, loss of glutamate and potassium buffering capacity, loss of astrocyte coupling, and chan

127 This decreased bicarbonate buffering capacity may contribute to the increased vulne

128 Ca2+ release mechanism, had little effect on buffering capacity measured over the first 200 ms of the

129 gentless pH control, acidity/alkalinity, and buffer capacity measurements in very small samples of bi

130 Together with ion substitution and buffer capacity measurements, we conclude that Cl(-) tra

131 This buffering capacity might explain the observed difference

132 gle biological cells to assess intracellular buffer capacities of different metal ions, such as Ca(II

133 unction at nonphysiological pH (at which the buffer capacity of biological samples is small) makes it

134 extracellular L(-) increased with increasing buffer capacity of extracellular compartment, (iii) the

135 solution at S/Fe = 0.112 is due to the redox buffer capacity of FeS, which is evidenced by the parall

136 reducing electrode, showing the insufficient buffer capacity of PBS to maintain a stable pH at the gi

137 actors controlling absorption are the pH and buffer capacity of the dose solution, the dissolution ra

138 different amounts of urea or by altering the buffer capacity of the system.

139 torage in adipose tissue, although the lipid-buffering capacity of adipocytes versus other cell types

140 characterized by sequestered domains with a buffering capacity of approximately 150 nmol H(+) mg(-1)

141 ermore, under normoxic conditions, glutamate-buffering capacity of astrocytes is increased upon cocul

142 ocean, resulting in increased alkalinity and buffering capacity of atmospheric CO(2).

143 ctic acid from anoxic tissues overwhelms the buffering capacity of blood.

144 ations include evidence that both the Ca(2+) buffering capacity of calsequestrin in solution and that

145 s in this pathway could compromise the redox buffering capacity of cells, which may in turn be relate

146 rmally absorbed by the intrinsic topological buffering capacity of chromatin, helping to avoid spurio

147 Indeed, increasing the buffering capacity of culture medium or frequency of med

148 y, and adjusting the serum concentration and buffering capacity of culture medium.

149 These findings highlight the buffering capacity of developmental systems, allowing ma

150 The buffering capacity of duplicates appears to be independe

151 g/lysis were accounted for by the greater H+ buffering capacity of endosomes containing PEI or PAM ve

152 thway, whose inhibition can enhance the K(+) buffering capacity of glia, which may be useful in disea

153 ng evidence suggests that changes in the ion buffering capacity of glial cells can give rise to neuro

154 However, the water quality and thermal buffering capacity of groundwater depends on the aquifer

155 (+)-H+ antiport, intracellular pH (pHi), and buffering capacity of hepatocytes obtained from rats aft

156 The pHi and the buffering capacity of hepatocytes were not different in

157 ty is important for cell uptake and that the buffering capacity of histidine facilitates endosomal me

158 eir virulence varied depending on the pH and buffering capacity of host tissue.

159 MCU-dependent cytosolic Ca(2+) clearance and buffering capacity of mitochondria reciprocally regulate

160 er, in a physiological situation, the Ca(2+)-buffering capacity of mitochondria was found not to be e

161 parison, diminishment of the endogenous Ca2+ buffering capacity of nerve endings by treatment with th

162 that may play a key role in setting the Ca2+ buffering capacity of Purkinje cells.

163 -producing S. gordonii is dominant while the buffering capacity of saliva is valid ( approximately pH

164 vironment can vary depending on the diet and buffering capacity of saliva, materials testing in const

165 ification in the surface ocean decreases the buffering capacity of seawater for CO2, whilst photosynt

166 f biodiesel wastewater and by increasing the buffering capacity of the anode medium.

167 Here we show that the calcium buffering capacity of the cell nucleus in mouse hippocam

168 f the system on its pH environment (e.g. the buffering capacity of the colon) and the pattern of inco

169 Adding 100 microM fluo-3, which doubles the buffering capacity of the cytoplasm, reduces peak averag

170 Simulation results also suggest that the buffering capacity of the ER, and not restricted diffusi

171 n a more significant optimality in the error-buffering capacity of the genetic code when compared to

172 obal temperature change based on the thermal buffering capacity of the germination phenotype.

173 antitative imaging experiments show that the buffering capacity of the nerve terminal is markedly low

174 in terrestrial biogeochemical cycles, in the buffering capacity of the oceans, and in the containment

175 urthermore, the decrease in C(c) reduces the buffering capacity of the other actin monomer binding pr

176 ion efficiency, presumably by increasing the buffering capacity of the polymer.

177 Alteration in the buffering capacity of the proteostasis network is an eme

178 ve diseases and is associated with decreased buffering capacity of the proteostasis network.

179 weathering has continued to deplete the acid buffering capacity of the terrestrial ecosystem while th

180 e second is an exploitation of the extensive buffering capacity of the turtle's shell and skeleton to

181 The mechanical stability and buffering capacity of this hydrogel can be adjusted by w

182 Furthermore, we show that the buffering capacity of torsinA is greatly diminished by t

183 We propose that the enhanced Ca(2+) buffering capacity of Wld(S+) mitochondria leads to incr

184 n the bacterial cells and facilitated by the buffering capacity of yogurt.

185 Manipulating Hsp90's buffering capacity offers a tool for harnessing cryptic

186 high-capacity immobile Ca(2+) buffer, with a buffer capacity on the order of 1000 and appropriate aff

187 ardium, and the role of extracellular pH and buffer capacity on this relationship.

188 In addition, increased cytosolic pH buffering capacity or elevated [Ca(2+)](i) reduces the r

189 lated to an intermediate polarization, their buffering capacity, or the result of a mixed population

190 The self-buffering capacity phenomenon was found to be a product

191 r sour taste sensitivity and higher salivary buffering capacity reported overall lower sour taste int

192 Together they lead to a poor acid buffering capacity, severe acidification and increased c

193 ere the molecule of interest has significant buffering capacity, such as a >100 uM protein sample.

194 of absolute Ca(2+) concentration and of rod buffering capacity suggest that the slower components of

195 ering or increasing the intracellular Ca(2+) buffering capacity, suggesting that this current was reg

196 alized structures with low endogenous Ca(2+) buffer capacity that allows large and extremely rapid [C

197 to be associated with the intracellular Ca2+ buffering capacity that could regulate the sensitivity t

198 pacity has been investigated: the higher the buffer capacity, the more time (and therefore proton cha

199 of the Earth system-namely, the ocean carbon buffer capacity, the radiative forcing of carbon dioxide

200 d be facilitated by maximizing intracellular buffering capacity through the presence of HCO(3)(-), HC

201 in releasing caged Ca(2+) but also increases buffer capacity to reduce [Ca(2+)](i) rises caused by Ca

202 ency inner hair cells must have a low Ca(2+) buffer capacity to sustain exocytosis, thus making them

203 ribution of the loss of mitochondrial Ca(2+)-buffering capacity to disease mechanism(s) by eliminatin

204 to adjust the SCV tolerance of proteostasis buffering capacity to provide an approach to mitigate sy

205 s of this neurocircuitry maintain sufficient buffering capacity to resist an effect on motivated beha

206 ng a mechanism to spatially match energy and buffering capacity to the demands imposed by transport.

207 In sharp contrast, enrichment of retinal pH-buffering capacity, to attenuate negative feedback from

208 contribution to glutathione-dependent redox-buffering capacity under ex vivo conditions in brain cel

209 The non-Pi, non-CO2 buffer capacity was calculated to be 27.0 +/- 6.2 slykes

210 Cytosolic buffer capacity was quantified for the first time non-in

211 BCs was enhanced when the intraterminal Ca2+ buffer capacity was reduced.

212 calcium, phosphate, acetate, propionate, and buffer capacity were not affected by the different amoun

213 s for climate stresses, soil and groundwater buffering capacities were defined using physical princip

214 en though arterial pH and [HCO(3)(-) ] (i.e. buffering capacity) were effectively altered.

215 Borate ions possess a buffer capacity which may help to protect the tooth stru

216 so due to heterogeneous soil and groundwater buffering capacities which protect against droughts.

217 ed receptor (GPCR) OctBR to upregulate glial buffering capacity, while under pathological K(+) stress

218 The marsh's buffering capacity will remain during extra-tropical sto

219 , it is challenging to predict how long this buffering capacity will remain functional.

220 g capacity by 2080-2100 but will retain some buffering capacity with a high accretion rate of 10 mm/y

221 Increasing retinal buffering capacity with HEPES attenuated the LM-ON surro

222 Enrichment of the extracellular buffering capacity with HEPES selectively attenuates sur

223 Reducing HSP90's buffering capacity with inhibitors or febrile temperatur

224 d were blocked by increasing cellular Ca(2+) buffering capacity with Quin-2.

225 o, the ability to map spatial differences in buffer capacity within a sample during the acid-base tit

226 (approximately 11 mM) of the total intrinsic buffering capacity within the myocyte (the other half be

227 and 9.25 for ammonium, provides very little buffering capacity within the physiological pH range of