ライフサイエンスコーパス: phosphate

1 y promiscuous phosphatases from d-ribulose 5-phosphate.

2 and the adsorption behavior of ammonium and phosphate.

3 ubstrate and TLR4 ligand, lipopolysaccharide-phosphate.

4 with the nonbridging oxygen of the scissile phosphate.

5 d a smaller amount of phosphatidylinositol-4-phosphate.

6 nd the enzyme cofactors NAD(+) and inorganic phosphate.

7 n, d-glycerol 3-phosphate and d-erythritol 4-phosphate.

8 n minimal medium supplemented with glucose-6-phosphate.

9 acceptor, releasing phosphate from glucose 1-phosphate.

10 lting alkenylnickel species onto the allylic phosphate.

11 onic allosteric activators such as inorganic phosphate.

12 isubstituted glycine aryl esters and allylic phosphates.

13 l injury via modulation of the sphingosine-1-phosphate 1 receptor (S1PR1).

14 Met oxidation studies (pH 7, D2O, 0.01 M phosphate, 25 degrees C) monitored by (1)H NMR spectrosc

15 (ribose 5-phosphate isomerase and ribulose 5-phosphate 3-epimerase) in the pentose phosphate pathway

16 kinase/phosphatase (PNKP), which generates 5-phosphate/3-hydroxyl DNA termini that are critical for l

17 ted Akt acted through phosphatidylinositol 3-phosphate 5-kinase and Rab11 to facilitate hERG recyclin

18 the export of Mss4, a phosphatidylinositol 4-phosphate 5-kinase, and required for ribosome biogenesis

19 s of PtdIns(4,5)P2 by phosphatidylinositol 4-phosphate 5-kinases (PI4P 5-kinases) is controlled by up

20 ndomly assigned 162 eligible patients (serum phosphate =6.0 to <10.0 mg/dl and a 1.5-mg/dl increase f

21 s regulated by phytohormones and by the soil phosphate abundance, and thus SL transport integrates pl

22 hosphate to vanadium(V) varying from 0 to 1, phosphate accelerated the reduction kinetics of V10 and

23 egment, facilitating placement of Ser65 in a phosphate-accepting position.

24 sential for designing strategies to increase phosphate accumulation and tolerance.

25 in a new gene regulatory network controlling phosphate accumulation in zinc-dependent manner.

26 , glyoxylate, and increased levels of acetyl phosphate, acetoacetyl coenzyme A (acetoacetyl-CoA), but

27 Lithium iron phosphate acts effectively as a reversible redox agent f

28 In this study, we targeted the glycerol-3-phosphate acyltransferase GPAM along with choline kinase

29 rmeable cuticle1 (pec1), cyp77a6, glycerol-3-phosphate acyltransferase6 (gpat6), and defective in cut

30 , the adsorption of ammonium increased while phosphate adsorption decreased.

31 Release of phosphate after phytate degradation and its association

32 enhanced as indicated by increased alkaline phosphates (ALP) activity and calcium deposition.

33 soil resources, such as water, nitrogen and phosphate, also act as signals that shape 3D root growth

34 Finally, we have shown that sphingosine 1-phosphate, an endogenous microglial signaling mediator t

35 ation of phosphodiester bonds between the 5'-phosphate and 3'-hydroxyl termini of single-stranded RNA

36 ntrations of ATP, ADP, AMP, cAMP, creatinine phosphate and ATP:AMP ratio were increased by diabetes a

37 radioactive element thorium and counterions phosphate and citrate were separated effectively from th

38 ly, by 1.0 M phosphite dianion, d-glycerol 3-phosphate and d-erythritol 4-phosphate.

39 The phosphate and diphosphate binding of the generated chann

40 hono(difluoromethyl) iminosugars as glycosyl phosphate and sugar nucleotide mimics.

41 ic ammonium salt generation from the allylic phosphate and the glycine aryl ester.

42 kers of refeeding syndrome (electrolytes and phosphate), and acute phase reactants, and recorded the

43 ugh phosphatidylinositol 4,5-bisphosphate, 3-phosphate, and 3,5-bisphosphate are commonly considered

44 sphate and nicotinamide adenine dinucleotide phosphate, and have become attractive biocatalysts for o

45 At a nearshore station, nitrate, phosphate, and silicate concentrations reached 19, 1.4,

46 ipid metabolite sphingosine to sphingosine-1-phosphate, and suggested a role for sphingosine phosphor

47 d to stabilise the negative charge of the 5'-phosphate, and thus three metals could be required for c

48 alnutrition, even with moderately low plasma phosphate, and, in particular, in children with edematou

49 is able to host concurrently two dihydrogen phosphate anions within a relatively large internal cavi

50 Our data identifies interstitial inorganic phosphate as a new TME marker for tumor progression.

51 ous or nanostructured zinc sulfides and zinc phosphate as compared to raw waste.

52 The importance of the 4'-phosphate at the distal end of the pantetheine arm is de

53 re caused solely by insufficient circulating phosphate availability for mineralization or also by a d

54 The negatively charged phosphate backbone increases (decreases) the DNA surface

55 The phosphate backbone oxygen is clearly the most common hal

56 lead to a clash between O8 of 8-oxoG and the phosphate backbone.

57 on of a family of aromatic hydrocarbons by a phosphate-bearing flavin mononucleotide (FMN) photocatal

58 ethyl-hexanoyl chitosan (CHC), beta-glycerol phosphate (beta-GP), and glycerol.

59 After a 1- to 3-week washout of phosphate binders, we randomly assigned 162 eligible pat

60 mplex with ATP (MDDEF-ATP) revealed that the phosphate-binding loop (amino acids 97-105) is not invol

61 The conformational behaviour of three phosphate-bridged dimannosides was studied by means of N

62 fication provided by 15 mM hydrazine in 5 mM phosphate buffer (PB; pH 7) over 100 to 300 s.

63 fugation, and mixing of the supernatant with phosphate buffer and sodium cyanide for derivatization i

64 ed strongly vitamin C degradation in citrate-phosphate buffer but not in the apple puree serum.

65 ng free spaces on surface via starting block phosphate buffer saline-tween20 blocker.

66 Ru(NH3)6(3+), and anionic Fe(CN)6(4-)) in a phosphate buffer solution (PBS) containing AFB1, the mag

67 from 0.2 to 1.3V using CV and DPV methods in phosphate buffer solution with pH 2.0.

68 as well as with hydrogen peroxide in aqueous phosphate buffer.

69 rds cardiac troponin I [1.7microA/(ng/mL) in phosphate buffer], but suffered from surface fouling in

70 in vivo compared to in vitro using agitated phosphate buffered saline +0.02% Tween 80 pH7.4, includi

71 25 head and neck squamous carcinoma cells in phosphate buffered saline.

72 technique for cell-free virus elution using phosphate-buffered saline (PBS) may provide an alternati

73 d 2-[(131) I] exhibit good stability in both phosphate-buffered saline and blood serum.

74 ells were formed into pellets and covered in phosphate-buffered saline at room temperature for 56 h.

75 The aerosol particles were then dispersed in phosphate-buffered saline for cytotoxicity and senescenc

76 wth and prolonged median survival from 13 d (phosphate-buffered saline) to 20 and 29 d for DAR2 and D

77 rmational transitions shifting the cleavable phosphate by one step.

78 ucleosides and nucleotide mono-, di- and tri-phosphates by capillary electrophoresis coupled to mass

79 tential for another sphingolipid, ceramide 1-phosphate (C1P), to modulate efflux pumps at the BBB.

80 d to a PPi-stabilized supersaturated calcium phosphate (CaP) solution containing 0 to 0.06 mg/mL LRAP

81 system for P removal and recovery as calcium phosphate (CaP).

82 This study suggests that phosphate complexation could enhance the reductive remov

83 imary efficacy end point was change in serum phosphate concentration from baseline (randomization) to

84 l assessed the effects of tenapanor on serum phosphate concentration in patients with hyperphosphatem

85 METHODS AND Resting SM high-energy phosphate concentrations and ATP flux rates were normal

86 Mean serum phosphate concentrations at baseline (after washout) wer

87 nificant, dose-dependent reductions in serum phosphate concentrations in patients with hyperphosphate

88 suggested species-specific adaptation to low phosphate conditions, which we confirmed with growth exp

89 es, involving the deposition of calcium- and phosphate-containing hydroxyapatite (HA) mineral within

90 (IGF2) receptor (IGF2R) recognizes mannose 6-phosphate-containing molecules and IGF2 and plays an imp

91 Compared with calcium phosphate control, a contraction of the unit cell in the

92 wo processes, as demonstrated for the cobalt phosphate (CoPi) water-splitting catalyst.

93 combinant cKL downregulated the renal sodium-phosphate cotransporter Npt2a in alphaKL-null mice suppo

94 tone phosphate (DHAP) and d-glyceraldehyde 3-phosphate (d-G3P) by an unresolved mechanism.

95 that sphingolipid signaling by sphingosine 1-phosphate decreases basal P-glycoprotein transport activ

96 rate induces less vertical lateral root GSA, phosphate deficiency results in a more vertical lateral

97 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is believed to

98 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most co

99 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most co

100 Glucose-6-phosphate dehydrogenase (G6PD) status was determined usi

101 lves interaction of nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) with apurinic/apyrimidin

102 rginine or creatine kinase, glyceraldehyde-3-phosphate dehydrogenase (GPDH), calcium-binding protein,

103 gresses from the host cell, glyceraldehyde-3-phosphate dehydrogenase 1 (GAPDH1), which is primary a g

104 malate/oxaloacetate shuttle and a glycerol-3-phosphate dehydrogenase 1(Gpd1p)-dependent shuttle are a

105 homeostasis, which is regulated by glucose-6-phosphate dehydrogenase and AMP kinase.

106 olving conversion to N(tz) ADPH by glucose-6-phosphate dehydrogenase and reoxidation to N(tz) ADP(+)

107 ified glucose transport and glyceraldehyde-3-phosphate dehydrogenase as the most selective antiparasi

108 er-expressing zwf gene (coding for glucose-6-phosphate dehydrogenase), WX-zwf, produced the highest g

109 A6, clathrin heavy chain 1, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase, filamin-A, and h

110 peS6PDH encodes a NADPH-dependent sorbitol-6-phosphate dehydrogenase, the key enzyme for biosynthesis

111 ific glycolytic proteins such as d-glucose-6-phosphate dehydrogenase.

112 inase and the rate-limiting enzyme glucose-6-phosphate dehydrogenase.

113 hyde (4-HPAA), Rhodiola contains a pyridoxal phosphate-dependent 4-HPAA synthase that directly conver

114 he pyrimidine beta-ribonucleosides and their phosphate derivatives that involves an extraordinarily e

115 ospecific aldol addition of dihydroxyacetone phosphate (DHAP) and d-glyceraldehyde 3-phosphate (d-G3P

116 reversible isomerization of dihydroxyacetone phosphate (DHAP) to d-glyceraldehyde phosphate (GAP), vi

117 cis-aldehyde carbonyl with the DHAP enamine phosphate dianion through a tetrahedrally coordinated wa

118 se (AChE), nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d), glutamic acid decarboxyl

119 ratios were observed for 6:2 polyfluoroalkyl phosphate diester (6:2diPAP) as well as well-known PFASs

120 fluorotelomer sulfonates or polyfluoroalkyl phosphate diesters accounted for a relatively minor prop

121 nitrification inhibitor 3,4-dimethylpyrazole phosphate (DMPP) significantly reduced the N2 O producti

122 e ability of casein kinase 2 to use GTP as a phosphate donor, may be a source of differences between

123 amma-ECS), phytochelatin synthase (PCS1) and phosphate effluxer (PHO1), and the heterologous expressi

124 Bis-o-nitrobenzyl protection of tyrosine phosphate enabled its incorporation into DHFR and Ikappa

125 phosphatidic acid and phosphatidylinositol-4-phosphate enhance association of chaperone-free CHIP wit

126 To overcome this problem, rock phosphate fertilisers are heavily applied, often with ne

127 Globally widespread phosphate fertilizer applications have resulted in long-

128 scular actions of certain molecules, such as phosphates, fibroblast growth factor 23, parathyroid hor

129 led to a significant upregulation in pentose phosphate flux and glycolytic intermediates in HCFs.

130 KCs showing consistently lower basal pentose phosphate flux.

131 of the biphasic force decay upon release of phosphate from caged phosphate was previously interprete

132 er than two as a glucose acceptor, releasing phosphate from glucose 1-phosphate.

133 must obtain all inorganic nutrients, such as phosphate, from the host.

134 The metabolism of glycerol-3-phosphate (G3P) is important for environmental stress re

135 acetone phosphate (DHAP) to d-glyceraldehyde phosphate (GAP), via general base catalysis by E165.

136 The (R)-BINOL Fc phosphate gave Fc-rearranged phosphonate in 91% de.

137 e-dependently increased the dihydroxyacetone phosphate/glycerol 3-phosphate ratio in INS-1(832/13) ce

138 to double-stranded nucleic acids via the 5' phosphate group these fluorophores stack onto the ends o

139 aining neutral nucleotides with a methylated phosphate group.

140 ed in receptor activation interacts with the phosphate groups.

141 tissue.The DNA methylation of 4875 Cytosine-phosphate-guanine (CpG) sites was affected differently b

142 Hence, connections from phosphate homeostasis (PHO) to TORC1 may differ between

143 s and affect expression of genes involved in phosphate homeostasis.

144 uggested that electrostatic interactions and phosphate-hydroxyl ligand exchanges drive protein adsorp

145 However, the concentration of phosphate in most natural habitats is low enough to limi

146 and carbon ratios, oxygen isotope ratios of phosphate in vegetation, and phosphatase enzyme activity

147 orylate sphingosine to produce sphingosine 1-phosphate, in kidney fibrosis induced by folic acid (FA)

148 monstrated that Raf kinases are required for phosphate-induced ERK1/2 phosphorylation in cultured hyp

149 on with conversion of the formed d-glucose-6-phosphate into mixtures of labeled methyl d-glucose-4,6-

150 Phosphate ions act as a catalyst in the ripening process

151 myo-Inositol phosphates (IPs) are important bioactive molecules that

152 Olivine lithium iron phosphate is a technologically important electrode mater

153 of this complex is highly pH-dependent; the phosphate is completely released from Gd-TREN-MAM below

154 Inorganic phosphate is the major bioavailable form of the essentia

155 inacolato) and (E)-1,2-disubstituted allylic phosphates is introduced.

156 side hydrolase 1 family (alpha/beta)8 triose-phosphate isomerase (TIM) barrel structure with a highly

157 suggested by this algorithm, genes (ribose 5-phosphate isomerase and ribulose 5-phosphate 3-epimerase

158 of two distinct modules: an N-terminal sugar phosphate isomerase-like domain associated with DSD acti

159 Type Igamma phosphatidylinositol phosphate kinase (PIPKIgamma), a phospholipid kinase gen

160 cture, conductive substrate, and Ni-Fe mixed phosphate lead to superior electrocatalytic activity tow

161 provided dose-dependent reductions in serum phosphate level from baseline (least squares mean change

162 ngle-site Ala substitutions reduced receptor phosphate levels more than expected for the loss of a si

163 ning AK and each of four different adenosine phosphate ligands.

164 uptake determined through 2-deoxy glucose 6 phosphate luminescence.

165 loss-of-function mutations in sphingosine-1-phosphate lyase (SGPL1).

166 of sphingosine kinase 1 and 2, sphingosine-1-phosphate lyase 1, and sphingosine-1-phosphate phosphata

167 a broad family of layered metal thio(seleno)phosphate materials that are moderate- to wide-bandgap s

168 Phosphate measurements confirmed that single-site Ala su

169 s decreased by in vitro non-enzymatic acetyl phosphate mediated lysine acetylation, and the presence

170 oscopy to measure whole-body VO2, quadriceps phosphate metabolism and pH during continuous and interm

171 t for COPD and asthma (genes in the inositol phosphate metabolism pathway and CHRM3) and describe tar

172 caused by disturbed vitamin D, calcium, and phosphate metabolism.

173 tion dynamics of single-crystal lithium iron phosphate microrods with long-axis along the [010] direc

174 Of particular interest is the Ca-phosphate mineral merrillite, the anhydrous end-member o

175 tal nodes of MOF nanoparticles with terminal phosphate-modified oligonucleotides.

176 aspase-9 activity, and the bulk of the added phosphate moiety appeared to directly block substrate bi

177 e of phosphorylated amino acids in which the phosphate moiety bears a chemical protecting group, thus

178 anding into the behavior and manipulation of phosphate monoesters in molecular biology.

179 Human inositol phosphate multikinase (HsIPMK) critically contributes to

180 Nicotinic acid adenine dinucleotide phosphate (NAADP) and cyclic ADP-ribose (cADPR) are Ca(2

181 eration of nicotinamide adenine dinucleotide phosphate (NADPH) in p53-deficient cancer cells.

182 o impaired nicotinamide adenine dinucleotide phosphate (NADPH) production and imbalanced redox homeos

183 r oxidized nicotinamide adenine dinucleotide phosphate/NADPH levels, phagocytic reactive oxygen speci

184 ntimicrobial, protein-repellent, and calcium phosphate nanoparticle remineralization was suggested to

185 We also evaluate the degree to which phosphate neutral loss occurs from phosphopeptide produc

186 osphosite localization algorithm) to include phosphate neutral losses can significantly improve local

187 it is limited by the rapid removal of the 5- phosphate of the guide strand by metabolic enzymes.

188 abels into product from both alpha and gamma phosphates of donor molecules.

189 This study examines the effect of phosphate on schwertmannite stability under reducing con

190 y week 4, with no differences in creatinine, phosphate, or TRP.

191 of neutrophil CXCR2, CD11b, and reduced NAD phosphate oxidase components (p22phox, p67phox, and gp91

192 The NOX (nicotinamide adenine dinucleotide phosphate oxidase) family includes seven unique members

193 ed form of nicotinamide adenine dinucleotide phosphate) oxidase-dependent killing and, in turn, host

194 decreased nicotinamide adenine dinucleotide phosphate-oxidase 2 and inducible nitric oxide synthase

195 kinase and nicotinamide adenine dinucleotide phosphate oxidases are also inhibited.

196 SOT18 in complex with 3'-phosphoadenosine 5'-phosphate (PAP) alone and together with the Gl sinigrin.

197 so measured plasma levels of FGF23, calcium, phosphate, parathyroid hormone, and vitamin D metabolite

198 ed endogenously from glucose via the pentose-phosphate pathway (PPP) in stable isotope-assisted ex vi

199 x towards glycolysis relative to the pentose phosphate pathway (PPP).

200 S) is a key enzyme in the methylerythritol 4-phosphate pathway and is a target for the development of

201 PH reflecting a higher activation of pentose phosphate pathway as this is accompanied with higher cyt

202 route for directing glucose into the pentose phosphate pathway that bypasses hexokinase and the rate-

203 lose 5-phosphate 3-epimerase) in the pentose phosphate pathway were overexpressed, and a geranyl diph

204 up-regulation of glucose influx, the pentose phosphate pathway, and NAD salvaging pathways.

205 complete non-oxidative phase of the pentose phosphate pathway, and others predicted to mediate lipop

206 glucose flux between glycolysis, the pentose phosphate pathway, and serine biosynthesis seems to be s

207 t together to shunt glucose into the pentose phosphate pathway, creating an alternative route for dir

208 which encode the first enzyme in the pentose phosphate pathway, have a more severe growth phenotype t

209 revealed a reduction in glycolysis, pentose phosphate pathway, polyamines and nucleotides, but an in

210 olism, glutamate metabolism, and the pentose phosphate pathway.

211 osine-1-phosphate lyase 1, and sphingosine-1-phosphate phosphatase 1 in normal human liver and cirrho

212 acking the LPA-degrading enzyme phospholipid phosphate phosphatase type 1 (PLPP1) had a 2-fold increa

213 ce and survival cues controlled by the lipid phosphate phosphatases Wunen and Wunen2.

214 Inorganic phosphate (Pi) accumulation within matrix vesicles (MVs)

215 gulated by levels of extracellular inorganic phosphate (Pi) and pyrophosphate (PPi).

216 Low phosphate (Pi) availability constrains plant development

217 a major developmental response of plants to phosphate (Pi) deficiency and is thought to enhance a pl

218 e hydrolysis of ATP and release of inorganic phosphate (Pi) from the nucleotide cleft of actin.

219 of extracellular and intracellular inorganic phosphate (Pi) levels is critical to most biochemical an

220 Two inorganic phosphate (Pi) uptake mechanisms operate in streptophyte

221 Phosphocreatine and inorganic phosphate (Pi) varied in opposite directions across gray

222 pholipids, especially phosphatidylinositol 3-phosphate (PI3P), via its SHR_BD and APT1 domains.

223 egulates the level of phosphatidylinositol 4-phosphate (PI4P) in the membranes of neuronal cells.

224 Low plasma concentrations of pyridoxal 5'-phosphate (PLP) are common in renal transplant recipient

225 The pyridoxal 5'-phosphate (PLP)-dependent transaminase BioA catalyzes th

226 by which phosphite (HPO3(2-)) is oxidized to phosphate (PO4(3-)), is the most energetically favorable

227 phate uptake and plant biomass production on phosphate-poor soils.

228 he glycolytic intermediates into the pentose phosphate (PPP) and serine pathways.

229 cosylsphingosine, sphingosine, sphingosine-1-phosphate) promote alpha-synuclein aggregation in vitro,

230 phylotype consistently carry a high-affinity phosphate pst transporter and the phoB-phoR regulatory s

231 M depletion of either phosphatidylinositol 4-phosphate (PtdIns4P) or PtdIns(4,5)P2 but not PtdIns(3,4

232 he involvement of covalently linked anomeric phosphates rather than oxocarbenium ion pairs as the rea

233 ed the dihydroxyacetone phosphate/glycerol 3-phosphate ratio in INS-1(832/13) cells, indicating a mor

234 oat bran and white bean had a lower calcium:phosphate ratio than barley bran and red kidney beans.

235 ransport of the cation-independent mannose 6-phosphate receptor (CI-MPR).

236 pact of fingolimod (FTY720), a sphingosine-1-phosphate receptor (S1PR) agonist, on 2 mouse models of

237 the clinically important GPCR, sphingosine-1-phosphate receptor 1 (S1P1).

238 independently of its receptor, Sphingosine-1-Phosphate receptor 2 (S1PR2).

239 via sortilin or cation-independent mannose 6-phosphate receptor, and facilitated the acidification of

240 Acid addition also allowed for 43% more phosphate recovery via struvite precipitation in the ace

241 le role of nicotinamide adenine dinucleotide phosphate reduced form oxidases (NOXs) in Mo-DC differen

242 te ATPase activity by inhibiting the rate of phosphate release of beta-cardiac myosin-S1, but the mol

243 reasing the rate-limiting step of the cycle (phosphate release), mavacamten reduced the number of myo

244 ase in the rate constant for actin-activated phosphate release, the biochemical step in myosin's ATPa

245 4ngmL(-1) for nucleotide mono-, di-, and tri-phosphates, respectively, were found.

246 Characterization of Excess Phosphate Response (EPiR) is essential for designing str

247 The development of such receptors that bind phosphate reversibly in a pH-dependent manner opens the

248 f Bioglass 45S5 (BAG) or fluoride-containing phosphate-rich bioactive glass (BAG-F).

249 In conclusion, fluoride-containing phosphate-rich bioactive glass incorporated as micromete

250 of fertilizers and in light of the fact that phosphate rock, the source of P fertilizer, is a finite

251 ion of olive mill wastewater (OMW) with rock phosphate (RP) in a field of olive trees, on olive fruit

252 cell (MC) activation and local sphingosine-1-phosphate (S1P) are significantly augmented after OVA tr

253 Chronic sphingosine-1-phosphate (S1P) infusion resulted in a development of si

254 Sphingosine 1-phosphate (S1P) is a multifunctional bioactive sphingoli

255 Sphingosine 1-phosphate (S1P) is a pleiotropic signaling molecule that

256 demonstrated the potential of sphingosine 1-phosphate (S1P) receptor (S1PR) agonism in the treatment

257 otein-coupled receptor agonist sphingosine-1-phosphate (S1P).

258 IP6 binds to the arrestin phosphate sensor, and is stabilized by trimerization.

259 scopy experiments on reactions using allylic phosphates showed the importance of allyl chloride inter

260 not alter 5-HT2C Galphaq-dependent inositol phosphate signaling, 5-HT2A or 5-HT2B receptor-mediated

261 d at SLC9A3R1, with mediators of calcium and phosphate signalling.

262 s device with dextran-free 0.1% riboflavin-5-phosphate solution with enhancers and by irradiating the

263 rces in this system was aided by a change in phosphate source rocks in 1998 AD, and a corresponding s

264 nly observed in the presence of an exogenous phosphate source.

265 Despite their large homology, the phosphate-specific OprP and the diphosphate-specific Opr

266 In S. cerevisiae, the phosphate starvation (PHO) responsive transcription fact

267 ired but Pho2 is dispensable for survival in phosphate starvation and is only partially required for

268 uired for gene induction and survival during phosphate starvation.

269 n repeat expansions in vivo, implying failed phosphate-steering promotes an unanticipated lagging-str

270 showed the greatest variety of high-mannose-phosphate structures.

271 The enzyme 1-deoxy-d-xylulose 5-phosphate synthase (DXPS) is a key enzyme in the methyle

272 These hydrolases acquire a mannose 6-phosphate tag by the action of the GlcNAc-1-phosphotrans

273 is not involved in ATP binding and that the phosphate tail of ATP in this structure is in an outward

274 relies on juxtaposition of 3 hydroxyl and 5 phosphate termini of the strand breaks for catalysis.

275 zations of substrates containing a Z-allylic phosphate tethered to an alkyne are described.

276 lity of NKA to transform ATP to ADP and free phosphate, the latter reacting with ammonium molybdate t

277 ability to sequester nanoclusters of calcium phosphate to form a core-shell structure, in a fluid tha

278 nate moiety represents a source of inorganic phosphate to microorganisms that live in environments th

279 With molar ratios of phosphate to vanadium(V) varying from 0 to 1, phosphate

280 /g dw for TMPP and 427 ng/g dw for triphenyl phosphate (TPhP).

281 udge were between 4.14 ng/g dw for tripropyl phosphate (TPP) and 7290 ng/g dw for TBOEP; for ash, the

282 enol (GlcNAc-P-P-Und) produced by the GlcNAc-phosphate transferase GacO and GlcNAc-phosphate-undecapr

283 n vitamin D metabolism and calcium and renal phosphate transport associated with differences in circu

284 type-Ib (GSD-Ib), deficient in the glucose-6-phosphate transporter (G6PT), is characterized by impair

285 atalysing Pi uptake in chlorophytes, whereas PHOSPHATE TRANSPORTER 1 (PHT1) proteins are the H(+) /Pi

286 sive disease caused by mutation of glucose-6-phosphate transporter and characterized by altered glyco

287 PHOSPHATE TRANSPORTER B (PTB) proteins are hypothesized

288 ession of Arabidopsis (Arabidopsis thaliana) phosphate transporter PHO1;H3 comprising MYB15, MYB84, b

289 by the action of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-IIc/Pit2.

290 GlcNAc-phosphate transferase GacO and GlcNAc-phosphate-undecaprenol (GlcNAc-P-Und) produced by the gl

291 PDR1 OE significantly enhanced phosphate uptake and plant biomass production on phospha

292 c syntheses relying on N-acetylglucosamine-1-phosphate uridylyltransferase (GlmU).

293 The phosphate was found to be involved in the phase transfer

294 h DI water and SRHA and no interference from phosphate was observed.

295 e decay upon release of phosphate from caged phosphate was previously interpreted as a signature of k

296 iesterase activity that leaves a terminal 3' phosphate which prevents overprocessing.

297 cleaved RNA(3'-rA) consists of 2',3'-cyclic phosphate which protects RNA(3'-rA) from ligation and fu

298 nto mixtures of labeled methyl d-glucose-4,6-phosphates, which were analyzed by (31)P NMR spectroscop

299 study of systematic replacement of a single phosphate with an amide linkage throughout the guide str

300 equent attachment of ATRP initiators via the phosphate-Zr(4+)-carboxylate chemistry.