ライフサイエンスコーパス: acid

1 ward the production of neurotoxic quinolinic acid.

2 otes the production of neurotoxic quinolinic acid.

3 ate) cores functionalized with phenylboronic acid.

4 he synthetic auxin 2,4-dichlorophenoxyacetic acid.

5 otal cellular protein and several free amino acids.

6 toins and unsaturated alpha-quaternary amino acids.

7 inducing Rsp5-mediated desaturation of fatty acids.

8 UPLC-MS/MS identified sixteen peptides/amino acids.

9 regates by tuning the concentration of fatty acids.

10 s heavily dependent on cholesterol and fatty acids.

11 and SRE, as well as with individual organic acids.

12 ta-fluorinated, and beta-arylated carboxylic acids.

13 human A3C S188I, but through different amino acids.

14 ly detected in oil samples, but not in fatty acids.

15 e of decarboxylation of 2,4-dimethoxybenzoic acid (1) is accelerated in parallel to the extent that t

16 phinothricin over the 20 proteinogenic amino acids (1) , indirect effects of BAR-containing transgene

17 oic acid (EPA; 20:5 n-3) and docosahexaenoic acid (22:6 n-3) has been associated with reduced adiposi

18 ylquinic acid (HC2) and 3,5-dicaffeoylquinic acid (3,5-diCQA).

19 nce peel and pulp, namely 3-O-caffeoylquinic acid (3-CQA), 4-p-coumaroylquinic acid (HC1), 4-O-caffeo

20 ransformation product, 3-quinolinecarboxylic acid (3-QCA), was identified by liquid chromatography hi

21 umaroylquinic acid (HC1), 4-O-caffeoylquinic acid (4-CQA), 5-O-caffeoylquinic acid (5-CQA), derivativ

22 e chlorogenic acid isomer 5-O-caffeoylquinic acid (5-CQA) on digestion of potato starch by porcine pa

23 feoylquinic acid (4-CQA), 5-O-caffeoylquinic acid (5-CQA), derivative of p-coumaroylquinic acid (HC2)

24 am of the S2' cleavage site is the FP (amino acids 798-818 SFIEDLLFNKVTLADAGFMKQY for SARS-CoV, FP1).

25 enolic compounds (4 anthocyanins, 9 phenolic acids, 9 flavonols, 7 flavan-3-ols), 3 triterpenoids, 7

26 in the cytoplasm when cultured with butyric acid, a principal short-chain fatty acid in the fermenta

27 ere we report that the addition of peracetic acid, a strong oxidant, to mild dilute acid pretreatment

28 structure (optical microscopy), and ascorbic acid (AA) degradation kinetics were performed.

29 chain amino acids (BCAAs) and aromatic amino acids (AAAs) have been shown to be associated with insul

30 type (WT) behaviour when exposed to abscisic acid (ABA) or CaCl2 .

31 microbiota bile acid metabolism, favor bile acid accumulation that contributes to AhR-mediated hepat

32 Based on our prior studies with the bile acid-activated nuclear hormone receptor farnesoid X rece

33 yocardial levels of 3 metabolites, nicotinic acid adenine dinucleotide, methylnicotinamide, and N1-me

34 mino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor and mammalian target of rapamycin (

35 ino-3-hydroxy-5-methylisoxazole-4-proprionic acid (AMPA) receptors.

36 Nucleic acid amplification testing (NAAT) is the preferred metho

37 infection in certain populations by nucleic acid amplification testing (NAAT), as they involve a les

38 owed the conjugation of fatty acid (palmitic acid analog) to Uox with the HSA binding capacity and re

39 led plasma mass spectrometry (ICP-MS), amino acid analysis, and spectroscopy (ATR-IR, Raman).

40 pid mediators revealed increased arachidonic acid and 12-lipoxygenase metabolites.

41 ressed, including a poor solubility of fatty acid and a substantial loss in the therapeutic activity.

42 er mice were given injections of deoxycholic acid and an increase after they were fed fenofibrate.

43 Fatty acid and bulk stable carbon isotope values of cave-adapt

44 two specific constituent components; gallic acid and carnosic acid were the cause for the synthetic

45 sition showed marked increase of taurocholic acid and decrease of tauro-alpha and beta-muricholic aci

46 ive C-S bond cleavage giving phenyl sulfinic acid and ionization to diphenyl sulfide radical cation t

47 dation, phospholipid catabolism, arachidonic acid and linoleic acid metabolism, sphingolipid metaboli

48 ic acid, catechin, chlorogenic acid, caffeic acid and p-coumaric acid varied among species and found

49 hatidylethanolamine inhibit and phosphatidic acid and sphingomyelin enhance SPCA1a activity.

50 ze the building blocks of HA, UDP-Glucuronic acid and UDP-N-Acetyl-Glucosamine, as well as hyaluronic

51 rocyanidins) as also hydroxycinnamoyl-quinic acids and phloretin derivatives were identified in the s

52 and energetics to be measured within nucleic acids and their complexes with proteins.

53 UFAs eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid were observed.

54 Carotenoid, ascorbic acid, and phenolic contents were unaffected by the 3-mon

55 trates including the natural indole-3-acetic acid, and the synthetic auxin 2,4-dichlorophenoxyacetic

56 studied by adding chlorogenic and rosmarinic acids, and food-grade phenolic apple and rosemary extrac

57 Both n-6 and n-3 polyunsaturated fatty acids are associated with lower CVD risk, although the e

58 caque A2*05 allotype prefers the basic amino acid arginine at the second position of the peptide, and

59 CE-MS data (5% ( approximately 0.8M) acetic acid as background electrolyte).

60 bed on the graphene as well as charged amino acids associated with the immobilized protein.

61 the peptide, and hydrophobic and polar amino acids at the C-terminal end.

62 kemogenesis, and inhibits all-trans-retinoic acid (ATRA)-induced AML cell differentiation, through re

63 These findings thus demonstrate that amino acid availability controls lysosome positioning through

64 ts have long known that CO2 directly affects acid-base and ion regulation, respiratory function and a

65 e (V-ATPase) and are extensively involved in acid-base homeostasis.

66 opurity and are prone to undergo deleterious acid-base side-reactions under the reaction conditions f

67 tubule is critical for blood pressure (BP), acid-base, and potassium homeostasis.

68 ased pharmaceutical development, and nucleic acid based biosensor device design.

69 ical insights into nuclear crowding, nucleic acid based pharmaceutical development, and nucleic acid

70 igh molecular weight amorphous poly-l-lactic acid-based BRS (APTITUDE, Amaranth Medical [AMA]) to Abs

71 catalyzing the oxygen evolution reaction in acid-based electrolyzers must be guided by the proper ba

72 Circulating branched-chain amino acids (BCAAs) and aromatic amino acids (AAAs) have been

73 am adipose development through dietary fatty acids before birth.

74 uded purine and pyrimidine metabolism, fatty acid beta-oxidation, phospholipid catabolism, arachidoni

75 Enzymes of amino acid biosynthesis were higher in coculture than in axeni

76 a potential regulatory role of ACPS in fatty acid biosynthesis.

77 ysine biosynthesis and degradation, and bile acid biosynthesis.

78 nic liquid) diblock copolymers, poly(acrylic acid)-block-poly(4-vinylbenzyl)-3-butyl imidazolium bis(

79 acrocycle threading kinetics, and (c) sialic acid blocking groups that prevent macrocycle threading u

80 For two nonamino acid buffers, TRIS had little effect while HEPES resulte

81 xtracellular loop, in the action of decanoic acid but not of 3,3'-diindolylmethane.

82 rd pathway for the metabolism of arachidonic acid by cytochrome P450 enzymes emerged.

83 nds, i.e. Gallic acid, catechin, chlorogenic acid, caffeic acid and p-coumaric acid varied among spec

84 Medium chain fatty acids can activate the pro-inflammatory receptor GPR84 b

85 Phenolic compounds, i.e. Gallic acid, catechin, chlorogenic acid, caffeic acid and p-cou

86 rcome this obstacle by utilizing the 6-amino-acid (CCPGCC) tetracysteine (TC) tag and FlAsH-EDT2 reag

87 lengths observed, suggesting that the fatty acid chain elongation process was not affected.

88 combinant pH1N1 virus encoding these 6 amino acid changes (pH1N1/NSs-6mut) induced lower levels of pr

89 y intrinsic local interactions between amino acids close to each other in the protein sequence.

90 Analysis of gallbladder bile acid composition showed marked increase of taurocholic a

91 oduced echium oil had the same omega-3 fatty acid composition than traditionally extracted oil.

92 in particular on hydrated perfluoro-sulfonic acid compounds employed as electrolytes in fuel cells.

93 igher and C18:2n-6 and monounsaturated fatty acid concentrations and n-6:n-3 PUFA ratio lower for GSP

94 However, for broad applications of fatty acid-conjugation, several issues should be addressed, in

95 often minute concentrations in vivo, d-amino acid containing peptides (DAACPs) are crucial to many li

96 igh levels of seed, nodule, and leaf stearic acid content.

97 tal polyunsaturated, total n-3 and n-6 fatty acid contents increased linearly (p<0.05) by raising the

98 the lysosomal efflux of most essential amino acids, converting the lysosome into a cellular depot for

99 oups on Wnt proteins to activated carboxylic acid (COOH) or glutaraldehyde (COH) groups functionalize

100 06155) was a key enzyme in its tricarboxylic acid cycle (TCA) pathway.

101 se complex, a rate-controlling tricarboxylic acid cycle enzyme.

102 by investigating the effects of deoxycholic acid (DCA) and ursodeoxycholic acid on the expression an

103 covered only by covalent attachment of amino acid deactivation agents to residual activated carboxy g

104 he recognition and internalization of sialic acid decorated apoptotic bodies and exosomes derived fro

105 AR bound to a polyethylene glycol-carboxylic acid derivative (Cmpd-15PA) of this modulator.

106 family of mediators that include arachidonic acid-derived lipoxins, omega-3 fatty acid eicosapentaeno

107 ipoxins, omega-3 fatty acid eicosapentaenoic acid-derived resolvins, docosahexaenoic acid-derived res

108 noic acid-derived resolvins, docosahexaenoic acid-derived resolvins, protectins, and maresins.

109 Topical application of docosahexaenoic acid (DHA), a representative omega-3 PUFA, in wild type

110 eed was developed based on infrared-assisted acid digestion.

111 We find that uric acid directly inhibits uridine monophosphate synthase (U

112 i.e., brackish vs. freshwaters), and nucleic acids (DNA vs. RNA), suggesting niche differentiation.

113 en the individual n-3 PUFAs eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid we

114 '-hydroxylase) and buildup of dehydrophaseic acid (DPA).

115 rrected three-dimensional gamma-aminobutyric acid-edited magnetic resonance (MR) spectroscopic imagin

116 hidonic acid-derived lipoxins, omega-3 fatty acid eicosapentaenoic acid-derived resolvins, docosahexa

117 hain, -(CH2)2-, and a hydrophilic carboxylic acid end group are found to be the most effective at ret

118 Maternal intake of eicosapentaenoic acid (EPA; 20:5 n-3) and docosahexaenoic acid (22:6 n-3)

119 tal polyphenols between 4.9 and 9.2mg gallic acid equivalents (GAE)/gDM.

120 products) can lead to the formation of fatty acid esters of 2-monochloropropane-1,3-diol, 3-monochlor

121 carotenoids and 11 were apocarotenoids fatty acids esters.

122 dentical with the first, except for an amino acid exchange in the stalk region abolishing the N-linke

123 sphonoethoxy)methyl)propoxy]methylphosphonic acid, exhibited Ki values of 6 and 70 nM for human HGPRT

124 Reference TAGs containing C14-C20 fatty acids (FAs) showed good linear response.

125 In comparison to spoligotyping of acid-fast-positive MGIT cultures, percent agreement betw

126 thyl-furfural (HMF) to 2,5-furandicarboxylic acid (FDCA) using aerial oxygen under mild reaction cond

127 lipidemia with elevated levels of free fatty acids (FFAs).

128 chemical synthesis of the fluorogenic amino acid Fmoc-Trp(C2-BODIPY)-OH (3-4 d), the preparation of

129 ero)cyclic alpha,beta-unsaturated carboxylic acids from 1,6- and 1,7-enyes and CO2.

130 it efficiently recovers proteins and nucleic acids from a variety of pathogenic bacteria and operates

131 ially restored total fecal short-chain fatty acids from the level significantly repressed in mice und

132 hat FatM increases the outflow of 16:0 fatty acids from the plastid, for subsequent use by RAM2 to pr

133 iew, we summarize recent advances of nucleic acid-functionalized transition metal nanosheets in biose

134 higher expression levels of the gibberellic acid (GA) catabolic enzyme StGA2ox1.

135 te *BEA, the metals that form stronger Lewis acids give greater selectivities and rates for the desir

136 (NO), nitrite (NO2-), and unsaturated fatty acids give rise to electrophilic nitro-fatty acids (NO2

137 and non-cell line specific changes in fatty acids, glycerophospholipids and carbohydrates over time,

138 ylation of the feedstock chemical isobutyric acid has enabled the asymmetric synthesis of a wide vari

139 eoylquinic acid (3-CQA), 4-p-coumaroylquinic acid (HC1), 4-O-caffeoylquinic acid (4-CQA), 5-O-caffeoy

140 cid (5-CQA), derivative of p-coumaroylquinic acid (HC2) and 3,5-dicaffeoylquinic acid (3,5-diCQA).

141 has been reported that topical hypochlorous acid (HOCl) formulations lead to relief of itch in human

142 proteins can be modified by different fatty acids; however, very little is known about how zDHHC enz

143 led understanding of the kinetics of nucleic acid hybridization.

144 Without oleic acid impurities, cadmium carboxylate can be completely d

145 iodosuccinimide and trifluoromethanesulfonic acid in dichloromethane and acetonitrile at -78 degrees

146 decrease of tauro-alpha and beta-muricholic acid in Tgr5(-/-) mice.

147 butyric acid, a principal short-chain fatty acid in the fermentation metabolites of S. epidermidis.

148 ochemical reaction mechanisms for alpha-keto acids in aqueous solution are robust and generalizable a

149 HCF222 encodes a protein of 99 amino acids in Arabidopsis (Arabidopsis thaliana) that has sim

150 of the relative proportion of duplex nucleic acids in mixed ds/ss nucleic acid solutions, demonstrati

151 kali metal hydride, HCF3, and borazine Lewis acids in quantitative yield at room temperature.

152 Five highly polar organic acids in serum were successfully quantified, and the SAL

153 is an anti-viral enzyme that cleaves nucleic acids in the cytosol, preventing accumulation and a subs

154 kely results in a further breakdown of amino acids in the liver, mediated by increased glucagon, with

155 n bark oil, zinc gluconate and trans-ferulic acid) in oil-in-water emulsions to control the fungal sp

156 ts of OVOCs, including high levels of formic acid, in the atmosphere (measured by an online high-reso

157 egulate the Rag GTPases in response to amino acids, including GATOR1, a GTPase activating protein for

158 port that the sensing of IAV RNA by retinoic acid inducible gene I (RIG-I) initiates ZBP1-mediated ce

159 Furthermore, amino acid infusion likely results in a further breakdown of a

160 wn risk factors for iron deficiency, gastric acid inhibitor use for >/=2 years was associated with an

161 with poultry animals; and the use of gastric acid inhibitors.

162 espiratory distress syndrome by hydrochloric acid instillation, animals underwent a decremental posit

163 The gallbladder excretes cytotoxic bile acids into the duodenum through the cystic duct and comm

164 archaea and bacteria by eliminating nucleic acid invaders in a crRNA-guided manner.

165 rane processing to concentrate omega-3 fatty acids is enhanced.

166 The effect of the chlorogenic acid isomer 5-O-caffeoylquinic acid (5-CQA) on digestion

167 gated transcriptomes using RNA-seq and amino acid levels with N treatment in tea (Camellia sinensis),

168 ansgenes in planta, including modified amino acid levels, have been seen but without the identificati

169 release into water of carboxylic and fulvic acid-like components.

170 We used sialic acid linkage-specific derivatization methods to improve

171 omega-6 (omega6) and omega-3 (omega3) fatty acids (linoleic and alpha-linolenic acid, respectively)

172 itro oleic acid (OA-NO2 ) and nitro linoleic acid (LNO2 ).

173 s as nerve activity produces large and rapid acid loads in presynaptic terminals.

174 ated Cy<Cy monoacylated with hydroxycinnamic acids<diacylated Cy.

175 ngue, mumps, and measles viruses) or nucleic acid material (Nipah and chikungunya viruses).

176 ulation, as well as host and microbiota bile acid metabolism, favor bile acid accumulation that contr

177 id catabolism, arachidonic acid and linoleic acid metabolism, sphingolipid metabolism, tryptophan met

178 rough physiologic functions apart from fatty acid metabolism.

179 II-A CRISPR-Cas immunity and central nucleic acid metabolism.

180 ere identified, including various free fatty acids, metabolites, and complex lipids such as ceramides

181 3-hexyl-thiophene) (P3HT)-phenyl-C61-butyric acid methyl ester (PCBM) mixture, and found to predict m

182 stitution test, proximate composition, amino acids, minerals and electrophoresis] were determined.

183 t the higher concentration of monocarboxylic acid MOFs were isostructural but suffered from increased

184 increased lambdamax of Cy chelates: malonic acid monoacylation<triglycosylated Cy<Cy monoacylated wi

185 ious studies have shown that methanesulfonic acid (MSA) reacts with amines and ammonia to form partic

186 acids give rise to electrophilic nitro-fatty acids (NO2 -FAs), such as nitro oleic acid (OA-NO2 ) and

187 The extracellular, active 180 amino acid Nogo-A region, named Nogo-A-Delta20, binds to hepar

188 -fatty acids (NO2 -FAs), such as nitro oleic acid (OA-NO2 ) and nitro linoleic acid (LNO2 ).

189 f deoxycholic acid (DCA) and ursodeoxycholic acid on the expression and release of HbetaD1 and HbetaD

190 of LDH activity by small hairpin ribonucleic acid or expression of phospho-deficient LDHA Y10F sensit

191 y for the reversible immobilization of amino acid or peptide derivatives on carbon nanomaterials such

192 ples were investigated by the degradation of acid orange 7 dye in aqueous solution under simulated so

193 This work investigates the effect of oxalic acid (OxA) on NPF from the reaction of MSA and methylami

194 c effects, particularly an increase in fatty acid oxidation, cannot be explained by decarboxylated os

195 intermediates that are important in nucleic acid oxidation.

196 ng-dependent switch from glycolysis to fatty acid oxidation.

197 orporates a photoreactive, non-natural amino acid, p-benzoyl-l-phenylalanine, into various positions

198 cloaddition allowed the conjugation of fatty acid (palmitic acid analog) to Uox with the HSA binding

199 The specific fatty acid pattern may be influenced by metabolic, genetic, an

200 We combine a 97-amino-acid peptide of human origin that binds hyaluronan, a ma

201 ransport elicited endocytosis of other amino acid permeases similarly involves unmasking of a cytosol

202 We found that the natural product caffeic acid phenethyl ester (CAPE) disrupts neural crest gene e

203 s of hyperaccumulation of the aromatic amino acid phenylalanine (Phe) in animals, known as phenylketo

204 les (CSLPHNPs) with poly (lactic-co-glycolic acid) (PLGA) core and lipid layer containing docetaxel a

205 rand replacement of dsDNA by peptide nucleic acid (PNA) and the in situ growth of electroactive polym

206 ene knockdown, we employed a peptide-nucleic acid (PNA) hybridization assay.

207 h suggests important roles of specific amino acid polymorphisms in the antigen-binding clefts.

208 translational labeling at the specific amino acid positions.

209 cetic acid, a strong oxidant, to mild dilute acid pretreatment reduces the temperature requirement to

210 xa isoforms (VEGF165a, 165 for the 165 amino acid product) and antiangiogenic VEGFxxxb (VEGF165b) iso

211 election and assessments of changes in amino acid properties provide evidence of positive selection o

212 TaADF4 encodes a 139-amino-acid protein containing five F-actin-binding sites and t

213 ecific locations within G-quadruplex nucleic acids, providing valuable probes for local structure, dy

214 3n-3 concentration and polyunsaturated fatty acid (PUFA) to saturated fatty acid (SFA) ratio were hig

215 We also demonstrate that the PML retinoic acid receptor-alpha (PML-RARalpha) oncofusion protein, w

216 We hypothesized that bile acids regulate colonic HbetaD expression and aimed to te

217 lude hypocretin and GABA (gamma-aminobutyric-acid)-releasing neurons of the lateral hypothalamus, whi

218 The effects of amino acid replacements on lipid association of the C-terminal

219 a-linked Kdo (3-deoxy-d-manno-oct-2-ulosonic acid) residue added by a third GT module belonging to th

220 show that interactions between charged amino acid residues are important both to directly stabilize t

221 ely charged DNA and positively charged amino acid residues, the translocation speed of DNA can be man

222 ted to a peptide resolution of 5 to 20 amino acid residues.

223 tain fucose, xylose and 4-O-methylglucuronic acid -residues.

224 presentative ZrPP-1 not only exhibits strong acid resistance (pH = 1, HCl) but also remains intact ev

225 3) fatty acids (linoleic and alpha-linolenic acid, respectively) in the cytochrome P450/soluble epoxi

226 enson-Bassham (CBB) and reverse tricaboxylic acid (rTCA) cycles.

227 etween Fzo1 turnover and the status of fatty acids saturation.

228 disease risk (including branched-chain amino acids, select unsaturated lipid species, and trimethylam

229 his study uncovered differences in the fatty acid selectivity profiles of cellular zDHHC enzymes and

230 e allows for UGA codons to specify the amino acid selenocysteine (Sec).

231 Cytosolic nucleic acid sensing elicits interferon production for primary a

232 haled CO2 to induce an acidosis and activate acid sensing ion channels.

233 ecoy peptides derived from the primary amino acid sequence in the SOD2-binding site in hsp70.

234 ance P (SP) [SP + 3H](3+) ion (SP(3+); amino acid sequence RPKPQQFFGLM-NH2).

235 A protocol for mapping amino-acid sequences to coarse-grained beads enables the direc

236 turated fatty acid (PUFA) to saturated fatty acid (SFA) ratio were higher and C18:2n-6 and monounsatu

237 ion of OG but not 5-(tetradecyloxy)-2-furoic acid significantly reduced hamster ear sebaceous gland s

238 lized hydrogen-bonded pi-complex at Bronsted acid sites, -36 kJ/mol.

239 ydrogenation and moderate to strong Bronsted acid sites.

240 can autonomously move on a spherical nucleic acid (SNA)-based 3D track.

241 acidic media or immersing MoS2 into certain acid solutions like TFSI.

242 duplex nucleic acids in mixed ds/ss nucleic acid solutions, demonstrating significant advantages ove

243 We aimed to identify the role of the enzyme acid sphingomyelinase in the aging of stored units of pa

244 Amino acid substitution mutations within a PMS2 C-terminal (72

245 We used an unbiased D-amino acid substitution strategy to determine structure-assemb

246 tion because trimming the Phe by small amino acid substitutions abolished alphaLbeta2 binding with so

247 The amino acid substitutions lie in two highly conserved loop regi

248 alpha:RGS protein pair based on single amino acid substitutions.

249 for a range of putative para-hydroxybenzoic acid substrates tested.

250 Consumption of amino acids such as arginine and tryptophan by immunoregulator

251 ic compounds by linking them to a glucuronic acid sugar for GI excretion.

252 the effect of omega-3 polyunsaturated fatty acid supplementation on clinical cardiovascular events,

253 evidence on the benefits and harms of folic acid supplementation.

254 ay, the Modified Carba NP assay, the boronic acid synergy test, and the metallo-beta-lactamase Etest,

255 -N-Acetyl-Glucosamine, as well as hyaluronic acid synthase which forms the disaccharide chain.

256 genes for cholesterol and unsaturated fatty acid synthesis.

257 ers of bovine serum albumin (BSA) and tannic acid (TA) were tested as Lf encapsulation system for ora

258 The antioxidant properties of trans-aconitic acid (TAA) alone or in the presence of usual antioxidant

259 cence-based biorthogonal non-canonical amino acid tagging (BONCAT) - for studying the activity and bi

260 e, we adapt bioorthogonal noncanonical amino acid tagging (BONCAT) to interrogate protein synthesis i

261 s in resource limited settings where nucleic acid testing is not practical or feasible.

262 effect of three antagonists, tetraiodoacetic acid (tetrac), triiodothyroacetic acid (triac) and 3-iod

263 it is controlled by a set of conserved amino acids that couple RNA and ATP binding to the protein (Mo

264 exible loop region containing aromatic amino acids, the caveolin-binding motif.

265 in combination cancer therapy using nucleic acids therapeutics for successful clinical translation.

266 a central growth regulator that senses amino acids through a pathway that converges on the Rag GTPase

267 n, the seeds were usually soaked in sulfuric acid to remove shells easily.

268 trafficking of the neuronal excitatory amino acid transporter 3 (EAAT3) blocks potentiation, suggesti

269 ntified increased translocation of the fatty acid transporter CD36 from its endosomal storage compart

270 as induction of potassium channels and amino acid transporters, derepression of genes marked with his

271 iodoacetic acid (tetrac), triiodothyroacetic acid (triac) and 3-iodothyronamine (T1AM), on cell proli

272 toward the shikimate-derived aromatic amino acids tyrosine and tryptophan.

273 ion of a photo-crosslinkable unnatural amino acid (UAA) cotranslationally incorporated into the paren

274 tert-butanesulfinyl aldimines with beta-keto acids under basic conditions at room temperature proceed

275 functions to integrate cholesterol and fatty acid uptake in Mtb.

276 rmed the functional relevance of these amino acids using a targeted mutagenesis strategy.

277 hlorogenic acid, caffeic acid and p-coumaric acid varied among species and found the maximum in Termi

278 ed in response to exogenously supplied fatty acids via the de novo synthesis of PA, a central metabol

279 ologically distinct models-in utero valproic acid (VPA) exposure, CNTNAP2 knockout and FMR1 knockout-

280 Valproic acid (VPA) is a proposed treatment for RP and other neur

281 best findings, while the use of 0.02% acetic acid was more appropriate in negative ionization mode.

282 inkage specific distribution of these sialic acids was quantitatively determined and unique for each

283 poration of a fluorescent noncanonical amino acid, we show that there is a rearrangement in the eag d

284 ics assays, whereby carotenoids and ascorbic acid were analyzed, not statistical differences between

285 Indospicine and 2-aminopimelic acid were more cytotoxic than arginine, displaying the h

286 , docosapentaenoic acid, and docosahexaenoic acid were observed.

287 tituent components; gallic acid and carnosic acid were the cause for the synthetic lethality.

288 Six hydroxycinnamic acids were identified and determined quantitatively in m

289 Fatty acids were influenced by breed and fertilizer applicatio

290 The fatty acids were quantified in rumen and plasma using targeted

291 Only natural amino acids were used as probes, and thus possible structural

292 l, especially for 20-hydroxyeicosatetraenoic acid, which has both vasoconstrictive and natriuretic ac

293 The enzyme interconverts d- and l-lactic acid, which is important for the assembly of cell walls

294 Glyphosate was converted into dithiocarbamic acid with CS2, followed by copper in the presence of amm

295 ective, copper-promoted couplings of boronic acids with carbohydrate derivatives.

296 iation between circulating C15:0/C17:0 fatty acids with disease risk, therefore, their origin needs t

297 TING protein define a novel cluster of amino acids with functional importance in the regulation of ty

298 in vascular occlusive events with tranexamic acid, with no heterogeneity by site of bleeding (p=0.595

299 g widespread delivery of therapeutic nucleic acids within brain tumors and provide a promising new de

300 steps along a pathway of redox active amino acids (Y122beta <--> [W48beta?] <--> Y356beta <--> Y731a

301 Conclusion With regard to optimizing nucleic acid yields in CT-guided lung core needle biopsies used