ライフサイエンスコーパス: butyric acid

1 compounds (acetone, butanol, propionic, and butyric acids).

2 response to biochemical differentiation with butyric acid.

3 enous auxins indole-3-acetic acid and indole-butyric acid.

4 er p-nitroaniline with the protonating agent butyric acid.

5 treatment with the exogenous auxin indole-3-butyric acid.

6 ced to differentiate toward eosinophils with butyric acid.

7 ll as reduced ability to utilize gamma-amino butyric acid.

8 ce with increased trend in the production of butyric acid.

9 and is resistant to the protoauxin indole-3-butyric acid.

10 ugh a two-carbon elongation forming indole-3-butyric acid.

11 thesis of indole-3-acetic acid from indole-3-butyric acid.

12 ed by acetic acid, followed by propionic and butyric acids.

13 in fatty acids (SCFAs) such as propionic and butyric acids.

14 s of SCFAs, including acetic, propionic, and butyric acids.

15 (range: 0-600 micromol) or the control odor butyric acid (0-1200 micromol) were presented to male Sp

16 tetradecanoylphorbol-13-acetate (30 nM) or n-butyric acid (0.3 mM) maximized the expression of lytic-

17 icromol/L), hydroxyurea (40 micromol/L), and butyric acid (0.5 mmol/L), significantly increase gamma-

18 r methyl mercaptan, 1 x 10(-3) mug/L air for butyric acid, 1 x 10(-4) mug/L air for p-cresol, 1 x 10(

19 , along with short chain fatty acids such as butyric acid (13 mg/g) explained the strong rancid, manu

20 ephrine ([(3)H]-NE]) and [(14)C]-gamma-amino-butyric acid ([(14)C]-GABA) from brain regions known to

21 reonine, 5.4%; D-valine, 3.4%; alpha-amino-n-butyric acid, 14%; alanine, 1.0%; and glycine, 0.32%.

22 Additionally, a co-drug, butyric acid 2-(2-butyryloxyethoxy) ethyl ester (BA-DEG-

23 nt peroxisomal processes, including indole-3-butyric acid/2,4-dichlorophenoxybutyric acid oxidation,

24 stress with the chemical chaperone 4-phenyl butyric acid (4-PBA).

25 z)]2+ (phen = 1,10-phenanthroline, bpy' = 4-(butyric acid)-4'-methyl-2,2'-bipyridine, and dppz = dipy

26 9,10-phenanthrenequinone diimine; bpy' = 4-(butyric acid)-4'-methyl-2,2'-bipyridine], provides DNA b

27 olic auxins and compounds including indole-3-butyric acid, 4-chloro-indole-3-acetic acid, and indole-

28 The plant growth regulators indole-butyric acid, 6-benzylaminopurine, and kinetin were also

29 tidine-2-carbonyl]-(3-chloro -benzyl)-amino]-butyric acid 99 (GLPG0974), is able to inhibit acetate-i

30 Importantly, 4-phenyl butyric acid, a chemical protein folding and trafficking

31 idopsis chy1 mutant is resistant to indole-3-butyric acid, a naturally occurring form of the plant ho

32 d lipids in the cytoplasm when cultured with butyric acid, a principal short-chain fatty acid in the

33 We examined the role of butyric acid, a short-chain fatty acid formed by ferment

34 beta3-containing subunit of the gamma-amino butyric acid-A receptor is likely to have the hypnotic e

35 showed differences mainly in acetic acid and butyric acid able to discriminate the groups Afmid and C

36 acing Cys 5, 30, 51, and 55 by alpha-amino-n-butyric acid (Abu) while retaining the disulfide between

37 e peptide synthesis to prepare alpha-amino-n-butyric acid (Abu)-PLB, the analogue in which all three

38 Cells treated with butyric acid acquired eosinophil characteristics; expres

39 contemporaneous facilitation of gamma-amino-butyric acid activity and inhibition of glutamate functi

40 d -730 A gamma were treated with alpha amino butyric acid (alpha ABA), and effects on gamma globin ex

41 with variants in the inhibitory gamma-amino butyric acid alpha2 receptor subunit (GABRA2) gene.

42 mate, aspartate) and inhibitory (gamma-amino butyric acid) amino acid neurotransmitters in brain, and

43 c acid, and resistance to protoauxins indole-butyric acid and 2,4-dichlorophenoxybutyric acid.

44 discovered that chemical chaperone 4-phenyl butyric acid and antioxidant N-acetylcysteine, which sig

45 Acetic acid, butyric acid and cyclohexanol with vinegar, cheese and c

46 y of CCR3, HL-60 clone 15 cells induced with butyric acid and IL-5 fused with HeLa cells expressing C

47 Treatment of the cell line with butyric acid and IL-5 results in a dose-dependent synerg

48 ctivity could rescue HLA-DR gene expression, butyric acid and MS-275, inhibitors of HDAC activity, we

49 ncharged carboxylic acid concentration for n-butyric acid and n-caproic acid at exposure times of 2,

50 ecal material as substrate, we accumulated n-butyric acid and n-caproic acid at total concentrations

51 e platform and chain elongation to produce n-butyric acid and n-caproic acid via the anaerobic fermen

52 o IAA, dfl1-D was less sensitive to indole-3-butyric acid and naphthaleneacetic acid, consistent with

53 analogs of these amino acids, alpha-amino-n-butyric acid and norvaline, were found to be racemates.

54 4-Phenyl butyric acid and taurine-conjugated ursodeoxycholic acid

55 , including toll-like receptors, gamma amino butyric acid and the lens protein alpha B crystallin, ha

56 ebellar neurotransmitters, GABA (gamma-amino-butyric acid) and glutamate are involved in the modulati

57 e, organophosphates, 4-[2,4-dichlorophenoxy] butyric acid, and insecticides) generated odds ratios of

58 of formic acid, acetic acid, propionic aicd, butyric acid, and pentanoic acid.

59 e oxidase (GOD) and poly[aniline-co-N-(1-one-butyric acid) aniline] (SPAnH) were then incorporated to

60 lic acids such as mandelic acid and alpha-Br-butyric acid are identified as promising compounds for t

61 ic acids (e.g., lactic acid, propionic acid, butyric acid) are metabolic by-products of bacterial met

62 of novel uracil phenylethylamines bearing a butyric acid as potent human gonadotropin-releasing horm

63 However propanoic, acetic and butyric acid as well as aldehydes compounds, phenol and

64 ed in STC colon tissue, and the abundance of butyric acid (BA) in colonic contents was significantly

65 Because butyric acid (BA) is the major short-chain fatty acid pr

66 r odor (cat fur) and a repulsive novel odor, butyric acid (BA), to awake rats.

67 parent ATRA and over 100000-fold lower than butyric acid (BA).

68 coating was used for propionic acid (PA) and butyric acid (BA).

69 rom lettuce leaves caused by dl-beta-amino-n-butyric acid (BABA) elicitation.

70 that had been either primed with beta-amino-butyric acid (BABA) or with an avirulent isolate of the

71 ginine, lysine, ornithine, and 2,4-diamino-n-butyric acid but not by 2,3-diaminopropionic acid.

72 ne tris-acid ethyl ester, [6,6]-Phenyl-C(61) butyric acid butyl ester and [6,6]-Thienyl C(61) butyric

73 -butyric acid methyl ester, [6,6]-phenyl-C61-butyric acid butyl ester, [6,6]-phenyl-C61-butyric acid

74 ory effect on beta-globin mRNA levels, while butyric acid caused a twofold inhibition of beta-globin

75 od for quantitation of gamma-(cholesteryloxy)butyric acid (CBA), a relatively new antitumor agent, in

76 of butyrate-producing bacteria and decreased butyric acid concentration in the cecum.

77 The propionic and butyric acid concentrations also associated significantl

78 The propionic and butyric acid concentrations were below detection limits

79 y or prevention, significantly increased the butyric acid content in the cecum and arrested hyperglyc

80 In BF infants higher levels of butyric acid, d-sphingosine, kynurenic acid, indole-3-la

81 Oleic acid, arachidonic acid, and butyric acid did not interact.

82 mpted alkylations of 2-(4-carboxy-1-naphthyl)butyric acid dimethyl ester with 1a failed as did attemp

83 n colon that was identified as a producer of butyric acid during growth on glucose, starch, or inulin

84 at drugs like hydroxyurea, 5-azacytidine and butyric acid each yielded increases in gamma/( gamma + s

85 rphology, electrophysiology, and gamma-amino-butyric acid expression.

86 mbedding immunocytochemistry for gamma-amino butyric acid (GABA) and glutamate.

87 s a rich drug affecting both the gamma-amino butyric acid (GABA) and glutamatergic neurotransmitter s

88 gonist SR 48692 on extracellular gamma-amino-butyric acid (GABA) and glycine in the striatum.

89 ate nucleus that also synthesize gamma-amino-butyric acid (GABA) and neuropeptide Y in adult mice lea

90 immunocytochemical staining for gamma amino butyric acid (GABA) and parvalbumin (PV) to characterize

91 ellular protons, and a glutamate:gamma-amino butyric acid (GABA) anti-porter (GadC) to expel GABA in

92 d gadB) and a putative glutamate:gamma-amino butyric acid (GABA) antiporter (gadC).

93 ound in both pyramidal cells and gamma-amino butyric acid (GABA) cells; GluR2/3 immunoreactivity is p

94 ding of real words is related to gamma-amino-butyric acid (GABA) concentration in the higher-order la

95 Gamma-butyric acid (GABA) dysfunction has been implicated in t

96 istribution of glycine (GLY) and gamma-amino butyric acid (GABA) immunoreactivities in the guinea pig

97 Here, we describe a role for gamma-amino butyric acid (GABA) in pollen tube growth and guidance.

98 The non-protein amino acid gamma-amino butyric acid (GABA) is produced by Arabidopsis and tomat

99 The inhibitory neurotransmitter gamma-amino butyric acid (GABA) is synthesized by two isoforms of th

100 be elucidated, noradrenergic and gamma-amino-butyric acid (GABA) neurones are implicated in the syste

101 2* nAChRs in VTA dopamine or VTA gamma-amino-butyric acid (GABA) neurons in beta2(-/-) mice to double

102 aling neuropeptide and marker of gamma-amino butyric acid (GABA) neurons, which specifically inhibit

103 s, and neurotransmitters such as gamma amino butyric acid (GABA) on neuronal and vascular development

104 uch as glycine, beta-alanine and gamma-amino-butyric acid (GABA) produce rapid transport and site sel

105 ments evaluated the role of RVLM gamma-amino butyric acid (GABA) receptor subtypes and glycine recept

106 Ionotropic gamma-amino butyric acid (GABA) receptors composed of heterogeneous

107 ay an important role in regulating g-amino-n-butyric acid (GABA) release from striatopallidal termina

108 artate show no such change while gamma-amino-butyric acid (GABA) shows a minor elevation.

109 precipitation studies identified gamma-amino butyric acid (GABA) type B receptor 2 (GABA(B)R2) as an

110 In tissue stained for gamma amino butyric acid (GABA) using postembedding immunocytochemic

111 ng 3 neurotransmitter systems--gamma-amino-n-butyric acid (GABA), dopamine, and serotonin--as well as

112 ate inhibitory neurotransmitter, gamma-amino butyric acid (GABA), has been limited by the propensity

113 Thus, we postulated that gamma-amino butyric acid (GABA)- and acetylcholine (ACh)-related gen

114 CPP-115, a next-generation gamma-amino butyric acid (GABA)-aminotransferase (AT) inhibitor, sho

115 formation through inhibition of gamma-amino butyric acid (GABA)-containing interneurons.

116 In addition, gamma-amino butyric acid (GABA)-ergic neurons were observed within t

117 optic tract and 93.1% contained gamma amino butyric acid (GABA).

118 re blocked by pre-injection with gamma-amino-butyric acid (GABA).

119 protein, muscimol binding to the gamma-amino butyric acid (GABA)A receptor, and levels of glutamic ac

120 We conclude that 1) if distinct gamma-amino butyric acid (GABA)ergic and cholinergic subclasses of l

121 3H-glutamate and 14C-gamma-amino-butyric-acid (GABA) release from isolated nerve terminal

122 (DSI) is a form of plasticity of gamma-amino-butyric acid (GABAA)-mediated (henceforth 'GABAergic') r

123 cholinergic) and those producing gamma-amino butyric acid (GABAergic).

124 ne, alanine, beta-alanine, and gamma-amino-n-butyric acid (gamma-ABA) were the most abundant amino ac

125 ed to be gated by acetylcholine, gamma-amino butyric acid, glutamate and histamine, as well as orthol

126 Arginine, citruline, gamma-amino butyric acid, glutamic acid, and aspartic acid always re

127 neurotransmitters, such as GABA (gamma-amino butyric acid), glycine, glutamate, ACh (acetylcholine) a

128 ducts possessing nine amino acid residues, a butyric acid group, and an internal acetate-derived unit

129 form exfoliated graphene with grafted 1-one-butyric acid (Gs-BA).

130 to form from propionic acid (H3CCH2COOH) and butyric acid (H3CCH2CH2COOH), respectively, on a catalys

131 no-3-carboxy-propylsulfanylmercuricsulfanyl) butyric acid (Hcy-S-Hg-S-Hcy).

132 ino-3-carboxy-propylsulfanylmercuricsulfanyl)butyric acid; Hcy-S-Hg-S-Hcy) are similar structurally,

133 defined composition with supplements such as butyric acid, hormones, growth factors, and other metabo

134 lar transport of the natural auxins indole-3-butyric acid (IBA) and indole-3-acetic acid (IAA) has be

135 Indole-3-butyric acid (IBA) is an endogenous auxin that acts in A

136 Indole-3-butyric acid (IBA) is an endogenous auxin used to enhanc

137 ) suggests that the auxin precursor indole-3-butyric acid (IBA) is converted into active indole-3-ace

138 Genetic evidence suggests that indole-3-butyric acid (IBA) is converted to the active auxin indo

139 Indole-3-butyric acid (IBA) is widely used in agriculture because

140 istant to the inhibitory effects of indole-3-butyric acid (IBA) on root elongation, but only lon2 mut

141 d a low dose of the auxin precursor indole-3-butyric acid (IBA) stimulated LRF in Brachypodium, while

142 Conversion of the auxin precursor indole-3-butyric acid (IBA) to active auxin (indole-3-acetic acid

143 on in the peroxisomal conversion of indole-3-butyric acid (IBA) to indole-3-acetic acid, because ech2

144 conversion of the endogenous auxin indole-3-butyric acid (IBA) to the active hormone indole-3-acetic

145 ecause it is resistant to the auxin indole-3-butyric acid (IBA), developmentally arrests when germina

146 of other endogenous auxins, such as indole-3-butyric acid (IBA), in Arabidopsis.

147 se haptenated peptides, Tax-5K-4-(3-Indolyl)-butyric acid (IBA), presented by HLA-A*0201.

148 inity column was prepared by coupling indole butyric acid (IBA), which has a monovalent affinity for

149 er of storage precursors, including indole-3-butyric acid (IBA), which is apparently shortened to act

150 One auxin precursor is indole-3-butyric acid (IBA), which undergoes peroxisomal beta-oxi

151 tic stress responses to cadmium and indole-3-butyric acid (IBA)-mediated auxin homeostasis in roots,

152 that suppressed ibr5 resistance to indole-3-butyric acid (IBA): those with restored responses to bot

153 h specificity for the conjugates of indole-3-butyric acid (IBA-Ala and IBA-Gly) and indole-3-propioni

154 Acetic, propionic, and butyric acid improved the ESI(-) responses of analytes t

155 the in vivo concentrations of propionic and butyric acid in the gingival crevices of periodontal sub

156 of either cysteine residue with alpha-amino butyric acid in the gp100 peptide, RLPRIFCSC, enhanced C

157 centrations of lactic, acetic, propionic and butyric acids in sour cassava starch wastewater using re

158 rats were exposed to TMT, or a control odor, butyric acid, in an open field.

159 as alpha-naphthalene acetic acid and indole-butyric acid increased the root dry weight of hydroponic

160 Applied auxin (indole-3-butyric acid) increased adventitious root formation on v

161 f amino acids, including Ala and gamma-amino butyric acid, indicating a role of oxygen-regulated RAP2

162 luorfen and the abiotic elicitor alpha-amino butyric acid induced responses similar to those induced

163 also diminished expression of GATA-1 in both butyric acid-induced HL-60 clone 15 cells and in differe

164 The profile of butyric-acid-induced changes on globin gene expression i

165 With ethanol as the alcohol substrate, added butyric acid inhibited ester synthesis.

166 onclassical peroxisome proliferator 4-phenyl butyric acid is an efficient inducer of peroxisomes in v

167 lysed for SCFA (acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, and isovale

168 Glu) receptor agonists L-2-amino-4-phosphono-butyric acid (L-AP4) and O-phospho-L-serine (L-SOP) both

169 tivity and led to an increase in gamma-amino butyric acid levels.

170 Rats were exposed to either caproic acid, butyric acid, limonene, or purified air and the spatial

171 (6) neurotransmitter metabolism (gamma-amino-butyric acid: lower in AD, p < 0.001).

172 2,3-diamino-L-propionic acid < 2,4-diamino-L-butyric acid < ornithine < lysine.

173 1(+/-) mice have increased GABA (gamma-amino butyric acid)-mediated inhibition and specific deficits

174 optimized solar cells with [6,6]phenyl-C(71)-butyric acid methyl ester ([70]PCBM) as acceptor, the ne

175 rojunction solar cells with [6,6]-phenyl-C71-butyric acid methyl ester ([70]PCBM) as acceptor.

176 ting copolymer (PDPP5T) and [6,6]-phenyl-C71-butyric acid methyl ester ([70]PCBM) cast from chlorofor

177 yric acid methyl ester, and [6,6]-phenyl-C71-butyric acid methyl ester ([70PCBM], in different aqueou

178 purified from an as-produced bis-phenyl-C61 -butyric acid methyl ester (bis-[60]PCBM) isomer mixture

179 isadduct (ICBA) or indene-[6,6]-phenyl-C(61)-butyric acid methyl ester (IPCBM) as the acceptor in the

180 ndem devices using the PDTIDTBT:Phenyl-C(61)-butyric acid methyl ester (PC(60)BM) blend in both serie

181 composite NPs of P3HT and [6,6]-phenyl-C(61)-butyric acid methyl ester (PC(60)BM) that is absent for

182 wo soluble fullerene acceptors, phenyl-C(61)-butyric acid methyl ester (PC(61)BM) and indene-C(60) bi

183 opyrrole) (P3HTT-DPP-10%), with phenyl-C(61)-butyric acid methyl ester (PC(61)BM) as an acceptor were

184 tigated in conjunction with [6,6]-phenyl-C61-butyric acid methyl ester (PC(61)BM) or [6,6]-phenyl-C71

185 -c-HBC) as a donor material and phenyl-C(70)-butyric acid methyl ester (PC(70)BM) as an acceptor.

186 iency of 4.2% for a PDHTT:[6,6]-phenyl-C(71)-butyric acid methyl ester (PC(71)BM) blend solar cell wi

187 aline), which when blended with phenyl-C(71)-butyric acid methyl ester (PC(71)BM) is capable of achie

188 hiadiazole)] (PCDTBT) and [6,6]-phenyl C(71) butyric acid methyl ester (PC(71)BM) were chosen for the

189 methyl ester (PC(61)BM) or [6,6]-phenyl-C71-butyric acid methyl ester (PC(71)BM).

190 Using phenyl-C61-butyric acid methyl ester (PC60BM) as an electron accept

191 ared to fullerene benchmark [6,6]-phenyl-C60-butyric acid methyl ester (PC60BM), and there are as yet

192 ance of similarly evaluated [6,6]-Phenyl-C61-butyric acid methyl ester (PC60BM)/PSEHTT devices.

193 eved with devices based on [6,6]-phenyl-C61 -butyric acid methyl ester (PC61 BM).

194 r the fullerene derivative, [6,6]-phenyl C71 butyric acid methyl ester (PC71 BM) as electron acceptor

195 from the BTTT oligomers and [6,6]-phenyl C71-butyric acid methyl ester (PC71BM) blends, the ones cont

196 TFTs were fabricated with [6,6]-phenyl-C(61) butyric acid methyl ester (PCBM) and Au source and drain

197 e derivatives such as [6,6]-phenyl-C61 or 71-butyric acid methyl ester (PCBM) are the ideal n-type ma

198 n blends of CuPC doped with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as the electron accepto

199 OPV cells using [6,6]-phenyl C(61)-butyric acid methyl ester (PCBM) as the electron accepto

200 ol polymer-fullerene devices with phenyl-C61-butyric acid methyl ester (PCBM) as the electron accepto

201 ology, and interaction with [6,6]-phenyl C61-butyric acid methyl ester (PCBM) as the molecular conjug

202 e OPVs based on the PDTIDTBT:Phenyl-C(61/71)-butyric acid methyl ester (PCBM) blend with maximum powe

203 f the blend film of HTCGemini and phenyl-C61-butyric acid methyl ester (PCBM) generates a prominent p

204 fer and separation at PbS QDs and phenyl-C61-butyric acid methyl ester (PCBM) interfaces using a comb

205 ne benzodithiophene) (PTB1)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is reported.

206 he poly(3-hexyl-thiophene) (P3HT)-phenyl-C61-butyric acid methyl ester (PCBM) mixture, and found to p

207 in the absence of the acceptor phenyl-C(61)-butyric acid methyl ester (PCBM) molecules.

208 and in blends (1:2) with [6,6]-phenyl-C(61)-butyric acid methyl ester (PCBM) on the use of the solve

209 hexylthiophene (P3HT) and [6,6]-phenyl-C(61)-butyric acid methyl ester (PCBM) photovoltaic blend thin

210 s in poly(3-hexylthiophene)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) photovoltaics.

211 ynthesized and blended with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) to function as an effic

212 n-channel semiconductor, [6,6]-phenyl C(61) butyric acid methyl ester (PCBM), can be effectively dop

213 3,2-b]thiophene (PBTTT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), to acquire a more comp

214 ganic solar cells using open-cage phenyl C61 butyric acid methyl ester (PCBM)-modified zinc oxide lay

215 relative to the blend with [6,6]-phenyl C61-butyric acid methyl ester (PCBM).

216 the fullerene derivative, [6,6]-phenyl-C(61)-butyric acid methyl ester (PCBM).

217 lectron acceptors such as (6,6)-phenyl C(61)-butyric acid methyl ester (PCBM).

218 ullerene (C60) and its derivative phenyl-C61-butyric acid methyl ester (PCBM).

219 -thiophene/benzodithiophene:[6,6]-phenyl C71-butyric acid methyl ester (PTB7:PC70 BM) solar cells can

220 2-carboxylate] as donor and [6,6]-phenyl-C71-butyric acid methyl ester as acceptor.

221 evice with poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester as an active layer and poly(3,

222 nt system compared to the use of phenyl-C71 -butyric acid methyl ester as an electron acceptor is sho

223 The carbonyl (C=O) stretch of the butyric acid methyl ester group of a functionalized full

224 bove 7% when blended with [6,6]-phenyl C(61)-butyric acid methyl ester in a typical bulk heterojuncti

225 -conducting species such as [6,6]-phenyl C61 butyric acid methyl ester in the periodic mesopores.

226 in combination with PCBM ([6,6]-phenyl C(61)-butyric acid methyl ester) as an electron acceptor based

227 nalized fullerenes, namely, [6,6]-phenyl-C61-butyric acid methyl ester, [6,6]-phenyl-C61-butyric acid

228 yric acid octyl ester, [6,6]-bis(phenyl)-C61-butyric acid methyl ester, [6,6]-thienyl-C61-butyric aci

229 butyric acid methyl ester, [6,6]-thienyl-C61-butyric acid methyl ester, and [6,6]-phenyl-C71-butyric

230 ric acid butyl ester and [6,6]-Thienyl C(61) butyric acid methyl ester, in airborne particulate from

231 luble fullerene derivative ([6,6]-phenyl C61-butyric acid methyl ester, PCBM), both blend morphology

232 or its soluble derivative, [6,6]-phenyl-C(61)butyric acid methyl ester, PCBM, have been studied by on

233 e 19 structural isomers of bis[60]phenyl-C61-butyric acid methyl ester, using them to elucidate impor

234 ith the electron acceptor [6,6]-phenyl-C(70)-butyric acid methyl ester.

235 oximately 4% in blends with [6,6]-phenyl-C61-butyric acid methyl ester.

236 ,1,3-benzothiadiazole)] and [6,6]-phenyl-C71-butyric acid methyl ester.

237 PTB1 and methanofullerene [6,6]-phenyl-C(71)-butyric acid methyl esters (PC(71)BM) exhibit a solar co

238 thiophene) (P3HT) donor and [6,6]-phenyl-C61-butyric acid methylester (PCBM) acceptor layers as the d

239 ved in fullerene-derivative [6,6]-phenyl-C71-butyric acid methylester-based Schottky junction devices

240 The difference between propionic and butyric acid (mmol/l) had the best diagnostic properties

241 peptide, substance P, serotonin, gamma-amino-butyric acid, neurokinins A and B, neurotensin, neuropep

242 ing auxins indole-3-acetic acid and indole-3-butyric acid, nor the synthetic auxin analogs 1-naphthal

243 1-butyric acid butyl ester, [6,6]-phenyl-C61-butyric acid octyl ester, [6,6]-bis(phenyl)-C61-butyric

244 2,3-diamino-L-propionic acid, 2, 4-diamino-L-butyric acid or L-ornithine, have been examined using ci

245 actor (TNF)-alpha, interleukin (IL)-1beta, n-butyric acid, or a cAMP analogue resulted in a 103- to 1

246 ristic analysis for the cancer-specific VFAs butyric acid ( P < 0.001) and pentatonic acid ( P = 0.00

247 We used fluorescent probe molecules, pyrene butyric acid (PBA), as guests in C-hexylpyrogallol[4]are

248 tant mice with the chemical chaperone phenyl butyric acid (PBA), which reduced adult ICH.

249 istered with 0.5 g/kg bodyweight of 4-phenyl butyric acid (PBA, a small chaperone known to ease endop

250 lactate platform to produce 196 kilograms of butyric acid per metric ton of beechwood.

251 The novel prodrug of butyric acid, pivaloyloxymethyl butyrate (AN-9), a histo

252 s much reduced in the Arabidopsis beta-amino-butyric acid priming mutant ibs1 (induced BABA sterility

253 Peroxisomal metabolism of indole-3-butyric acid, propionate, and isobutyrate also is disrup

254 ably demonstrate that a shift in gamma-amino-butyric acid receptor B (GABABR) function, from inhibito

255 the Glutamate-family GPCR dimer, gamma-amino butyric acid receptor b2, whereas two Rhodopsin-family G

256 sthetics, which act primarily as gamma-amino-butyric acid receptor modulators and N-methyl-D-aspartic

257 The treatment with muscimol, a gamma amino butyric acid receptor-A (GABA(A)) agonist, mitigates the

258 ger mode of approximately GABAb (gamma amino butyric acid receptor-type b) duration.

259 cal stimulation or puffing GABA (gamma-amino butyric acid) receptor blockers in the inner retina also

260 All compounds, except Indole-3-butyric acid, repressed the recovery of the PIN2-Dendra2

261 ys55 are replaced by isosteric alpha-amino-n-butyric acid residues.

262 We isolated ibr5 as an Arabidopsis indole-3-butyric acid-response mutant, but it also is less respon

263 BA-to-IAA conversion, including the indole-3-butyric acid response1 (ibr1) ibr3 ibr10 triple mutant,

264 y intramolecular hydrogen bonding in the bis-butyric acid rubin (1b).

265 l)-amino]-ethyl)-carbamoyl)-2-decanoylami no butyric acid (SC-alpha alpha delta 9), was previously id

266 +/- 1.8 mM, and mild = 0.8 +/- 0.3 mM; mean butyric acid-severe = 2.6 +/- 0.4 mM, and mild = 0.2 +/-

267 had little effect on apoptosis (P>0.05), but butyric acid significantly accelerated apoptotic changes

268 ihydro-2H-pyrimidin-1-yl]-1-phenylethylamino}butyric acid sodium salt, 10b (elagolix), was identified

269 no-9-benzyl-8-hydroxy-9H-purin-2-ylsulfanyl)-butyric acid succinimidyl ester was analyzed by using ma

270 most efficient enzymes for the activation of butyric acid (Taxol D side chain), TmAAE13 as the best c

271 Interestingly, short chain fatty acids (butyric acid), the product of lactic acid bacteria (LAB)

272 lication of the chemical elicitor beta-amino butyric acid, the non-pathogenic bacteria Pseudomonas fl

273 With the exception of alpha-amino-n-butyric acid, these amino acids are either unknown or of

274 This was confirmed by exogenously adding butyric acid to 824(pAADB1) fermentations to increase th

275 acterized in vitro by delivering gamma-amino butyric acid to a target solution, and demonstrates low-

276 ways, converting IAA conjugates and indole-3-butyric acid to free IAA.

277 is of jasmonic acid and conversion of indole butyric acid to indole acetic acid.

278 esults from a reduced conversion of indole-3-butyric acid to indole-3-acetic acid.

279 hibits the increase of betaine/gamma-amino-n-butyric acid transporter 1 and heat shock protein 70 mRN

280 nes (aldose reductase, betaine/gamma-amino-n-butyric acid transporter 1, and heat shock protein 70) i

281 se of the inhibitory glycine and gamma-amino-butyric acid type A (GABA(A)) receptors this interaction

282 While gamma amino-butyric acid Type A (GABAA) receptors are the primary mo

283 as they allosterically modulate gamma-amino-butyric acid type A (GABAA) receptors.

284 Expression of gamma-amino butyric acid type B (GABA[B]) receptor gene transcripts

285 entation of TMT (> or =75 micromol), but not butyric acid (up to 1200 micromol), significantly increa

286 fatty acids (SCFAs, including propionic and butyric acids) using Pickering emulsions stabilised by h

287 s (formic acid, acetic acid, propionic acid, butyric acid, valeric acid, isovaleric acid, and trimeth

288 or formic acid, acetic acid, propionic acid, butyric acid, valeric acid, isovaleric acid, and trimeth

289 Serum values for a-amino-butyric acid, valine, isoleucine, leucine, tyrosine, phe

290 a small molecule 4-[N-(1,8-naphthalimide)]-n-butyric acid, virstatin, that inhibits virulence regulat

291 tested, 4-[4-[(2-hydroxybenzoyl)amino]phenyl]butyric acid was identified as a preclinical candidate a

292 eurons to the neurotransmitter gamma-amino-n-butyric acid was normal, the response of these same neur

293 bstrate, no significant inhibitory effect by butyric acid was observed.

294 while the capability of producing SCFAs and butyric acid was superior to the control rice noodles; t

295 crystal MALDI matrix of paranitroaniline and butyric acid was used to enhance the mass spectral respo

296 ids (VFAs) were produced and acetic acid and butyric acid were the key components.

297 S)-[10(alpha or beta)-dihydroartemisininoxy]butyric acids were synthesized as new potential antimala

298 xy) ethyl ester (BA-DEG-BA), released active butyric acid when it was intradermally injected into mou

299 y screening for reduced response to indole-3-butyric acid, which is metabolized to active auxin in pe

300 lolly pine seedlings in response to indole-3-butyric acid, with peak expression occurring 24 to 48 h