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

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

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

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

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

17 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(

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

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

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

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

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

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

24 9,10-phenanthrenequinone diimine; bpy' = 4-(butyric acid)-4'-methyl-2,2'-bipyridine], provides DNA b

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

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

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

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

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

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

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

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

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

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

35 Cells treated with butyric acid acquired eosinophil characteristics; expres

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 4-Phenyl butyric acid and taurine-conjugated ursodeoxycholic acid

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 The propionic and butyric acid concentrations also associated significantl

71 The propionic and butyric acid concentrations were below detection limits

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 3H-glutamate and 14C-gamma-amino-butyric-acid (GABA) release from isolated nerve terminal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 2,3-diamino-L-propionic acid < 2,4-diamino-L-butyric acid < ornithine < lysine.

156 1(+/-) mice have increased GABA (gamma-amino butyric acid)-mediated inhibition and specific deficits

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

194 3,2-b]thiophene (PBTTT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), to acquire a more comp

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

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

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

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

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

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

201 2-carboxylate] as donor and [6,6]-phenyl-C71-butyric acid methyl ester as acceptor.

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

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

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

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

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

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

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

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

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

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

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

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

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

215 ,1,3-benzothiadiazole)] and [6,6]-phenyl-C71-butyric acid methyl ester.

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

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

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

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

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

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

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

223 1-butyric acid butyl ester, [6,6]-phenyl-C61-butyric acid octyl ester, [6,6]-bis(phenyl)-C61-butyric

224 2,3-diamino-L-propionic acid, 2, 4-diamino-L-butyric acid or L-ornithine, have been examined using ci

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

242 +/- 1.8 mM, and mild = 0.8 +/- 0.3 mM; mean butyric acid-severe = 2.6 +/- 0.4 mM, and mild = 0.2 +/-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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