ライフサイエンスコーパス: taurine

1 ating taurine) to >1.6 mM (after conjugating taurine).

2 solution of naphthalene dialdehyde (NDA) and taurine.

3 radiolabelled d-[(14) C]aspartate and [(3) H]taurine.

4 glycine, pyruvate, and the Ca(2+) regulator taurine.

5 ogic evidence of rapid reepithelization with taurine.

6 ulates the agonist properties of glycine and taurine.

7 ue to GAT2, and this uptake was inhibited by taurine.

8 2-transfected HEK293 cells transported [(3)H]taurine.

9 pha-CEHC glycine glucuronide, and alpha-CEHC taurine.

10 the oxo group and the C1 proton of substrate taurine.

11 a result of the efflux of the intracellular taurine.

12 ximately 295 nm is identified for binding of taurine.

13 nitine, thiamine, and amino acids, including taurine.

14 zed cysteine metabolites such as sulfate and taurine.

15 ansporter which accepts beta-alanine but not taurine.

16 either protonated or specifically deuterated taurine.

17 ures, which can be related to the amino acid taurine.

18 mited permeability to Na+ and the zwitterion taurine.

19 d neurotransmitters glutamate, aspartate and taurine.

20 the endogenous intracellular L-glutamate and taurine.

21 w breeds that shared ancestry with the Asian taurines.

22 Low concentrations of taurine (10-100 microM) decreased neuronal input resista

23 eased dramatically including glycine (700%), taurine (185%), and serine (215%).

24 Taurine (2-aminoethanesulphonic acid) is an amino acid-l

25 its detection limits of 21 nM silicate, 3 nM taurine, 3 nM sulfide, and 13 nM cyanide.

26 he density in the mature neurons, except for taurine; 4) under hypoxia, all these amino acids decreas

27 tion, 27 metabolites (tryptophan, serotonin, taurine, 8 acylcarnitines, 13 glycerophospholipids, and

28 h sexes were a decrease in concentrations of taurine (a major organic osmolyte), carnitine (involved

29 Here we show that taurine, a natural amino acid, drastically boosts the ce

30 The physiological roles of taurine, a product of cysteine degradation and one of th

31 uration behavior with considerable levels of taurine accumulation inside the cells (as much as 40% of

32 ree possible substrates of NAT biosynthesis (taurine, acetyl-CoA, and acetate), the level of taurine

33 n sum, this study provides new evidence that taurine activates a serotonin system, apparently via 5-H

34 N-terminal taurine acylations allowed synthesis of a number of taur

35 attack by N(2)O(3); (iii) the nitrosation of taurine affords ethanesultone (ES), which displays alkyl

36 ng three pairwise comparisons among European taurine, African taurine, and indicine groups, we furthe

37 urinary clearance of beta-PEA, agmatine and taurine after oral intake by healthy individuals demonst

38 capping moiety was shown to be comprised of taurine, alanine, and glycine.

39 Residue F159 in taurine alpha-ketoglutarate dioxygenase (TauD) is demons

40 Taurine alpha-ketoglutarate dioxygenase (tauD) is one of

41 te taurine and the non-heme Fe(II) center of taurine/alpha-ketoglutarate (alphaKG) dioxygenase (TauD)

42 Taurine, an agonist of glycine receptor chloride (GlyR C

43 e we tested the hypothesis that supplemental taurine, an amino acid that functions as a chemical chap

44 the treatment of alcohol withdrawal, and by taurine, an ingredient of certain 'energy drinks' often

45 ch differences are observed for the European taurine ancestry (P=0.1357).

46 imals (n=425) show an unfluctuating zebu and taurine ancestry of 0.84+/-0.009 s.d. and 0.16+/-0.009 s

47 tions of tissues and cellular fractions with taurine and acetate indicated that the kidney has the hi

48 e expressed in human embryonic kidney cells, taurine and AL34662, a non-specific 5-HT(2) receptor act

49 , high-affinity, low-capacity transporter of taurine and beta-alanine; ATB(0,+) (SLC6A14) is a Na(+)-

50 low-affinity, high-capacity transporter for taurine and beta-alanine; TauT (SLC6A6) is a Na(+)- and

51 he contents of free hydrophobic amino acids, taurine and carnosine/anserine were elevated after hydro

52 of a large amount of the ester conjugate of taurine and D-peptide allows intracellular esterase to t

53 which gives antioxidant metabolites such as taurine and glutathione.

54 icity and oxidative stress including reduced taurine and glutathione; (3) inhibition of several devel

55 metabolism, aminoacyl-tRNA biosynthesis and taurine and hypotaurine metabolism were enriched after P

56 e the accuracy of future CNV studies in both taurine and indicine cattle.

57 ope, actually exhibit ancestry from both the taurine and indicine lineages.

58 rope and the Indian subcontinent resulted in taurine and indicine lines of cattle, respectively.

59 neurochemical markers of neuronal function, taurine and lactate, suggesting altered PFC metabolism i

60 ed release of the uncharged osmolytes [(3) H]taurine and myo-[(3) H]inositol, without major impact on

61 the antioxidant enzyme, catalase, as well as taurine and N-acetyl-cysteine attenuate the TNF-alpha-in

62 tions of the concurrence of high contents of taurine and nitrite/nitrate in the diet.

63 We speculate that organic osmolytes such as taurine and possibly novel processes such as extracellul

64 be attributed to the increased production of taurine and reduced glutathione.

65 ation products, as well as N-acetylcysteine, taurine and sulfo-conjugates in both rats and humans.

66 he structural relationship between substrate taurine and the non-heme Fe(II) center of taurine/alpha-

67 neration was demonstrated by chlorination of taurine and tyrosine using mass spectrometry.

68 ry of these populations with the presence of taurine and zebu genetic backgrounds.

69 rachidonoyl dopamine), NATau (N-arachidonoyl taurine), and NA-5HT (N-arachidonoyl serotonin), all dis

70 ated unusual hepatic amino acid, fatty acid, taurine, and carnitine profiles.

71 ysfunction in pathway of amino acid, purine, taurine, and choline metabolisms.

72 d on the reaction of naphthalene dialdehyde, taurine, and cyanide, yielding a fluorescent beta-isoind

73 o acids, including glutamate, GABA, glycine, taurine, and D-serine, in 21.5 s.

74 ed glutamate, aspartate, glutamine, alanine, taurine, and GABA.

75 ine to cysteine, a precursor of glutathione, taurine, and H2S.

76 ine to cysteine, a precursor of glutathione, taurine, and H2S.

77 comparisons among European taurine, African taurine, and indicine groups, we further identified 78 u

78 A panel of 4 biomarkers-formate, citrulline, taurine, and isocitrate-were identified as markers of SS

79 trong hard-sphere-like self-exclusion; urea, taurine, and myo-inositol have a tendency toward self-as

80 ake of compatible osmolytes such as betaine, taurine, and myo-inositol is a protective response share

81 coefficients of glycerophosphocholine (GPC), taurine, and myo-inositol.

82 nd citrulline, and elevated serum glutamate, taurine, and serotonin.

83 ulators beta-phenylethylamine (beta-PEA) and taurine are important biogenic amines of the sympathetic

84 These findings establish taurine as a physiological gliotransmitter and show that

85 in the brain, in the local concentration of taurine at or near cellular spatial resolution in vivo o

86 ely, with significant differences in African taurine (AT) and Asian zebu backgrounds across chromosom

87 tical run, easily distinguishing glycine and taurine BA conjugates.

88 gesting the possible involvement of GADL1 in taurine biosynthesis.

89 Exogenous GlyR agonists (glycine, taurine) block RDE by preventing the closure of postsyna

90 ween most of the Russian cattle and European taurine breeds, apart from a few breeds that shared ance

91 mparing them to the genomes of 53 commercial taurine breeds.

92 me multiple nutrients, including glucose and taurine, but prefer proline, and they actively synthesiz

93 These cells show immunoreactivity to taurine, but they do not express GABA or somatostatin, n

94 d the potencies of glycine, beta-alanine and taurine by 9-, 6- and 3-fold respectively, and that of t

95 rate comparable to that of the oxidation of taurine by the TauD-J enzyme intermediate after adjustme

96 ibitor of taurine transport, suggesting that taurine can act as an endogenous activator of these rece

97 onclude that physiological concentrations of taurine can inhibit VB neurons via activation of extrasy

98 supply to the intestinal epithelium and for taurine capture between meals.

99 h herds, and/or from subsequent movements of taurine cattle through the African slave trade.

100 land, then ~120 years ago the first European taurine cattle were introduced to the island, and finall

101 ted in the Nelore individual relative to the taurine cattle, while genes involved in lipid transport

102 ixture with Asian zebu, African and European taurine cattle.

103 apidus, while homarine, lactate, betaine and taurine characterized E. verrucosa and C. pagurus.

104 their effects were assessed on MPO-mediated taurine chlorination and low-density lipoprotein oxidati

105 The relationship between GABA and taurine concentrations suggests that whole camel milk ma

106 ent TauT-mediated uptake predominates at low taurine concentrations, whereas at higher concentrations

107 thylated arginines and either glutathione or taurine concentrations.

108 olic acid, which in vivo is converted to its taurine conjugate tauroursodeoxycholic acid (TUDC), is a

109 ic acid and absence of the usual glycine and taurine conjugated primary bile acids.

110 on of the structural isomers of glycine- and taurine-conjugated BAs and unconjugated tetra-hydroxy BA

111 The serum concentration of taurine-conjugated BAs was essentially the same in the t

112 Principally, taurine-conjugated BAs were greatly elevated ( approxima

113 75% by this dose, dominated by increases in taurine-conjugated bile acids (t-CBAs).

114 port here a radiosynthesis of N-(11)C-methyl-taurine-conjugated bile acids and biodistribution studie

115 ers behave in a manner similar to endogenous taurine-conjugated bile acids in vivo and are thus promi

116 The radiosyntheses of the N-(11)C-methyl-taurine-conjugated bile acids proceeded with radiochemic

117 A radiosynthesis of N-(11)C-methyl-taurine-conjugated bile acids was developed and used to

118 In particular, taurine-conjugated bile acids were significantly decreas

119 developed a radiosynthesis of N-(11)C-methyl-taurine-conjugated bile acids.

120 on shifted from C24 bile alcohol sulfates to taurine-conjugated C24 bile acids.

121 which were accompanied by increased hepatic taurine-conjugated cholic acid and beta-muricholic acid

122 Glycine/taurine-conjugated primary BAs increased over time in IC

123 Moreover, phenylbutyric acid and taurine-conjugated ursodeoxycholic acid attenuated HNE-i

124 exposed to chenodeoxycholate and its glycine/taurine conjugates at different pH levels.

125 developed and used to prepare N-(11)C-methyl-taurine conjugates derived from cholic, chenodeoxycholic

126 ulating genes, leading to an accumulation of taurine conjugates in the rat liver.

127 Glycine or taurine conjugates were absent in the urine, bile, and s

128 side from an increased accumulation of their taurine conjugates.

129 ts are mediated by milk-derived-fat-promoted taurine conjugation of hepatic bile acids, which increas

130 food-deprived animals, with a novel class of taurine-containing lipids and the essential polyunsatura

131 acylations allowed synthesis of a number of taurine-containing peptides.

132 compositions, leading to the suggestion of a taurine-containing peptidylamido-glycan structure.

133 Taurine-containing water-soluble peptidomimetics were de

134 Taurine content of jerky samples was found to increase w

135 The amplitude of the taurine current was larger in neurons from adult mice th

136 lysine, isoleucine, leucine, phenylalanine, taurine, cysteine, and glucose uptake rates to enhance h

137 ant analytes was detected including glycine, taurine, D-serine, and glutamate.

138 In subcutaneous adipose tissue, taurine decreased ethanol-induced oxidative stress and c

139 eurons; 3) during normoxia GABA, glycine and taurine decreased GABA(A)Ralpha and GlyRalpha1 density i

140 Taurine deficiency leads to heart dysfunction, brain dev

141 ally high, then fell, possibly indicative of taurine dependency in seals, and progressive depletion o

142 armacological blockade of VRACs, by cellular taurine depletion, by metabolic inactivation of glia wit

143 Parallel measurements taken for taurine deuterated at both C1 and C2 show an additional

144 nated by a 2-His-1-carboxylate facial triad: taurine dioxygenase (TauD), (S)-(2)-hydroxypropylphospho

145 Combined with parallel studies of taurine dioxygenase and past studies of clavaminate synt

146 similarity to proteins annotated as alpha-KG:taurine dioxygenases (TauD), a well characterized member

147 l glycine receptor agonists beta-alanine and taurine directly activated alpha6beta2delta receptors wi

148 represents the first undistorted imaging of taurine distribution in brain at 20 mum resolution.

149 A method to image taurine distributions within the central nervous system

150 ed the E ring (2a-5a) or were synthesized by taurine-driven E-ring opening (2b-5b).

151 ictive modeling calculations and showed that taurine-driven E-ring opening and increasing negative ch

152 -driven E-ring opening, we hypothesized that taurine-driven E-ring opening of bacteriochlorophyll der

153 ed from type 2 to type 1 for 1b (WST11) upon taurine-driven E-ring opening, we hypothesized that taur

154 line of osmolytes like betaine, homarine and taurine during storage.

155 the response of oral gingival epithelium to taurine during wound healing remains unclear.

156 Moreover, we found that taurine enhanced K(V) channels via intracellular protein

157 Taurine-evoked currents were absent in relay neurons fro

158 ed brain taurine levels by 20%, suggesting a taurine-exporting role for GAT2 in the brain.

159 uring sleep deprivation compared with sleep (taurine, formate, citrate, 3-indoxyl sulfate, carnitine,

160 The location-specific loss of taurine from CA1 but not CA3 neurons following ischemia

161 ated release of D-[(3)H]aspartate and [(14)C]taurine from non-swollen astrocytes.

162 e of inulin, more bacterial deconjugation of taurine from primary bile acids was observed along with

163 Taurine, gamma-aminobutyric acid, and beta-alanine (subs

164 trogressed (1.56%) according to the European taurine genetic proportion.

165 nd free amino acids, and a large decrease of taurine, glucose, lactate, and creatine/phosphocreatine.

166 Some bioactive substances like coenzyme Q10, taurine, glutamine, creatine, creatinine, carnosine and

167 -MS/MS), and thiols (homocysteine, cysteine, taurine, glutamylcysteine, total glutathione, and cystei

168 There was greater release of taurine, glycine and glutamate in the NAC of the high-do

169 egative correlation with inflammation in the taurine group (P = -0.712; P <0.05).

170 Taurine has been demonstrated to play a role as an endog

171 In a number of studies, taurine has been reported to activate glycine receptors

172 The essential amino acid taurine has important physiologic and pathologic roles,

173 Taken together, these data demonstrate that taurine has important protective effects against ethanol

174 ribute to pathogenesis and that cysteine and taurine have the potential to serve as adjunctive treatm

175 e that the microbiota-associated metabolites taurine, histamine, and spermine shape the host-microbio

176 ere divided into two groups: gingiva with 1% taurine-hydrated collagen membrane (n = 8) and saline-hy

177 The local application of taurine-hydrated collagen membrane on human gingival wou

178 chemically specific XFI to study the role of taurine in brain disease.

179 ulfur K-edge to image the sulfonate group in taurine in situ in ex vivo tissue sections.

180 quantitative technique validation by imaging taurine in the cerebellum and hippocampus regions of the

181 The levels of glutamine, glutamate, and taurine in the gb hemolymph were significantly lower at

182 lutamate, glutamine, N-acetyl aspartate, and taurine in the prefrontal cortex.

183 resulted in the detection of hypotaurine or taurine in the reaction mixtures, suggesting the possibl

184 port findings that indicate a novel role for taurine in the regulation of voltage-gated delayed recti

185 that glial cells are the exclusive source of taurine in this nucleus.

186 n of radioactivity from [(35)S]cysteine into taurine, in primary murine astrocytes and neurons, and i

187 exposure, while alanine increased by 46% and taurine increased by 37%.

188 Taurine increased GH-dependent IGF1 synthesis in the liv

189 ed the time and dose dependence of uptake of taurine into MDCK cell monolayers.

190 also investigated the polarity of uptake of taurine into MDCK cells, and our results confirmed that

191 The non-European taurine introgressed animals (n=425) show an unfluctuati

192 Taurine is an abundant component of meat and fish-based

193 Taurine is an essential amino acid in some mammals and i

194 Combining numerous indirect measurements, taurine is known to play critical roles in brain functio

195 Taurine is one of the most abundant amino acids in the r

196 Taurine is one of the most abundant free amino acids in

197 Since taurine is small and mobile, it cannot be chemically "ta

198 N-arachidonoyl taurine is therefore an interesting prototype compound t

199 ur data reveal that inorganic S compounds or taurine is unlikely to serve as an S source during invas

200 roscopy, demonstrated increased abundance of taurine, isoglutamine, choline, lactate, phenylalanine a

201 Plasma levels of taurine, lathosterol, bile acids (taurocholate and glyco

202 Deletion of GAT2 increased brain taurine levels by 20%, suggesting a taurine-exporting ro

203 Deletion of GAT2 reduced liver taurine levels by 50%, without affecting the expression

204 Hepatic and blood taurine levels in HCU animals were decreased by 21 and 3

205 ee serine and glycine levels were higher and taurine levels lower in all tissues examined.

206 Taurine levels were initially high, then fell, possibly

207 Taurine levels, measured using MRS, showed a very strong

208 otaurine without a corresponding increase in taurine levels, suggesting that oxidation of hypotaurine

209 y with respect to preservation of myocardial taurine levels.

210 ropean cattle are largely descended from the taurine lineage, gene flow from African cattle (partiall

211 erally have been considered to belong to the taurine lineage.

212 than any other nutrient, including glucose, taurine, lipids, vitamins, or other amino acids.

213 Further, we apply the technique to image taurine loss from the vulnerable CA1 (cornus ammonis 1)

214 creased levels of serotonin, tryptophan, and taurine may explain the antidepressive effect of acute s

215 ivation of extrasynaptic GABA(A)-Rs and that taurine may function as an endogenous regulator of excit

216 rences in genes involved in carbohydrate and taurine metabolism.

217 lity, and simplicity of the enzyme-cleavable taurine motif promise new ways to promote the uptake of

218 Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present

219 esters, dipeptides and nucleophiles provided taurine N- and O-conjugates and sulfonopeptides.

220 ation between HPLC and ELISA for glycine and taurine (n = 10) showed regression coefficients of 0.97

221 nclude amides of long-chain fatty acids with taurine [N-acyl-taurines (NATs)].

222 osanoyl-taurine [NAT(24:0)] and N-eicosanoyl-taurine [NAT(20:0)]-as primary substrates for FAAH in mo

223 wo long-chain saturated NATs-N-tetracosanoyl-taurine [NAT(24:0)] and N-eicosanoyl-taurine [NAT(20:0)]

224 amides regulated by FAAH in vivo: the N-acyl taurines (NATs).

225 long-chain fatty acids with taurine [N-acyl-taurines (NATs)].

226 ents often present in energy drinks, such as taurine, niacin, and pyridoxine, is less well defined.

227 Among metabolites, nutrients as taurine, nicotinamide and beta-alanine, were found.

228 gival epithelium after direct application of taurine on incised human gingival samples.

229 mines formed by the interaction of HOCl with taurine or glycine decreased I(Na) in a similar fashion.

230 tly increased levels of lactate (P < 0.005), taurine (P < 0.005), and isoglutamine (P < 0.005) and de

231 Taurine prevented ethanol-induced decreases in serum adi

232 In the liver, taurine prevented ethanol-induced oxidative stress and a

233 Taurine prevented ethanol-induced oxidative stress and i

234 Taurine prevented the ethanol-induced decrease in CCAAT/

235 and metabolic changes in total creatine and taurine previously reported to be associated with amyloi

236 deficiency in the offspring decreases liver taurine production and associates with abrogation of a g

237 In this study, we show that taurine reduced the excitability of thalamocortical rela

238 ediate swelling-activated Cl(-) currents and taurine release in human non-neural cells.

239 s (VRACs), and it has been hypothesized that taurine released from glial cells is capable of inhibiti

240 We found that glutamine and taurine repressed the induction of both transcription fa

241 -deficient offspring, oral administration of taurine rescued their growth retardation and osteoporosi

242 steic acid to beta-alanine, hypotaurine, and taurine, respectively.

243 The metabotropic taurine response was insensitive to the Cl(-) channel bl

244 that the fatty acid analogue N-arachidonoyl taurine restores channel gating of many different mutant

245 onal roles, the precise mechanism underlying taurine's actions has not yet been identified.

246 Elucidation of taurine's neurochemical roles and importance would be su

247 keeping with its broad tissue distribution, taurine serves as a modulator of numerous basic processe

248 After UDCA removal cholestatic parameters, taurine species of cholic acid and chenodeoxycholic acid

249 CDO, and GOT1 expression were normalized by taurine supplementation, indicating that cysteine is not

250 ing a meal whereas TauT may be important for taurine supply to the intestinal epithelium and for taur

251 ostweaning growth and bone formation through taurine synthesis and suggests potential therapies to in

252 In this study, we analyzed taurine synthesis capability as reported by incorporatio

253 gesting that oxidation of hypotaurine limits taurine synthesis in cells.

254 rons, establishing the presence of an intact taurine synthesis pathway in these cells.

255 istent with its role as an organic osmolyte, taurine synthesis was stimulated under hypertonic condit

256 The taurine synthetic pathway is proposed to be incomplete i

257 lfonic acids: 2-aminoethane-1-sulfonic acid (taurine, T), 3-aminopropane-1-sulfonic acid (homotaurine

258 Here the interaction of taurine (Tau) with nitrite was investigated.

259 he acetyl group with the sulfonic amino acid taurine (Tau-LPFFD-NH2) and a second novel one in which

260 For taurine that was deuterated at the C1 position (adjacent

261 radation of coenzyme A, and the synthesis of taurine, the final product of cysteamine oxidation and t

262 nome-wide copy number differences among five taurine (three Angus, one Holstein, and one Hereford) an

263 Cells can release the free amino acid taurine through volume-regulated anion channels (VRACs),

264 addition of divalent metal ions or substrate taurine to TauD, an alpha-ketoglutarate-dependent dioxyg

265 >10-fold, from 118 muM (without conjugating taurine) to >1.6 mM (after conjugating taurine).

266 otypes that suggest changes in NO-associated taurine transport and bile acid metabolism.

267 c inhibition was enhanced by an inhibitor of taurine transport, suggesting that taurine can act as an

268 xpression of glucose transporter 1 (GLUT-1), taurine transporter (TAUT), sodium-dependent neutral ami

269 Cisplatin downregulates expression of the taurine transporter gene (TauT) in LLC-PK1 proximal tubu

270 ions but potently induced, together with the taurine transporter TauT, in response to depletion of ne

271 50%, without affecting the expression of the taurine transporter TAUT.

272 nduced injury and adaptive regulation of the taurine transporter, we hypothesized that TauT functions

273 macropinocytosis, but likely not relying on taurine transporters.

274 new epithelial formation was observed in 1% taurine-treated gingivectomy specimens, whereas incomple

275 e current study, we showed that knockdown of taurine up-regulated gene 1 (TUG1) induces marked inhibi

276 of the conserved long noncoding RNAs MALAT1, taurine upregulated gene 1 (TUG1), maternally expressed

277 report that the long noncoding RNA (lncRNA) taurine-upregulated 1 (Tug1) contributes to CKD developm

278 c1a) is functionally regulated by the lncRNA taurine-upregulated gene 1 (Tug1).

279 Taurine uptake across the brush-border membrane of human

280 tions of the solute transporters involved in taurine uptake across the luminal membrane of human ente

281 PAT1 may be responsible for bulk taurine uptake during a meal whereas TauT may be importa

282 esults suggest an important role for GAT2 in taurine uptake from portal blood into liver.

283 this study is the first to demonstrate both taurine uptake via PAT1 and functional coexpression of P

284 affinity ammonium amtB transporter, urea and taurine utilization systems.

285 d copepodamides, are polar lipids connecting taurine via an amide to isoprenoid fatty acid conjugate

286 in particular omega-3 fatty acids, selenium, taurine, vitamins D and B12, in the context of the devel

287 Taurine was a more potent agonist at recombinant alpha4b

288 as a source of anserine, phosphocreatine and taurine was discussed.

289 n of radioactivity from [(35)S]cysteine into taurine was observed in rat glioma cells as well as in p

290 ternofetal clearance of (14)C-MeAIB and (3)H-taurine was reduced and uterine arteries showed increase

291 rine, acetyl-CoA, and acetate), the level of taurine was significantly reduced, whereas the levels of

292 lux of uncharged osmolytes (myo-inositol and taurine) was suppressed by deletion of LRRC8A or LRRC8D,

293 putatively identified while one metabolite, taurine, was definitively identified.

294 Currents elicited by 50 microM taurine were abolished by gabazine, insensitive to midaz

295 aline, GABA, glutamine, alanine, glycine and taurine were separated and detected at concentrations si

296 organic osmolyte 2-aminoethylsulfonic acid (taurine), which reduces liver endoplasmic reticulum stre

297 thesis involves conjugation with glycine and taurine, which promotes a high intraluminal micellar con

298 N-protection of taurine with Cbz and SO2-activation with benzotriazole f

299 ed us to define the orientation of substrate taurine with respect to the magnetic axes of the Fe(II)-

300 analysis revealed an ancient stable African taurine x Asian zebu admixture.