ライフサイエンスコーパス: taurine

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

2 the endogenous intracellular L-glutamate and taurine.

3 of radiolabeled selenium-75 homocholic acid taurine.

4 solution of naphthalene dialdehyde (NDA) and taurine.

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

6 ogic evidence of rapid reepithelization with taurine.

7 ulates the agonist properties of glycine and taurine.

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

9 2-transfected HEK293 cells transported [(3)H]taurine.

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

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

12 a result of the efflux of the intracellular taurine.

13 d neurotransmitters glutamate, aspartate and taurine.

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

15 (TM3) side chain, important for transport of taurine.

16 w breeds that shared ancestry with the Asian taurines.

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

18 ived organic sulfonate substrate in the gut, taurine (2-aminoethanesulfonate).

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

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

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

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

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

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

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

26 ated Schiff base adduct of retinaldehyde and taurine (A1-taurine, A1T) that forms reversibly by nonen

27 base adduct of retinaldehyde and taurine (A1-taurine, A1T) that forms reversibly by nonenzymatic reac

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

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

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

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

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

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

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

35 Taurine alleviates repression of betaine-homocysteine S-

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

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

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

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

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

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

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

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

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

45 which gives antioxidant metabolites such as taurine and glutathione.

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

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

48 al genomic ancestry analyses, we reconstruct taurine and indicine ancestry genome-wide and along chro

49 nsity SNP genotyping data to investigate the taurine and indicine ancestry in southern European cattl

50 ce independently and gave rise to the modern taurine and indicine cattle breeds.

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

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

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

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

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

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

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

58 findings indicate that a combination of past taurine and recent indicine admixture-derived genetic re

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

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

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

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

63 chromosome-level genome assemblies of Angus (taurine) and Brahman (indicine) cattle subspecies from c

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

65 palmitic acid, L-tryptophan, kynurenic acid, taurine, and 25-hydroxyvitamin D compared with controls.

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

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

68 d nutrients, such as long-chain fatty acids, taurine, and choline.

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

70 Plasma concentrations of serotonin, taurine, and glycerophosphocholine were significantly lo

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

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

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

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

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

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

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

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

79 ded dipeptides, polyunsaturated fatty acids, taurine, and xanthine.

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

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

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

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

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

85 gesting the possible involvement of GADL1 in taurine biosynthesis.

86 table, contrasting phenotypes of tick loads, taurine breeds carrying higher loads of the parasite tha

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

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

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

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

91 of physiological concentrations of GABA and taurine, but, surprisingly, that receptor activity is on

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

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

94 We also show that N-oleoyl taurine (C18:1 NAT), the most abundant NAT in human plas

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

96 ns that have introgressed from indicine into taurine cattle under positive selection, harbouring gene

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

98 n cattle diversity is generally dominated by taurine cattle, although elevated levels of indicine anc

99 entify one highly divergent locus in African taurine cattle, which is putatively linked to trypanotol

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

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

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

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

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

105 thylated arginines and either glutathione or taurine concentrations.

106 ding two novel products, that is, diclofenac taurine conjugate (DCF-M403) and unexpected diclofenac m

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

108 ition of chenodeoxycholic acid (CDCA) or its taurine conjugate, which was fully blocked by CFTR inhib

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 Taurine-conjugated bile acids, which have reduced membra

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

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

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

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

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

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

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

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

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

129 side from an increased accumulation of their taurine conjugates.

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

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

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

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

134 Taurine-containing water-soluble peptidomimetics were de

135 Taurine content of jerky samples was found to increase w

136 laskensis G20, which use isethionate but not taurine; corresponding knockout mutants of D. alaskensis

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

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

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 in aquafeeds, but one of the limitations is taurine deficiency that can be especially detrimental fo

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

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

144 Here we decipher the complete taurine desulfonation pathway in Bilophila wadsworthia 3

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

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

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

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

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

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

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

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

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

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

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

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

157 iff base conjugate that the primary amine of taurine forms with retinaldehyde would readily hydrolyze

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

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

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

161 n 0 (C-), 5 (T5), 10 (T10) or 20 (T20) added taurine (g/kg), while a control diet (C+) included two-f

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

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

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

165 absolute amounts and mol% of certain AA (eg: Taurine, glutamine, tyrosine, phenylalanine) in the drie

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

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

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

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

170 w intestinal bacteria to access sulfite from taurine have not yet been identified.

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

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

173 elenium, vitamin D(3), vitamin C, trytophan, taurine, histidine and hydroxyproline were below the ref

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

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

176 nvestigation of the 2OG-dependent oxygenase, taurine hydroxylase (TauD), revealed a strong link betwe

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

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

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

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

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

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

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

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

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

186 Taurine increased GH-dependent IGF1 synthesis in the liv

187 ing 508 individuals from 23 cattle breeds of taurine, indicine and mixed ancestry, including three br

188 s a key role in converting bile salt-derived taurine into H(2)S in the disease-associated gut bacteri

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

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

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

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

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

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

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

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

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

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

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

200 Taurine levels paralleled these differences in A1T.

201 Taurine levels were initially high, then fell, possibly

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

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

204 ardiomyopathy and almost undetectable plasma taurine levels.

205 y with respect to preservation of myocardial taurine levels.

206 /day resulted in maintenance of normal blood taurine levels.

207 itional copies in the indicine compared with taurine lineage and an indicus-specific extra copy of fa

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

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

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

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

212 ed lipids, as well as antioxidant molecules [taurine (m/z 124.0068), uric acid (m/z 167.0210), ascorb

213 peak open probability (P(Open,peak)) of 0.4, taurine (maximal P(Open,peak) = 0.4), or the endogenous

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

215 rences in genes involved in carbohydrate and taurine metabolism.

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

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

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

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

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

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

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

223 s, the N-acylethanolamines (NAEs) and N-acyl taurines (NATs), in central and peripheral tissues.

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

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

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

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

228 VRAC permeability to organic substances like taurine or cisplatin.

229 cross crossbred animals showing an excess of taurine or indicine ancestry.

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

231 nositol (mI), scyllo-inositol (sI), glycine, taurine, phosphoethanolamine (PE) and increase in the le

232 Cloning the taurine PRDM9 gene, which is the common form carried by

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

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

235 ity in the presence of combinations of GABA, taurine, propofol, allopregnanolone and/or the inhibitor

236 n of taurine to sulfoacetaldehyde by a known taurine:pyruvate aminotransferase is followed, unexpecte

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

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

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

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

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

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

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

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

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

246 e themselves, such as pyridoxine/vitamin B6, taurine, some essential amino acids, and a conditionally

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

248 Overall, it seems that high dietary taurine supplementation acted as a growth promoter and c

249 In this study, taurine supplementation in high plant protein diets (low

250 Oral taurine supplementation of 100 mg/kg/day resulted in mai

251 Taurine supplementation significantly reduced fillet dri

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

253 fold higher amount of fishmeal (30%) with no taurine supplementation.

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

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

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

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

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

259 The taurine synthetic pathway is proposed to be incomplete i

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

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

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

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

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

265 An initial deamination of taurine to sulfoacetaldehyde by a known taurine:pyruvate

266 >10-fold, from 118 muM (without conjugating taurine) to >1.6 mM (after conjugating taurine).

267 rea, nitrate, dimethylsulfoniopropionate and taurine transformation were identified that interlink me

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

269 Hepatic ammonia handling was analyzed in taurine transporter (TauT) KO mice.

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

271 al in the eighth transmembrane domain of the taurine transporter SLC6A6 was identified resulting in a

272 50%, without affecting the expression of the taurine transporter TAUT.

273 macropinocytosis, but likely not relying on taurine transporters.

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

275 vely, our findings indicate that adjuvantial taurine treatment has the potential to significantly imp

276 Taurine treatment induced BHMT expression in HCU mice by

277 DM9, whereas all others were variants of the taurine type.

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

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

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

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

282 alysis of the highly conserved lncRNA locus, taurine-upregulated gene 1 (Tug1).

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

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

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

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

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

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

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

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

294 an amino acid associated with tissue damage (taurine), which may be useful as a joint marker of the t

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

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

297 specific cysteic acid decarboxylase produces taurine, while hydrogen sulfide is recycled into cystein

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

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

300 the main cattle groups, we identify a major taurine x indicine cattle admixture event dated to circa