ライフサイエンスコーパス: glycine

1 with soybean cyst nematode (SCN; Heterodera glycines).

2 hannels upon binding glutamate and coagonist glycine.

3 heir response to equilibrium applications of glycine.

4 rder characterized by accumulation of excess glycine.

5 line sequence, this residue is replaced by a glycine.

6 nt amino acids l-glutamate, l-cysteine and l-glycine.

7 ecame less sensitive to the neurotransmitter glycine.

8 ening events in the absence of extracellular glycine.

9 nd condensed with a second CO(2) to generate glycine.

10 e (pentose phosphate pathway) and serine and glycine (1-carbon metabolism) were also decreased in Pos

11 Glutamine-148->histidine (Q148H) and glycine-140->serine (G140S) amino acid substitutions in

12 predicted the active ligands interacted with glycine 165, located in loop D gating domains surroundin

13 Here, we show that glycine-305 and the homologous site in IFITM3, glycine-9

14 a regulator of neurotransmitter release, at glycine-305 was previously linked to paroxysmal neurolog

15 mors reportedly harbor missense mutations at glycine 34 in genes encoding histone variant H3.3.

16 Histone H3.3 glycine 34 to arginine/valine (G34R/V) mutations drive d

17 ation of glycine-95 (and to a lesser extent, glycine-91) disrupted IFITM3 oligomerization and reduced

18 Mutation of glycine-95 (and to a lesser extent, glycine-91) disrupte

19 ycine-305 and the homologous site in IFITM3, glycine-95, drive protein oligomerization from within a

20 that IFITM3 promotes membrane rigidity in a glycine-95-dependent and amphipathic helix-dependent man

21 arginine sandwiched between two neighboring glycines (a Gly-Arg-Gly, or "GRG," sequence).

22 erein, we present a versatile acetyl-alanine-glycine (Ac-AG) tag that conceals quantitative informati

23 tive antagonist, and high affinity homomeric glycine activated glutamate receptors.

24 icantly inhibits cannabinoid potentiation of glycine-activated currents in cultured spinal neurons an

25 The discovery of this glycine additive in TFA mobile phases provides a simple

26 consecutive PNA monomers of N-(2-aminoethyl)glycine (aeg) scaffolds (the sequential architecture) we

27 l alkenyl arylsulfones as dipolarophiles and glycine/alanine iminoesters as azomethine ylide precurso

28 mpared to the genes associated with wet, and glycine-amended conditions.

29 t are uniquely associated with dry, wet, and glycine-amended conditions.

30 nverts l-serine and (6S)-tetrahydrofolate to glycine and 5,10-methylenetetrahydrofolate.

31 rmed by injecting HP gamma-glutamyl-[1-(13)C]glycine and acquiring dynamic (13)C data on a preclinica

32 Addition of glycine and alanine together doubled high impact pyrazin

33 the N-methyl-D-aspartate receptor coagonists glycine and D-serine and N-methyl-D-aspartate receptor h

34 whose malfunction results in accumulation of glycine and diminished supply of glycine-derived 1-carbo

35 herein two homologous aptamers interact with glycine and each other to regulate gene expression.

36 on, and the reversal potential of inhibitory glycine and GABA(A) receptors.

37 domain in GluN1 is more closed when bound to glycine and glutamate relative to what is observed in th

38 osed of GluN1 and GluN2 subunits, which bind glycine and glutamate, respectively, to activate their i

39 s induced by PG degradation products such as glycine and glycine-rich oligopeptides.

40 oise (SNR) ratios of gamma-glutamyl-[1-(13)C]glycine and its product [1-(13)C]glycine were evaluated.

41 The serine glycine and one-carbon pathway (SGOCP) is a crucially im

42 Serine, glycine and other nonessential amino acids are critical

43 ciated with MacTel, and showed low levels of glycine and serine in the serum of MacTel patients.

44 o acids were unchanged in levels, except for glycine and serine that increased as a percentage of all

45 Glycine and small amino acid residues allow close-packin

46 ynthesis, generating 5'-aminolevulinate from glycine and succinyl-CoA.

47 difications is the heterogeneous addition of glycine and/or glutamate residues to the disordered C-te

48 with those of the dicot parasites Heterodera glycines and Globodera rostochiensis to understand the c

49 endothelial cells by NMDA agonists (NMDA or glycine) and the serine protease tissue plasminogen acti

50 CA cycle with increased synthesis of serine, glycine, and glutathione.

51 ive overexpression of glutamine, valine, and glycine, and relative suppression of glutamate and lipid

52 data suggest that defects in the urea cycle, glycine, and serine metabolism may be underrecognized in

53 sized by three proteins: FemX adds the first glycine, and the homodimers FemA and FemB sequentially a

54 h in mice fed diets restricted in serine and glycine, and the reduction of circulating serine by inhi

55 mys gene cluster encoding up to mycosporine-glycine are also upregulated under FR light.

56 ing dipeptide repeat proteins (R-DPRs), poly-glycine arginine (GR) and poly-proline arginine (PR), an

57 inine-rich dipeptide repeats, including poly glycine-arginine and poly proline-arginine, as the main

58 quences (90% amino acid identity) revealed a glycine-arginine rich N-terminal extension of ~100 amino

59 In this study, we discovered glycine as a simple additive for TFA mobile phases, whic

60 gion of human IgG, including the lack of one glycine as found in IgG2.

61 se against the parasitic nematode Heterodera glycines as it attempts to develop a multinucleate nurse

62 CM) proteins, and reveal tripeptide Arginine-Glycine-Aspartate (RGD) domains that bind and signal thr

63 (68)Ga-labeled arginine-glycine-aspartate tripeptide sequence (RGD) PET/CT imagi

64 onformationally-constrained, cyclic arginine-glycine-aspartic acid (cRGD) to enable highly selective

65 urface decorated with two different arginine-glycine-aspartic acid (RGD) peptides: one is cyclic (RGD

66 e high-affinity amino acid sequence arginine-glycine-aspartic acid-phenylalanine-cysteine (RGDFC) att

67 The dihedral angles of the glycine at the end of the second polyP region are very v

68 he crucial role of the highly conserved dual glycines at position 236-237 in the lower hinge region o

69 hains with different chemical properties and glycine-based variants, were also evaluated.

70 ough the rapid biosynthesis of predominantly glycine betaine and an increased root-to-shoot ratio to

71 Additionally, PDX increased the levels of glycine betaine and L-carnitine in plasma samples, which

72 that one-carbon metabolism, associated with glycine betaine and L-carnitine, and bile acid and trypt

73 K(+) concentrations the organism switches to glycine betaine as its major osmoprotectant.

74 lation of organic compatible solutes such as glycine betaine does not perturb the functioning of cyto

75 ) concentration (~10 mM) at which the KCl to glycine betaine osmoprotectant switch in H. halophila oc

76 Clamp association is also promoted by glycine betaine, a zwitterionic compound that accumulate

77 erforms both de novo synthesis and uptake of glycine betaine, matching the biosynthesis and transport

78 Therefore, the pre-harvest application of glycine-betaine and A. nodosum can be a good alternative

79 Glycine-betaine and A. nodosum treated cherries presente

80 r pre-harvest application of salicylic acid, glycine-betaine complex and seaweed extract (Ascophyllum

81 ed mutations were in opuD, encoding the main glycine-betaine transporter, and alsT, encoding a predic

82 of His-583 revealed that it is essential for glycine binding, and the structure of H583C PlGoxA had n

83 enzyme exhibits strong cooperativity toward glycine binding.

84 , with the regulated gene(s) dictating which glycine-binding aptamer is conserved.

85 ment is shorter and the bilobed cleft of the glycine-binding domain in GluN1 is more closed when boun

86 hat are captured in the unliganded (closed), glycine-bound (open and desensitized), and allosteric mo

87 ter preferred glucose to exogenous serine or glycine but not the former.

88 ers were reactive toward the amine substrate glycine, but only WT A2ML1 reacted with the hydroxyl sub

89 nonical inhibitory neurotransmitters GABA or glycine, but several expressed neither or both.

90 All of these were derived from GGX for glycine by single-base substitutions.

91 Here, we modify the simple acyl-glycine by synthesizing lipid analogues with a range of

92 ving over time compared to neutral cues, and Glycine carriers of the Ser9Gly D3R variant seem to expe

93 essed in genetically grouped (Glycine vs. No Glycine carriers) current smokers (n = 104, >= 10 cigare

94 d DNA and observed that a sublethal bolus of glycine chloramine, but not H(2)O(2), significantly inhi

95 idants produced by neutrophils, H(2)O(2) and glycine chloramine, on maintenance DNA methylation in Ju

96 r these data suggested the inhibition of the glycine cleavage (GCV) system caused the synthetic letha

97 e, alpha-ketoglutarate dehydrogenase and the glycine cleavage complex.

98 cellular BOLA3 deficiency downregulated the glycine cleavage system protein H, thus bolstering intra

99 Gldc functions in the glycine cleavage system, a mitochondrial component of fo

100 alus associated with loss of function of the glycine cleavage system.

101 , glutamic acid (coded by GAZ [Z = A or G]), glycine (coded by GGX), Ser (coded by AGY), and Arg (cod

102 that a rare 6-bp natural deletion of lysine-glycine codons, endemic to wheat landraces of Shaanxi Pr

103 tem protein H, thus bolstering intracellular glycine content.

104 The spike aspartic acid-614 to glycine (D614G) substitution is prevalent in global seve

105 Consistent with these observations, the glycine deactivation rate is slower in the presence of c

106 Loss of glycine decarboxylase (GLDC) can severely impact neurolo

107 alus are associated with loss of function of glycine decarboxylase (Gldc) in mice and in humans suffe

108 son) of a triplication of the gene encoding glycine decarboxylase, GLDC, presumably resulting in red

109 Peptoids (oligomers of N-substituted glycines) demonstrate proteolytic stability and better b

110 (exSer)-dependent PDAC cells during Ser/Gly (glycine) deprivation.

111 mulation of glycine and diminished supply of glycine-derived 1-carbon units to the folate cycle.

112 The serine-glycine dipeptide lipid classes, including lipid 430 and

113 similarly to the previously reported serine-glycine dipeptide lipids.

114 asses are structurally related to the serine-glycine dipeptide lipids.

115 o test the effect of the PHI dimethyl oxalyl glycine (DMOG) in the pathophysiology of graft versus ho

116 t minerals to mediate the oligomerization of glycine during iterative wet-dry cycles.

117 c gene expression with consequent serine and glycine elevation in the brain.

118 We analyzed the stability of glycine embedded within nontronite samples previously ex

119 oteins, and carboxyl group footprinting with glycine ethyl ester, were further applied to determine B

120 possible to measure Pb concentrations in the glycine extract solutions on a continuous scale using a

121 estration, nor blockade of the phenylalanine-glycine (FG)-rich nuclear pore complex.

122 hyperpolarized (HP) gamma-glutamyl-[1-(13)C]glycine for non-invasive imaging of glioblastoma.

123 A serine- and glycine-free diet rescues the transient motor impairment

124 strate that ALS/FTLD-linked FUS mutations in glycine (G) strikingly drive formation of droplets that

125 domain involving three amino acid residues, glycine (G), serine (S), and glutamic acid (E) at positi

126 Additionally, the glycine (G6) and lysine (K7) residues of the Walker A mo

127 Glycine (Gly) is used as a model system to evaluate the

128 n thought to occur exclusively at N-terminal glycines (Gly).

129 tions show that TNPO1 recognizes an arginine-glycine(-glycine) (RG/RGG)-rich region, whereas TNPO3 re

130 choline and valine gradients, but a positive glycine gradient.

131 Aza-glycine has proven to be a valuable tool in the design o

132 r approaches (e.g., repair and stabilize and glycine-helix breaking) yields well-behaved clade C-Env

133 from the C-terminal cleavage domain by a di-glycine hinge.

134 proper brain development and a regulator of glycine homeostasis, uncovering hyperglycinemia as a dri

135 short beta-sheet by incorporating N-(hydroxy)glycine (Hyg) residues into the backbone of peptides.

136 e describe a method for incorporation of aza-glycine in collagen peptides, and we apply the method to

137 id loss of fluidity, emphasizing the role of glycine in promoting fluidity.

138 techniques showed higher photodegradation of glycine in the acid-treated nontronite, triggered by dec

139 lts in simultaneous release of glutamate and glycine in the lateral interpeduncular nucleus (LIPN).

140 ivity between the two agonists glutamate and glycine in the NMDA receptor.

141 By replacing leucine with glycine in the zebrafish MetRS-binding pocket (MetRS-L27

142 plasticity in neural networks; extracellular glycine increases probability of postsynaptic response o

143 BA controls threshold excitability, wherreas glycine increases the strength of inhibition under condi

144 uids with different pH values influences how glycine is adsorbed into their interlayer regions, affec

145 Glycine is further reduced in D. desulfuricans by glycin

146 Soybean cyst nematode (SCN; Heterodera glycines) is the largest pathogenic cause of soybean yie

147 equate 1-carbon supply, as opposed to excess glycine, is the cause of hydrocephalus associated with l

148 In particular, the proline/glycine kink in helical peptides was reported to both in

149 The position of the proline/glycine kink in the sequence further controls the specif

150 (mPEG) was conjugated to quinidine through a glycine linker, making a monovalent quinidine-polymer co

151 Two glycine lipid classes were identified, termed lipid 567

152 Both serine-glycine lipid classes were previously shown to engage hu

153 Both glycine lipid classes were shown to promote TLR2-depende

154 s demonstrate that P. gingivalis synthesizes glycine lipids and that these lipids engage TLR2 similar

155 not clear if other lipids related to serine-glycine lipids are also produced by P. gingivalis The go

156 ditional lipid classes similar to the serine-glycine lipids that possess biological properties.

157 o officinalis L.; 37% LA and 23% GLA) or SO [Glycine max (L.) Merr.; 50% LA and 0% GLA] for 4 wk, fol

158 h the intensity of greenness of the soybean [Glycine max (L.) Merr.] canopy as determined by the Dark

159 We collected soybean [Glycine max (L.) Merr.] data were collected from field e

160 Soybean [Glycine max (L.) Merr.] is the most important oilseed cr

161 a and Lotus japonicus, and two crop species, Glycine max (soybean) and Phaseolus vulgaris (common bea

162 l dynamics of lighting for a rendered mature Glycine max (soybean) canopy to review the relative impo

163 Glycine max (soybean) Sec4 functions in the root during

164 information concerning the relevant genes in Glycine max (soybean).

165 use transcriptome data from various soybean (Glycine max and Glycine soja) tissues treated under diff

166 ns at within-membrane residues in the legume Glycine max Cox2 could enable yeast COX2 allotopic expre

167 A consistent risk for soybean (Glycine max L.) production is the impact of drought on g

168 to screen PS-SGCL against two plant lectins, Glycine max soybean agglutinin and Vicia villosa.

169 We developed a soybean (Glycine max) assay, BARCSoySNP6K, containing 6000 marker

170 onsible for the damage it causes in soybean (Glycine max) crop.

171 CR and proteomics to study putative soybean (Glycine max) iron transporters GmVTL1a and GmVTL1b and h

172 metabolites (i.e. phytoalexins) of soybean (Glycine max) that, collectively with other 5-deoxyisofla

173 , as well as the DGAT2 enzymes from soybean (Glycine max), and castor (Ricinus communis), followed by

174 leaf size in both M. truncatula and soybean (Glycine max), indicating functional conservation.

175 olonization of maize (Zea mays) and soybean (Glycine max), respectively.

176 ntial for proper trichome growth in soybean (Glycine max).

177 GABA and glycine mediate fast inhibitory neurotransmission and ar

178 locks synaptic AMPAR accumulation induced by glycine-mediated depolarization.

179 ion is exemplified by faster accumulation of glycine-modified lipopolysaccharide (LPS) and depletion

180 While the glycine moiety of GCA is exposed into a highly polar poc

181 In constrast, our experiments showed that glycine molecules were preferably incorporated by ion ex

182 Glycine mutations undergo rapid loss of fluidity, emphas

183 glycine riboswitch aptamers with and without glycine, Mycobacterium SAM-IV riboswitch with and withou

184 ng the endoplasmic reticulum, via N-terminal glycine myristoylation.

185 that NMT acts both as N-terminal-lysine and glycine myristoyltransferase.

186 Unexpectedly, we find that human N-terminal glycine myristoyltransferases (NMT) 1 and 2 can efficien

187 ation by OCM intermediates and repression of glycine N-methyltransferase (Gnmt).

188 s of tonic inhibition of SR by intracellular glycine observed in vitro, primary cultures, and in vivo

189 lase that cleaves the bond between the fifth glycine of cross-bridges and the alanine of the adjacent

190 The results demonstrated that glycine offered the best response boosting on peptides.

191 ty acids (PUFAs) level and the active serine-glycine-one-carbon (SGOC) pathway.

192 es evoked by brief, quasi-synaptic pulses of glycine onto outside-out patches were impaired in mutant

193 Glycine or D-cycloserine augmentation of psychotropic dr

194 The quinoprotein glycine oxidase from the marine bacterium Pseudoalteromo

195 mechanism for the reductive half-reaction of glycine oxidation.

196 thesis of amino acids by transamination with glycine, paralleling the extant metabolic mechanisms and

197 n important role in defense in the G. max-H. glycines pathosystem, with some of the spatially and tem

198 furicans assimilates CO(2) via the reductive glycine pathway, a seventh CO(2) fixation pathway.

199 0 MBq of (68)Ga-IMP288, a histamine-succinyl-glycine peptide given after initial targeting of a triva

200 They share a glycine-phenylalanine-hydroxyproline/alanine (GFO/A) mot

201 le small molecule binding site in the DNAJA1 glycine/phenylalanine-rich region.

202 TTLL glycylases add glycines post-translationally to internal glutamates, an

203 Restriction of dietary serine and glycine potently induces the accumulation of deoxysphing

204 structure of H583C PlGoxA had no active-site glycine present in glycine-soaked crystals.

205 ort evidence for the consumption of soybean (Glycine), probable banana (Musa), and turmeric (Curcuma)

206 ma levels of glutamic acid (GLU), glutamine, glycine, proline (PRO), tryptophan (TRP), tyrosine, seri

207 Peptides designed to include a glycine-proline-hydroxyproline (GPO) amino acid triad ar

208 catabolism, such as glutamic acid, alanine, glycine, pyrimidine, and creatine.

209 The mPEG-glycine-quinidine conjugate retained its ability to inhi

210 20 nM for quinidine and 4.61 nM for the mPEG-glycine-quinidine conjugate).

211 esence of several subunits of the inhibitory glycine receptor (GlyR) in the reward system, specifical

212 an startle disease is caused by mutations in glycine receptor (GlyR) subunits or in other proteins as

213 , most commonly in the alpha1 subunit of the glycine receptor (GlyR), cause the startle disease/hyper

214 t the intracellular domain of the inhibitory glycine receptor alpha1 subunit contributes to trafficki

215 Thus, the proline-rich stretch from the glycine receptor alpha1 subunit represents a multifuncti

216 and myoclonus or stiff person syndrome, and glycine receptor autoantibodies, were observed to disrup

217 glutamate, AP5, and NMDA positively modulate glycine receptor currents.

218 A T258F mutation of the glycine receptor increases the receptor affinity to endo

219 ors and involved an increase in postsynaptic glycine receptor-mediated currents.

220 aracterizing high-affinity modulators of the glycine receptor.

221 regulation and release (GAD65, amphiphysin); glycine receptors (GLY-R); water channels (AQP4).

222 Glycine receptors (GlyRs) are anion-permeable pentameric

223 Glycine receptors (GlyRs) are key players in mediating f

224 Glycine receptors (GlyRs) are the major mediators of fas

225 Glycine receptors (GlyRs) mediate fast inhibitory neurot

226 hronic pain and startle disease by targeting glycine receptors (GlyRs).

227 ade of GABA(A) receptors (GABA(A) Rs) and/or glycine receptors demonstrated no GABAergic synaptic com

228 Tonic conductance through glycine receptors of cerebellar granule cells is a yet u

229 te their relative scarcity, tonically active glycine receptors of cerebellar granule cells make a sig

230 hibitory synapses can directly interact with glycine receptors to enhance inhibitory signalling.

231 teins, and gamma-aminobutyric acid (GABA) or glycine receptors.

232 positive allosteric modulators of inhibitory glycine receptors.

233 ors and decreases this probability acting at glycine receptors.

234 spartate modulation of native or recombinant glycine receptors.

235 laevis oocytes expressing recombinant human glycine receptors.

236 ne is further reduced in D. desulfuricans by glycine reductase to acetyl-P, and then to acetyl-CoA, w

237 glycine, seizures and failure to thrive, but glycine reduction often fails to confer neurological ben

238 Unexpectedly, we also discovered that glycine regulates d-serine metabolism by a dual mechanis

239 an additional N-degron pathway specific for glycine regulates the stability of metazoan proteomes.

240 obtained in anaesthetized rats revealed that glycine released in the rostral ventrolateral medulla (R

241 which bind the beta-spike of trimeric valine-glycine repeat protein G (VgrG) and are important for T6

242 sphosites on LAT, is governed by a preceding glycine residue (G131) but can be accelerated by substit

243 Two conserved glycine residues (G335 and G338) are potent inhibitors o

244 Introducing 3 glycine residues that disrupt a rigid IS6-alpha-interact

245 es repositions to expose previously shielded glycine residues to the pore without significant rotatio

246 of collagen peptides containing multiple aza-glycine residues.

247 w that TNPO1 recognizes an arginine-glycine(-glycine) (RG/RGG)-rich region, whereas TNPO3 recognizes

248 Vibrio cholerae and Fusobacterium nucleatum glycine riboswitch aptamers with and without glycine, My

249 The glycine riboswitch is among the most well-studied due to

250 oach, we show that one aptamer of the tandem glycine riboswitch pair is typically much more highly co

251 n together, our findings suggest that tandem glycine riboswitches degrade into functional singletons,

252 Sorghum glycine rich proline rich protein (SbGPRP1) exhibit anti

253 In Arabidopsis, AtSRBP1 is a glycine-rich (GR) RNA-binding protein, also known as AtG

254 ompasses the cytoskeleton-associated protein glycine-rich domain, the basic domain, and serine/prolin

255 of Streptococcus gordonii) have shown that a glycine-rich motif in its hydrophobic core is essential

256 egions (IDRs) from a family of phenylalanine-glycine-rich nucleoporins (FG-Nups) to control nucleocyt

257 highly enriched in disordered phenylalanine/glycine-rich nucleoporins (FG-Nups), which form a permea

258 PG degradation products such as glycine and glycine-rich oligopeptides.

259 he parasite cell wall and identified it as a glycine-rich protein (GRP).

260 composition, and the role of the apoplastic glycine-rich protein 1 (CpGRP1) were analysed.

261 ion and hyperconjugative interactions in aza-glycine's backbone directly preorganizes the collagen pe

262 unnatural side chains were also accessed via glycine Schiff base alkylation, further increasing the s

263 eroviruses; however, a conserved proline and glycine seem to be key residues.

264 It is characterized by elevation of glycine, seizures and failure to thrive, but glycine red

265 phatidylethanolamines and sphingomyelin, and glycine-serine and sphingomyelin, observed in controls,

266 inker region was substituted with a flexible glycine-serine linker of the same length underwent effic

267 tudy found variants in genes associated with glycine-serine metabolism (PSPH, PHGDH and CPS1) to be a

268 es that are directly or indirectly linked to glycine-serine metabolism, further validating our previo

269 Insertion of additional flexible glycine-serine repeats had no effect on S-acylation, but

270 evelopment, including NMDA channel blockers, glycine site agents, and allosteric modulators, as well

271 A), an N-methyl-D-aspartate receptor (NMDAR) glycine site antagonist, and of 4-chloro-3-hydroxyanthra

272 In contrast, [1-(13)C]glycine SNR was significantly higher in tumor-bearing ra

273 wed no difference in gamma-glutamyl-[1-(13)C]glycine SNR, pointing to similar delivery to tumor and n

274 Structures for glycine-soaked crystals were obtained for each.

275 PlGoxA had no active-site glycine present in glycine-soaked crystals.

276 e data from various soybean (Glycine max and Glycine soja) tissues treated under different conditions

277 383 ) and EPA Method 1340, and uses a 0.4 M glycine solution at pH 1.5.

278 heterozygous mutations in Col3a1 that encode glycine substitutions analogous to those found in patien

279 Single glycine substitutions in collagen III, which predominate

280 +)-permeable channels gated by glutamate and glycine that are essential for central excitatory transm

281 ing tripeptide (l-gamma-glutamyl-l-cysteinyl-glycine) that can function as a reversible reducing agen

282 e with the mutant human superoxide dismutase glycine to alanine point mutation at amino acid 93 (hSOD

283 one (CTQ) cofactor to catalyze conversion of glycine to glyoxylate and ammonia.

284 sibility of using HP gamma-glutamyl-[1-(13)C]glycine to monitor GGT expression in the brain and thus

285 by synaptic-like millisecond applications of glycine to outside-out patches were much shorter (7- to

286 ified a mutation in the Ins2 gene, causing a glycine-to-serine substitution at position 32 on the B c

287 ding to the serotonin transporter and to the glycine transporters (GlyT1 and GlyT2).

288 Glycine treatment augmented the prednisolone-induced red

289 centrations of 4 formate precursors (serine, glycine, tryptophan, and methionine) were increased in c

290 d acyclic forms, alone or in the presence of glycine under moderate temperature drying conditions.

291 aviors were assessed in genetically grouped (Glycine vs. No Glycine carriers) current smokers (n = 10

292 Importantly, higher [1-(13)C]glycine was associated with higher GGT expression and hi

293 yl-[1-(13)C]glycine and its product [1-(13)C]glycine were evaluated.

294 but can be accelerated by substituting this glycine with aspartate or glutamate.

295 Substitution of the glycine with leucine converted the resting-state R2lox c

296 ncreases in plasma arginine, citrulline, and glycine, with decreases in total and D-serine, cholester

297 lood orange juice, and for phenylalanine and glycine, with regards to orange juice.

298 l carboxylate metal ligand is conserved as a glycine within the R2lox group but not in R2c.

299 ng rotational orientation places an extended glycine zipper motif (G(40)xxxS(44)xxxG(48)) together wi

300 n estimated diameter of 2 nm, as long as the glycine zipper motif remains intact.