ライフサイエンスコーパス: PG

1 PG also showed blunted amphetamine-induced euphoria and

2 PG demonstrated significant blunting of opioid release c

3 PG is rare in the cellular membranes that carry CD1b pro

4 PG synthesis at the cell division septum is necessary fo

5 PG-QC formulations were prepared by mixing a QC ethanol

6 PG-QC formulations with various PG to QC ratios were pre

7 PGs, bile acids, and tryptophan metabolites are importan

8 isruption of model membranes by protegrin-1 (PG-1), a cationic AMP from pig leukocytes.

9 s buffer and discovered two compounds (PG-1, PG-2) exhibited exceptional selectivity for progesterone

10 Thirty-nine participants (15 PG, 7 BED, and 17 controls) were scanned with [(11)C]car

11 rain activity in 103 participants (30 CD, 28 PG, and 45 controls) while they watched videos depicting

12 We used the process-based growth model 3-PG, to provide estimates of tree species responses to ch

13 The 3-PG model predicted that aboveground biomass growth and n

14 l climate models (GCMs) were used with the 3-PG model to predict the future productivity and water us

15 ty to the folding-deficient mutant SERT-(601)PG(602)-AA.

16 stalled on tri-N-acetylglucosamine (NAG)3, a PG mimic, as well as PG isolated from various Gram (+) a

17 d that the protein's C-terminal domain has a PG-binding-competent conformation.

18 pared by mixing a QC ethanol solution with a PG aqueous solution followed with vacuum drying of the s

19 Here, with a PG-labelling approach utilizing timed pulses of multiple

20 using p-nitrophenyl acetate and O-acetylated PG as substrates.

21 P < .001), but not in moderate and advanced PG.

22 NFL thinning slowed dramatically in advanced PG, but GCC thinning rate remained relatively steady and

23 rence in the rate of grade B/C fistula after PG versus PJ (20% vs 22%, P = 0.617).

24 The rate of grade B/C fistula after PG versus PJ was not different.

25 an independent cohort and in meta-analysis (PG x E=3.6 x 10(-9)), but is not replicated in Caucasian

26 (CD) analyses of daptomycin with Ca(2+) and PG-containing membranes, we found that there are only tw

27 BED and PG are thus dissociable as a function of dopaminergic an

28 antitative analysis of mouse hepatic BMP and PG species and their changes induced by long-term high-f

29 trategy for quantitative analysis of BMP and PG species was developed after one-step methylation of l

30 f drug cravings and gambling urges in CD and PG.

31 a direct glycosidic linkage between CPS and PG and showed that a single CPS repeat unit can be trans

32 s of purified CPS-PG identified only CPS and PG sugars in the appropriate ratios, suggesting the abse

33 oxygenase-2 into PG-ethanolamide (PG-EA) and PG-glycerol (PG-G), respectively.

34 ion by altering the balance between PG-G and PG levels in vivo.

35 action of peptidoglycan (PG) hydrolases and PG-synthesizing/modifying enzymes.

36 hloride; n = 7; Protocol 1); NO (l-NMMA) and PG (ketorolac) inhibition alone, or combined NO, PGs, Na

37 esis that inhibition of KIR channels, NO and PG synthesis, and Na(+) /K(+) -ATPase would not alter th

38 PJ and PG are established methods for reconstruction in pancrea

39 rent utilization of l-Asp for pyrimidine and PG synthesis may be part of the regulatory scheme, ensur

40 onding between the hydroxyl groups of QC and PG.

41 ctivity also resulted in cell separation and PG fragment release defects, indicating that activation

42 or how AmiC functions in cell separation and PG fragment release.

43 quantification and localization of SQDG and PG molecular species, among mesophyll (M) and bundle she

44 rong cocaine cravings to cocaine videos, and PG participants reporting strong gambling urges to gambl

45 ry lipid mediators (i.e., leukotriene B4 and PGs) in omental adipose tissue from Ob patients.

46 and epigenetic changes in fetal life and are PG targets, we investigated if exposure of pregnant rats

47 terial (carbon nanofibers (CNF)), denoted as PG-C and CNF-C nanocomposites, respectively, were synthe

48 ylglucosamine (NAG)3, a PG mimic, as well as PG isolated from various Gram (+) and Gram (-) bacterial

49 the solubility of QC reached 241.76mug/mL at PG/QC ratio of 30/1 compared with approximately 4.32mug/

50 that distinguish mammalian PG from bacterial PG.

51 of Gram-positive and Gram-negative bacterial PG utilizing metabolic cell wall recycling and biosynthe

52 ers, respectively, by removing of the benzyl-PG.

53 inflammation by altering the balance between PG-G and PG levels in vivo.

54 MOR availability did not differ between PG and HV groups.

55 detected progression earlier than VF in both PG and GS/PPG groups.

56 t there should be more compounds produced by PG and GLY than have been reported in e-cigarette aeroso

57 n-like), including receptors for chemokines, PGs, histamine, platelet activating factor, and anaphyla

58 aqueous buffer and discovered two compounds (PG-1, PG-2) exhibited exceptional selectivity for proges

59 lasts are mostly composed of 16:0-containing PGs.

60 Overall, 16:1-containing PGs primarily contribute to the thylakoid membranes of M

61 rovide the most detailed descriptions of CPS-PG linkages for any microorganism.

62 Component sugar analysis of purified CPS-PG identified only CPS and PG sugars in the appropriate

63 -type epitopes of a newly identified cypress PG.

64 ractions and downstream effects of different PGs and their assorted sulfated epitopes.

65 onic membranes of dimyristoylphosphocholine, PG-1 first induced edge instability at low concentration

66 Inside cells, FtsZ directs PG insertion at the division plane, though it is unclear

67 ith plasma concentrations too low to disrupt PG biosynthesis.

68 though we could detect six of the documented PG-G hydrolases in neutrophils by quantitative PCR, only

69 h rs11161721 (PG x E=1.8 x 10(-8); empirical PG x E=1.2 x 10(-8)) as the top hit.

70 by a homogalacturonan unit linked to an endo-PG resistant unit.

71 , the molecular pathways leading to enhanced PG/GLY reactivity are described, along with the most imp

72 osynthesis of prostaglandin glycerol esters (PG-Gs) from 2-arachidonoylglycerol.

73 ed by cyclooxygenase-2 into PG-ethanolamide (PG-EA) and PG-glycerol (PG-G), respectively.

74 UV-A exposed PG caused oxidative damage to the cell and significantly

75 months for GS/PPG eyes and 56.7 +/- 16.0 for PG eyes.

76 , we identified an alternative mechanism for PG synthesis in E. coli that is PgsA independent.

77 tification of this alternative mechanism for PG synthesis not only expands our knowledge of bacterial

78 The receptors for PGs, which have yet to be fully characterized, display a

79 Such stem peptides do not form PG cross-bridges, resulting in a decrease in PG cross-li

80 Fourteen PG and 15 healthy volunteers (HV) underwent two [(11)C]c

81 and 2-propen-1-ol were produced mostly from PG, while other compounds (e.g., formaldehyde) originate

82 Furthermore, PG 32:0 shows genotype-specific differences in cellular

83 llic acid (GA) and its ester propyl gallate (PG) in the presence of UV-A light against Escherichia co

84 ous opioid release in pathological gamblers (PG) using [(11)C]carfentanil PET with an oral amphetamin

85 addiction phenotypes: pathological gambling (PG) and binge eating disorder (BED).

86 e dependence (CD) and pathological gambling (PG), few studies have directly investigated neurobiologi

87 (TS), with or without being pre-gelatinized (PG), on the growth, feeding efficiencies, plasma and mus

88 a (GS/PPG) eyes and 153 perimetric glaucoma (PG) eyes.

89 nto PG-ethanolamide (PG-EA) and PG-glycerol (PG-G), respectively.

90 nd aerosolize the solvents propylene glycol (PG) and glycerol (GLY), thereby affording unique product

91 nt refill "e-liquids" were propylene glycol (PG), glycerin, nicotine, ethanol, acetol, and propylene

92 sis leaves have the machinery to glycosylate PG to form phlorin, which can be hydrolyzed enzymaticall

93 ought-after molecular mechanisms that govern PG action in the cervix.

94 We have recently developed pollen grains (PGs) as a unique method to deliver vaccines orally.

95 decorated onto 2D material (porous graphene (PG)) and 1D material (carbon nanofibers (CNF)), denoted

96 lators by expanding the understanding of how PG is processed by lytic enzymes.

97 ss of leaf development or genotype; however, PG shows photosynthetic cell-specific differential local

98 = 14), 2) peri-implant pyogenic granuloma (I-PG) (n = 5), 3) peri-implant peripheral giant cell granu

99 play a role with subsequent development of I-PG and I-PGCG-like lesions.

100 Yeast two-hybrid experiments identified PG core proteins ABC1K3, PES1, and CCD4 as PGM48 interac

101 Previous studies identified PG-Gs as signalling molecules involved in inflammation.

102 In PG and SA cells, brief (1-4 s) raphe stimulation elicite

103 In PG patients, [(11)C]carfentanil BPND was reduced in the

104 eractions in C. jejuni Therefore, changes in PG greatly impact the physiology of this organism.

105 PG cross-bridges, resulting in a decrease in PG cross-linking and, consequently, reduced PG thickness

106 Deltaape1 resulted in marked differences in PG biochemistry, including O-acetylation, anhydromuropep

107 PGs as AKR1B1 inhibitors and the interest in PG-related molecules as leads for the development of nov

108 osphodiester bonds, which typically occur in PG-polysaccharide linkages.

109 ideos in CD participants, gambling videos in PG participants, and sad videos in control participants.

110 Eicosanoids, including PGs, produced by cyclooxygenases (COX), and leukotrienes

111 alacturonase (PG) gene, ADPG2, and increases PG activity in Arabidopsis leaves, which in turn reduces

112 Finally, the PGP-independent PG synthesis in E. coli may also have important implicat

113 can be metabolized by cyclooxygenase-2 into PG-ethanolamide (PG-EA) and PG-glycerol (PG-G), respecti

114 f phosphatidylethanolamine and glycerol into PG and is catalyzed by ClsB, a phospholipase D-type card

115 ntrast to conventional morphine, intravenous PG-M exclusively activated peripheral opioid receptors t

116 rthogonal modifications protect the isolated PG against lysozyme degradation in vitro.

117 0-dihydroxy-DPA and n-6 PUFA derived 15-keto-PG E2 (15-keto-PGE2).

118 trast, we found an L234A, L235A, P329G (LALA-PG) variant that eliminates complement binding and fixat

119 an and murine antibodies containing the LALA-PG variant have typical pharmacokinetics in rodents and

120 These LALA-PG substitutions allow a more accurate translation of re

121 the translocation of the final lipid-linked PG precursor called lipid II across the cytoplasmic memb

122 contributions of radial versus longitudinal PG insertion at the septum.

123 The three-dimensional structure of the LytA/PG complex provides a novel structural basis for ligand

124 creased enzymatic activity on macromolecular PG and on the synthetic PG derivative.

125 at gonococcal AmiC can act on macromolecular PG to liberate cross-linked and non-cross-linked peptide

126 mical differences that distinguish mammalian PG from bacterial PG.

127 chemistry to fluorescently label the mature PG in whole bacterial cells of Bacillus subtilis.

128 cantly higher detection rate than VF in mild PG (63.1% vs. 38.7%, P < .001), but not in moderate and

129 domly assigned in pairs to watch a 20-minute PG-rated movie containing or not containing guns in a un

130 Modifying PG postsynthetically can aid in the development of antib

131 n is replicated in African-American mothers (PG x E=0.01) from an independent cohort and in meta-anal

132 (beta-ME), Trolox (TX), n-propyl gallate (n-PG), and ascorbic acid (AA).

133 ave the cross-links for insertion of nascent PG material.

134 cells cannot elongate without inserting new PG in the side-wall.

135 However, KIR channels, NO, PGs and Na(+) /K(+) -ATPase activity are not obligatory

136 ia pathways independent of KIR channels, NO, PGs and Na(+) /K(+) -ATPase in humans, consistent with a

137 ketorolac) inhibition alone, or combined NO, PGs, Na(+) /K(+) -ATPase (ouabain) and KIR channel inhib

138 tal muscle would be independent of KIR , NO, PGs and Na(+) /K(+) -ATPase activity.

139 IR channels alone or in combination with NO, PGs and Na(+) /K(+) -ATPase significantly reduced the va

140 e of KIR channels alone or combined with NO, PGs and Na(+) /K(+) -ATPase, attenuated ATP-mediated vas

141 Progression was detected in 62.1% of PG eyes and 59.8% of GS/PPG eyes by OCT, significantly (

142 script level showed the most accumulation of PG.

143 rase B (PatB) catalyzes the O-acetylation of PG in Gram (-) bacteria, which aids in bacterial surviva

144 In severity-stratified analysis of PG eyes, OCT had significantly higher detection rate tha

145 Different classes of PG function via overlapping families of receptors and si

146 Expansion of PG is tightly coupled to growth of a bacterial cell and

147 ithout the need to control the expression of PG synthesis genes.

148 ed capacity for evolving novel inhibitors of PG biogenesis despite their limited coding potential.

149 enetic manipulations to enhance the level of PG with implications for the commercial production of th

150 , LtgD was necessary for wild-type levels of PG precursor incorporation and produced fragments predom

151 n the hybrids, such that the localization of PG 32:0 in B73 x Mo17 is similar to the distribution in

152 -G/P2Y6 pair uncovers the signalling mode of PG-Gs as previously under-appreciated products of cycloo

153 rate that this postsynthetic modification of PG can be extended to use click chemistry to fluorescent

154 Phytoproduction of PG using a bacterial gene paves the way for further gene

155 ic lines were analyzed for the production of PG using gas and liquid chromatography coupled to mass s

156 we describe a more sustainable production of PG using plants expressing a native bacterial or a codon

157 Quantitative proteomics of PG from senescing rosettes of PGM48 overexpression lines

158 ral element for innate immune recognition of PG fragments.

159 on of expression of the WalRK TCS regulon of PG hydrolases.

160 th normal cell separation and the release of PG fragments by gonococci during growth.

161 sting and emerging evidence for the roles of PG sulfation and receptor interactions in determining ho

162 ntibiotics, polymerize the glycan strands of PG and crosslink them into the cell wall meshwork via at

163 Recent studies of PG sulfation illustrate the challenges of attributing bi

164 ortant implications for the understanding of PG biosynthesis in eukaryotes that remains incomplete.

165 Different classes of PGs may support or inhibit cell growth, and their functi

166 ogether, these results highlight the role of PGs as AKR1B1 inhibitors and the interest in PG-related

167 e cell wall with reduced PG cross-linking on PG units that have stems terminating in d-Ala-d-Lac, ser

168 vision regulator GpsB appears to co-ordinate PG synthesis at the septum during division and at the si

169 as PGM48 interactors, whereas several other PG-localized proteins and chlorophyll degradation enzyme

170 How the control over PG synthesis is exerted is unknown.

171 -negative prey bacteria, modifying their own PG as they grow inside prey.

172 descending facilitatory actions of intra-PAG PGs play a direct and central role in the maintenance of

173 ol 400 0.4 % and propylene glycol 0.3 % (PEG/PG) (n = 72).

174 3 +/- 7.4 vs 7.3 +/- 5.9; p = 0.001) and PEG/PG (19.3 +/- 7.5 vs 7.9 +/- 8.2; p = 0.001) respectively

175 +/- 2.2 vs 11.0 +/- 6.6; p = 0.002) and PEG/PG (6.5 +/- 2.5 vs 10.5 +/- 5.6; p = 0.019) respectively

176 whether the combination of serum pepsinogens(PGs), IgG anti-Helicobacter pylori (HpAb), and osteopont

177 Peptidoglycan (PG) is a highly cross-linked, protective mesh-like saccu

178 Peptidoglycan (PG) is important for helical shape, colonization, and ho

179 Peptidoglycan (PG), an essential stress-bearing component of the bacter

180 ia surround themselves with a peptidoglycan (PG) exoskeleton synthesized by the penicillin-binding pr

181 d cell separation and altered peptidoglycan (PG) fragment release, but little else is known about how

182 rounded by a polymer known as peptidoglycan (PG), which protects the cell from changes in osmotic pre

183 ifications onto its bacterial peptidoglycan (PG), the coat woven into bacterial cell wall.

184 cation of essential bacterial peptidoglycan (PG)-containing cell walls can lead to antibiotic resista

185 tic Z-ring, which coordinates peptidoglycan (PG) remodeling and envelope constriction.

186 s to synthesize the essential peptidoglycan (PG) cell wall during growth and division.

187 s previously shown to inhibit peptidoglycan (PG) biosynthesis, but its molecular mechanism of action

188 d peripheral (side-wall like) peptidoglycan (PG) synthesis in Streptococcus pneumoniae (pneumococcus)

189 eved by a concerted action of peptidoglycan (PG) hydrolases and PG-synthesizing/modifying enzymes.

190 E) through the replacement of peptidoglycan (PG) stem terminal d-Ala-d-Ala with d-Ala-d-Lac.

191 highly polymeric molecule of peptidoglycan (PG), pose a major problem for the release of progeny vir

192 lysis by a cell wall made of peptidoglycan (PG).

193 cosamine (GlcNAc) residues of peptidoglycan (PG).

194 ccus), side-wall (peripheral) peptidoglycan (PG) synthesis emanates from midcells and is catalyzed by

195 ly by the architecture of the peptidoglycan (PG) cell wall, a mesh-like layer that encases the cell.

196 y a proton influx through the peptidoglycan (PG)-tethered stator ring MotA/B.

197 e mouse OB glomerular layer, periglomerular (PG) and short axon (SA) cells, as well as mitral/tufted

198 not all (mltG), genes involved in peripheral PG synthesis and in the gpsB regulatory gene.

199 n which GpsB negatively regulates peripheral PG synthesis by PBP2b and positively regulates septal ri

200 Phosphatidylglycerol (PG) makes up 5-20% of the phospholipids of Escherichia c

201 olipids, we identified phosphatidylglycerol (PG) as the immunodominant lipid antigen.

202 membrane's content of phosphatidylglycerol (PG).

203 osphatidylserine (PS), phosphatidylglycerol (PG), phosphatidylinositol (PI), and sulfatides (ST).

204 ructural isomer (i.e., phosphatidylglycerol, PG, another low-abundance class of phospholipids).

205 lglycerols (SQDG) and phosphatidylglycerols (PG).

206 dy examined the capability of phytoglycogen (PG) to improve the water solubility of quercetin (QC).

207 Compared with PJ, PG was associated with an increased rate of grade A/B bl

208 motes the expression of a polygalacturonase (PG) gene, ADPG2, and increases PG activity in Arabidopsi

209 n allergens, especially a polygalacturonase (PG), were further characterized using double one-dimensi

210 ntly attached to hyperbranched polyglycerol (PG-M) by a cleavable linker.

211 cal properties of drum dried pregelatinized (PG) and granular cold-water-swelling (GCWS) corn starch

212 -amino acid modifications strengthening prey PG during Bdellovibrio invasion, and a zonal mode of pre

213 nderlying mechanisms that help the processed PGs to achieve this goal were not fully understood.

214 nce that plants can be engineered to produce PG using a bacterial gene.

215 h can be hydrolyzed enzymatically to produce PG.

216 /MS analysis showed that ATII cells produced PGs.

217 igation suggests a model where LtgD produces PG monomers in such a way that these fragments are relea

218 sponsible for the release of proinflammatory PG fragments.

219 Prostaglandin (PG) D2 is the dominant COX product of mast cells and is

220 Prostaglandin (PG) E2 is a bioactive lipid that plays protective roles

221 Prostaglandin (PG) E2 is involved in the Mo/Mp-mediated inflammatory re

222 Prostaglandin (PG)E2 accumulates in inflamed periodontal tissue and ind

223 xpression/production of COX-2/prostaglandin (PG) E2 and diminished expression of E-prostanoid (EP) 2

224 Analgesics which affect prostaglandin (PG) pathways are used by most pregnant women.

225 [LT] C4, LTD4, and LTE4), and prostaglandin (PG) E2 are generated at the site of inflammation, it is

226 ance on nitric oxide (NO) and prostaglandin (PG) synthesis.

227 y identified this compound as prostaglandin (PG)E2.

228 tinguished by thromboxane B2, prostaglandin (PG) E2, and PGD2 production, in addition to lysophosphol

229 tion (between 50% and 90%) in prostaglandin (PG) profiles in fish tissues and plasma with disruptions

230 erior to global inhibition of prostaglandin (PG) biosynthesis by aspirin-like drugs.

231 olving mediators, such as the prostaglandin (PG) D2-derived cyclopentenone metabolite, 15d-PGJ2, prod

232 vical ripening and labor with prostaglandin (PG) E2 or PGE analogs, often requiring many hours of hos

233 sis of nitric oxide (NO) and prostaglandins (PG).

234 Interestingly, other prostaglandins (PGs) inhibited the enzyme, including non-electrophilic P

235 Proteoglycans (PGs) in the extracellular matrix (ECM) play vital roles

236 Proteoglycans (PGs), a family of glycosaminoglycan (GAG)-protein glycoc

237 The pseudogap (PG) state and its related intra-unit-cell symmetry break

238 d carbon nanotubes (MWCNTs), and pyrogallol (PG) was fabricated and utilized for the sensitive determ

239 Accurate quantitative PG composition analysis provided compositional insights

240 In naive rats, PG EP3 receptor (EP3R) antagonism in vlPAG modulated nox

241 PG cross-linking and, consequently, reduced PG thickness and rigidity.

242 The analysis indicates reduced PG cross-linking, increased carboxypeptidase activities,

243 red in regions of the cell wall with reduced PG cross-linking on PG units that have stems terminating

244 tion microscopy, revealing higher resolution PG structural details and allowing the cell wall biosynt

245 weight/obesity on PTB risk, with rs11161721 (PG x E=1.8 x 10(-8); empirical PG x E=1.2 x 10(-8)) as t

246 und NMR-based solution structure of the same PG-fragment.

247 During senescence, PGs increase in size, reflecting their role in dismantli

248 The divisome controls septal PG synthesis and separation of daughter cells.

249 ese multi-enzymatic processes on two similar PG walls have proved challenging to elucidate.

250 or a polyglutamine repeat with site-specific PG mutations that favor the hairpin form, giving results

251 Current methods to synthesize PG are not sustainable due to the requirement for carbon

252 ration amidase can utilize a small synthetic PG fragment as substrate (GlcNAc-MurNAc(pentapeptide)-Gl

253 ty on macromolecular PG and on the synthetic PG derivative.

254 ), 5) tooth-associated pyogenic granuloma (T-PG) (n = 21), and 6) tooth-associated peripheral giant c

255 Degradation of tetrasaccharide PG fragments by LtgA is the first demonstration of a fam

256 and turbidity of GCWS were also higher than PG starch.

257 paste viscosity and textural parameters than PG starch and these parameters were enhanced with additi

258 cell monolayer permeation tests showed that PG-QC formulations resulted in substantially enhanced ce

259 The PG diets had significantly higher water stability, bulk

260 The PG muropeptide profile of 11168-GS was identical to that

261 as been demonstrated that LpoB activates the PG polymerization activity of PBP1b in vitro, the mechan

262 isualized as the energy scale approaches the PG.

263 -Lac, serving as markers to prevent both the PG-stem modification by carboxypeptidases and the cell w

264 utolysins such as lysozyme from cleaving the PG.

265 II, and Lipid II(A)(WTA), substrates in the PG and wall teichoic acid (WTA) biosynthetic pathways.

266 that Lys(M) inhibits a distinct step in the PG synthesis pathway from the A2 and E proteins indicate

267 In the PG treatments, intestinal SCFA significantly decreased w

268 ith their unique subcellular location in the PG.

269 rospective trials suggest superiority of the PG regarding perioperative complications.

270 that inhibit the MurA and MraY steps of the PG synthesis pathway (2-4) .

271 n be made robust to mis-specification of the PG using an SVM based classifier.

272 Among these, the pattern of sulfation on the PG sugar chains is a paramount determinant of a diverse

273 mycin to PG is approximately 1:1 if only the PG lipids in the outer leaflets of membranes are accessi

274 We and others have shown that the PG synthases PBP1b and PBP1a of Escherichia coli require

275 e isolated mutants that are resistant to the PG hydrolase lysozyme.

276 a strong n-type doping behavior, whereas the PG showed a weak n-type doping behavior.

277 ered expression of genes associated with the PG or tryptophan metabolism.

278 FtsW is thought to work in concert with the PG synthases penicillin-binding proteins PBP3 and PBP1b.

279 ol of spinal A-nociceptor processing through PG EP3 receptors.

280 Thus, PG-M may serve as prototype of a peripherally restricted

281 oes not conduct protons and does not bind to PG until it is inserted into the flagellar motor.

282 an importance of the multivalent binding to PG saccharides.

283 e comprehensively investigate the changes to PG composition in vancomycin-resistant Enterococcus faec

284 the lipoprotein adaptor NlpI contributes to PG enlargement by regulating cellular levels of MepS, a

285 and dynamics are mechanistically coupled to PG metabolism.

286 The stoichiometric ratio of daptomycin to PG is approximately 1:1 if only the PG lipids in the out

287 A direct glycosidic linkage to PG was also demonstrated for serotypes 8 and 31, whose r

288 phosphate (Und-P), (iii) diverting Und-P to PG synthesis or (iv) promoting Und-P recycling.

289 single CPS repeat unit can be transferred to PG.

290 Phloroglucinol (1,3,5-trihydroxybenzene; PG) and its derivatives are phenolic compounds that are

291 This study showed the potential of using PG to formulate poorly water-soluble ingredients such as

292 tion of the products derived from vaporizing PG and GLY under mild, single puff conditions.

293 PG-QC formulations with various PG to QC ratios were prepared; the solubility of QC reac

294 binary mixture of lipids and peptides, where PG-1 acts as a line-active agent in lowering interfacial

295 c and transcriptional analyses combined with PG structure determination of the guaA mutant enabled us

296 energy transfer measurements, combined with PG-binding assays and fitting of the crystal structures

297 rodopa Ki was 20% lower in BED compared with PG and controls (p<0.002).

298 Compared with PG, BED patients show widespread losses of mu-opioid rec

299 were more postoperative bleeding events with PG.

300 on of QC crystallinity upon formulating with PG that was associated with the intermolecular hydrogen