ライフサイエンスコーパス: C6

1 on occurs with retention of configuration at C6'.

2 mic-like parallel factor analysis component (C6).

3 heme-containing substitute, cytochrome (Cyt) c6.

4 ed at the midvertebral levels of C1, C3, and C6.

5 y a modest effect on the replication of HAdV-C6.

6 We used yeast lysate labeled with either (13)C6(15)N2-lysine or (2)H8-lysine, isotopologues of lysine

7 and perfluoroalkyl carboxylic acids (PFCAs; C6-15) along with six perfluoro-octane sulfonic acid (PF

8 ing significant amounts of C4 (35.8% yield), C6 (28.2% yield), and C8 (9.4% yield) alcohols.

9 Two phenyl substituents on C6 (2i), or a phenyl and a methyl substituent (2g, 2h),

10 EPEV replicated in C6/36 mosquito cells, yielding high infectious titers, b

11 ulturing mosquito pools on Aedes albopictus (C6/36) cell cultures.

12 e collected in 2012; 13 PFASs (C6-C12 PFCAs; C6, 8, 10 PFSAs; MeFOSAA and EtFOSAA; and FOSA) were rou

13 The approximately 9-14% yearly decline of C6-8 perfluoroalkyl sulfonates (PFSAs) following the cea

14 yl sulfonates (PFSAs) following the cease in C6-8 PFSA precursor production in 2001 indicates that th

15 dual dipolar couplings (DeltaRDCs) involving C6/8-H6/8, C3'-H3' and C4'-H4' vectors are correlated to

16 b]indole (N-acetoxy-AalphaC), and their [(13)C6]AalphaC-labeled homologues were reacted with albumin.

17 the ABCC6 (ATP binding cassette transporter C6) ABC transporter are associated with pseudoxanthoma e

18 6 aldehydes that seem to be more stable than C6 alcohols and esters.

19 one leaf removal had no consistent impact on C6 alcohols, volatile phenols, lactones, fermentation-de

20 increase in particular important phenols and C6 alcohols, while C6 aldehydes mostly decreased.

21 In addition, C6-alcohols accumulated before veraison and decreased to

22 lar important phenols and C6 alcohols, while C6 aldehydes mostly decreased.

23 ted by the genetic origin of the olives with C6 aldehydes that seem to be more stable than C6 alcohol

24 products of the lipoxygenase pathway (mainly C6-aldehydes) and of glucosinolate hydrolysis (mainly is

25 n separation of a 11-component mixture of C1-C6 alkanes, the hierarchical phase outperforms the struc

26 A Rh(III)-catalyzed highly efficient C6-alkylation of 2-pyridones has been achieved successfu

27 A methyl substituent on C6 along with a single phenyl causes the phenyl to twist

28 GEOV1, MERIS, and MODIS C6 also exhibited an increasing trend, but to a much sma

29 In Sickle mice, C6' also attenuated the increased ROS markers gp91(phox)

30 mination with 2-aminobenzoic acid and 2-(13)[C6]-aminobenzoic acid, respectively.

31 ferences in intracellular growth relative to C6 and C14.

32 rparts 1-4 were proven to self-assemble into C6 and C7 pseudocycles by intramolecular H-bonds in solu

33 s the attachment of two sulfhydryl groups to C6 and C8 of a pendant octanoyl chain.

34 factor, the insertion of two sulfur atoms at C6 and C8 of an n-octanoyl chain.

35 radicals, which abstract hydrogen atoms from C6 and C8 of the substrate.

36 rtion of two sulfur atoms at the unactivated C6 and C8 positions of a protein-bound octanoyl chain to

37 in the ipsilateral DH of the spinal segment C6 and corresponding neuronal responses in typical pain-

38 In particular, fingerprinting revealed that C6 and F98 glioma models have similar signatures while 9

39 The expressed DbpA/C6 and OspC proteins were useful in detecting anti-Borre

40 Here we analyze rat C6 and patient-derived glioma cell motility in vitro usi

41 ting the more readily accessible hydroxyl at C6 and the more reactive anomeric hydroxyl.

42 (dihexyl-N-nitrosoamino)-2,4-dinitrobenzene (C6') and an inactive form of the compound [1,5-bis-(dihe

43 e invariable region 6 of the vlsE gene (DbpA/C6) and (b) the full-length ospC gene (OspC).

44 ssible directions were tested (C1-->C2, C1-->C6), and two different mechanisms were sought (stepwise

45 hyperintensity and volume alterations of C5, C6, and C7 nerve roots were observed in patients with AL

46 ransfer occurs after Cys(1226) attack to Cyt C6, and the methyl transfer step is chemically rate-limi

47 Likewise, lack of C6, and thereby deficient terminal complement complex, w

48 tide that blocks MAC formation by inhibiting C6, and we compared its therapeutic effect to that of Or

49 y certain catalysts favour bond formation at C6, and-although there are a small number of catalytic e

50 By contrast, anti-C6 antibodies were detected in pretreatment sera from 17

51 We generated a C6 antisense oligonucleotide that blocks MAC formation b

52 1:1 mixture of acetaminophen (APAP) and (13)C6-APAP resulted in mass spectra that contained "twin" i

53 ophen (N-acetyl-p-aminophenol, APAP) and (13)C6-APAP were incubated with rat liver microsomes, which

54 This included complement components C3, C5, C6, apolipoproteins A-I, A-IV, C-I and M, histidine-rich

55 An efficient, direct C6-arylation of 2-pyridones has been successfully accomp

56 to diversify the stereochemical outcomes at C6 as well as C10a.

57 d KMO, but not IDO, in vitro in BDV-infected C6 astroglioma cells.

58 a dimethylallyl moiety to the flavin N5 and C6 atoms.

59 ensity-based functionals, (ii) semiclassical C6-based, and (iii) one-electron effective potentials.

60 nfiguration to the stereogenic center of the C6-benzylic position in both cellular and enzymatic test

61 mately to formation of the dimethylallyl C3'-C6 bond.

62 ible for assembly of the ethyl side chain at C6, bridgehead epimerization at C5, installation of the

63 N5 mechanism in which 5 binds to S2 with its C6-C11 group poised to attack C1 in GPP to form the moen

64 er samples were collected in 2012; 13 PFASs (C6-C12 PFCAs; C6, 8, 10 PFSAs; MeFOSAA and EtFOSAA; and

65 cosmetics while medium chain fatty alcohols (C6-C12) could be used as diesel-like biofuels.

66 Medium-size alkyl gallates (C6-C12) were the best antioxidants.

67 separation of 50 analytes, including alkane (C6-C12), alkene, alcohol, aldehyde, ketone, cycloalkane,

68 that the range of alkylimidazole homologues (C6-C13) observed in atmospheric HULIS would be 1.5-4.4 t

69 ropyridines (DHPs) bearing changes at the C2/C6, C3/C5, C4, or N1 position.

70 C8/C7 and C6/C5 polyfluorinated sulfonates from br-PFOS and br-PFH

71 n of C6, C8, and C10 monoalkylated PFPAs and C6/C6, C6/C8, and C8/C8 dialkylated PFPiAs was investiga

72 roxy group was selectively introduced to the C6, C7, C10 and the central C21 position of diazafenestr

73 C8-C6' coupling and four O-methyl groups at C6, C7, C3', and C4' as numbered on the 1-benzylisoquino

74 llowed by the sequential condensation of the C6, C7, C8.

75 After 12 weeks, axons from C6-C7 dorsal root ganglia regenerated through the tenasc

76 Although TRPC3/C6/C7 can be directly activated by diacylglycerols produ

77 The sorption of C6, C8, and C10 monoalkylated PFPAs and C6/C6, C6/C8, an

78 -appended self-assembled monolayers with C2, C6, C8, and C12 space-filling alkyl chains, which captur

79 increasing chain length for C8-C14 PFCAs and C6-C8 perfluoroalkyl sulfonates.

80 ned during the last two days of the culture (C6-C8) resulted in a significant decrease in PF formatio

81 , C8, and C10 monoalkylated PFPAs and C6/C6, C6/C8, and C8/C8 dialkylated PFPiAs was investigated in

82 reactions (J-K), for the formation of the C5-C6, C9-C10, and C17-C18 double bonds, a Suzuki-Molander

83 (C6-C9)-acyl chains with a distal phenyl group proved to

84 cis-diastereoselectivity providing access to C6-carbon-functionalized dihydrothymidine cis-alcohols,

85 alent phosphate as monoesters of C2, C3, and C6 carbons of glucose residues based on analyses of phos

86 membrane lipid order disruption byd-ceramide-C6 causes Golgi pH alkalization.

87 ho-Az to detect differences in H2S levels in C6 cells and those treated with AOAA, a common inhibitor

88 The viability of C6 cells remained unchanged, indicating that these surfa

89 rigenic process and increased the ability of C6 cells to form colonies in soft agar or spheres when g

90 C6 ceramide increases IQGAP1 protein levels by preventin

91 We report here that C6 ceramide increases serum-stimulated ERK1/2 activation

92 osmotic shock, bacterial sphingomyelinase or C6 ceramide.

93 igenic lipid, and treatment with short-chain C6-ceramide decreased the number of ovarian cancer cells

94 Exogenous C6-ceramide did not alter Bcl-x 5'SS selection in INS-1

95 In addition, exogenously added C6-ceramide mimicked the effects of TNFalpha that lead t

96 ed that long-chain ceramide regenerated from C6-ceramide through the salvage/recycling pathway, at le

97 nanoparticle-based delivery, fluorescent NBD C6-ceramide was efficiently converted to NBD C6-glucosyl

98 ay, at least in part, mediated the action of C6-ceramide.

99 Azido-functionalized C6-ceramides were incorporated into and localized within

100 C6 compounds such as 1-hexanol, (E)-2-hexenal, (E)-2-hex

101 and TAS) and volatiles compounds (alcohols, C6 compounds, ethyl esters, terpenes, aldehydes, acids,

102 correlations between the ripening ratio and C6 compounds, resveratrol and carbonyl compounds.

103 the highest acetaldehyde, ethyl acetate and C6-compounds levels, and had increased ester levels in r

104 orphine alkaloid glaucine, which displays C8-C6' coupling and four O-methyl groups at C6, C7, C3', an

105 8x, respectively), than Ti-C2-Cr(SNS) and Ti-C6-Cr(SNS).

106 etnUiO-66-S gives the highest selectivity to C6-cyclic products (62.4% and 28.6% for cyclohexane and

107 Pt subsetnUiO-66-N decreases selectivity for C6-cyclic products to <50% while increases the acyclic i

108 NMR studies of dimerization in C6 D6 find aromaticity-modulated H-bonding (AMHB) energy

109 C6-deficient C57BL/6 mice were also inoculated with E. c

110 l functional connectivity between the spinal C6-DH and the thalamus, primary somatosensory cortex, bi

111 se- (C6-MAN) and ethylene-glycol-terminated (C6-EG) diluents.

112 We then compared the performance of the C6 EIA alone and as a first-tier test followed by immuno

113 The C6 EIA alone had sensitivity similar to that of standard

114 undergoing evaluation for Lyme disease, the C6 EIA could guide initial clinical decision making, alt

115 However, the C6 EIA has not been extensively studied in pediatric pat

116 We performed a C6 EIA on all collected specimens, followed by a supplem

117 followed by a supplemental immunoblot if the C6 EIA result was positive but the whole-cell sonicate E

118 l immunoblot improved the specificity of the C6 EIA to 98.6%.

119 thm, where immunoblotting is replaced by the C6 EIA, performs as well or better than STTT.

120 T) approach where the second-tier test was a C6 EIA.

121 equence, expressed (VlsE) CLIA followed by a C6 EIA.

122 whole-cell sonicate (WCS) EIA followed by a C6 EIA; (2) a WCS EIA followed by a VlsE chemiluminescen

123 At the 2 laboratories that performed the C6 ELISA, the percentage of positive tests was comparabl

124 the results of standard serological assays (C6, ELISA, and Western blot).

125 A biogenetically inspired dehydrative C6-etherification reaction proved highly effective to se

126 rms sequential methylations to build out the C6-ethyl side chain in a stereocontrolled manner.

127 Cys residues (four disulfide bonds), whereas C6 evasins have only three of these disulfide bonds.

128 isplays an additional, stabilizing Cu-Cipso (C6 F5 ) interaction.

129 2,6-Ph2 -4-tBuC6 H2 ) with Piers' borane (HB(C6 F5 )2 ).

130 is(alkyl) hydridoborato Ce{C(SiHMe2 )3 }2 HB(C6 F5 )3 (2).

131 eaturing the unusual [HBEt3 ](-) (5) and [HB(C6 F5 )3 ](-) (6) ligands is described.

132 plex supported by a diphosphine ligand and B(C6 F5 )3 act cooperatively, in a manner reminiscent of a

133 ers enable C-C bond formation as catalytic B(C6 F5 )3 can be used to effect formal 1,5-alkyl migratio

134 ation of alkyne-containing substrates with B(C6 F5 )3 enabled the first catalytic intramolecular cycl

135 l-known frustrated Lewis pair (FLP) PtBu3 /B(C6 F5 )3 in varying stoichiometries.

136 reaction with the hard Lewis acidic borane B(C6 F5 )3 initiates a cascade reaction to yield a complex

137 complex Ce{C(SiHMe2 )3 }3 (1) reacts with B(C6 F5 )3 to produce the zwitterionic bis(alkyl) hydridob

138 Magnetic measurements reveal that [2Dy ][B(C6 F5 )4 ] is an SMM with a record anisotropy barrier up

139 (2Dy ) as a salt of the non-coordinating [B(C6 F5 )4 ](-) anion.

140 plex [(TiX3 )2 (mu2 -OCHO-kappaO:kappaO')][B(C6 F5)4], 4[B(C6 F5)4], was simply deprotonated with the

141 (mu2 -OCHO-kappaO:kappaO')][B(C6 F5)4], 4[B(C6 F5)4], was simply deprotonated with the strong base K

142 15), divided in 3 models: brain tumors (9 L, C6, F98), permanent stroke, and a control group of healt

143 MR approaches in healthy tissues and in the C6, F98, and permanent stroke models.

144 imethylsilyl-alpha-D-cholesterylglucoside at C6 followed by phosphoramidite coupling.

145 products (GEOV1, MERIS, MODIS C5, and MODIS C6) from 2003 through 2011 to help clarify the performan

146 C6 functionalization inhibits access to the (1)npi* stat

147 Instead, C6 functionalization plays an important role in regulati

148 erted a dipeptide precursor into the desired C6-functionalized azabicycloalkane scaffolds.

149 lta-C8, delta-C10) and gamma-lactones (gamma-C6, gamma-C8, gamma-C10).

150 gnificant apoptotic and cytotoxic effects in C6 GBM cells.

151 The trisaccharides prepared from (13)C6(glc) sucrose and lactose were analyzed by ESI-MS(n),

152 +) exchanger NHE5 is abundantly expressed in C6 glioma cells and plays an important part in regulatin

153 able differences in channel activity between C6 glioma cells and tsA201 cells expressing L166Q and A1

154 acellular Ca(2+) concentration in 1321N1 and C6 glioma cells without altering TRAP-6 and carbachol Ca

155 reduced proliferation and increased death of C6 glioma cells, effects that can be partially rescued b

156 ronic antidepressant treatment of rats or of C6 glioma cells, tracks with the delayed onset of therap

157 Sustained treatment of C6 glioma cells, which lack 5-hydroxytryptamine transpor

158 rived tsA201 cells and in glial cell-derived C6 glioma cells.

159 Immunization of C6 glioma-bearing rats with DCs pulsed with Hsp70-SPIONs

160 ormed in athymic mice bearing NIS-expressing C6-glioma subcutaneous xenografted tumors to determine t

161 was observed in human NIS (hNIS)-expressing C6-glioma xenografts as well as expected NIS-mediated up

162 , oral glucose absorption (RaO) with [U-(13) C6 ]-glucose, and hepatic glucose production (EGP) with

163 ns in mouse tissues during 12 to 48 h of (13)C6-glucose feeding.

164 e, we report noninvasive introduction of (13)C6-glucose via a stress-free, ad libitum liquid diet.

165 , 2) 10% D-[(13)C6]glucose, and 3) 1% D-[(13)C6]glucose co-provisioned with 10% sucrose.

166 tes, which generate M2 acetyl-CoA (e.g. [(13)C6]glucose or [1,2-(13)C2]palmitate) or/and M1 acetyl-Co

167 es for 7 days: 1) 10% sucrose, 2) 10% D-[(13)C6]glucose, and 3) 1% D-[(13)C6]glucose co-provisioned w

168 C6-ceramide was efficiently converted to NBD C6-glucosylceramide in live cells or in mouse tissues, w

169 enabled detection and quantification of NBD C6-glucosylceramide in the low-femtomolar range.

170 labeled metabolites, namely, (14)C- and (13)C6-glucuronides and sulfates.

171 The lack of a C6 H-bond donor while maintaining A3AR affinity and effi

172 The base and sugar (H6,C6, H1',C1') chemical shifts of C43 for the dominant con

173 dipolar zwitterionic p-benzoquinonemonoimine C6 H2 (-cdots, three dots, centered NH2 )2 (-cdots, thre

174 lidene; Cp*=eta(5) -C5 Me5 ; Trip=2,4,6-iPr3 C6 H2 ) with a variety of organic substrates are describ

175 2 ; R=1,12-xanthendiyl spacer; Mes=2,4,6-Me3 C6 H2 ), acting as a frustrated Lewis pair (FLP) in smal

176 diazametallocyclobutene 8 (Ar=4-Ph-2,6-iPr2 C6 H2 ).

177 (kappa(2) -N,O-AZADO) ((Ar) L=1,9-(2,4,6-Ph3 C6 H2 )2 -5-mesityldipyrromethene).

178 f saturated NHC SIMes (SIMes=[:C{N(2,4,6-Me3 C6 H2 )CH2 }2 ]) with Group 1 alkyl bases suggest this d

179 Addition of N3 Ar(X3) (Ar(X3) =2,4,6-X3 C6 H2 ; X=Cl or Me) to [(i) Pr2 NN]Cu(NCMe) results in t

180 reated with NaOH/Na(+) BArf (-) (BArf =B(3,5-C6 H3 (CF3 )2 )4 ) to give lipophilic Lambda- and Delta-

181 The protonation of 4 by [H(OEt2 )2 ][B{C6 H3 (CF3 )2 }4 ] yields [(3H,4H-pyr-ONO)(3H-pyr-ONO)Zr

182 isocyanates (iPr2) ArNCO ((iPr2) Ar=2,6-iPr2 C6 H3 ) and (Ph2tBu) ArNCO ((Ph2tBu) Ar=2,6-Ph2 -4-tBuC6

183 he dicopper(II) diketimide 4 (Ar=2,6-(i) Pr2 C6 H3 ) or undergo nitrile insertion to give diazametall

184 ] (cAACMe =:C(CMe2 )2 (CH2 )NAr, Ar=2,6-iPr2 C6 H3 ) with H2 SiI2 in a 3:1 molar ratio in DME afforde

185 2) )2 ] (Ar(Dipp2) =2,6-(2,6-(iPr)2 C6 H3 )2 C6 H3 ).

186 CNAr(Dipp2) )2 ] (Ar(Dipp2) =2,6-(2,6-(iPr)2 C6 H3 )2 C6 H3 ).

187 duct L:Si=Si[Fe(CO)4 ]:L (L:=C{N(2,6-Pr(i) 2 C6 H3 )CH}2 ) (2) at room temperature.

188 ][NTf2 ], where Ar${{^{{\rm Dipp}{_{2}}}}}$=C6 H3 -2,6-(C6 H3 -2,6-iPr2 )2 and R=Me (3), CHCH2 (4),

189 here Ar${{^{{\rm Dipp}{_{2}}}}}$=C6 H3 -2,6-(C6 H3 -2,6-iPr2 )2 and R=Me (3), CHCH2 (4), or CCH (5).

190 [(3H,4H-pyr-ONO)TiCl2 (OEt2 )][B{3,5-(CF3 )2 C6 H3 }4 ] (3-Et2 O) states through remote protonation o

191 (3H,4H-pyr-ONO)(3H-pyr-ONO)Zr][B{3,5-(CF3 )2 C6 H3 }4 ] (5), thus demonstrating the storage of three

192 here PO(Bp,OMe) =(2-MeOC6 H4 )(2-{2,6-(MeO)2 C6 H3 }C6 H4 )(2-SO3 -5-MeC6 H3 )P, inserts vinyl fluori

193 lSi: ((TMS) L=N(SiMe3 )Dipp; Dipp=2,6-Pr(i)2 C6 H4 ) and two NHC ligands (N-heterocyclic carbene=:C[(

194 (Bp,OMe) =(2-MeOC6 H4 )(2-{2,6-(MeO)2 C6 H3 }C6 H4 )(2-SO3 -5-MeC6 H3 )P, inserts vinyl fluoride (VF)

195 Me3 )ClSi:-->Ni(NHC)2 ] (1; Dipp=2,6-(i) Pr2 C6 H4 ; N-heterocyclic carbene=C[((i) Pr)NC(Me)]2 ) with

196 e CAr -H bond activation product [1-F-2-IMe -C6 H4 ](+) I(-) (3).

197 of a tripodal nitroxide ligand [{(2-(t) BuNO)C6 H4 CH2 }3 N](3-) (TriNOx(3-) ), feature a size-sensit

198 taining the redox-active ligand [{2-(tBuN(O))C6 H4 CH2 }3 N](3-) .

199 -imine [Cp*(IXy)(H)2 RuSn(kappa(2) -N,O-NSO2 C6 H4 Me)Trip] (6) complexes was achieved by treatment o

200 and lactam functionalities using IrCl(CO)[P(C6 H5 )3 ]2 (Vaska's complex) in the presence of tetrame

201 ed Cu(II) complex Cu{N(SiMe3 )Dipp}2 (1 Dipp=C6 H5 -2,6Pr(i) 2 ) and its Cu(I) counterpart [Cu{N(SiMe

202 not detected with reactive cations such as [C6 H5 ](+) .

203 Treatment of Zr2 with one equivalent of KCH2 C6 H5 and two equivalents of benzo-15-crown-5 ether (B15

204 Treatment of 2 with one equivalent of KCH2 C6 H5 and two equivalents of benzo-15-crown-5 ether (B15

205 1, Tren(TIPS) =N(CH2 CH2 NSiPr(i)3 )3 ) with C6 H5 CH2 K and [U(Tren(TIPS) )(THF)][BPh4 ] (2) afforde

206 Treatment of 3 with C6 H5 CH2 K and two equivalents of benzo-15-crown-5 ethe

207 ddition of H3 BNMeR'H2 to [Rh(L(R) )(eta(6) -C6 H5 F)][BAr(F) 4 ].

208 din A by taking advantage of a direct indole C6 halogenation of the related ketopremalbrancheamide.

209 4-HSL, promote plant growth, treatments with C6-HSL, oxo-C10-HSL, or oxo-C14-HSL resulted in differen

210 growth, characterized by acetylation of the C6 hydroxyl group of N-acetylmuramic acid in the PG glyc

211 roduction of a vinyl group as a masked OH at C6, (iii) an oxymercurative aldol to synthesize the tric

212 of genes encoding both plastocyanin and Cyt c6 in algal and cyanobacterial genomes might be because

213 in, and transient receptor potential channel C6 in the podocyte was significantly altered in 1,25-vit

214 The virus burdens in the livers of HAdV-C6-infected hamsters are higher than the virus burdens i

215 Similarly to mouse models, in hamsters, HAdV-C6 is sequestered by macrophages to a lesser degree than

216 radio ((14)C) isotopologue and a stable ((13)C6) isotopologue of acetaminophen as substrates for in v

217 The radiocalibrated (13)C6-isotopologues were in turn used to quantitate acetami

218 During the pulse, rats (n = 5) were fed (13)C6-labeled lysine ("heavy") feed for 23 days to label pr

219 Experiments with (13)C6 labelled Gal and Glc showed that both monosaccharides

220 C-MS) method to measure the fraction of [(13)C6]leucine-labeled alpha-tubulin-derived surrogate pepti

221 The performance of 8Ah C6/LiFePO4 pouch cells were measured following periods o

222 amsters are infected intravenously with HAdV-C6, live, infectious virus can be isolated from the lung

223 The commercially-available C6 Lyme enzyme immunoassay (EIA) has been approved to re

224 e, especially when compared to the mannose- (C6-MAN) and ethylene-glycol-terminated (C6-EG) diluents.

225 Because the initial C6-Me and C6-styryl derivatives had unexpectedly high A3

226 Of these, the C6-Me-(2-phenylethynyl) and C2-(5-chlorothienylethynyl)

227 The sensor fabricated with C6-MEG has a specificity factor ( approximately 13.5) su

228 this study, the methoxy-terminated diluent (C6-MEG) is the most effective in alleviating both nonspe

229 andards, traditionally used to calibrate (13)C6-metabolites via liquid chromatography-tandem mass spe

230 phy-tandem mass spectrometry (LC-MS/MS), (13)C6-metabolites were radiocalibrated by their (14)C-isoto

231 n enzyme assays, the simultaneous C5(methyl)/C6(methyl/ethyl) substitution in the 2-Cl-6-F- and 2,6-F

232 philic attack of Cys(1226) to cytosine (Cyt) C6, methyl transfer from S-adenosyl-l-methionine (SAM) t

233 rutinoside, ranging from 258 (C6) to 10,729 (C6) mg kg(-1).

234 but not female mice exposed in utero to the C6 monoclonal antibody, binding to contactin-associated

235 entified in the genes coding for C5 (n = 4), C6 (n = 5), C7 (n = 12), C8 (n = 7), and C9 (n = 2).

236 ratio in the dorsal nerve root ganglion and C6 nerve (P < .001) with the multiecho TSE-mDixon sequen

237 onation at N5 of H2F and hydride transfer to C6 occur in a stepwise mechanism.

238 at full maturity were characterised by gamma-C6 of high enantiomeric purity remaining stable during t

239 f the cluster becomes covalently attached to C6 of the octanoyl substrate.

240 al isomers (C1alpha, C1beta, C2, C3, C4, and C6) of a Glc-Pt.

241 gioselectively a fructosyl residue to either C6-OH group of the glucose residues in Tre.

242 or five-membered H-bonded pseudocycles (C8, C6 or C5), depending on the steric bulk of both N(alpha)

243 by using either the mice deficient in C5 and C6, or MAC's regulator CD59.

244 However, the DbpA/C6-OspC ELISA was markedly better (80% versus 63%) than

245 The two methods (DbpA/C6-OspC versus 2-tier test) were equivalent in identifyi

246 The MW 226 C6-OSs were chemically elucidated, along with structural

247 The presence of a conformationally flexible C6 oxygen atom in the sugar-derived lactol donors is req

248 t solvents: one, ~10 years old, receiving C5-C6 paraffins and the other, ~35 years old, receiving nap

249 , specifically for contributions made to the C6 peak, data from the simulations suggest that the 18-

250 rformance is comparable to the commonly used C6 peptide by lab-based ELISA.

251 omer sulfonamide alkylamine (FTAA) and C3 to C6 perfluoroalkane sulfonamido amphoterics.

252 oding dose (50 mg . kg(-1) ) of l-[ring-(13) C6 ]phenylalanine was administered via i.p. injection.

253 l-[ring-(13)C6]Phenylalanine was infused.

254 ore, our results suggest that C2, C3, and/or C6 phosphate could all contribute to abnormal glycogen s

255 C6 phosphorylation also accounted for approximately 20%

256 l phosphate, we determined the proportion of C6 phosphorylation in rabbit muscle glycogen to be appro

257 d with wild type mice, but the proportion of C6 phosphorylation remained unchanged at approximately 2

258 ansient receptor potential (TRP) ion channel C6 plays a pivotal role in hereditary and sporadic glome

259 at both the C2 position (2-O-sulfation) and C6 position (6-O-sulfation).

260 enabled their regiospecific ring-opening at C6 position by organometallic nucleophiles.

261 ations that could generate a new bond at the C6 position of a dienoate are particularly desirable bec

262 ing to be a general way to functionalize the C6 position of an N,C3-disubstituted indole for the synt

263 ew azabicycloalkane scaffolds endowed at the C6 position with a para-substituted phenethyl side chain

264 o the major product PA-A is oxidation at the C6 position.

265 zole, squaramide or a benzamide group at the C6' position.

266 d with a hydrogen bond donating group at the C6' position.

267 a regioselective fashion at the challenging C6-position of 2-pyridone intermediates.

268 ) the number of fluorine atoms at the C2 and C6 positions, and (3) the number of pairs of fluorine at

269 lization, but a single phenyl substituent on C6 produces a greater increase.

270 els in athymic nude mice: a human PC-3 M-luc-C6 prostate tumor and a human BxPc3-luc2 pancreatic tumo

271 h the tricyclic core and the adjacent C5 and C6 quaternary stereocenters.

272 the ligand and reaction conditions used, the C6 regioisomer a can be obtained in 4:1 ratio and excell

273 ng system and the attendant C5 (quaternary), C6 relative stereochemistry; a malonate enolate conjugat

274 pes belonging to species C, HAdV-C5 and HAdV-C6, replicate to significantly different extents and cau

275 ignificantly different severities, with HAdV-C6 replicating better and inducing more severe and more

276 l carboxylates and sulfonates (>/=C8 and >/= C6, respectively).

277 cules adsorb bowl opening-up with the center C6 ring parallel to the surface.

278 SpnF because interconversion between the C5-C6 s-trans and s-cis conformers is facile.

279 n contrast, the enantiomeric purity of gamma-C6 significantly decreased during post-harvest storage o

280 metric hydrogenation was employed to set the C6 stereochemistry, resulting in an especially efficient

281 Because the initial C6-Me and C6-styryl derivatives had unexpectedly high A3AR affinit

282 ion of the N-(p-methoxybenzyl) group and the C6 substituent in the lactam ring of the free-radical in

283 evelopment of catalysts and processes for C5-C6 sugar reforming into chemical intermediates and produ

284 drate polymers into their constituent C5 and C6 sugars, and subsequent heterogeneously catalyzed tran

285 In particular, the C6' sulfonamides catalyzed the reaction with the alpha,b

286 SF from the excimer state of Me, C6, TEG, and EH takes place in tauSF = 22, 336, 195, and

287 iable major protein-like sequence expressed (C6)-that were performed at 1 university laboratory, 1 co

288 series of Cinchona alkaloids includes known C6' (thio)urea and sulfonamide derivatives and several n

289 depleted of individual complement components C6 to C9.

290 hat completely reversed specificity from the C6 to the C3 position.

291 quercetin-3-O-rutinoside, ranging from 258 (C6) to 10,729 (C6) mg kg(-1).

292 95 (C4), Cys148 (C5) to Cys219 (C8), Cys151 (C6) to Cys243 (C9), and Cys161 (C7) to Cys266 (C10).

293 ved from the fifth to the sixth cervical (C5-C6) to the seventh cervical to first thoracic (C7-T1) le

294 DPP) chromophores with methyl (Me), n-hexyl (C6), triethylene glycol (TEG), and 2-ethylhexyl (EH) sub

295 Transient receptor potential channel C6 (TRPC6) gain-of-function mutations and increased TRPC

296 ing the transient receptor potential channel C6 (TRPC6).

297 especially for 3,4-DHPEA-EDA, p-HPEA-EDA and C6 volatiles.

298 ater to humic-rich freshwater ecosystems but C6 was only present at trace to background levels.

299 Chromosomes C2, C4 and C6 were the result of complex reshuffling of syntenic bl

300 [1,5-bis-(dihexylamino)-2,4-dinitrobenzene (C6)] were tested in neuronal cell cultures and penile ly