ライフサイエンスコーパス: Me

1 Me(2+) also promotes an increase in the backward translo

2 Me(2+) ions are intimate architectural components of eac

3 Me(2+) modulates the translocation rates but not their r

4 Med., and indicate strong oil biodegradation potential.

5 ted to glioma risk (AMORIS, P trend = 0.002; Me-Can, P trend = 0.04) and pre-diagnostic diabetes (AMO

6 ine groups have been synthesized (R = H (1), Me (2), and allyl (3)), and their electrocatalytic prope

7 The complexes, ((Mes)PDI(Me))UI3(THF) (1), ((Mes)PDI(Me))UI2(THF)2 (2), [((Mes)PDI(Me))UI]2 (3), and

8 al complexes Ti((Me)PDP)2 and Zr((Me)PDP)2 ((Me)PDP = 2,6-bis(5-methyl-3-phenyl-1H-pyrrol-2-yl)pyridi

9 form trans-bis(imido) species, Cp(P)U(NAr)2((Mes)PDI(Me)) (Ar = Ph, 2-Cp(P); Ar = p-Tol, 3-Cp(P)) and

10 -Cp(P); Ar = p-Tol, 3-Cp(P)) and Cp*U(NPh)2((Mes)PDI(Me)) (2-Cp*), only 1-Cp* can cleave diazene N ho

11 p* with AgSbF6 affords cationic [Cp*U(NPh)2((Mes)PDI(Me))][SbF6] (5-Cp*) from a metal-based U(V)/U(VI

12 from phenyl to p-tolyl, forming Cp*U(NTol)2((Mes)PDI(Me)) (3-Cp*), changes the electronic structure,

13 (I) forms cationic uranium(VI) [Cp*U(NTol)2((Mes)PDI(Me))][SbF6] (4-Cp*) and [Cp*U(NTol)2((t)Bu-(Mes)

14 beta-iodo- and beta-chloroenones 9a,c; (2) (Me)2Phen(OMe)2.NiCl2 13b is a better Ni-catalyst than (M

15 I3(THF) (1), ((Mes)PDI(Me))UI2(THF)2 (2), [((Mes)PDI(Me))UI]2 (3), and [((Mes)PDI(Me))U(THF)]2 (4), w

16 and (C5Me5)3ThMe, 1, rather than (C5Me5)2Th(Me)I.

17 tepwise oxo silylation to form (Me3SiO)2UI2((Mes)PDI(Me)) (5) or (Me3SiO)UI2((t)Bu-(Mes)PDI(Me)) (5-(

18 3-Me-2,6-diazaindole ((2,6-aza)Ind) was strategically desi

19 yl substituent led to the discovery of the 3-Me,5-acrylonitrile-phenyl analogue RP-13s (IDX899) havin

20 = 0; MoF3, x = 1; MoF6, x = 2; MoF9, x = 3; Mes = 2,4,6-trimethylphenyl) and their silica-supported

21 he production of both 4-Me-5-NO2-L-Trp and 4-Me-7-NO2-L-Trp uncovered remarkable regio-promiscuity of

22 air-sensitive cobalt(III) dihydride boryl 4-Me-((iPr)PNP)Co(H)2BPin (1) and the air-stable cobalt(II

23 The production of both 4-Me-5-NO2-L-Trp and 4-Me-7-NO2-L-Trp uncovered remarkable

24 s with methyl protected phenolic moieties (4-Me), displaying a Ag(I) center incapable of O2 binding (

25 nitration process was developed to nitrate 4-Me-DL-Trp.

26 The reaction of 4-Me with dioxygen at low temperature produces a species (

27 nd the air-stable cobalt(II) bis(pivalate) 4-Me-((iPr)PNP)Co(O2C(t)Bu)2 (2) compounds were effective

28 ricyclic nucleosides 6'-F-tc-T and 6'-F-tc-5(Me)C, as well as the corresponding building blocks for o

29 ermediate 5-methylphenazine-1-carboxylate (5-Me-PCA), a reactive compound that has eluded detection i

30 electrochemical methods to directly detect 5-Me-PCA and find that it is transported by MexGHI-OpmD in

31 onsistent with the high redox potential of 5-Me-PCA, which distinguishes it from other well-studied P

32 We also show that 5-Me-PCA is sufficient to fully induce MexGHI-OpmD express

33 ers, [((Ar)Nacnac)Mg-]2 (Ar = C6H2Me3-2,4,6 (Mes); C6H3Et2-2,6 (Dep)), yielding 1,2-dimagnesioethane

34 idyl)-1-butanone (NNK), O(6)-methyl-dG (O(6)-Me-dG) and O(6)-pyridyloxobutyl-dG (O(6)-POB-dG), formed

35 Addition of MeCN, CNAr(2,6-Me) , or O2 to 3 releases N2 with formation of (iPr2) Tp

36 U((t)Bu-(Mes)PDI(Me)) (THF) (1-(t)Bu) (2,6-((Mes)N horizontal lineCMe)2-p-R-C5H2N, Mes = 2,4,6-trimet

37 gen at low temperature produces a species (8-Me) analogous to Int1 demonstrating that initial dioxyge

38 The compromised 9,Me-GlcCer production in the DeltasmtB strain was not acc

39 asmtA and wild-type cells showed a similar 9,Me-GlcCer content, reduced by 50% in the smtB disruptant

40 lkyldT lesions, with the alkyl group being a Me, Et, nPr, iPr, nBu, iBu, (R)-sBu and (S)-sBu, are rec

41 ns with several case studies and developed a Me-PaMuFind-It web tool to estimate the number and possi

42 Absent Me(2+), the primer strand transfer pathway between the p

43 methyl-perfluorooctane sulfonamido) acetate (Me-PFOSA-AcOH) were 26-36% lower in children of black mo

44 ccurring in Methylobacterium extorquens AM1 (Me).

45 olated from the reaction between SiBr4 and [(Mes)2 P]Li, the latter of which acts as a sacrificial re

46 2(THF)2 (2), [((Mes)PDI(Me))UI]2 (3), and [((Mes)PDI(Me))U(THF)]2 (4), were examined using electronic

47 The 6-[pyrid-2-yl]-B-Me-1,2-azaborine ligand has been demonstrated to form an

48 Implicating factors during bacteria-Me(O)NP interactions such as aggregation, surface functi

49 In contrast, both Bar-Me and CF3DODA-Me induce reactive oxygen species in HL-6

50 an-1,9-dien-28-oate [bardoxolone-methyl (Bar-Me)] and methyl 2-trifluoromethyl-3,11-dioxoolean-1,12-d

51 Only Bar-Me forms a Michael addition adduct with glutathione (GSH

52 A Wing domain, absent in other betabetaalpha-Me members, suppresses endonuclease activity, but confer

53 The major differences between Me-4FDG and 2-FDG were that Me-4FDG did not enter the br

54 The synthetic value of 1,4-bis-Mes/Dipp-1,2,4-triazolylidenes is further demonstrated b

55 In particular the 1,4-bis-Mes/Dipp-1,2,4-triazolylidenes overcome the above limita

56 tyl-substituted analogue, Cp*U(NTol)2((t)Bu-(Mes)PDI(Me)) (3-(t)Bu), displays the same electronic str

57 2UI2((Mes)PDI(Me)) (5) or (Me3SiO)UI2((t)Bu-(Mes)PDI(Me)) (5-(t)Bu), respectively.

58 ntamethylcyclopentadienide), and Cp*U((t)Bu-(Mes)PDI(Me)) (THF) (1-(t)Bu) (2,6-((Mes)N horizontal lin

59 yl; R = H, (Mes)PDI(Me); R = C(CH3)3, (t)Bu-(Mes)PDI(Me)), has been investigated.

60 (Me))][SbF6] (4-Cp*) and [Cp*U(NTol)2((t)Bu-(Mes)PDI(Me))][SbF6] (4-(t)Bu), respectively, as confirme

61 Complementary dNTP binding is affected by Me(2+) identity, with Ca(2+) affording the highest affin

62 nted f-block MIC complexes [M(N'')3 {CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N''=N(SiMe3 )2 ) are repor

63 We have developed (11)C-Me-NB1 as a PET tracer for imaging GluN1/GluN2B-containi

64 (11)C-Me-NB1 binding in rat brain was blocked in vitro and in

65 In vitro, (11)C-Me-NB1 binding was independent of the sigma-1 receptor (

66 ating an indirect effect of Sigma1R on (11)C-Me-NB1 binding.

67 Furthermore, (11)C-Me-NB1 enables imaging of GluN1/GluN2B NMDA receptor cro

68 Conclusion:(11)C-Me-NB1 is suitable for the in vivo imaging of NMDA GluN1

69 Methods:(11)C-Me-NB1 was synthesized and characterized by in vitro dis

70 Results:(11)C-Me-NB1 was synthesized at 290 +/- 90 GBq/mumol molar act

71 g/kg dose of (+)-pentazocine abolished (11)C-Me-NB1-specific binding, indicating an indirect effect o

72 y by eliprodil was studied by PET with (11)C-Me-NB1.

73 2'-C-Me-DAPN-TP and 2'-C-Me-GTP were chain terminators for ge

74 tide incorporation assays revealed that 2'-C-Me-DAPN-TP was incorporated opposite U.

75 2'-C-Me-DAPN-TP and 2'-C-Me-GTP were chain terminators for genotype 1b HCV-pol, a

76 merically pure (R)- and (S)-5'-C-methyl (C5'-Me) substituted nucleosides and their incorporation into

77 structural analyses showed that the (S)-C5'-Me epimers are spatially and structurally more similar t

78 3'-end of an ON with either (R)- or (S)-C5'-Me nucleotides.

79 l-2'-deoxy-2'-fluorouridine [(R)- or (S)-C5'-Me-2'-FU, respectively] revealed that the stereochemical

80 at the stereochemical orientation of the C5'-Me and the steric effects that emanate from the alkyl su

81 (2,6-((Mes)N horizontal lineCMe)2-p-R-C5H2N, Mes = 2,4,6-trimethylphenyl; R = H, (Mes)PDI(Me); R = C(

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

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

84 tsD (Pepstatin A) but not B inhibitor (Ca074-Me), in two mouse CKD models, UUO and chronic ischemia r

85 l studies into the mechanism of the catalyst Me-1a (N-methylated 1a) revealed that C-H coordination t

86 ystal form of the simple molecular cavitand, Me,H,SiMe2, is shown to be intrinsically porous, possess

87 ionic pincer bis(carbene) ligand, (Mes)CCC ((Mes)CCC = bis(mesityl-benzimidazol-2-ylidene)phenyl), is

88 yano 3,12-dioxooleano-1,9-dien-28-oate; CDDO-Me) (4) are potent inducers of antioxidant and anti-infl

89 In contrast, both Bar-Me and CF3DODA-Me induce reactive oxygen species in HL-60 and Jurkat le

90 ic hindrance by the 11-keto group in CF3DODA-Me, which prevents Michael addition by the conjugated en

91 l-3,11-dioxoolean-1,12-dien-30-oate (CF3DODA-Me) contain 2-cyano-1-en-3-one and 2-trifluoromethyl-1-e

92 )Benz)]MgX [X = F, Cl, Br, I, SH, N(H)Ph, CH(Me)Ph, O2CMe, S2CMe].

93 CH3NO2, I2), and a propyne clathrate (CH3CCH@Me,H,SiMe2.2CHCl3), have been prepared and characterized

94 ligand forming {MeC(NC6H3(i)PrCH(Me)CH2)CHC(Me)NCH2CH2NMe2}Sc{NHB(NAr'CH)2} (21).

95 2,6-C6H3(i)Pr2, NacNac(NMe2) = Ar'NC(Me)CHC(Me)NCH2CH2NMe2).

96 ted cyclohexanes c-C6H(x)R(12-x) (R = F, Cl, Me; x = 0, 2, 4, 8, 10, 12) using homodesmotic reaction

97 ecedented f-block MIC complexes [M(N'')3 {CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N''=N(SiMe3 )2 ) are

98 mide using 2-carbomethoxynorbornene (NBE-CO2 Me) as a transient mediator are realized by using a newl

99 ized using 2-carbomethoxynorbornene (NBE-CO2 Me) as a transient mediator.

100 igands and 2-carbomethoxynorbornene (NBE-CO2 Me) as the mediator, arylation, amination, and chlorinat

101 The resulting complete Med-PIC structure reveals two components of functional s

102 or-RNA polymerase II pre-initiation complex (Med-PIC) was assembled and analyzed by cryo-electron mic

103 of coordinated axial NO ligand in complex [((Me)DDB)Fe(NO)2((*)NO)](+), the simple addition of MeCN/H

104 The complexes, ((Mes)PDI(Me))UI3(THF) (1), ((Mes)PDI(Me))UI2(THF)2 (2), [

105 olated in the molecular form of composition (Me-cAAC:)2Si2H2 (1) and (Cy-cAAC:)2Si2H2 (2) at room tem

106 C-terminal domain of the polymerase, control Med-PIC interaction and transcription.

107 FOSAA and its methyl and ethyl derivatives (Me- and EtFOSAA), and 6:2/6:2 diPAP were detected in sed

108 However, in this case, Ru-dihydride Me-3 is much more stable to protonation and can even be

109 n 2012 when we found that saturated bis-Dipp/Mes imidazolidinylidenes readily form isolable, though r

110 halichondrin B series, a hydroxyl-directed (Me)4NBH(OAc)3 reduction of E- and Z-beta-alkoxy-enones 3

111 il in the deep Eastern Mediterranean Sea (E. Med.) water column and to minimize potential bias associ

112 n to be taken up by single crystals of empty Me,H,SiMe2 at room temperature, but sorption rates are s

113 ion of the para-substituent (NO2, CF3, H, F, Me, OMe, NMe2) was confirmed by (15)N NMR and by computa

114 The NacNac-Fe-MOF catalyst, I*Fe(Me), efficiently catalyzed the challenging intramolecula

115 l-4-[F-18]-fluoro-4-deoxy-d-glucopyranoside (Me-4FDG), a substrate for SGLTs; 4-deoxy-4-[F-18]-fluoro

116 the steric demand of the polymer end-group (Mes vs Et) transferred during the initiation step determ

117 Over 20 isostructural x(gas/guest)@Me,H,SiMe2 (x </= 1) clathrates (guest = H2O, N2, Ar, CH

118 from various 2-(N-R-amino)biphenyls (R = H, Me, CF3CO, MeSO2, CF3SO2) react with hydrogen peroxide i

119 0)(Idipp)][B(Ar(F))4] (1R[B(Ar(F))4]; R = H, Me, Et; Ar(F) = C6H3-3,5-(CF3)2; Idipp = C[N(C6H3-2,6-iP

120 coordination compounds (X = F, Cl, I; R = H, Me; BDI = 2,6-diisopropylphenyl-beta-diketiminate).

121 (L(R) =R2 P(CH2 )3 PR2 ; R=Ph, (i) Pr; R'=H, Me) form by addition of H3 BNMeR'H2 to [Rh(L(R) )(eta(6)

122 and (eta(5)-C5R5)(CO)3Cr-H ([Cr](R)-H, R= H, Me) were evaluated for formal H atom transfer reactivity

123 lecarboxylate) with varying substituents (H, Me, F, CF3, MeO, NO2, and Ph) in the R4 position of the

124 et by growing aliphatic P1' substituents (H, Me, iPr, iBu) reveals a dramatic, enthalpy-dominated gai

125 Electropositive groups X (X = H, Me, TMS, TES) gave preferentially the linear isomer (reg

126 -C5H2N, Mes = 2,4,6-trimethylphenyl; R = H, (Mes)PDI(Me); R = C(CH3)3, (t)Bu-(Mes)PDI(Me)), has been

127 y Me-(14)C and (36)S and secondary Me-(3)H3, Me-(2)H3, 5'-(14)C, and 5'-(3)H2 kinetic isotope effects

128 However, Me-4FDG was not reabsorbed in the kidney in Glut2(-/-) m

129 ical aerobic oxidation of n-Pr4N[(dpms)Pd(II)Me(OH)] (5) and (dpms)Pd(II)Me(OH2) (8) (dpms = di(2-pyr

130 Pr4N[(dpms)Pd(II)Me(OH)] (5) and (dpms)Pd(II)Me(OH2) (8) (dpms = di(2-pyridyl)methanesulfonate) in wa

131 Thermolysis of the Rh(III)-Me complex (DPEphos)RhMeI2 (1) results in reductive elim

132 stent with SN2 attack by I(-) at the Rh(III)-Me group via two separate competing paths.

133 There were no differences in Me-4FDG uptake into the heart of wild-type, Sglt1(-/-) a

134 Inform Me use was associated with greater KTC knowledge about I

135 efficacy of a mobile Web application, Inform Me, for increasing knowledge about IRDs.

136 were used to test the significance of Inform Me exposure after controlling for covariates.

137 splant centers were randomized to use Inform Me after routine transplant education (intervention) or

138 record depth profiles of alkali metal ions (Me(+)) within thin SiO2 layers.

139 repared modified myoglobins containing an Ir(Me) site that catalyse the functionalization of C-H bond

140 containing an iridium porphyrin cofactor (Ir(Me)-PIX) in place of the heme catalyze enantioselective

141 y by evaluating CYP119 mutants containing Ir(Me)-PIX in cell lysates, rather than as purified enzymes

142 We conducted directed evolution of the Ir(Me)-myoglobin and generated mutants that form either ena

143 Variants of the Ir(Me)-PIX CYP119 displaying these properties were identifi

144 utsugamushi were identified by injecting Kun Ming (KM) mice peritoneally with the organs of either Ap

145 ian Ried, and in the Rhine, up to 0.56 mug/L Me-Ph3P(+) was detected.

146 y a monoanionic pincer bis(carbene) ligand, (Mes)CCC ((Mes)CCC = bis(mesityl-benzimidazol-2-ylidene)p

147 the redox-active pyridine(diimine) ligand, (Mes)PDI(Me) ((Mes)PDI(Me) = 2,6-(2,4,6-Me3-C6H2-N horizo

148 [( identical withSiO)2Ta( horizontal lineCH2)Me] and [( identical withSiO)Ta( horizontal lineCH2)Me2]

149 ases that release the alpha- (1-->2)-linked (Me)GlcAp side groups.

150 ive pyridine(diimine) ligand, (Mes)PDI(Me) ((Mes)PDI(Me) = 2,6-(2,4,6-Me3-C6H2-N horizontal lineCMe)2

151 r nuclei and the rostral part of the medial (Me) nuclei contained a moderate concentration of 5-HT fi

152 the desired homogeneous composition of MeN4 (Me = metal) sites in the carbon that is accompanied by a

153 (NHC)2]Cl (1a, 2a; R = m-Ter = 2,6-Mes2C6H3, Mes = 2,4,6-Me3C6H2 and 1b, 2b; R = Tipp = 2,4,6-iPr3C6H

154 ides of type (Me)2O3 with the primary metal (Me) constituent being Fe (66 atomic (at.) %) along with

155 (Et), R = methoxymethyl (MeOMe), R = methyl (Me), and R = phenyl (Ph)] were found in German rivers an

156 rolopyrrole (TDPP) chromophores with methyl (Me), n-hexyl (C6), triethylene glycol (TEG), and 2-ethyl

157 ing (MRM) and identified as methylcobalamin (Me-Cbl).

158 itional kinetic states not observed at >1 mm Me(2+).

159 t separated ion pair complex [Li(THF)4] [Mo2(Me)2(mu-Me){mu-HC(NDipp)2}2] (4c), where Dipp stands for

160 ted ion pair complex [Li(THF)4] [Mo2(Me)2(mu-Me){mu-HC(NDipp)2}2] (4c), where Dipp stands for 2,6-iPr

161 A computational analysis of the Mo2(mu-Me)2Li core of complexes 3a and 3b has been developed, w

162 imolybdenum complexes of composition [Mo2{mu-Me}2Li(S)}(mu-X)(mu-N^N)2] (3a-3c), where S = THF or Et2

163 N,N'-Dipp [2,6-di(2-propyl)phenyl] and N,N'-Mes [2,4,6-trimethylphenyl] substitution on the carbene

164 A demonstrated [(NPr)2 TTz]Cl4 /N(Me) -TEMPO AORFB delivered an energy efficiency of 70 %

165 Ar =:C{N(Ar)CH}2 ) with 4 equiv of IMe (:C{N(Me)CMe}2 ), which proceeded through the formation of a s

166 m on the aminomethyl radical functionality N(Me)-CH2. presumably arising at copper oxidation/deproton

167 f-block MIC complexes [M(N'')3 {CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N''=N(SiMe3 )2 ) are reported.

168 y characterized derivative, [Fe(III)S2(Me2)N(Me)N2(amide)(Pr,Pr)](-) (8), shows that oxo atom donor r

169 Paired with 4-trimethylammonium-TEMPO (N(Me) -TEMPO) as catholyte, [(NPr)2 TTz]Cl4 enables a 1.44

170 Rs) by the specific agonist DAMGO ([D-Ala2,N-Me-Phe4,Gly5-ol]-Enkephalin) hyperpolarizes medially loc

171 imidazole substrate shows that compared to N-Me, N-iPr and N-Ph variants, the N-o-tolyl variant of th

172 our earlier mechanistic studies, a set of N-Mes- or N-Dipp-substituted 1,2,4-triazolium salts were s

173 tion of metal and metal oxide nanoparticles [Me(O)NPs] in consumer products has led to a growth in co

174 , Ar' = 2,6-C6H3(i)Pr2, NacNac(NMe2) = Ar'NC(Me)CHC(Me)NCH2CH2NMe2).

175 igands (N-heterocyclic carbene=:C[(Pr(i) )NC(Me)]2 ) was synthesized in high yield and structurally c

176 C6 H4 ; N-heterocyclic carbene=C[((i) Pr)NC(Me)]2 ) with N2 O furnishes the first Si-metalated imino

177 ns-bis(imido) species supported by neutral [(Mes)PDI(Me)](0) ligands formed by complete oxidation of

178 is the iridium-methyl bond in the [Cp*Ir(NHC)Me(CD2Cl2)][BAr(F)4] starting material.

179 amide (RC)-Ph2P( horizontal lineNCO2Me)NHCH(Me)Ph (5; dr of 95:5) with tert-butyllithium in THF has

180 koxysilanes using cationic (alpha-diimine)Ni(Me)(CH3CN)(+) complexes 4a,b/B(C6F5)3 yield high molecul

181 at well-defined complex 3b (alpha-diimine)Ni(Me)(OEt2)(+) reacts rapidly at -60 degrees C with vinylt

182 ith [U{N(CH2 CH2 NSiMe2 Bu(t) )2 CH2 CH2 NSi(Me)(CH2 )(Bu(t) )}] (6) produced the diuranium mu-phosph

183 aE(PhC(O)H) = -4.38 eV and DeltaDeltaE(PhC(O)Me) = -3.97 eV.

184 Here we challenged rRNA 2'-O-Me globally by inhibiting the rRNA methyl-transferase fi

185 However, whether rRNA 2'-O-Me is an adjustable feature of the human ribosome and a

186 translate mRNAs is modulated through a 2'-O-Me pattern and not by nonribosomal actors of the transla

187 Our data establish rRNA 2'-O-Me plasticity as a mechanism providing functional specif

188 nal domains of ribosomes are targets of 2'-O-Me plasticity.

189 2'-O-Me, we identified a repertoire of 2'-O-Me sites subjected to variation and demonstrate that fun

190 2'-O-Me was shown to be essential for accurate and efficient

191 Ribose 2'-O-methylation (2'-O-Me) is the most abundant rRNA chemical modification, and

192 eq, a nonbiased quantitative mapping of 2'-O-Me, we identified a repertoire of 2'-O-Me sites subjecte

193 Rap1 by 8-(4-chlorophenylthio)adenosine-2'-O-Me-cAMP prevented TNF-alpha-induced CEC migration and re

194 amide-containing medicinal drugs, such as O-Me-alibendol and -buclosamide.

195 veral Epac-specific antibodies tested, Phi-O-Me-cAMP exhibited dramatically reduced signals in DKO my

196 Phi-O-Me-cAMP is a weak partial agonist for purified Epac, but

197 Phi-O-Me-cAMP readily entered intact myocytes, but did not act

198 ladenosine-3',5'-cyclic monophosphate (Phi-O-Me-cAMP) in mice lacking either one or both isoforms (Ep

199 more, insight into the migration behavior of Me(+) during O2(+) sputtering is given by switching the

200 3 equiv of KC8 in the presence of 1 equiv of Me-cAAC: and Cy-cAAC:, respectively.

201 There was urinary excretion of Me-4FDG in Sglt1(-/-) and Sglt2(-/-) mice.

202 toxicity, fate, and process implications of Me(O)NPs within wastewater treatment, specifically durin

203 The incollapsible 0D pores of Me,H,SiMe2 have been exploited for the enclathration and

204 tivated sludge achieves high removal rate of Me(O)NPs by the formation of aggregates through adsorpti

205 lity of Me-3 rationalizes the lower rates of Me-1a compared to 1a, and also explains why the reaction

206 Complete reabsorption of Me-4FDG from the glomerular filtrate in wild-type mice a

207 on of 5-HT fibers, whereas caudal regions of Me as well as the central nuclei and the intercalated nu

208 film systems can achieve complete removal of Me(O)NPs, thus allowing for long-term environmental expo

209 The greater stability of Me-3 rationalizes the lower rates of Me-1a compared to 1

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

211 0) ligands formed by complete oxidation of [(Mes)PDI(Me)](3-) ligands of 1-Cp(P) and 1-Cp*.

212 4R12](6-) nodes in ZrR2-BTC (R = CH2SiMe3 or Me).

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

214 cinchona alkaloid derivative (TMS-quinine or Me-quinidine).

215 The tetraphosphadisilene {(Mes)2 P}2 Si=Si{P(Mes)2 }2 (7) is readily isolated from the reaction betwe

216 ting Ph3Al with iodoarenes containing p-H, p-Me, p-F, and p-CF3 substituents, which shows a linear cu

217 taining the Cry1Ab protein) from its parent (Ming Hui 63).

218 ox-active pyridine(diimine) ligand, (Mes)PDI(Me) ((Mes)PDI(Me) = 2,6-(2,4,6-Me3-C6H2-N horizontal lin

219 dine(diimine) ligand, (Mes)PDI(Me) ((Mes)PDI(Me) = 2,6-(2,4,6-Me3-C6H2-N horizontal lineCMe)2C5H3N) h

220 Ar = p-Tol, 3-Cp(P)) and Cp*U(NPh)2((Mes)PDI(Me)) (2-Cp*), only 1-Cp* can cleave diazene N horizontal

221 tituted analogue, Cp*U(NTol)2((t)Bu-(Mes)PDI(Me)) (3-(t)Bu), displays the same electronic structure.

222 nyl to p-tolyl, forming Cp*U(NTol)2((Mes)PDI(Me)) (3-Cp*), changes the electronic structure, generati

223 oxo silylation to form (Me3SiO)2UI2((Mes)PDI(Me)) (5) or (Me3SiO)UI2((t)Bu-(Mes)PDI(Me)) (5-(t)Bu), r

224 s)PDI(Me)) (5) or (Me3SiO)UI2((t)Bu-(Mes)PDI(Me)) (5-(t)Bu), respectively.

225 ns-bis(imido) species, Cp(P)U(NAr)2((Mes)PDI(Me)) (Ar = Ph, 2-Cp(P); Ar = p-Tol, 3-Cp(P)) and Cp*U(NP

226 lcyclopentadienide), and Cp*U((t)Bu-(Mes)PDI(Me)) (THF) (1-(t)Bu) (2,6-((Mes)N horizontal lineCMe)2-p

227 P)U((Mes)PDI(Me))]2 (1-Cp(P)), Cp*U((Mes)PDI(Me))(THF) (1-Cp*) (Cp(P) = 1-(7,7-dimethylbenzyl)cyclope

228 H, (Mes)PDI(Me); R = C(CH3)3, (t)Bu-(Mes)PDI(Me)), has been investigated.

229 pyridine(diimine) ligands, [Cp(P)U((Mes)PDI(Me))]2 (1-Cp(P)), Cp*U((Mes)PDI(Me))(THF) (1-Cp*) (Cp(P)

230 bF6] (4-Cp*) and [Cp*U(NTol)2((t)Bu-(Mes)PDI(Me))][SbF6] (4-(t)Bu), respectively, as confirmed by met

231 s cationic uranium(VI) [Cp*U(NTol)2((Mes)PDI(Me))][SbF6] (4-Cp*) and [Cp*U(NTol)2((t)Bu-(Mes)PDI(Me))

232 AgSbF6 affords cationic [Cp*U(NPh)2((Mes)PDI(Me))][SbF6] (5-Cp*) from a metal-based U(V)/U(VI) oxidat

233 (2), [((Mes)PDI(Me))UI]2 (3), and [((Mes)PDI(Me))U(THF)]2 (4), were examined using electronic and X-r

234 lexes, ((Mes)PDI(Me))UI3(THF) (1), ((Mes)PDI(Me))UI2(THF)2 (2), [((Mes)PDI(Me))UI]2 (3), and [((Mes)P

235 The complexes, ((Mes)PDI(Me))UI3(THF) (1), ((Mes)PDI(Me))UI2(THF)2 (2), [((Mes)PD

236 (1), ((Mes)PDI(Me))UI2(THF)2 (2), [((Mes)PDI(Me))UI]2 (3), and [((Mes)PDI(Me))U(THF)]2 (4), were exam

237 Mes = 2,4,6-trimethylphenyl; R = H, (Mes)PDI(Me); R = C(CH3)3, (t)Bu-(Mes)PDI(Me)), has been investig

238 mido) species supported by neutral [(Mes)PDI(Me)](0) ligands formed by complete oxidation of [(Mes)PD

239 ds formed by complete oxidation of [(Mes)PDI(Me)](3-) ligands of 1-Cp(P) and 1-Cp*.

240 r(H)OMes (Cp* = pentamethylcyclopentadienyl, Mes = mesityl) with Piers' borane [HB(C6F5)2] and carbon

241 arkovnikov products, Ph(Me)C(H)SiH2Ph and Ph(Me)C(H)Bpin, and (ii) hydroboration of carbodiimides and

242 yrene to afford the Markovnikov products, Ph(Me)C(H)SiH2Ph and Ph(Me)C(H)Bpin, and (ii) hydroboration

243 The formation of (IMe4 )PMes (Mes=mesityl) is also catalyzed by the phosphinidene-brid

244 -(CF3)2C6H3}4]AgFe(CO)5 with Et2O and PMes3 (Mes = 2,4,6-trimethylphenyl) has also been investigated,

245 acNac(NMe2) ligand forming {MeC(NC6H3(i)PrCH(Me)CH2)CHC(Me)NCH2CH2NMe2}Sc{NHB(NAr'CH)2} (21).

246 Primary Me-(14)C and (36)S and secondary Me-(3)H3, Me-(2)H3, 5'-

247 d the Metabolic syndrome and Cancer project (Me-Can) cohorts (n = 269,365).

248 Publications were searched on Pub Med and EMBASE up to December 30, 2015.

249 in the formation of [L(R)Ni(SCPh3)] (1: R = Me; 2: R = tBu) in good yields.

250 complexes (DNICs) [((R)DDB)Fe(NO)2](+) (R = Me, Et, Iso; (R)DDB = N,N'-bis(2,6-dialkylphenyl)-1,4-di

251 )NiCl] (L(R) = {(2,6-iPr2C6H3)NC(R)}2CH; R = Me, tBu) in C6H6 results in the formation of [L(R)Ni(SCP

252 alyzes the conversion of N2 to N(SiR3)3 (R = Me, Et) at room temperature, representing the highest tu

253 s, ring A) and 13(2) carboalkoxy groups (R = Me or Et) were constructed in 37-61% yield from the hydr

254 (P,C) = 8-diisopropylphosphino-naphthyl; R = Me, nPr, nBu] have been synthesized and spectroscopicall

255 reactions of Cp*Ti{MeC(N(i)Pr)2}(NNR2) (R = Me or Ph) with HBPin or 9-BBN gave borylhydrazido-hydrid

256 Mo(OC(CH3)(CF3)2)3] featuring a mesityl (R = Mes) or an ethyl (R = Et) substituent initiate the livin

257 silylene complexes Cp*(IXy-H)(H)RuSiH2R (R = Mes (3) and Trip (4); IXy = 1,3-bis(2,6-dimethylphenyl)i

258 2}}}}}$=C6 H3 -2,6-(C6 H3 -2,6-iPr2 )2 and R=Me (3), CHCH2 (4), or CCH (5).

259 h less studied, but show potential to resist Me(O)NP inhibition and achieve removal through possible

260 Complexes [PhBP3]RuH(eta(3)-H2SiRR') (RR' = Me,Ph, 1a; RR' = Ph2, 1b; RR' = Et2, 1c) react with XylN

261 is of the methyl-borylamide (NacNac(NMe2))Sc(Me){NHB(NAr'CH)2} (18) generated transient imide 25 via

262 Interestingly, the structures of [H(sebenzim(Me))]xHgX2 exhibit a variety of different hydrogen bondi

263 Primary Me-(14)C and (36)S and secondary Me-(3)H3, Me-(2)H3, 5'-(14)C, and 5'-(3)H2 kinetic isoto

264 not only does the opposite hold true, since Me substitution leads to substantially higher enantiosel

265 The size (Me, Et, iPr, and tBu) and position (meta and para) of th

266 L=PhC(N(t) Bu)2 ; R=1,12-xanthendiyl spacer; Mes=2,4,6-Me3 C6 H2 ), acting as a frustrated Lewis pair

267 esis of spiroindolenines from 2-substituted (Me, Et) indoles and 2-(pyrrolidin-1-yl)benzaldehydes has

268 us complexes Pt(SnR3)2(CNBu(t))2 (R = Bu(t), Mes, Ph, or Pr(i)), only the Bu(t) analogue does both H2

269 Although the dinuclear complex [(Tp(tBu,Me)Cr)2(mu-O)2] exists, mechanistic experiments suggest

270 The tetraphosphadisilene {(Mes)2 P}2 Si=Si{P(Mes)2 }2 (7) is readily isolated from

271 Me)2.NiCl2 13b is a better Ni-catalyst than (Me)2Phen(H)2.NiCl2 13a; and (3) a low Ni-catalyst loadin

272 not their response to force, suggesting that Me(2+) does not affect the distance to the transition st

273 ferences between Me-4FDG and 2-FDG were that Me-4FDG did not enter the brain and was not excreted int

274 amount of charge was required suggests that Med*+ initiates a chain reaction.

275 This drastically mitigates the Me(+) migration artifact, commonly observed in depth pro

276 (HR = 0.78, 95% CI 0.66 to 0.93) but not the Me-Can cohort (HR = 0.99, 95% CI 0.63 to 1.56).

277 ry sits adjacent rather than opposite to the Me-Cbl cofactor with respect to the substrate in the enz

278 ovaried, respectively, with the "I" and the "Me" dimensions of the self, even at the single-trial lev

279 ventromedial prefrontal cortex encoded the "Me" self-dimension.

280 degree they were thinking about themselves ("Me").

281 Therefore Me(2+) ions can influence the noncovalent transitions th

282 Thus, Me,H,SiMe2 exhibits very low, but measurable, gas permea

283 The neutral complexes Ti((Me)PDP)2 and Zr((Me)PDP)2 ((Me)PDP = 2,6-bis(5-methyl-3-

284 idazol-2-ylthio)methyl zinc complexes, [Titm(Me)]ZnX, demonstrate how the Zn-C bond lengths are highl

285 sity functional theory calculations on [Titm(Me)]ZnCl demonstrate that the interaction is very flexib

286 xposure of diverse biological communities to Me(O)NPs in streams receiving wastewater effluents.

287 heteroarenes mediated by a triarylimidazole (Med) was investigated by cyclic voltammetry (CV) and con

288 ivation of molecular hydrogen by a trimeric (Me-DuPhos)3Ni3(OAc)5I complex was established as turnove

289 we report that ternary metal oxides of type (Me)2O3 with the primary metal (Me) constituent being Fe

290 ds, [Cp(P)U((Mes)PDI(Me))]2 (1-Cp(P)), Cp*U((Mes)PDI(Me))(THF) (1-Cp*) (Cp(P) = 1-(7,7-dimethylbenzyl

291 x-active pyridine(diimine) ligands, [Cp(P)U((Mes)PDI(Me))]2 (1-Cp(P)), Cp*U((Mes)PDI(Me))(THF) (1-Cp*

292 f Meldrum's acid acceptors is reported using Me-StackPhos.

293 ely grafting two organometallic complexes [W(Me)6 (1) followed by ZrNp4 (2)] on a single silica suppo

294 Two compatible organometallic complexes, W(Me)6 (1) and TiNp4 (2), were successively anchored on a

295 etallic precatalyst [( identical withSi-O-)W(Me)5( identical withSi-O-)Ti(Np)3] (4).

296 nometallic catalyst [( identical withSi-O-)W(Me)5] (3), with a TON of 98, for propane metathesis at 1

297 imetallic precatalyst [ identical withSi-O-W(Me)5 identical withSi-O-Zr(Np)3] (4) has been synthesize

298 ls with the 1,3-enyne, TMSC identical withCC(Me) horizontal lineCH2, to form secondary homopropargyl

299 (1a, X = CF3; 1b, X = Cl; 1c, X = H; 1d, X = Me; 1e, X = OMe) were successfully applied in the regios

300 mplex 3a, X = MeCO2, while in 3b and 3c, X = Me.

301 Zr((Me)PDP)2 exhibits photoluminescent behavior and its exci

302 The neutral complexes Ti((Me)PDP)2 and Zr((Me)PDP)2 ((Me)PDP = 2,6-bis(5-methyl-3-phenyl-1H-pyrrol-

303 ctions, the earth-abundant metal complex Zr((Me)PDP)2 acts as a substitute for the precious metal pho