ライフサイエンスコーパス: Am

1 Am J Obstet Gynecol.

2 Am umbilical vein blood sample at 22 weeks gestation sho

3 Am) SIV were developed and implemented at CDC for rapid

4 ic complex, [PtCl(Am)2(ACRAMTU)](NO3)2 (1) ((Am)2 = ethane-1,2-diamine, en; ACRAMTU = 1-[2-(acridin-9

5 Am complexes, [Am{N(E=PPh(2) )(2) }(3) ] (1-Am, E=Se; 2-Am, E=O) are compared to isoradial [Nd{N(E=P

6 gnetotransport measurements, is 1.0 x 10(11) Am(-2), almost an order of magnitude lower than in a fer

7 ty increases approximately to a value of 2.2 Am M(-1) cm(-2) in the range of 0.01 to 20 muM and to 0.

8 reomeric form of the complexes cis-[Pt(NH3)2(Am)(R-Gua)](2+), where R-Gua is 9-methyl- or 9-ethylguan

9 presence of phenanthriplatin, cis-[Pt(NH3)2(Am)Cl](+) where Am is phenanthridine.

10 A subset of the TRANS(2)Am flights investigated easterly wind conditions capable

11 s, [Am{N(E=PPh(2) )(2) }(3) ] (1-Am, E=Se; 2-Am, E=O) are compared to isoradial [Nd{N(E=PPh(2) )(2) }

12 ual axial dipole moment > 160 ZAm(2) (10(21) Am(2))] is further constrained by the new data, which in

13 veloped for determining five actinides ((241)Am, (239)Pu, (237)Np, (232)Th, and (238)U) at ng/L level

14 We used alpha particles from an (241)Am source as a proxy for the neutron-capture reaction an

15 (241)Am alpha particles (5.49 MeV) and (241)Am gamma-rays (59.5 keV), with full widths at half-maxim

16 centrations of (137)Cs, (210)Pb(un) and (241)Am in cryoconite were 2,123 +/- 74, 7,535 +/- 224 and 11

17 of FRNs (i.e. (137)Cs, (210)Pb(un) and (241)Am) and other contaminants (i.e. metal(loids), phosphoru

18 Pu, (235)U/(239)Pu, (236)U/(240)Pu, and (241)Am/(241)Pu model purification ages as well as other mult

19 Pu, (235)U/(239)Pu, (236)U/(240)Pu, and (241)Am/(241)Pu model purification ages obtained at four inde

20 oscopic resolution is achieved for both (241)Am alpha particles (5.49 MeV) and (241)Am gamma-rays (59

21 series of radiation sources, including (241)Am and (57)Co radiation.

22 A novel method was developed to measure (241)Am/(241)Pu in complex sample matrices using an O(2)/He r

23 en found to be linear over the range of (241)Am activity studied.

24 )Pu, 9.4 GBq of (240)Pu and 29.7 GBq of (241)Am were released from both fire events corresponding to

25 rement of neutron capture properties of (241)Am.

26 V at excitation with alpha-particles of (241)Am.

27 factors of nearly 100 for (154)Eu over (241)Am were achieved.

28 CFM samples most probably representing (241)Am and (244)Pu employed in a previous tracer test demons

29 on efficiency has been obtained for the (241)Am-loaded poly(ethersulfone)-based grafted membrane comp

30 50% was found for (237)Np, (242)Pu, and (243)Am concentrations determined with the two analytical met

31 havior of (233)U, (237)Np, (242)Pu, and (243)Am was investigated in a water conductive shear zone und

32 (236)U, (237)Np, and Pu isotopes and (243)Am were determined in ground- and seawater samples at le

33 ow for the determination of (237)Np and (243)Am, for which isotopic tracers either are rarely availab

34 ofunctional platinum complex cis-[Pt(NH3)2Cl(Am)](+), also known as phenanthriplatin, where Am is the

35 rt the structural characterization of (Cp'(3)Am)(2)(mu - 4,4'-bpy) and its lanthanide analogue, (Cp'(

36 that were collected for K(3)Nd(PO(4))(2)/K(3)Am(PO(4))(2), K(3)NdSi(2)O(7)/K(3)AmSi(2)O(7), and NdBO(

37 and Pu(2)[B(13)O(19)(OH)(5)Cl(2)(H(2)O)(3)], Am[B(9)O(13)(OH)(4)].H(2)O, or Cm(2)[B(14)O(20)(OH)(7)(H

38 exes were synthesized: 4a (Am2 = en) and 4b (Am = NH3), in which N-[2-(acridin-9-ylamino)ethyl]-N-met

39 1); 25 mM) from CO2 at a fixed current of -5 Am(-2) in fed-batch bioelectrochemical reactors at high

40 transcriptome-wide maps that distinguish m(6)Am and m(6)A.

41 transcriptome-wide and demonstrate that m(6)Am can repress translation while increasing the stabilit

42 e primary somatosensory cortex abolishes m(6)Am gain on maf1 homolog, negative regulator of RNA polym

43 PCIF1 depleted T cells, we identify 2237 m(6)Am genes and 854 are affected by HIV infection.

44 Among the m(6)Am genes, we find that PCIF1 inhibits HIV infection by e

45 ings show that the methylation status of m(6)Am in the 5' cap is a dynamic and reversible epitranscri

46 Moreover, we find that m(6)Am is selectively demethylated by fat mass and obesity-a

47 unequivocally uncover the association of m(6)Am methylation with increased mRNA stability, translatio

48 Here, we demonstrate that loss of m(6)Am methyltransferase phosphorylated CTD interacting fact

49 We find that m(6)A and m(6)Am misannotations arise from mRNA isoforms with alternat

50 019) use complementary approaches to map m(6)Am modification sites transcriptome-wide and demonstrate

51 IF1 in HIV-host interactions, identifies m(6)Am modified genes in T cells which are affected by viral

52 ne (m(6)A), and reduces the stability of m(6)Am mRNAs.

53 Conversely, mimicking this increase adds m(6)Am onto Maf1, reduces MAF1, and induces comorbidity symp

54 FTO preferentially demethylates m(6)Am rather than N(6)-methyladenosine (m(6)A), and reduces

55 e dynamics and reprogramming of the host m(6)Am RNA methylome during HIV infection.

56 can remove either m(6)A or cap-adjacent m(6)Am RNA modifications, has previously been associated wit

57 ription-start nucleotides and quantifies m(6)Am stoichiometry for each 5' isoform that initiates with

58 These isoforms contain m(6)Am that maps to "internal" sites, increasing the likelih

59 Using a transcriptome-wide map of m(6)Am we find that m(6)Am-initiated transcripts are markedl

60 acilitate future studies to characterize m(6)Am's function.

61 A MTase for N(6)-2'-O-dimethyladenosine (m(6)Am) in vivo that regulates flowering time, and specifica

62 (m(6)A) and N(6),2'-O-dimethyladenosine (m(6)Am) modifications (m(6)A/m) of messenger RNA mediate div

63 nucleotide, N(6),2'-O-dimethyladenosine (m(6)Am), is a reversible modification that influences cellul

64 mRNAs, and N(6),2'-O-dimethyladenosine (m(6)Am), which is found at the first transcribed nucleotide.

65 difications (m(6)A, m(1)A, m(5)C, m(5)U, m(6)Am, m(7)G, W, I, Am, Cm, Gm, and Um), but also returns t

66 ed with reduced stability of a subset of m(6)Am-annotated mRNAs.

67 criptome-wide map of m(6)Am we find that m(6)Am-initiated transcripts are markedly more stable than m

68 We show that the enhanced stability of m(6)Am-initiated transcripts is due to resistance to the mRN

69 F1, the methyltransferase that generates m(6)Am.

70 he preparation and structure of Am-GWMOF-6, [Am(2) (C(6) H(8) O(4) )(3) (H(2) O)(2) ][(C(10) H(8) N(2

71 ge proportions of both actinides (Pu, 97.7%; Am, 86.8%) were associated with mobile colloids in the s

72 5 x increase in magnetisation (from 22 to 96 Am(2)/kg) coincides with this nanoprecipitate formation-

73 e discovered that all M(3+) cations (M = Ac, Am, Cm, La) were completely encapsulated within the bind

74 The complexes of trivalent actinide (Am(III) and Cm(III)) and lanthanide (Nd(III) and Sm(III)

75 selectivities for trivalent minor actinides (Am and Cm) in the presence of trivalent lanthanides.

76 ng our understanding of the minor actinides (Am, Cm) versus lanthanides is key for developing advance

77 he interactions between the heavy actinides, Am(3+) and Cm(3+), and the natural lanthanide-binding pr

78 determined on the 317th and 674th day after Am separation, and the residual amount of Am in the solu

79 This Note of Concern relates to Ezzat et al Am J Pathol 163:1177-1184.

80 s Note of Concern relates to Al-Gayyar et al Am J Pathol 177:1187-1197 and Correction 185:1795-1796.

81 s, such as in the setting of Barberio et al (Am J Epidemiol.

82 eview the accompanying paper by Desai et al (Am J Epidemiol.

83 spectives on 3 findings of DeVilbiss et al. (Am J Epidemiol.

84 series analysis proposed by Flanders et al. (Am J Epidemiol.

85 this issue of the Journal, DeVilbiss et al. (Am J Epidemiol.

86 In this issue of the Journal, Chen et al. (Am J Epidemiol.

87 cent issue of the Journal, DeVilbiss et al. (Am J Epidemiol.

88 n this issue of the Journal, Baranyi et al. (Am J Epidemiol.

89 In this issue of the Journal, Reeves et al. (Am J Epidemiol.

90 n this issue of the Journal, Elbogen et al. (Am J Epidemiol.

91 DeVilbiss et al. (Am J Epidemiol.

92 this issue of the Journal, Chiolero et al. (Am J Epidemiol.

93 The accompanying paper by Rudolph et al. (Am J Epidemiol.

94 The article by Prentice et al. (Am J Epidemiol.

95 In this issue, DeVilbiss et al. (Am J Epidemiol.

96 In this issue of the Journal, Feder et al. (Am J Epidemiol.

97 rican Journal of Epidemiology, Huang et al. (Am J Epidemiol.

98 heir accompanying paper, Schildcrout et al. (Am J Epidemiol.

99 d later inflammatory profiles, Huang et al. (Am J Epidemiol.

100 n this issue of the Journal, Gaskins et al. (Am J Epidemiol.

101 ductor package developed by Schiffer et al. (Am J Epidemiol.

102 this issue of the Journal, Caniglia et al. (Am J Epidemiol.

103 this issue of the Journal, Cardenas et al. (Am J Epidemiol.

104 iant of this approach, used by Regan et al. (Am J Epidemiol.

105 2009;96(1):187-199), Sturmer et al. (Am J Epidemiol.

106 current issue of the Journal, Torres et al. (Am J Epidemiol.

107 ing in this issue of the Journal, Yu et al. (Am J Epidemiol.

108 urrent issue of the Journal, Buckley et al. (Am J Epidemiol.

109 Women's Health Initiative, Prentice et al. (Am J Epidemiol.

110 Masarwa et al. (Am J Epidemiol.

111 all amounts of plutonium (Pu) and americium (Am) was disposed in shallow trenches at the Little Fores

112 aration of long-lived isotopes of americium (Am) and curium (Cm) for recycle into fast reactors.

113 2009 after chemical separation of americium (Am) on October 27, 2009.

114 Plutonium (Pu), americium (Am), and curium (Cm) activities were measured in sedimen

115 Selective oxidation of trivalent americium (Am) could facilitate its separation from lanthanides in

116 The amygdala (Am), one of the most sensitive structures from which to

117 oms at 2.44(1) A, and can be explained by an Am incorporation at Fe structural sites at the magnetite

118 results include the first measurement of an Am-S bond length, with a mean value of 2.921(9) A, by si

119 itio wave function theory calculations on an Am(3+) organometallic complex, [Am(C(5) Me(4) H)(3) ] (1

120 as a One Health detection method for Ac and Am.

121 owed that the distributions of m(5)C, Cm and Am are tissue-specific.

122 the 2'-O-methylated ribonucleosides (Cm and Am) are present at higher levels than the corresponding

123 also found that the levels of m(5)C, Cm, and Am are significantly lower (by 6.5-43-fold) in mRNA than

124 spectroscopy comparisons between Ac(III) and Am(III) in HCl solutions indicate Ac(III) coordinates mo

125 u and Am species were found to be Pu(IV) and Am(III), and large proportions of both actinides (Pu, 97

126 ively compare the ionicities of the Nd-O and Am-O bonds.

127 M(4) edge CC-RIXS data for 21 U, Np, Pu and Am compounds, we demonstrate the ability to compare the

128 wing of the former disposal trenches, Pu and Am have been transferred from the buried wastes into the

129 yed for the sequential measurement of Pu and Am in environmental surveillance programs, potentially r

130 nvestigate the chemical speciation of Pu and Am in the trench water by combining fluoride coprecipita

131 esence of readily detected amounts of Pu and Am in the trench waters provides a unique opportunity to

132 , simple rocksalt compounds formed by Pu and Am lie on the boundary between metals and insulators.

133 ominant oxidation states of dissolved Pu and Am species were found to be Pu(IV) and Am(III), and larg

134 uclide interferences (Ra, Th, U, Np, Pu, and Am) for long-lived polonium isotopes ((208)Po, (209)Po,

135 and to the oxidation of Am(III) to Am(V) and Am(VI) in nitric acid.

136 chistriatum (AAv), the medial archistriatum (Am) and the medial HV.

137 In the accompanying article (Am J Epidemiol.

138 the presence of a trivalent actinide such as Am(III), and (iii) preferential sorption of Pu(IV) in th

139 ting the growth of either T4 motA(Am)or asiA(Am) and for impairing transcription from MotA/AsiA-activ

140 T4 motA amber [motA(Am)] or asiA(Am) phage grows poorly in wild-type E. coli.

141 The patient asks, "Am I going to fall apart?" She had numerous fractures in

142 Att/Am hybrids were created for each Am strain and then back

143 m (met(lab)) results in metamorphosis in Att/Am hybrids, and met(Att)/met(lab) and met(lab)/met(lab)

144 Blackburn (Am J Epidemiol.

145 The article by Blackburn (Am J Epidemiol.

146 We propose that Blackburn (Am J Epidemiol.

147 forms a secondary structure while EKEKEKE-C-Am has a random structure.

148 ling peptide EKEKEKE-PPPPC-Am with EKEKEKE-C-Am.

149 iation while protein adsorption on EKEKEKE-C-Am/gold is high with large variation.

150 Cell viability was measured using calcein Am and ethidium homodimer-1.

151 In all significantly different cases, Am workers were 4.5- to 6.2-fold more strongly attracted

152 the Ac results, comparisons with +3 cations (Am, Cm, and La) that could be handled on the mg scale we

153 raints on Epidemiology in an Age of Change" (Am J Epidemiol.

154 ations on an Am(3+) organometallic complex, [Am(C(5) Me(4) H)(3) ] (1).

155 Herein, two Am complexes, [Am{N(E=PPh(2) )(2) }(3) ] (1-Am, E=Se; 2-Am, E=O) are co

156 graphic, the measured analyte concentration (Am) approaches the accurate value (A0) when matrix effec

157 effects, the measured analyte concentration (Am) was inaccurate at high matrix concentrations, but ac

158 ypropylenimine dendrimers (DAB-Am-16 and DAB-Am-64) were modified at the exterior to impart different

159 on 3 and 5 polypropylenimine dendrimers (DAB-Am-16 and DAB-Am-64) were modified at the exterior to im

160 imine) dendrimers coordinated to Cu(II), DAB-Am(n)-Cu(II)x (n = 4, 8, 16, 32, 64, x = n/2), was studi

161 FS and XANES measurements on the reduced DAB-Am(n)-Cu(0)(cluster) corroborate the TEM data, and provi

162 rs is a function of the n/x ratio of the DAB-Am(n)-Cu(II)x precursor, with highly monodisperse, extre

163 I)-dendrimer complexes with NaBH4 yields DAB-Am(n)-Cu(0)(cluster) species.

164 The mu(e) values of Am(III) (mu(e)(Am(III)) = 3.86 x 10(-4) cm(2)/(Vs)), U(IV) (mu(e)(U(IV)

165 Att/Am hybrids were created for each Am strain and then backcrossed to their respective Am li

166 Upon contact with preformed Fe3O4, Am(III) forms surface complexes with cosorbed Fe at the

167 Although the genome of FLE-Am is almost the same size as the genomes of pathogenic

168 e sequenced the genome of an FLE, termed FLE-Am, present in the Gulf Coast tick, Amblyomma maculatum.

169 We show that FLE-Am likely evolved from a pathogenic strain of Francisell

170 ive metabolic capabilities indicate that FLE-Am transitioned recently to its current endosymbiotic li

171 of 2D amorphous FePO4 nanosheets on Ni foam (Am FePO4 /NF).

172 rs that are isomorphous with those found for Am(III), Cf(III), and with lanthanides that possess simi

173 RNA(His(GUG)) for Um, and tRNA(Pro(GGG)) for Am. tRNA(Ser(UGA)), previously observed as a TrmJ substr

174 well as excellent chemical separations, for Am, Pu, U, and Th through the entire procedure for sever

175 tion 32 was confirmed as the TrmJ target for Am in tRNA(Pro(GGG)) and Um in tRNA(Gln(UUG)) by mass sp

176 These compounds adopt the general formula [Am]Mn(H2POO)3, where Am = guanidinium (GUA), formamidini

177 idia, whether the cultures were derived from Am- or Am+ isolates.

178 mily of f-element compounds (Ce, Nd, Sm, Gd; Am, Bk, Cf) of the redox-active dioxophenoxazine ligand

179 f the common methylated nucleo-sides Cm, Gm, Am or Um or for specific cases in which the base or suga

180 As noted by Galea and Hernan (Am J Epidemiol.

181 In an accompanying article, Hofmann (Am J Epidemiol.

182 A, m(1)A, m(5)C, m(5)U, m(6)Am, m(7)G, W, I, Am, Cm, Gm, and Um), but also returns the key sequence c

183 eneral formula RS(CH2CH2)nH (R = Et, t-Bu, i-Am; n = 1-3) and thiodiethanol monomethyl ether (9) have

184 emblies with Case 3 BPs (IFBA+Pu-240 or IFBA+Am-241) for reactivity control while reducing 20% IFBA u

185 extraordinary sensitivity of the amide III (Am III) vibration and the C(alpha)H bending vibration to

186 Inhibition of hepatic mTOR in Am mice increased hepatic lipid deposition and HIRI.

187 g Social Epidemiology and Causal Inference" (Am J Epidemiol.

188 ) to americium introduces unexpectedly ionic Am-N bonding character and unique spectroscopic properti

189 he lanthanides and minor actinides (that is, Am, Cm), with limited success.

190 J Am Geriatr Soc.

191 S proteins, we have previously suggested [J. Am.

192 hall and Galea in this issue of the Journal (Am J Epidemiol.

193 spark new conversations (e.g., see Kawachi (Am J Epidemiol.

194 t (met(Att)) and a recessive allele from lab Am (met(lab)) results in metamorphosis in Att/Am hybrids

195 . mexicanum (Am; paedomorph), and laboratory Am (paedomorph).

196 companying article, Samoilenko and Lefebvre (Am J Epidemiol.

197 metries ranging from bent to close to linear Am-O-Fe bonds.

198 us species tested except for A. mackerrasae (Am), a neurotropic species limited to Australia that wou

199 sted except for Angiostrongylus mackerrasae (Am), a neurotropic species limited to Australia that wou

200 ight-saturated photosynthetic rate per mass (Am ) was related negatively to leaf mass per area and po

201 Both Apis cerana (Ac) and Apis mellifera (Am) share an evolutionarily conserved set of QMP compoun

202 have identified a honey bee [Apis mellifera (Am)] odorant receptor (Or) for the queen substance 9-oxo

203 adenosine (m(6)A), and 2'-O-methyladenosine (Am) in RNA isolated from mammalian cells and tissues.

204 es N(6)-methylation of 2'-O-methyladenosine (Am) within a single-stranded RNA in vitro.

205 (Att; metamorph), wild-caught A. mexicanum (Am; paedomorph), and laboratory Am (paedomorph).

206 ined using Rothman's sufficient cause model (Am J Epidemiol.

207 l data analysis or systems science modeling (Am J Epidemiol.

208 ssy polymeric state of pure-chain molecules (Am-S(P)).

209 were related to the risk of early mortality (Am J Epidemiol.

210 T4 motA amber [motA(Am)] or asiA(Am) phage grows poorly in wild-type E. coli

211 owever, previous work has found that T4 motA(Am)does not grow in the E. coli mutant strain TabG.

212 for restricting the growth of either T4 motA(Am)or asiA(Am) and for impairing transcription from MotA

213 using Alb-TSC1(-/-) (AT) and Alb-mTOR(-/-) (Am) transgenic mice.

214 When the black-grass A. myosuroides (Am) AmGSTF1 was expressed in Arabidopsis thaliana, the t

215 Black-grass (Alopecurus myosuroides; Am) populations, displaying no overt disease symptoms, c

216 t became the ancestors of North American (N. Am.) cultivars, and 25 Elite Cultivars from N. Am.

217 .) cultivars, and 25 Elite Cultivars from N. Am.

218 erein, we describe the preparation of (NBu4 )Am[S2 P((t) Bu2 C12 H6 )]4 and two isomorphous lanthanid

219 arating heat generating minor actinides (Np, Am, Cm) from spent nuclear fuel solution to reduce the r

220 rats, and in the medial amygdaloid nucleus (Am), GAD(67) mRNA was higher in male rats.

221 er Am separation, and the residual amount of Am in the solution was estimated.

222 tion of Pu and uranium (U) and the amount of Am were estimated by thermal ionization mass spectrometr

223 ctronic differences between the complexes of Am(III) and the lanthanides.

224 Coordination of Am(III) by a combination of thenoyltrifluoroacetonate an

225 een studied with regard to the extraction of Am(III) from Eu(III) and Cm(III) from 0.1-3 M HNO3.

226 thod for analysis of sub-femtogram levels of Am and Cm in large-volume urine samples was developed.

227 formation pathway dictates the magnitude of Am(III) incorporation within this solid.

228 A neuroanatomical model of Am-induced seizure propagation is proposed suggesting th

229 Here, we report the oxidation of Am in two systems, perchloric acid and nitric acid and t

230 .6 V potential for one-electron oxidation of Am(III) to Am(IV) in 1 molar acid.

231 ith a terpyridine ligand to the oxidation of Am(III) to Am(V) and Am(VI) in nitric acid.

232 rust (GR) was synthesized in the presence of Am(III), and subsequently converted to Fe(OH)2(s) interm

233 ation were correlated with the proportion of Am+ conidia, whether the cultures were derived from Am-

234 rine samples spiked with known quantities of Am and Cm isotopes in the range of attogram to femtogram

235 The elemental ratio of Am to Pu in the produced particles was determined on the

236 The retention of Am(III) by coprecipitation with or adsorption onto prefo

237 pyridyl-based ligands for the separation of Am(III) from lanthanide(III) ions is considered, as well

238 Furthermore, the sorption of Am(III) to these minerals is strongly impacted by LanM,

239 hod to access the higher oxidation states of Am in noncomplexing media for the study of the associate

240 The preparation and structure of Am-GWMOF-6, [Am(2) (C(6) H(8) O(4) )(3) (H(2) O)(2) ][(C

241 n environment markedly distinct from that of Am(III) in Fe3O4.

242 The mu(e) values of Am(III) (mu(e)(Am(III)) = 3.86 x 10(-4) cm(2)/(Vs)), U(I

243 s constitutes the first quantitative data on Am-C bonding in a molecular species.

244 um thickness ZrB(2) IFBA; (Case 2) Pu-240 or Am-241 mixed homogeneously with the fuel; and (Case 3) a

245 and (Case 3) another composite BP: Pu-240 or Am-241 with 150 mum thickness ZrB(2) IFBA.

246 hether the cultures were derived from Am- or Am+ isolates.

247 contrasting magnetism in two of the phases, Am = GUA and FA, that arises from structural distortions

248 of 1 for all rice varieties except Mn in Pka Am Pun rice and As in Pka Am Pun rice, Jek Chuey Sao Hai

249 s except Mn in Pka Am Pun rice and As in Pka Am Pun rice, Jek Chuey Sao Hai rice, and Leb Nok rice.

250 r dynamics results showed that EKEKEKE-PPPPC-Am forms a secondary structure while EKEKEKE-C-Am has a

251 tion of the nonfouling peptide EKEKEKE-PPPPC-Am with EKEKEKE-C-Am.

252 Finally, we extended EKEKEKE-PPPPC-Am with the cell-binding sequence RGD and demonstrated c

253 wed that protein adsorption on EKEKEKE-PPPPC-Am/gold is very low with small variation while protein a

254 As predicted, Am was more sensitive than Ac in all cases (1.3- to 2.7-

255 architecture is used as a platform to probe Am(3+) coordination chemistry and guest-enhanced lumines

256 A heteromeric nuclear protein Am Alpha Binding protein (AAB) binds specifically to a C

257 ss of platinum(IV) complexes of the type [Pt(Am)(R(COO)2)2], where Am is a chelating diamine or two m

258 The cytotoxic complex, [PtCl(Am)2(ACRAMTU)](NO3)2 (1) ((Am)2 = ethane-1,2-diamine, en

259 The reactions of AnCl(3) (An = Pu, Am, Cm) with molten boric acid under the same conditions

260 Kuller and Reisler's 1971 publication (Am J Epidemiol.

261 DPA by ozonation or use of Fenton's reagent, Am, Pu, U, and Th are separated from each other and the

262 ain and then backcrossed to their respective Am line.

263 Risch (Am J Epidemiol.

264 C, but aggregated extensively in an rpoH165 (Am) mutant.

265 e according to phenotype: RGC, Ho, CPr, RPr, Am, BP, MG.

266 The ligand separates Am(III) and Cm(III) from the lanthanides with remarkably

267 n increase in structural order around sorbed Am.

268 ty and Estimation in Case-Referent Studies" (Am J Epidemiol.

269 inner-sphere Cl(1-) ligands (3.2+/-1.1) than Am(III) (0.8+/-0.3).

270 ave higher levels of ovarian activation than Am workers.

271 workers responded less strongly to QMP than Am workers, and 9-HDA and 10-HDA consistently elicited s

272 lts confirmed Seaborg's 1954 hypothesis that Am(III) 5f-orbital covalency was more substantial than 4

273 e were detected at distances suggesting that Am and Fe polyhedra share corners in geometries ranging

274 ensity on basal oxygen atoms contrasting the Am(III) and Cm(III) borates, where a basal O 2p orbital

275 Our results explain the Am III frequency dependence on conformation as well as t

276 Isolation of the Am and Pu is then achieved using a combination of extrac

277 ich results in a psi dependent mixing of the Am III and the (C)C(alpha)H bending motions.

278 The sum of the impurities of the Am/Cm product stream using the simulated raffinate was f

279 of the most difficult systems to study, the Am-Cl interaction within AmCl6(3-).

280 bitals was similar to that observed with the Am(III) 6d-orbitals.

281 ons at higher HNO3 concentration compared to Am(3+).

282 ial for one-electron oxidation of Am(III) to Am(IV) in 1 molar acid.

283 ridine ligand to the oxidation of Am(III) to Am(V) and Am(VI) in nitric acid.

284 ve larger Pu 5f atomic occupancy relative to Am and Cm 5f, as well as unique involvement and occupanc

285 molecular orbitals for Bk and Cf relative to Am and Cm.

286 We report that reversion to Am+ depends on DNA methylation within and upstream of Ta

287 Reversion to Am+ did not occur when conidia were plated on 5-azacytid

288 DNA methylation, also prevented reversion to Am+.

289 Both TraK and TraV accumulated in traB2[Am] cells; however, the TraB2 amber fragment could be de

290 ion factor activation was assayed with Trans-Am kits.

291 Herein, two Am complexes, [Am{N(E=PPh(2) )(2) }(3) ] (1-Am, E=Se; 2-

292 simultaneous determination of Pu, Np, Th, U, Am, Cm, Pm, Y, and Sr isotopes, as well as iron-55, by i

293 mobilities (mu(e)) of the actinides Th and U-Am in different oxidation states (prepared in 1 M HCl an

294 yzes formation of Cm, Um, and, unexpectedly, Am.

295 a two-electrode electrolyzer assembled using Am FePO4 /NF as an electrocatalyst at both electrodes gi

296 In the article by Chen and VanderWeele (Am J Epidemiol.

297 acental abruption by Ananth and VanderWeele (Am J Epidemiol.

298 ratios introduced by Ananth and VanderWeele (Am J Epidemiol.

299 presence of other competing actinides, viz., Am(III), U(VI), and Np(V).

300 plexes of the type [Pt(Am)(R(COO)2)2], where Am is a chelating diamine or two monodentate am(m)ine li

301 pt the general formula [Am]Mn(H2POO)3, where Am = guanidinium (GUA), formamidinium (FA), imidazolium,

302 nanthriplatin, cis-[Pt(NH3)2(Am)Cl](+) where Am is phenanthridine.

303 )](+), also known as phenanthriplatin, where Am is the N-heterocyclic base phenanthridine, has promis