ライフサイエンスコーパス: La

1 La and 17 other elements (Na, K, V, Ni, Co, Cu, Zn, Ga,

2 La involvement in regulating the type I interferon (IFN)

3 La ribonucleoprotein domain family, member 6 (LARP6) is

4 La-related protein 1 (LARP1) binds TOP mRNAs, regulating

5 La-related protein 1 (LARP1) is a conserved RBP that int

6 La-related protein 1 (LARP1) regulates the stability of

7 La-related protein-4 (LARP4) binds poly(A) and PABP.

8 La/SS-B (or La) is a 48 kDa RNA-binding protein and an a

9 gated the microstructural features of 0.001% La doped BaSnO3 thin film using both conventional and ab

10 7.1 vs. 49.4 +/- 6.9 mmol (kg d.w.)(-1) ], [La(-) ] [34.8 +/- 12.6 vs. 35.5 +/- 13.2 mmol (kg d.w.)(

11 ear spin relaxation rates of (2) H and (139) La in LaCl3 +(2) H2 O and La(ClO4 )3 +(2) H2 O solutions

12 The (139) La T1 values vary both with solution chemistry and press

13 level using a combination of (31)P and (139)La solid state NMR spectroscopy (SSNMR), extended X-ray

14 </= 3), which was further supported by (139)La SSNMR and EXAFS.

15 2-La and 2-Ce show the same unusual structural feature of

16 2-La and 2-Ce were also prepared to allow the first compar

17 k and rainfall associated with the 2010-2011 La Nina.

18 Relative to the 2011 La Nina, the pantropical biosphere released 2.5 +/- 0.34

19 The chemo-ensemble, [2L+La(3+)], is shown responsible for providing intracellula

20 The structural features of the [2L+La(3+)] complex were established by DFT computational ca

21 ed using GraphPad Prism software (version 6, La Jolla, CA).

22 is comparable to the theoretical value of a La-La covalent bond and is shorter than reported values

23 os is followed by a super El Nino and then a La Nina.

24 was formed by the reaction of laser-ablated La atoms with acetylene molecules in a molecular beam so

25 .4-2 Log cycles of Lactobacillus acidophilus La-5 and Bifidobacterium animalis BB12.

26 Using ground- and lidar-measurements across La Rioja province (Spain) and Denmark, we investigate ho

27 creased contents of alpha-lactalbumin (alpha-La) were associated with increased sensitivity to ultras

28 ring gelation, where higher amounts of alpha-La lead to a gel more dependent on disulfide bonds.

29 The alpha-La:beta-lactoglobulin (beta-Lg) ratio greatly affected t

30 tion) of the Devil's Tower (Gibraltar 2) and La Quina 18 Neanderthals and four SH hominins, all sub-a

31 2)], La(cyclobut-1-en-3-yne) [La(C4H2)], and La(benzyne) [(La(C6H4)].

32 Hence, using La:Ce:V tertiary diagrams and La/V ratios is necessary to distinguish ship plumes from

33 7334, SKF 96365, clemizole hydrochloride and La(3+), but not ML204.

34 from the Greater Nicoya sites of Jicaro and La Cascabel in northwest Costa Rica (n = 9; A.D. 800-125

35 o infection with neuroinvasive West Nile and La Crosse encephalitis viruses.

36 tic ENSO cycle with intermittent El Nino and La Nina events of varying intensity and strength as well

37 n (ENSO)--in particular, extreme El Nino and La Nina events that modulate California's climate not on

38 El Nino and La Nina events, the extremes of ENSO climate variability

39 he two end members of the cycle, El Nino and La Nina, force anomalous oceanographic conditions and co

40 nvestigate the global impacts of El Nino and La Nina.

41 of (2) H and (139) La in LaCl3 +(2) H2 O and La(ClO4 )3 +(2) H2 O solutions were determined as a func

42 Oropouche virus (OROV) and La Crosse virus (LACV) are orthobunyaviruses that are tr

43 ion, we evaluated Oropouche virus (OROV) and La Crosse virus (LACV) pathogenesis and immune responses

44 unoccupied La d-states and occupied O p- and La d-states changes during CO2 chemoresistive sensing of

45 ties, namely La(1-x)Sr(x)BO3 perovskites and La(2-x)Sr(x)BO4 layered perovskites (B = Fe, Co, Ni, or

46 ng receptor modeling, lanthanoid ratios, and La-Ce-Sm ternary diagrams pointed to petroleum refinerie

47 and establish a causal link between Ro60 and La proteins and integrity of structural RNAs.

48 es, silencing of the genes encoding Ro60 and La proteins gives rise to these same defects in surveill

49 Ro60 and La proteins, which exist in ribonucleoprotein particles

50 cal studies show that, on Mg, Zr, Sm, W, and La catalysts, which strongly coke during the reaction, l

51 p) pi-back-bond, but for the d(0) f(0) Y and La and 4f(3) Nd congeners only MIC-->M sigma-bonding is

52 ations between whole-rock values of Sr/Y and La/Yb and crustal thickness for intermediate rocks from

53 We propose that coupled use of Sr/Y and La/Yb is a feasible method for reconstructing crustal th

54 rrelations between their whole-rock Sr/Y and La/Yb ratios and modern crustal thickness.

55 tic criteria for SS utilize anti-Ro and anti-La as serological markers.

56 Anti-Ro and anti-La identify patients with SS and more severe disease tha

57 se than patients expressing anti-Ro and anti-La.

58 diagnostic criteria for SS, anti-Ro and anti-La.

59 pholipid antibody, and anti-Ro/SS-A and anti-La/SS-B antibodies.

60 The reduced expression of anti-La in the F0 group compared to the F <1 and F > 3 groups

61 ild dry eyes did not express anti-Ro or anti-La, while 25% expressed anti-SP1.

62 zed to evaluate these sera for anti-Ro, anti-La, anti-SP1, anti-CA6, and anti-PSP.

63 transcripts interact with the lupus antigen (La) ribonucleoprotein, avoiding cytoplasmic RNA sensors.

64 zuelan equine encephalitis virus, as well as La Crosse bunyavirus.

65 At La content of 1.0 wt.%, the tensile strength and elongat

66 understanding of the selective adsorption at La site and may enable the design of new materials for C

67 e were decreased under glacial conditions at La Brea, and these have compensating effects on the ci/c

68 d drought stress under glacial conditions at La Brea.

69 MB1 protein in a Sjogren syndrome antigen B (La/SSB)-dependent manner in a murine metastasis model.

70 avy stable elements (Rb, Sr, Zr, Ba, Cs, Ba, La, Ce, Nd, Sm, Dy, Lu, U, Th) in glassy fallout from th

71 ut-1-en-3-yne) [La(C4H2)], and La(benzyne) [(La(C6H4)].

72 The linkage between La Nina and western US stratospheric intrusions can be e

73 (ion selectivity, affinity for Ca(2+) block, La(3+) sensitivity, unitary current magnitude), and phar

74 amely, Na, Mg, Al, K, Ca, Ti, V, Cr, Mn, Br, La, W, and Au.

75 e found using distantly related bunyaviruses La Crosse virus and California encephalitis virus, sugge

76 ur data show that electron doping induced by La substitution leads to an insulator-to-metal transitio

77 The complexation of L by La(3+) was shown by absorption spectra wherein isosbesti

78 identified: lanthanacyclopropene [La(C2H2)], La(cyclobut-1-en-3-yne) [La(C4H2)], and La(benzyne) [(La

79 o Front Range and heavily impacted the Cache La Poudre River watershed.

80 eadily controlled by adjusting the catalyst (La)/initiator (ROH) ratio, which is determined by the un

81 nov., from Early Cenomanian La Buzinie amber (France), preserved with its marsupial

82 We showed previously that conditional La knockout (La cKO) from mouse cortex neurons results i

83 Notably, the high conducting La and Pr complexes have the largest particle sizes.

84 apped lanthanum hydroxide nanoparticles [Cys-La(OH)3 NPs] towards the fabrication of efficient immuno

85 The characterization of Cys-La(OH)3 NPs was carried out by different techniques incl

86 These Cys-La(OH)3 NPs were electrophoretically deposited onto an i

87 imilar volcanic systems (e.g. Etna, Piton de La Fournaise, Kilauea).

88 ith OROV or a selective (flox/flox) deletion La Crosse virus, a closely related encephalitic orthobun

89 biguous evidence for the formation of direct La-La bond.

90 During La Nina years, maximum June temperatures were higher tha

91 Heat-stress events are more frequent during La Nina events, but occur under all climatic conditions,

92 l westerly ducts and subtropical jets during La-Nina and weaker during El-Nino.

93 and with positive anomalies occurring during La Nina periods.

94 ) central Pacific Ocean, particularly during La-Nina conditions.

95 In this article, we show that during La Crosse Virus-induced encephalitis, egress of iMOs was

96 the stocks and flows of Ag, Au, Pd, Ru, Dy, La, Nd, and Co in automotive embedded EEE.

97 f thirty-two hydrogen atoms surrounding each La atom.

98 es as being largely responsible for enhanced La and total lanthanoid concentrations in the majority o

99 to 8 days when challenged with either excess La(3+) ions or human serum, and did not accumulate in an

100 Extracellular La(3+) and Gd(3+) rapidly and reversibly blocked the ind

101 rromagnetic LaFeO(3) (LFO) and ferromagnetic La(0.7)Sr(0.3)MnO(3) (LSMO), we find that a net magnetic

102 ately coupled to an epitaxial ferromagnetic (La,Sr)MnO3 film, electric field pulse sequences of less

103 brication of a LaB6 nanowire with only a few La atoms bonded on the tip that emits collimated electro

104 of hydroxy quinoline and the amine group for La(3+) ion binding and the glyco-moiety to bring water s

105 of 140 nM (16 +/- 2 ppb) was shown by L for La(3+) in the buffer at physiological pH.

106 er, our results demonstrate a novel role for La in mediating RIG-I-driven responses downstream of vir

107 ron count in keeping with that expected from La substitution.

108 ated vaccine strain based on an isolate from La Reunion incorporating an internal ribosome entry sequ

109 Structures of L proteins from La Crosse orthobunyavirus and vesicular stomatitis virus

110 Water from La Pampa, Argentina, was used for washing and cooking ri

111 hock state and some REE+Y systematics (e.g., La/Y and Sm/Nd ratios).

112 Ba, Ca, Cd, Ce, Co, Cr, Cs, Cu, Dy, Fe, Ga, La, Li, Mg, Mn, Na, Nd, Ni, Pb, Pr, Rb, Sc, Se, Sr, Tl,

113 nts (Ag, As, Ce, Co, Cs, Cu, Eu, Fe, Ga, Gd, La, Lu, Mn, Mo, Nb, Nd, Ni, Pr, Rb, Sm, Te, Ti, Tl, Tm,

114 iquitination are preferentially bound by GFP-La(WT) and are less enriched in GFP-La(SD) RIPs.

115 hat STAT3 protein levels were reduced in GFP-La(SD) cells due to an increase in STAT3 ubiquitination

116 d by GFP-La(WT) and are less enriched in GFP-La(SD) RIPs.

117 ssing a sumoylation-deficient mutant La (GFP-La(SD)), suggesting a proproliferative function of La in

118 scent protein (GFP)-tagged wild-type La (GFP-La(WT)) grow faster than cells expressing a sumoylation-

119 with time >CP such that they were greater [[La(-) ] 95.6 +/- 14.1 mmol (kg d.w.)(-1) ] and lower [[P

120 ere clearly resolved together with the heavy La atoms in the reconstructed phase.

121 Hoffmann-La Roche Ltd, Basel, Switzerland) versus ranibizumab (Lu

122 Hoffmann-La Roche Ltd, Genentech, Inc.

123 229 solid form screens conducted at Hoffmann-La Roche and Eli Lilly and Company over the course of 8+

124 ealth; with drug supply provided by Hoffmann-La Roche and Genentech.

125 F Hoffmann-La Roche-Genentech and the Breast Cancer Research Founda

126 We therefore sought to clarify how La regulates IFN production in response to viral infecti

127 Human La antigen (Sjogren's syndrome antigen B [SSB]) is an ab

128 The human La-related protein group 7 (hLARP7) is a constitutive co

129 -sense RNA viruses (influenza A virus [IAV], La Crosse virus [LACV], Oropouche virus [OROV], and Ebol

130 of California, San Diego, Medical Center in La Jolla.

131 n in comparison to the equivalent domains in La and revealing an unprecedented fold for the RRM1.

132 reased from 100 nm to 50 nm with increase in La-content from 0.2 to 1.4 wt.%.

133 With further increase in La-content to 1.0 wt.%, the length of the plate-shaped c

134 m nuclear reprocessing facilities located in La Hague (France) and Sellafield (Great Britain).

135 consistent biotic signature was observed in La:phosphate and mobilization: solid pool ratios, and in

136 compounds were identified and quantified in La Mancha Verdejo wines oven this five year period.

137 chment of immune and astrocyte reactivity in La cKO cortex.

138 berrant nuclear accumulation of 5.8S rRNA in La cKO is supported by a 10-fold increase in a pre-5.8S

139 who pointed me to Frank Dixon at Scripps in La Jolla, California, for postdoctoral training.

140 The charge stripes in La-438 are weakly correlated along c to form a staggered

141 ral urban community in 6 US Census tracts in La Puente, California.

142 ficantly affected protein binding, including La, P54nrb and NPM.

143 activity; however, some proteins, including La/SSB, NPM1, ANXA2, VARS and PC4, appeared to enhance A

144 controlled through Sr(2+) substitution into La(1-x)Sr(x)CoO(3-delta) .

145 the Middle Pleistocene layers of the Isernia La Pineta site (Italy).

146 wed previously that conditional La knockout (La cKO) from mouse cortex neurons results in defective t

147 The quasi-2D nickelate La4Ni3O8 (La-438), consisting of trilayer networks of square plana

148 have been identified: lanthanacyclopropene [La(C2H2)], La(cyclobut-1-en-3-yne) [La(C4H2)], and La(be

149 Lanthanum (La)-doped BaSnO3 (LBSO) perovskite would be an ideal rep

150 al enzyme-bound Ca(2+) ion with a lanthanum (La(3+)) ion.

151 Phosphate (Pi) sequestration by a lanthanum (La) exchanged clay mineral (La-Bentonite), which is exte

152 he recovery of neodymium (Nd) and lanthanum (La) from monazite ore that combines microbially based le

153 We elucidate the effect of lanthanum (La) on the microstructure and mechanical properties of M

154 2,4,5-tetrakis(phosphonomethyl)benzene, Ln = La, Ce, Pr, Nd, Sm, Eu, Gd) have been synthesized and ch

155 romatic anions, [Ln(eta(4) -Sb4 )3 ](3-) (Ln=La, Y, Ho, Er, Lu), which were isolated as the K([2.2.2]

156 has demonstrated that the light REEs (LREEs: La, Ce, Pr, and Nd) are essential for at least some meth

157 he Pr dopant in a colossal magnetoresistant (La(1-y)Pr(y))(1-x)Ca(x)MnO3 (LPCMO) system, which has be

158 by a lanthanum (La) exchanged clay mineral (La-Bentonite), which is extensively used in chemical lak

159 The Li-O2 battery based on gradient Mn-La-Pt catalysts shows high discharge specific capacity (

160 Gradient Mn-La-Pt catalysts with three-layered structure of manganes

161 Also, the Modoki El Ni no and the Modoki La Ni na phases have greater impact.

162 ls expressing a sumoylation-deficient mutant La (GFP-La(SD)), suggesting a proproliferative function

163 m1Wjl)/SzJ mice liver of both aggressive (My-La, HUT78, HH, MAC2A, and MAC2B) and indolent (FE-PD and

164 easily tunable electronic properties, namely La(1-x)Sr(x)BO3 perovskites and La(2-x)Sr(x)BO4 layered

165 of localized activity vary from one El Nino (La Nina) event to another; still, some El Nino (La Nina)

166 Nina) event to another; still, some El Nino (La Nina) events are more similar to each other.

167 e western portion of the ENP during El Nino (La Nina), but reduced (enhanced) TC frequency in the eas

168 W), which intensify (weaken) during El Nino (La Nina), producing low-level anticyclonic (cyclonic) re

169 wever, inconsistencies exist between El Nino/La Nina (ENSO) cycles and precipitation in the historica

170 That is, when the influences of El Nino/La Nina are strong enough to isolate more than 48% of th

171 the understanding and prediction of El Nino/La Nina events and also may be applied in the investigat

172 o basin and are warmer/cooler during El Nino/La Nina periods.

173 level and translation of Netrin-1 in a NS5A-La-related protein 1 (LARP1)-dependent fashion.

174 aling triggered the translocation of nuclear La/SSB into the cytoplasm, enhanced the protein synthesi

175 In the nucleoplasm, La binds to and protects from 3' exonucleases, the ends

176 st alpha1 expression in the lateral nucleus (La), whereas alpha3 was prominent in intercalated nuclei

177 ific cooling was modest, similar to observed La Nina excursions of 1(o) to 2 degrees C.

178 ttempt to rationalize the high activities of La(1-x)Sr(x)CoO(3-delta) through the electronic structur

179 nce changes as a function of the addition of La(3+) followed by F(-) and HPO4(2-) ions.

180 Binding of La ribonucleoprotein domain family, member 6 (LARP6) to

181 first complete aromatic characterisation of La Mancha Verdejo white wines, also the data suggest tha

182 Cocrystallization of La(3+)-bound enzymes with Man9GlcNAc2 substrate analogs

183 infiltration of the lung is a consequence of La-specific CD4(+) T cell autoimmunity.

184 Thus, deletion of La from postmitotic neurons results in defective pre-tRN

185 Depletion of La and NPM1 reduced nuclear ASO levels, suggesting poten

186 Depletion of La in various types of cancer cell lines impairs cell pr

187 omains of RIG-I and the N terminal domain of La.

188 lattice constant together with an excess of La can stabilize an antiferromagnetic LaMnO3-type phase

189 ), suggesting a proproliferative function of La in HEK293 cells.

190 ing experiment between the Canary Islands of La Palma and Tenerife, verifying the presence of quantum

191 ShRNA knockdown of La in HEK 293 T cells increased Sendai virus infection e

192 with up to 392 mg of Nd L(-1) and 281 mg of La L(-1) leached during seven consecutive 24 h cycles.

193 RIG-I activation and that overexpression of La enhances RIG-I-ligand binding.

194 , RNA chaperoning and AKT phosphorylation of La protein regulates CCND1 IRES-mediated translation.

195 of approximately 75 fold in the presence of La(3+) among the nine lanthanide ions studied in the HEP

196 dress the question of whether sumoylation of La contributes to cell proliferation of HEK293 cells.

197 ort a novel mechanism whereby sumoylation of La promotes cell proliferation by averting ubiquitinatio

198 Sumoylation of La regulates not only the trafficking of La in neuronal

199 of La regulates not only the trafficking of La in neuronal axons but also its association with speci

200 t the charge stripes within each trilayer of La-438 are stacked in phase from one layer to the next,

201 re, we present photocatalyst sheets based on La- and Rh-codoped SrTiO3 (SrTiO3:La, Rh; ref.

202 La/SS-B (or La) is a 48 kDa RNA-binding protein and an autoantigen i

203 of CaCo2As2, substituting even 10% of Eu or La into the Ca site causes ferromagnetic ordering of Co

204 e course but had no such effect on LARP4B or La protein or on LARP4 in the TTP KO cells.

205 ls-Alder cyclization catalyzed by Me2AlCl or La(OTf)3.

206 t intermittently triggers regular El Nino or La Nina events, super El Nino events, or no events at al

207 No other La or Pi phases were detected by SSNMR and EXAFS indicat

208 ble Viru outposts in the Moche Valley, Pampa La Cruz, and Huaca Las Estrellas, and as part of a broad

209 Here we show that in unpoled Co/PbTiO3/(La,Sr)MnO3 ferroelectric tunnel junctions, the polarizat

210 highly functionalized heteroleptic cis-[Pd2(La)2(Lb)2](4+) cages.

211 sed on the functional role of the PDGFRalpha-La/SSB-LAMB1 pathway and its molecular link to K19 expre

212 t the signaling components of the PDGFRalpha-La/SSB-LAMB1 pathway were strongly expressed at the inva

213 , contradicting the paradigm of a persistent La Nina pattern.

214 El Nino-Southern Oscillation (ENSO) phases (La Nina, neutral, and El Nino years) appear to be a weak

215 aneously facilitating access to the (1)pipi*(La)/S0 conical intersection, such that population of the

216 of the cancer-associated RNA-binding protein La has been linked to translation of viral and cellular

217 The cancer-associated RNA-binding protein La is posttranslationally modified by phosphorylation an

218 e is at present restricted to the prototypic La protein, which acts as an RNA chaperone binding to 3'

219 s been discovered in the family MnRMnSbO6 (R=La, Pr, Nd, Sm).

220 oyotes competed for prey resources at Rancho La Brea (RLB).

221 e performed on RE1/RE2 mixtures, where RE1 = La-Sm and RE2 = Gd-Lu, with emphasis on Eu/Y separations

222 71143-0.73448 and concentrations of 10 REEs (La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er, Yb) in ppb levels.

223 rtantly, knockdown of the negative regulator La-related protein 7 (LaRP7) increased neutrophilic infl

224 The vast range of lanthanide salts (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Y) catalyzes

225 sitively correlated with some REEs (i.e. Sc, La, Ce, Pr, Nd, Lu, Th).

226 our places (Taipei, Taiwan; South China Sea; La Jolla, United States; Jerusalem, Israel) in the north

227 todissociation spectroscopy of size-selected La(3+)(H2O)n nanodrops containing up to 550 water molecu

228 gh and low conducting members of the series (La, Pr for high and Ce for low) affirm the structural si

229 that Pinatubo-like eruptions tend to shorten La Ninas, lengthen El Ninos and induce anomalous warming

230 s based on La- and Rh-codoped SrTiO3 (SrTiO3:La, Rh; ref.

231 ely to be negative for anti-SSA/Ro, anti-SSB/La, and antinuclear antibodies than women (36% men vs 11

232 MDI that recruits a translation stimulator, La-related protein (Larp), to the mitochondrial outer me

233 tive growth patterns occurring during strong La Nina years.

234 ited States, such as occurs following strong La Nina winters (Nino3.4<-1.0 degrees C).

235 tropical wetland emissions during the strong La Nina were at least by 5% larger than the long-term me

236 ements to estimate the impact of this strong La Nina on the global atmospheric CH4 budget.

237 rn and central Pacific co-occurs with strong La Nina's.

238 first half of 2011 experienced the strongest La Nina since the early 1980s, when global surface netwo

239 cattering in stripe-ordered superconductors (La,M)2CuO4 to probe the relationship between electronic

240 sink in 2011 during the strongest sustained La Nina since 1917.

241 The hLARP7 N-terminal La module binds and protects the 3' end from degradation

242 edging weights in the breeding grounds) than La Nina years.

243 Here, we demonstrate that La is stably associated with a spliced pre-tRNA intermed

244 o the CCND1 start codon and demonstrate that La's RNA chaperone activity can change the folding of it

245 ents, thus contradicting the hypothesis that La Voulte was a deep-water environment.

246 is frustration of crystallinity reveals that La(3+) disrupts the hydrogen-bonding network of water mo

247 Herein, we show that La binds close to the CCND1 start codon and demonstrate

248 Mechanistically, we show that La directly binds RIG-I and have mapped this interaction

249 The La(naphthalene) complex was formed by the reaction of la

250 The La-related proteins (LARPs) form a diverse group of RNA-

251 As the La content was increased to 0.6 wt.%, a new plate-shaped

252 central Pacific (CP) El Nino as well as the La Nina with realistic features.

253 rium in protein structure is governed by the La Chatelier's principle of chemical equilibrium.

254 tion over the Tropical continents during the La Nina.

255 uld be enabled by small particles (i.e., the La and Pr complexes would be the worst conductors).

256 The proton conductivities for the La and Pr complexes were roughly an order of magnitude h

257 Asian CHIKV genotype, which differs from the La Reunion LR2006 OPY1 isolate belonging to the Indian O

258 -year-old thylacocephalan arthropod from the La Voulte exceptional fossil biota in SE France.

259 In this study, we identify the La-related protein 1 (LARP1) as a key novel target of mT

260 s is considerably different from that in the La(naphthalene) complex, as suggested by accurately meas

261 ha1, showing the strongest expression in the La, and alpha3, with the strongest expression in the IC

262 A systematic structure search in the La-H and Y-H systems under pressure reveals some hydroge

263 measurements of a ball milled sample of the La complex corroborate this result.

264 ty and plasticity in the architecture of the La module within LARPs.

265 e undergoes a rhombohedral distortion of the La sublattice.

266 rmined by the unique chemoselectivity of the La-X (X = OR, NR2, R) group.

267 Structural information regarding the La module is at present restricted to the prototypic La

268 In this species, the La-La distance is comparable to the theoretical value of

269 re observed in the Caribbean compared to the La Reunion outbreaks in 2005 and 2006.

270 session of a composite RNA binding unit, the La module.

271 es of the target perovskite families via the La(3+)/Sr(2+) ratio.

272 rature dependences for the structure of the (La,M)2O2 layers and the electronic nematicity of the CuO

273 ity of the Cu 3d orbitals, structure of the (La,M)2O2 layers, and CDW order.

274 Ln resin for isolating Sr and Pb, LREE then La-Ce-Nd-Sm, Lu(Yb), and Hf, Th, and U, respectively) al

275 Thus, La has a positive role in enhancing type I and type III

276 n fluorescent protein (GFP)-tagged wild-type La (GFP-La(WT)) grow faster than cells expressing a sumo

277 outhern Oscillation), with more events under La-Nina and less under El-Nino conditions.

278 identify that the distribution of unoccupied La d-states and occupied O p- and La d-states changes du

279 Hence, using La:Ce:V tertiary diagrams and La/V ratios is necessary t

280 etanic stimulation rely on calcium entry via La(3+)- and nifedipine-sensitive calcium channels.

281 generalizes to Hispanic children of the Viva La Familia Study.

282 growth inhibition potentials of both 0.06%w La(NO3)3 and La2O3 were found to be superior to formalde

283 on; however, the molecular mechanism whereby La supports cell proliferation is not clearly understood

284 the underlying molecular mechanism by which La stimulates CCND1 IRES-mediated translation, and we pr

285 y the first (second) type is associated with La Nina (El Nino) like conditions, suggesting that both

286 elation with adult growth chronologies, with La Nina years (characterised by warmer temperatures and

287 atic compound was observed in a complex with La.

288 ydrides of lanthanum can be synthesized with La atoms in an fcc lattice at 170 GPa upon heating to ab

289 At x = 0.2 wt.%, La dissolved completely in the alpha-Mg matrix.

290 in above the dome in single-layered Bi2Sr2-x La x CuO6.

291 riments on the electronic response in (Sr1-x La x )2IrO4 (x = 0, 0.021, and 0.067).

292 the anomalous charge dynamics in the (Sr1-x La x )2IrO4 system.

293 k electron-doped perovskite iridate, (Sr(1-x)La(x))3Ir2O7.

294 namely [K(2.2.2-cryptand)][Cp'3Ln] (Ln = Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm; Cp' = C5

295 m and a 4f(n)5d(1) configuration for Ln = Y, La, Gd, Tb, Dy, Ho, Er.

296 Rare-earth elements and minor metals (Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu)

297 BINOLate (REMB) catalysts (REMB; RE = Sc, Y, La - Lu; M = Li, Na, K; B = 1,1-bi-2-naphtholate; RE/M/B

298 exes [M(N'')3 {CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N''=N(SiMe3 )2 ) are reported.

299 We studied YLOID (Y, La and lanthanoids), recognized as very useful tracers d

300 propene [La(C2H2)], La(cyclobut-1-en-3-yne) [La(C4H2)], and La(benzyne) [(La(C6H4)].