ライフサイエンスコーパス: lambda

1 the expression of type III interferons (IFN-lambda).

2 cus-Gerischer analysis of this data provided lambda.

3 observed for Family X siblings Pols beta or lambda.

4 rinkage is controlled by a penalty parameter lambda.

5 om unique immunomodulatory properties of IFN-lambda.

6 In addition, DA method clarified (Lambda = 0.02 and chi(2) = 63.74) variations between sam

7 was near zero at close electrode proximity, lambda = 0.11 eV at a distance of ~4 angstrom, as manife

8 TiO(2) thin film with broad transparency at lambda = 0.4-8 um and an optimized refractive index n =

9 as positioned at a distance of ~27 angstrom (lambda = 0.94 eV).

10 resolution of less than lambda(0)/40, where lambda(0) is the free-space wavelength.

11 h a sensor can determine a material constant lambda(0) of an elastic medium is approximately [Formula

12 rture having dimensions of approximately 0.6 lambda(0) x 0.4lambda(0).

13 ), Delta(lambda) is the local variability of lambda(0), and D is the dimension of the medium.

14 is the correlation length of fluctuations in lambda(0), Delta(lambda) is the local variability of lam

15 s propagation with a resolution of less than lambda(0)/40, where lambda(0) is the free-space waveleng

16 d Nd:YAG laser at the fundamental frequency (lambda = 1,064 nm) to ablate Ag and graphite composite t

17 an exceed the blackbody limit by >8 times at lambda = 1.7 mum resonant wavelength in the far-field.

18 or optimized to operate at the wavelength of lambda = 10.6 mum.

19 y a second non-resonant near-infrared pulse (lambda = 1064 nm) for energy addition into the gas via i

20 was directly fed by the fundamental output (lambda = 1064 nm) of a current state-of-the-art diode-pu

21 st of GST, we realize broadband (Deltalambda/lambda ~ 15%) mode shifting between an electric dipole r

22 t absorption resonances within an ultrathin (lambda/165) metasurface to develop broadband absorption

23 r 2017 to October 2018 were analyzed using a lambda (2)-based technique for vorticity visualization a

24 A sharp waveguide mode was obtained at lambda = 2.5 um without scattering or mode distortion fo

25 A bright fundamental mode was obtained at lambda = 2.50-2.65 um without mode distortion or scatter

26 of silicon by single femtosecond MIR pulses (lambda = 2.7-4.2 mum).

27 Under these conditions, due to the lambda(2) scaling, the ponderomotive energy of laser-dri

28 n (REMPI) scheme targeting molecular oxygen (lambda ~ 287.6 nm).

29 k with degree distribution k(-lambda), where lambda = 3 for a large number of nodes N.

30 at their characteristic C-H absorption from lambda = 3.40 to 3.50 mum.

31 The yet unknown 2-amino-substituted lambda(3) ,sigma(2) -phosphinines are phosphorus-contain

32 tonitrile (ACN) and tetrahydrofuran (THF), a lambda(3)-boranephosphonate intermediate can also coordi

33 two-step mechanism involving generation of a lambda(3)-boranephosphonate intermediate that immediatel

34 yl halides, epoxides, Michael acceptors, and lambda(3)-iodanes in moderate to good yields.

35 ard deviation of the position accuracy below lambda/300 at room temperature and ambient conditions.

36 , to directly view on a widefield microscope lambda/31-scale (25-nm radius) objects in the near-field

37 ne catalyst (monitored via NMR) with an LED (lambda = 365 nm) drastically changes the chemical enviro

38 The interferon lambda 4 gene (IFNL4) regulates immune responses by cont

39 e, we examined the role played by interferon lambda-4 (IFN-lambda4) on HCV diversity; IFN-lambda4 pla

40 on exposure to cytocompatible visible light (lambda ~ 400 nm) in a dose-dependent manner.

41 (-1) h(-1) and a quantum yield of 50+/-4 % (lambda=400 nm) under visible light illumination (AM 1.5G

42 We argue that a resolving power of ~lambda/4000, the typical size of an atom, may be achieva

43 y was studied upon sensitized irradiation at lambda = 420 nm.

44 the entire visible spectrum from wavelength lambda = 460 nm to 700 nm, while maintaining diffraction

45 tively yields the respective dihalo-sigma(4),lambda(5)- and tetrahalo-sigma(5),lambda(6)-diazaphospho

46 The dihalo-sigma(4),lambda(5)-diazaphospholium triflate salt serves well as

47 tolysis of the [C-S] bond under green light (lambda=530 nm) excitation, producing an ion pair interme

48 f focused 500 ps duration laser radiation at lambda = 532 nm within fibrin hydrogels at pulse energie

49 (blue, ~lambda(605nm)) to resorufin (pink, ~lambda(570nm)) dye.

50 mbda(660nm) for resorufin, absorbance ratio (lambda(570nm)/lambda(605nm)), and change in color (blue

51 o-sigma(4),lambda(5)- and tetrahalo-sigma(5),lambda(6)-diazaphospholium triflate salts.

52 led with the conversion of resazurin (blue, ~lambda(605nm)) to resorufin (pink, ~lambda(570nm)) dye.

53 r resorufin, absorbance ratio (lambda(570nm)/lambda(605nm)), and change in color (blue to pink).

54 d by measuring the fluorescence intensity at lambda(660nm) for resorufin, absorbance ratio (lambda(57

55 resolving power of better than 1 nanometer (lambda/800, where lambda is the wavelength of light) at

56 rption well beyond the Lambertian limit over lambda = 950-1,200 nm.

57 5))(3) resulted in significant red shifts of lambda(abs) and lambda(fl).

58 Rather, IFN-lambda activates keratinocytes and mesangial cells to pr

59 rons of type I (IFN-alpha) and type III (IFN-lambda) against SARS-CoV-2 and compared them with those

60 In vivo IFN-lambda airway levels during viral infections were correl

61 ts with RSV infection showed the highest IFN-lambda airway levels; and (c) individuals with the highe

62 ts (<18 months) had higher virus-induced IFN-lambda airway secretion; (b) subjects with RSV infection

63 ferential shifts in population growth rates (lambda) among coral populations during both stress and n

64 ethinking the pathophysiological role of IFN-lambda and its possible use in clinical practice against

65 ore accurate best-practice representation of Lambda and its uncertainty.

66 Adjustments of g(m) , lambda and photosynthetic capacity were shown to be cons

67 Pollen significantly diminished interferon-lambda and pro-inflammatory chemokine responses of airwa

68 However, practices to calculate and report Lambda and related uncertainty are not universal, leadin

69 s and their cognate receptors, such as phage lambda and the Escherichia coli LamB (EcLamB) protein.

70 Independently measuring Lambda and the f-mode frequency enables tests of gravity

71 n General Relativity and for nuclear matter, Lambda and the f-modes are related by universal relation

72 ratory failure and death, we reveal that IFN-lambda and type I IFN production were both diminished an

73 patients with flu with milder symptoms, IFN-lambda and type I IFN were robustly induced earlier, at

74 ial dimensions (x, y, z), multiple channels (lambda) and time (t).

75 osis was 88% and 68%, respectively, with One Lambda, and 78% and 86%, respectively, with Immucor.

76 e DNA binding affinities of WT pol beta, pol lambda, and pol mu, and several variants of pol beta, fo

77 deactivation to reduce the excess air ratio, lambda, and vessel operation changes to minimize operati

78 Type III IFNs, or IFN-lambda, are the newest members of the IFN family and wer

79 Based on our findings, we propose lambda as an effective way of monitoring the efficacy of

80 exercised in the possible future use of IFN-lambda as therapy for influenza.

81 he antiviral cytokine interferon lambda (IFN-lambda) as a therapeutic for influenza, as administratio

82 of the electron-phonon interaction parameter lambda at metal and metal-overlayer surfaces.

83 (EoS)-related tidal deformability parameter Lambda, but at late times is also characterised by the f

84 between his breathing zone and bedroom air (lambda(BZ)).

85 tical large Lambda(C/Cl) values for cis-DCE (Lambda(C/Cl) = 10.0 to 17.8) that contrasted with identi

86 ntical smaller Lambda(C/Cl) for TCE and PCE (Lambda(C/Cl) = 2.3 to 3.8).

87 17.8) that contrasted with identical smaller Lambda(C/Cl) for TCE and PCE (Lambda(C/Cl) = 2.3 to 3.8)

88 microorganisms and observed identical large Lambda(C/Cl) values for cis-DCE (Lambda(C/Cl) = 10.0 to

89 Large Lambda(C/Cl) values for cis-DCE reflected cob(I)alamin a

90 ion followed by protonation, whereas smaller Lambda(C/Cl) values for PCE evidenced cob(I)alamin addit

91 imilar slopes of dual element isotope plots (Lambda(C/Cl) values of 2.4 +/- 0.1 to 3.6 +/- 0.1) sugge

92 to chlorine isotope effects (as expressed by Lambda(C/Cl), the slope of delta(13)C versus delta(37)Cl

93 icantly between the tetrasporophytes (mainly lambda-carrageenan) and the gametophytes (mainly kappa/i

94 accommodation of the sulfate groups found on lambda-carrageenan.

95 arine bacteria suggests a role in processing lambda-carrageenan.

96 building block of the marine algal galactan lambda-carrageenan.

97 ing to opposing dual element isotope slopes (lambda(CF) = 6.64 +/- 0.14 vs lambda(UNSWDHB) = -1.20 +/

98 on method involving replication of the phage lambda cI repressor gene.

99 LexA repressor, like the lambda CI repressor, is inactivated during the SOS respo

100 Moreover, separated cis enantiomers revealed Lambda-cis to have a preference for the i-motif, whereas

101 reated with the chiral solvating agent (CSA) Lambda-[Co((S,S)-dpen)(3)](3+) 2I(-)B(C(6)F(5))(4)(-) (L

102 The Lambda complex crystallises with the normally parallel s

103 Notably, higher IFN-lambda concentrations in patients with COVID-19 correlat

104 The long flexible tail tube of bacteriophage lambda connects its capsid to the tail tip.

105 y, we assessed how type III interferons (IFN-lambda) contribute to the pathogenesis induced by RNA vi

106 hows that the solvent reorganization energy (lambda) correlates well with the oxygen diffusion coeffi

107 the missing M = Ti, Zr members of the Delta,Lambda-[Cu(bpy)(2)(H(2)O)](2)[MF(6)](2).3H(2)O (M = Ti,

108 amined breeding sites were contaminated with lambda-cyhalothrin residues.

109 Lambda-cyhalothrin was the main insecticide (97.5%) used

110 ole, triflumizole, flonicamid, imidacloprid, lambda-cyhalothrin, cyproconazole, fludioxinil and cypro

111 e a shortened AGD in male pups, whereas two (lambda-cyhalothrin, pyrimethanil) were anticipated to be

112 ctin, Chlorpyrifos, Imidacloprid, Iprodione, lambda-cyhalothrin, Spinosad A, and Spinosad D were quan

113 here mosquitoes have developed resistance to lambda-cyhalothrin, suggests the involvement of copper i

114 The presence of copper in lambda-cyhalothrin-free breeding sites, where mosquitoes

115 .81; P = 0.0017) with mosquito resistance to lambda-cyhalothrin.

116 ies was resistant (30-63% mortality rate) to lambda-cyhalothrin.

117 While it is thought that IFN-lambda cytokines are the exclusive ligands for signaling

118 , which lack all known functional murine IFN-lambda cytokines.

119 s of PS formation and destruction (lambda(f)/lambda(d)) determined.

120 have enabled high-resolution examination of lambda decision-making to provide new insights and excit

121 ther, these data support the theory that IFN-lambda decreases neutrophil motility and function in the

122 crystallography, we show that the complexes Lambda/Delta-[Ru(TAP)(2) (11-CN-dppz)](2+) (TAP=1,4,5,8-

123 st antiviral cytokine interferon-lambda (IFN-lambda) determine the persistence of murine norovirus in

124 investigate how organization underpins phage lambda development and decision-making by characterizing

125 olecular-level characterization of events in lambda development.

126 o the 3 main types, their average effects on lambda did not differ.

127 However, IFN-lambda displays unique traits that delineate them as pri

128 ging at the single-molecule level to examine lambda DNA replication, transcription, virion assembly,

129 all organic molecules to long nucleic acids (lambda DNA).

130 The time-dependent extensions of single lambda-DNA molecules were monitored at constant applied

131 during influenza recovery in mice, with IFN-lambda driving these effects most potently.

132 nal (space xy + discrete time t + wavelength lambda) DS dynamics imaged by STS compressed ultrafast p

133 nt pH molecular dynamics using the multisite lambda-dynamics approach (CpHMD(MSlambdaD)) to investiga

134 Computationally, multisite lambda-dynamics simulations add clear support for mTPP e

135 azole (4), and 4-amino dinaphthodiazepine 5 (lambda(em) = 315-400 nm) is strongly quenched in the pre

136 s, M2biQ acts as a nearly universal emitter (lambda(em) = 468-690 nm) with large Stokes shifts (116-3

137 C(2)H(5)OH-HEPES (v/v, 9/1, pH 7.0) media at lambda(em) = 475 nm.

138 e blue-green region of the visible spectrum (lambda(em) up to 560 nm) and show extremely large Stokes

139 he deep-blue region of the visible spectrum (lambda(em) ~ 440 nm) upon excitation at 255 nm with quan

140 es in the solid state and in PMMA films with lambda(em)(max) = 621-784 nm.

141 architectural protein Fis recruits multiple lambda-encoded Xis proteins to the attR recombination si

142 Bacteriophage lambda encodes a DNA recombination system that includes

143 the appearance of a weak blue luminescence (lambda(ex) = 370 nm) due to an increased concentration o

144 a dual role of the CTD, first in binding to lambda Exo to facilitate loading of Redbeta directly ont

145 sent a 2.3 angstrom crystal structure of the lambda Exo trimer bound to three copies of the Redbeta C

146 on system that includes a 5'-3' exonuclease (lambda Exo) and a single strand annealing protein (Redbe

147 the single-stranded 3'-overhang generated by lambda Exo.

148 monstrate that an engineered temperate phage lambda expressing a programmable dCas9 represses a targe

149 , and rates of PS formation and destruction (lambda(f)/lambda(d)) determined.

150 datasets: 88% and brain datasets: 66%) using LAmbDA Feedforward 1 Layer Neural Network with bagging.

151 in significant red shifts of lambda(abs) and lambda(fl).

152 using the finite element method show a 0.24 lambda focal spot with 21.8 dB of polarization purity an

153 izes two key regularization constants, i.e., lambda for L2 regularization and t for L1 regularization

154 We used the lambda-mu-sigma (lambda for skewness, mu for median, sigma for the coeffi

155 The reorganization energy, lambda, for interfacial electron transfer (ET) and for p

156 The total reorganization energy, lambda, for interfacial electron transfer, ET, from a co

157 NA recombination reaction that excises phage lambda from the chromosome, the bacterial DNA architectu

158 paired values of the population growth rate (lambda) from high and low levels of an identified driver

159 eltaG(gamma), and the reorganization energy, lambda(gamma), both of which become smaller.

160 and new questions regarding how the isolated lambda genetic circuit acts, what biological events tran

161 work of previous and current generations of lambda geneticists.

162 tyl radicals produced during the photolysis (lambda >= 305 nm) of 5-100 mM PA under steady state [O(2

163 Nevertheless, except at lambda >= 600 nm, the observed alpha(b) values far excee

164 under UV/Vis light (AM 1.5G, 100 mW cm(-2) , lambda>300 nm) with a cobalt-based turnover number of 90

165 light illumination (AM 1.5G, 100 mW cm(-2) , lambda>400 nm).

166 Type III IFN lambdas (IFN-lambda) have recently been described as important mediat

167 ghboring plants had the strongest effects on lambda However, when drivers were combined into the 3 ma

168 eling reveals that small values of the ratio lambda (i.e., [Formula: see text]) can bias hematocrit d

169 -sphere reorganization energy, lambda(o), as lambda(i) << lambda(o) such that lambda = lambda(i) + la

170 as lambda(i) << lambda(o) such that lambda = lambda(i) + lambda(o) ~ lambda(o).

171 The small inner-sphere reorganizations, lambda(i), for Ru(III/II)P and TPA(+/0) make them excell

172 two stable behaviours are possible for phage lambda if the main constraints of lambda switch are pres

173 the use of the antiviral cytokine interferon lambda (IFN-lambda) as a therapeutic for influenza, as a

174 biota and host antiviral cytokine interferon-lambda (IFN-lambda) determine the persistence of murine

175 ft-cell tropism and resistance to interferon-lambda (IFN-lambda)-mediated clearance during persistent

176 Type III IFN lambdas (IFN-lambda) have recently been described as imp

177 Interferon lambda (IFNL) is expressed at high levels by intestinal

178 ight and heavy chains) based on Ig alpha, Ig lambda, Ig kappa, Ig u, and Ig heavy chain subunits in n

179 translocations involving the immunoglobulin lambda (IgL) locus are present in 10% of patients, and i

180 e to stimulation by IFN-gamma, IFN-beta, IFN-lambda, IL-4, IL-13, and IL-10 cytokines to better under

181 Genetic elements in the bacteriophage lambda immunity region contribute to stable maintenance

182 wever, our data suggest that therapeutic IFN-lambda impairs bacterial clearance during influenza supe

183 nfluenza, as administration of pegylated IFN-lambda improves lung function and survival during influe

184 e poly(I:C)-induced innate production of IFN lambda in human infant AECs is regulated by (a) p38-MAPK

185 ere, we identify a nonredundant role for IFN-lambda in immune dysregulation and tissue inflammation i

186 Finally, we show an increase in the value of lambda in tumor vascular networks following treatment wi

187 that is the work to produce a cavity of size lambda in water, and 3) the long-range contribution that

188 d, whereas the marginal water use efficiency lambda increased linearly.

189 agreement with dielectric continuum theory, lambda increased to values expected in CH(3)CN solution

190 Type I (IFN-alpha and IFN-beta) and III (IFN-lambda) interferons are host-produced antiviral cytokine

191 We show that protein kinase C (PKC) lambda/iota loss in hepatocytes promotes autophagy and o

192 cell differentiation program through an aPKC lambda/iota-Erk dependent Etv5/Satb2 chromatin repressiv

193 We report that IFN-lambda is present in the lower, but not upper, airways o

194 f better than 1 nanometer (lambda/800, where lambda is the wavelength of light) at a wavelength of 80

195 n length of fluctuations in lambda(0), Delta(lambda) is the local variability of lambda(0), and D is

196 'bright side' (BS) view along the direction lambda(=k(1) x eta(1)).

197 mbda(o), as lambda(i) << lambda(o) such that lambda = lambda(i) + lambda(o) ~ lambda(o).

198 ire sequencing [RACE-RepSeq]), we detected a lambda LC monoclonal expansion in the bone marrow (BM) o

199 thogenic transformation of a patient-derived lambda LC, by recombinantly expressing variants in E. co

200 dividuals with the highest virus-induced IFN-lambda levels (>90th percentile) had higher viral loads

201 isotype in all patients, with a predominant lambda light chain (73%).

202 Apart from phage lambda, little is known about other phages that target E

203 ules at many wavelengths in the range 122 <= lambda <=155 nm offer a rationale for this apparent depl

204 s repressed by the bacterial LexA protein in lambda lysogens.

205 harmful proinflammatory effects, whereas IFN-lambda mainly signals in epithelia, thereby inducing loc

206 nt sources were associated with increases in lambda(max) (up to 4.1 nm), colour density (up to 22%),

207 road absorption in the near-infrared region (lambda(max) = 1187 nm).

208 dG(N(1)-H)(*) was generated photochemically (lambda(max) = 350 nm) from an N-aryloxy-naphthalimide pr

209 iMe(2)) (3), which was identified by UV-vis (lambda(max) = 385, 460, 890 nm), Mossbauer (delta = 0.21

210 m UV light) with blue LED light (410-490 nm, lambda(max) = 465 nm) through an energy transfer (EnT) p

211 as been found to be an exceptional deep red (lambda(max) = 621 nm, = 0.32, tau(av) = 366 ns) thermall

212 hotooxidations in the presence of red light (lambda(max) = 640 nm).

213 Complex 3 also absorbs low-energy light (lambda(max) = 779 nm).

214 Both compounds produce emission at lambda(max) = 938-944 nm.

215 ) O(7) :Eu exhibits a broad emission band at lambda(max) =622 nm under 450 nm excitation, and structu

216 ution, the receptor shows cyan fluorescence (lambda(max)(em) = 485 nm, Phi(F) = 33%), which is partly

217 When the changes in A(max), lambda(max), polymeric colour, colour density, and turbi

218 opsied because of the presence of dnDSA (One Lambda, mean fluorescence intensity [MFI], >1000).

219 ism and resistance to interferon-lambda (IFN-lambda)-mediated clearance during persistent infection r

220 onductivity/PFG-NMR method and the rho, eta, lambda method.

221 Consequently, beta- and lambda-MnO(2) are likely to be good candidates as oxidat

222 gnose plasma cell dyscrasia failed to detect lambda+ monoclonal PCs.

223 We used the lambda-mu-sigma (lambda for skewness, mu for median, sig

224 After outlier removal, the LMS (Lambda-Mu-Sigma) function within R's GAMLSS package was

225 nism of transcription antitermination by the lambda N protein, subjects of my thesis work.

226 elective monoalkylated amines using Ni(II)-N(Lambda)N(Lambda)O pincer type complexes through the borr

227 h modal volumes of the order of few tens of (lambda/n)(3) .

228 anization energy, lambda(o), as lambda(i) << lambda(o) such that lambda = lambda(i) + lambda(o) ~ lam

229 Significantly, lambda(o) was near zero at close electrode proximity, la

230 << lambda(o) such that lambda = lambda(i) + lambda(o) ~ lambda(o).

231 robes of outer-sphere reorganization energy, lambda(o), as lambda(i) << lambda(o) such that lambda =

232 ) such that lambda = lambda(i) + lambda(o) ~ lambda(o).

233 monoalkylated amines using Ni(II)-N(Lambda)N(Lambda)O pincer type complexes through the borrowing hyd

234 Values of lambda obtained using He atoms compare favorably with kn

235 stereogenic metal center featuring either a Lambda or Delta absolute configuration.

236 HC ligands, the metal center adopts either a Lambda or Delta absolute configuration.

237 ined stereochemistry (here overhand knots of Lambda- or Delta-handed entanglement) is reminiscent of

238 tion modalities, the continuous expansion of lambda-orthogonal tandem photoclick chemistry, and the i

239 light-induced mutations in the cII gene from lambda phage in transgenic mouse embryonic fibroblasts d

240 PKCtau/lambda plays a central role in NT-mediated alpha-defensi

241 report amino acids associated with both IFN-lambda polymorphism and HCV load across multiple viral g

242 In mice, we demonstrate that IFN-lambda produced by lung dendritic cells in response to a

243 High in vivo IFN-lambda production is influenced by virus type and associ

244 IFN-lambda protein is increased in murine lupus and IFN-lamb

245 IFN-lambda protein levels were quantified: (a) in human infa

246 of better fitting within the chiral cavity (Lambda/R pair), whereas (DeltaDeltaDeltaDelta)T3 favored

247 ctive T-cell lymphopenia with inverted kappa/lambda ratio in several kindreds.

248 ith no significant difference in Ig kappa/Ig lambda ratios or heavy chain levels.

249 y working in the field of type III IFNs (IFN-lambda) realized that this class of IFNs could play an i

250 ntestine and the lung, signaling via the IFN-lambda receptor (IFNLR) controls clinically important vi

251 Mice lacking the IFN-lambda receptor (Ifnlr1(-/-)) had blunted CD8(+) T cell

252 protein is increased in murine lupus and IFN-lambda receptor (Ifnlr1) deficiency significantly reduce

253 s both from the restricted expression of IFN-lambda receptor, confined to epithelial cells and to a l

254 ed knockout (KO) HIE lines for IFN alpha and lambda receptors and the signaling molecules, MAVS, STAT

255 esignER, which incorporates (i) a refactored lambda-Red recombination system that reduces toxicity an

256 s, and bioinformatic analyses identified IFN-lambda regulation of a DC IL-10 immunoregulatory network

257 velop a monomeric C-terminal fragment of the lambda repressor as a novel fluorescent probe that speci

258 creted viral protein that is central for IFN-lambda resistance.

259 tter understand the regulation of innate IFN-lambda responses in vitro in primary human infant airway

260 IFN-lambda responses to dsRNA in the human infant airway epi

261 infection globally suppresses intestinal IFN-lambda responses, which is attributable to secreted NS1.

262 he nature of the stereoisomer employed, with Lambda Ru(II) centers showing a better intercalation fit

263 In addition, we report the structure of Lambda-[Ru(phen)(2) (11-CN-dppz)](2+) bound to d(TCGGCGC

264 ral taxa, projected stochastic growth rates (lambda(s) ) were found to be lowest under higher emissio

265 ((S,S)-dpen)(3)](3+) 2I(-)B(C(6)F(5))(4)(-) (Lambda-(S,S)-1(3+) 2I(-)B(C(6)F(5))(4)(-)), baseline-res

266 The new CSAs are prepared in two steps from Lambda-(S,S)-1(3+) 3Cl(-) by standard anion metathesis r

267 Thus, IFN-lambda serves a critical role in bridging innate and ada

268 rved in HHV-6B, distinguishing from the 255 "Lambda"-shaped dimeric CATCs observed in murine cytomega

269 (IFN-alpha, IFN-beta) and type III IFNs (IFN-lambda) share many properties, including induction by vi

270 Analysis of DCs revealed IFN-lambda signaling directed the migration and function of

271 Here we found that IFN-lambda signaling in dendritic cell (DC) populations was

272 alpha and the spin-orbit scattering constant lambda(SO).

273 for phage lambda if the main constraints of lambda switch are preserved - these behaviours correspon

274 We determined structures of the lambda tail tube in free tails and in virions before and

275 as regulation of early gene transcription in lambda, the study of which began with the discovery of t

276 thway confers immunity against bacteriophage lambda through an abortive infection mechanism.

277 terahertz field to a small volume of 10(-8)(lambda(THz)/2)(3).

278 gs that establish the unique capacity of IFN-lambda to act at the barriers of the host to balance tis

279 The propensity for Lambda to overlap for a variety of conditions and mechan

280 efits and potential limitations of using IFN-lambda to prevent, limit, and treat these dangerous vira

281 Here, the theory is developed, linking lambda to the thermal attenuation of atom scattering spe

282 and faster viral clearance and a higher IFN-lambda to type I IFN ratio correlated with improved outc

283 set-independent transfer learning framework (LAmbDA) to train models on multiple datasets (even from

284 neumoniae was significantly reduced upon IFN-lambda treatment during influenza superinfection in vivo

285 IFN lambda (type III-IFN-lambda1) is a molecule primarily pr

286 sotope slopes (lambda(CF) = 6.64 +/- 0.14 vs lambda(UNSWDHB) = -1.20 +/- 0.18).

287 d selection operators with minimum or one SE lambda values were 0.74 (95% CI, 0.67-0.82), 0.74 (95% C

288 because of the highly restrictive usage of 2 lambda variable (V) domains (IGLV1-40 and IGLV1-44) and

289 d within the active site of a DNA polymerase lambda variant.

290 By demonstrating that IFN-lambda variation leaves a large footprint on the viral p

291 37)Cl(Vitamin B12) = -4.0 +/- 0.2 per mille, lambda(Vitamin B12) = 6.46 +/- 0.20).

292 lambda was almost entirely a genetic item a few years be

293 h the average and variability of the driver, lambda was marginally more sensitive to 1 SD of change i

294 her immunoglobulin (Ig) light chain kappa or lambda, we designed a second-generation CAR targeting Ig

295 nd to study gene regulation in bacteriophage lambda when I was there.

296 tachment network with degree distribution k(-lambda), where lambda = 3 for a large number of nodes N.

297 l(-1) (1.4 eV) in the reorganization energy (lambda), which constitutes the major portion of the prot

298 sity, and ionic conductivity data (rho, eta, lambda), which is readily available in the literature fo

299 Unlike phage lambda, which is a member of the Siphoviridae family, th

300 tivity surface plasmon resonance wavelength, lambda, while the change in Deltalambda/Deltan with diff