ライフサイエンスコーパス: lambda

1 either right-handed (Delta) or left-handed (Lambda).

2 he temporal difference learning algorithm TD(lambda).

3 IFN-stimulated gene expression and IFN-beta/lambda.

4 at fully characterize 8-oxo-dG bypass by Pol lambda.

5 uires the capacity of IECs to respond to IFN-lambda.

6 esponse to both endogenous and exogenous IFN-lambda.

7 ired HCV clearance by both IFN-alpha and IFN-lambda.

8 arrative for the life cycle of bacteriophage lambda.

9 s: sigma-2 followed by kappa, then sigma and lambda.

10 tial for establishing the SI traceability of lambda.

11 approximately 2-fold higher than that of Pol lambda.

12 to an RNA binding peptide from bacteriophage lambda.

13 ection (MOI) without or with IFN-beta or IFN-lambda.

14 eeders vs. nonbreeders differentially affect lambda.

15 we report that neutrophils responded to IFN-lambda.

16 enhance the induction of IFN-alphas and IFN-lambdas.

17 s discriminated PRs from GRs and HVs (Wilks' lambda = 0.499, P <0.012).

18 dipolar mode at the telecommunication band (lambda 1.55 mum), which is considered as the OFF state.

19 f a distinct CTP peak at longer wavelengths (lambda 1.85 mum) far from the telecommunication waveleng

20 Likewise, overexpression of IFN-lambda (1 to 4) in C/C cells induced basal ISG expressio

21 within very small dimensions (lambda/1,250 x lambda/1,250 in our device), resulting in a miniature ra

22 metry breaking within very small dimensions (lambda/1,250 x lambda/1,250 in our device), resulting in

23 tor, designed to have maximum sensitivity at lambda = 10.6 mum, was designed, fabricated, and charact

24 (conventional) single-pulse laser ignition (lambda = 1064 nm) and a novel dual-pulse method based on

25 d near-infrared (NIR) energy addition pulse (lambda = 1064 nm).

26 ion measured by dispase fragmentation assay (lambda = 15.1 min).

27 amorphous silicon photonic wires at telecom (lambda 1550 nm) and mid-IR (lambda >/= 2100 nm) wavele

28 erved over a wide range of pump wavelengths (lambda = 1580-1650 nm).

29 it exhibits a broad transparent window from lambda = 2.5 mum up to 7 mum.

30 ol detection, we track the -OH absorption at lambda = 2.8-2.9 mum.

31 lf of reorganization (lambda), that is, Hab =lambda/2.

32 UV-irradiation (lambda = 254 nm) of our assemblies induces a photochemic

33 as damaged using ultraviolet (UV) radiation (lambda=254nm) and hydroxyl radicals, the intensity of th

34 ng an ultraviolet (UV) pre-ionization pulse (lambda = 266 nm) with an overlapped near-infrared (NIR)

35 The interferon (IFN) lambda 3/4 (IFNL3/4) locus, influencing innate immunity

36 ed by measuring the intensity attenuation at lambda = 3.0-3.2 mum, which is associated with -CH absor

37 Frequently, the reactivity of lambda(3) iodanes is further enhanced by acids (Lewis or

38 less than (5 nm)(3) or approximately 10(-6) lambda(3), comparable to the size of the smallest electr

39 formation of the initial complex between the lambda(3)-iodane and a nucleophile, which can be a solve

40 s shows that the sigma-hole bond between the lambda(3)-iodane and the nucleophile is not necessarily

41 Alkynyl-lambda(3)-iodanes have been established as alkynyl catio

42 heteroarene ligands of unsymmetrical diaryl-lambda(3)-iodanes is a key step in the developed one-pot

43 intermediacy of two distinct dicarboxy aryl-lambda(3)-iodanes is hypothesized in the mechanism.

44 Key for the observed reactivity of lambda(3)-iodanes, powerful reagents for the selective t

45 pivotal switch in reactivity induced by aryl-lambda(3)-iodanes.

46 Optimal results are obtained with Lambda-3 c(3+) 3 BArf (-) (CH2 Cl2 , -35 degrees C; 98-8

47 guide pair with an edge-to-edge distance of lambda/3 at the telecommunication wavelength.

48 , and an external quantum efficiency of 15% (lambda = 360 +/- 10 nm).

49 nzyl phosphate-functionalized microcapsules, lambda = 365 nm, or subjecting the pH-responsive microca

50 We analysed the association of interferon lambda 4 (IFNL4)-related polymorphisms and HLA-B haploty

51 s: We analysed the association of interferon lambda 4 (IFNL4)-related polymorphisms and HLA-B haploty

52 u were quantified at lambda = 424.408 nm and lambda = 402.148 nm, respectively.

53 oaddition with electron-deficient olefins at lambda = 419 nm.

54 als of (234)U and (238)Pu were quantified at lambda = 424.408 nm and lambda = 402.148 nm, respectivel

55 bpy)3](2+) at lambda = 620 nm and luminol at lambda = 425 nm, respectively).

56 (OCT) to measure the CTE of an InGaN-based (lambda = 450 nm) high-power LED encapsulated in polystyr

57 revealed Dsg3 order decreased more rapidly (lambda = 5.5 min), indicating that cadherin order is not

58 reaction promoted by a chiral salen-type bis(lambda(5)-iodane) reagent, followed by an in situ regio-

59 compounds characterized by the presence of a lambda(5)-phosphorus functionality at the alpha-position

60 ect to the diazo moiety, here referred to as lambda(5)-phosphorus-containing alpha-diazo compounds (P

61 Absorption data spanning from lambda = 500 to 840 nm were collected using a photoacous

62 endorff reagent and scanning densitometry at lambda - 520nm in reflectance/absorption mode.

63 section (MAC) of 7.89 +/- 0.25 m(2) g(-1) at lambda = 550 nm and an absorption Angstrom exponent (AAE

64 -2) m(2) g(-1) to 7.9 x 10(-2) m(2) g(-1) at lambda = 550 nm with absorption Angstrom exponents (AAE)

65 in the electronic absorption spectrum of 1 (lambda = 610 nm, epsilon = 1375 L.mol(-1).cm(-1); lambda

66 a = 610 nm, epsilon = 1375 L.mol(-1).cm(-1); lambda = 613 nm (calcd)).

67 of different luminophores ([Ru(bpy)3](2+) at lambda = 620 nm and luminol at lambda = 425 nm, respecti

68 ta 32%) for the 1(st) order is only 4.4 V at lambda = 633 nm as compared to 70 V for a conventional F

69 The median measured MAC at lambda = 660 nm for smoldering oak particles was 1.1 (0.

70 ices that couple visible-wavelength light at lambda = 674 nm from single-mode, high index-contrast di

71 n from a metamaterial thickness of less than lambda/7.

72 overing a spectral coverage of 110 cm(-1) at lambda 8 mum.

73 substrate that locally modify near-infrared (lambda=915 nm) optical wavefronts.

74 ive index sensitivities (1,091 nm RIU(-1) at lambda=921 nm) and FOMs (>2,800 RIU(-1)).

75 ts consisting of polymerases (Pol mu and Pol lambda), a nuclease (the Artemis.DNA-PKcs complex), and

76 n LTP maintenance in wild-type mice, PKCiota/lambda, a gene-product closely related to PKMzeta, persi

77 examine how human DNA polymerase lambda (Pol lambda) achieves medium fidelity by determining 12 cryst

78 Thus, IFN-lambda acted as a unique immunomodulatory agent by modif

79 LTP and long-term memory, persistent PKCiota/lambda activation compensates for PKMzeta loss in PKMzet

80 l types, however, the cell(s) upon which IFN-lambda acts to exert its antiviral effects is unclear.

81 s a large electron-phonon coupling parameter lambda and critical temperature of several K.

82 Electron-phonon coupling constant lambda and electronic density of states at the Fermi lev

83 On ICU day 1, high free light chain lambda and high free light chain kappa were seen in 46.5

84 LAD2 MCs induced expression of IFN-beta, IFN-lambda and IFN-stimulated genes.

85 GHG2), and IgA (IGHA), and the light chains (lambda and kappa).

86 o the interaction patterns of E. coli phages lambda and T7.

87 t certified reference materials (CRMs), both lambda and the partition volume, V, must be metrological

88 itional prognostic value of free light chain lambda and the significance of allelic inclusion in B ce

89 IP3R model, we establish the dependencies of lambda and xi on two important IP3R model parameters, IP

90 sity function involving only two parameters, lambda and xi, which represent the basal rate of puff ge

91 emarkable 111% increase in magnetostriction (lambda) and 435% increase in strain sensitivity (dlambda

92 t in finding both the reorganization energy (lambda) and electronic coupling (|M|) through ultrafast

93 tes of deterministic population growth rate, lambda, and demographic variance, sigmad2, from models w

94 both the low-density intrinsic growth rate, lambda, and the carrying capacity density, K, which is a

95 f the IFN-lambdaR1 subunit, specific for IFN-lambdas, and interleukin-10Rbeta (IL-10Rbeta), which is

96 =B(3,5-C6 H3 (CF3 )2 )4 ) to give lipophilic Lambda- and Delta-3 a-d(3+) 3 BArf (-) , which are scree

97 Conversely, a PKCiota/lambda-antagonist disrupts late-LTP and spatial memory i

98 estine and colon is required for enteric IFN-lambda antiviral activity.

99 erted region with a reorganization energy of lambda approximately 1 eV.

100 Light chains kappa and lambda are immunoglobulin constituents but also circulat

101 Type III IFNs (IFN-lambdas) are secreted factors that are well-known for th

102 educing the excitation probability of spins (lambda), are compared on two distinct bacterial mechanos

103 study of the C-dots and the DNA fragment of lambda bacteriophage was performed, and the DNA binding

104 ained equimolar mixtures of genomic DNA from lambda bacteriophage, Escherichia coli (strain K12, MG16

105 addition to inducing ISG transcription, IFN-lambda (but not IFN-beta) specifically activated a trans

106 as shown previously, it is attenuated in Pol lambda by a hydrophobic core including Leu431, Ile492, a

107 the sterilizing innate immune effects of IFN-lambda by extending these findings in Rag1-deficient mic

108 HK022 Nun blocks superinfection by coliphage lambda by stalling RNA polymerase (RNAP) translocation s

109 IFN-lambda can induce antiviral interferon-stimulated genes

110 n and a region where each parameter set (xi, lambda) can be caused by using two different combination

111 lambda-Carrageenan and xanthan gum were selected in this

112 blends, in particular in the low elasticity lambda-carrageenan.

113 idative stress response DNA polymerase (Pol) lambda caused by hyperactive HUWE1 p.R4187C.

114 kappa(+) B cells relative to nonautoreactive lambda(+) cells, we show that tolerance of human B cells

115 In all populations tested, there was a lambda chain bias for HIV Env binding antibodies, compar

116 the directed evolution of the bacteriophage lambda cI TF against two synthetic bidirectional promote

117 thogonal logic gates, based on bacteriophage lambda cI variants and multi-input promoter architecture

118 shape of the emissivity spectrum varepsilon(lambda) closely matches that of absorptance alpha(lambda

119 ble constant uncertainty of 0.68% for a flat lambda cold dark matter universe in the era of third-gen

120 more CD19 B cells expressing both kappa and lambda compared with healthy controls (median [interquar

121 In the enolate derived from the Lambda-configured catalyst, the tert-butyl group that sh

122 Type III interferons (IFN-lambda) control enteric viral infections in the gut and

123 systemic replication, and type III IFN (IFN-lambda) controls MNV persistence in the intestinal epith

124 In J774A.1 cells, lambda-cyhalothrin, resmethrin, 3-PBA, o,p'-DDT, p,p'-DD

125 amilies, to a 90 min pulse of the pyrethroid lambda-cyhalothrin.

126 ta,Lambda)-Piz to a Kd of 622 +/- 55 nM for (Lambda,Delta)-Piz.

127 ciated with the five membered chelate rings (lambda/delta), alignment modes of the C-C bonds with the

128 rent dual element C-Cl isotope correlations (Lambda = Deltadelta(13)C/Deltadelta(37)Cl approximately

129 e removed through DNA polymerase lambda (Pol lambda)-dependent MUTYH-initiated base excision repair (

130 the lysis-lysogeny decision of bacteriophage lambda despite variable infection times being likely in

131 ctor protein (IHF) is required for efficient lambda-development in vivo and a specific IHF recognitio

132 ction to controllably and completely stretch lambda DNA in a two-dimensional nanofluidic network comp

133 ymerase (RNAP) translocation specifically on lambda DNA.

134 structures, and chemical modifications into lambda-DNA remains technically challenging.

135 Condensation of lambda-DNA with hexamminecobalt(III) ions completely pro

136 sequences and structures incorporated within lambda-DNA.

137 ar toolkit for rapid preparation of modified lambda-DNA.

138 It accounts for the experimental Lambda-doublet populations via explicit consideration of

139 Here we present a method to calculate the Lambda-doublet ratio when concurrent potential energy su

140 have shown a clear preference for the Pi(A') Lambda-doublet states, in apparent contradiction with ab

141 l structures are available, most include the Lambda enantiomer and there is very little structural in

142 ll-matched DNA, in the absence of the other, Lambda enantiomer.

143 ounteract the latter activity, bacteriophage lambda encodes a small protein inhibitor called Gam that

144 Importantly, rIFN-lambdas enhanced epithelial barriers in vitro, preventin

145 free energy perturbation (FEP) coupled with lambda-exchange molecular dynamics method to calculate t

146 Redbeta interacts with lambda exonuclease (lambdaexo), the other component of t

147 s conveniently prepared from PCR products by lambda-exonuclease digestion and streptavidin magnetic b

148 d emphasize the therapeutic potential of IFN-lambda for treating mucosal viral infections.

149 Estimates of lambda from empirical observations of breeders only are

150 nO2 phases-beta, gamma, R, alpha, delta, and lambda-from aqueous solution.

151 more recently identified type III IFNs (IFN-lambda) function as the first line of defense against vi

152 I IFN (IFN-alpha/beta) and type III IFN (IFN-lambda) function at the epithelial level, and their resp

153 rticle, we report that the regulation of IFN-lambda genes did not track with mechanisms that control

154 isplayed evidence of positive selection, the lambda genes in sIgkappa(+) cells accumulated bystander

155 o acid sequences and/or Vkappa,lambda-Jkappa,lambda genes.

156 lies of the 4.6 Mb E. coli genome, 48.5 kb lambda genome, and a representative M. musculus sequence

157 aracteristics, and catalytic activity of the lambda-genome maturation complex.

158 We examined the relationship between IFN-lambda genotypes and significant liver fibrosis in HIV-H

159 IFN-lambda genotypes may be useful to target HCV treatments

160 t count ratio index [APRI] of >/=1.5) by IFN-lambda genotypes was analyzed using Cox proportional haz

161 itrophenyl to stimulate nitrophenyl-specific lambda(+) germinal center B cells and sequenced the unex

162 markably electrotonically compact (estimated lambda > 1.5 mm).

163 n detail under UV-A and visible irradiation (lambda > 320 nm) to avoid direct phototransformation.

164 oxalate complexes absorb near-UV radiation (lambda > 350 nm), providing a potentially powerful sourc

165 Upon excitation with visible light (lambda > 400 nm) in methanolic solutions, they undergo p

166 r light irradiation (AM 1.5G, 100 mW cm(-2), lambda > 400 nm, pH 6.7, 25 degrees C).

167 brid as a photocatalyst under visible light (lambda > 420 nm) irradiation.

168 cocatalyst under visible-light irradiation (lambda > 420 nm).

169 for explosive low-density population growth (lambda > 5) and complex density fluctuations under herbi

170 es at telecom (lambda 1550 nm) and mid-IR (lambda >/= 2100 nm) wavelengths is demonstrated and anal

171 -fidelity pols follow a common paradigm, Pol lambda has developed specific conformations and mechanis

172 aPKC-lambda has recently been implicated in epidermal differe

173 Lambda interferon (IFN-lambda) has potent antiviral effects against multiple en

174 to injection of purified IFN-alpha/beta or -lambda, IECs in EW-infected mice exhibited impaired STAT

175 Interferon-lambda (IFN-lambda) is a central regulator of mucosal im

176 In addition, interferon-lambda (IFN-lambda) is a key host determinant blocking M

177 ge-specific deletion of the receptor for IFN-lambda, Ifnlr1 We found that expression of IFNLR1 on int

178 Type I (alpha and beta) and type III (lambda) IFNs are induced upon viral infection through ho

179 with specificity for the kappa (Igkappa) and lambda (Iglambda) L chains of ferret Ig.

180 e have developed a five-dimensional (x,y,z,t,lambda) imaging system that leverages a snapshot hypersp

181 a) closely matches that of absorptance alpha(lambda), implying that the Kirchhoff's law can adequatel

182 of interferon (IFN)-alpha, IFN-beta and IFN-lambda in bronchial epithelial and bronchial lavage cell

183 (ISGs) in epithelia, while the effect of IFN-lambda in non-epithelial cells remains unclear.

184 , selective deletion of the aPKC isoform Pkc-lambda in proopiomelanocortin (POMC) neurons disrupts le

185 pression also determines the efficacy of IFN-lambda in resolving persistent murine norovirus (MNoV) i

186 The final step of lysis in phage lambda infections of Escherichia coli is mediated by the

187 genes encoding components of the interferon lambda innate immune system drive viral polymorphism.

188 Thus, NS1 and IFN-lambda interactions govern IEC tropism and persistence o

189 Lambda interferon (IFN-lambda) has potent antiviral effe

190 Lambda interferons (IFNlambdas) or type III IFNs share h

191 The bacteriophage lambda is a convenient source of high quality long (48.5

192 In particular, lambda is most sensitive to nonbreeder parameters in lon

193 has an area of 0.7lambda x 0.7lambda, where lambda is the free-space wavelength.

194 Interferon-lambda (IFN-lambda) is a central regulator of mucosal immunity; howe

195 In addition, interferon-lambda (IFN-lambda) is a key host determinant blocking MNoV infectio

196 rates contribute to population growth rate (lambda) is key to understanding how animal populations w

197 n this spectral range, its absorptance alpha(lambda) is spectrally flat and differentiates from unity

198 scherichia coli and its virus, bacteriophage lambda, is paradigmatic for gene regulation in cell-fate

199 (CDR-L3) amino acid sequences and/or Vkappa,lambda-Jkappa,lambda genes.

200 against HA exhibited an inherent bias toward lambda L chain usage.

201 nt as an RV144 V2 Ab but paired with a mouse lambda L chain.

202 tion resulted in human VH pairing with mouse lambda L chains instead of allowing otherwise subdominan

203 absolute configurations of which are denoted Lambda (left handed helix) or Delta (right handed helix)

204 sed rhinovirus replication and increased IFN-lambda levels at the gene and protein levels.

205 Rhinovirus replication was higher and IFN-lambda levels were lower in AECs from asthmatic patients

206 observed across species and suggest that the lambda light chain bias against HIV provides the host an

207 l for the understanding the various kappa to lambda light chain ratios observed across species and su

208 In this report, we describe biased lambda light chain use during the HIV Env glycoprotein (

209 he normal B cells expressing the nontargeted lambda light chain, thus potentially minimizing humoral

210 Kappa and lambda light chains and IgH genes are main partners in a

211 , herbivore access drove population decline (lambda < 1), suppressing complex fluctuations.

212 tandard PELDOR measurement, and confirm that lambda < 1/(n-1) is needed to sufficiently suppress mult

213 The mid-infrared (2.5 < lambda < 25 mum) spectral region is utilized for many pu

214 ping of 2,5-diphenyltetrazoles (possible for lambda </= 322 nm) proceeds best at a wavelength shorter

215 igations with N-ethylmaleimide (possible for lambda </= 390 nm) are ideally performed at 330 nm, wher

216 gs provide insight into the mechanism of IFN-lambda-mediated antiviral activity.IMPORTANCE Human noro

217 r1(-/-) mice, suggesting that NS1 evades IFN-lambda-mediated antiviral immunity.

218 t supports an essential role for IECs in IFN-lambda-mediated control of enteric viral infection, and

219 tage dependence of ZIKV pathogenesis and IFN-lambda-mediated immunity at the maternal-fetal interface

220 Moreover, IFN-lambda-mediated sterilizing immunity against murine noro

221 ism for a unique catalytic behavior of cubic lambda-MnO2 .

222 fferences in the electrochemical behavior of lambda-MnO2 depend on the preparation method and provide

223 Chemically prepared lambda-MnO2 has not been intensively studied as a materi

224 Lambda-mode laser scanning microscopy confirms this fluo

225 he roles of P-loop residues in bacteriophage lambda motor function.

226 s downregulated, whereas upregulation of IFN-lambda mRNA was found in the epithelium of cattle that h

227 of infection, the level of expression of IFN-lambda mRNA was higher in follicle-associated epithelium

228 Functional lambda mRNA was obtained, as expected, from the LK14-dep

229 r-displacement plethysmography (ADP) and the lambda-mu-sigma method for percentile estimation.

230 Bacteriophage lambda of Escherichia coli has two alternative life cycl

231 n was detected in 86%; the remainder had IgM lambda or IgG kappa.

232 feline heavy (IGHG1a) together with a light (lambda or kappa) chain.

233 t power P av of 650 mW and center wavelength lambda p of 810, 820, 830, and 840 nm are coupled into t

234 riming is presented for three DNA templates: Lambda phage, Synechocystis sp. PCC 6803 rbcL gene, and

235 Here we demonstrate the use of lambda-phage displaying Cry1Aa13 toxin variants modified

236 uction of recombinant DNA sequences into the lambda-phage genome with 90-100% yield.

237 ffinity, from a Kd of 27 +/- 3 nM for (Delta,Lambda)-Piz to a Kd of 622 +/- 55 nM for (Lambda,Delta)-

238 ically plausible ranges, we find that the xi-lambda plane is comprised of only two disjoint regions,

239 Here we examine how human DNA polymerase lambda (Pol lambda) achieves medium fidelity by determin

240 mispairs are removed through DNA polymerase lambda (Pol lambda)-dependent MUTYH-initiated base excis

241 responses by exogenous IFN-beta, but not IFN-lambda, protected MCs against HRV infection.

242 e hepatocytes expressed higher levels of IFN-lambda proteins (IL28B, IL-29), preactivated IFN-stimula

243 becomes refractory after hours, whereas IFN-lambda provides a long-lasting IFN-stimulated gene induc

244 ndings show that RNR controls ET by lowering lambda, raising HDA, and directing PT both within and be

245 f the intracellular domain of the interferon-lambda receptor 1 (IFNLR1) has been determined at the no

246 -KO), mice with disruption of the interferon lambda receptor 1 gene (Il28ra(-/-)), and mice with disr

247 episomal replicon by CRISPR/Cas9, coupled to lambda-red-mediated recombination and simultaneous posit

248 We show that the lambda-related phage 82 Q protein (82Q) can also engage

249 ltaneously measured the concentration of the lambda repressor CI and the number of messenger RNAs (mR

250 ately 2-fold higher than that of Pols mu and lambda, respectively.

251 Here, we sought to identify IFN-lambda-responsive cells by generation of mice with linea

252 mice, we identified IECs as the dominant IFN-lambda-responsive cells in control of enteric virus infe

253 rd of noncrystalline LCPT patients displayed lambda-restriction or acute tubular injury.

254 based on the presence of an immunoglobulin G lambda serum M protein (4,784 mg/dL) and confirmed by th

255 stress propagation (the hydrodynamic length lambda) sets the length scale of slow deformations, and

256 Finally, early normalization of kappa:lambda sFLC ratio but not negative uIFE predicted achiev

257 gnostic samples (100%) had an abnormal kappa:lambda sFLC ratio, and involved (monoclonal) FLC (iFLC)

258 sharks express four L chain isotypes, kappa, lambda, sigma, and sigma-2, encoded by 35 functional min

259 Type III interferons (IFN-lambdas) signal through a heterodimeric receptor complex

260 , we found that fetuses lacking type III IFN-lambda signaling had increased ZIKV replication in the p

261 nockout cell lines and mice to show that IFN-lambda signaling is regulated by SOCS1 but not by SOCS3

262 IFN-lambda SNPs rs12979860, rs8099917, and rs81013142 were i

263 Whereas lambda somatic mutants from the depleted sample displaye

264 Here, we report a suppressor analysis of lambda spanin function.

265 sis identified the functional domains of the lambda spanins, which are similar to class I viral fusio

266 HC P/M stereochemistry and the iridium Delta/Lambda stereochemistry.

267 ents (age 64.6 +/- 11.3 years, 63% male, 76% lambda subtype), 40 received the 3-drug regimen and 66 r

268 nistically induces a Raman transition in the Lambda system and excites the qubit.

269 s positions in the genomes of bacteriophages lambda, T5, T7, T4 and R1-37 and investigated the abilit

270 The lambda-terminase protomer is composed of one large catal

271 he Red recombination system of bacteriophage lambda that promotes a single strand annealing (SSA) rea

272 upling (Hab ) is one half of reorganization (lambda), that is, Hab =lambda/2.

273 e Maxwell time tauM, the hydrodynamic length lambda, the ratio of active stress zetaDeltamu, and per-

274 trimming the DNA ends; DNA polymerase mu and lambda to add nucleotides; and the DNA ligase IV complex

275 are the critical cell type responding to IFN-lambda to control multiple enteric viruses.

276 mong mature females, the total elasticity of lambda to the projection kernel generally increased with

277 ferences in sensitivities, or changes of log lambdas to changes in autocorrelation among two major ax

278 Interestingly, a time ratio lambda = tp/tm (tp is the aggregate characteristic time,

279 h cdPCR and ddPCR platforms can transfer the lambda traceability characteristics of a cdPCR assay to

280 t study, we use a transgenic fish model, the lambda transgenic medaka, to evaluate the potential muta

281 A monochromatic beam of wavelength lambda transmitted through a periodic one-dimensional di

282 IFN-lambda treatment analogously diminished ZIKV infection i

283 ma) treatment, but not IFN-alpha, -beta, or -lambda treatment, dramatically decreased infection of hu

284 beta) (type I), IFN-gamma (type II), and IFN-lambda (type III).

285 vian quantum dynamics of the dark state in a Lambda-type three-level system coupled to two bosonic ba

286 For the Lambda-type three-level system, this dark state is gener

287 late stochastic population growth rates (log lambdas ) under different temporal autocorrelations in d

288 nment tools: BLASTX, RAPSearch2, DIAMOND and Lambda, using empirically obtained reads.

289 A new parameter, the separation ratio Lambda = v drift /v gas , is employed to determine the b

290 suggest that the difference on the obtained Lambda values for biodihaloelimination could be associat

291 Lambda values of 1,2-DCA were, for the first time, deter

292 ce display to engineer a higher-affinity IFN-lambda variant, H11, which enabled crystallization of th

293 In mice, IFN-lambda was elicited by enteric viruses and acted on neut

294 However, lambda was largely insensitive to this effect, even when

295 Dramatic increase in lambda was observed for MC samples ( -360 ppm and -380

296 ll subsets expressing cell surface kappa and lambda were quantified by flow cytometry; their frequenc

297 of DNA target copies per reaction partition, lambda, where the partitions are fixed-location chambers

298 volume of >10(5)lambda x 10(5)lambda x 10(3)lambda, which enables natural light to be processed dire

299 edirected in a volume of >10(5)lambda x 10(5)lambda x 10(3)lambda, which enables natural light to be

300 ntrolled and redirected in a volume of >10(5)lambda x 10(5)lambda x 10(3)lambda, which enables natura