ライフサイエンスコーパス: wild-type

1 step in ethylene biosynthesis compared with wild type.

2 ut 10(-9.0) m produced the same effect as in wild type.

3 silencing as direct transformation into the wild type.

4 xpress mCherry, which distinguishes from the wild type.

5 nt was more susceptible to NaCl than was the wild type.

6 r brief bouts of activity and sleep than the wild-types.

7 lammatory cytokines than those infected with wild-type 874391.

8 gineered strain with a strain containing the wild-type ACT1 promoter.Genetic isolation of a genetical

9 ated by examining the effect of E6APC820A on wild-type activity and single-turnover pulse-chase kinet

10 sponse to ischemic stress that is similar to wild-type aged hearts (i.e., impaired ischemic AMPK acti

11 h FcRn-binding albumin variant compared with wild-type albumin.

12 To what extent the wild-type allele contributes to leukemogenesis is unclea

13 putative Wag31 target demonstrated that the wild-type allele was dominant and showed no synergy with

14 7) or a low ratio (0.05 to 0.7) of mutant to wild-type alleles (ITD [high] and ITD [low], respectivel

15 pha-synuclein overexpressing model harboring wild-type alleles of GBA, A53T-SNCA mouse model) were ex

16 llen and associated food allergies, a single wild-type allergen does not provide a complete solution.

17 id radical cation signal was detected in the wild type, although it was lost in the mutant.

18 tion and reduced IL-6 production compared to wild type and esat-6 complemented Mtb strains.

19 GFR was assessed in conscious TRPC6 wild type and knockout mice, and in anesthetized rats wi

20 Finally, we showed that overexpression of wild type and mutant 4R-Tau isoform in neuroblastoma SH-

21 carefully selected genes with their drugs in wild type and mutant forms.

22 some EBV-associated cancers, p53 tends to be wild type and overly expressed; however, the effects of

23 displays a hyperactive phenotype relative to wild type and overproduces a number of compound families

24 itro, however, IFN-gamma production by naive wild type and tristetraprolin-deficient CD8(+) T-cells i

25 study of both cancer-bearing mouse models in wild types and their corresponding control types, emphas

26 nt cluster analyses of microarray data using wild-type and c-Jun-deleted macrophages highlight the ce

27 Wild-type and cathepsin K knockout mice were rendered di

28 on Ca(2+) imaging in hippocampal area CA1 of wild-type and Df(16)A(+/-) mice, an animal model of 22q1

29 Wild-Type and dominant-negative-DISC1 (DN-DISC1) mice we

30 Comparative infection with wild-type and epithelial cell receptor-blind viruses dem

31 ing GCaMP6s, we found no differences between wild-type and Fmr1 KO mice in overall whisker-evoked act

32 ucleus accumbens (NAc) shell ensembles using wild-type and Fos-GFP mice, which express green fluoresc

33 IL-15 equally sustains wild-type and Il7ra(-/-) ILC survival in vitro and compe

34 Both wild-type and mutant ANO5 protein localize to the endopl

35 e wild type, however, the mRNA levels of the wild-type and mutant cells were comparable.

36 h-clamp to explore biophysical properties of wild-type and mutant KV 3.1 channels.

37 Viruses containing wild-type and mutant MN/10 or BJ/92 hemagglutinins (HAs)

38 n (Gfap(R236H)(/+)) (and thus expresses both wild-type and mutant protein).

39 essing no MECP2 (MECP2-KO), congenic pair of wild-type and mutant RTT patient-specific induced plurip

40 By combining wild-type and mutant subunits in various asymmetric conf

41 We transfected HEK293T cells with pyrin and wild-type and mutated WDR1 Mutant protein formed aggrega

42 ed Huh7 cell lines which ectopically express wild-type and NEDDylation-deficient HBx and found that N

43 thotopically injected breast cancer cells in wild-type and RAGE-knockout C57BL6 mice.

44 By analyzing activated murine wild-type and Rheb-deficient CD4(+) T cells, as well as

45 Furthermore, SSRIs protected both wild-type and SERT knockout mice from behavioral despair

46 and proteomes of primary mouse B cells from wild-type and STAT6-deficient mice cultured for 4 d in t

47 o infection of gastric epithelial cells with wild-type and VacA-deficient H. pylori strains, treatmen

48 ted isolated intestinal tissue from C57BL/6 (wild-type) and Cftr(-/-) mice in Ussing chambers and mea

49 more physiological excitation rates than the wild-type, and the generation of early-after-depolarisat

50 ytokeratin-19-positive cells in the liver of wild-type animals was slightly reduced in Nlrp3(-/-) mic

51 gher in the lungs of CC10-IL-13 Tg mice than wild-type animals.

52 t when the fitness values of the mutants and wild types are anti-correlated across environments.

53 e immunity against subsequent infection with wild-type bacteria.

54 ells in the lung and draining lymph nodes in wild-type BALB/c mice after RSV infection.

55 delayed germination as compared to grains of wild type barley.

56 it was suboptimal compared with that seen in wild-type bone marrow (BM)-transplanted OS mice in perip

57 elease, was detected during acute hypoxia in wild-type but not Cox4i2(-/-) PASMCs.

58 embryonic fibroblasts by reconstitution with wild-type but not mutant FKBP65 that lacks intact PPIase

59 fects were reversed upon reconstitution with wild-type, but not enzyme-active site-deficient DHHC3.

60 Complementation with wild-type, but not mutagenized, C1qbp restored OXPHOS pr

61 ted colonic HbetaD1 and HbetaD2 release from wild-type, but not Takeda GPCR 5(-/-), mice.

62 ld-type samples were correctly classified as wild type by this method with the remaining three sample

63 These experiments utilized wild-type C57BL/6 mice, IL33-/- mice, B6.C3(Cg)-Rorasg/s

64 Furthermore, in wild-type C57BL/6J mice fed a high fat diet, 2-weeks sup

65 ent (Nlrp3(-/-)) and NLRP3 inhibitor-treated wild-type (C57BL/6) mice.

66 Overexpression of FoxO in wild type cardiomyocytes induced murf1 expression and ca

67 In isolated wild-type cardiomyocytes, Cx43 protein content decreased

68 ffer between tumour samples from variant and wild-type carriers.

69 fficient and less deleterious alternative to wild-type Cas9 for gene-knockout studies.

70 acterize the magnetosome arrangement in both wild-type cells and DeltamamJ mutants, which exhibit dif

71 Wild-type cells are required for the active elimination

72 athways in the stem cell compartment and how wild-type cells limit the proliferation of mutant cells

73 ial drug susceptibilities of KRAS mutant and wild-type cells, and predict relapse based on increased

74 n2 is constantly localized to the nucleus in wild-type cells.

75 Rgamma expression in knock-out cells than in wild-type cells.

76 SMARCA4/BRG1 mutant but not of SMARCA4/BRG1 wild-type cells.

77 ration curve shifted to the left relative to wild type channels and the ICl was nearly insensitive to

78 gnificantly less MHCII, and grew faster than wild-type clones in s.c. and orthotopic xenograft models

79 cally significant changes between pallid and wild-type control.

80 central nervous system, and their respective wild-type controls to photothrombotic stroke.

81 Compared with wild-type controls, HAT-L4-deficient newborn mice had gr

82 Compared with wild-type controls, striatal synaptosomes isolated from

83 hyperplasia compared with similarly injured wild-type controls.

84 female late-stage R6/2 mice and age-matched wild-type controls.

85 ectrophoresis from A36V mutant than from the wild-type core protein.

86 NF or TNF receptors are outcompeted by their wild-type counterpart.

87 ells proliferate more efficiently than their wild-type counterparts in response to BCR cross-linking.

88 n cryo electron microscopy (cryo-EM) maps of wild type CPMV containing RNA-2, and of naturally-formed

89 unction in NOD2(-/-) CVB3 mice compared with wild-type CVB3 mice.

90 mice induced a severe myocarditis similar to wild-type CVB3 mice.

91 Mice harboring wild-type Cyp24a1 (BVE(Cyp24a1-wt)) developed PTC at 5 w

92 C1-64 on the plasma membrane distribution of wild-type DAT and two non-functional DAT mutants, R60A a

93 F conformation, reduced the concentration of wild-type DAT in filopodia.

94 pression and activity of TACE were lower, in wild-type DCs (wtDCs) than in TNF knockout (TNFko) DCs.

95 igated the VtE-induced amelioration of DN in wild-type (DGKalpha(+/+)) and DGKalpha-deficient (DGKalp

96 Although virtually all AMLs with wild-type DNMT3A displayed CpG island hypermethylation,

97 genotype followed by introgression into the wild type does not result in the same level of silencing

98 cortical patches that rapidly disassemble in wild-type embryos.

99 grik1-2 grik2-1) that grows similarly to the wild-type, enabling us to evaluate the function of GRIKs

100 By comparing the FTIR spectra of wild-type enzyme and two mutagenesis variants, we are ab

101 d ligand binding affinity, compared with the wild-type enzyme, demonstrating that substrate binding t

102 etic complementation of patient's cells with wild-type FANCM improved their resistance to MMC re-esta

103 TM is sufficient to promote DNA synthesis in wild-type fat body cells.

104 solubility-enhancing mutations that maintain wild-type fitness with an accuracy of 90%.

105 dominant negative effect on the function of wild-type FLCN in regulating kidney cell proliferation a

106 ested primary FLT3-ITD NK-AML in contrast to wild-type FLT3 NK-AML.

107 and for the intermediate risk genotype NPM1 wild-type/FLT3 without internal-tandem duplications (EFS

108 s that are caused by these perturbations the wild-type function of genes can be elucidated.

109 Remarkably, upon restoration of near wild-type FXN levels, we observed significant recovery o

110 % increase in fusion compared to that of the wild-type gBcyt while arginine substitutions had wild-ty

111 ress this deficit, we generated samples of a wild-type GPCR (A2AR) that are deuterated apart from (1)

112 (line M20) injected in the hippocampus with wild-type, H50Q, G51D or A53E alphaS fibrils displayed i

113 ently detected by antibodies elicited by the wild-type HA from viruses selected as the vaccine candid

114 cid (DHA), a representative omega-3 PUFA, in wild type hairless mice induced expression of the Nrf2 t

115 tions of inflammatory cytokines, compared to wild type hearts.

116 is the first detailed case report suggesting wild-type HIV-1 infection despite good adherence, eviden

117 remarkably reduced compared with that of the wild type, however, the mRNA levels of the wild-type and

118 tant phenotypes can be rescued by expressing wild-type HRPU-2 in neurons.

119 Q mutations have serum half-lives as long as wild-type human IgG1.

120 Importantly, secretion of wild-type human SOD1 and the ALS-linked mutant in human

121 metabolic alterations in glioblastomas with wild-type IDH are poorly understood.

122 n and cynomolgus FcgammaRs compared with the wild-type IgG1 antibody.

123 We also found that wild-type immature thymocytes can be separated into dist

124 have led to a SLO3 variant that differs from wild type in both pH and intracellular Ca(2+) sensitivit

125 ed currents that inactivate more slowly than wild type, indicating that increased cation permeability

126 As compared with wild-type infected mice, CD151-null infected mice exhibi

127 hree orders of magnitude for the full-length wild-type KcsA, a pH-gated bacterial channel, in membran

128 Uremic wild-type (KL(fl/fl) ) and knockout (Prx1-Cre;KL(fl/fl)

129 yzing the expression of pRGA::GFP-RGA in the wild-type Landsberg erecta background, we demonstrate th

130 e in Flower-deficient CTLs and is rescued to wild-type level by reintroducing Flower or by raising ex

131 in animals with striatopallidal knock-out to wild-type levels, suggesting a dependence on adenosine r

132 -type gBcyt while arginine substitutions had wild-type-like fusion levels in an in vitro gB/gH-gL cel

133 ed by comparing melanoma cells infected with wild-type-like VZV or hyperfusogenic mutants.

134 While wild-type lint fiber trichome cells contained long longi

135 , and myeloperoxidase activity compared with wild-type littermates.

136 ted to the Golgi and activated by Rab29 than wild-type LRRK2.

137 ion, and cells lacking NRP2 are deficient in wild-type LUJV infection.

138 lative to the sensor electrode prepared from wild-type M13, Y3E peptides engineered M13 and without M

139 In wild-type mammals, approximately 60% of cells have recom

140 sult stems from local obstruction of flow by wild-type matrix producers, which generates regions of n

141 Lentiviral complementation with wild-type MDH2 cDNA restored MDH2 levels and mitochondri

142 Conversely, overexpression of wild-type METTL3, but not of a catalytically inactive fo

143 TRAF3IP2 expression and myocardial injury in wild type mice post-I/R.

144 observed in cortical pyramidal neurons from wild type mice was conspicuously reduced in TASK(-/-) mi

145 nce distribution was estimated in 8-week-old wild type mice, and stochastically varied for each condi

146 o the vasculature or diluted into blood from wild type mice.

147 owed less neurological deficit compared with wild-type mice (n=6).

148 amin D) each increased serum FGF23 levels in wild-type mice and in mice with global deficiency of the

149 were lower in Brd4 heterozygous mice than in wild-type mice at 21 days after birth.

150 Kalpha2(DeltaMC) mice was lower than that in wild-type mice despite being higher after 24 hours.

151 he differential CT responses in IgA(-/-) and wild-type mice disappeared after intestinal microbiota e

152 In wild-type mice fed an unsupplemented ad libitum diet, ag

153 Wild-type mice initially learnt, but with prolonged trai

154 eosinophils from fungal allergen-challenged wild-type mice maintain a distinct cytokine profile, and

155 Moreover, overexpression of DLST in wild-type mice protected against cardiac hypertrophy and

156 Wild-type mice showed increased myocilin expression in t

157 Wild-type mice subjected to IL-17A neutralization and IL

158 2 innate lymphoid cells (ILC2), and C57BL/6 wild-type mice treated with anti-IL5 antibody.

159 not observed in Ig-treated Rag1(-/-) mice or wild-type mice treated with anti-type I IFNR alone.

160 sponse element of Gpr64 gene in the uteri of wild-type mice treated with P4.

161 ly, both the renal injury and dysfunction in wild-type mice undergoing iAKI is significantly ameliora

162 knock-out and heterozygous mice compared to wild-type mice using RNA-seq; and (iii) morphological an

163 ally, the administration of exogenous NGF to wild-type mice was found to significantly increase load-

164 nia, we found that goal-oriented learning in wild-type mice was supported by stable spatial maps and

165 monas species directly impair wound healing, wild-type mice were infected with Pseudomonas aeruginosa

166 toward either M1 or M2 macrophages in vivo, wild-type mice were injected with gamma interferon (IFN-

167 [KO]), iNOS-deficient (iNOS KO), and C57BL/6 wild-type mice were orally infected with A. actinomycete

168 was significantly reduced after treatment of wild-type mice with CSP, and uPA-deficient mice were unr

169 IL-6R by CD4(+) T cells and by treatment of wild-type mice with neutralizing anti-IL-6 mAb.

170 ing the peripheral macrophage populations of wild-type mice with Nrp1-depleted bone marrow-derived ma

171 mage at doses that caused minimal effects in wild-type mice, and adoptive transfer of gammadelta T ce

172 lanar cell polarity genes Vangl2 and Ptk7 In wild-type mice, collagen-fibril bundles appear within a

173 Indeed, compared with wild-type mice, MLKL knockout mice displayed more severe

174 nificantly decreased on pressure overload in wild-type mice, paralleling a decreased oxidative metabo

175 increased serum glycolate concentrations in wild-type mice, rats, and nonhuman primates.

176 expression caused no significant changes in wild-type mice, suggesting that Hjv is not a limiting fa

177 Compared with wild-type mice, the cell surface levels of Cav1.2 in the

178 V-Cre, and in NBQX- and rapamycin-pretreated wild-type mice, these compounds blocking alpha-amino-3-h

179 lso sufficient to improve these behaviors in wild-type mice, when circulating levels of OCN decline a

180 reater percentage of affected limbs than the wild-type mice.

181 ttractant CXCL1 in their lungs compared with wild-type mice.

182 rse was significantly attenuated compared to wild-type mice.

183 oduction and sperm motility in knock-out and wild-type mice.

184 of PKA were increased by glucocorticoids in wild-type mice.

185 ate sodium for 7 days and were compared with wild-type mice.

186 -treated mutant but not in similarly treated wild-type mice.

187 e-primed reinstatement in OCT3-deficient and wild-type mice.

188 e more resistant to bacterial infection than wild-type mice.

189 express low NR2E3 relative to the livers of wild-type mice.

190 ferent in Ormdl3(Delta2-3/Delta2-3)/CC10 and wild-type mice.

191 ofoundly reduced rapid eye movement sleep in wild-type mice; these effects were eliminated in Taar1 k

192 eaker signal from the mutant compared to the wild-type MIP.

193 sis opposite to the pattern observed for the wild-type miR-200b expression.

194 By using both IL-10-deficient and wild-type mothers, we showed that both inoculum and geno

195 Given that wild-type mouse myosin VIIa is a slow, high-duty ratio,

196 study, Calhm1 knockout, Panx1 knockout, and wild-type mouse nasal septal epithelial cells were grown

197 levels of MT1-MMP were engineered to express wild-type MT1-MMP, a phosphomimetic mutant (T567E), or a

198 eport the first successful transformation of wild-type NCCs into NBL by enforced expression of N-Myc,

199 otentials for a given stimulus compared with wild-type neurons.

200 doplasmic reticulum (ER) stress in both KRAS wild-type normal pancreas cells, as well as in KRAS muta

201 HA digestion in wild type NSC cultures or in the SGZ induces increased N

202 ation, and CD44-null as well as HA-disrupted wild type NSCs demonstrate delayed neuronal differentiat

203 decreased nucleosome interactions similar to wild-type nucleosome arrays.

204 and postnatal n-6/n-3 PUFA ratio exposure in wild-type offspring under standard maternal dietary fat

205 Studies on NS1 wild type or mutant alone or in recombinant RSVs demonst

206 that in glioma cells expressing either EGFR wild type or the mutant EGFRvIII, EGFR inhibition trigge

207 rated transgenic zebrafish models expressing wild-type or A152T-tau, where A152T caused neurodegenera

208 C57BL/6 wild-type or CD73(-/-) mice received a single dose of wh

209 Expression of the wild-type or edited allele of AMD1 but not un-editable a

210 rated Abcc6(-/-) and Enpp1(asj) mice, either wild-type or hemizygous for human ENPP1.

211 Primary cultures of hepatocytes derived from wild-type or hepatocyte-specific furin, PC5/6, or comple

212 efects were rescued upon the reexpression of wild-type or kinase-dead CDK19.

213 Indeed, BCL6 represses the expression of wild-type p53 and its target genes in GBM cells.

214 a conditional AP2-G knockdown line and NF54 wild-type parasites at multiple stages of development, w

215 rization in Cox4i2(-/-) PASMCs compared with wild-type PASMCs, which could be normalized by the appli

216 predicted resistance to ibrutinib with only wild-type patients responding (P = .002).

217 Ectopic expression of wild-type Pdcd4 and Pdcd4(157-469), a deletion mutant th

218 Interestingly, overexpression of the wild-type PDGFRA was even more potent in promoting trans

219 ause 78% of human MPNSTs have expression of wild-type PDGFRA, whereas only 5% harbor activating muta

220 afish embryos overexpressing mutant, but not wild-type, PDGFRA, suggesting a mechanism through which

221 rotron-based in vivo imaging technique, that wild-type pigs display both a basal and a Toll-like rece

222 gain and biochemical analyses comparable to wild-type pigs.

223 getative SAM In agreement, SP-overexpressing wild-type plants exhibited precocious doming of vegetati

224 Overexpressing PEX1 in wild-type plants impaired growth, suggesting that excess

225 in higher endogenous iron concentration than wild-type plants in both brown and white grains.

226 y are morphologically indistinguishable from wild-type plants.

227 e NTD equilibrium can be shifted back to its wild-type position by mutation at a secondary site with

228 Notably, overexpression of the wild-type PRKACA was unable to fully recapitulate the on

229 = 533 nm) absorption maxima relative to the wild-type protein (lambdamax = 527 nm).

230 f fibroblasts with a lentivirus encoding the wild-type protein partially rescued the deficiency of GP

231 nts decreased cell proliferation relative to wild-type protein.

232 econstitution of PTEN-null cells with either wild-type PTEN or a catalytically dead mutant stabilizes

233 Relative to wild-type pups receiving high perinatal n-6/n-3 ratios,

234 s, subcutaneous adipose tissue in 14-day-old wild-type pups receiving low n-6/n-3 ratios had more adi

235 s similar to those for animals infected with wild-type R. typhi and develop comparable pathology and

236 We show that wild-type RAS amplification increases receptor tyrosine

237 orporation into DHFR and IkappaB-alpha using wild-type ribosomes, and the elaborated proteins could s

238 GreA factors activate RNA cleavage by wild-type RNAPs to similar levels.

239 Accordingly, the activity of the wild type RUNX2 promoter was decreased upon methylation

240 ed more efficiently by IFN-beta than was the wild-type S. aureus, and immunoblotting showed that IFN-

241 .9% (2786/2789, 95% CI [0.997, 1.00]) of the wild-type samples were correctly classified as wild type

242 ption factors, particularly in SDHD promoter wild-type samples.

243 icantly lower for SERT-DeltaN32 than that of wild type SERT and SERT-DeltaN22.

244 px-mediated SAMHD1 degradation and inhibited wild-type SIVmac (simian immunodeficiency virus of macaq

245 We found that injection of fluorescent wild-type SOD1 (wt SOD1YFP) or monomeric mutant G85R SOD

246 acteria-specific (P25 CD4(+) TCR transgenic) wild-type spleen cells into sanroqueRag1(-/-) mice actua

247 EVS evoked relaxation of wild type stomachs, but the predominant response of W/W(

248 rated in different genetic backgrounds (e.g. wild-type strain versus knockout strain).

249 rt succumbed to infection with a more recent wild-type strain, indicating that immune responses to th

250 on increased cytarabine resistance of a KRAS wild-type subclone.

251 Wild-type T. denticola and the purified PF triggered act

252 lation-dependent mediator of the toxicity of wild-type tau and of all the FTDP-17 mutants tested.

253 Whereas wild-type Teff cells upregulated Mdr1 in the ileum, thos

254 143K were found to be more thermostable than wild-type TK.

255 cause the ohr mutant was more sensitive than wild type to 3-morpholinosydnonimine hydrochloride (SIN-

256 control mice (NT) and in mice carrying human wild-type torsinA (hWT) or mutant torsinA (hMT).

257 ly, this mutation was able to sustain 15% of wild-type transport activity, when the catalytic glutama

258 ein synthesis and abolished proliferation in wild-type tubular cells, but only reduced proliferation

259 M) are known to be more aggressive than KRAS wild-type tumors.

260 tion at a secondary site with restoration of wild-type two-pronged binding of the UBXD1 adaptor prote

261 antly in its deprotonated form when bound to wild-type VAO, but predominantly in its protonated form

262 ors display a different behavior against the wild-type versus V27A mutant A/M2 channels, and (ii) the

263 growth of the escape mutant viruses with the wild-type virus revealed that some escape mutants posses

264 346 mutant maintains similar antigenicity to wild-type virus, opening the possibility for its use as

265 ection of cells with UnaG and infection with wild-type virus, passage of UnaG through progeny was sig

266 K166Q showed superior growth to that of the wild-type virus.

267 retained fitness during coinfection with the wild-type virus.

268 Comparisons of cells from wild-type vs. AE3(-/-) mice show that AE3 (present in hi

269 (irAGO8) plants but did not differ from the wild type when consuming plants silenced in AGO1 (a, b,

270 er binding to CNS synaptosomes isolated from wild type (wt) mice treated with NIR light was significa

271 sue) were found in LanCL1 knock-out, TKO and wild type (WT) mouse brains, suggesting that LanCL prote

272 plaque morphologies similar to those of the wild-type (WT) A24 Cruzeiro strain in BHK cells, and bot

273 Wild-type (WT) and B cell-deficient mice received ovalbu

274 Male wild-type (WT) and Cyp2e1-null mice were fed standard ch

275 Ear thickness of wild-type (wt) and Sucnr1-deficient (Sucnr1(-/-) ) mice,

276 Wild-type (WT) and TG mice received vehicle or BACE inhi

277 ssion of FOXO transcription factors in three wild-type (WT) and three HD induced-pluripotent stem cel

278 Nephrotoxic serum nephritis was induced in wild-type (WT) and ubiquitin-binding deficient ABIN1[D48

279 t close in response to darkness but exhibits wild-type (WT) behaviour when exposed to abscisic acid (

280 hrombosis model, we found that compared with wild-type (WT) control and nonhematopoietic DREAM knocko

281 ice exhibited enhanced mortality compared to wild-type (WT) controls, while mice lacking the necropto

282 s by RNA sequencing of ATXN2Q127 mice versus wild-type (WT) littermates.

283 es by an increase of 10-300 fold compared to wild-type (WT) merozoites.

284 time corresponding to peak LCN2 induction in wild-type (WT) mice injected with LPS, Lcn2(-/-) mice ch

285 b1)-deficient and FXII-deficient mice and in wild-type (WT) mice pretreated with a PKal inhibitor pri

286 adiponectin gene knockout (Adipoq(-/-) ) and wild-type (WT) mice were crossed to produce pregnant mou

287 ressure during rest and activity compared to wild-type (WT) mice, and smaller responses to chemorecep

288 In wild-type (WT) mice, LY2828360 (3 mg/kg per day i.p. x 1

289 When inoculated into naive wild-type (WT) mice, this persistently circulating CHIKV

290 Compared with the wild-type (WT) rat, Cyp3a1/2 expression was completely a

291 Unexpectedly, in wild-type (WT) TSCs these genes are transcribed and are

292 eratures above the conversion temperature of wild-type (wt) virions.

293 aptive immunity, and protection of mice from wild-type (WT) WNV infection.

294 rdial infarction (PMI) HF model evaluated in wild-type (wt-PMI) and Nod1(-/-) mice (Nod1(-/-)-PMI).

295 Patients and Methods Mutation analyses (wild-type [WT] and mutant) for TP53, KRAS, and EGFR were

296 e, the high pelleting temperatures challenge wild-type xylanases.

297 Third, treatment of wild-type yeast cells with E9591 or LMT generated cellul

298 ntrations of K(+) and Na(+) , as compared to wild-type Z. xanthoxylum grown under 50 mm NaCl.

299 ures issued from embryos that expressed only wild-type Zeb2 (Zeb2(+/+) EPCs) or were heterozygous for

300 one in one centre, assessed plasmid VRC5283 (wild-type Zika virus).