ライフサイエンスコーパス: wild-type

1 ) of 88 degrees C (+45 degrees C relative to wild type).

2 hat of heteromeric GlyRs (0.96; cf. 0.99 for wild type).

3 tant, NRAS-mutant, NF1-deficient, and triple wild-type).

4 t C/P efficiency of CSTF2D50A was lower than wild type.

5 ncy of root hair formation compared with the wild type.

6 ficantly less stable and infectious than the wild type.

7 G and fusion (F) protein levels than for the wild type.

8 pta and more nuclei per compartment than the wild type.

9 te influx in cadt1 was 2.4 times that of the wild-type.

10 lated in overexpressing fruits compared with wild-type.

11 instead of localising at myofibre ends as in wild-type.

12 nt reduction in MNRR1 levels compared to the wild type (0% heteroplasmy) (CL9), we evaluated the effe

13 ation (half-widths: 0.25 +/- 0.08 ms, n = 19 wild-type, 0.60 +/- 0.17 ms, n = 21 Kv3.3KO, p = 0.0001)

14 ecombinant virus lacking these miRNAs to the wild type (17syn+), we found that during acute infection

15 rent contraction kinetics in knockout versus wild-type; (2) Aberrant activation of the glucose/lipid

16 In the test sample of 49 gliomas (nine IDH wild type, 21 IDH mutant/1p19q intact, and 19 IDH mutant

17 antibodies that have reduced reactivity to a wild-type 3c3.A strain and very limited reactivity to 3c

18 hanced by about 2 and 8 K when compared with wild-type A(1)-receptor and A(1)R-Y288A(7.53) (a folding

19 A(1)R-G279S(7.44) than in those coexpressing wild-type A(1)R.

20 rectly injecting adenoviruses expressing CaM-wild type, a loss-of-function CaM mutation, CaM (1-4), a

21 , recombinant RSV strains harboring either a wild-type A2 strain G gene (one stop codon preceding a w

22 up to nonhuman primates, a natural host for wild-type AAV.

23 Compared with wild type, ablation of the miR-144/451 cluster increased

24 direct RNA sequencing to examine RNA from a wild-type accession of the model plant Arabidopsis thali

25 bound to the RBD 170-fold more tightly than wild-type ACE2.

26 l through FOP-mutant ACVR1 or form NSCs with wild-type ACVR1.

27 Genome-wide analyses also revealed that wild-type AID localized to MHCII genes, and AID expressi

28 n of the ACKR2-V41A receptor compared to the wild type allele by measuring its ligand binding affinit

29 Combining SE deletion and KO and wild-type alleles in a genotypic series, we determined t

30 Overexpression of C/EBPbeta in human wild-type alpha-Syn transgenic mice facilitates PD patho

31 nes are enriched in TP53-mutated versus TP53-wild-type AML.

32 -causing C. gloeosporioides in comparison to wild type and empty-vector control plants.

33 bining infection studies of L. monocytogenes wild type and isogenic mutants together with biochemical

34 -deficient mutant plant line compared to the wild type and JA- insensitive line.

35 We analyse 2,717 genomes from wild-type and 53 DNA repair defective backgrounds, expos

36 te hippocampal and cortical slices from male wild-type and amyloid precursor protein (APP) knock-out

37 ssing APP in EVs isolated from the brains of wild-type and APP overexpressing Tg2576 mice.

38 tly, equally inhibits ring-stage survival of wild-type and artemisinin-resistant parasites harboring

39 d the immune response were analyzed by using wild-type and B-cell-deficient (muMT) mice and transfer

40 Sensitized wild-type and CD8-deficient (CD8(-/-)) mice were challen

41 e, a differential study was carried out with wild-type and CT-1 null mice in fed (ad libitum) and foo

42 day 5 postinfection (d p.i.), although both wild-type and DUBmut virus infections resulted in simila

43 at the N- and C- terminus of peptides using wild-type and engineered ribosomes.

44 ic analysis of hematovascular development in wild-type and etv2 mutant zebrafish embryos.

45 combination strategies that can target BRCA wild-type and homologous recombination (HR) DNA repair-p

46 he rate and pattern of iAs metabolism in the wild-type and humanized mice.

47 mice displayed increased weight relative to wild-type and increased food intake at 20 months of age,

48 further examined these agents in vivo using wild-type and mdx mouse models.

49 tal periodontitis was induced for 30 days in wild-type and Msx2 knock-in Swiss mice using Porphyromon

50 Wild-type and MUC2-knockdown colonoids infected with EAE

51 s in touch-induced mechanical strain between wild-type and mutant animals.

52 Immunoprecipitation of wild-type and mutant constructs showed that IQGAP1 assoc

53 mutation caused a splicing defect, we tested wild-type and mutant mRNA substrates, containing 333 nt

54 s challenged with normalized secretomes from wild-type and mutant S. marcescens derivatives.

55 Using adenoviral gene transfer, wild-type and mutant SK2 channels were overexpressed in

56 uorescence in NIH/3T3 cells transfected with wild-type and mutated human L1 genes.

57 sphorylation of AGO2(Y393) disrupts both the wild-type and oncogenic KRAS-AGO2 interaction, albeit un

58 he onset of rapid cell rearrangement in both wild-type and snail twist mutant embryos, where our theo

59 ated Vi (165 kDa) induced a response in both wild-type and T cell-deficient mice, suggesting that it

60 Transcriptome analysis of wild-type and T357I-mutant cells identified 36 different

61 es of glutamate were conducted with MAOIs in wild-type and TAAR1-knockout (KO) mice.

62 carried out parallel CRISPR-Cas9 screens in wild-type and TP53 knockout human retinal pigment epithe

63 in young (14-16 weeks) and old (57-60 weeks) wild-type and transgenic mice.

64 ange mass spectrometry (HXMS) are applied to wild-type and VWD variants of the single A1, A2, and A3

65 Notably, the titer of the IgG in wild-type animals could be increased by more than 200-fo

66 the dentate gyrus, which was not the case in wild-type animals, and worsens impairment in spatial lea

67 report describes the effects of full-length, wild-type APC (fl-APC) on cell-cell adhesion genes and p

68 n tested the impact of expressing either the wild type APH-1B or the APH-1B T27I variant on gamma-sec

69 odelling towards the heterozygous regions in wild type Arabidopsis, but not in msh2 mutants.

70 rt a novel transgenic mouse expressing human wild-type asyn under control of the noradrenergic-specif

71 ities in mice intranasally challenged with a wild-type B anthracis strain or with an isogenic mutant

72 to a prototype reporter-KSHV, KSHVr.219, and wild-type BAC16 virus.

73 In a wild-type background, exo70a2 reduced male transmission

74 cellular survival rates compared to those of wild-type bacteria in the infected macrophages.

75 Although all wild-type bacterial populations exhibit antibiotic toler

76 he protective efficacy of BCG-disA-OE versus wild-type BCG and measured lung weights, pathology score

77 r concentrated at row 2 tips like they do in wild-type bundles.

78 ty of homomeric GlyRs (to 0.16; cf. 0.99 for wild type) but reduced only marginally that of heteromer

79 within the primordia of tt7-2 compared with wild-type, but not in the tt4 mutant, consistent with op

80 P mice (CD31(+) CD45(-) GFP(+) cells), or in wild type C57BL/6 mice (CD31(+) CD45(-) endoglin(+) cell

81 Retinal endothelial cell sorting in wild type C57BL/6 mice was validated by comparative tran

82 we used streptozotocin to induce diabetes in wild-type C57BL/6 and knockout mice lacking the genes en

83 comparison to the HSV-1 0DeltaNLS-vaccinated wild-type C57BL/6 counterpart.

84 ilateral superior cervical ganglionectomy in wild-type C57BL/6 mice, we showed that sympathetic nerve

85 de in cells that potently block infection by wild-type capsid, demonstrating that HIV-1 can use disti

86 transformation of AA to HMD (via 6-ACA), the wild type CAR was combined with the L342E variant and tw

87 3D genome folding using Hi-C experiments on wild type cells and ataxia telangiectasia mutated (ATM)

88 oss of 1C enzymes increased the longevity of wild type cells.

89 orthogonal methods we validated that PIK3CA wild-type cells adopt MAPK-dependent circuitries in brea

90 e activator aphB, and ompR overexpression in wild-type cells also repressed virulence through aphB We

91 Use of these methods shows that wild-type cells move in the same direction as their neig

92 Transplanted wild-type cells rescued gonad development but not germ c

93 tation to indole caused a bipartite response-wild-type cells were attracted to regions of high indole

94 control of the pathogen after infection with wild-type cells.

95 levels of Rho1-GTP at the division site than wild-type cells.

96 vioral effects without necessarily restoring wild-type circuit states, while highlighting the potenti

97 ted using tissue-specific GA inactivation in wild-type (Col-0) or rescue of GA-deficient dwarf mutant

98 re abundant and myofiber size was larger for wild-type compared with Icam1(-/-) mice during 28 days o

99 baga/+ and octbeta1r/+ flies behave like the wild-type control.

100 f neonatal Magel2-deficient mice compared to wild-type controls.

101 ty of the other four containing at least one wild-type copy of Ppal15kDa was compromised at varying l

102 if the recipient bacterium already carries a wild-type copy of the gene.

103 infected with adenoviruses expressing either wild-type CryAB (CryAB(WT)) or CryAB(R120G).

104 lone should be offered to patients with BRAF wild-type cutaneous melanoma, while those three regimens

105 Here, we trained wild-type, D1-Cre, A2A-Cre, or vGluT2-Cre:Ai9 male and f

106 activity in a manner indistinguishable from wild-type D2R, indicating that arrestin recruitment can

107 tent neutralizing antibody responses to both wild-type (D614) and D614G mutant(2) SARS-CoV-2 as well

108 nches light-induced rhodopsin signaling like wild type, demonstrating that in vivo monomeric arrestin

109 assembly of equimolar mixtures of mutant and wild-type desmin generated chimeric filaments of seeming

110 reased rhodopsin packing density compared to wild-type discs.

111 the aortas of young and aged normolipidemic wild type, disease-free mice and found that aging led to

112 ation between mutated DNA from patients over wild-type DNA from healthy volunteers was obtained thus

113 molecule intermolecular FRET measurements of wild-type E-cadherin and cis-interaction mutants combine

114 ed colonization of the colonic epithelium by Wild-type EAEC than its isogenic Pic mutant.

115 EBNA3A hypomorph mutant virus (Delta3A) and wild-type EBV.

116 Overexpression of wild-type EHD1 accelerated internalization of Cx43 and e

117 We addressed this by injecting labeled wild-type embryonic stem cells into blastocysts derived

118 r cell death can have the opposite effect on wild-type epithelia by inducing, via a non-autonomous IL

119 ions induce distinct expression changes from wild-type ETV6 and enhance cell motility and invasivenes

120 indicate that the dominant structure in the wild type exhibits a triplet involving the unpaired nucl

121 orised by EZH2 status: mutant (EZH2(mut)) or wild-type (EZH2(WT)).

122 The wild-type fibril structure, solved to 3.6- angstrom reso

123 ly rearranged, lower energy fold compared to wild-type fibrils.

124 D8s; however, gB-CD8s primed by a concurrent wild-type flank infection infiltrated the TG and were re

125 Whether the wild-type form of the protein, however, has a role in no

126 y a panel of gB monoclonal antibodies than a wild-type gC rescuant virus.

127 A2 strain G gene (one stop codon preceding a wild-type gene end signal), an A4G gene end signal prece

128 Mitochondria harboring wild-type genomes have functional electron transport cha

129 In nonstimulated EHEC, wild-type GrlA associates with cardiolipin membrane doma

130 r all three viral challenges compared to the wild-type H2 vaccines.

131 FX6(HA) reporter allele by gene targeting in wild-type H9 cells to precisely define RFX6 expression a

132 he frequency of homozygous TSG disruption in wild-type hosts compared to those with an inherited driv

133 chanically evoked currents is similar to the wild type; however, the proportions of rapidly adapting

134 f megakaryocyte-associated genes compared to wild-type HSPCs, and we provide early validation of G6B

135 d a DNase I cleavage assay we found that the wild type hTERT core promoter folds into a stacked, thre

136 assay in HEK-293 cells stably expressing the wild-type human P2X7 variant (HEK-hP2X7 cells).

137 Overall, wild-type HVT and HVT-DeltavNr-13 showed similar growth

138 In the wild-type HVT-infected cells, vNr-13 expression appeared

139 of interferon responses than were seen with wild-type icPEDV infection.

140 for RSV-driven AHR, since reconstitution of wild-type ILC2 rescued RSV-driven AHR in IL-13-deficient

141 3% enzymatic activity when compared with the wild-type immunotoxin in an adenosine diphosphate-ribosy

142 dimers in their variable domains and remain wild-type in their antibody constant domains.

143 ance of PUN RNA in the cytoplasm compared to wild-type-infected cells.

144 rand invasion occurs in uls1Delta cells with wild-type kinetics, arguing that global histone depletio

145 L-1-dependent increased survival relative to wild-type knock-in mice.

146 rom nonfailing and HF hearts, 4 mouse lines: wild-type, KO (CaMKIIdelta-knockout), CaMKIIdeltaC trans

147 r in mitochondria from YAC128 mice and their wild-type littermates as well as in mitochondria from po

148 1 deletion (EC-AGO1-knockout [KO]) and their wild-type littermates to a fast food-mimicking, high-fat

149 e inside the airway of Dp16 mice compared to wild-type littermates, showing the potential risk of upp

150 Cys17Ser) PKARIalpha knock-in mice and their wild-type littermates.

151 e single phase found for amantadine block of wild-type M2.

152 Here, we exposed wild-type male mice to 5-60 min of 40 Hz or control flic

153 action to a live human host, a behavior that wild-type males never display, suggesting that male mosq

154 Wild-type mesoderm cells have long polarized filopodia-l

155 l muscle from global Zip14 knockout (KO) and wild-type mice (WT).

156 However, wild-type mice and all existing humanized mouse models c

157 resistant to growth of various cancers than wild-type mice and are more responsive to anti-PD-1 immu

158 ntotemporal dementia (FTD) as well as in the wild-type mice and tau knock-out and P301L tau mouse mod

159 pts were expressed at very low levels in the wild-type mice and were significantly upregulated in the

160 S100-knockout mice weighed 21% more than wild-type mice at age 8 weeks and a higher proportion de

161 posure acutely suppresses BAT temperature in wild-type mice but not in Opn5-null mice.

162 thermore, melanopsin-activated astrocytes in wild-type mice enhanced the firing rate of cortical neur

163 nic in wild-type (TG), or KO background, and wild-type mice exposed to TAC.

164 mized female GPR30(-/-) , ERalpha(-/-) , and wild-type mice injected intramuscularly with the potent

165 jection of two antisense oligonucleotides in wild-type mice leads to a dose-dependent increase in pro

166 Here, we subjected adult, wild-type mice to distinct chronic jet-lag paradigms, wh

167 We also used wild-type mice treated with the SULT1E1 inhibitor triclo

168 Treating wild-type mice with an anti-CCL2 mAb attenuated the seve

169 Notably, treatment of infected wild-type mice with apoptotic cells significantly increa

170 ein, and Il10 and Tgfb1 mRNAs, compared with wild-type mice, and fewer T-regulatory cells.

171 serotypes were injected intrathymically into wild-type mice, and gene transfer efficiency was monitor

172 C/MS, in normal small intestines of C57BL/6J wild-type mice, and in normal and tumour samples from Ap

173 ination are attenuated in human cells and in wild-type mice, but not in live mosquitoes.

174 Compared with wild-type mice, IL-1R(-/-) mice have more severe liver a

175 histone mark H3K9me3 in mdx mice compared to wild-type mice, indicating a chromatin conformation less

176 el intensity and subcellular distribution in wild-type mice, knockout mice, and receptor-positive and

177 Compared with nontransgenic wild-type mice, mice with neuronal Mfn2 overexpression a

178 In wild-type mice, oral metformin increased circulating GDF

179 ponses that were comparable in magnitudes to wild-type mice, suggesting that this B cell response was

180 on, and reduced circulating C3 compared with wild-type mice.

181 ic lamina propria macrophages, compared with wild-type mice.

182 less efficient in the humanized mice than in wild-type mice.

183 suppressed in Gpr81-null mice compared with wild-type mice.

184 se in portal hypertension compared to BDL in wild-type mice.

185 critical for LPS-induced endotoxic shock in wild-type mice.

186 3R(+)) Treg cells develop as are observed in wild-type mice.

187 s of MLN increased IL-12/23p40 compared with wild-type mice.

188 are less susceptible to superinfection than wild-type mice.

189 sions in the Ahr knockout in comparison with wild-type mice.

190 cells, compared with healthy individuals or wild-type mice.

191 erebral infiltration of ACE10 as compared to wild-type monocytes (~3-fold increase; P < 0.05) led to

192 mutant superoxide dismutase-1 (mutSOD1) kill wild-type motor neurons (MNs) by an unknown mechanism.

193 the causative bacterial species in different wild-type mouse backgrounds as well as in knockout, tran

194 uces ECM and integrin alpha5 proteins in K41 wild-type mouse embryo fibroblasts (MEFs), CRT null MEFs

195 xposure to all-trans retinoic acid (ATRA) on wild-type NK and CD38KO NK cell function and highlighted

196 yzed the interaction between transformed and wild-type NSCs isolated from the adult mouse subventricu

197 ds and their sequence homology with abundant wild-type nucleic acids.

198 the Gs heterodimeric protein (GalphaS) into wild-type oocytes phenocopied the MIHR mutants.

199 anterior wall of the left ventricle of RyR2 wild type or mutant mouse hearts.

200 based on their mode of action and effects in wild-type or in other neurodegenerative disease models m

201 s identified by pigment presence or absence (wild-type or knock-out lineages, respectively) followed

202 uide RNA library in HL lines carrying either wild-type or mutant A20.

203 Six-day-old wild-type or NRLP3-/- mice were inoculated with sham or

204 given injections of mast cells derived from wild-type or Ptgs2(Y385F) mice.

205 ransfer (FRET) to determine the influence of wild-type or S34F-substituted U2AF1 on the conformationa

206 (39 muW/cm(2)), which is higher than that of wild-type P. aeruginosa and even the strongly electrogen

207 eomic comparison of TbDYRK null mutants with wild-type parasites identified molecules that operate on

208 r levels of alkylation-induced DNA breaks as wild type, PARP-1 activation is undetectable in AAG-defi

209 Wild-type PfCRT (PfCRT3D7) lacks significant chloroquine

210 by using cyanide to block Pi assimilation in wild-type plants and a vacuolar Pi transport mutant, and

211 tants were not affected compared to stressed wild-type plants, suggesting that alterations in PA leve

212 20% that of wild-type plants.

213 igher in the rfa1 rfa4 double mutant than in wild-type plants.

214 ression level of RHD3 is higher than that in wild-type plants.

215 s in leaves, more than 4-fold higher than in wild-type plants.

216 ue is essential for the proximal activity of wild-type PLCgamma1, but we provide evidence that activa

217 on of InsP(8) levels through transfection of wild-type PPIP5K1; transfection of kinase-dead PPIP5K1 w

218 ayed similar subcellular localization as the wild-type progranulin protein.

219 tructural analyses of the PIs complexed with wild-type Protease (PR(WT)) and highly-multi-PI-resistan

220 signature, as do cells that overexpress the wild-type protein.

221 Critically, supplementation with extra wild-type Prph2 protein elicited improvements in Prph2 p

222 enerate a similar inflammatory response to a wild-type rabbit strain and, therefore, validated this m

223 We measured airway inflammation and AHR in wild-type, RAGE(-/-) , TLR4(-/-) and TLR4(-/-) RAGE(-/-)

224 The role of the nonmutated, wild-type RAS proteins in the context of mutant RAS is i

225 agonists have no effect on dopamine (DA) in wild type rats, we used the methylzoxymethanol acetate (

226 genomic databases showed that patients with wild-type RBM10 and p53 survive longer than do those wit

227 tal defect, completely rescued in irradiated wild-type recipients of PDIA6-deficient bone marrow cell

228 nd in naive BALB/c mice compared to that for wild-type RSV, the r2stop+A4G RSV was better able to inf

229 We found that both wild-type S. aureus and a DeltahemB SCV prototype potent

230 One mAb, 2B04, neutralized wild-type SARS-CoV-2 in vitro with remarkable potency (h

231 ultaneously to the S protein and neutralized wild-type SARS-CoV-2 virus in a synergistic manner.

232 to 25 degrees introduces variability in the wild-type seam cell lineage, with a proportion of animal

233 was lowered by about 3% when compared to the wild-type seeds.

234 n plants when compared to the non-transgenic wild-type seeds.

235 Adult rat ventricular myocytes expressing wild-type SERCA2b or a redox-insensitive mutant in which

236 the SFTSV-A46 mutant replicated similarly to wild-type SFTSV (SFTSV-WT), it showed weaker pathogenic

237 Consistently, the application of auxin to wild-type shoots induced a steeper GSA and auxin transpo

238 t that is stronger than that adjacent to the wild-type site.

239 By E15.5, wild-type skin had undergone angiogenesis and formed a h

240 s able to tolerate 100 mM serine whereas the wild type strain was already inhibited by 1 mM of the am

241 per(Bd-Kah) element isolated from the Kahuku wild-type strain was highly degenerate and appeared to h

242 reased ethanol levels in comparison with the wild-type strain.

243 ly engineered strains, but incompatible with wild-type strains that lack resistant alleles.

244 minants associated with the pathogenicity of wild-type strains.

245 e until a reference genome of autotetraploid wild type sugarcane specie, Saccharum spontaneum is avai

246 into the plant tissue are as virulent as the wild type, suggesting that this is due to alterations in

247 By comparing the MSM of the wild-type system with those of the D4A and D4P mutations

248 Finally, wild-type T. thermophilus outcompetes an otherwise isoge

249 lipoxygenase mutant, lox10, colonized by the wild-type T. virens (TvWT) lacked ISR response against C

250 Here we show that, when challenged with wild-type temperate phages (which can become lysogenic),

251 Idelta-knockout), CaMKIIdeltaC transgenic in wild-type (TG), or KO background, and wild-type mice exp

252 attainment of structural information on the wild-type TM287/288 expressed in cellular membranes with

253 the monomer-to-dimer ratio of the unliganded wild-type TNFR1 but exhibited no ligand binding.

254 Lentiviral expression of wild-type TRAPPC4 in these fibroblasts restored traffick

255 Reintroduction of wild-type TTK rescued both radioresistance and HR repair

256 idosis, a nongenetic disease associated with wild-type TTR misfolding.

257 SF3B1 mutations, we also detected nine SF3B1 wild-type tumors (including five lung adenocarcinomas).

258 ficantly outcompeted during cochallenge with wild-type UMH9 in the kidneys and spleen after inoculati

259 ch postulates that reexposure to circulating wild-type varicella delays the onset of herpes zoster, p

260 Compared with wild-type, VHL-deficient Th17 cells had elevated glycoly

261 e of D/N Vif mutants with A3G degradation by wild-type Vif.

262 hogenesis of the DUBmut virus to that of the wild-type virus and found that the DUBmut-infected mice

263 cally stable and replicates similarly to the wild-type virus in cell culture.

264 ylation and grew to 2-log-higher titers than wild-type virus in human Caco-2 cells and simian Vero ce

265 ed immortalization potential relative to the wild-type virus.

266 es might invade despite the highly prevalent wild-type virus.

267 Several pathways activated by heat stress in wild type were induced to a lesser extent in Mgat4d[-/-]

268 nzyme showed no loss in activity compared to wild type, while displaying a T(m) of 88 degrees C (+45

269 er times to respiratory arrest compared with wild type, without altering blood chemistry or displayin

270 We characterized GEC from wild type (WT) and col4alpha5 knockout AS mice, a heredi

271 tafakA mutant causes larger lesions than the wild type (WT) during murine skin infection.

272 stores growth and inflammatory phenotypes to wild type (WT) profiles.

273 Wild-type (WT) and SXRKO mice were chronically or perina

274 tation increased chromosome instability in a wild-type (WT) background, suggesting that such mutants

275 murine DMD) embryonic stem cells (ESCs) into wild-type (WT) blastocysts (mdx/WT chimera).

276 When compared to wild-type (WT) cardiomyocytes, ARDKO displayed reduced f

277 rient-induced mitochondrial respiration than wild-type (WT) cells.

278 r that, AnxA1, Fpr2/3 knockout (KO) mice and wild-type (WT) controls were infected intranasally with

279 ssessed and compared to those in age-matched wild-type (WT) controls.

280 essed in HuH7 cells were less sensitive than wild-type (WT) enzyme to degradation evoked by DPTA, sug

281 ER+, PR+ T47D breast cancer cells expressing wild-type (WT) ER or an activating ESR1 mutation, Y537S-

282 tions in the expression of the corresponding wild-type (WT) gene, due to either variations in copy nu

283 ative damage were greater in Taz(KD) than in wild-type (WT) hearts, but there were no differences in

284 ere, we report that overexpression of either wild-type (WT) LIN28B or a LIN28B mutant that is unable

285 ction with Citrobacter rodentium compared to wild-type (WT) mice evidenced by more severe intestinal

286 mmation, and apoptosis when compared to P2X4 wild-type (WT) mice subjected to renal IR.

287 from about 4 postnatal weeks, SOD1-G93A and wild-type (WT) mice were evaluated in the rotarod test,

288 nthase and stimulator of interferon genes in wild-type (WT) mice.

289 ound that all NHE isoforms were expressed in wild-type (WT) mouse cochlea.

290 h zymosan or immune complexes, compared with wild-type (WT) neutrophils.

291 AdrA wild-type (wt) or its inactive version AdrA mutant (mut)

292 Heterozygous TLR2(+/-) pups from wild-type (WT) or TLR2(-/-) dams were fed either by thei

293 smaller leaves, and lower grain yields than wild-type (WT) plants.

294 -DDDHA infection than after infection with a wild-type (WT) strain.

295 and pathogenicity in DBA/2 mice compared to wild-type (WT) virus (activation pH, 5.5).

296 d IgG binding to red blood cells (RBCs) from wild-type (WT), alpha1,3-galactosyltransferase gene-knoc

297 FMRP regulates leak closure in wild-type (WT), but not FX synapses, by stimulus-depende

298 s xenograft growth of PIK3CA-mutant, but not wild-type (WT), colorectal cancers.

299 ice and AMPKalpha1alpha2lox/lox littermates (wild-type [WT]).

300 OV-neutralizing and binding antibodies using wild-type Zaire EBOV (ZEBOV) or pseudovirion assays were