ライフサイエンスコーパス: wild

1 , lasting roughly between 1 d and 3 d in the wild.

2 is known about their social behaviour in the wild.

3 expenditure, but requires calibration in the wild.

4 is known of their social organization in the wild.

5 dry and semi-dry areas, in contrast to their wild ancestor, the Red junglefowl, which lives in humid

6 Bumble bees are both a major group of wild and commercially-reared pollinators.

7 of the distinct evolutionary trajectories of wild and domesticated plants and, at least in part, is e

8 ges and supports a clear distinction between wild and domesticated trees, with only limited gene flow

9 The interaction of pathogens between wild and farmed aquatic animal populations is a concern

10 ing disease (CWD) is a prionopathy affecting wild and farmed cervids.

11 n declines and to improve the health of both wild and managed bee populations.

12 ation of changes in oxidative balance within wild animals across time, space and major life-history c

13 y in response to changes in temperature, yet wild animals often experience multiple environmental flu

14 ught to have been transmitted to humans from wild animals.

15 utational effects with variation seen in the wild are teasing apart the role of neutral and non-neutr

16 We test our model using long-term data from wild banded mongooses, a species characterized by freque

17 he rhizosphere microbiota when compared with wild barley genotypes adapted to desert environments wit

18 nhancing habitat adjacent to crops increases wild bee diversity and abundance on and off crops.

19 cations of parasites for annual mortality in wild bird populations using phylogenetic comparative met

20 Viruses with the wild bird virus backbone and either PB1, NP, or the enti

21 In two field experiments using wild birds and humans, we measured both the "survival" a

22 luenza A viruses continue to circulate among wild birds and poultry worldwide, posing constant pandem

23 cting poultry in Asia have spilled over into wild birds and spread via bird migration to countries in

24 eage can cause severe disease in poultry and wild birds, and occasionally in humans.

25 We relied on a wild boar experimental model, analysing 24 wild-born spe

26 This study evaluated cataracts in wild boar exposed to chronic low-dose radiation.

27 h showed 99-100% similarity with Sus scrofa (Wild boar) species.

28 a wild boar experimental model, analysing 24 wild-born specimens raised in captivity from 6 months to

29 lobal differences in GI between domestic and wild canids, certain regional differences in gyrificatio

30 ell numbers indicated that the two groups of wild-caught bats had significantly higher numbers of imm

31 We presented wild-caught great tits (Parus major) with a problem-solv

32 tightened behavioural trait correlations in wild-caught stickleback from high- compared to low-risk

33 Overall, this study of wild-caught, juvenile American alligator tails identifie

34 Here, using a dataset of 144 wild chimpanzee (Pan troglodytes) communities, we show t

35 six olive leaves cultivars, including three wild cultivars, and two extraction processes (an innovat

36 target site in collections of colonized and wild-derived African mosquitoes do not prevent cleavage

37 information, within the brain of the African wild dog closely resembles that observed in other carniv

38 uotient of 1.73, indicating that the African wild dog has a relatively large brain size.

39 re, we used hidden Markov models to test how wild dog movements were affected by the Human Footprint

40 extreme altitude (>4,000 m) of the highland wild dogs' (HWD) observed range and confirmed vocalizati

41 enting WCSRG did not take into account > 120 wild/exotic clones maintained at the USDA-ARS Sugarcane

42 nes within WCSRG and Louisiana (commercials, wild/exotic) using 423 SSR alleles showed an average gen

43 Here, we tested innovation in a wild group of Barbary macaques (Macaca sylvanus).

44 alysed selected minerals (Fe-Mn-Zn-Cu-Mg) in wild-harvested and commercially available termites.

45 e-scale survey and sampling of infections on wild hosts in several populations, we then identified a

46 h-mortality trade-off via risk-taking in the wild in two subpopulations of juvenile lemon sharks Nega

47 epigenetic landscapes and can be overcome by wild introgression.

48 re established for one of the most sensitive wild isolates, and deletion of the only G-protein beta-s

49 RNAs remained unchanged and many miRNAs from wild mice gained target site.

50 calizations indicate their potential to be a wild NGSD population.

51 Differences between wild Norway rats and their laboratory counterparts were

52 ing that freely interacting animals (whether wild or captive) rely on social learning has proved rema

53 This is predicted to affect wild organisms, particularly because of the central role

54 e grown at the surface of the estuary, while wild oysters typically grow at the bottom of the water c

55 Here, we use longitudinal data from wild Phayre's leaf monkeys to test the hypothesis that f

56 levels and post-hatching nest temperature in wild pied flycatchers (Ficedula hypoleuca) using a full

57 e costs to remove wild pigs averaged $50 per wild pig (6.8 effort hours per wild pig) for removing th

58 raged $50 per wild pig (6.8 effort hours per wild pig) for removing the first 99% of the animals.

59 Invasive wild pigs (Sus scrofa) are known to depredate nests, and

60 Finally, the costs to remove wild pigs averaged $50 per wild pig (6.8 effort hours pe

61 2200 experimental studies and more than 1200 wild plants, we ask if land use intensification is causi

62 U accumulation was limited in these wild populations due to a combination of factors includi

63 would be facilitated by long-term studies in wild populations experiencing different ecological condi

64 between social context and gene flow within wild populations.

65 nsequences of domestication-introgression in wild populations.

66 st evidence of male-mediated maturation in a wild primate, the gelada (Theropithecus gelada).

67 ll as de novo assemblies of a landrace and a wild relative.

68 Strains of the wild rice species Oryza rufipogon also exhibited differe

69 genomic diversity in the cultivated but not wild rubber trees despite a relatively short domesticati

70 Four jams were made using two wild species of Physalis spp., two containing seeds (P1W

71 roblem-solving is a stable, general trait in wild spotted hyenas.

72 e with free-living stages between farmed and wild stocks.

73 Here, by resequencing 1,506 wild sunflowers from 3 species (Helianthus annuus, Helia

74 We compared the genetic makeups of wild survivors versus non-survivors of WNS, and found si

75 ompression resistance between cultivated and wild tomato accessions.

76 Solanaceae, including 15 accessions of five wild tomato species.

77 nly limited gene flow being detected between wild trees and domesticated landraces.

78 xpanding throughout the distributed range of wild turkeys in North America.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 Although all wild-type bacterial populations exhibit antibiotic toler

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

202 3% enzymatic activity when compared with the wild-type immunotoxin in an adenosine diphosphate-ribosy

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

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

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

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

207 1 deletion (EC-AGO1-knockout [KO]) and their wild-type littermates to a fast food-mimicking, high-fat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

250 (39 muW/cm(2)), which is higher than that of wild-type P. aeruginosa and even the strongly electrogen

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

252 Wild-type PfCRT (PfCRT3D7) lacks significant chloroquine

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

254 20% that of wild-type plants.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

295 lated in overexpressing fruits compared with wild-type.

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

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

298 e transition from separate sexes (dioecy) in wild Vitis vinifera ssp. sylvestris (V. sylvestris) to h

299 on in the frequency of the two states across wild yeast strains.

300 We used long-term data from wild yellow-bellied marmots (Marmota flaviventer) living