ライフサイエンスコーパス: wildtype

1 tial amplitude in peripheral mouse C-fibres (wildtype).

2 afety) in the order Nav 1.8 KO > Nav 1.9KO > wildtype.

3 ical constriction in acellular embryos as in wildtype.

4 be more sensitive to foot-shock compared to wildtype.

5 ell as far more pronephric cells compared to wildtype.

6 reduced selectivity for Ca(2+) compared with wildtype.

7 expression between fiberless mutant and its wildtype.

8 O mice showed a decrease in rod sensitivity (wildtype =-1.97 log units, KO =-1.81 log units; p = .014

9 implicit time was observed in Tph2-KI mice (wildtype = 24.25 msec, KI = 25.22 msec; p = .011).

10 gnificantly higher activation rates than the wildtype (90-fold versus 20-fold) and interacted with an

11 Analysis of wildtype AcrB and four functionally-inactive variants re

12 monitored and compared to control mice carry wildtype Adenomatous polyposis coli gene.

13 Coexpression of T122K with wildtype AGA results in processing of the precursor into

14 In contrast, expression of the wildtype allele of wag31 in APYS1-resistant M. tuberculo

15 d high-throughput phenotype data from 14,250 wildtype and 40,192 mutant mice (representing 2,186 knoc

16 ANO1 expression was examined in wildtype and Ano1(/+egfp) mice with immunohistochemical

17 and glucose tolerance did not differ between wildtype and Cox7a1 knockout mice fed with high fat or c

18 We subjected wildtype and Cox7a1 knockout mice to different temperatu

19 lacking, we compared the Cx50 expression in wildtype and Cx57-deficient mice.

20 ed CB2R mRNA expression in VTA DA neurons in wildtype and DAT-Cnr2 cKO heterozygous but not in the ho

21 The biocatalytic versatility of wildtype and engineered carboxymethylproline synthases (

22 guishing of individual VM and FB tissue from wildtype and FGF-2-deficient embryonic day (E)14.5 embry

23 to potential mechanistic differences between wildtype and FTDP-17 Tau variants, as well as different

24 Remarkably, PAR1 wildtype and glycosylation-deficient mutant were equally

25 of isogenic soluble Env trimers, designated wildtype and gV3, which differ only in their potential t

26 NA-binding and target gene regulation in the wildtype and haploinsufficient states.

27 bryonic fibroblasts (MEF) cells derived from wildtype and heterozygous mice.

28 h no significant difference observed between wildtype and heterozygous patients in the majority of th

29 mparisons, no significant difference between wildtype and heterozygous patients were found.

30 cells in the dorsal thalamus was similar in wildtype and knockout mice but there was a notable reduc

31 ypothesized to control MG formation, in both wildtype and Lhx2-deficient RPCs.

32 Cholestasis was induced in wildtype and liver-specific p38alpha knockout mice by bi

33 n human atrial myocardium and in both intact wildtype and M2 or M1/3-receptor knockout mouse Langendo

34 dianion binding to the transition state for wildtype and many mutant TIM-catalyzed reactions of subs

35 aining either wildtype or a 65% mix of K206I/wildtype and measured force generation.

36 istribution and brain PET imaging studies in wildtype and mGluR2 knockout rats in a primate and in hu

37 macrophages and activated complement in both wildtype and MIF-/- mice.

38 njury, we investigated the early response of wildtype and MIF-/- to ethanol.

39 Here, we show that wildtype and mutant activated forms of FGFR3 increase ex

40 This model faithfully reproduces wildtype and mutant behaviors by simulating individual p

41 r understanding RTT pathophysiology, wherein wildtype and mutant neurons are intermixed throughout th

42 Cell adhesion assays on wildtype and mutant PECAM-1 further characterized the st

43 comparison of rNTP incorporation kinetics by wildtype and mutant Pol mu indicates that rNTP accommoda

44 s the stability difference score between the wildtype and mutant protein.

45 large proportion of mammalian traits both in wildtype and mutants are influenced by sex.

46 is in concert with physiological data of G20 wildtype and mutants demonstrated that pyruvate fermenta

47 eases force at submaximal activation in both wildtype and NEB KO fiber bundles and, importantly, that

48 d TLR4 responses in human hepatoma cells and wildtype and Nox4-deficient mice.

49 Lean wildtype and obese db/db mice were pretreated with antib

50 distribution of Panx1 in the mouse retina of wildtype and Panx1-null mice by reverse-transcription po

51 However, repression was noted in both wildtype and Ppp1r15a deleted cells and in cells rendere

52 lacking T, B, and NK cells) when compared to wildtype and Rag1-null mice (lacking T and B cells but r

53 We deep sequenced wildtype and Tbx5-mutant mouse atria, identifying 2600

54 orted that elucidate differences between the wildtype and this mutant form of human GALE, little is k

55 nce APAP evoked hypothermia was identical in wildtype and Trpv1(-/-) mice, and not reduced by adminis

56 ation of APAP evoked a marked hypothermia in wildtype and Trpv1(-/-) mice, but only restored normal b

57 triggered activation of hepatic NK cells in wildtype and tumor-bearing mice.

58 agonists (glutamate and quisqualate) in the wildtype and two mutant receptors.

59 of SIfTER-computed energy landscapes for the wildtype and two oncogenic variants, G12V and Q61L, sugg

60 formed molecular dynamics simulations on the wildtype and V94M enzyme in different states of substrat

61 aging experimentally-available structures of wildtype and variant sequences of a protein to define a

62 of SBMA, a myogenic model that overexpresses wildtype androgen receptor (AR) exclusively in muscle fi

63 x from PE to PC of Gnmt(-/-) mice to that of wildtype animals and normalized DG and TG content preven

64 lagl1 and Sox9 did not induce gliogenesis in wildtype animals, but nonetheless activated expression o

65 CD electroporation, inhibited gliogenesis in wildtype animals, but rescued MG development in Lhx2-def

66 s evolved the binucleation rate decreased in wildtype animals, whereas it remained high in p38alpha-d

67 dium channel (Nav 1.8, Nav 1.9) knockout and wildtype animals.

68 rus were inoculated into Rad54-deficient and wildtype Arabidopsis thaliana plant lines to compare the

69 lly rescued by concomitant overexpression of wildtype Arf4 or Arf4-Q71L.

70 spine density to an even greater extent than wildtype Arf4, whereas the inactive Arf4-T31N mutant doe

71 ed with sorafenib (25 mg/kg)-treated C57BL/6 wildtype as well as hepatitis B virus (HBV) and lymphoto

72 n the fliL strain was similar to that in the wildtype, at high loads.

73 when RAD52 was depleted in a BRCA1- or PALB2-wildtype background, a negligible decrease in colony sur

74 e EcR pathway appears to be dispensable in a wildtype background.

75 f these bacterial deletion strains as on the wildtype bacteria.

76 n Vdr(-/-) mice subjected to BDL compared to wildtype BDL mice.

77 displayed increased liver damage compared to wildtype BDL mice.

78 ding of the mutant was nearly similar to the wildtype; binding of Mg2+ occurred with higher affinity.

79 P-1LeuKO mice compared to mice that received wildtype bone marrow.

80 trongly associated with tumors that are KRAS wildtype, BRAF wildtype, have no or a low CpG island met

81 expression in the (peri-)archicortex of the wildtype brain.

82 docetaxel in comparison to 71.1% in men with wildtype BRCA2 (p = 0.019).

83 ) induces cellular senescence in the lung of wildtype but not caveolin-1-null mice.

84 Chronic ethanol feeding also sensitized wildtype, but not MIF-/-, mice to lipopolysaccharide, in

85 ate aminotransferase (AST) were increased in wildtype, but not MIF-/-, mice.

86 Restoration of wildtype, but not mutant ZNF750 protein uniquely inhibit

87 Among wildtype C. elegans, individual nucleolar size varies, b

88 neration in the spinal cord in comparison to wildtype C3(+/+) mice.

89 w that the modified Prox-1-GFP mice carrying wildtype C57BL/6 background provide a valuable tool for

90 Ventricular myocytes were isolated from wildtype (C57Bl/6) and NOS1 knockout (NOS1(-/-)) mice, a

91 ALB/c 3T3 cells compared with BMI1- or SUZ12-wildtype cells after arsenic exposure.

92 We showed that CBL wildtype cells have lower MET expression than CBL mutant

93 moderate inhibition of PI3K-AKT signaling in wildtype cells was sufficient to cause AJ alterations.

94 In p53-wildtype cells, both drugs induced significant G2 cell c

95 cells were longer and more flagellated than wildtype cells, which may explain their predominance on

96 so decreased in CBL mutant cells compared to wildtype cells.

97 increases the steady-state levels of mature wildtype CFTR in a CFTR-associated ligand (CAL)- and TC1

98 Only wildtype choline-supplemented mice showed improvement wi

99 Pre-treatment of wildtype cochleae with the calcium chelator 1,2-bis(o-am

100 ly increased mDA fiber outgrowth compared to wildtype cocultures, proving a regulatory role of FGF-2

101 mbling advanced human disease in contrast to wildtype controls.

102 ce deficient in gammadelta T cells and their wildtype controls.

103 had a less activated phenotype, unlike their wildtype counterparts that expressed IFN-gamma and espec

104 Wildtype, COX-2 knockout and COX-2 heterozygous mice wer

105 3H/HeJ mice were sensitized with recombinant wildtype Cyp c 1 or carp extract by intragastric gavage.

106 proliferation experiments using recombinant wildtype Cyp c 1, and overlapping peptides spanning the

107 hat crypts (one or two) are a normal part of wildtype development but they almost all resolve by birt

108 Wildtype Dictyostelium amoebae feed on bacteria, but for

109 echanism in the presumptive retina region in wildtype embryos, thus accounting for the apparent up-re

110 porter gene in sphk2(MZ) embryos compared to wildtype embryos.

111 erior chamber, and tested for restoration of wildtype energetics.

112 cific response compared with that induced by wildtype Env and could be explained by a loss of V3-dire

113 These results suggest that wildtype Ewsa inhibits LOH induction, possibly by mainta

114 bsequently, we showed that C. jejuni 81-176 (wildtype) exhibited enhanced chemoattraction to and resp

115 could follow the double pulsed stimulus with wildtype fibres blocking first and Nav 1.8 KO fibres end

116 lockade on the wheel-running performances of wildtype (gamma-aminobutyric acid [GABA]-CB(1)(+)/(+)) a

117 obal gene expression patterns in livers from wildtype, Gcn2 (-/-), and Atf4 (-/-) mice treated with a

118 NOD 2 wildtype genes were protective with respect to the survi

119 edict whether an unknown mouse has a CF or a wildtype genotype with 1.0, 0.84, and 0.9 accuracy for e

120 rkB receptors mimics the MeCP2 deficiency in wildtype glutamatergic neurons, while re-expression of B

121 2.4 kcal/mol by their covalent attachment at wildtype GPDH.

122 riven by a significant genotype main effect (wildtype>heterozygote>null mutant).

123 ted with tumors that are KRAS wildtype, BRAF wildtype, have no or a low CpG island methylator phenoty

124 exhibit light responses very similar to the wildtype HBC(R/MC)s, suggesting that the mixed rod-cone

125 hagy was inhibited chemically in ER-stressed wildtype hepatocytes, which resulted in cytoplasmic vacu

126 eles was compared as well as those that were wildtype, heterozygous, or homozygous for the TSLPrs1898

127 GS(double dagger))GA+HPi = 3.3 kcal/mol, for wildtype hlGPDH-catalyzed reaction of GA + HPi, and for

128 lues of kcat/KGAKX for dianion activation of wildtype hlGPDH-catalyzed reduction of GA and kcat/KGAKX

129 ted for the interactions between the 180 kDa wildtype homotrimeric tailspike protein of the bacteriop

130 In embryonic hearts from wildtype, homozygous (HO) and heterozygous (HET) Mybpc3-

131 sociated virus pseudotype 2/5 to overexpress wildtype human alpha-synuclein (rAAV2/5 alpha-syn).

132 ng fibres in knockout animals as compared to wildtypes, in combination with reduced per-pulse sodium

133 oliferation led us to explore the biology of wildtype KLF6 (KLF6(WT) ) and its antagonistic, alternat

134 Patients with either wildtype KRAS or CDKN2A/p16 lived significantly longer t

135 ury, and function were altered compared with wildtype larvae.

136 e, we find that inducing the DosR regulon to wildtype levels in aerobic, replicating M. tuberculosis

137 nant and restored susceptibility to APYS1 to wildtype levels.

138 red with cells co-expressing cathepsin B and wildtype LFABP.

139 -)) mice gained less body weight compared to wildtype littermate control (M-JAK2(+/+)) mice and were

140 p2tm1.1bird-/+), as compared to their female wildtype littermate controls.

141 ogy (3 months of age) in comparison to their wildtype littermates and assessed changes in cognition,

142 occurred even in 73%, while only 7% of their wildtype littermates developed HCC.

143 mozygotes are deaf, whereas heterozygous and wildtype littermates have normal hearing.

144 and trebled thrombus formation compared with wildtype littermates in tumor-bearing mice.

145 l thalamic nucleus) when compared with their wildtype littermates.

146 ce of both sexes and compare it with that of wildtype littermates.

147 sis and VEGF/VEGFR2 expression compared with wildtype littermates.

148 icient mice, global HCN1 knockouts and their wildtype littermates.

149 atty acid-binding protein (LFABP) than their wildtype littermates.

150 umor suppressor gene in TUSC2 deficient EGFR wildtype lung cancer cells increased sensitivity to erlo

151 idently identified 22 gene products from the wildtype M. marinum secretome in a single CZE-tandem mas

152 ondrial DRP1, but requires FADD/caspase-8 in wildtype macrophages to remove RIPK3 inhibition.

153 l mice developed 50% fewer colon tumors than wildtype mice after exposure to azoxymethane and dextran

154 Forced overexpression of UCP2 protected wildtype mice against APAP-induced hepatotoxicity in the

155 d the effects of environmental enrichment in wildtype mice and in a mouse model of Abeta neuropatholo

156 ed by the scavenging of extracellular ATP in wildtype mice and in Rag2/common gamma-null mice after a

157 travenously inoculated in IL-15 knockout and wildtype mice and in wildtype mice treated with anti-IL-

158 tted fewer working memory errors compared to wildtype mice but had normal reference memory.

159 4))-induced liver fibrosis in Cxcr3(-/-) and wildtype mice by histological, molecular, and functional

160 However, Adult FX and wildtype mice did not exhibit consistent differences in

161 During eccentric contractions, wildtype mice exhibited a 36% loss in torque about the a

162 increased Ptp4a3 expression in the colon of wildtype mice immediately following treatment with the c

163 significantly when the study was repeated in wildtype mice made deficient in eosinophils with a deple

164 Anterior crural muscles from mdx and wildtype mice performed a single bout of 100 electricall

165 At 12 months of age, wildtype mice showed altered synaptic protein levels and

166 In transgenic humanized UGT1A SNP and wildtype mice this UGT1A haplotype led to lower UGT1A me

167 his study we used FMR1 knockout and isogenic wildtype mice to systematically map the distribution of

168 d in IL-15 knockout and wildtype mice and in wildtype mice treated with anti-IL-15 antibodies (aIL-15

169 Wildtype mice treated with azoxymethane and dextran sodi

170 an increased a- and b-wave compared to Panx1 wildtype mice under scotopic conditions.

171 sed transcriptomic analysis in Tob1(-/-) and wildtype mice upon EAE.

172 e cranial base of newborn Pax7-deficient and wildtype mice using a computational shape modeling techn

173 the study of D1-MSN dendrite development in wildtype mice, and its degeneration in a mouse model of

174 eding, chemokine expression was increased in wildtype mice, but not MIF-/- mice.

175 in p55(Deltans/Deltans) mice, but absent in wildtype mice, confirming that the p55(Deltans/Deltans)

176 Compared to wildtype mice, MMP-12 KO mice had decreased levels of ad

177 Compared to wildtype mice, these responses are altered in melanopsin

178 Compared to wildtype mice, TIMP-1(-/-) mice showed further impaired

179 In slice cultures from wildtype mice, we found that chemical LTP increased the

180 duction in M-wave root mean square (RMS) for wildtype mice, which was in stark contrast to mdx mice t

181 lt mice, but also may extend the lifespan of wildtype mice.

182 t pronounced in Nav 1.8 KOs and the least in wildtype mice.

183 ased in homozygous fiber bundles compared to wildtype mice.

184 se dependent decrease in body temperature in wildtype mice.

185 (TNF-alpha) expression was increased only in wildtype mice.

186 of hepatic lesions in IRF3-deficient versus wildtype mice.

187 scheme on three different cohorts of CF and wildtype mice.

188 neuroanatomical expression profiling of En2 wildtype mice.

189 ubsided in Nox4-deficient mice compared with wildtype mice.

190 es implanted into Slco2a1 (-/-), compared to wildtype mice.

191 cantly decreased bone strength compared with wildtype mice.

192 bone fracture healing quality compared with wildtype mice.

193 two significant alterations when compared to wildtype mice: They die at birth due to a malformed diap

194 ated by these mutations, is expressed at the wildtype Michaelis complex, and ca. 50% is only expresse

195 reportedly develop lower torque compared to wildtype motors.

196 In VDR wildtype mouse corneal epithelial cells (WT), 1,25(OH)2D

197 nized transgenic UGT1A-SNP and corresponding wildtype mouse model were established carrying the GS-as

198 EMEPO had no effect in wildtype myocytes.

199 y cages, APPSWE /PS1dE9 (n = 27) and healthy wildtype (n = 21) mice were randomly assigned to either

200 BDNF acts cell autonomous and autocrine, as wildtype neurons are not capable of rescuing growth defi

201 We also found that overexpressing wildtype NFAT3, but not mutant NFAT3-S259A, promoted A43

202 ations in KRAS [KRAS wildtype] or BRAF [BRAF wildtype], no or a low CpG island methylator phenotype,

203 Male wildtype offspring developed a milder metabolic phenotyp

204 nderlying the effect of paternal diabetes on wildtype offspring is unclear.

205 ermined metabolic and skeletal phenotypes in wildtype offspring of Akita mothers and fathers.

206 lopment of metabolic and skeletal changes in wildtype offspring, with a greater effect of maternal di

207 l diabetes resulted in phenotypic changes in wildtype offspring.

208 in metabolic and skeletal phenotypes in male wildtype offspring.

209 ith reconstituted troponin containing either wildtype or a 65% mix of K206I/wildtype and measured for

210 xpression profiles of planulae with either a wildtype or an experimentally expanded apical organ, we

211 fects of the novel variant, we expressed the wildtype or mutant hEAAT1 in mammalian cells and perform

212 using green fluorescent protein-tagged PKD (wildtype or mutant S427E) and targeted fluorescence reso

213 ate increase was blunted in PDE4D but not in wildtype or PDE4B knockout mice.

214 ne residue, is severely impaired compared to wildtype or the mutant viruses encoding K77R or K113R.

215 ype human troponin complex, 50% mix of K206I/wildtype, or 100% K206I.

216 lecular subtypes (no mutations in KRAS [KRAS wildtype] or BRAF [BRAF wildtype], no or a low CpG islan

217 In contrast, wildtype PAR1 displayed a greater efficacy at G12/13-dep

218 nents can occasionally reverse the cell near wildtype periodicity, but frz- cells are otherwise in a

219 s showed that repeated rounds of swarming by wildtype Pf-5 drives the accumulation of gacS/gacA spont

220 inate on the edge and that initial DeltagacA:wildtype Pf-5 ratios of at least 2:1 lead to a collapse

221 but they do co-swarm with orfamide-producing wildtype Pf-5.

222 psi2-1 and psi3-1 seedlings have a wildtype phenotype but overexpression of PSI1 or PSI2 pr

223 w reduced growth and seed yields relative to wildtype plants in fluctuating light and/or temperature.

224 not show any visible difference compared to wildtype plants.

225 g [Ca(2+)] at normal resting levels while in wildtype PNs mGluR1 EPSCs are enhanced by elevated [Ca(2

226 hibition of histone deacetylases, mutant and wildtype promoters were induced to the same level, indic

227 , importantly, all appear to destabilise the wildtype protein in co-transfection experiments in a hum

228 However the wildtype protein must be engineered to incorporate all o

229 through a mutant that closely resembles the wildtype protein, but not through a mutant engineered fo

230 conformational changes in comparison to the wildtype protein.

231 pore expansion beyond the rate found for the wildtype protein.

232 iles more similar to each other than did the wildtype proteins.

233 enotype was restored by expression of either wildtype PSI1 or PSI1 G2A with a mutated myristate attac

234 D1-N87A PSII variant was similar to that of wildtype PSII.

235 ed in recently available mGluR2 knockout and wildtype rats and in a monkey using a structurally disti

236 riments in Wistar and in mGluR2 knockout and wildtype rats as well as in vivo biodistribution and bra

237 feration, associated with Gq signaling, than wildtype receptor.

238 ositide signaling compared with glycosylated wildtype receptor.

239 However, co-inoculation with wildtype rescued DeltaspeC growth, indicating R. solanac

240 ormation in Lhx2-deficient cells, but not in wildtype retinas.

241 Sf9 cell lines stably expressing either the wildtype RyR or the G4946E variant, in order to test the

242 In contrast, wildtype RyR1 was closed and not activated by luminal Ca

243 In wildtype skeletal muscle EHD1 localizes to the transvers

244 Wildtype Slr1-GFP is predominantly nuclear, but also co-

245 hematopoiesis in the presence of endogenous wildtype Stat5 alleles.

246 al G12/13 coupling, thrombin-stimulated PAR1 wildtype strongly induced RhoA-mediated stress fiber for

247 th Dnmt3a-null bone marrow in the absence of wildtype support cells succumbed to bone marrow failure

248 phosphodiesterase activity as NO binding to wildtype SwH-NOX.

249 xhibited characteristics similar to those of wildtype Synechocystis PSII core complexes.

250 The affinity of wildtype TbbTIM for I(3-) increases 20,000-fold upon dec

251 f substrate pieces shows that ca. 50% of the wildtype TIM dianion binding energy, eliminated by these

252 splayed loss of heterozygosity (LOH) for the wildtype tp53 locus.

253 omplex, and ca. 50% is only expressed at the wildtype transition state.

254 Wildtype, Ucp1-KO and Fgf21-KO mice were placed on contr

255 tributions of RMP were not different between wildtype uninjured and injured muscle cells (median: -73

256 th two-photon laser scanning for analysis of wildtype, Val/Met, and Met/Met mice both at baseline and

257 s associated with higher- or lower-level, or wildtype variants, depending on genotype.

258 transplant patients (3 year survival: 66.8% wildtype vs. 42.6% gene mutation, p = 0.026).

259 1,000 Da) for differential expression in XOR wildtype vs. mice with inactivated XOR, arising from gen

260 high-resolution structures, so comparison of wildtype-vs.-mutant crystal structure pairs is not suffi

261 eared in the order NaV 1.8 KO > NaV 1.9 KO > wildtype, which is most likely explained by the relative

262 e cyanobacterium Synechocystis sp. PCC 6803 (wildtype) with alanine, present in higher plants, or wit

263 set specific (NS)-Pten heterozygous (HT) and wildtype (WT) adult mice received either intraperitoneal

264 the NCX KO exhibited higher SK current than wildtype (WT) and apamin prolonged their APs.

265 bution of ASS to the pathophysiology of ALD, wildtype (WT) and Ass(+/-) mice (Ass(-/-) are lethal due

266 Wildtype (WT) and DP1(-/-) mice were subjected ICH and n

267 expression of TWEAK after I/R in SM of Nrf2-wildtype (WT) and knockout (KO) mice.

268 roteins did not significantly differ between wildtype (WT) and KO mice at each time point, the timing

269 ee genomic transgenic mouse lines expressing wildtype (WT) and L151F mutant mouse GCAP1 with or witho

270 tely high fat plus cholesterol diet (HFC)-on wildtype (WT) and liver-specific Foxo1/3/4 triple knocko

271 in skinned fast skeletal muscle fibers from wildtype (WT) and nebulin deficient (NEB KO) mice.

272 Using wildtype (WT) and Nf1(-/-) chondrocyte cultures in vitro

273 Here, using male wildtype (WT) and Pxr-null mice, we examined PXR-mediate

274 ing the whole dataset (399 transgenic HD and wildtype (WT) brains, from mice aged 9-80 weeks) publicl

275 tent after 24-48 h reperfusion compared with wildtype (WT) counterparts.

276 erozygous knockout (Foxp2+/-) mice and their wildtype (WT) littermates from juvenile to adult ages, a

277 and accumulation of free fatty acid (FFA) in wildtype (WT) livers, which were significantly reduced i

278 was isolated from p58(IPK) knockout (KO) and wildtype (WT) mice and treated with lipopolysaccharide (

279 terone-induced uterine gland (PUGKO) but not wildtype (WT) mice on day 5 post-mating.

280 of HPbetaCD resulted in OHC death in prestin wildtype (WT) mice whereas OHCs were largely spared in p

281 was significantly lower in Flt3L KO than in wildtype (WT) mice with lower alanine aminotransferase (

282 A), and IL-17A mRNA in IRF3-deficient versus wildtype (WT) mice, whereas IL-27p28 mRNA expression was

283 ng primary hepatocytes isolated from HET and wildtype (WT) mice.

284 e liver injury and liver carcinogenesis than wildtype (WT) mice.

285 CD39-transgenic (CD39tg) and wildtype (WT) mouse livers were transplanted into WT rec

286 cles display the same number of myofibers as wildtype (WT) muscles, but by E18.5 dyW-/- muscles are s

287 s of db mutant, which overexpress leptin, to wildtype (WT) or genetically obese (ob) mice has been re

288 , mediated prominent 2-APB-induced Ip on the wildtype (WT) Orai1 channels of narrow pore sizes, while

289 evel by costaining for native D1R and D2R in wildtype (WT) PD0 animals.

290 88(L265P)CXCR4(WHIM/FS) or MYD88(L265P)CXCR4(WILDTYPE (WT)) had intermediate BM and serum immunoglobu

291 vity was monitored in cells transfected with wildtype (WT), Cys42Ser or Cys117/195Ser PKGIalpha that

292 ter the induction of ConA-acute hepatitis in wildtype (WT), perforin(-/-) , tumor necrosis factor rel

293 Cs had lower mitochondrial calcium than Ucp2 wildtype (WT)-PASMCs at baseline and during histamine-st

294 and 57% with neither NRAS nor BRAF mutation (wildtype [WT]).

295 ided into those carrying >/=3 major alleles (wildtype [WT]+: G-C/G-C, G-C/T-C, G-C/G-A, N = 100) and

296 other Xoo and 10 Xoc strains virulent toward wildtype Xa27 plants.

297 In wildtype Xu-142, 26 miRNAs are involved in cotton fiber

298 tegrin, we compared the sterol dependence of wildtype Y. pseudotuberculosis internalization with that

299 MS), we analysed the retina of adult longfin wildtype zebrafish at 0, 3 and 18 days after Ouabain inj

300 numbers and mitotic dysfunction compared to wildtype zebrafish embryos.