ライフサイエンスコーパス: wildtype

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

2 G mutant were similar to those obtained with wildtype.

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

4 expression between fiberless mutant and its wildtype.

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

6 ical constriction in acellular embryos as in wildtype.

7 iation was only retained in astrocytoma, IDH-wildtype.

8 , and in a short day photoperiod compared to wildtype.

9 d prognostic information in astrocytoma, IDH-wildtype.

10 fold higher in the N408K mutant, than in the wildtype.

11 ypes between heterozygotes, homozygotes, and wildtypes.

12 aptive substitutions, but poorly neutralized wildtype 2019-2020 A/Kansas/14/2017 (H3N2) HA-pseudoviru

13 Male knockouts and wildtypes (6-8 weeks old) were then injected with NMDA (

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

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

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

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

18 ced apoptosis in multiple TP53-null and TP53-wildtype AML cell lines.

19 2 Arabidopsis shoot architectures, including wildtype and 10 mutant strains, and we uncovered a desig

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

21 Wildtype and a phosphomimetic mutant of GAPVD1, but not

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

23 m the superfused murine retina isolated from wildtype and Ca(v)2.3-deficient mice.

24 g kainic acid, KA) on the neural retina from wildtype and Ca(v)2.3-deficient mice.

25 We subjected wildtype and Cox7a1 knockout mice to different temperatu

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

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

28 and recovery, we generated littermate PVG C6 wildtype and deficient rats and tested functional and hi

29 to differential footpad DTH responses using wildtype and four core genotypes (FCG) mice and poplitea

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

31 was prevented by a GluN2C/2D potentiator in wildtype and GluN2C heterozygous mice but not in GluN2C

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

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

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

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

36 Both wildtype and Keap1(f/f) pups at PND1 were exposed to hyp

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

38 Uterine arteries from late pregnant wildtype and LOX-1 overexpressing mice were incubated ov

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

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

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

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

43 detergent-resistant membrane fractions from wildtype and mutant cells, consistent with the predictio

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

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

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

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

48 tatively recapitulates branching of cultured wildtype and mutant ureteric buds, and achieves similar

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

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

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

52 nstrated tumor growth inhibition in both p53 wildtype and p53 mutant cancer cell lines, demonstrating

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

54 hanism, we studied gene expression of single wildtype and rnf2 mutant hearts.

55 Comparison of the miRNA profiles between wildtype and SUN1 null myotubes identified a cluster of

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

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

58 atellite stable/MSI-low, CIMP-negative, BRAF-wildtype, and KRAS-wildtype tumors (P (trend) range from

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

60 This sexual dimorphism in wildtype animals manifested pre-pubertally, was enhanced

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

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

63 iR-223 3p mimic or infusing neutrophils from wildtype animals.

64 -HT signaling relative to cocaine actions on wildtype animals.

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

66 of the red-shifted protein from that of the wildtype are observed by Fourier transform infrared spec

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

68 ion of host immunity is advantageous for the wildtype bacteria.

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

70 Wildtype BCs make both ribbon-containing and ribbon-free

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

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

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

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

75 ted basal ATPase activity similar to that of wildtype BRG1 (wtBRG1).

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

77 frequency and burst firing of nRT neurons in wildtype but not GluN2C knockout.

78 This effect was observed in wildtype but not in GluN2C knockout mice demonstrating t

79 mical experiments demonstrate the binding of wildtype but not mutant E2F promoters by repressive PRC1

80 Strikingly, wildtype, but not Hebp1-deficient, neurons showed elevat

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

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

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

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

85 Ad5.TGFbeta2 induced ocular hypertension in wildtype C57BL/6J mice and further amplified the IOP in

86 id ccm strain increased 121% relative to the wildtype ccm strain, with an electron flux per cell of 1

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

88 e observed a strong expression of MT1-MMP in wildtype cells of both primary tumors and lung metastase

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

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

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

92 (DNMT1(-/-) cells), were compared to HCT116 wildtype cells.

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

94 ells are more lethal and brain invasive than wildtype cells.

95 Phosphorylation-dependent potentiation of wildtype CFTR and other variants also was observed in ep

96 VX-770 potentiated wildtype CFTR and several disease mutants expressed in o

97 tein carrying the T303E mutation but not the wildtype claudin-16 or the T303R mutant protein increase

98 Unlike wildtype claudin-16, phosphomimetic claudin-16 is deloca

99 distinguished pathogenic TNNT2 variants from wildtype controls using a sarcomere functional reporter

100 hese mice displayed lower pH in neurons than wildtype controls, determined by intracellular pH in hip

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

102 remarkably lower in Keap1(f/f) pups than in wildtype counterparts (28.9% vs 2.4%, wildtype vs Keap1(

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

104 1.22, 1.99; Pheterogeneity = 0.04), and KRAS-wildtype CRC (OR per 5 kg/m2: 1.35; 95% CI: 1.17, 1.54;

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 Wildtypes developed severe tonic-clonic seizures, wherea

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

109 T790M (L/T) mutant Ba/F3 cells while leaving wildtype EGFR Ba/F3 cells unaffected.

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

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

112 ered in their subsite specificities from the wildtype enzyme.

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 xpression profiles in perinatal ovaries from wildtype, FiglaNull, Lhx8Null and Sohlh1Null mice.

117 Wildtype floral organ number in early formed flowers is

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

119 combinant molecular clone TR3 representing a wildtype genome.

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

121 Wildtype GRK2 reversed the increase in cisplatin- and et

122 rotection from cisplatin that was similar to wildtype GRK2, suggesting that this protection may be me

123 icantly worse QOL score when compared to the wildtype group after sildenafil treatment.

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

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

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

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

128 ents with superior therapeutic efficacy over wildtype hMSCs in the diabetic mouse model without repla

129 increase its half-life in plasma compared to wildtype hOCN.

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

131 e time points through retransplantation into wildtype hosts mediates B cell recruitment into lymphoid

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

133 We expressed wildtype human Nav1.7, the I848T mutant, or other mutati

134 tial for GABA(A)-evoked currents compared to wildtype in the third postnatal week.

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

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

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

138 stituted beta-hairpin PriA variant displayed wildtype levels of DNA unwinding and PriB binding in vit

139 nant and restored susceptibility to APYS1 to wildtype levels.

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

141 king the IDR (DeltaIDR prestin) demonstrated wildtype-like nonlinear capacitance (NLC) in HEK293T cel

142 nt CRC cell lines but not in the majority of wildtype lines nor in fibroblasts.

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

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

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

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

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

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

149 acle for fertilisation is similar for SR and wildtype male sperm, both over short and long time-frame

150 has been adjusted to match sperm delivery by wildtype males.

151 ge in type I IFN receptor-deficient mice and wildtype mice administered neutralizing Abs against type

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

153 posterior tissues isolated from Fkbp8-/- and wildtype mice at E9.5 and E10.5 showed that Fkbp8-/- emb

154 ce had reduced mucous expression compared to wildtype mice following mucous induction.

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

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

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

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

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

160 ene was sexually differentially expressed in wildtype mice, glycosylation-dependent cell adhesion mol

161 In young wildtype mice, rats, and NHPs, but not in M(1) mAChR KO

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

163 reased angiotensin II responsiveness only in wildtype mice, which coincided with decreased AT1 contri

164 he kidney capsules of 5 weeks old female NOD wildtype mice.

165 n ratio in both serum and islets compared to wildtype mice.

166 ased in homozygous fiber bundles compared to wildtype mice.

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

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

169 e encephalomyelitis (EAE) course compared to wildtype mice.

170 cantly decreased bone strength compared with wildtype mice.

171 bone fracture healing quality compared with wildtype mice.

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

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

174 se dependent decrease in body temperature in wildtype mice.

175 antly delayed in TSG-6-null mice relative to wildtype mice.

176 ulated production of IL-1beta was evident in wildtype mice.

177 ated decreases in REM sleep duration in aged wildtype mice.

178 arrel organization also degrades with age in wildtype mice.

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

180 switches (i.e., a few substitutions act like wildtype, most abolish function).

181 reportedly develop lower torque compared to wildtype motors.

182 e, increased with ex-vivo phosphorylation of wildtype mouse bones and declined with ex-vivo dephospho

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

184 The hmTert gene, encoding the wildtype mTert protein, was fully functional, as a mESC

185 non-codeleted (n = 54); (3) astrocytoma, IDH-wildtype (n = 20).

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

187 erse group of minimally permeant cations for wildtype NaChBac, ranging in sizes from ammonium to guan

188 idine have much less effect on the growth of wildtype neural stem cells and Prospero neural tumours.

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

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

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

192 al genetic determinants of PARPi response in wildtype or BRCA2-knockout cells.

193 nalization, but no spine shrinkage in either wildtype or Fmr1(-/y) mice.

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

195 ignalling axis promotes resistance on a TP53 wildtype or null background, but not a mutant TP53 backg

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

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

198 ippocampal neurons expressing Cre and either wildtype, or mutants mimicking or preventing phosphoryla

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

200 ction, high risk p53 mutation (p53HRmut) and wildtype p53 (p53WT) inactivated by the human papillomav

201 ese mutant p53 (mutp53) either directly lose wildtype p53 (wtp53) tumor suppressor function or exhibi

202 Wildtype PAO1, recycling-defective AmpG and NagZ mutants

203 discoveries is critical because, while PTEN wildtype patients can be diagnosed clinically, they do n

204 herefore, non-PTEN aetiologies exist in PTEN wildtype patients.

205 titial fluid at pH 7.4, whereas the one with wildtype Pcyb-AfGDH was not.

206 y 1.70- and 9.0-fold faster IET than that of wildtype Pcyb-AfGDH, respectively.

207 d higher DET current values than that of the wildtype Pcyb-AfGDH-immobilized electrodes at pH 6.5, wh

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

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

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

211 n affinity led to almost equal inhibition of wildtype PfFNT and the Gly107Ser mutation.

212 Reactions pairing wildtype PKS modules with non-native substrates primaril

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

214 d slower growth rates and lower fitness than wildtype pMB2.

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

216 e viruses can efficiently target and replace wildtype populations in cell culture experiments.

217 he catalytic activity of PRC2-EED-I363M over wildtype-PRC2.

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

219 ffolds of missense protein variants from the wildtype protein structure.

220 uced changes to drug binding relative to the wildtype protein structure.

221 conformational changes in comparison to the wildtype protein.

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

223 ns the complement regulatory activity of the wildtype protein.

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

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

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

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

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

229 In comparison to wildtype replicon, mutants expressing IL-2 injected into

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

231 s81-Mms4 to M phase but not S phase allows a wildtype response to various forms of replication pertur

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

233 Wildtype ribosomes isolated from CHO cells, but not thos

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

235 ns are detectable in the majority of healthy wildtype samples.

236 The pD rate profiles for wildtype ScOMPDC and the Q215A variant are identical, ex

237 rger increases in the activation barrier for wildtype ScOMPDC-catalyzed deuterium exchange compared w

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

239 Escherichia coli strains in which wildtype SSB is replaced by SSB-IDL fusions are viable a

240 far exceeding those inhibiting growth of the wildtype strain, even in the presence of the enzyme inhi

241 phenotypes nearly identical to those of the wildtype strain.

242 rdingly, lowest numbers were seen in the IDH-wildtype subpopulation.

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

244 tocontrol of cardiac function in translucent wildtype tadpoles.

245 , an effect that is rescued by re-expressing wildtype Tau.

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

247 ng loss-of-function mutants within otherwise wildtype tissues.

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

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

250 -low, CIMP-negative, BRAF-wildtype, and KRAS-wildtype tumors (P (trend) range from 0.03 to 3.4e-03),

251 onfidence interval, 0.65-1.04)] but not BRAF-wildtype tumors [1.09 (0.97-1.22); P difference as shown

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

253 MERS-CoV were resistant to superinfection by wildtype virus, likely due to reduced levels of the viru

254 han in wildtype counterparts (28.9% vs 2.4%, wildtype vs Keap1(f/f)).

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

256 metic dCENP-A mutants is reduced relative to wildtype, while non-phosphorylatable dCENP-A retention i

257 genes were decorated by broad PcG domains in wildtype whole embryo lysates.

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

259 ic Hedgehog TP53-mutant, Sonic Hedgehog TP53-wildtype, WNT, Group 3, and Group 4, defined by the Worl

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

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

262 Using competitive autoradiography in wildtype (WT) and AVPR1A knockout (KO) postnatal day 0 (

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

264 ble cell lines expressing fluorescent-tagged wildtype (WT) and E22G Abeta42 to study the aggregation

265 Pregnant wildtype (WT) and eNOS(-/-) mice were supplemented with

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

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

268 RA and wildtype (WT) animals were treated with vehicle (RA/WT)

269 NH encoded by HAE-causing SERPING1 acts upon wildtype (WT) C1INH in a dominant-negative manner and fo

270 had more severe colon lesions compared with wildtype (WT) controls.

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

272 active for excision of eG compared with the wildtype (WT) enzyme.

273 y, and growth of their offspring compared to wildtype (WT) fish.

274 imilar substrate affinity (Km) values to the wildtype (WT) Km value but had a lower turnover number a

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

276 s disease (AD)-like transgenic (Tg) mice and wildtype (WT) littermates with a single, whole-body dose

277 re of mutant mice was indistinguishable from wildtype (WT) littermates.

278 19:5 L:D) photoperiod exposure versus their wildtype (WT) littermates.

279 t-induced mortality (P = 0.02) compared with wildtype (WT) littermates.

280 nctional Prom1 knockout (KO) mice, and their wildtype (WT) littermates.

281 -USP20 was significantly increased in LVs of wildtype (WT) mice after a 1-week catecholamine infusion

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

283 ment reduced plasma LDL-C, TC and TG in LDLR wildtype (WT) mice fed a high fat and high cholesterol d

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

285 that LFABP(-/-) mice become more obese than wildtype (WT) mice upon high-fat feeding.

286 Fancd2 (-/-) and wildtype (WT) mice were fed a standard diet (SD), a diet

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

288 They have extended lifespans compared to wildtype (WT) mice, and male mice show enhanced fecundit

289 l age-related microbiome changes compared to wildtype (WT) mice, including an increase in Bacteroides

290 tein acetylation following a HFD relative to wildtype (WT) mice.

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

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

293 um vulgare L. cv Optic) mutant (NRH) and its wildtype (WT) parent were grown in tubes of sieved (<250

294 oth sign and degree of change) compared with wildtype (WT) values.

295 of MNTB physiological properties observed in wildtype (WT) was abolished in L9'T mice.

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

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.