ライフサイエンスコーパス: wild-type mouse

1 during the dark in both the Crx(-/-) and the wild type mouse.

2 c, NPS 2143, inhibited secretion only in the wild-type mouse.

3 hereas a blunted response is observed in the wild-type mouse.

4 en fluorescent protein (GFP) (delta neo) and wild-type mouse.

5 gp91(phox-/-)) mice as much as it was in the wild-type mouse.

6 that are between 9 and 40% of the Gclm(+/+) wild-type mouse.

7 t mouse was approximately double that of the wild-type mouse.

8 conditions in which it had no effect in the wild-type mouse.

9 0-fold lower in the mutant mouse than in the wild-type mouse.

10 the ADG to the levels found in the HG of the wild-type mouse.

11 from Osx-expressing cells isolated from the wild-type mouse.

12 m-operated site and the sites in the injured wild-type mouse.

13 ansplantation of skin from a transgenic to a wild-type mouse.

14 hages decreased with age at 18 months in the wild-type mouse.

15 Wild-type mouse AChE and mouse mutants Y330F and Y330A a

16 tants ( approximately 14 fold) over those of wild-type mouse AChE, indicating that these residues may

17 /ml wild-type mouse BChE, and 0.06 microg/ml wild-type mouse AChE.

18 GAD67-GFP (Deltaneo) mouse compared with the wild type mouse after prolonged exposure to kainate.

19 Our results indicated that wild-type mouse alphabetagammaENaC has intrinsic Na(+) s

20 eral lines of transgenic mice overexpressing wild-type mouse amyloid precursor protein (moAPP) either

21 We show that overexpression of wild-type mouse and human c-rel genes suffices to malign

22 oteolytically inactive thrombin can activate wild-type mouse and human platelets after treatment with

23 tiserum to the C-terminus (CT-2) labels both wild-type mouse and human Purkinje cell nuclei, but not

24 Oligonucleotides from the wild-type mouse and mole rat alphaB-crystallin promoter

25 G1alpha disulfide formation was increased in wild-type mouse aortas by in vivo nitroglycerin treatmen

26 Treatment of wild-type mouse aortic smooth muscle cells with 8-Br-cGM

27 iated with homogeneous sized alpha-HDL, when wild-type mouse apoA-I was present (in TgDelta6 +/+ and

28 iary structure and stability as those of the wild-type mouse apoAI.

29 cess, we determined the crystal structure of wild-type mouse apoE, which, like apoE4, forms a four-he

30 dy used a beta(3) integrin (-/-) mouse and a wild-type mouse as a control for in vivo PO by transvers

31 In contrast to cultured adult wild-type mouse astrocytes, adult Apoe(-/-) astrocytes d

32 Direct cDNA selection performed on a wild-type mouse BAC clone spanning the OVE459 insertion

33 s not expressed preferentially in layer 4 of wild-type mouse barrel cortex.

34 disruption by systemic LPS than the control wild-type mouse BBB.

35 0.5 microg/ml human G117H BChE, 2 microg/ml wild-type mouse BChE, and 0.06 microg/ml wild-type mouse

36 In wild-type mouse blood vessels, estrogen attenuates vasoc

37 on cathepsin K expression in the MOCP-5 and wild-type mouse bone marrow co-culture systems by Northe

38 duce the formation of PrP(Sc) molecules from wild type mouse brain homogenate substrate in serial pro

39 ctively stained intact myelinated regions in wild type mouse brain.

40 -synuclein as a novel interactor of PSEN1 in wild-type mouse brain tissue.

41 nerating regions of pcd mouse brain, but not wild-type mouse brain, show elevated autophagy, which ca

42 these peptides, designated WE-15, exists in wild-type mouse brain, thus validating the approach to i

43 creased in mutant mouse brain as compared to wild-type mouse brain.

44 ovel 33 kDa protein in both normal human and wild-type mouse brain.

45 or hippocampus of the transgenic compared to wild type mouse brains.

46 mceph mouse brains are enlarged and - unlike wild-type mouse brains - they keep growing throughout ad

47 significantly decreased in BACE1-null versus wild-type mouse brains, remaining unchanged in BACE1-het

48 f these transcription factors between HD and wild-type mouse brains.

49 ns and ages in Huntington's disease (HD) and wild-type mouse brains.

50 Treating cortical neurons of the wild-type mouse, but not the Kal7(KO) mouse, with an Abl

51 mensional structure of myosin filaments from wild-type mouse cardiac muscle and from a MyBP-C knockou

52 of CAG repeats during repair of 8-oxoG in a wild-type mouse cell extract.

53 It is robust in wild-type mouse cells (observed in 50% of outside-out pa

54 yo fibroblasts from Fbxw7-deficient mice, or wild-type mouse cells expressing Fbxw7 small interfering

55 d3(-/-) mouse cells migrate more slowly than wild-type mouse cells, a change in cell behaviour that p

56 Ectopic expression of wild-type mouse class I MHC (H-2K(b)) but not degradable

57 roblasts with kinetics equivalent to that of wild-type mouse CMV, did not negatively affect replicati

58 Transient expression of wild-type mouse coilin in knockout cells results in form

59 ation of Angptl4 and Adrp mRNA expression in wild-type mouse colon but not in Pparbeta/delta-null mou

60 expression patterns for Cdx-2 and PTEN along wild-type mouse colon, as well as in colon tumors occurr

61 napA strain showed normal (like that of the wild type) mouse colonization efficiency in the conventi

62 ls were elevated after infection only in the wild-type mouse cornea.

63 alization and enhanced cell proliferation of wild-type mouse corneal epithelial cells in an organ cul

64 th factor (VEGF) in matrilysin-deficient and wild-type mouse corneas (experiment IV).

65 lantation and naked MT1-MMP DNA injection in wild-type mouse corneas compared with either bFGF pellet

66 l electrophoresis were present in mutant and wild-type mouse cortex and hypothalamus at comparable le

67 the only two sites basally phosphorylated in wild-type mouse cTnI with full sequence coverage, which

68 L-FABP mouse cytosol had 60% the activity of wild type mouse cytosol.

69 ouse-derived brown adipocytes, compared with wild-type mouse-derived brown adipocytes, displayed an i

70 In a wild-type mouse, during auditory and vestibular hair cel

71 rs analysed DNA binding affinity data of the wild-type mouse EGR1 protein and four variants differing

72 for such cleavage, it is shown that, whereas wild type mouse embryo fibroblasts (MEFs) produce cleave

73 a superfamily) induce p19(Arf) expression in wild type mouse embryo fibroblasts (MEFs), and they enha

74 1,25(OH)(2)D(3) induces p27 accumulation in wild type mouse embryo fibroblasts and arrests wild type

75 essing of endogenous pro-alpha1(V) chains by wild type mouse embryo fibroblasts and by fibroblasts de

76 B1 is similar to that occurring in infected wild-type mouse embryo fibroblast cells but the levels o

77 UV light inhibits translation of IkappaB in wild-type mouse embryo fibroblasts (MEF(S/S)) and that t

78 We stimulated wild-type mouse embryo fibroblasts (MEF) or MEF with a h

79 Moreover, whereas wild-type mouse embryo fibroblasts (MEFs) produce primar

80 results in accelerated TRAF2 degradation in wild-type mouse embryo fibroblasts (MEFs), as compared w

81 stribution from polysomes to subpolysomes in wild-type mouse embryo fibroblasts (MEFs).

82 y decreased in HIF-1alpha-null compared with wild-type mouse embryo fibroblasts (MEFs).

83 induced nuclear Nrf2 and HO-1 effectively in wild-type mouse embryo fibroblasts (wt MEFs) and in B-Ra

84 Here, intralitter comparisons between wild-type mouse embryo fibroblasts and mouse embryo fibr

85 roteins, DNA, and mRNA and virus yields from wild-type mouse embryo fibroblasts and sibling cells lac

86 Although cultures of wild-type mouse embryo fibroblasts set Myc levels precis

87 IFN-gamma suppresses c-myc in wild-type mouse embryo fibroblasts, but not in Stat1-nul

88 p53 knockout mice, which was not the case in wild-type mouse embryo fibroblasts, suggesting that p53

89 94002 induced apoptosis of MKK4-null but not wild-type mouse embryo fibroblasts.

90 mouse embryo fibroblasts when compared with wild-type mouse embryo fibroblasts.

91 cancer treatment, could induce aneuploidy in wild type mouse embryonic fibroblasts.

92 hanced the expression of geminin relative to wild type mouse embryonic fibroblasts.

93 overexpression of miR-199 or miR-214 in the wild-type mouse embryonic brains was sufficient to distu

94 We found that in wild-type mouse embryonic fibroblast (MEF), TNF induced

95 properties of 26S proteasomes purified from wild-type mouse embryonic fibroblast cells and those lac

96 In wild-type mouse embryonic fibroblast cells under a caspa

97 ssion in tuberous sclerosis complex 2 (TSC2) wild-type mouse embryonic fibroblasts (MEF) but not in T

98 s virus led to higher levels of autophagy in wild-type mouse embryonic fibroblasts (MEF) than in RNas

99 IL-8) and IL-6 mRNA and protein secretion in wild-type mouse embryonic fibroblasts (MEF).

100 MrgX-deficient and wild-type mouse embryonic fibroblasts (MEFs) also had si

101 We demonstrate that while wild-type mouse embryonic fibroblasts (MEFs) are complet

102 hat veliparib enhanced the effects of CPT in wild-type mouse embryonic fibroblasts (MEFs) but not Par

103 In wild-type mouse embryonic fibroblasts (MEFs), the Arf pr

104 Compared with wild-type mouse embryonic fibroblasts (MEFs), Usp4-/- ME

105 ated Rac1 was lower in Icmt-deficient versus wild-type mouse embryonic fibroblasts (MEFs).

106 Nuclear translocation was observed in wild-type mouse embryonic fibroblasts (WT MEFs), Tg2576

107 in human umbilical vein endothelial cells or wild-type mouse embryonic fibroblasts because of an inte

108 AP 2, Bcl-x(L), Bfl-1/A1, TRAF1, and FLIP in wild-type mouse embryonic fibroblasts but not in GSK-3be

109 minantly to the nuclear compartment, whereas wild-type mouse embryonic fibroblasts localize survivin

110 Infection of UNG(-/-) and wild-type mouse embryonic fibroblasts with KSHV did not

111 ormation and anchorage-independent growth in wild-type mouse embryonic fibroblasts, and that these an

112 paB activation as measured by DNA binding in wild-type mouse embryonic fibroblasts, but deletion of G

113 Overexpression of Six1 in wild-type mouse embryonic fibroblasts, but not in knocko

114 NF-kappaB and JNK are activated by LIGHT in wild-type mouse embryonic fibroblasts, no activation of

115 city for adipogenesis in vitro compared with wild-type mouse embryonic fibroblasts.

116 ockout mice are radioresistant compared with wild-type mouse embryonic fibroblasts.

117 re of cystogenesis was assessed in explanted wild-type mouse embryonic metanephroi, using 8-Br-cAMP a

118 erate unstable chromosomal rearrangements in wild-type mouse embryonic stem (ES) cells.

119 sed to generate the mutant mice and with the wild-type mouse embryonic stem cell line.

120 nduced cell migration in FN-null, but not in wild-type, mouse embryonic cells.

121 SCD2 expression is high in liver of wild-type mouse embryos and neonates between embryonic d

122 Finally, palatal shelves from prefusion wild-type mouse embryos cultured in the presence of a sy

123 Analysis of wild-type mouse embryos demonstrated co-expression of Ga

124 In wild-type mouse embryos, beta-actin expression was promi

125 In wild-type mouse embryos, PrV axons cross the midline and

126 rom endothelin receptor A (EdnrA) mutant and wild-type mouse embryos, we identified Dlx6, a member of

127 ed amiloride-sensitive Na(+) currents of the wild type mouse ENaC in a dose-dependent manner.

128 to alphaAsp-206-Arg-231, reversibly inhibits wild-type mouse ENaCs expressed in Xenopus oocytes, as w

129 vo, miR-exon4 was most highly amplified from wild-type mouse enamel organs at the secretory stage.

130 Interestingly, increasing cytosolic GSH in wild-type mouse endothelial cells decreased constitutive

131 CR1 on their erythrocytes to the results for wild-type mouse erythrocytes that do not express CR1.

132 psonized pneumococci similarly injected with wild-type mouse erythrocytes.

133 Thus, 5-aza-dC induces Dnmt1 degradation in wild-type mouse ES cells, but not in Dnmt [3a(-/-), 3b(-

134 In wild-type mouse ESCs, 5fC/5caC accumulates to detectable

135 co-enriched at tandem repetitive elements in wild-type mouse ESCs.

136 y in situ hybridization using wholemounts of wild-type mouse eyes and by immunofluorescence staining

137 eal injection of TRPM1-positive MAR IgG into wild-type mouse eyes, and the appearance of the IgG in t

138 Using cultured neurospheres from PPT1-KO and wild-type mouse fetuses, we further demonstrate that the

139 Bovine or wild type mouse fibroblasts were able to bind and intern

140 was observed in p53-deficient but not in p53 wild-type mouse fibroblasts treated with the DNA demethy

141 Additionally, treatment of wild-type mouse fibroblasts with a selective COX-2 inhib

142 n transgenic mouse fibroblasts compared with wild-type mouse fibroblasts.

143 d at points of cell-cell contact in cultured wild-type mouse FLS.

144 rrelated with FLVCR1 expression, we examined wild-type mouse Flvcr1 mRNA levels in the posterior colu

145 This study includes wild-type mouse [Formula: see text] and a variant with t

146 ng brain stem and in the vagal nuclei in the wild-type mouse further supports this hypothesis.

147 Secretagogue-induced acid secretion in wild-type mouse gastric glands could be significantly re

148 rticle tracking to study the mobility of the wild-type mouse H-2L(d) class I MHC molecule and of seve

149 derwent transplantation heterotopically with wild-type mouse heart expressing alpha-gal epitopes and

150 orms of cTnT purified from healthy human and wild-type mouse heart tissue.

151 -ND hearts was at a level similar to that of wild type mouse hearts under beta-adrenergic stimulation

152 omyocyte telomere length decrease sharply in wild-type mouse hearts after birth, resulting in cardiom

153 e performed RNA Seq analysis of AE3-null and wild-type mouse hearts and evaluated the data with respe

154 as relatively preserved, whereas function in wild-type mouse hearts declined substantially.

155 iac damage and impaired function relative to wild-type mouse hearts following ischemia reperfusion.

156 g a 20 min ischemic period in transgenic and wild-type mouse hearts was assessed using an ex vivo wor

157 ol hearts and in 60-week-old knockin than in wild-type mouse hearts.

158 increased risk of ventricular tachycardia in wild-type mouse hearts.

159 ion in individual mitochondria isolated from wild-type mouse hearts.

160 Furthermore, human apoE was resecreted from wild-type mouse hepatocytes after a pulse with human VLD

161 mma in vitro inhibited cell proliferation of wild-type mouse hepatocytes, but not STAT1(-/-) hepatocy

162 This was done by growing wild-type mouse hepatoma cells (HEPA-1) and their HIF-1-

163 alpha (PGC1alpha), to the Adam10 promoter in wild-type mouse hippocampal neurons and shifted APP proc

164 e (10 mum for 30 min) reduced FMRP levels in wild-type mouse hippocampal slices.

165 ned field EPSPs and whole-cell recordings in wild-type mouse hippocampal slices.

166 gh dose of recombinant human ADAMTS13 into a wild-type mouse immediately before reperfusion reduces i

167 transplantation of a D(5)(-/-) kidney into a wild-type mouse increased the expression of both, sugges

168 gene expression in E14 and P0 aganglionic or wild type mouse intestine.

169 Real-time RT-PCR of wild-type mouse intestine showed that only UcnII, but no

170 p65 formed a complex with VDR in noninfected wild-type mouse intestine.

171 These mouse iPSCs, along with wild-type mouse iPSCs, were compared with the targeted m

172 Glucose normally does not produce TDP in wild-type mouse islets except under forced intracellular

173 ibited and compared with the TDP response in wild-type mouse islets with and without forced intracell

174 l during glucose deprivation was observed in wild-type mouse islets.

175 in frequency of [Ca(2+)](i) oscillations in wild-type mouse islets.

176 , and beta-cell functional markers in TG and wild-type mouse islets.

177 ressed in glomeruli purified from Alport and wild-type mouse kidneys.

178 R246Q-mutant rat laminin beta2 replaced the wild-type mouse laminin beta2 in the GBM.

179 CS expression were analyzed in transgenic or wild-type mouse lens and lens epithelial cells stimulate

180 Appropriate controls were used, including wild-type mouse lens, scrambled oligonucleotides, and a

181 oped normally and were remarkably similar to wild-type mouse lenses.

182 Wild-type mouse LES maintained a basal pressure (24 +/-

183 Finally, unlike the wild-type mouse limb bud, the Shh(-/-) mutant posterior

184 use hepatocytes were incubated (pulsed) with wild-type mouse lipoproteins, and cells and media were c

185 We performed partial hepatectomy of wild-type mouse liver and induced a regenerative respons

186 as well as in Smad4, and their reduction to wild-type mouse liver levels in AHR -/- mice fed the ret

187 ibody inhibited RA 4-hydroxylase activity of wild-type mouse liver microsomes to the levels of AHR-nu

188 n 3-week-old Ercc1 null and 1- to 2-year-old wild-type mouse liver.

189 Livers of SPTBN1(+/-) mice, compared to wild-type mouse livers, display a significant increase i

190 ppressed by zinc treatment in both MT-KO and wild-type mouse livers.

191 hallenge, Siglec-F ligands were increased in wild-type mouse lungs but less so in St3gal3 mutants, wh

192 tly lower in TLR2(-/-) and TLR4(-/-) than in wild type mouse macrophage cell lines.

193 nd tumor tissue) but is barely detectable in wild-type mouse mammary glands.

194 We show here that the wild-type mouse mammary tumor virus MMTV(C3H) persisted

195 affects mammary tumorigenesis, we generated wild-type mouse mammary tumor virus/polyoma middle-T (WT

196 e found that a primary stable cell line from wild-type mouse marrow cells expressing BCR-ABL caused s

197 nse that can be rescued by overexpression of wild type mouse MKP-1.

198 rotein-PACSIN2 were concentrated in midstage wild-type mouse MKs in a well-defined invagination of th

199 ATP-facilitated sIPSCs were also recorded in wild-type mouse MNTB neurones, but were absent in the MN

200 ing oligomers and the mThy-1 alpha-synuclein wild-type mouse model (Line 61), which accumulates vario

201 duced gastric intraepithelial neoplasia in a wild-type mouse model and show no additive effect of hig

202 In this preliminary study in a wild-type mouse model, DNA Abeta42 trimer immunization p

203 ogenesis have been hindered by the lack of a wild-type mouse model.

204 riminating scar versus unwounded tissue in a wild-type mouse model.

205 ELISA in the cerebrum, as compared with TLR4 wild-type mouse models.

206 rimental as well as in spontaneous syngeneic wild-type mouse models.

207 Wild-type mouse Muller cells treated with increasing con

208 proximately 20% of the covalent phosphate in wild type mouse muscle glycogen.

209 We found that prior AICAR stimulation of wild-type mouse muscle increases insulin sensitivity to

210 of mutated human MYOC prevented secretion of wild-type mouse Myoc but did not dramatically affect sec

211 In wild-type mouse myocytes, PDBu increased PLM phosphoryla

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

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

214 When injected into a wild-type mouse, necrotic liver from Ppia(-/-) mice indu

215 orm a complex similar in size to that of the wild-type mouse oligonucleotide.

216 to the kinetochores of polar chromosomes of wild-type mouse oocytes, in which polar chromosomes are

217 ely restored after the addition of exogenous wild-type mouse or human alpha-synuclein, but not by A30

218 34-deficient platelets, ex vivo treatment of wild-type mouse or human platelets with the Vps34-specif

219 stics and response to TGF-beta1 with that of wild-type mouse oral keratinocytes (MOK(WT)).

220 rative transcriptomic analysis of mutant and wild-type mouse organs revealed lipid metabolic changes

221 P and 100 times more sensitive to BzATP than wild-type mouse P2X7R.

222 hepatocytes, we transplanted suspensions of wild-type mouse pancreatic cells into syngeneic recipien

223 rhodopsin in native membranes obtained from wild-type mouse photoreceptors and opsin isolated from p

224 he 50 known targets from the knockout versus wild-type mouse plasma, class-specific precursor/fragmen

225 Most human and wild-type mouse platelets had 1 to 2 distinct PACSIN2 fo

226 LTC4 induced surface expression of CD62P by wild-type mouse platelets in platelet-rich plasma (PRP)

227 Wild-type mouse platelets in the presence of mAb 1B5 (an

228 Deposition patterns of untreated human and wild-type mouse platelets were consistent with random di

229 Relative to wild-type mouse platelets, ADAP-deficient platelets exhi

230 In wild-type mouse platelets, Munc13-4 levels were lower th

231 Unlike wild-type mouse platelets, platelets from Galphaq-defici

232 With untreated human and wild-type mouse platelets, soon after the initial adhesi

233 tions compared to the amplitude of S-IJPs in wild-type mouse preparations.

234 Interestingly, immunoblot analysis of wild type mouse primary cortical neurons treated with Ab

235 iPS-RPE cells compared with that of isolated wild-type mouse primary RPE (mpRPE) cells in vitro and i

236 We conclude that (a) AA metabolism in wild-type mouse prostate differs from humans in the basa

237 ), protective mutants (Q167R and Q218K), and wild-type mouse PrP(89-230) at pH 5.5 and 3.5.

238 Sc) compared with that of the epitope-tagged wild-type mouse PrP(C).

239 tion (mouse- equivalent) abolished FRET with wild-type mouse PrP, whereas mutant PrP-P101L displayed

240 disease to Tg(MoPrP)4053 mice overexpressing wild-type mouse PrP-A in approximately 540 days.

241 y to identify the manganese binding sites in wild-type mouse PrP.

242 ds to Hh ligands with an affinity similar to wild-type mouse Ptch1 (mPtch1).

243 zol-induced seizures in postnatal day 7 (P7) wild-type mouse pups and that transgenic knock-in mice h

244 cles containing the mouse opsin promoter and wild-type mouse Rds gene were injected subretinally into

245 mmary gland explants into cleared fat pad of wild type mouse recipients indicates that the observed a

246 ayed clearance of porcine RBCs compared with wild-type mouse recipients.

247 oft agar can be reverted by re-expression of wild-type mouse RelA, but not by expression of RelA muta

248 VLDLR mRNA was detected in the wild-type mouse retina and in purified RECs and RPE cell

249 Fluorescence microscopy of wild-type mouse retina disclosed a strong DNM1L expressi

250 RT-PCR was performed on total RNA from wild-type mouse retina to identify the Dynamin-1 isoform

251 Therefore, VLDLR expression in the wild-type mouse retina was investigated and the retinal

252 VLDLR is expressed in the wild-type mouse retina, especially in RECs and RPE cells

253 of the total photoreceptor population in the wild-type mouse retina, we generated mouse lines with CN

254 of the total photoreceptor population in the wild-type mouse retina, we used Cngb3(-/-)/Nrl(-/-) mice

255 reprogrammable mice grown in aggregates with wild-type mouse retinal cells.

256 ARPE-19 and primary RPE cells isolated from wild type mouse retinas from H(2)O(2)-induced cell death

257 e pik3r1 KO mice was slower than that in the wild-type mouse retinas at 5 minutes of exposure to ligh

258 sgene in a line that was hemizygous null for wild-type mouse rhodopsin (mrho(+/-)), and the eyes of t

259 emission, 457 or 540 nm) appears in frog and wild-type mouse rod outer segments reaching a maximum in

260 When a wild-type mouse rod was illuminated with light sufficien

261 Wild-type mouse rods illuminated continuously with laser

262 th a time constant of approximately 40 ms in wild-type mouse rods, much faster than previous estimate

263 To test this hypothesis, wild-type mouse Ron and three mutant forms of Ron contai

264 RyR2 cDNA were constructed, one encoding the wild type mouse RyR2 (RyR2(wt)) and the other encoding m

265 The wild-type mouse sclera consisted of irregularly arranged

266 ferocytosis) is bolstered in the presence of wild-type mouse serum, through the C3 deposition on the

267 ocytes moved significantly more rapidly than wild-type mouse skin cells.

268 was suppressed in TNF-alpha(-/-) compared to wild-type mouse skin in response to the tumour promotor

269 (VD3) and/or all-trans retinoic acid (RA) on wild-type mouse skin induces a human atopic dermatitis-l

270 ted PKCalpha and other kinases were lower in wild-type mouse skin treated with 12-O-tetradecanoylphor

271 nflammation in both PPAR-gamma-deficient and wild-type mouse skin, indicating that the inhibition of

272 ditional pairs of highly branched SGs, or in wild-type mouse skin, K6a expression consistently coinci

273 In comparison with wounded wild-type mouse skin, Smad4-deficient wounds had delayed

274 points in Tabby (Eda-deficient) compared to wild-type mouse skin.

275 arrier disruption) occurs in CD44 k/o versus wild-type mouse skin.

276 ing to a marked thinning of epidermis versus wild-type mouse skin.

277 mouse skin in response to TPA compared with wild-type mouse skin.

278 rimary cortical neurons from mice expressing wild-type mouse SNCA, wild-type human SNCA, or mutant A5

279 Immunized mast cell-deficient and wild-type mouse spleen cells produced IFN-gamma and IL-1

280 ntiation of monocyte-derived fibrocytes from wild-type mouse spleen cells, but not from SIGN-R1(-/-)

281 he vast majority of exons harboring m(6)A in wild-type mouse stem cells is spliced the same in cells

282 c segregation of afferents, we now show in a wild-type mouse strain that the visual pathway can be su

283 Here we use a long-lived wild-type mouse strain to show that the ability to segre

284 Here we report the observed changes for two wild type mouse strains commonly used in transgenic stud

285 In contrast, wild-type mouse strains and Djungarian hamsters were not

286 original collected mice but not in the nine wild-type mouse strains that were examined.

287 reater expression of activation markers than wild-type mouse T cells.

288 ven by a BAC transgene containing the entire wild-type mouse tau locus, including the endogenous prom

289 a and provide details of their expression in wild-type mouse tissues.

290 n of the axons in the corpus callosum from a wild-type mouse to a knockout mouse showed that myelin i

291 ely 40% larger than the response observed at wild-type mouse trachea tissue.

292 nd RT-PCR experiments of NKCC1-deficient and wild type mouse transcriptomes, we confirmed the absence

293 The wild-type mouse ultraviolet (UV) and bovine blue cone vi

294 CRISPR/Cas system in comparison to that of a wild-type mouse used as a control.

295 e determine the plasma clearance rate in the wild-type mouse, using time-resolved fluorescence on a s

296 The wild-type mouse was either uninjured or lethally irradia

297 essed in the basolateral membrane of the RPE wild-type mouse, was expressed at very low levels in bot

298 of target transcripts in RNA extracted from wild-type mouse whole eyes or retinas between embryonic

299 ssion profile of the rod-dominated retina of wild type mouse with that of the cone-only retina of Nrl

300 HCN1/HCN2/HCN3/HCN4 = 9:9:1:89 in OC of the wild-type mouse, with HCN4 protein primarily attributabl