ライフサイエンスコーパス: adult mouse

1 ar smooth muscle cells in multiple organs of adult mouse.

2 igands (GFLs), during development and in the adult mouse.

3 essential role for cochlear function in the adult mouse.

4 s of serotonin axons in the neocortex of the adult mouse.

5 0 is critical for the normal behavior of the adult mouse.

6 tinal colonization of a streptomycin-treated adult mouse.

7 nctionally equivalent to normal HSPCs in the adult mouse.

8 n to be essential for gluconeogenesis in the adult mouse.

9 ine conduction defects or arrhythmias in the adult mouse.

10 as been successfully applied to the study of adult mouse, adult zebrafish and adult human brains, and

11 leting one copy of FGF receptor 2 (FGFR2) in adult mouse airway basal cells results in self-renewal a

12 Pdgfra gene was systemically inactivated in adult mouse (alpha-KO mouse), and the role of PDGFRalpha

13 pe to colocalize with all cell types in both adult mouse and adult human brain tissue.

14 vo remyelination in mouse and increases both adult mouse and adult human oligodendrocyte progenitor c

15 visual (V1) and frontal (FC) cortices of the adult mouse and compared findings to those in the rhesus

16 a model of severe insulin resistance in the adult mouse and defined how beta-cells adapt.

17 NA (shRNA) to acutely knock down Sgce in the adult mouse and found that this approach produced dyston

18 novel cell type specificity profiles in the adult mouse and human brain.

19 early postnatal cortex, mostly persisted in adult mouse and human cortex.

20 that modest cardiomyocyte turnover occurs in adult mouse and human hearts, mediated primarily by prol

21 ional diffuse cytosolic expression in normal adult mouse and human hearts.

22 s distinct target genes in developing versus adult mouse and human intestinal cells.

23 detailed protocol that describes how to grow adult mouse and human liver and pancreas organoids, from

24 a novel model of beta-cell neogenesis in the adult mouse and identify the presence of neogenic factor

25 The adult mouse and rat brain flatmaps provide layered diagr

26 45(-)) cardiac stem cells (eCSCs) from whole adult mouse and rat hearts.

27 a description of the orofacial nuclei of the adult mouse and to ascertain the influence of excitatory

28 phingosine 1-phosphate receptor-1 (S1PR1) in adult mouse aortic endothelial cells.

29 in 20,921 individual cells in and around the adult mouse Arc-ME using Drop-seq.

30 Kcne3 transcript was undetectable in adult mouse atria, ventricles, and adrenal glands, but K

31 ain from individual principal neurons in the adult mouse auditory cortex over a 50-day period surroun

32 on to pyramidal cells in layer 2/3 (L2/3) of adult mouse barrel cortex during sensory deprivation and

33 Successful cultures were prepared using adult mouse basal cells selected for expression of c-KIT

34 Spry2 deletion in the adult mouse beta-cell caused hyperglycemia and hypoinsul

35 Inducible deletion of Bcl-x(L) in adult mouse beta-cells also increased glucose-stimulated

36 Thus, CTGF can induce replication of adult mouse beta-cells given a permissive microenvironme

37 Thus, MANF expression in adult mouse beta-cells is needed for their maintenance i

38 a mouse model to ectopically express MafB in adult mouse beta-cells using MafA transcriptional contro

39 is expressed as two separate isoforms in the adult mouse brain and that each differentially regulates

40 Two areas in the adult mouse brain contain neural stem cells: the subvent

41 ce, and in silico modeling approaches in the adult mouse brain following 9 Gy cranial RT.

42 trate editing of post-mitotic neurons in the adult mouse brain following injection of Cas9 ribonucleo

43 Hoxa5 expression in the adult mouse brain has been reported, suggesting that thi

44 Finally, HH and AQ inhibit ZIKV infection in adult mouse brain in vivo.

45 iple genes (Dnmt1, Dnmt3a and Dnmt3b) in the adult mouse brain in vivo.

46 s, including cell culture, chick embryos and adult mouse brain tissue.

47 ever, the limited expression of CD157 in the adult mouse brain undermined confidence that CD157 is an

48 iotemporal presence of PEDF and PEDFR in the adult mouse brain, and to determine the PEDF blood level

49 VSVDeltaG-H5N1, and VLV were all safe in the adult mouse brain, as were VSVDeltaG viruses expressing

50 rotocol takes from 7-28 d to complete for an adult mouse brain, including hydrogel embedding, full li

51 In the adult mouse brain, newly born Sema5A-/- GCs show an incr

52 We show that SH2D5 is highly enriched in adult mouse brain, particularly in Purkinjie cells in th

53 In the adult mouse brain, RGS14 mRNA and protein are found almo

54 In the adult mouse brain, three Tau isoforms are expressed that

55 siently depleting microglia from the healthy adult mouse brain, we show that microglia are necessary

56 omplexes and show they were effective in the adult mouse brain, with minimal off-target effects.

57 map their expression patterns throughout the adult mouse brain.

58 mber than previously estimated in the normal adult mouse brain.

59 r zone (SVZ) of the lateral ventricle of the adult mouse brain.

60 ed neurotropism and were safe in the healthy adult mouse brain.

61 (PEI) as a gene carrier was investigated in adult mouse brain.

62 genous NMDA receptors (NMDARs) directly from adult mouse brain.

63 in are expressed ubiquitously throughout the adult mouse brain.

64 of mouse brain, we identified piRNAs only in adult mouse brain.

65 32H) in the subventricular zone (SVZ) of the adult mouse brain.

66 igh-resolution 3D fluorescence images of the adult mouse brain.

67 Wake mRNA, protein, and cells throughout the adult mouse brain.

68 icroglia shape the synaptic landscape in the adult mouse brain.

69 levant mRNA levels detectable throughout the adult mouse brain.

70 ulate GluN1 and GluN2A subunit levels in the adult mouse brain.

71 pocampus and primary olfactory cortex in the adult mouse brain.

72 e activity in both neurogenic regions of the adult mouse brain.

73 erior ventral V-SVZ of both the neonatal and adult mouse brain.

74 oding canonical TET1 are co-expressed in the adult mouse brain.

75 ombinase-expressing (Cre(+)) nuclei from the adult mouse brain.

76 ery of cell types and regulatory elements in adult mouse brain.

77 se to appropriate stimuli and engraft in the adult mouse brain.

78 eurons, astrocytes and microglia from single adult mouse brains and analyse their transcriptomes by R

79 ue clearing to image the vascular network of adult mouse brains and developed a pipeline to segment t

80 + microglia were also present in non-treated adult mouse brains and exhibited immature transcriptomic

81 neuronal and glial cells in the striatum of adult mouse brains via stereotaxic injection of AAV vect

82 tricted progenitors myelinated dysmyelinated adult mouse brains within one month.

83 In adult mouse brains, p39 deficiency results in dysregulat

84 ately 4,900 RNAs enriched for GGUA motifs in adult mouse brains.

85 efficiently transduce specific cell types in adult mouse brains.

86 s regions of embryonic, early postnatal, and adult mouse brains.

87 Telomerase is expressed in adult mouse, but not in most human, tissues and mouse te

88 ssion levels in the nucleus accumbens of the adult mouse, but selectively restricted the upregulation

89 A proteomic analysis of the secretome of adult mouse cardiac fibroblasts upon digestion by CatA i

90 We used isolated adult mouse cardiac myocytes and fibroblasts, as well as

91 Ablating Drp1 in adult mouse cardiac myocytes not only interrupts mitocho

92 ical Wnt and JAK/STAT signaling reprogrammed adult mouse cardiac, lung, and tail tip fibroblasts into

93 ging and in vitro cyclic stretch of isolated adult mouse cardiomyocytes as a model system to investig

94 We found that unstressed Hippo-deficient adult mouse cardiomyocytes re-enter the cell cycle and u

95 ablished conditions for long-term culture of adult mouse cardiomyocytes that are genetically labeled

96 n vitro culture system, we demonstrated that adult mouse cardiomyocytes were able to dedifferentiate

97 iled to repair after apex resection, whereas adult mouse cardiomyocytes with Pitx2 gain-of-function e

98 ial metabolism and promotes proliferation in adult mouse cardiomyocytes, resulting in increased regen

99 ange in ion currents or action potentials in adult mouse cardiomyocytes, which lack IKr.

100 ase in intracellular cAMP levels in isolated adult mouse cardiomyocytes, with heart-directed expressi

101 medium bathing a pure population of isolated adult mouse cardiomyocytes.

102 ne programs that can induce proliferation of adult mouse cardiomyocytes.

103 We find that, in adult mouse cells, hypomethylated CpG dinucleotides pres

104 ts that efficiently and widely transduce the adult mouse central nervous system (CNS) after intraveno

105 of presenilins in excitatory neurons of the adult mouse cerebral cortex results in progressive memor

106 coproteins, we purified glycoproteins of the adult mouse cerebral cortex using a combination of anion

107 of 5,081 and 10,309 cells from neonatal and adult mouse cerebral cortices, respectively.

108 iferation, and gene expression using primary adult mouse CFs, which spontaneously transdifferentiate

109 tor YAP, termed YAP5SA, partially reprograms adult mouse CMs to a more fetal and proliferative state.

110 way is sufficient to drive mature OLs in the adult mouse CNS to reinitiate myelination, leading to ne

111 nd promotes axon regeneration in the injured adult mouse CNS, demonstrating feasibility of in silico-

112 nohistochemistry for protein localization in adult mouse cochlea implicate metabolic, sensory, and ne

113 ek and Ppp3r1 genes are all expressed in the adult mouse cochlea including the spiral ganglion neuron

114 r development and in supporting cells of the adult mouse cochlea.

115 n induction from lentiviral vectors in young adult mouse colon (YAMC) cells.

116 In the adult mouse colon, TLR2 promotes colonic neurogenesis, r

117 ick embryo and extensive colonization of the adult mouse colon.

118 Conditionally immortalized, young adult mouse colonic (YAMC) epithelial cells demonstrate

119 Our study demonstrates that adult mouse colonic tissue undergoes acute physiological

120 OhrA is critical for V. cholerae adult mouse colonization but is dispensable when the mic

121 nation following demyelinating injury to the adult mouse corpus callosum.

122 criptomically distinct astrocyte subtypes in adult mouse cortex and hippocampus.

123 found that PV cells still express p75NTR in adult mouse cortex of both sexes and that its activation

124 utamate imaging and electrophysiology in the adult mouse cortex, we show that glutamate uptake is slo

125 te layer-specific cis-regulatory elements in adult mouse cortex.

126 of cortical interneurons (CINs) are found in adult mouse cortices, but the mechanism generating their

127 mpared chromatin accessibility landscapes of adult mouse dentate granule neurons in vivo before and a

128 ve radial glia-like neural stem cells in the adult mouse dentate gyrus and made the surprising discov

129 he single base-resolution DNA methylome from adult mouse dentate neurons consists of both CpG (~75%)

130 Microglia in the healthy adult mouse depend on colony-stimulating factor 1 recept

131 adipocyte differentiation in developing and adult mouse dermis.

132 expressed in early neural progenitors in the adult mouse DG and mediates the inhibitory effects of Se

133 Tbx20(OE) was induced specifically in adult mouse differentiated CMs.

134 functional effects of this restoration in an adult mouse displaying retinal permeability.

135 glycemia on mitochondrial transport, primary adult mouse DRG neuron cultures were treated with physio

136 Deletion of Arid1a with Ltf-iCre in the adult mouse endometrial epithelium preserves the gland d

137 a tractable approach for fully reprogramming adult mouse endothelial cells to haematopoietic stem cel

138 Activation of Wnt/beta-catenin signaling in adult mouse epidermis leads to expansion of the stem cel

139 We have used the adult mouse facial nerve crush model and adult-onset con

140 uppress the cardiogenic activity of AGHMT in adult mouse fibroblasts.

141 induction of beating iCMs from neonatal and adult mouse fibroblasts.

142 nstration, we further applied Destin to 2088 adult mouse forebrain cells and identified cell-type-spe

143 CD133(+)/GFAP(-) ependymal (E) cells in the adult mouse forebrain neurogenic zone.

144 l functions since deletion of Satb2 from the adult mouse forebrain prevents the stabilization of syna

145 es, from either collagen-tagged zebrafish or adult mouse GFPtpz-collagen donors, enhances scar format

146 ion of inducibly expressed beta-actin-GFP in adult mouse hair cells in vivo and by directly measuring

147 ulature undergoes dramatic remodeling during adult mouse hair cycle.

148 implicate the transcription factor Gata6 in adult mouse hair follicle regeneration where it controls

149 ics following induction of CELF1 or CELF2 in adult mouse heart and of CELF1 in muscle by RNA-seq, com

150 ved that MCUb protein is undetectable in the adult mouse heart at baseline, but mRNA and protein are

151 th the isolation of viable myocytes from the adult mouse heart.

152 ence of the most prominent cell types in the adult mouse heart.

153 rdiac myocytes and nonmyocytes from the same adult mouse heart.

154 their genome-wide occupancy in the fetal and adult mouse heart.

155 banding that induced cardiac hypertrophy in adult mouse hearts and was also elevated in left ventric

156 We induced high FAO in adult mouse hearts by cardiac-specific deletion of ACC2

157 that tamoxifen-induced deletion of Slc8b1 in adult mouse hearts causes sudden death, with less than 1

158 y, we investigated the metabolic response of adult mouse hearts expressing ssTnI to chronic pressure

159 Isolated adult mouse hearts or cardiomyocytes were perfused for 5

160 tional Parkin deletion with Drp1 ablation in adult mouse hearts prevented Parkin upregulation in mito

161 n of proteins involved in calcium cycling in adult mouse hearts, and that lack of PKP2 can cause arrh

162 Our results show that Prdm16 deletion in the adult mouse hematopoietic system has a less severe effec

163 l knockout mouse model and deleted Prdm16 in adult mouse hematopoietic system using the IFN-inducible

164 k components REV-ERBalpha and REV-ERBbeta in adult mouse hepatocytes disrupts diurnal rhythms of a su

165 erate activation of IKK2-NF-kB in unstressed adult mouse hepatocytes produces a cytoprotective gene e

166 ntiation, neurite outgrowth, and survival of adult mouse hippocampal neural progenitors and their pro

167 sy fiber termini of dentate gyrus neurons in adult mouse hippocampal slices.

168 we show that neural stem cells (NSCs) in the adult mouse hippocampus actively transcribe the pro-acti

169 urosphere-forming neural precursors from the adult mouse hippocampus and examined the responsiveness

170 r fluoxetine suppressed BMP signaling in the adult mouse hippocampus both by decreasing levels of BMP

171 receptor B (PirB) from pyramidal neurons in adult mouse hippocampus results in deficient LTD at CA3-

172 n of an NS-associated allele PTPN11(D61G) in adult mouse hippocampus results in increased baseline ex

173 In this study, we show in the adult mouse hippocampus that expression of the granin fa

174 required for proliferating stem cells of the adult mouse hippocampus to return to quiescence.

175 in neural progenitor cells isolated from the adult mouse hippocampus, cell cycle-linked phosphorylati

176 asticity markers cofilin and synapsin in the adult mouse hippocampus.

177 he dendrites of CA1 pyramidal neurons in the adult mouse hippocampus.

178 n pattern of TSPO at basal conditions in the adult mouse hippocampus.

179 gy and Lkb1 work synergistically to maintain adult mouse homeostasis and survival.

180 nmt3a protein levels are undetected in young adult mouse HSCs until forced into cycle.

181 ss spectrometry of mouse young adult and old adult mouse HSCs, multipotent progenitors and oligopoten

182 ent post-transcriptional repression in young adult mouse HSCs.

183 e transplantation capacity of both fetal and adult mouse HSPCs.

184 hat sensory functions can be restored in the adult mouse if avulsed sensory fibers are bridged with t

185 severe defect in the proximal region of the adult mouse incisor after loss of BMP signaling in the G

186 Using the adult mouse incisor as a model for a continuously renewi

187 In this study, we used the adult mouse incisor as a model to uncover how BMP signal

188 We found that epigenomes in adult mouse intestine and other self-renewing tissues sh

189 In the adult mouse, intravenous administration of 1 x 10(11) ve

190 l stem cell (MSC)-like population within the adult mouse kidney that displays long-term colony-formin

191 To examine the roles of Pax2 and Pax8 in the adult mouse kidney, we deleted either Pax2, Pax8, or bot

192 eq, DroNc-seq, and 10X Chromium platforms on adult mouse kidney.

193 identified, and isolated by flow cytometry, adult mouse lateral ventricle subventricular zone (SVZ)

194 G2(+) cells) that were isolated from healthy adult mouse liver by using a "Percoll-Plate-Wait" proced

195 al cells (Cxcr7(iDeltaEC/iDeltaEC)) from the adult mouse liver impaired liver regeneration by diminis

196 Nme2Cas9 with a guide RNA targeting Pcsk9 in adult mouse liver produces efficient genome editing and

197 tissue-specific ablation of FOXA1/2/3 in the adult mouse liver results in the collapse of the epigene

198 tes dramatically reduced regeneration in the adult mouse liver, further supporting the notion that bo

199 a quantitative study of microRNA function in adult mouse liver, suggesting that the natural abundance

200 ry network, we ablated all FoxA genes in the adult mouse liver.

201 in human and mouse cell lines as well as the adult mouse liver.

202 and how moderate activation of IKK2-NF-kB in adult mouse livers alters hepatic gene expression and pa

203 genitors that were transplanted into injured adult mouse lungs differentiated into all major airway a

204 isolate highly pure and functional ECs from adult mouse lungs.

205 The adult mouse mammary epithelium contains self-sustained c

206 and luminal keratin-8-positive cells of the adult mouse mammary gland evokes cell dedifferentiation

207 ve shown that driving expression of Ascl1 in adult mouse MG stimulates neural regeneration.

208 vivo efficacy was further supported with an adult mouse model of Cryptosporidium infection.

209 The only protective antibody for CCHFV in an adult mouse model reported to date, 13G8, bound GP38 wit

210 opaR, and aphA for in vivo fitness using an adult mouse model.

211 r hair cells (OHCs) in a chemically-deafened adult mouse model.

212 These data from adult mouse models and in vitro models of human brain de

213 V. cholerae colonization in both infant and adult mouse models, particularly in the presence of othe

214 Here, we identified Gli1+ cells in adult mouse molar PDL as multi-potential stem cells (PDL

215 ransplanted immediately after lesions in the adult mouse motor cortex restored damaged cortical pathw

216 ransplanted immediately after lesions in the adult mouse motor cortex restored damaged motor cortical

217 transcriptome changes from late embryonic to adult mouse muscle and demonstrate that alternative spli

218 rotein 2 (IMP2) was selectively deleted from adult mouse muscle; two phenotypes were observed: decrea

219 g CRISPR-generated beta-catenin-null primary adult mouse myoblasts, we found that beta-catenin was es

220 ulations of cardiac progenitor/stem cells in adult mouse myocardium all sharing stem cell antigen-1 (

221 tein shows a distinct laminar pattern in the adult mouse neocortex and that their cell type-specific

222 here we use rapid, high-pressure freezing on adult mouse neocortex to quantify the extent to which th

223 Here, we report that embryonic and adult mouse neural stem/progenitor cells (NSCs/NPCs) exh

224 blating terminal Schwann cells (tSCs) at the adult mouse neuromuscular junction (NMJ) by using mice e

225 c functional receptors and channels found in adult mouse nociceptor neurons, as well as native subtyp

226 ons (VGLUT3+) in the glomerular layer of the adult mouse OB as well as several of their synaptic targ

227 We addressed this question in the adult mouse olfactory system by combining odor discrimin

228 ent plasticity can occur in the periphery of adult mouse olfactory system, which should improve odor

229 haracterized cells with ALDH activity in the adult mouse or human pancreas during physiological condi

230 rting cells of an ex vivo preparation of the adult mouse organ of Corti, and these waves were found t

231 signalling in an ex vivo preparation of the adult mouse organ of Corti.

232 c imaging of tissue up to the scale of whole adult mouse organs and should be useful for a wide range

233 some IMP2 expression is retained in several adult mouse organs, IMP1 and IMP3 are either absent or e

234 DH1(+)/CD90(-)/Ecad(-) cells residing in the adult mouse pancreas have the ability to initiate Pancre

235 nt Ptf1a-lineage cells in the developing and adult mouse pancreas.

236 az using a Cre-lox recombination strategy in adult mouse pancreatic acinar cells (Yap1fl/fl;Tazfl/fl;

237 an improved method for in vivo conversion of adult mouse pancreatic acinar cells toward beta cells, w

238 diated gene transfer to express LINC00473 in adult mouse PFC neurons, we mirrored the human sex-speci

239 data suggest that short-term loss of CRB2 in adult mouse photoreceptors, but not in Muller glial cell

240 RNA sequencing of more than 1,300 neurons in adult mouse primary motor cortex, providing a morpho-ele

241 x) reactivates robust synaptic plasticity in adult mouse primary visual cortex (V1), which allows sub

242 ibe a comprehensive single-cell atlas of the adult mouse prostate epithelium, which displays extensiv

243 The adult mouse prostate luminal cells contain both castrati

244 he periurethral region of the developing and adult mouse prostate, and distinct from the previously i

245 itro does not reflect gene expression in the adult mouse; rather it is predominantly the expression p

246 Moreover, we show that the adult mouse retina displays a surprising degree of plast

247 consequences of targeted loss of CRB2 in the adult mouse retina using adeno-associated viral vectors

248 ssion patterns of TPBG in the developing and adult mouse retina using two antibodies, one against the

249 ted allele-specific mRNA-seq analysis in the adult mouse retina, a disease-relevant neural tissue.

250 We used the model of the adult mouse retina, a part of the CNS amenable to struct

251 Using the model of the adult mouse retina, we examined the constitutive role of

252 ried dramatically in different layers of the adult mouse retina, with alpha equaling ~0.050 in the ga

253 erize Copine expression in the postnatal and adult mouse retina.

254 d a 4-step immunopanning protocol to extract adult mouse RGCs with high fidelity and used it to isola

255 Knockout of Yap1 in the adult mouse RPE caused cell depolarization and tight jun

256 Specific deletion of Smad4 in adult mouse SCs led to increased propensity for terminal

257 injury on primary afferent synaptic input to adult mouse SDH interneurons using in vitro patch-clamp

258 tamatergic drive onto DYN neurons within the adult mouse SDH while increasing the appearance of affer

259 Organoids are established robustly from adult mouse skin and expand over at least 6 mo, while ma

260 e H3 K4/K9/K27me3 levels actively reduced in adult mouse skin and hair follicle stem cells (HFSCs) du

261 During wound healing in adult mouse skin, hair follicles and then adipocytes reg

262 n by modulating responses to beta-catenin in adult mouse skin.

263 ntrations reduced the pacemaker precision of adult mouse SN DA neurons but did not affect their somat

264 iological analysis of postnatal juvenile and adult mouse SN DA neurons in in vitro brain-slices, we o

265 om the medial ganglionic eminence (MGE) into adult mouse spinal cord ameliorates mechanical and therm

266 al-induced expression of Wnt3a in the normal adult mouse spinal cord induces an injury-like response

267 ort a novel preparation of acute slices from adult mouse spinal cord, allowing visualized whole cell

268 potentially functional, integration into the adult mouse spinal cord.

269 dentified lamina I projection neurons of the adult mouse spinal cord.

270 axon regeneration and density in unsectioned adult mouse spinal cord.

271 neurogenic subventricular zone (SVZ) of the adult mouse striatum.

272 for LRRK2 phosphorylation, including in the adult mouse striatum.

273 osine hydroxylase (TH) in tissue sections of adult mouse striatum.

274 hat serve as neural stem cells (NSCs) in the adult mouse subventricular zone (SVZ) express the histon

275 sformed and wild-type NSCs isolated from the adult mouse subventricular zone niche.

276 , we performed single-nucleus RNA-Seq on the adult mouse SV in conjunction with sample preservation t

277 eural stem cell and OPC proliferation in the adult mouse SVZ following demyelination.

278 ilization in neural stem cells (NSCs) of the adult mouse SVZ, but its role there has not been elucida

279 pressing joint interzone cells identifies in adult mouse synovium an MSC population largely negative

280 In adult mouse testes, most piRNAs are derived from long si

281 progenitor spermatogonia in prepubertal and adult mouse testes.

282 s), which comprise >80% of small RNAs in the adult mouse testis, have been proposed to bind and regul

283 ing small RNAs abundant in spermatids of the adult mouse testis.

284 Our results demonstrate that, in the intact adult mouse, the postsynaptic inhibitory effects in spin

285 RNA in the 3' region of ITS1 is prevalent in adult mouse tissues and quiescent cells, as it is in hum

286 tion of Fgfr1 or Spry2 in basal cells of the adult mouse trachea caused an increase in steady-state p

287 ssion profiles of major SV cell types in the adult mouse, transcriptional profiles of rare SV cell ty

288 study, we conditionally deleted FOXA2 in the adult mouse uterus using the lactotransferrin Cre (Ltf-C

289 Closer analysis of adult mouse utricles demonstrated that the basolateral p

290 ous YAP and led to striolar proliferation in adult mouse utricles.

291 alone is sufficient to promote plasticity in adult mouse V1.

292 validated the in silico modeling in cultured adult mouse ventricular cardiomyocytes by modulating PGI

293 ergy transfer measurements of cGMP in intact adult mouse ventricular myocytes.

294 NSCs in the adult mouse ventricular-subventricular zone (V-SVZ) exhi

295 e 'native' biophysical properties of IK,L in adult mouse vestibular type I hair cells.

296 d seven inhibitory types of neurons in L4 of adult mouse visual cortex (V1).

297 was sufficient to enhance plasticity in the adult mouse visual cortex.

298 itory parvalbumin-expressing interneurons in adult mouse visual cortex.

299 e show that single-dose ketamine reactivates adult mouse visual cortical plasticity and promotes func

300 sts promoted HF regeneration in neonatal and adult mouse wounds, whereas beta-catenin activation redu