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1 0 is critical for the normal behavior of the adult mouse.
2 tinal colonization of a streptomycin-treated adult mouse.
3 nctionally equivalent to normal HSPCs in the adult mouse.
4 n to be essential for gluconeogenesis in the adult mouse.
5 ine conduction defects or arrhythmias in the adult mouse.
6 expression in neural progenitor cells of the adult mouse.
7 s being the critical regulator of Epo in the adult mouse.
8 ey components of a hypothalamic niche in the adult mouse.
9 find that they reside in most tissues of the adult mouse.
10 nyl-1,2,3,6-tetrahydropyridine (MPTP) in the adult mouse.
11 ent NSCs from the SVZ and the DG of the same adult mouse.
12 igands (GFLs), during development and in the adult mouse.
13 ar smooth muscle cells in multiple organs of adult mouse.
14 essential role for cochlear function in the adult mouse.
15 s of serotonin axons in the neocortex of the adult mouse.
16 as been successfully applied to the study of adult mouse, adult zebrafish and adult human brains, and
17 leting one copy of FGF receptor 2 (FGFR2) in adult mouse airway basal cells results in self-renewal a
18 Pdgfra gene was systemically inactivated in adult mouse (alpha-KO mouse), and the role of PDGFRalpha
21 vo remyelination in mouse and increases both adult mouse and adult human oligodendrocyte progenitor c
23 visual (V1) and frontal (FC) cortices of the adult mouse and compared findings to those in the rhesus
24 Although the existence of committed MCp in adult mouse and human blood has been postulated, they ha
26 that modest cardiomyocyte turnover occurs in adult mouse and human hearts, mediated primarily by prol
27 expressed in an age-dependent manner in both adult mouse and human hepatic macrophages and plays an i
28 detailed protocol that describes how to grow adult mouse and human liver and pancreas organoids, from
30 a description of the orofacial nuclei of the adult mouse and to ascertain the influence of excitatory
34 ain from individual principal neurons in the adult mouse auditory cortex over a 50-day period surroun
35 on to pyramidal cells in layer 2/3 (L2/3) of adult mouse barrel cortex during sensory deprivation and
40 have isolated a rare population of cells in adult mouse blood, committed to the mast cell lineage.
44 k5 specifically in neural progenitors of the adult mouse brain attenuated adult hippocampal neurogene
46 pecifically in the neurogenic regions of the adult mouse brain delays the normal progression of neuro
47 trate editing of post-mitotic neurons in the adult mouse brain following injection of Cas9 ribonucleo
49 s morphine-like compound distribution in the adult mouse brain has been recently improved, and new hy
56 VSVDeltaG-H5N1, and VLV were all safe in the adult mouse brain, as were VSVDeltaG viruses expressing
58 rotocol takes from 7-28 d to complete for an adult mouse brain, including hydrogel embedding, full li
59 onstrated the expression of ephrin-B1 in the adult mouse brain, indicating a sustained role beyond ea
61 We show that SH2D5 is highly enriched in adult mouse brain, particularly in Purkinjie cells in th
63 ined to astrocytes and neural progenitors in adult mouse brain, the synchronized cycling pattern of F
65 we describe a reliable approach, applied on adult mouse brain, to generate specific STP and STN neur
66 ion of CaN in vivo favors 5-HT uptake in the adult mouse brain, whereas CaN inhibition reduces cerebr
67 rising presence of non-CG methylation in the adult mouse brain, with some showing evidence of imprint
92 eurons, astrocytes and microglia from single adult mouse brains and analyse their transcriptomes by R
93 neuronal and glial cells in the striatum of adult mouse brains via stereotaxic injection of AAV vect
98 ssion levels in the nucleus accumbens of the adult mouse, but selectively restricted the upregulation
101 ical Wnt and JAK/STAT signaling reprogrammed adult mouse cardiac, lung, and tail tip fibroblasts into
102 ging and in vitro cyclic stretch of isolated adult mouse cardiomyocytes as a model system to investig
103 We found that unstressed Hippo-deficient adult mouse cardiomyocytes re-enter the cell cycle and u
104 stribution of seven histone modifications in adult mouse cardiomyocytes subjected to a prohypertrophy
105 n vitro culture system, we demonstrated that adult mouse cardiomyocytes were able to dedifferentiate
106 iled to repair after apex resection, whereas adult mouse cardiomyocytes with Pitx2 gain-of-function e
107 ial metabolism and promotes proliferation in adult mouse cardiomyocytes, resulting in increased regen
109 ase in intracellular cAMP levels in isolated adult mouse cardiomyocytes, with heart-directed expressi
111 ts that efficiently and widely transduce the adult mouse central nervous system (CNS) after intraveno
112 of presenilins in excitatory neurons of the adult mouse cerebral cortex results in progressive memor
113 coproteins, we purified glycoproteins of the adult mouse cerebral cortex using a combination of anion
114 nd OL production in different regions of the adult mouse CNS including the 4-month-old optic nerve, i
115 way is sufficient to drive mature OLs in the adult mouse CNS to reinitiate myelination, leading to ne
116 nd promotes axon regeneration in the injured adult mouse CNS, demonstrating feasibility of in silico-
119 factor (TGF)alpha or amphiregulin, in young adult mouse colon cells and ADAM17(-/-) MCE cells overex
120 0-conditioned medium activates EGFR in young adult mouse colon epithelial cells and human colonic epi
128 utamate imaging and electrophysiology in the adult mouse cortex, we show that glutamate uptake is slo
130 of cortical interneurons (CINs) are found in adult mouse cortices, but the mechanism generating their
131 mpared chromatin accessibility landscapes of adult mouse dentate granule neurons in vivo before and a
132 ve radial glia-like neural stem cells in the adult mouse dentate gyrus and made the surprising discov
133 he single base-resolution DNA methylome from adult mouse dentate neurons consists of both CpG (~75%)
136 expressed in early neural progenitors in the adult mouse DG and mediates the inhibitory effects of Se
140 e have herein examined the responsiveness of adult mouse dopamine neurons in vivo to overexpression o
141 glycemia on mitochondrial transport, primary adult mouse DRG neuron cultures were treated with physio
142 a tractable approach for fully reprogramming adult mouse endothelial cells to haematopoietic stem cel
143 Activation of Wnt/beta-catenin signaling in adult mouse epidermis leads to expansion of the stem cel
149 l functions since deletion of Satb2 from the adult mouse forebrain prevents the stabilization of syna
152 ion of inducibly expressed beta-actin-GFP in adult mouse hair cells in vivo and by directly measuring
153 implicate the transcription factor Gata6 in adult mouse hair follicle regeneration where it controls
155 ics following induction of CELF1 or CELF2 in adult mouse heart and of CELF1 in muscle by RNA-seq, com
156 n were evaluated in the normal embryonic and adult mouse heart as well as in control and failing huma
163 banding that induced cardiac hypertrophy in adult mouse hearts and was also elevated in left ventric
164 that tamoxifen-induced deletion of Slc8b1 in adult mouse hearts causes sudden death, with less than 1
165 y, we investigated the metabolic response of adult mouse hearts expressing ssTnI to chronic pressure
167 tional Parkin deletion with Drp1 ablation in adult mouse hearts prevented Parkin upregulation in mito
168 n of proteins involved in calcium cycling in adult mouse hearts, and that lack of PKP2 can cause arrh
171 erate activation of IKK2-NF-kB in unstressed adult mouse hepatocytes produces a cytoprotective gene e
172 nd optogenetics, we found that proliferating adult mouse hippocampal neural precursors received immat
173 ntiation, neurite outgrowth, and survival of adult mouse hippocampal neural progenitors and their pro
175 urosphere-forming neural precursors from the adult mouse hippocampus and examined the responsiveness
176 r fluoxetine suppressed BMP signaling in the adult mouse hippocampus both by decreasing levels of BMP
177 n of an NS-associated allele PTPN11(D61G) in adult mouse hippocampus results in increased baseline ex
180 in neural progenitor cells isolated from the adult mouse hippocampus, cell cycle-linked phosphorylati
192 hat sensory functions can be restored in the adult mouse if avulsed sensory fibers are bridged with t
198 l stem cell (MSC)-like population within the adult mouse kidney that displays long-term colony-formin
199 identified, and isolated by flow cytometry, adult mouse lateral ventricle subventricular zone (SVZ)
200 e discovered that Trim28 genetic loss in the adult mouse leads to defective immature erythropoiesis i
202 G2(+) cells) that were isolated from healthy adult mouse liver by using a "Percoll-Plate-Wait" proced
203 al cells (Cxcr7(iDeltaEC/iDeltaEC)) from the adult mouse liver impaired liver regeneration by diminis
206 e mitochondrial ATP-Mg/Pi carrier present in adult mouse liver, in the control of mitochondrial AdN l
207 a quantitative study of microRNA function in adult mouse liver, suggesting that the natural abundance
210 and how moderate activation of IKK2-NF-kB in adult mouse livers alters hepatic gene expression and pa
212 genitors that were transplanted into injured adult mouse lungs differentiated into all major airway a
214 and luminal keratin-8-positive cells of the adult mouse mammary gland evokes cell dedifferentiation
218 V. cholerae colonization in both infant and adult mouse models, particularly in the presence of othe
219 ransplanted immediately after lesions in the adult mouse motor cortex restored damaged cortical pathw
220 ransplanted immediately after lesions in the adult mouse motor cortex restored damaged motor cortical
221 transcriptome changes from late embryonic to adult mouse muscle and demonstrate that alternative spli
222 thepsins L and Z in different cell lines and adult mouse muscles confirmed that they are critical in
223 ulations of cardiac progenitor/stem cells in adult mouse myocardium all sharing stem cell antigen-1 (
224 tein shows a distinct laminar pattern in the adult mouse neocortex and that their cell type-specific
225 here we use rapid, high-pressure freezing on adult mouse neocortex to quantify the extent to which th
227 c functional receptors and channels found in adult mouse nociceptor neurons, as well as native subtyp
228 ons (VGLUT3+) in the glomerular layer of the adult mouse OB as well as several of their synaptic targ
230 However, here we demonstrate that, in the adult mouse olfactory system, a 1-week-long exposure to
231 ent plasticity can occur in the periphery of adult mouse olfactory system, which should improve odor
232 haracterized cells with ALDH activity in the adult mouse or human pancreas during physiological condi
233 c imaging of tissue up to the scale of whole adult mouse organs and should be useful for a wide range
234 some IMP2 expression is retained in several adult mouse organs, IMP1 and IMP3 are either absent or e
235 tivated by ductal ligation-induced injury of adult mouse pancreas and apparently act in a cell-autono
236 DH1(+)/CD90(-)/Ecad(-) cells residing in the adult mouse pancreas have the ability to initiate Pancre
238 az using a Cre-lox recombination strategy in adult mouse pancreatic acinar cells (Yap1fl/fl;Tazfl/fl;
239 an improved method for in vivo conversion of adult mouse pancreatic acinar cells toward beta cells, w
240 s, an Hdac1 transgene was expressed in young adult mouse PFC, followed by behavioral assays for worki
241 data suggest that short-term loss of CRB2 in adult mouse photoreceptors, but not in Muller glial cell
245 itro does not reflect gene expression in the adult mouse; rather it is predominantly the expression p
246 Heterozygous deletion of Mll2 induced in the adult mouse results in a normal phenotype suggesting tha
248 consequences of targeted loss of CRB2 in the adult mouse retina using adeno-associated viral vectors
249 ted allele-specific mRNA-seq analysis in the adult mouse retina, a disease-relevant neural tissue.
251 bit established, mature blood vessels in the adult mouse retina, suggesting that only proliferating r
256 A mild focal cortical contusion model in adult mouse sensory-motor cortex was implemented by the
258 e H3 K4/K9/K27me3 levels actively reduced in adult mouse skin and hair follicle stem cells (HFSCs) du
260 ntrations reduced the pacemaker precision of adult mouse SN DA neurons but did not affect their somat
261 iological analysis of postnatal juvenile and adult mouse SN DA neurons in in vitro brain-slices, we o
263 om the medial ganglionic eminence (MGE) into adult mouse spinal cord ameliorates mechanical and therm
264 se medial ganglionic eminence (MGE) into the adult mouse spinal cord completely reverses the mechanic
265 al-induced expression of Wnt3a in the normal adult mouse spinal cord induces an injury-like response
266 d/or its glucuronides and/or codeine) in the adult mouse spinal cord using a well-validated antibody.
267 ort a novel preparation of acute slices from adult mouse spinal cord, allowing visualized whole cell
274 hat serve as neural stem cells (NSCs) in the adult mouse subventricular zone (SVZ) express the histon
275 ehensively analyze lncRNA expression for the adult mouse subventricular zone neural stem cell lineage
276 egulation of the pace of neurogenesis in the adult mouse SVZ and in the migration of neuroblasts alon
277 ilization in neural stem cells (NSCs) of the adult mouse SVZ, but its role there has not been elucida
278 pressing joint interzone cells identifies in adult mouse synovium an MSC population largely negative
279 MEF2C and TBX5, can cooperatively reprogram adult mouse tail-tip and cardiac fibroblasts into beatin
282 Our results demonstrate that, in the intact adult mouse, the postsynaptic inhibitory effects in spin
284 RNA in the 3' region of ITS1 is prevalent in adult mouse tissues and quiescent cells, as it is in hum
285 by mapping base-resolution methylomes in 17 adult mouse tissues at shallow coverage, we identify 302
286 old reductions in full-length transcripts in adult mouse tissues, thereby disrupting protein expressi
287 tion of Fgfr1 or Spry2 in basal cells of the adult mouse trachea caused an increase in steady-state p
288 study, we conditionally deleted FOXA2 in the adult mouse uterus using the lactotransferrin Cre (Ltf-C
289 and selective ablation of hair cells in the adult mouse utricle by inserting the human diphtheria to
298 ecapitulated during hair regeneration in the adult mouse, when K79(+) cells migrate out of the reacti
299 patterns from the Allen Brain Atlas for the adult mouse with panels of cell type-specific genes for
300 sts promoted HF regeneration in neonatal and adult mouse wounds, whereas beta-catenin activation redu
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