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1 natures of hepatic steatosis and fibrosis in juvenile mice.
2 olectin injections increased femur length in juvenile mice.
3 imaging in acute slices from male and female juvenile mice.
4 ole of Iba1 in excitatory synaptic growth in juvenile mice.
5 tibody enhancement of signals in newborn and juvenile mice.
6 e cell synaptic connectivity is increased in juvenile mice.
7 ional programs in perinatal fentanyl exposed juvenile mice.
8 tions, bacterial burden, and inflammation in juvenile mice.
9 s lipid, cholesterol, and iron metabolism in juvenile mice.
10 These knockout experiments were performed on juvenile mice.
11 itors, which form the articular cartilage in juvenile mice.
12 se to characterize calsyntenin-1 function in juvenile mice.
13 chaffer collateral-CA1 synapses in adult and juvenile mice.
14 ic connections between the Purkinje cells of juvenile mice.
15 t was larger in neurons from adult mice than juvenile mice.
16 adult mice but not in the IC of experimental juvenile mice.
17 tween Hb9 INs in spinal cords of newborn and juvenile mice.
18 om layer I interneurons in brain slices from juvenile mice.
19 during the first wave of spermatogenesis in juvenile mice.
20 ses UCP levels and activity in hippocampi of juvenile mice.
21 l fibre synapses in the cerebellar cortex of juvenile mice.
22 e (nucleus) of growing oocytes isolated from juvenile mice.
23 nuated following intracranial inoculation of juvenile mice.
24 h the first wave of germ cell development in juvenile mice.
25 ed representational drift similar to that of juvenile mice.
26 erited Cdkn1c in the brains of embryonic and juvenile mice.
27 n of CR6 from infected dams occurred only in juvenile mice.
28 the visceral precursor cell pool in overfed juvenile mice.
29 ns and decreased hepatic bacterial burden in juvenile mice.
30 diomyocyte proliferation and regeneration in juvenile mice.
31 y MNTB-LSO synapses in brainstem slices from juvenile mice.
33 a A virus is highly age-sensitive: robust in juvenile mice (4-6 wk old) but attenuated in mature mice
34 Conditional deletion of beta-cell Ezh2 in juvenile mice also reduced H3 trimethylation at the Ink4
35 nflammatory markers were already elevated in juvenile mice although at this age the number of dopamin
36 eterious effects of reducing EphA4 levels in juvenile mice and do not provide support for the hypothe
37 Vigorous pancreatic beta-cell replication in juvenile mice and humans declines with age, and elucidat
38 ids are incorporated into various tissues in juvenile mice and in a concentration dependent manner.
39 both in the first wave of spermatogenesis in juvenile mice and in ongoing spermatogenesis of adult mi
42 oth endogenous production of anti-GBS IgG in juvenile mice and vertical transfer of antibodies to off
43 aneous absence-like epileptiform activity in juvenile mice, and increased seizure susceptibility in r
44 Previously, we showed that some podocytes in juvenile mice are recruited from cells lining Bowman's c
47 anscriptome is significantly less complex in juvenile mice as compared to adult controls and, possibl
49 inister fractionated hindlimb irradiation to juvenile mice bearing implanted rhabdomyosarcoma (RMS) t
50 ntraepithelial lymphocytes), in suckling and juvenile mice before and after weaning, respectively.
52 significant effect on synaptic plasticity in juvenile mice but impairs some forms of long-term potent
53 l numbers fall rapidly in the hippocampus of juvenile mice but stabilize during adulthood, ensuring l
55 at Schaffer-collateral synapses monitored in juvenile mice, but again decreased NMDA-receptor mediate
56 ype 9 loss-of-function decreased survival in juvenile mice, but increased survival in adult mice with
57 d extends the cardiac regenerative window in juvenile mice by activating YAP-mediated transcriptional
59 suggest that isolated GnRH-EGFP neurons from juvenile mice can generate episodes of repetitive burst
61 follicle development have been identified in juvenile mice deficient in heterologous oocyte-granulosa
63 The Abcb4(-/-) mice model of PFIC3, with juvenile mice developing progressive cholestatic liver i
64 elated differences in immunologic responses; juvenile mice displayed a sustained myeloid infiltrate (
65 ined influx of myeloid cells in the lungs of juvenile mice during acute RSV infection could potentiat
66 ry layer 2/3 neurons in the visual cortex of juvenile mice during the critical period, adult mice aft
70 t daily intranasal insulin administration to juvenile mice for 7 days prior to repeated isoflurane an
73 f7 and, to lesser extent, E2f8 transgenes in juvenile mice impaired cell proliferation, caused replic
81 n slices of the neocortex and hippocampus of juvenile mice of both sexes, using widefield and multiph
82 ccumulated in the calyx of Held terminals of juvenile mice of either sex during high-frequency spikin
84 g, the cochlear nucleus, fusiform cells from juvenile mice (of either sex) generate robust 1-2 Hz osc
85 Here we examined the effect of HI injury in juvenile mice on retinal structure and function, in part
86 d that ablation of neuroligins in newborn or juvenile mice only modestly impaired basal synaptic func
87 ic morphology varies as a function of sex in juvenile mice or primary neuronal cell cultures is large
89 y, with widespread fMRI hyperconnectivity in juvenile mice reconfiguring to hippocampal hypoconnectiv
90 ocal malformation of cortical development in juvenile mice reduced neuronal cytomegaly and corrected
92 y of RDH10 in both Sertoli and germ cells in juvenile mice results in a blockage of spermatogonial di
93 tion of the first wave of spermatogenesis in juvenile mice results in agametic seminiferous tubules.
94 predominantly nonintegrating rAAV vectors to juvenile mice results in loss of persistent transgene ex
95 h-fat-low-fat diet regimen in adult, but not juvenile, mice results in an impoverished eVAT, but not
96 Patch-clamp recordings in layer 5 neurons of juvenile mice revealed increased intrinsic excitability.
97 te hippocampal slices and fixed tissues from juvenile mice revealed that Aif1(-/-) microglia display
98 climbing fiber/Purkinje cell connectivity in juvenile mice, showing the complexity of PCP action.
99 notypic preparations from the hippocampus of juvenile mice, stimulation of 5-HT(7)R/G(12) signaling p
100 re, we show that hippocampal astrocytes from juvenile mice subjected to social isolation exhibit incr
102 elium led to a reversible delay in growth in juvenile mice that was associated with epithelial archit
104 wave of spermatogenesis in 12- to 28-day old juvenile mice to determine more precisely when HSP70-2 i
105 posure in childhood on LUT function by using juvenile mice treated with VCR (4 mg/kg) or saline and e
107 t likely to be antibody positive (26.9%) and juvenile mice weighing between 13 and 14 g least likely
108 Serum metabolite profiles of adult lean and juvenile mice were comparable, while that of adult obese
109 doxorubicin-induced cardiotoxicity in which juvenile mice were exposed to doxorubicin, using a cumul
112 ns and levels of BDNF protein are highest in juvenile mice when adult motor patterns are shaped, whil
113 -term depression was selectively impaired in juvenile mice when NR2D overexpression was moderate.
114 ments for partner discrimination observed in juvenile mice which also show cognitive defects in adult
116 distinct peripheral inflammatory profile in juvenile mice, which may impact the injury and repair re
117 ial defeat stress in males or females and in juvenile mice, which typically are excluded from classic