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1 ency was predicted to be highest at the mean birthdate.
2 s could be used as a proxy to infer neuronal birthdate.
3 ojection neurons were similarly organized by birthdate.
4 timulus selectivity follow projection neuron birthdate.
5 er-layer neurons, independently of niche and birthdate.
6 y superficial cortical layers independent of birthdate.
7 his is organized in accordance with cellular birthdate.
8 of SPN in the spinal cord was independent of birthdate.
9 factual result of measurement error in child birthdates.
10 ged in a spatial gradient according to their birthdates.
11 cordings and fluorescent retroviral reporter birthdating.
12 tin, and newly generated cells by using BrdU-birthdating.
13                We generated digital neuronal birthdating 3D-maps and revealed that the temporal order
14 eurons, as proof-of-concept that the digital birthdating 3D-maps could be used as a proxy to infer ne
15                             We recorded from birthdated abDGCs in mice and photoactivated parvalbumin
16 ) male and female mice was used to label and birthdate adult-born neurons for morphological and elect
17                                              Birthdating analyses in control and Blimp1 CKO mice show
18 atives, biochemical, immunocytochemical, and birthdating analyses were conducted.
19                                         BrdU birthdating analysis revealed that many late-born neuron
20 imetable of early neurogenesis, indicated by birthdating analysis, was delayed.
21 ure to nutritional deficiency based on their birthdate and birthplace.
22 e directly examined the relationship between birthdate and CA1 pyramidal neuron diversity, focusing o
23 d cell subtype specific markers to determine birthdate and cell cycle exit more precisely than previo
24 cent protein Kaede to simultaneously analyze birthdate and cell fate in live zebrafish embryos.
25 ecting retroviruses to either "birthdate" or birthdate and knock-out Pten in granule neurons of the m
26 ed, and up to 2 controls per case nearest by birthdate and matched on sex were identified from the FP
27 ve investigated the relationship between the birthdate and the onset of differentiation of neurons in
28 pyramidal neurons reflected a combination of birthdate and the rate of neurogenesis.
29                      The correlation between birthdate and tonotopic position suggests testable mecha
30 n-induced tag exchange-based genetic tool to birthdate and track the segregation of centrosomes over
31 lass II Kenyon cells, defined by their early birthdate and unique dendritic arborizations, have been
32                Children 3-59 months old with birthdates and surveillance hospital arrival dates were
33                            Bromodeoxyuridine birthdating and anti-IgG double-labeling studies showed
34                             Our results from birthdating and in utero electroporation experiments dem
35                                      Genetic birthdating and morphological and molecular analyses pin
36                       The current study used birthdating and pathway-tracing methods to investigate t
37           All participants provided name and birthdate, and 94% provided a complete social security n
38 from among survey participants using gender, birthdate, and location.
39 ationship between enteric neuron subtype and birthdate, and suggest that some enteric neurons exhibit
40 e utricle, labeling hair cells following EdU birthdating, and demonstrates that sub-type identity is
41 imp1 CKO mice showed that bipolar cells were birthdated as early as E13.5 in Blimp1 CKO mice, five da
42                                              Birthdate before or after the age threshold for elementa
43                              Differentiation birthdating by label dilution using [(3)H]thymidine also
44                                           We birthdated CA1 pyramidal neurons with in utero electropo
45                                 We find that birthdates called for induction appear with unusually hi
46                         By bromodeoxyuridine birthdating cells in green fluorescent protein-expressin
47 scribed here use a novel genetic approach to birthdate centrosomes in human cells and identify asymme
48                                  Strikingly, birthdated cholinergic projections within the cortex fol
49 nment of DACA eligibility among mothers with birthdates close to the DACA age qualification cutoff.
50 lamination, while EdU incorporation aided in birthdating cortical neurons.
51 eurons generated, rather than strictly their birthdate, determines the specific types of interneurons
52 eous excitatory and inhibitory currents from birthdated DGCs.
53                          Neurons of the same birthdate displayed distinct connectivity, coactivity ac
54 imilar to that of GAD67 mRNA, for cells with birthdates (E14) of many of the mature GAD-containing ne
55 tegration in a model of TLE, we retrovirally birthdated either early-born [EB; postnatal day (P)7] or
56          Oligodendrocyte lineage markers and birthdating experiments indicated a precocious oligodend
57 l differentiation domain by in vivo neuronal birthdating experiments.
58 a somewhat inverted "outside-in" sequence of birthdates for cortical neurons that is similar to that
59            At adulthood, gentle mediolateral birthdate-gradients in S cells were still evident, but M
60                                              Birthdating in male and female mice showed that tuberal
61 lineage, and sequential neuronal formation ("birthdate") in postmortem human cerebral cortex.
62                             Autoradiographic birthdating indicates that almost all of these early app
63 ing, and cFos staining in mice, we show that birthdate is a strong predictor of CA1 principal cell di
64      In the present study we determined that birthdate is not a factor contributing to the abnormal p
65                            Cortical neuronal birthdate is partly controlled by an intrinsic clock-typ
66 we used 2-photon calcium imaging in neuronal birthdate-labeled Mash1-CreER;Ai14 mice to image simulta
67 odies, and includes subgroups that differ in birthdate, location, and proprioceptive input.
68 Syrian hamsters daily injections of the cell birthdate marker bromodeoxyuridine throughout puberty (p
69 es and associated projections, we used newer birthdating methods and cell subtype specific markers to
70 f cortical neuron development including cell birthdates, migration patterns and lineage relationships
71      To examine the relationship between DGC birthdate, morphology, and network integration in a mode
72 tionary origin, gene expression, cell types, birthdates, neurogenesis, lineage and migration, circuit
73                                         Same-birthdate neurons exhibited overlapping spatial represen
74                     By measuring activity in birthdated neurons, we revealed a functional map within
75 rch that have applied distinct approaches to birthdate newly generated neurons and to validate marker
76 suggest that during neuronal development the birthdate of a neuron appears to have significant conseq
77 hdate of occipital subplate neurons) or G18 (birthdate of layers III-IV neurons) demonstrate loss of
78 ked to the olfactory cortices in part by the birthdate of mitral cells.
79  BRDU treatment on gestational day 14 (G14 - birthdate of occipital subplate neurons) or G18 (birthda
80  E55) in the claustrum, corresponding to the birthdates of layers 6 and 5 of the insular cortex, esta
81 nsidered together with results regarding the birthdates of neurochemically defined classes of V gangl
82             Although detailed studies of the birthdates of neurons populating the ferret visual corte
83  the ferret visual cortex are available, the birthdates of neurons that reside in somatosensory corte
84  (exit the cell cycle) in the mouse, but the birthdates of some major enteric neuron subtypes are sti
85                                Moreover, the birthdates of the claustrum and Layer 6b are similarly p
86     Specifically, Wnt1 deletion disrupts the birthdating of MbDA neurons and causes a depletion of Mb
87                                  Early-born (birthdated on E11.5) neurons ectopically expressed subce
88 ished by coinjecting retroviruses to either "birthdate" or birthdate and knock-out Pten in granule ne
89 41 (95% CI 0.18-0.93) adjusted for age, sex, birthdate, parental diabetes, and birthweight.
90                  The changes in the mRNA and birthdating patterns from E20-PN15 suggest that some of
91                            We also find that birthdate predicts cholinergic innervation patterns with
92 le out this possibility by examining whether birthdates randomly called for induction in the Vietnam-
93 dies reveal an intimate relationship between birthdate, response to migration cues and neuronal fate
94                                     Finally, birthdate revealed spatial patterns of axonal arborizati
95                                              Birthdating revealed generation of ectopically placed de
96                                         BrdU birthdating revealed retarded and modestly disorganized
97  classes of enteric neuron differed in their birthdates; serotonin neurons were born first with peak
98                                   Dual-color birthdating shows the ECM assembly process in culture an
99                      Here, we used a precise birthdating strategy to study aGC differentiation using
100                 Using a Tet-On-based genetic birthdating strategy, we identify a "sequential stacking
101                                              Birthdating studies of neurons labeled with bromodeoxyur
102 ere we used a panel of molecular markers and birthdating studies to show that in MAM-exposed rats the
103                                  We use BrdU birthdating studies to show that scrambler cortex shows
104 ing to the timing of rod genesis revealed by birthdating studies.
105                     A thorough retinal cell "birthdating" study has not been performed for the labora
106 ated in a defined sequence dictated by their birthdate such that early-born neurons settle in deep co
107 nd, using scRNA-seq and subtype-specific OSN birthdating, that exposure to male and exogenous musk od
108  that neuronal subtype fate is determined by birthdate through progressive restriction of the neuroge
109  generate here the first 4-dimensional (3D + birthdating time) map of pallium construction in the adu
110 estimate hazard ratios (HRs), stratifying by birthdate to control for age, year, and seasonality and
111 ome-wide expression profiling, and classical birthdating to (i) identify specific molecular types of
112                 Using 5-bromo-2-deoxyuridine birthdating to identify newborn cells, we found that the
113 orescent markers for motoneuron location and birthdate, to probe spatial and temporal organization of
114                                              Birthdate was positively associated with proportion mass
115  newborn rods and by 5-bromo-2'-deoxyuridine birthdating, we demonstrate that early-born post-mitotic
116                                              Birthdates were established by a single injection of bro
117 al to ventral progression according to their birthdates, which are aligned with the tonotopic axis.
118 -virus tracing strategy combining retroviral birthdating with rabies virus-mediated putative retrogra
119 tors (PRs) migrate to positions according to birthdate, with early-born cells localizing to the basal
120 ion along the length of the cochlea based on birthdates, with neurons in the base (responding to high

 
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