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1 er-layer neurons, independently of niche and birthdate.
2 y superficial cortical layers independent of birthdate.
3 of SPN in the spinal cord was independent of birthdate.
4 tin, and newly generated cells by using BrdU-birthdating.
5 ) male and female mice was used to label and birthdate adult-born neurons for morphological and elect
6                                              Birthdating analyses in control and Blimp1 CKO mice show
7 atives, biochemical, immunocytochemical, and birthdating analyses were conducted.
8                                         BrdU birthdating analysis revealed that many late-born neuron
9 imetable of early neurogenesis, indicated by birthdating analysis, was delayed.
10 ure to nutritional deficiency based on their birthdate and birthplace.
11 cent protein Kaede to simultaneously analyze birthdate and cell fate in live zebrafish embryos.
12 ecting retroviruses to either "birthdate" or birthdate and knock-out Pten in granule neurons of the m
13 ve investigated the relationship between the birthdate and the onset of differentiation of neurons in
14 lass II Kenyon cells, defined by their early birthdate and unique dendritic arborizations, have been
15                            Bromodeoxyuridine birthdating and anti-IgG double-labeling studies showed
16                             Our results from birthdating and in utero electroporation experiments dem
17                                      Genetic birthdating and morphological and molecular analyses pin
18                       The current study used birthdating and pathway-tracing methods to investigate t
19           All participants provided name and birthdate, and 94% provided a complete social security n
20 from among survey participants using gender, birthdate, and location.
21 ationship between enteric neuron subtype and birthdate, and suggest that some enteric neurons exhibit
22 imp1 CKO mice showed that bipolar cells were birthdated as early as E13.5 in Blimp1 CKO mice, five da
23                              Differentiation birthdating by label dilution using [(3)H]thymidine also
24                         By bromodeoxyuridine birthdating cells in green fluorescent protein-expressin
25 nment of DACA eligibility among mothers with birthdates close to the DACA age qualification cutoff.
26 eurons generated, rather than strictly their birthdate, determines the specific types of interneurons
27 imilar to that of GAD67 mRNA, for cells with birthdates (E14) of many of the mature GAD-containing ne
28 a somewhat inverted "outside-in" sequence of birthdates for cortical neurons that is similar to that
29            At adulthood, gentle mediolateral birthdate-gradients in S cells were still evident, but M
30                             Autoradiographic birthdating indicates that almost all of these early app
31      In the present study we determined that birthdate is not a factor contributing to the abnormal p
32                            Cortical neuronal birthdate is partly controlled by an intrinsic clock-typ
33 we used 2-photon calcium imaging in neuronal birthdate-labeled Mash1-CreER;Ai14 mice to image simulta
34 Syrian hamsters daily injections of the cell birthdate marker bromodeoxyuridine throughout puberty (p
35 f cortical neuron development including cell birthdates, migration patterns and lineage relationships
36 suggest that during neuronal development the birthdate of a neuron appears to have significant conseq
37 hdate of occipital subplate neurons) or G18 (birthdate of layers III-IV neurons) demonstrate loss of
38 ked to the olfactory cortices in part by the birthdate of mitral cells.
39  BRDU treatment on gestational day 14 (G14 - birthdate of occipital subplate neurons) or G18 (birthda
40 nsidered together with results regarding the birthdates of neurochemically defined classes of V gangl
41             Although detailed studies of the birthdates of neurons populating the ferret visual corte
42  the ferret visual cortex are available, the birthdates of neurons that reside in somatosensory corte
43  (exit the cell cycle) in the mouse, but the birthdates of some major enteric neuron subtypes are sti
44     Specifically, Wnt1 deletion disrupts the birthdating of MbDA neurons and causes a depletion of Mb
45                                  Early-born (birthdated on E11.5) neurons ectopically expressed subce
46 ished by coinjecting retroviruses to either "birthdate" or birthdate and knock-out Pten in granule ne
47 41 (95% CI 0.18-0.93) adjusted for age, sex, birthdate, parental diabetes, and birthweight.
48                  The changes in the mRNA and birthdating patterns from E20-PN15 suggest that some of
49 dies reveal an intimate relationship between birthdate, response to migration cues and neuronal fate
50                                         BrdU birthdating revealed retarded and modestly disorganized
51  classes of enteric neuron differed in their birthdates; serotonin neurons were born first with peak
52                 Using a Tet-On-based genetic birthdating strategy, we identify a "sequential stacking
53                                              Birthdating studies of neurons labeled with bromodeoxyur
54 ere we used a panel of molecular markers and birthdating studies to show that in MAM-exposed rats the
55                                  We use BrdU birthdating studies to show that scrambler cortex shows
56 ing to the timing of rod genesis revealed by birthdating studies.
57                     A thorough retinal cell "birthdating" study has not been performed for the labora
58 ated in a defined sequence dictated by their birthdate such that early-born neurons settle in deep co
59  that neuronal subtype fate is determined by birthdate through progressive restriction of the neuroge
60  generate here the first 4-dimensional (3D + birthdating time) map of pallium construction in the adu
61 estimate hazard ratios (HRs), stratifying by birthdate to control for age, year, and seasonality and
62 ome-wide expression profiling, and classical birthdating to (i) identify specific molecular types of
63                 Using 5-bromo-2-deoxyuridine birthdating to identify newborn cells, we found that the
64 orescent markers for motoneuron location and birthdate, to probe spatial and temporal organization of
65  newborn rods and by 5-bromo-2'-deoxyuridine birthdating, we demonstrate that early-born post-mitotic
66                                              Birthdates were established by a single injection of bro
67 -virus tracing strategy combining retroviral birthdating with rabies virus-mediated putative retrogra

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