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1 an chondroitin sulfate proteoglycon-positive glial progenitor.
2 or recycling sustains Akt phosphorylation in glial progenitors.
3 dly the behavior of this ubiquitous class of glial progenitors.
4 P+ and GFP- tumor cells expressed markers of glial progenitors.
5 ebellar projection to this abundant class of glial progenitors.
6 studied primarily as migratory scaffolds and glial progenitors.
7 e induction of GFAP+ cells from normal human glial progenitors.
8  days after SCI increased the number of NG2+ glial progenitors.
9 ed by specified NT-3-responsive neuronal and glial progenitors.
10 otent neuroepithelial (NEP) cells and spinal glial progenitors.
11 inhibiting the proliferation of neuronal and glial progenitors.
12 differentiation, and migration of neural and glial progenitors.
13 erned gene expression in dividing neural and glial progenitors.
14 m cells and the proliferation of parenchymal glial progenitors.
15  bowel (ENCDC) contains proliferating neural/glial progenitors.
16 are engaging in glutamatergic signaling with glial progenitors.
17 ant, exhibits dynamic distribution in radial glial progenitors.
18 ways as central to the regulation of radial 'glial' progenitors.
19                                   Regions of glial progenitor ablation occurred corresponding to the
20 e numbers and high proportions of both human glial progenitors and astrocytes.
21 to its function in neurogenesis, Ascl1 marks glial progenitors and controls the number and distributi
22                  The roles that neuronal and glial progenitors and mature cells play in CNS angiogene
23 vo reveals heterogeneity in Ascl1-expressing glial progenitors and shows that Ascl1 defines cells tha
24  The identity and degree of heterogeneity of glial progenitors and their contributions to brain tumor
25 e-Cell Transcriptomics Resolves Intermediate Glial Progenitors and Uncovers a Pivotal Determinant of
26 e to astrocytes as well as oligodendrocytes, glial progenitors appear to be of potential great utilit
27                             These new radial glial progenitors are capable of giving rise to new neur
28  neuroepithelial cells and neurogenic radial glial progenitors are coexisting.
29 rapid apoptosis of those cells, while radial glial progenitors are less affected.
30 , but not glial, output of individual radial glial progenitors as revealed by mosaic analysis with do
31       These data point to hyperproliferative glial progenitors as the source of the optic tumors and
32 loblastomas, and identified OLIG2-expressing glial progenitors as transit-amplifying cells at the tum
33 ta-gal-positive cells identified in vivo are glial progenitors, as defined by their ability to surviv
34 hreonine 301, and La nuclear export in mouse glial progenitors, as well as its association with polys
35 al AMPA receptor-mediated currents in NG2(+) glial progenitors at anatomically distinct axo-glial syn
36 d an EGFR-GFP fusion protein in white matter glial progenitors at postnatal day 3 of the rat forebrai
37                         Crest-derived nodose glial progenitors can additionally generate autonomic ne
38 SOD1(G93A) glial-restricted precursor cells--glial progenitors capable of differentiating into astroc
39 e set out to study their function during the glial progenitor cell (GPC) to astrocyte transition.
40  distinct THY1(hi)EGFR(hi)PDGFRA(-) bipotent glial progenitor cell (GPC), which is lineage-restricted
41 on and/or birth of new neurons during radial glial progenitor cell (RGPC) neurogenesis, but its role
42 H3 domains in a yeast two-hybrid screen of a glial progenitor cell cDNA library, we isolated the rat
43 a profound decrease in the expression of the glial progenitor cell marker A2B5 and a corresponding in
44 ene loss is coupled with bi-allelic somatic (glial progenitor cell) Nf1 gene inactivation develop bra
45 nded set of malignant cell states, including glial progenitor cell-like, neuronal-like and cilia-like
46 lls (GFP(+) cells) as well as the uninfected glial progenitor cells (GFP(-) cells) that are recruited
47  myelin loss in HD, we generated bipotential glial progenitor cells (GPCs) from human embryonic stem
48 this question, we compared the properties of glial progenitor cells (GPCs) from the cortices of healt
49 h humanized white matter by engrafting human glial progenitor cells (GPCs) into neonatal immunodefici
50 properties of human glia, we engrafted human glial progenitor cells (GPCs) into neonatal immunodefici
51 stablish humanized glial chimeric mice using glial progenitor cells (GPCs) produced from induced plur
52                                 As a result, glial progenitor cells (GPCs), which can give rise to ne
53 al disorders may be amenable to treatment by glial progenitor cells (GPCs), which give rise to astrog
54                Neonatally transplanted human glial progenitor cells (hGPCs) densely engraft and myeli
55                                        Human glial progenitor cells (hGPCs) exhibit diminished expans
56 es to analyse RNA-sequencing data from human glial progenitor cells (hGPCs) produced from disease-der
57 forebrain, we engrafted wild-type (WT) human glial progenitor cells (hGPCs) produced from human embry
58                RNA-seq of cultured SCZ human glial progenitor cells (hGPCs) revealed disrupted glial
59 th mutant huntingtin (mHTT)-expressing human glial progenitor cells (hGPCs), derived from either huma
60                                       Radial glial progenitor cells (RGCs) in the dorsal telencephalo
61 ng neocortex relies on the ability of radial glial progenitor cells (RGCs) to switch from proliferati
62                                       Radial glial progenitor cells (RGPs) are the major neural proge
63 ed Cre recombinase expression to a subset of glial progenitor cells after spinal cord injury, yieldin
64                      JCV replicates in human glial progenitor cells and astrocytes, which undergo vir
65 a common marker for sympathetic neuronal and glial progenitor cells and delineate the cellular basis
66 ghly elongated basal processes of the radial glial progenitor cells and impairment of postmitotic neu
67                                              Glial progenitor cells are abundant in adult human white
68 ing system that allows the study of isolated glial progenitor cells both in vitro and in vivo was use
69  tumor-initiating progenitor cells (TPCs) to glial progenitor cells derived from normal adult human b
70 f miR-491-5p in primary Ink4a-Arf-null mouse glial progenitor cells exacerbated cell proliferation an
71                                       Radial glial progenitor cells exhibit bidirectional cell cycle-
72 itch et al. (2019) show that patient-derived glial progenitor cells fail to properly differentiate an
73 ymmetric division cycles of polarized radial glial progenitor cells for proper development.
74 electively deletes the Tsc2 gene from radial glial progenitor cells in the developing cerebral cortex
75 pproximately 30% decrease in dividing radial glial progenitor cells in the hippocampal VZ and DG in t
76 alities in the differentiation competence of glial progenitor cells lead to failure in the morphologi
77 e adult brain and increased proliferation of glial progenitor cells leading to enlarged optic nerves.
78 zophrenia but suggest that the physiology of glial progenitor cells may be altered in schizophrenia.
79 l cycle progression or survival in iPSCs and glial progenitor cells or astrocyte differentiation.
80 e co-activation of RTK and PI3K signaling in glial progenitor cells recapitulates key features of hum
81 drogliomas may be comprised of proliferating glial progenitor cells that are blocked in their ability
82 xpressed identical oncogenes in two types of glial progenitor cells, glial-restricted precursor (GRP)
83 rise from a p2-like domain of ependymoradial glial progenitor cells, indicated by coexpression of Pax
84  addition, distinct populations of nominally glial progenitor cells, which also have the capacity to
85 d dysplastic neurons are derived from radial glial progenitor cells.
86 n via autocrine and paracrine stimulation of glial progenitor cells.
87 n of activated forms of both KRas and Akt in glial progenitor cells.
88  were found in the percentage of neuronal or glial progenitor cells.
89 e to defective differentiation competence of glial progenitor cells.
90 r of the adult human brain harbors a pool of glial progenitor cells.
91 rovide evidence that glial tumors arise from glial progenitor cells.
92 elination and its associated mobilization of glial progenitor cells.
93 es/J), we deleted Tsc1 and/or Tsc2 in radial glial progenitor cells.
94 c role in apical nuclear migration in radial glial progenitor cells.
95 to elicit AMPA receptor-mediated currents in glial progenitor cells.
96 n both neuroepithelial stem cells and radial glial progenitor cells.
97  that GLUL is widely expressed in neuro- and glial-progenitor cells and mature astrocytes but not in
98 ein Nde1 (mNudE) regulate the fate of radial glial progenitors collaboratively.
99                                              Glial progenitors colonize the CNS widely in the perinat
100 a timed migration of a ridge of neuronal and glial progenitors directed toward the region of the TGFa
101 demonstrate that prolonged mitosis of radial glial progenitors directly alters neuronal fate specific
102 e dynamic repertoire of common and divergent glial progenitors during development and tumorigenesis a
103 neurite formation and proliferation of neuro-glial progenitors during embryonic spinal cord developme
104 ) is upregulated primarily by astrocytes and glial progenitors early after SCI.
105 d than has previously been observed and that glial progenitors exist in the outer circumference of th
106 drives the switch in Notch output and radial glial progenitor fate as part of the larger developmenta
107 nts of both neuroepithelium cells and radial glial progenitors follow the same developmental trajecto
108 ble-positive cells represent a population of glial progenitors for sympathetic satellite cells.
109 s), a population of abundant, highly dynamic glial progenitors, frequently surrounded small branches
110  ectopic expression of mPar3 prevents radial glial progenitors from dividing asymmetrically yet gener
111 ial for long term survival and protection of glial progenitors from glutamate toxicity.
112 Cell, Windrem et al. (2017) transplant human glial progenitors from schizophrenia patients into mouse
113 em cells and lineage-restricted neuronal and glial progenitors from the embryonic rat telencephalon u
114 EK1/2 inhibition selectively rescued primary glial progenitors from TMX toxicity in vitro while enhan
115 ed to a 10-fold increase in the abundance of glial progenitors, giving rise to a progenitor "hyperpla
116  in the optic nerve, brain-derived migrating glial progenitors (GPs), but not local progenitors.
117         One of the basic problems with human glial progenitors (hGRPs) replacement strategies is the
118 erve phospho-tyrosine EGFR immunostaining of glial progenitors in culture.
119 y contain, in addition to NSCs, neuronal and glial progenitors in different states of differentiation
120  discusses the role of adult-born neural and glial progenitors in drug seeking associated with the di
121 le of producing the appropriate neuronal and glial progenitors in ES cell culture.
122 eal a previously unrecognized role of radial glial progenitors in stabilizing nascent brain vascular
123                            Individual radial glial progenitors in the developing thalamus actively di
124 ng from low-titre retrovirus-infected radial glial progenitors in the embryonic medial ganglionic emi
125 e roles, and even act as neuronal as well as glial progenitors in the enteric nervous system.
126 nderlying asymmetric cell division of radial glial progenitors in the mammalian neocortex.
127                                       Unlike glial progenitors in the subventricular zone, differenti
128 es dose-dependent growth inhibition of mouse glial progenitors in which Akt and/or Ras-Erk 1/2 pathwa
129 onal analysis resolves greater complexity of glial progenitors, including transient glial intermediat
130 sient expression of Rbfox proteins in radial glial progenitors induces neuronal splicing events prefe
131 tem Cell, Han et al. (2013) transplant human glial progenitors into mouse brains and thereby improve
132                                          The glial progenitor is not maintained by GDNF.
133 cept that loss of function of Tsc2 in radial glial progenitors is one initiating event in the develop
134 lian CNS contains a ubiquitous population of glial progenitors known as NG2+ cells that have the abil
135        We thus asked whether these nominally glial progenitors might include multipotential progenito
136                                        Thus, glial progenitors migrate across the CC, presumably in c
137 t allows growth of neuroepithelial cells and glial progenitors, mutant cells hyper-respond to FGF2, h
138 g cells, quaking (QKI) to identify embryonic glial progenitors, NG2 to identify neonatal oligodendroc
139 are not widely available and the dynamics of glial progenitor niche remodelling at sites of neurovasc
140  Tsc1 inactivation or Rheb overexpression in glial progenitors of Nf1(+/-) mice does not lead to glio
141 roneural factor is itself required in radial glial progenitors only for proper orientation of cell di
142  in both CNS and PNS, via transplantation of glial progenitors or the implantation of tissue scaffold
143 rA and pMeA displayed either a neuronal or a glial progenitor phenotype, but no species or treatment
144                                       Radial glial progenitors play pivotal roles in the development
145  the vagal neural crest maintains a neuronal/glial progenitor pool, whereas this cluster is depleted
146 cs, we uncover an unanticipated diversity of glial progenitor pools with unique molecular identities
147  ultimately generating mice with a humanized glial progenitor population.
148 ion to drive K-ras(G12D) expression in neuro-glial progenitor populations at different developmental
149           Asymmetric cell division of radial glial progenitors produces neurons while allowing self-r
150 Cs, suggesting ET-1's role as a regulator of glial progenitor proliferation may be conserved in human
151    Brain progenitors, including neuronal and glial progenitors, respond to stroke and initiate a part
152                                       Radial glial progenitors (RGPs) are elongated epithelial cells
153                                       Radial glial progenitors (RGPs) are responsible for producing n
154 st metabolic production of lactate by radial glial progenitors (RGPs) co-regulates vascular developme
155 ally along the glial fibers of mother radial glial progenitors (RGPs) in a birth-date-dependent insid
156                   Orderly division of radial glial progenitors (RGPs) in the developing mammalian cer
157 om those in the dorsal telencephalon, radial glial progenitors (RGPs) in the ventral telencephalon re
158 ortex depends on extensive mitoses of radial glial progenitors (RGPs) residing in the ventricular zon
159              Brain neural stem cells (radial glial progenitors, RGPs) undergo a mysterious form of ce
160 ojection neurons (PNs) generated from radial glial progenitors (RGs) through either direct neurogenes
161 adult neurons and glia originate from radial glial progenitors (RGs), a type of stem cell typically e
162                                       Radial glial progenitors span the neuroepithelium, extending lo
163 1 function does not appear to affect overall glial progenitor specification, suggesting that a later
164 ve expansion of both infected and uninfected glial progenitors, suggesting that PDGF was driving tumo
165 ral gliomas can arise from transformation of glial progenitors that are driven to proliferate via mit
166 ese observations suggest that in addition to glial progenitors that commit to a specific lineage prio
167 yer of the cerebellar cortex is populated by glial progenitors that express ionotropic glutamate rece
168 lation of neural precursor cells, namely the glial progenitors that give rise to oligodendrocytes in
169 belong to a distinct population, most likely glial progenitors, that are less affected by aging than
170 sion gradients in neuroepithelial and radial glial progenitors (the 'protomap').
171 rate a valuable and specific contribution of glial progenitors to normalizing gliogenic levels, rescu
172 demonstrates that these crest-derived nodose glial progenitors transiently express Phox2b, give rise
173 ctionally, we found that localized niches of glial progenitors undergo EMT after spinal cord injury i
174   To test the gliomagenic potential of adult glial progenitors, we infected adult rat white matter wi
175 erkinetic nuclear oscillations in the radial glial progenitors were also abolished, as were cell divi
176 liferation of musashi1-immunoreactive radial glial progenitors, while visual experience increased neu
177                                    Infecting glial progenitors with Cre-recombinant retrovirus simult

 
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