コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 es/J), we deleted Tsc1 and/or Tsc2 in radial glial progenitor cells.
2 c role in apical nuclear migration in radial glial progenitor cells.
3 to elicit AMPA receptor-mediated currents in glial progenitor cells.
4 e to defective differentiation competence of glial progenitor cells.
5 n both neuroepithelial stem cells and radial glial progenitor cells.
6 d dysplastic neurons are derived from radial glial progenitor cells.
7 n via autocrine and paracrine stimulation of glial progenitor cells.
8 n of activated forms of both KRas and Akt in glial progenitor cells.
9 were found in the percentage of neuronal or glial progenitor cells.
10 r of the adult human brain harbors a pool of glial progenitor cells.
11 rovide evidence that glial tumors arise from glial progenitor cells.
12 elination and its associated mobilization of glial progenitor cells.
13 ed Cre recombinase expression to a subset of glial progenitor cells after spinal cord injury, yieldin
15 a common marker for sympathetic neuronal and glial progenitor cells and delineate the cellular basis
16 ghly elongated basal processes of the radial glial progenitor cells and impairment of postmitotic neu
17 that GLUL is widely expressed in neuro- and glial-progenitor cells and mature astrocytes but not in
19 ing system that allows the study of isolated glial progenitor cells both in vitro and in vivo was use
20 H3 domains in a yeast two-hybrid screen of a glial progenitor cell cDNA library, we isolated the rat
21 tumor-initiating progenitor cells (TPCs) to glial progenitor cells derived from normal adult human b
22 f miR-491-5p in primary Ink4a-Arf-null mouse glial progenitor cells exacerbated cell proliferation an
24 itch et al. (2019) show that patient-derived glial progenitor cells fail to properly differentiate an
26 lls (GFP(+) cells) as well as the uninfected glial progenitor cells (GFP(-) cells) that are recruited
27 xpressed identical oncogenes in two types of glial progenitor cells, glial-restricted precursor (GRP)
28 e set out to study their function during the glial progenitor cell (GPC) to astrocyte transition.
29 distinct THY1(hi)EGFR(hi)PDGFRA(-) bipotent glial progenitor cell (GPC), which is lineage-restricted
30 myelin loss in HD, we generated bipotential glial progenitor cells (GPCs) from human embryonic stem
31 this question, we compared the properties of glial progenitor cells (GPCs) from the cortices of healt
32 h humanized white matter by engrafting human glial progenitor cells (GPCs) into neonatal immunodefici
33 properties of human glia, we engrafted human glial progenitor cells (GPCs) into neonatal immunodefici
34 stablish humanized glial chimeric mice using glial progenitor cells (GPCs) produced from induced plur
36 al disorders may be amenable to treatment by glial progenitor cells (GPCs), which give rise to astrog
39 es to analyse RNA-sequencing data from human glial progenitor cells (hGPCs) produced from disease-der
40 forebrain, we engrafted wild-type (WT) human glial progenitor cells (hGPCs) produced from human embry
42 th mutant huntingtin (mHTT)-expressing human glial progenitor cells (hGPCs), derived from either huma
43 electively deletes the Tsc2 gene from radial glial progenitor cells in the developing cerebral cortex
44 pproximately 30% decrease in dividing radial glial progenitor cells in the hippocampal VZ and DG in t
45 rise from a p2-like domain of ependymoradial glial progenitor cells, indicated by coexpression of Pax
46 alities in the differentiation competence of glial progenitor cells lead to failure in the morphologi
47 e adult brain and increased proliferation of glial progenitor cells leading to enlarged optic nerves.
48 nded set of malignant cell states, including glial progenitor cell-like, neuronal-like and cilia-like
49 a profound decrease in the expression of the glial progenitor cell marker A2B5 and a corresponding in
50 zophrenia but suggest that the physiology of glial progenitor cells may be altered in schizophrenia.
51 ene loss is coupled with bi-allelic somatic (glial progenitor cell) Nf1 gene inactivation develop bra
52 l cycle progression or survival in iPSCs and glial progenitor cells or astrocyte differentiation.
53 e co-activation of RTK and PI3K signaling in glial progenitor cells recapitulates key features of hum
55 ng neocortex relies on the ability of radial glial progenitor cells (RGCs) to switch from proliferati
56 on and/or birth of new neurons during radial glial progenitor cell (RGPC) neurogenesis, but its role
58 drogliomas may be comprised of proliferating glial progenitor cells that are blocked in their ability
59 addition, distinct populations of nominally glial progenitor cells, which also have the capacity to