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1 nal degeneration is accompanied by primarily oligodendrocytic accumulation of alpha-synuclein (alphas
4 -positive tau aggregates were generated in a oligodendrocytic cell line after treatment with peroxyni
5 ne system, gamma-aminobutyric acidergic, and oligodendrocytic changes are all integral parts of the d
6 dy, we have investigated the contribution of oligodendrocytic connexin47 (Cx47) and astrocytic Cx30 t
7 ates, probably caused by the upregulation of oligodendrocytic Cx32 in Cx30/Cx47 double-deficient mice
8 rated specific Cx47 antibodies revealed that oligodendrocytic Cx47 is phosphorylated in vivo dependin
9 idence that phosphorylation and stability of oligodendrocytic Cx47 proteins is dependent on astrocyti
11 ined neuronal and oligodendrocytic or purely oligodendrocytic defects that closely match their respec
14 r cell migration, predominantly neuronal and oligodendrocytic donor cell differentiation, and functio
16 ck Cx47 expression and therefore cannot form oligodendrocytic gap junctions, which explains the pheno
17 analyses showed that some of the upregulated oligodendrocytic genes contain an RE1 motif and are dire
18 T showed upregulation of neuronal as well as oligodendrocytic genes, specifically those involved in m
21 to the exclusive generation of cells of the oligodendrocytic lineage at the expense of newborn neuro
24 g of clones for ChAT and glial, neuronal, or oligodendrocytic lineage markers shows that motoneurons
25 -cyclic mononucleotide 3'-phosphodiesterase (oligodendrocytic marker) demonstrated expression of NBC
29 esting that interaction and stabilization of oligodendrocytic myelin-associated glycoprotein by neuro
32 ither purely neuronal, combined neuronal and oligodendrocytic or purely oligodendrocytic defects that
33 iating to neurons and glia, the neuronal and oligodendrocytic pools were significantly enlarged and t
34 ned as axons surrounded by only one layer of oligodendrocytic process, were first seen at P2 and P4 i
35 including induced maturation of rat primary oligodendrocytic progenitor cells (OPCs) in vitro and my
36 ral precursors and their mature neuronal and oligodendrocytic progeny in many CNS regions, including
37 GFP expressed under the control of an early oligodendrocytic promoter, these oligodendrocyte progeni
38 rol of the human early promoter (P2) for the oligodendrocytic protein cyclic nucleotide phosphodieste
39 plastic cells, whose decision to initiate an oligodendrocytic rather than astrocytic or neuronal prog
41 n was observed in a subset of astrocytic and oligodendrocytic tau inclusions as well as the neuropil
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