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2 1/neuron-restrictive silencing element (RE-1/NRSE) mediates transcriptional repression by the repress
3 essor of Crh transcription, via the Crh RE-1/NRSE, and an enhancer of Crh transcription, via a mechan
4 ts was down-regulated by REST/NRSF in a RE-1/NRSE-dependent fashion in both muscle-derived L6 and RES
13 um channel H6, another gene with a bipartite NRSE, were up-regulated by dominant-negative REST in C6-
14 mputational analysis revealed many bipartite NRSE variants conserved between mouse and human genomes.
19 erformed data base searches with a composite NRSE to identify additional candidate NRSF target genes.
21 neuronal transcription factor genes contain NRSEs, suggesting that NRSF may repress neuronal differe
24 hat the neuron-restrictive silencer element (NRSE) of MOR functions as a critical regulator to repres
25 hat the neuron-restrictive silencer element (NRSE) of mu opioid receptor (MOR) functions as a critica
26 that a neural restrictive silencer element (NRSE) was critical for preventing ectopic expression of
27 that a neuron restrictive silencer element (NRSE) was implicated in transcriptional repression of th
28 that a neural restrictive silencer element (NRSE) within the second intron prevented expression of L
34 quence (neuron restrictive silencer element [NRSE]), in vitro and in vivo, reduced NRSF binding to Hc
35 f experimentally validated binding sites for NRSE can be found at http://www.cse.ucsd.edu/groups/bioi
37 ved in pancreas development that also harbor NRSE-like motifs, including pdx-1, Beta2/NeuroD, and pax
46 se in the acetylation of histones around RE1/NRSE and that this decrease requires the N-terminal Sin3
47 in the brain contain a silencer element (RE1/NRSE) that limits transcription in nonneuronal cells by
48 ite/neuron-restrictive enhancer element (RE1/NRSE), activate plasmid-encoded neuronal promoters in va
53 re cross-competed with a characterized SCG10 NRSE probe and do not bind to the AVP probe with a speci
54 re extensive evolutionary survey showed that NRSE sites matching the PSFM model exist in roughly simi
59 g transcription factor (REST)/NRSF, both the NRSE and sequences in the first intron were required.
60 timal silencing of L1 gene expression by the NRSE-binding factor RE-1-silencing transcription factor
64 In contrast, a similar construct lacking the NRSE produced precocious expression in the peripheral ne
66 study, we have investigated the role of the NRSE in the regulation of L1 expression during postnatal
70 These data support the conclusion that the NRSE not only plays a role in the silencing of L1 expres
71 co-transfection studies, we showed that the NRSE of the MOR promoter is functional in NRSF-positive
73 enic mice, an L1lacZ gene construct with the NRSE generated a neurally restricted expression pattern
75 NRSF/REST from A126.1B2 exhibited binding to NRSE/RE-1, nuclear extracts from PC12 cells did not.
77 ST), the transcription factor which binds to NRSE/RE-1, was expressed at similar levels in both PC12
80 functionally synergic repressor element with NRSE in NS20Y cells, but not in the NRSF negative PC12 c
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