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1 ivated receptor gamma coactivator 1 (PGC-1), nuclear respiratory factor-1).
2 ctivator 1alpha and the transcription factor nuclear respiratory factor 1.
3 itive transcription factors: AP-1, CREB, and nuclear respiratory factor 1.
4 locked EPO-mediated nuclear translocation of nuclear respiratory factor-1.
5 gene expression and nuclear accumulation of nuclear respiratory factor-1, -2alpha (Gabpa), and perox
7 encoded by nrf is a close homologue of human Nuclear Respiratory Factor 1 and avian Initiation Bindin
8 ry mitochondrial biogenesis (no induction of nuclear respiratory factor 1 and mitochondrial transcrip
9 ear localization of 2 transcription factors, nuclear respiratory factor 1 and nuclear factor-E2-relat
10 vator 1alpha, the transcriptional activators nuclear respiratory factor 1 and nuclear respiratory fac
11 own to orchestrate mitochondrial biogenesis, nuclear respiratory factor-1 and peroxisome-proliferator
13 reduced levels of the PGC-1alpha downstream nuclear respiratory factors 1 and 2, mitochondrial trans
14 vated receptor-gamma coactivator 1 alpha and nuclear respiratory factors 1 and 2, or to enhanced expr
15 al transduction and recruitment of the NRF1 (nuclear respiratory factor 1) and THRB to the promoters
16 ptor-gamma coactivator-1alpha (PGC-1 alpha), nuclear respiratory factor-1, and mitochondrial transcri
17 activated receptor-gamma coactivator 1-beta, nuclear respiratory factor-1, and transcription factor A
18 that the gene encoding the homolog of human Nuclear respiratory factor 1, erect wing (ewg), is auton
19 eceptor gamma coactivator 1alphaand 1betaand nuclear respiratory factor 1 mRNA and mitochondrial DNA
21 tochrome c promoter mutants showed that both nuclear respiratory factor 1 (NRF-1) and cAMP-response e
22 re conserved in EWG homologs including human nuclear respiratory factor 1 (NRF-1) and the sea urchin
29 The present study tested our hypothesis that nuclear respiratory factor 1 (NRF-1) serves such a role
30 othesis, binding of the transcription factor nuclear respiratory factor 1 (NRF-1) to the cytochrome c
31 expression of a dominant negative allele of nuclear respiratory factor 1 (NRF-1), and glucose depriv
32 regulated by the same transcription factor, nuclear respiratory factor 1 (NRF-1), found recently by
33 in other COX genes, namely binding sites for nuclear respiratory factor 1 (NRF-1), nuclear respirator
35 oregulated by the same transcription factor, nuclear respiratory factor 1 (NRF-1), which regulates al
37 nscriptional activation [c-fos, c-jun, JunB, nuclear respiratory factor 1 (NRF-1)], mitochondrial pro
38 responsive to reactive oxygen species, i.e. nuclear respiratory factor-1 (NRF-1) and mitochondrial t
39 t I RE1-like silencer and functional Sp1 and nuclear respiratory factor-1 (NRF-1) elements within a G
42 he polio virus receptor that is bound by the nuclear respiratory factor-1 (NRF-1) transcription facto
43 We reported that estradiol (E(2)) induces nuclear respiratory factor-1 (NRF-1) transcription throu
44 that control the expression of these genes - nuclear respiratory factor-1 (NRF-1) was significantly u
45 ssociate with reduced expression of multiple nuclear respiratory factor-1 (NRF-1)-dependent genes enc
50 ing of EglN2 under hypoxic conditions reveal nuclear respiratory factor 1 (NRF1) motif enrichment in
51 X gene minimal promoter-binding activity as nuclear respiratory factor 1 (NRF1), a previously known
52 ecific DNA-binding transcriptional activator nuclear respiratory factor 1 (NRF1), in promoting contex
53 inding algorithms predicted the existence of nuclear respiratory factor-1 (NRF1) binding sites in E2F
54 ed receptor-gamma coactivator-1alpha [PGC1], nuclear respiratory factor 1 [NRF1], mitochondrial trans
55 c mitochondrial biogenesis by enhancement of nuclear respiratory factor-1, PGC-1alpha (peroxisome pro
57 activator 1alpha, PGC1 related co-activator, nuclear respiratory factor 1, transcription factor A of
58 ors including estrogen-related receptors and nuclear respiratory factor 1, yet its physiological role
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