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1                                              hnRNP F had a higher frequency of expression than CKB in
2                                              hnRNP F may be a potential target in the treatment of hy
3                                              hnRNP F stimulated Sirtuin-1 transcription via hnRNP F-r
4       Interestingly, AS targets of the QKI-6-hnRNP F/H pathway in OLs are differentially affected in
5                 The sumoylation of hnRNP A1, hnRNP F, and hnRNP K were confirmed in vivo by coimmunop
6 ophy, and glomerulotubular fibrosis in Akita hnRNP F-Tg mice.
7 TB, Fox, Muscleblind, CELF/CUG-BP, TIA-1 and hnRNP F/H, respectively.
8                                      CKB and hnRNP F were expressed in 78% and 89% of colon tumors, r
9          These results establish hnRNP H and hnRNP F as being repressors of exon inclusion and sugges
10                     We show that hnRNP H and hnRNP F proteins are present in a complex with Fox2 and
11       In this study, we identify hnRNP H and hnRNP F proteins as being novel silencers of fibroblast
12 ess is known, however, about how hnRNP H and hnRNP F silence exons.
13 cated multiple binding sites for hnRNP H and hnRNP F within these cis-regulatory elements.
14 ence was used to knock down both hnRNP H and hnRNP F.
15  at least seven SR proteins and repressed by hnRNPs F, H and I, supporting an extensive antagonism of
16 d with control plasmid or plasmid containing hnRNP F cDNA in vitro.
17                           Our results define hnRNP F as a regulatory element of MBP expression in oli
18 reviously shown that Glorund, the Drosophila hnRNP F/H homolog, contributes to anterior-posterior axi
19 , heterogeneous nuclear ribonucleoprotein F (hnRNP F) and high mobility group box 1 protein (HMGB1) i
20 g heterogeneous nuclear ribonucleoprotein F (hnRNP F) in their RPTCs and immortalized rat renal proxi
21 fection of heterogenous ribonucleoprotein F (hnRNP F) or small interfering RNA resulted in lower abun
22 f heterogeneous nuclear ribonucleoprotein F (hnRNP F) overexpression on angiotensinogen (Agt) gene ex
23 f heterogeneous nuclear ribonucleoprotein F (hnRNP F) renoprotective action in a type 2 diabetes (T2D
24 ified a broad spectrum of in vivo functional hnRNP F/H targets in OLs that contain conserved exons fl
25 lement were identified as hnRNP A1, hnRNP H, hnRNP F, and SF2/ASF by site-specific cross-linking and
26 port of additional hnRNP proteins, including hnRNP F.
27 binding motifs related to those in mammalian hnRNP F and H, which play roles in regulated RNA splicin
28     These results demonstrate that mammalian hnRNP F can act as a negative regulator in the pre-mRNA
29  DCS has been shown to assemble hnRNP H, not hnRNP F, from HeLa cell extracts, and we show that hnRNP
30  not consistent with the observed effects of hnRNP F.
31  more RPTC apoptosis and lower expression of hnRNP F, SIRTUIN-1, and FOXO3alpha than nondiabetic kidn
32 ndrocytes and imply an important function of hnRNP F in the control of myelin synthesis.
33      These results suggest an involvement of hnRNP F and CKB in colorectal cancer.
34 we demonstrate that a change in the level of hnRNP F is an important determinant in the regulated use
35 s studied both showed high protein levels of hnRNP F in colon tumors compared with normal colon tissu
36 inase activity results in phosphorylation of hnRNP F in the cytoplasm and its release from MBP mRNA a
37  analyses of cellular proteins, the ratio of hnRNP F to H or H' was found to be higher in memory B ce
38 ion was down-regulated with up-regulation of hnRNP F.
39 ence that cytoplasmic QKI-6 acts upstream of hnRNP F/H, which forms a novel pathway to control AS in
40 hat the overexpression of either hnRNP H1 or hnRNP F resulted in the dramatic silencing of exon IIIc.
41               Transfection of p44/42 MAPK or hnRNP F small interfering RNA (siRNA) prevented insulin
42  in Akita mice and Akita mice overexpressing hnRNP F suppressed Bmf expression and RPTC apoptosis.
43 sgenic (Tg) mice specifically overexpressing hnRNP F in their RPTCs were created, and the effects on
44 sgenic (Tg) mice specifically overexpressing hnRNP F in their RPTCs.
45 of Sirtuin-1 small interfering RNA prevented hnRNP F stimulation of Foxo3alpha and downregulation of
46    Here, we identify the RNA-binding protein hnRNP F as a novel component of MBP mRNA transport granu
47 nRNP H can interact with the related protein hnRNP F, suggesting that hnRNPs H and F may exist as a h
48 ts of this enhancer complex are the proteins hnRNP F, KSRP, and an unidentified protein of 58 kDa (p5
49        Fourth, overexpression of recombinant hnRNP F in plasma cells resulted in a decrease in the en
50 B), heterogeneous nuclear ribonucleoprotein (hnRNP) F/H and E/K are identified as interacting SRE pai
51 rs, heterologous nuclear ribonucleoproteins (hnRNPs) F and H.
52                 Our results demonstrate that hnRNP F protects kidneys against oxidative stress and ne
53                 Our results demonstrate that hnRNP F suppression of Bmf transcription is an important
54 , using a recombinant protein we showed that hnRNP F could bind to the region downstream of a poly(A)
55                      The results showed that hnRNP F overexpression attenuated systemic hypertension,
56              Additionally, they suggest that hnRNP F is a potential marker for colorectal cancer prog
57                      These data suggest that hnRNP F plays a modulatory role and can ameliorate hyper
58 mRNA in late-stage Drosophila oocytes by the hnRNP F/H homolog, Glorund (Glo), is important for embry
59      HnRNP F inhibited Bmf transcription via hnRNP F-responsive element in the Bmf promoter.
60 RNP F stimulated Sirtuin-1 transcription via hnRNP F-responsive element in the Sirtuin-1 promoter.
61                                    In vitro, hnRNP F overexpression prevented the high-glucose stimul
62                                    In vitro, hnRNP F overexpression stimulated Sirtuin-1 and Foxo3alp