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1                                              CUG-BP and ETR-3 like factor (CELF) proteins are regulat
2                                              CUG-BP and ETR-3-like (CELF) family RNA-binding proteins
3                                              CUG-BP and ETR-3-like factor proteins control developmen
4                                              CUG-BP was found to bind to the human cardiac troponin T
5                                              CUG-BP, Elav-like family member 1 (CELF1, also called CU
6                                              CUG-BP, ETR-3, and CELF4 are more broadly expressed, and
7 reening of a mouse liver cDNA library with a CUG-BP probe identified two mETR-3 cDNAs.
8                                     Although CUG-BP in nuclear extracts preferentially photocrosslink
9 ediated down-regulation of MBNL1, MBNL2, and CUG-BP in DM1 myoblasts demonstrated that MBNL1 plays a
10 The relative importance of MBNL1, MBNL2, and CUG-BP in DM1 pathogenesis is, however, unclear.
11                                         Both CUG-BP and mETR-3 bind to mETR-3 mRNA via CUG repeats, s
12  of genes regulated posttranscriptionally by CUG-BP therefore may contribute to DM pathogenesis.
13 is predicted to encode a member of the CELF (CUG-BP- and ETR-3-like factors) family of RNA-binding pr
14 cting regulators PTB, Fox, Muscleblind, CELF/CUG-BP, TIA-1 and hnRNP F/H, respectively.
15 s tightly controlled by RNA splicing factors CUG-BP and hnRNPM through direct binding.
16 This family, which we call CELF proteins for CUG-BP- and ETR-3-like factors, specifically bound MSE-c
17 t region in Mt-PK mRNA is a binding site for CUG-BP/hNab50 in vivo, and triplet repeat expansion lead
18 lear concentration of the hypophosphorylated CUG-BP/hNab50 isoform is increased in DMPK knockout mice
19                                    Moreover, CUG-BP localized to the base of the RNA hairpin and not
20  elevation of the hypophosphorylated form of CUG-BP/hNab50.
21 eats, suggesting the possible involvement of CUG-BP-like proteins in the regulation of mETR-3 process
22                       Steady-state levels of CUG-BP, a regulator of pre-mRNA splicing proposed to med
23 0, thus facilitating nuclear localization of CUG-BP/hNab50.
24 ed in DM1 skeletal muscle; overexpression of CUG-BP in normal cells induces a switch to IR-A.
25  of MBNL1 and MBNL2 or the overexpression of CUG-BP in normal myoblasts results in abnormal IR splici
26 the key event, whereas the overexpression of CUG-BP plays a secondary role in the aberrant alternativ
27 in nuclear foci, the localization pattern of CUG-BP in both normal and DM cells was similar.
28             DMPK-mediated phosphorylation of CUG-BP/hNab50 results in dramatic reduction of the CUG-B
29 r distribution and RNA-binding properties of CUG-BP.
30 ld be, in part, a result of sequestration of CUG-BP/hNab50 and, in part, of lowered DMPK levels, whic
31 f DMPK could alter phosphorylation status of CUG-BP/hNab50, thus facilitating nuclear localization of
32  DMPK also interacts with and phosphorylates CUG-BP/hNab50 protein in vitro.
33  also demonstrated that CUG-binding protein (CUG-BP) binds a conserved CUG motif within a human cTNT
34 ion, elevated levels of CUG-binding protein (CUG-BP) have been shown to result in altered IR splicing
35 the binding of purified CUG-binding protein (CUG-BP) to these RNAs.
36 lear ribonucleoprotein, CUG-binding protein (CUG-BP), may mediate the trans-dominant effect of the RN
37 inding protein, identical to hNab50 protein (CUG-BP/hNab50), are altered in homozygous DM patient and
38                           The novel protein, CUG-BP, is particularly interesting since it binds to tr
39  of the members of the CUG-binding proteins, CUG-BP, has been identified previously.
40 ated the role of three RNA-binding proteins, CUG-BP, hnRNP C and MBNL, as possible sequestered factor
41 th specific binding to CUG repeat sequences (CUG-BP/hNab50) that possibly plays a role in mRNA proces
42 re altered in homozygous DM patient and that CUG-BP/hNab50 is a substrate for DMPK both in vivo and i
43 g/photocrosslinking studies demonstrate that CUG-BP/hNab50 binds to RNAs containing the Mt-PK 3'-UTR.
44                          Here we report that CUG-BP is one of a novel family of developmentally regul
45 escent protein (GFP) tags we have shown that CUG-BP and hnRNP C do not co-localise with expanded repe
46                           We have shown that CUG-BP levels are elevated in DM1 cells by mechanisms th
47 ms an RNA hairpin structure and suggest that CUG-BP is unlikely to be a sequestered factor.
48                     Our results suggest that CUG-BP regulates the equilibrium of splice site selectio
49                                          The CUG-BP and ETR-3 like factors (CELF) are a family of six
50                                          The CUG-BP protein mediates this switch through an intronic
51                                          The CUG-BP, Elav-like family (CELF) of RNA-binding proteins
52                                          The CUG-BP/hNab50 protein is localized predominantly in the
53                             Furthermore, the CUG-BP exhibited no binding to an RNA oligonucleotide of
54                               Members of the CUG-BP and ETR-3 like factor (CELF) protein family bind
55                               Members of the CUG-BP, Elav-like family (CELF) regulate alternative spl
56 lation and intracellular localization of the CUG-BP/hNab50 protein.
57  These domains have common features with the CUG-BP and ETR3-like Factor (CELF) family of splicing re
58 kDa and displays a high level of homology to CUG-BP protein.
59  the ETR-3 molecule is similar to one within CUG-BP.