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1 -like 1 (MBNL1) protein and up-regulation of CUG binding protein 1 (CUGBP1).
2                         RNA-binding proteins CUG-binding protein 1 (CUGBP1) and HuR are highly expres
3 n-dependent kinase 4 (CDK4) by the action of CUG-binding protein 1 (CUGBP1) and microRNA-222 (miR-222
4                                      The RBP CUG-binding protein 1 (CUGBP1) destabilizes and represse
5 MT1 IRES-specific trans-acting factor (ITAF) CUG-binding protein 1 (CUGBP1) from in vitro translation
6 e we report that miRNA 195 (miR-195) and RBP CUG-binding protein 1 (CUGBP1) jointly regulate IGF2R ex
7                                              CUG-binding protein 1 (CUGBP1) was identified as the maj
8                     The RNA-binding protein, CUG-binding protein 1 (CUGBP1), regulates gene expressio
9 family member 1 (CELF1), also referred to as CUG-binding protein 1 (CUGBP1), regulates the stability
10 ding proteins muscleblind-like 1 (MBNL1) and CUG-binding protein 1 (CUGBP1).
11  and to the increased steady-state levels of CUG-binding protein 1 (CUGBP1).
12 ng regulators muscleblind-like 1 (MBNL1) and CUG-binding protein 1 (CUGBP1).
13 , and mass spectrometry that is bound by the CUG-binding protein 1 (CUGBP1).
14 he functions of RNA-binding proteins such as CUG-binding protein 1 (CUGBP1).
15 ctivities of RNA-binding proteins, including CUG-binding protein 1 (CUGBP1).
16 otein H2 expression and the translocation of CUG-binding protein 1 from the nucleus to the cytoplasm.
17     Here we highlight the roles of RBPs HuR, CUG-binding protein 1, AU-binding factor 1, and several
18 erogeneous nuclear ribonucleoprotein H2, and CUG-binding protein 1-responsive internal ribosome entry
19           We found that the splicing factor, CUG-binding-protein-1 (CUGBP1), bound to a consensus seq
20 osphorylation of the RNA-associated protein, CUG-binding protein 2 (CUGBP2), which appears to enhance
21 lly through a mechanism involving endogenous CUG-binding protein 2 (CUGbp2).
22 tability and translation is regulated by the CUG-binding protein 2 interacting with AU-rich sequences
23 re, we present the solution NMR structure of CUG-binding protein 2 RRM3 in complex with 5'-UUUAA-3' o
24 l vision-type RNA-binding protein 3, and the CUG-binding protein and embryonic lethal abnormal vision
25                    We also demonstrated that CUG-binding protein (CUG-BP) binds a conserved CUG motif
26 el line of investigation, elevated levels of CUG-binding protein (CUG-BP) have been shown to result i
27  repeats and studied the binding of purified CUG-binding protein (CUG-BP) to these RNAs.
28                       Its closest homologue, CUG-binding protein (CUG-bp), is a human RBP that has be
29 ved heterogeneous nuclear ribonucleoprotein, CUG-binding protein (CUG-BP), may mediate the trans-domi
30     However, we observed increased levels of CUG-binding protein (CUG-BP1) in skeletal muscle, as see
31                    One of the members of the CUG-binding proteins, CUG-BP, has been identified previo
32  pyrimidine tract-binding protein (PTB), and CUG-binding protein (CUGBP) interact in vivo, as demonst
33 1 (DM1) patients leads to the induction of a CUG-binding protein, CUGBP1, which increases translation
34 cific pre-mRNAs by altering the functions of CUG-binding proteins (CUGBPs).
35 ribed a family of five RNA-binding proteins: CUG-binding protein, embryonic lethal abnormal vision-ty
36 of tropomyosin reporters with members of the CUG-binding protein family, which are candidate URE-bind
37 us and intracellular distribution of the RNA CUG-binding protein, identical to hNab50 protein (CUG-BP
38                                        Poly-(CUG) binding proteins in the Muscleblind-like (MBNL) fam
39                               Of 10 putative CUG binding proteins tested for colocalization with muta
40                                          The CUG binding protein was localized to the cytoplasm, wher

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