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3 n-dependent kinase 4 (CDK4) by the action of CUG-binding protein 1 (CUGBP1) and microRNA-222 (miR-222
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
9 family member 1 (CELF1), also referred to as CUG-binding protein 1 (CUGBP1), regulates the stability
16 otein H2 expression and the translocation of CUG-binding protein 1 from the nucleus to the cytoplasm.
18 erogeneous nuclear ribonucleoprotein H2, and CUG-binding protein 1-responsive internal ribosome entry
20 osphorylation of the RNA-associated protein, CUG-binding protein 2 (CUGBP2), which appears to enhance
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
26 el line of investigation, elevated levels of CUG-binding protein (CUG-BP) have been shown to result i
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
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
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
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