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1 minal oligopyrimidine tract containing mRNA, Elongation factor 1alpha.
2 rotein synthesis by targeting the eukaryotic elongation factor-1alpha.
3 ylogeny based on 2,243 bp from both nuclear (elongation factor 1alpha and carbomoylphosphate synthase
4 F) protein and transcription enzymes such as elongation factor 1alpha and EF-2.
5 er hosts that have very similar or identical elongation factor 1alpha and mitochondrial small subunit
6  DNA sequences were obtained for translation elongation factor 1alpha and the mitochondrial small sub
7 eins, and two cellular proteins, translation elongation factor-1alpha and heat-shock protein 60.
8 caused pre-existing complexes involving Vav, elongation factor-1alpha, and F-actin to increase in siz
9 n induces the Aplysia eukaryotic translation elongation factor 1alpha (Ap-eEF1A) as a late gene that
10  DNA primase) (GANP), CD74, CD22, NF-kappaB, elongation factor 1alpha, CD79b, octamer binding factor
11    We discovered that a C parvum translation elongation factor 1alpha (CpEF1alpha) was discharged fro
12                                   Eukaryotic elongation factor 1alpha (eEF-1A) is a multifunctional p
13 ZPR1 proteins bind to eukaryotic translation elongation factor-1alpha (eEF-1alpha).
14                                   Eukaryotic elongation factor 1alpha (eEF1A) can be post-translation
15                                              Elongation factor 1alpha (eEF1A) is one of these protein
16                       We discovered that the elongation factor-1alpha (eEF1A) inhibitor, ternatin-4,
17 mouse), with Int6sh under the control of the elongation factor-1alpha (eEF1A) promoter.
18        Tef1/2 (the yeast form of translation elongation factor 1alpha [eEF1A]) aids the specificity o
19 including two previously described proteins, elongation factor 1alpha (EF-1alpha) and the polypyrimid
20 oaches identified the eukaryotic translation elongation factor 1alpha (EF-1alpha) as the primary targ
21 -largest subunit (RPB2), and the translation elongation factor 1alpha (EF-1alpha) gene.
22 omegalovirus and the human polypeptide chain elongation factor 1alpha (EF-1alpha) promoters in the pc
23 uences from three nuclear genes: translation elongation factor 1alpha (EF-1alpha), the largest subuni
24 ing of aa-tRNA, is the actin-binding protein elongation factor 1alpha (EF-1alpha).
25 -mitochondrial cytochrome b (cyt b), nuclear elongation factor-1alpha (EF-1alpha) and two anonymous n
26                                  Polypeptide elongation factor-1alpha (EF-1alpha) is a multifunctiona
27 ange of the expression cassette to the human elongation factor-1alpha (EF-1alpha) promoter has permit
28 ha1) has high similarity with the eukaryotic elongation factor-1alpha (EF-1alpha).
29 ts transcription of an integrated, proviral, elongation factor 1alpha (EF1A) promoter-green fluoresce
30 lslacZ) with a splice acceptor, or the human elongation factor 1alpha ( EF1alpha) gene enhancer/promo
31                          We report here that Elongation Factor 1alpha (EF1alpha) forms a complex with
32 ell as an actin/microtubule-binding protein, elongation factor 1alpha (EF1alpha) is a candidate linke
33 n of reporter genes driven by the same human elongation factor 1alpha (EF1alpha) promoter in murine l
34 e to an enhanced interaction with Eukaryotic Elongation Factor 1alpha (EF1alpha), whose protein level
35 hF.IX expression was controlled by the human elongation factor 1alpha [EF1alpha] enhancer-promoter) w
36 al/contractile proteins (paxillin, vimentin, elongation factor-1alpha, F-actin, tropomyosin, and myos
37  L, P, and the nucleocapsid (N), but lacking elongation factor-1alpha, heat-shock protein 60, and gua
38 ted in other eukaryotes (ribosomal subunits, elongation factor 1alpha, histone H1, HSP70 and CDC48),
39 elongation reactions catalysed by eukaryotic elongation factor-1alpha in vitro.
40 lyses of DNA sequences from the nuclear gene elongation factor-1alpha place echiurans and pogonophora
41  in which the strong human polypeptide chain elongation factor 1alpha promoter drives a bicistronic m
42 ors were constructed that utilized the human elongation factor 1alpha promoter, a human growth factor
43 tial C-terminal domain resembling eukaryotic elongation factor 1alpha respectively.
44  molecular data set included protein coding (elongation factor-1alpha, RNA polymerase II, and LW rhod
45 NA, with the 60S ribosomal subunit, and with elongation factor 1alpha, suggesting that granules repre
46         Based on DNA sequence of translation elongation factor 1alpha (tef-1alpha), and morphological
47 e that encodes a truncated and mutated human elongation factor 1alpha (Trun-EF).
48 enzyme is reported to interact directly with elongation factor 1alpha, which carries charged tRNA to