ライフサイエンスコーパス: elongation factor 1

1 a mutation in YKL160W, hereafter named ELF1 (elongation factor 1).

2 s of the potential of therapeutics targeting elongation factor 1.

3 class of novel cyclic lactone inhibitors of elongation factor 1.

4 Stretching the GUVs in the range of elongation factors 1-1.3 led to an overall decrease in c

5 drial fission factor (Mff) and mitochondrial elongation factor 1/2 (MIEF1/2) interact with and recrui

6 Herein, eukaryotic elongation factor-1 A1 (eEF1A1) is identified as an inte

7 the translation elongation factor eukaryotic elongation factor 1 alpha (eEF1A) is necessary for AID c

8 The human elongation factor 1 alpha (EEF1A1) promoter fragment int

9 NA), as well as fragments of the translation elongation factor 1 alpha (EF-1alpha) and actin (Act) ge

10 livery of aminoacyl-tRNAs to the ribosome by elongation factor 1 alpha (EF-1alpha).

11 Elongation factor 1 alpha (EF1 alpha) is an abundant pro

12 rometry (LC-MS/MS)-based proteomics revealed elongation factor 1 alpha (EF1a) as a protein binding to

13 We demonstrate here that the mRNA for the elongation factor 1 alpha (EF1alpha) is present in vivo

14 ion by at least 100-fold with the use of the elongation factor 1 alpha (EF1alpha) promoter and a stro

15 ted protein levels of eukaryotic translation elongation factor 1 alpha (EF1alpha), an Mdm2-interactin

16 beta-actin (Actin), beta-tubulin (Tubulin), elongation factor 1 alpha (EF1alpha), glyceraldehyde-3 p

17 bosomal DNA and fragments of the translation elongation factor 1 alpha (Tef1), endochitinase CHI18-5

18 re we discovered that eukaryotic translation elongation factor 1 alpha 1 (eEF1A1) interacted with PpI

19 staining intensity of eukaryotic translation elongation factor 1 alpha 1 (eEF1A1), one of the candida

20 Eight target proteins, including translation elongation factor 1 alpha 1 (EF1A1), deleted in azoosper

21 of these proteins, the actin-binding protein elongation factor 1 alpha 1 (EF1alpha1), blocks neural c

22 ic to the 5' UTR region and the other to the elongation factor 1 alpha coding region, amplifies PTI-1

23 nuclear large-subunit rRNA, the translation elongation factor 1 alpha gene (EF-1alpha), and the seco

24 eement with species sequence identification (elongation factor 1 alpha gene).

25 ppears to be dampened by the secretion of an elongation factor 1 alpha protein (EF1alpha), which inte

26 hondrial (cytochrome oxidase I) and nuclear (elongation factor 1 alpha) DNA sequence data.

27 PTI-1 encodes a truncated and mutated human elongation factor 1 alpha, and its 5' untranslated regio

28 N-terminus and lysine 55 (K55) of eukaryotic elongation factor 1 alpha.

29 e of charged tRNA and its direct transfer to elongation factor 1 alpha; however, whether the extensio

30 mining reaction is facilitated by the GTPase elongation factor-1 alpha (eEF1A), which escorts aa-tRNA

31 entified the cellular protein as translation elongation factor-1 alpha (EF-1 alpha).

32 s, basic fibroblast growth factor (bFGF) and elongation factor-1 alpha (EF1alpha), targeted to the he

33 The cytochrome oxidase I, 16S, 18S, and elongation factor-1 alpha genes have been widely used an

34 MA was found to interact with elongation factor 1-alpha (EF1alpha), an essential compo

35 comprise the peptide sequence of translation elongation factor 1-alpha 1 (eEF1A1).

36 both vectors used the Xenopus translational elongation factor 1-alpha enhancer/promoter regulatory c

37 portions of the beta-tubulin and translation elongation factor 1-alpha genes indicated that the isola

38 oly(A)-binding protein], and glp-3/eft-3 (an elongation factor 1-alpha homolog).

39 virus (CMV) promoter (AAV-C-AT) or the human elongation factor 1-alpha promoter (AAV-E-AT) were exami

40 included ferritin H, eukaryotic translation elongation factor 1-alpha, ferritin L, fibronectin, and

41 enes, such as actin, alpha/beta-tubulin, and elongation factor 1-alpha.

42 IT included increased eukaryotic translation elongation factor-1-alpha-1 (apoptosis related) and redu

43 otein kinase-p38, and eukaryotic translation elongation factor-1-alpha-1) and decreases repair/cytopr

44 ted and disulfide-bonded proteins, including elongation factor 1-alpha1 and mouse serum albumin, and

45 S) 18, vacuolar ATPase subunit A (VhaA), and elongation factor 1-beta (EF1b).

46 inery were identified, including translation elongation factor 1-beta (PfEF-1beta).

47 The translation elongation factor 1 complex (eEF1) plays a central role

48 s have indicated that eukaryotic translation elongation factor 1 delta (eEF1D) may associate with RNP

49 oned and was identified as mouse translation elongation factor-1 delta subunit (TEF-1 delta; GenBank

50 include genes for RPL6/mRNA for TAX REB 107, elongation factor-1 delta, 26S protease S4 regulatory su

51 zipper motif, characteristic of translation elongation factor-1 delta, was also found in the mouse T

52 t the eEF1A and eEF1G subunits of eukaryotic elongation factor 1 (eEF1) are important components of t

53 When elongation factor 1 (EF-1) from rabbit reticulocytes was

54 Here, we focused on the elongation factor 1 (EF1) family of viral translational

55 We developed a lentiviral vector with an elongation factor 1 (EF1alpha) promoter to drive nNOS or

56 we show that the C-terminal domain (CTD) of elongation factor-1 (Elf1) plays a critical role in TC-N

57 In our model, CSB, CSA, UVSSA, elongation factor 1 (ELOF1), and specific Pol II and UVS

58 es with the eEF1Bbeta subunit of translation elongation factor 1 for binding to KTN1, and eEF1Bbeta k

59 lipid-binding protein (CPBP), a homologue of elongation factor-1 gamma, is a component of a complex t

60 potential factors involved in SHM, including elongation factor 1 homolog (ELOF1), a component of the

61 tone acetylase p300 and positive translation elongation factor 1 (p-TEFb) and phosphorylation of the

62 month after transduction, however, the human elongation factor 1 promoter mediated 10-fold higher sta

63 or beta-galactosidase under control of human elongation factor 1 promoter or CMV immediate early-1 pr

64 In subpopulations requiring activation, the elongation factor 1 promoter was far superior to a hCMV

65 uorescent protein (GFP) under the control of elongation factor-1 promoter was used to study infection