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2 also show that eIF4AIII associates with both polysomal and monosomal RNA in S2 cell extracts, whereas
7 s of genes exhibiting increased or decreased polysomal association after Argonaute or RPG knockdowns,
8 of the MLL1 and MLL4 mRNAs increasing their polysomal association and translation, resulting in the
12 pts are functional mRNAs, the expression and polysomal association of natural La1 and La1' RNAs were
14 repressed BCL2 mRNA was associated with non-polysomal, but dense fractions on sucrose density gradie
17 reveal that these proteins are excluded from polysomal complexes in exponentially growing cells, indi
18 the proportion of individual mRNA species in polysomal complexes in leaves of Arabidopsis thaliana un
19 , levels of miR169 pronouncedly decreased in polysomal complexes, concomitant with the increased accu
20 RNAs were associated with the epitope-tagged polysomal complexes, with an average relative level of a
24 lutionarily conserved process leading to the polysomal degradation of thousands of 'non-aberrant' mRN
27 ith [35S]cysteine/methionine or [14C]NaHCO3, polysomal distribution analyses and ribonuclease protect
28 arisons of protein and mRNA abundance and by polysomal distribution analyses, the uORF represses tran
33 ha(1)-subunit transcript associated with the polysomal fraction in beta(1)-subunit expressing MSV-MDC
34 , eNOS transcripts were enriched in the free polysomal fraction of nonproliferating cells and enriche
36 studies that demonstrated enrichment of the polysomal fraction of reticulocytes with gamma-globin mR
37 hown by the increase of CD20 mRNA within the polysomal fraction, indicating a new role of HDAC6 in th
46 mplification of endogenous ATR transcript on polysomal fractions immunoprecipitated with hnRNP A18.
47 7 induced the coshift of Act1 and HuR to the polysomal fractions in a sucrose gradient, HuR deficienc
49 predominantly polysomal fractions toward non-polysomal fractions in cells transfected with the chimer
51 oximately 140 kDa in size and is enriched in polysomal fractions of cytoplasmic extracts from HeLa ce
53 Quantification of alpha-TM mRNA bound in polysomal fractions reveals that both wild-type and hete
54 bution of luciferase mRNA from predominantly polysomal fractions toward non-polysomal fractions in ce
55 at endogenous Nrf2 mRNAs were recruited into polysomal fractions under oxidative stress conditions.
56 xcess mRNAs in rnr1 are often present in non-polysomal fractions, and half-life measurements demonstr
57 the distribution of receptor mRNA toward the polysomal fractions, favoring increased translation.
58 P41a and/or CSP41b, which are not present in polysomal fractions, stabilize ribosome assembly interme
64 ARP6 by small interfering RNA also decreased polysomal loading of collagen mRNAs, suggesting that it
65 eIF4E1 protein level by reducing eIF4E1 mRNA polysomal loading without affecting total mRNA level or
69 g (RDM), that uses site-specific cleavage of polysomal mRNA followed by separation on a sucrose gradi
70 n on genic regions with fragmented total and polysomal mRNA illuminated numerous aspects of posttrans
71 introduces a new technique for cell-specific polysomal mRNA isolation in kidney injury models that is
74 ges in the maternal component of the zygotic polysomal mRNA population during the transition from ooc
75 quantitative comparison of steady-state and polysomal mRNA populations revealed that over half of th
76 usly a cDNA library made from membrane-bound polysomal mRNA prepared from breast and prostate cancer
78 ided a high level of reproducibility between polysomal mRNA samples immunopurified from two independe
82 Quantitative comparison of steady-state and polysomal mRNAs for 15 genes involved in nodulation iden
83 d a methodology for affinity purification of polysomal mRNAs from genetically defined cell population
84 bules from adult testes, and the presence of polysomal mRNAs in sucrose gradient analyses of testes f
85 d metabolites demonstrated that profiling of polysomal mRNAs strongly augments the prediction of cell
88 iments with free 40 S ribosomal subunits and polysomal preinitiation complexes, but not with free or
93 the proportion of individual mRNA species in polysomal (PS) complexes in leaves of non-stressed and m
95 ment with these data, Cot/tpl2 increases the polysomal recruitment of the 5 TOP eEF1alpha and eEF2 mR
97 somal subunits but not with 80S monosomes or polysomal ribosomes, indicating that it is not a ribosom
98 somal subunits but not with 80S monosomes or polysomal ribosomes, indicating that it is not a ribosom
99 Rat U34A GeneChips with either total RNA or polysomal RNA at one and six hours following contraction
100 eloped a one-step procedure for isolation of polysomal RNA from collagen1alpha1-eGFPL10a mice subject
102 wever, comparison of the absolute amounts of polysomal RNA indicates that polysome association is not
103 oligonucleotide microarray hybridization of polysomal RNA of untreated and STI571-treated 32D-BCR/AB
104 Quantitative analysis of sRNAs in total and polysomal RNA samples revealed that mature microRNAs (mi
106 omoter (ProLAT52) to generate epitope-tagged polysomal-RNA complexes that could be affinity purified,
109 enom exonuclease was used to demonstrate the polysomal RNase generates products with a 3' hydroxyl.
114 undance in the cytoplasmic fraction, and its polysomal sedimentation profile do not change in respons
115 is report, the major proteins binding to non-polysomal testicular mRNAs were isolated and analyzed.
119 e and chemokine mRNAs in translation-active (polysomal) versus translation-inactive (free ribosomes)
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