戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 han a 100-fold change compared to that for a constitutive gene.
2  that plays a role in the expression of many constitutive genes.
3  that of tissue-specific genes and resembles constitutive genes.
4 te approximately 2-fold in S/G2/M similar to constitutive genes.
5 g to their target gene promoters and causing constitutive gene activation in the absence of stimulati
6 enin, leading to elevated protein levels and constitutive gene activation, has been proposed as an im
7 y of mRNAs for elastin and collagen I with a constitutive gene after ascorbate supplementation or wit
8                                The impact of constitutive gene-body methylation is mostly explained b
9  structural foci for spatial organization of constitutive genes concordant with CTCF-motif orientatio
10  using human specific primers, was used as a constitutive gene control; iNOS mRNA was similarly detec
11 nd considerable interindividual variation in constitutive gene expression and inducibility, indicatin
12 l LC are targeted selectively for high-level constitutive gene expression by Dec2FR in vitro and in v
13  that the observed growth-rate dependence of constitutive gene expression can be explained by a simpl
14 se elements located at -833 is essential for constitutive gene expression in MCF-7 cells.
15 trast to the contribution of NFI proteins to constitutive gene expression in other systems, we demons
16 o +72, was previously shown to direct strong constitutive gene expression in transgenic plants.
17 initiation by a sigma factor responsible for constitutive gene expression indicates that undefined ac
18  In summary, gene translocation can modulate constitutive gene expression levels due to changes in ch
19 a(70) binding bacterial promoters to predict constitutive gene expression levels from any sequence.
20                                          The constitutive gene expression of the proangiogenic factor
21  primary fibroblast cell lines all exhibited constitutive gene expression of two receptor chains that
22                   These results suggest that constitutive gene expression profiles, in which the gene
23 Because mutations in the RRF motif result in constitutive gene expression throughout the cell cycle,
24 hile TFBS that contain a CpG are involved in constitutive gene expression with some CpG containing se
25 nsient and stable transformation vectors for constitutive gene expression, gene silencing, protein ta
26 1beta are likely members of the same family, constitutive gene expression, synthesis, and processing
27 ene expression over 3 orders of magnitude in constitutive gene expression, to within a factor of 3 in
28 at methylation provides a general signal for constitutive gene expression, whereas other sex-specific
29  H3K36me3 are preferentially associated with constitutive gene expression, while an H3K27me3-containi
30 r information results for the simple case of constitutive gene expression.
31 ow activating epigenetic marks and generally constitutive gene expression.
32 , suggesting that GATA4 is required for Bcl2 constitutive gene expression.
33 ion that chromium inhibits inducible but not constitutive gene expression.
34 in-protein interactions needed to facilitate constitutive gene expression.
35 thylation of the promoter is correlated with constitutive gene expression.
36 llations, not just in cell size, but also in constitutive gene expression.
37 , in contrast to reporter systems relying on constitutive gene expression.
38 in most vegetative tissues corresponded with constitutive gene expression.
39 ther lineage (B) included both inducible and constitutive genes from diverse phyla.
40  used strategy that circumvents pathological constitutive gene induction by physiologically regulated
41 mutations are in previously identified dauer-constitutive genes involved in transducing environmental
42 nclear since the CB2R gene knockout mice are constitutive gene knockout.
43  involvement in context-specific rather than constitutive gene regulation.
44 ed via transgenic modification of plants for constitutive gene silencing.
45 ed genes tend to have focused promoters, and constitutive genes typically have dispersed promoters.
46  Glyceraldehyde-3-phosphate dehydrogenase (a constitutive gene) was quantified in the same way as CAM
47 ranscriptional activity was restricted to RT-constitutive genes, whereas two-thirds of the genes that