ライフサイエンスコーパス: constitutive gene

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1 that plays a role in the expression of many constitutive genes.

2 te approximately 2-fold in S/G2/M similar to constitutive genes.

3 g to their target gene promoters and causing constitutive gene activation in the absence of stimulati

4 enin, leading to elevated protein levels and constitutive gene activation, has been proposed as an im

5 y of mRNAs for elastin and collagen I with a constitutive gene after ascorbate supplementation or wit

6 structural foci for spatial organization of constitutive genes concordant with CTCF-motif orientatio

7 using human specific primers, was used as a constitutive gene control; iNOS mRNA was similarly detec

8 nd considerable interindividual variation in constitutive gene expression and inducibility, indicatin

9 l LC are targeted selectively for high-level constitutive gene expression by Dec2FR in vitro and in v

10 that the observed growth-rate dependence of constitutive gene expression can be explained by a simpl

11 se elements located at -833 is essential for constitutive gene expression in MCF-7 cells.

12 trast to the contribution of NFI proteins to constitutive gene expression in other systems, we demons

13 o +72, was previously shown to direct strong constitutive gene expression in transgenic plants.

14 initiation by a sigma factor responsible for constitutive gene expression indicates that undefined ac

15 In summary, gene translocation can modulate constitutive gene expression levels due to changes in ch

16 The constitutive gene expression of the proangiogenic factor

17 primary fibroblast cell lines all exhibited constitutive gene expression of two receptor chains that

18 These results suggest that constitutive gene expression profiles, in which the gene

19 Because mutations in the RRF motif result in constitutive gene expression throughout the cell cycle,

20 hile TFBS that contain a CpG are involved in constitutive gene expression with some CpG containing se

21 nsient and stable transformation vectors for constitutive gene expression, gene silencing, protein ta

22 1beta are likely members of the same family, constitutive gene expression, synthesis, and processing

23 ene expression over 3 orders of magnitude in constitutive gene expression, to within a factor of 3 in

24 at methylation provides a general signal for constitutive gene expression, whereas other sex-specific

25 H3K36me3 are preferentially associated with constitutive gene expression, while an H3K27me3-containi

26 ow activating epigenetic marks and generally constitutive gene expression.

27 , suggesting that GATA4 is required for Bcl2 constitutive gene expression.

28 llations, not just in cell size, but also in constitutive gene expression.

29 ion that chromium inhibits inducible but not constitutive gene expression.

30 in-protein interactions needed to facilitate constitutive gene expression.

31 thylation of the promoter is correlated with constitutive gene expression.

32 in most vegetative tissues corresponded with constitutive gene expression.

33 used strategy that circumvents pathological constitutive gene induction by physiologically regulated

34 mutations are in previously identified dauer-constitutive genes involved in transducing environmental

35 nclear since the CB2R gene knockout mice are constitutive gene knockout.

36 ed genes tend to have focused promoters, and constitutive genes typically have dispersed promoters.

37 Glyceraldehyde-3-phosphate dehydrogenase (a constitutive gene) was quantified in the same way as CAM

38 ranscriptional activity was restricted to RT-constitutive genes, whereas two-thirds of the genes that

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