ライフサイエンスコーパス: autonomous replication

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1 r of the genomic islands and may even encode autonomous replication.

2 d that this element is sufficient to promote autonomous replication.

3 and orc8) are not able to promote efficient autonomous replication.

4 egion 3' to the gene, which is essential for autonomous replication.

5 l oriC contains features that support stable autonomous replication.

6 seven plasmids tested, only p82 shows strong autonomous replication activity in an in vitro replicati

7 ity to function as oriC, confirming that the autonomous replication activity of these plasmids is due

8 ble inheritance of plasmids depends on their autonomous replication and efficient partition to daught

9 e phage functions are required for excision, autonomous replication and encapsidation of the element

10 hogens and genetic units that are capable of autonomous replication and systemic trafficking and offe

11 , indicating that all elements necessary for autonomous replication are probably located on this 3.3

12 zed the circular plasmid regions that confer autonomous replication, but the genetic elements necessa

13 in this interaction is sufficient to confer autonomous replication competence to AAV in 293 cells.

14 ulate to a high copy number because of their autonomous replication during the DNA synthesis phase of

15 nal regions of linear plasmids necessary for autonomous replication in B. burgdorferi.

16 B. burgdorferi CA-11.2A cp32 was capable of autonomous replication in both high-passage B. burgdorfe

17 in of hepatitis C virus (HCV) are capable of autonomous replication in cultured Huh7 cells.

18 t from IncP-9 plasmid pM3 was sufficient for autonomous replication in Pseudomonas putida but not in

19 atives of the plasmid prD1 failed to support autonomous replication in Tetrahymena.

20 ly replicating sequence elements that permit autonomous replication in the promoter region of this ge

21 ability of oriC plasmids to maintain stable autonomous replication in wild type and MtrA-overproduci

22 encing and mapping of elements which support autonomous replication in yeast.

23 The target-triggered isothermal autonomous replication/nicking process on the modified t

24 e amplified detection of a target DNA by the autonomous replication of a nucleic acid reporter unit t

25 In an attempt to mimic the apparently autonomous replication of extrachromosomal DNA in the ch

26 rdant resistance (P = 0.007), reflecting the autonomous replication of HIV and the independent evolut

27 he function of the origin, as judged by both autonomous replication of plasmids during T4 infection a

28 We suggest that autonomous replication of SMCs may be essential for norm

29 were also observed in Huh7 cells supporting autonomous replication of subgenomic GBV-B RNAs.

30 in 293 cells, presumably because rescue and autonomous replication of the AAV genome from these plas

31 ies revealed that (i) a low-level rescue and autonomous replication of the wild-type AAV genome occur

32 expression from recombinant AAV but also to autonomous replication of the wild-type AAV genome.

33 ed and 80% contained consensus sequences for autonomous replication origins that could explain their

34 could maintain plasmids containing the yeast autonomous replication sequence replication element but

35 units of RNA polymerases I, II or III or an autonomous replication sequence were independently purif

36 Escherichia coli and was characterized as an autonomous replication sequence, ars.

37 The latter contain an autonomous replication sequence, suggesting that DNA rep

38 e the replication efficiency of a variety of autonomous replication sequences (ARSs) in the presence

39 nic region functioned as oriC, i.e., allowed autonomous replication to otherwise nonreplicative plasm

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