ライフサイエンスコーパス: plant DNA

コーパス検索結果 (１語後でソート)

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1 in a sample in comparison to the endogenous plant DNA.

2 o the cell nucleus and integrate it into the plant DNA.

3 C5DNA methyltransferase homologs in various plant DNAs.

4 Iron increases ferritin synthesis, targeting plant DNA and animal mRNA.

5 Using the plant DNA barcode markers rbcL and matK, we have assembl

6 Using plant DNA barcoding regions (trnL and rpoC) coupled with

7 s a protein with similarity to mammalian and plant DNA binding proteins.

8 Currently, the Plant DNA C-values database (Release 6.0, Dec. 2012) con

9 Currently, the Plant DNA C-values database contains data for 8510 speci

10 e been recently updated and/or extended: the Plant DNA C-values database, and GSAD, the Genome Size i

11 In plants, DNA damage accumulated in the embryo of seeds is

12 However, it is unclear whether plant DNA demethylases can promote the transposition of

13 d a copy of hsp26 (marked with a fragment of plant DNA designated pt), we have identified domains tha

14 ation, they may function in the recycling of plant DNA during late stages of PCD when the integrity o

15 r an entire guild of insect herbivores using plant DNA extracted from insect gut contents.

16 Plant DNA flanking the insertion site was cloned and use

17 cing technologies now permit the analyses of plant DNA from fossil samples (ancient plant DNA, plant

18 po and pattern of mitochondrial gene loss in plants, DNAs from 280 genera of flowering plants were su

19 ant beta-tubulin gene family as a target for plant DNA identification.

20 nt dynamic interplay between geminivirus and plant DNA in evolution.

21 in the Arabidopsis genome by analyzing T-DNA/plant DNA junctions generated under non-selective condit

22 In plants, DNA methylation patterns are faithfully inherite

23 In plants, DNA methylation, histone modifications, and RNA

24 raveling complex sugar signaling networks in plants, DNA microarray analysis was used to determine th

25 es of plant DNA from fossil samples (ancient plant DNA, plant aDNA), and thus enable the molecular re

26 pe RFP sequence, implying the involvement of plant DNA repair machinery.

27 ng plants will be useful tools in dissecting plant DNA repair processes.

28 ess, established a specific role for TAF1 in plant DNA repair processes.

29 Plant DNA-repair machinery predominantly uses non-homolo

30 In fbl17 mutant plants, DNA replication is severely impaired and endorep

31 The sensor was tested using real animal and plant DNA samples in which the hydrolysis of T and C cou

32 The resulting transgenic locus may have plant DNA separating the transgenic sequences.

33 In a sample of 40 G. tabacina plants, DNA sequence variation at one homoeologous histo

34 However, plant DNA sequences that encode proteins with similarity

35 ctors (ZFP TFs) that minimize the use of non-plant DNA sequences.

36 effects' by, or 'readthrough' from, flanking plant DNA sequences.

37 See1 is required for the reactivation of plant DNA synthesis, which is crucial for tumor progress

38 In this study, a plant DNA virus was used to explore the constraints impo

39 substitution rates, the first reported for a plant DNA virus, are in line with those estimated previo

40 The plant DNA viruses also exhibit diversity, but the source

41 In this article, features of plant DNA viruses are discussed in relation to gene sile

42 explanation for why relatively few types of plant DNA viruses have evolved: they would have had to o

43 Plant DNA viruses-- both the ssDNA geminiviruses and the

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