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  sigma, are evident in both intragenomic and intergenomic analyses of rice and sorghum.
2 s the following analytical capabilities: (i) intergenomic and intragenomic comparative analysis of ex
3 Conjugative plasmids are typically locked in intergenomic and sexual conflicts with co-resident rival
4                             Additionally, an intergenomic approach to investigating the mechanical pr
5  plant biology that do not account for these intergenomic associations are incomplete.
6 the requisite genetic variation required for intergenomic coevolution exists in the CYC-COX system in
7                                          The intergenomic coevolution of interacting gene products ha
8                                              Intergenomic comparison found marked differences in cyto
9                                              Intergenomic comparisons identified lineage-specific gen
10 PCR), allows both intragenomic profiling and intergenomic comparisons of cytosine methylation.
11 of qTeller now supports multiple genomes for intergenomic comparisons, and includes capabilities for
12 vel variation in developmental rate and that intergenomic compatibility is critical for high fitness.
13                                              Intergenomic conflict can affect the distribution of gen
14 tic processes, and all the opportunities for intergenomic conflict that arise due to divergence in in
15 ordinates expression of enzymes that require intergenomic control.
16                                          The intergenomic dependency between the two variants may con
17 in the assembled linkage map with an average intergenomic distance of 7.5 cM.
18 f orthologous proteins, matrices of pairwise intergenomic distances based on genome-wide analysis of
19 iana populations, which revealed much higher intergenomic diversity than for the considerably more un
20  investment arises from a complex intra- and intergenomic duel.
21 e proportion of these individuals depends on intergenomic epistasis between larvae and nursing adults
22                     Our results suggest that intergenomic epistasis can be the proximate mechanism fo
23 , we examine the structure and mechanisms of intergenomic epistasis in the Paramecium-Chlorella symbi
24 pled with metabolomics, we show evidence for intergenomic epistasis wherein low fitness is associated
25                                   Because of intergenomic epistasis, partner-switched symbioses may p
26 between subgenomes, gene conversion or other intergenomic exchanges that escaped detection by genetic
27 t allelic silencing may be a way to overcome intergenomic gene expression interaction conflicts, and
28                          Although intra- and intergenomic heterogeneities in crossover distribution h
29 ge of allopolyploidy through the fixation of intergenomic heterozygosity.
30                            Models to explain intergenomic incompatibilities incorporate both genetic
31 on of auto- and allopolyploids suggests that intergenomic incompatibilities play the major role.
32          Using a co-GWA approach, devil-DFTD intergenomic interactions explained ~3x more variation i
33                         The possibility that intergenomic interactions govern hybrid vigor through ep
34 nitor regulatory interactions from the novel intergenomic interactions that arise from genome merger
35 ur results highlight the need to account for intergenomic interactions when investigating host-pathog
36 y through the acquisition of new traits, new intergenomic interactions, and buffering of mutations, a
37 tative trait mapping approaches ignore these intergenomic interactions.
38 nding animal-microbe mutualism increased its intergenomic network without gaining any new genomes.
39 enes might be dependent on maternal-paternal intergenomic or interallelic interactions.
40 nomic recombination, manifested as extensive intergenomic phylogenetic conflict and patchily distribu
41 overlapping but distinct functions involving intergenomic (primarily DprB) and intragenomic (primaril
42 , MutS2 plays a significant role in limiting intergenomic recombination across a range of donor DNA t
43 iding statistically significant evidence for intergenomic recombination and acquisition of a genetic
44 iversity is generated by intragenomic and/or intergenomic recombination between sequence variants.
45                        Our results show that intergenomic recombination can occur in the structural r
46  results suggest a role for intragenomic and intergenomic recombination in regulating plant mitochond
47 upporting a role for horizontal transfer and intergenomic recombination in the evolution of emm genes
48 Y mutants did not show higher frequencies of intergenomic recombination or greater sensitivity to UV-
49 tween flaA genes of different strains (i.e., intergenomic recombination).
50 e genetic background of the input R5 SHIV by intergenomic recombination, creating an X4 virus with no
51 ons between DNA repeat sequences, as well as intergenomic recombination, facilitated by their natural
52 To study the spatiotemporal requirements for intergenomic recombination, we developed an assay with d
53 by the alien genome occurs in the absence of intergenomic recombination.
54 tation, deletion between direct repeats, and intergenomic recombination.
55  semiconserved loci, indicative of extensive intergenomic recombination.
56 uals, persistence over time, and evidence of intergenomic recombination.
57 alian transgene cassette is inserted into an intergenomic region.
58 nce for varying selection between intra- and intergenomic regions.
59                              Homophila is an intergenomic resource linking the human and fly genomes
60 uent folding to the final dimer state, these intergenomic RNA interactions convert to a high affinity
61 mouse model lacking both genes including the intergenomic sequence.
62                          Budding yeast have "intergenomic signaling" pathways that sense the amount o
63 g a robust model system to interrogate human intergenomic signaling.
64 -recapture data, and 960 genomes to identify intergenomic signatures of coevolution between devils an
65                              Construction of intergenomic symmetrical best matches (SymBets) and join
66 that originate in young polyploids (here, an intergenomic translocation) may become fixed in populati
67 nt fragments of maize chromosome 9 including intergenomic translocations and modified maize addition
68 lar karyotype; 76% of the individuals showed intergenomic translocations, and 69% were aneuploid for
69 coding sequences indicates that considerable intergenomic variation also occurs between microsporidia