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 ition are correlated across lines, revealing concerted evolution.
2 pidly between species, a phenomenon known as concerted evolution.
3 icate transcription as a driver of rRNA gene concerted evolution.
4 ccur as tandem arrays and are homogenised by concerted evolution.
5  this basis are predicted to undergo reduced concerted evolution.
6 rRNA gene families have become a paradigm of concerted evolution.
7  provide a tool to investigate mechanisms of concerted evolution.
8 ination by the recombinational mechanisms of concerted evolution.
9 meologue, possibly resulting from interlocus concerted evolution.
10 dent evolution of duplicated genes is called concerted evolution.
11  process of duplicated regions that involves concerted evolution.
12 hown to evolve neutrally and be subjected to concerted evolution.
13 ed repeats and the nad9 genes are undergoing concerted evolution.
14 strong intrastrain similarity, indicative of concerted evolution.
15 mined that the repeat regions have undergone concerted evolution.
16 balance between amino acid substitutions and concerted evolution.
17 mosomes that may account for this pattern of concerted evolution.
18 h cascades have been subjected to a long and concerted evolution.
19 ter-locus recombination, gene conversion, or concerted evolution.
20 f the flagelliform gene underwent intragenic concerted evolution.
21 a tandemly repeated sequence that evolves by concerted evolution.
22 ined in each nucleus signals a relaxation of concerted evolution, a recombination-driven process that
23                              The duration of concerted evolution after gene duplication is highly var
24 sovers lead to repeat homogenization through concerted evolution, although the degree of unequal cros
25     VERL repeats 3-22 have been subjected to concerted evolution and consequently have almost identic
26 We discuss the definition and description of concerted evolution and describe whether incomplete conc
27     Moreover, the gene cluster has undergone concerted evolution and homogenization within primates.
28  cycles in order to determine the effects of concerted evolution and sexual reproduction upon the div
29                     We estimated the rate of concerted evolution and the degree of sequence homogeniz
30          The average length of the period of concerted evolution and the gene conversion rate are est
31 positive correlation between the duration of concerted evolution and the gene expression level.
32 hod is developed to estimate the duration of concerted evolution and the time to the whole-genome dup
33 rrays is influenced by intra- and interlocus concerted evolution and their expression is characterize
34 evel of genetic activity required to sustain concerted evolution, and propose a model to explain why
35 unction, alpha-satellite is also a model for concerted evolution, as alpha-satellite repeats are more
36 ese families is quite different from that of concerted evolution but is in agreement with the birth-a
37 uplicated gene pairs) exhibit no evidence of concerted evolution, but instead appear to evolve indepe
38 e internal transcribed spacers (ITS) exhibit concerted evolution by the fast homogenization of these
39 n of the Drosophila dumpy gene is undergoing concerted evolution by the process of unequal crossing o
40 roteins by positive selection are known, and concerted evolution can influence the differentiation of
41 nserved amino acid repeat structure promotes concerted evolution due to the high probability of misre
42 he current models to explain this process of concerted evolution, emphasizing early studies of recomb
43 onomic families, indicating that independent concerted evolution events have homogenized different mo
44                              The models with concerted evolution fit the data significantly better th
45 ormation, thereby indicating that interlocus concerted evolution has not been an important factor in
46 ndings with the fossil record indicates that concerted evolution has occurred since Bos/ Bison and Sy
47 isting phylogenetic trees and indicate where concerted evolution has taken place.
48 dition, we find that purifying selection and concerted evolution have acted to conserve Aliatypus spi
49                We show that the processes of concerted evolution have been operating on all species o
50 dicates that cellular processes underpinning concerted evolution have homogenized populations and spe
51                    In addition, processes of concerted evolution have radically altered the codon usa
52 ation results demonstrate that the length of concerted evolution (i.e., phase II) is highly variable,
53             Here, we studied the dynamics of concerted evolution in 85 individuals of seven plant spe
54 ore of the same product, which could enhance concerted evolution in dosage-sensitive genes.
55 e is a limiting factor in the observation of concerted evolution in some pairwise comparisons.
56                          The higher level of concerted evolution in the 5-7 MY-old segmental duplicat
57                                              Concerted evolution in the egg receptor could explain th
58  We also examine the prevalence and scale of concerted evolution in the histone and Stellate clusters
59 than 35 million years ago and are subject to concerted evolution in the long term.
60 quivocally demonstrates the pervasiveness of concerted evolution in the rrn gene family.
61  for polyploid samples, indicating a lack of concerted evolution in these taxa.
62 two subgenera, suggesting different rates of concerted evolution in two subgenera which could be attr
63 riants was largely consistent with models of concerted evolution in which there is uniform recombinat
64 igene families were thought to be subject to concerted evolution, in which all member genes of a fami
65  when it is based on the molecular clock but concerted evolution is common.
66                                              Concerted evolution is normally used to describe paralle
67                                              Concerted evolution is often invoked to explain the dive
68  rRNA sequences supports the hypothesis that concerted evolution is reduced when copies of a gene are
69                                  Remarkably, concerted evolution is so well orchestrated that even tr
70                                However, some concerted evolution is suggested by clustering of rDNA s
71 apid evolutionary change between species and concerted evolution leading to molecular homogeneity wit
72                                              Concerted evolution maintains at near identity the hundr
73                                              Concerted evolution makes one duplicated chromosomal seg
74  and propose that, as in the abalone system, concerted evolution may be involved in adaptive changes
75 e duplication (WGD) or retroposition under a concerted evolution mode, plant CRP genes evolved primar
76                             The way in which concerted evolution occurred appears to be determined by
77 s of unequal crossing-over, altering the way concerted evolution occurs.
78                   This revealed evidence for concerted evolution of all three cytoplasmic domains wit
79                                              Concerted evolution of different regulatory mechanisms f
80 al dispersal and highlight the potential for concerted evolution of dispersal and animal personality
81 GC plays in various genetic diseases and the concerted evolution of gene families, the parameters tha
82 tion of the translation apparatus, including concerted evolution of Gln-tRNA synthetase and Glu-tRNAG
83 h recombination and breakpoint repair, while concerted evolution of IR1 is driven by gene conversion
84                                          The concerted evolution of morphological and behavioral spec
85 ation of molecular mechanisms that cause the concerted evolution of multigene families such as rDNA.
86                   We propose a model for the concerted evolution of opsin genes and the elaboration o
87                                  Evidence of concerted evolution of paralogous 2'-5' oligoadenylate s
88 me and different chromosomes, supporting the concerted evolution of rDNA units.
89 ed evolution and describe whether incomplete concerted evolution of rDNAs predominantly affects codin
90               These data suggest that in the concerted evolution of rRNA genes, homogenization is a c
91 bA/babB gene conversions likely underlie the concerted evolution of the 3' segments, in an experiment
92 oles of conversion interact to drive dynamic concerted evolution of the hsp70 genes.
93              Still, support for this idea of concerted evolution of the morphology of the lizard sens
94 ider whether these LTRs might play a role in concerted evolution of the primate RNU2 locus.
95                               The process of concerted evolution of the rDNA locus should give rise t
96 recombinational events that give rise to the concerted evolution of the rDNA locus.
97  sequence variation resulting from imperfect concerted evolution of the ribosomal DNA region follows
98 ation of RNU2 has remained unchanged despite concerted evolution of the tandem array.
99 e propose that the primary driving force for concerted evolution of the tandem U2 genes is intrachrom
100 iple theoretical studies have focused on the concerted evolution of the tandemly repeated rRNA genes
101                                         Thus concerted evolution of the U2 tandem array occurs in sit
102 ences is the product of the much more recent concerted evolution of this satellite DNA.
103                   These patterns support the concerted evolution of tRNA-binding sites in the two sub
104 higher in ITS2 than in ITS1, suggesting that concerted evolution operates more efficiently on the for
105    To determine whether these genes defy the concerted evolution paradigm, we examined the patterns o
106 ates that the molecular drive leading to the concerted-evolution pattern of this satellite DNA is a t
107 may maintain similarities with each other by concerted evolution, possibly involving gene conversion-
108 ive units within species suggests intragenic concerted evolution, presumably through gene conversion
109 tified an additional seven families in which concerted evolution probably occurs.
110 ufogriseus is likely due to duplications and concerted evolution rather than a high number of indepen
111 cross species reveal the strong influence of concerted evolution, resulting in intragenic homogenizat
112 ith a previous observation of the interlocus concerted evolution (sequences corresponding to A and D
113  red abalone VERL have not been subjected to concerted evolution since the divergence of the red spec
114 l DNA (rDNA) repeats evolve together through concerted evolution, some genomes contain a considerable
115                       The classical model of concerted evolution states that hundreds to thousands of
116                                       Unlike concerted evolution, the model of birth-and-death evolut
117 cus) of arthropods, a locus known to undergo concerted evolution, the recombinational processes that
118                      We investigated whether concerted evolution through conversion and crossing over
119  five chromosome pairs and is homogenized by concerted evolution through recombination and gene conve
120  epigenetic phenomena influencing incomplete concerted evolution, to give a comprehensive understandi
121 ar clock model, indicating a crucial role of concerted evolution via gene conversion after gene dupli
122    This difference is explained by extensive concerted evolution via gene conversion between duplicat
123 ns, two gene families that appear to undergo concerted evolution were studied in detail.
124 d nonribosomal peptide synthetases evolve by concerted evolution, which generates sets of sequence-ho
125 believed that this gene family is subject to concerted evolution, which homogenizes the member genes
126 d some ampliconic genes exhibit evidence for concerted evolution with the acquisition and purging of
127 se members possess a single dsRBM that shows concerted evolution with the most C-terminal dsRBM domai
128 at the two orthologous t-unit arrays undergo concerted evolution within each taxa and are likely fluc

 
Page Top