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1 ts part of the tasks of their parental gene (subfunctionalization).
2 ed zebrafish genes that do not show temporal subfunctionalization.
3 tain the structural signature of splice form subfunctionalization.
4  forms among the duplicate genes - a form of subfunctionalization.
5 , higher transcript dosage, and evidence for subfunctionalization.
6 PE LIKE1 (GRL1), creating the possibility of subfunctionalization.
7 ed from ancient duplications associated with subfunctionalization.
8 s of certain roles in a process described as subfunctionalization.
9 nce of their promoter activities and protein subfunctionalization.
10  more instances of neofunctionalization than subfunctionalization.
11  in function through neofunctionalization or subfunctionalization.
12 of expression for gar genes, consistent with subfunctionalization.
13 nce of both overlapping redundancy and early subfunctionalization.
14  in a complementary fashion, perhaps driving subfunctionalization.
15 g silenced in other organs, suggesting rapid subfunctionalization.
16 ular localization are similar to cis-element subfunctionalization.
17 whole-genome duplication and, paradoxically, subfunctionalization after duplication can lead to relat
18     We describe the scope of transcriptional subfunctionalization and 15 cases of probable neofunctio
19 resulted in independent instances of paralog subfunctionalization and maintained functional redundanc
20               However, the relative roles of subfunctionalization and neofunctionalization in the ret
21  are modified by gene gain and loss, by gene subfunctionalization and neofunctionalization, and by ch
22 nctional specialization, with roles for both subfunctionalization and neofunctionalization.
23  CDY genes in simians spurred the process of subfunctionalization and possibly neofunctionalization.
24 tation, transposability of individual genes, subfunctionalization and/or fractionation of syntenic ge
25 tion compared to BZR1, hallmarks of neo- and subfunctionalization, and dynamic HSP90 client status ac
26  after duplication because they are prone to subfunctionalization, and gene complexity is regained vi
27 roles of conservation, neofunctionalization, subfunctionalization, and specialization in the preserva
28                                              Subfunctionalization appears to be a common phenomenon i
29                    Retargeting or regulatory subfunctionalization are common in the studied nucleus-e
30 , missing CNSs and a large insertion support subfunctionalization as a reflection of fractionation of
31  eudicot euAP1 and euFUL genes, we postulate subfunctionalization as the functional outcome after the
32 ng sequences of AUX/LAX genes have undergone subfunctionalization based on their distinct patterns of
33 nary novelties not based on gene duplication/subfunctionalization but by interactions in complex netw
34  preservation, increasing the probability of subfunctionalization but decreasing the probability of n
35 his paper, which could be termed subcellular subfunctionalization, complementary null mutations can o
36                               In cis-element subfunctionalization, complementary null mutations occur
37 ose that differential regulation and isoform subfunctionalization define starch-adaptive plasticity,
38 lication-Retention-Non/Neofunctionalization, subfunctionalization/duplication-degeneration-complement
39 k, likely reflecting the pathways of paralog subfunctionalization during evolution.
40                                 The multiple subfunctionalization events that have occurred in this s
41 that expression reduction, a special type of subfunctionalization, facilitates the retention of dupli
42 and MYB42 syntelogs appear to have undergone subfunctionalization following gene duplication and dive
43             Together, these data reveal that subfunctionalization following gene duplication may be i
44 onserved target genes, suggesting that their subfunctionalization has evolved primarily via diverse p
45 rts and that lineage specific expansions and subfunctionalization have fashioned regulatory proteins
46 allel duplications and subsequent convergent subfunctionalization have resulted in the segregation to
47  epigenetic modifications can drive neo- and subfunctionalization in evolution by gene duplication.
48 ted genes evolved separate functions through subfunctionalization in growth/development and stress re
49 3 lineage has undergone gene duplication and subfunctionalization in poppy, with one gene copy requir
50  and differential expression pattern suggest subfunctionalization in providing GGPP to specific tissu
51 ion may be related is through the process of subfunctionalization, in which an alternatively spliced
52             One consequence of polyploidy is subfunctionalization, in which the ancestral expression
53 tic pathways, partition ancestral functions (subfunctionalization) into divergent developmental modul
54                                           If subfunctionalization is common, one expects duplicate ge
55                                              Subfunctionalization is evidenced by the observation tha
56                                              Subfunctionalization is the process by which a pair of d
57 at functional divergence between duplicates (subfunctionalization) is caused by the loss of regulator
58 n gene duplication followed by co-option and subfunctionalization led to the emergence of globin fami
59 the complete function of the ancestral gene (subfunctionalization) may result in a requirement for bo
60 pulations, (ii) is quite consistent with the subfunctionalization model when degenerative but complem
61 and have provided evidence in support of the subfunctionalization model.
62 n-functionalization of one duplicate copy or subfunctionalization, neither of which yields novel func
63 including lineage-specific gene duplication, subfunctionalization, neofunctionalization and pseudogen
64                                  Relative to subfunctionalization, neofunctionalization is expected t
65 nd floral determinacy, unlike the pronounced subfunctionalization observed in Arabidopsis thaliana an
66 ization of 5AQ, pseudogenization of 5Bq, and subfunctionalization of 5Dq, all contributing to the dom
67                  These results might reflect subfunctionalization of a PcG protein during evolution.
68 ingle-stripe elements arose by splitting and subfunctionalization of ancestral dual-stripe elements.
69  can include neofunctionalization as well as subfunctionalization of ancestral functions.
70 zebrafish and use it to provide evidence for subfunctionalization of Aqp0a and b, as well as to show
71 me duplication, suggesting the potential for subfunctionalization of chromatin regulation of paralogs
72 ion in Populus is driven by a combination of subfunctionalization of duplicate pairs and purifying se
73 ts provide new insights into tissue-specific subfunctionalization of duplicated exons in vertebrate e
74  mechanisms that may underlie germ-line/soma subfunctionalization of duplicated genes, taking into ac
75  46 human and 26 mouse tissues indicate that subfunctionalization of expression evolves slowly and is
76  present two hepcidin types show a degree of subfunctionalization of its functions, with hamp1 more i
77  system for studying neofunctionalization or subfunctionalization of talin following the vertebrate t
78                              We also noticed subfunctionalization of the four Arabidopsis A1-type HSF
79  Schizosaccharomyces lineage may have led to subfunctionalization of the Mid1 orthologs.
80                               Therefore, the subfunctionalization of the O. tauri enzyme was differen
81                 From this analysis, we found subfunctionalization of the receptors in the control of
82 starch-related gene families and resulted in subfunctionalization of the respective gene products.
83                      This study affirms that subfunctionalization of the transcriptional regulatory e
84 d the recently proposed alternatives such as subfunctionalization or duplication-degeneration-complem
85 ns, altered tissue expression, and potential subfunctionalization or neofunctionalization of HYDIN2 e
86 ifferential division of ancestral functions (subfunctionalization) or emergence of novel functions (n
87  evolve by gene duplication, divergence, and subfunctionalization" parallel to models for the evoluti
88 en together, our results are consistent with subfunctionalization partitioning alternatively spliced
89 cal description of a system with alternative subfunctionalization paths.
90 evolutionary outcomes by independent neo- or subfunctionalization processes during the evolution of t
91                             In contrast, the subfunctionalization (SF) hypothesis argues that duplica
92 popular models include neofunctionalization, subfunctionalization (SUBF) by degenerative mutations, a
93  non-coding sequences, false positive noise, subfunctionalization, synteny, annotation errors, invers
94 ication, which can be accomplished by either subfunctionalization (the partitioning of ancestral func
95 e become temporally restricted under partial subfunctionalization to particular stages of floret deve
96 volved through gene duplication, followed by subfunctionalization to specialize in repairing the nucl
97  hypothesis that the evolutionary process of subfunctionalization was responsible for the preservatio
98  gene duplicates are frequently preserved by subfunctionalization, whereby both members of a pair exp
99 eviously, it has been shown that splice form subfunctionalization will result in duplicate pairs with
100              PSY gene duplication has led to subfunctionalization, with each paralog exhibiting diffe

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