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1 nt transcription factor gene families in the plant kingdom.
2 d distribution of RSH gene expression in the plant kingdom.
3 cular evolution of this lectin family in the plant kingdom.
4 ated by the absence of this vitamin from the plant kingdom.
5 GIP-like genes are widely distributed in the plant kingdom.
6 T, C, or G) methylation and is unique to the plant kingdom.
7 processes they regulate, are specific to the plant kingdom.
8 logs of this gene are present throughout the plant kingdom.
9 d algae; they appear to be ubiquitous in the plant kingdom.
10 fforts to harness the chemical wealth of the plant kingdom.
11 es representing most of the divisions of the plant kingdom.
12 r geometric patterns observed throughout the plant kingdom.
13 ed transcription are highly conserved in the plant kingdom.
14 functions in oxidative stress sensing in the plant kingdom.
15 and that appears to function broadly in the plant kingdom.
16 reproduction strategy axes is general in the plant kingdom.
17 ects a conserved, universal mechanism in the plant kingdom.
18 se (TGS1), previously uncharacterized in the plant kingdom.
19 y, comprises the smallest angiosperms in the plant kingdom.
20 heme enzymes, which might also apply to the plant kingdom.
21 n the evolution of chemical diversity in the plant kingdom.
22 t is not widely distributed elsewhere in the plant kingdom.
23 ogical importance of gene positioning in the plant kingdom.
24 transcription factors (TF) ubiquitous in the plant kingdom.
25 ted by CYP79s is a general phenomenon in the plant kingdom.
26 , but is absent in the algae and outside the plant kingdom.
27 ologues, ubiquitously distributed throughout plant kingdom.
28 s in regulating programmed cell death in the plant kingdom.
29 TFIIB gene family has been conducted in the plant kingdom.
30 t of cyclotide-encoding sequences within the plant kingdom.
31 f and domain structure within and across the plant kingdom.
32 subfamilies that are present throughout the plant kingdom.
33 examples of convergent evolution across the plant kingdom.
34 ivities will also vary widely throughout the plant kingdom.
35 0.1 s is one of the fastest movements in the plant kingdom.
36 plant species representing major branches of plant kingdom.
37 BA biosynthesis pathway among members of the plant kingdom.
38 ent gap in studies of TF families across the plant kingdom.
39 a void in studies of TF families across the plant kingdom.
40 did not have introns, perhaps outside of the plant kingdom.
41 complex developmental strategies within the plant kingdom.
42 ts a ubiquitous adaptive response within the plant kingdom.
43 EGases, with members present throughout the plant kingdom.
44 ctural diversity of triterpenoids across the plant kingdom.
45 s, there are other classes restricted to the plant kingdom.
46 tails of their structure and function in the plant kingdom.
47 ine-rich glycoproteins, occur throughout the plant kingdom.
48 tive pressure appears to be conserved in the plant kingdom.
49 teoglycans and are widely distributed in the plant kingdom.
50 of 7TM receptor action also functions in the plant kingdom.
51 nance is highly conserved in both animal and plant kingdoms.
52 rol synthesis across the fungal, animal, and plant kingdoms.
53 hen acquired independently in the animal and plant kingdoms.
54 sory behaviors in the bacterial, fungal, and plant kingdoms.
55 y responses across the bacterial, fungal and plant kingdoms.
56 ibute to the chemical diversity found in the plant kingdom, (2) genes encoding biochemical pathway co
57 f identified miRNAs for other species in the plant kingdom, a large number of potential miRNAs remain
58 ly and functionally conserved throughout the plant kingdom and emerge as key actors in the specificat
59 tic strategies are widely distributed in the plant kingdom and frequently involve coupling parasite o
60 tion of viral sequences is widespread in the plant kingdom and has been occurring for a long period o
62 he most abundant and diverse families in the plant kingdom and its unique developmental patterns have
63 m HHPred to search for TFIIB homologs in the plant kingdom and performed a comprehensive analysis of
66 data identify the first KASH members in the plant kingdom and provide a novel function of SUN-KASH c
67 ling ATPases are conserved in the animal and plant kingdom and regulate transcriptional programs in r
68 e PG activity and H2O2 are widespread in the plant kingdom and that the response may be associated wi
69 ibution of volatile aldoximes throughout the plant kingdom and the presence of CYP79 genes in all seq
70 wide distribution of these sequences in the plant kingdom and their prevalence in the Arabidopsis an
71 and architecture vary greatly throughout the plant kingdom, and even within an individual plant durin
72 he presence of members of this family in the plant kingdom, and investigate the two Arabidopsis SUN-d
73 ne pathways are extremely diverse across the plant kingdom, and most specialized diterpenes are taxon
74 re enriched in ELIP promoters throughout the plant kingdom, and showed a clade-specific pattern of ga
75 rhizal fungi is almost ubiquitous within the plant kingdom, and the early stages of the association a
76 of chloroplast signaling is conserved in the plant kingdom, and the plant protein has evolved enhance
77 hosphate groups, occur throughout animal and plant kingdoms, and are synthesized by a recently cloned
78 mong the most compositionally variant in the plant kingdom, arise from specialized fatty acid biosynt
79 to hsp90 via TPR domains is conserved in the plant kingdom as well as in the animal kingdom and that
81 2/WDL family are found widely throughout the plant kingdom, but are not similar to non-plant proteins
83 ands of such terpenes have been found in the plant kingdom, but each species is capable of synthesizi
85 tative Vapyrin orthologs exist widely in the plant kingdom, but not in Arabidopsis, or in non-plant s
86 terpenoid phytoalexins occur throughout the plant kingdom, but until recently were not known constit
87 s sequences were identified from outside the plant kingdom, but weak sequence similarity was found be
88 opment and physiology in both the animal and plant kingdoms, but little is known concerning mechanism
89 e detected selenoproteins in a member of the plant kingdom, Chlamydomonas reinhardtii, and directly i
90 ellular homologues throughout the animal and plant kingdoms contain a conserved DNA binding domain.
92 tural, load-bearing role of cellulose in the plant kingdom, countless efforts have been devoted to de
93 tion of trxG function between the animal and plant kingdoms despite the different structural nature o
94 as well as non-secreted peptides outside the plant kingdom (e.g., the alpha-amanitin toxin gene famil
97 cal diversity and catalytic potential in the plant kingdom for human uses, but this effort is often e
98 a plant-specific domain found throughout the plant kingdom from the alga Chlamydomonas to grasses and
99 abundance of wall structures present in the plant kingdom gives hope that this challenge can be met.
102 mpatibility expands between the metazoan and plant kingdoms, illustrating striking conservation of th
103 ent, leaf shape is highly diverse across the plant kingdom, implying that patterning of growth must b
104 yzed a variety of kinesin sequences from the plant kingdom including 12 from Zea mays and 29 from Ara
105 tabolites that are widely distributed in the plant kingdom, including many plants that are commonly c
106 despite the wide distribution of PC-8 in the plant kingdom, including species consumed by humans.
107 , which is widely distributed throughout the plant kingdom, is a significant component of many floral
108 We identified two NRH subclasses in the plant kingdom; one preferentially targets the purine rib
109 patterns of genic DNA methylation across the plant kingdom or about the evolutionary processes that s
110 of these enzymes, their distribution in the plant kingdom, or the mechanisms by which they act in th
113 lation of LS Rubisco is not universal in the plant kingdom, suggesting a species-specific protein sub
114 one of these clones had homologs outside the plant kingdom, suggesting that most Arabidopsis ncRNAs a
115 unique to nonepsilon 14-3-3 isoforms of the plant kingdom, suggesting that this region constitutes a
116 vation of the 110-kD PETs polyprotein in the plant kingdom suggests that PSRP-7 and EF-Ts function to
117 ns of the FT/TFL1 gene family throughout the plant kingdom, summarize new findings regarding the uniq
118 ridophyta) are very important members of the plant kingdom that lag behind other taxa with regards to
119 group of proteins widely distributed in the plant kingdom that participate in the tolerance to water
120 Ds has been shown to transpose widely in the plant kingdom, the activation vector system developed in
121 and abundance of this protein family in the plant kingdom, the biochemical function remains largely
123 ents at all timescales, from the base of the plant kingdom, to intraspecific or hybridization events
125 ranscript assemblies from 184 species in the plant kingdom, we have identified a set of 861 rice gene
126 l as in green algae; homologs outside of the plant kingdom were identified as members of the MARVEL p
127 ay, this endosymbiosis occurs broadly in the plant kingdom where it has a pronounced impact on plant
128 ase inhibitors are widespread throughout the plant kingdom where they play an important role in prote
129 protein-based surface defense system in the plant kingdom, wherein protein biosynthesis in short, pr
130 lulose synthases are highly conserved in the plant kingdom with five gene family members in maize and
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