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1 oteins (PGIPs) are widely distributed in the plant kingdom.
2 e for a ubiquitous class of receptors in the plant kingdom.
3  complex developmental strategies within the plant kingdom.
4 ts a ubiquitous adaptive response within the plant kingdom.
5  EGases, with members present throughout the plant kingdom.
6 s, there are other classes restricted to the plant kingdom.
7 tails of their structure and function in the plant kingdom.
8 ine-rich glycoproteins, occur throughout the plant kingdom.
9 tive pressure appears to be conserved in the plant kingdom.
10 tannins (HTs), are widely distributed in the plant kingdom.
11 teoglycans and are widely distributed in the plant kingdom.
12 of 7TM receptor action also functions in the plant kingdom.
13 nt transcription factor gene families in the plant kingdom.
14 d distribution of RSH gene expression in the plant kingdom.
15 cular evolution of this lectin family in the plant kingdom.
16 ated by the absence of this vitamin from the plant kingdom.
17 GIP-like genes are widely distributed in the plant kingdom.
18 T, C, or G) methylation and is unique to the plant kingdom.
19 processes they regulate, are specific to the plant kingdom.
20  greatest repositories of information on the plant kingdom.
21 logs of this gene are present throughout the plant kingdom.
22 d algae; they appear to be ubiquitous in the plant kingdom.
23 es representing most of the divisions of the plant kingdom.
24 r geometric patterns observed throughout the plant kingdom.
25 ed transcription are highly conserved in the plant kingdom.
26 ar content and are widely distributed in the plant kingdom.
27 urated sequences collected across the entire plant kingdom.
28 Eukaryota but with a special emphasis on the plant kingdom.
29 e abiotic and biotic stress responses in the plant kingdom.
30 the broad existence of this mechanism in the plant kingdom.
31 re conserved among VRN5 orthologs across the plant kingdom.
32  rice, Arabidopsis, and other species in the plant kingdom.
33 n insects, some helminths and throughout the plant kingdom.
34 n and underlying enzymatic mechanisms in the plant kingdom.
35  of eukaryotic translational fidelity in the plant kingdom.
36 ion similarly to their homologues across the plant kingdom.
37 gulate growth and development throughout the plant kingdom.
38 ns are heterosides widely distributed in the plant kingdom.
39 bacteria, they remain uncharacterized in the plant kingdom.
40 ic bacteria that can infect hosts across the plant kingdom.
41  vast array of triterpenoid diversity in the plant kingdom.
42  produces the largest floating leaves in the plant kingdom.
43 out its macroecological variation across the plant kingdom.
44 ction as iron sensors that are unique to the plant kingdom.
45 y manipulation by plant pathogens across the plant kingdom.
46 utes to the acylation of flavan-3-ols in the plant kingdom.
47 ny physical and chemical defenses across the plant kingdom.
48 s of which exist across multiple taxa in the plant kingdom.
49 is arose independently numerous times in the plant kingdom.
50  of tandem kinase proteins (TKPs) across the plant kingdom.
51 scaffold modifications are widespread in the plant kingdom.
52  by selfish elements for survival within the plant kingdom.
53 se (TGS1), previously uncharacterized in the plant kingdom.
54 e presence of numerous DP subfamilies in the plant kingdom.
55 transcription factors (TF) ubiquitous in the plant kingdom.
56 ologues, ubiquitously distributed throughout plant kingdom.
57  examples of convergent evolution across the plant kingdom.
58 ctural diversity of triterpenoids across the plant kingdom.
59 fforts to harness the chemical wealth of the plant kingdom.
60 functions in oxidative stress sensing in the plant kingdom.
61  and that appears to function broadly in the plant kingdom.
62 reproduction strategy axes is general in the plant kingdom.
63 ects a conserved, universal mechanism in the plant kingdom.
64 y, comprises the smallest angiosperms in the plant kingdom.
65  heme enzymes, which might also apply to the plant kingdom.
66 n the evolution of chemical diversity in the plant kingdom.
67 t is not widely distributed elsewhere in the plant kingdom.
68 ogical importance of gene positioning in the plant kingdom.
69 ost successful adaptations to drought in the plant kingdom.
70 ted by CYP79s is a general phenomenon in the plant kingdom.
71 , but is absent in the algae and outside the plant kingdom.
72 s in regulating programmed cell death in the plant kingdom.
73  TFIIB gene family has been conducted in the plant kingdom.
74 t of cyclotide-encoding sequences within the plant kingdom.
75 f and domain structure within and across the plant kingdom.
76  subfamilies that are present throughout the plant kingdom.
77 ivities will also vary widely throughout the plant kingdom.
78 veys for comparable reactions throughout the plant kingdom.
79 0.1 s is one of the fastest movements in the plant kingdom.
80 plant species representing major branches of plant kingdom.
81 BA biosynthesis pathway among members of the plant kingdom.
82 ent gap in studies of TF families across the plant kingdom.
83  a void in studies of TF families across the plant kingdom.
84 did not have introns, perhaps outside of the plant kingdom.
85 hen acquired independently in the animal and plant kingdoms.
86 sory behaviors in the bacterial, fungal, and plant kingdoms.
87 y responses across the bacterial, fungal and plant kingdoms.
88 nance is highly conserved in both animal and plant kingdoms.
89 hanisms are conserved through the animal and plant kingdoms.
90 hanosensitive ion channels across animal and plant kingdoms.
91 ted functions across the animal, fungal, and plant kingdoms.
92  cell diversification in both the animal and plant kingdoms.
93 ion pathways is essential in both animal and plant kingdoms.
94 rol synthesis across the fungal, animal, and plant kingdoms.
95 ibute to the chemical diversity found in the plant kingdom, (2) genes encoding biochemical pathway co
96 red their investigation, particularly in the plant kingdom [3-5].
97 f identified miRNAs for other species in the plant kingdom, a large number of potential miRNAs remain
98  have shown that TRB proteins evolved in the plant kingdom after the transition to a terrestrial habi
99 hat aldoxime production occurs widely in the plant kingdom, aldoxime-derived auxin biosynthesis is li
100  reproductive systems can be observed in the plant kingdom and applied in crop breeding; however, the
101  patterns of replicated evolution across the plant kingdom and discuss the processes responsible for
102 ly and functionally conserved throughout the plant kingdom and emerge as key actors in the specificat
103 ed that the CSLC genes are widespread in the plant kingdom and evolved from an ancient family.
104 tic strategies are widely distributed in the plant kingdom and frequently involve coupling parasite o
105 tion of viral sequences is widespread in the plant kingdom and has been occurring for a long period o
106 ng E3 ligases have massively expanded in the plant kingdom and have diversified into plant U-box prot
107 mannose units have been found throughout the plant kingdom and have numerous industrial applications.
108 n glycans than alpha-Gal or glycans from the plant kingdom and insects of importance in allergy.
109 o one of the fastest radiating clades in the plant kingdom and is characterized by the repeated evolu
110 t TA is discovered for the first time in the plant kingdom and is shown to be valuable to improve tan
111 he most abundant and diverse families in the plant kingdom and its unique developmental patterns have
112 m HHPred to search for TFIIB homologs in the plant kingdom and performed a comprehensive analysis of
113 e of an sn-2 G3P acyltransferase outside the plant kingdom and PlsB2 the first example of a 2-acyl-G3
114       Polyploidy is remarkably common in the plant kingdom and polyploidization is a major driving fo
115  are bioactive polyphenols widespread in the plant kingdom and present in the human diet.
116  data identify the first KASH members in the plant kingdom and provide a novel function of SUN-KASH c
117 ling ATPases are conserved in the animal and plant kingdom and regulate transcriptional programs in r
118 iscovery of telomerase RNA components in the plant kingdom and some algae groups revealed new insight
119 e PG activity and H2O2 are widespread in the plant kingdom and that the response may be associated wi
120 ibution of volatile aldoximes throughout the plant kingdom and the presence of CYP79 genes in all seq
121  wide distribution of these sequences in the plant kingdom and their prevalence in the Arabidopsis an
122 and architecture vary greatly throughout the plant kingdom, and even within an individual plant durin
123 he presence of members of this family in the plant kingdom, and investigate the two Arabidopsis SUN-d
124 ne pathways are extremely diverse across the plant kingdom, and most specialized diterpenes are taxon
125  can help to predict invasiveness across the plant kingdom, and should guide international policy on
126 re enriched in ELIP promoters throughout the plant kingdom, and showed a clade-specific pattern of ga
127 rhizal fungi is almost ubiquitous within the plant kingdom, and the early stages of the association a
128 of chloroplast signaling is conserved in the plant kingdom, and the plant protein has evolved enhance
129 hosphate groups, occur throughout animal and plant kingdoms, and are synthesized by a recently cloned
130 mong the most compositionally variant in the plant kingdom, arise from specialized fatty acid biosynt
131 y, characterization, and distribution in the plant kingdom as well as a detailed analysis of their se
132 to hsp90 via TPR domains is conserved in the plant kingdom as well as in the animal kingdom and that
133  with one of the most rapid movements in the plant kingdom, as described by Darwin.
134 nstrate that BXDs independently arose in the plant kingdom at least three times.
135         As one of the great survivors of the plant kingdom, barnyard grasses (Echinochloa spp.) are t
136       Despite their wide distribution in the plant kingdom, biosynthesis of only a small subset of th
137                                   Across the plant kingdom, biosynthesis of such defense compounds is
138                Rapid movement is rare in the plant kingdom, but a prerequisite for ballistic seed dis
139 2/WDL family are found widely throughout the plant kingdom, but are not similar to non-plant proteins
140 ng pathways diversified independently in the plant kingdom, but documented examples are rare.
141 ands of such terpenes have been found in the plant kingdom, but each species is capable of synthesizi
142         This phenomenon is widespread in the plant kingdom, but has not been studied at the molecular
143 tative Vapyrin orthologs exist widely in the plant kingdom, but not in Arabidopsis, or in non-plant s
144 e proteins, MDLs) are present throughout the plant kingdom, but remain experimentally unexplored in t
145  terpenoid phytoalexins occur throughout the plant kingdom, but until recently were not known constit
146 s sequences were identified from outside the plant kingdom, but weak sequence similarity was found be
147 opment and physiology in both the animal and plant kingdoms, but little is known concerning mechanism
148 fferent modes of gene duplication across the plant kingdom by comparing 141 genomes, which provides a
149 e detected selenoproteins in a member of the plant kingdom, Chlamydomonas reinhardtii, and directly i
150               Despite their abundance in the plant kingdom, chlorophyll catabolites have been overloo
151 f the most ancient cell wall polymers in the plant kingdom, consisting of beta-(1-4)-linked backbones
152 ellular homologues throughout the animal and plant kingdoms contain a conserved DNA binding domain.
153                                          The plant kingdom contains a stunning array of complex morph
154 lized metabolites is the main reason why the plant kingdom contains such a wide and rich array of div
155                                    While the plant kingdom continues to serve as an important source
156 f pigments because they are prevalent in the plant kingdom, contributing to colors over a wide range
157 tural, load-bearing role of cellulose in the plant kingdom, countless efforts have been devoted to de
158 tion of trxG function between the animal and plant kingdoms despite the different structural nature o
159 e cilia are widespread across the animal and plant kingdoms, displaying complex collective dynamics c
160 as well as non-secreted peptides outside the plant kingdom (e.g., the alpha-amanitin toxin gene famil
161                               Throughout the plant kingdom expression of the flavonoid biosynthetic p
162                                       In the plant kingdom, few genes encoding RING zinc-finger prote
163 cal diversity and catalytic potential in the plant kingdom for human uses, but this effort is often e
164 a plant-specific domain found throughout the plant kingdom from the alga Chlamydomonas to grasses and
165  abundance of wall structures present in the plant kingdom gives hope that this challenge can be met.
166                         Thus, hsp70 from the plant kingdom has conserved the ability to interact func
167         Many actin-binding proteins from the plant kingdom have been characterized and their function
168 ounds evolved and are distributed across the plant kingdom, hindering a systematic view and understan
169 mpatibility expands between the metazoan and plant kingdoms, illustrating striking conservation of th
170 ent, leaf shape is highly diverse across the plant kingdom, implying that patterning of growth must b
171 rowth is a ubiquitous process throughout the plant kingdom in which the cell elongates in a self-simi
172 yzed a variety of kinesin sequences from the plant kingdom including 12 from Zea mays and 29 from Ara
173 tabolites that are widely distributed in the plant kingdom, including many plants that are commonly c
174 despite the wide distribution of PC-8 in the plant kingdom, including species consumed by humans.
175 y defense responses that have evolved in the plant kingdom independent of EDS1.
176  review, we explore the extent of HGT in the plant kingdom, indicating the widespread occurrence of m
177 , which is widely distributed throughout the plant kingdom, is a significant component of many floral
178  secondary metabolites in species across the plant kingdom, most notably in the family Asteraceae.
179 oteins are well conserved between animal and plant kingdoms; nevertheless, because plant cells exhibi
180      We identified two NRH subclasses in the plant kingdom; one preferentially targets the purine rib
181 patterns of genic DNA methylation across the plant kingdom or about the evolutionary processes that s
182  of these enzymes, their distribution in the plant kingdom, or the mechanisms by which they act in th
183  arising from their relative scarcity in the plant kingdom, particularly in edible plants.
184 roles of the OsKAI2 signaling pathway in the plant kingdom, particularly in grasses.
185                                   Across the plant kingdom, phytochrome (PHY) photoreceptors play an
186              When viewed at the scale of the plant kingdom, plant genome evolution has been punctuate
187                                          The plant kingdom produces hundreds of thousands of low mole
188                                 Although the plant kingdom provides an enormous diversity of metaboli
189  pathogen and that NHP is present across the plant kingdom, raising the possibility that an engineeri
190 l to early diverging eukaryotes, such as the plant kingdom, remains unclear.
191 ticularly successful during evolution of the plant kingdom, representing a substantial proportion of
192 nding the phylogenomic scrutinization of the plant kingdom should reveal the full extent of HGT.
193 lation of LS Rubisco is not universal in the plant kingdom, suggesting a species-specific protein sub
194 one of these clones had homologs outside the plant kingdom, suggesting that most Arabidopsis ncRNAs a
195  unique to nonepsilon 14-3-3 isoforms of the plant kingdom, suggesting that this region constitutes a
196 vation of the 110-kD PETs polyprotein in the plant kingdom suggests that PSRP-7 and EF-Ts function to
197 ns of the FT/TFL1 gene family throughout the plant kingdom, summarize new findings regarding the uniq
198 ridophyta) are very important members of the plant kingdom that lag behind other taxa with regards to
199  group of proteins widely distributed in the plant kingdom that participate in the tolerance to water
200 Ds has been shown to transpose widely in the plant kingdom, the activation vector system developed in
201  and abundance of this protein family in the plant kingdom, the biochemical function remains largely
202 loring trait relationships across the entire plant kingdom, the dominant traits underpinning these un
203                                       In the plant kingdom, the maximum lifespans described for clona
204 pecies representative of major clades of the plant kingdom to enhance its generalizability.
205 from ancestral genes across the metazoan and plant kingdoms to establish multicellularity.
206 ents at all timescales, from the base of the plant kingdom, to intraspecific or hybridization events
207 s across the Tree of Life, especially in the plant kingdom, very few computational methods have been
208 rn ecosystems and the diversification of the Plant Kingdom, Viridiplantae, into over 374,000 describe
209                                   Within the plant kingdom W/SRC is a broadly used effector that conv
210 ranscript assemblies from 184 species in the plant kingdom, we have identified a set of 861 rice gene
211 l as in green algae; homologs outside of the plant kingdom were identified as members of the MARVEL p
212 ay, this endosymbiosis occurs broadly in the plant kingdom where it has a pronounced impact on plant
213 is essential in eukaryotes, not least in the plant kingdom where it plays key roles in cell expansion
214 ase inhibitors are widespread throughout the plant kingdom where they play an important role in prote
215  protein-based surface defense system in the plant kingdom, wherein protein biosynthesis in short, pr
216                           Here, we present a plant kingdom-wide sequence mining approach based on seq
217 lulose synthases are highly conserved in the plant kingdom with five gene family members in maize and
218                      It is widespread in the plant kingdom with important functions in development an
219 f specialized metabolites is produced in the plant kingdom, with each individual plant synthesizing t
220 domesticated diverse species from across the plant kingdom, yet much of our foundational knowledge of

 
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