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1 plast genome of members of the grass family (Poaceae).
2 lant families (Convolvulaceae, Fabaceae, and Poaceae).
3 aracteristic of monocots, including grasses (Poaceae).
4  and switchgrass (Panicum virgatum, monocot, Poaceae).
5 tems of 26 species, mainly European grasses (Poaceae).
6 the Pooideae sub-family of the grass family (Poaceae).
7 stemborer egg-laying in maize Zea mays (L.) (Poaceae).
8 onservation for this set of genes within the Poaceae.
9 onserved within, as well as specific to, the Poaceae.
10 ce similarity with plant species outside the Poaceae.
11 sequence similarity in a species outside the Poaceae.
12 ly reported for core eudicots and members of Poaceae.
13  duplication event preceded evolution of the Poaceae.
14 and eudicots, CslF genes are specific to the Poaceae.
15 ribes Bromeae and Triticeae but not in other Poaceae.
16 ollowed the order: Brassicaceae > Fabaceae > Poaceae.
17 on studies within Stipa and the grass family Poaceae.
18 model for genetic and genomic studies in the Poaceae.
19 angiosperm families outside the Fabaceae and Poaceae.
20 in Brachypodium distachyon, a model plant of Poaceae.
21 e C4 crop and a model for research in family Poaceae.
22 hogen biology during virus infections of the Poaceae.
23 that likewise enable discoveries outside the Poaceae.
24 umber to ZEP1 in rice, another member of the Poaceae.
25 plant miRNAs in general, particularly in the Poaceae.
26 as maize (Zea mays) and other grasses in the Poaceae.
27 arrangements and nucleotide substitutions in Poaceae, a phenomenon that has been noted recently throu
28    Intriguingly, the ACA-targeting miRNAs in Poaceae also direct PTGS for calmodulin-like proteins wh
29                                           In Poaceae, although species belonging to different subfami
30                                     Airborne Poaceae, Amaranthaceae, Cannabaceae, Uriticaceae.
31                                              Poaceae, among the most abundant plant families, include
32 were similar to that of the actual monocots (Poaceae and Asparagaceae).
33 rgenic pollen families Betulaceae, Oleaceae, Poaceae and Asteraceae across Europe.
34 ensity and duration of Betulaceae, Oleaceae, Poaceae and Asteraceae pollen seasons were examined.
35 class I gene activity between members of the Poaceae and Brassicaceae.
36 n diverse angiosperm lineages, including the Poaceae and Brassicaceae.
37 AP1/FUL-like genes duplicated at the base of Poaceae and codon substitutions occurred under relaxed s
38 after the divergence of the Bromeliaceae and Poaceae and comprises from 2 to 75 members in sequenced
39 ait transitions in the species-rich families Poaceae and Cyperaceae.
40                                 Species from Poaceae and Fabaceae exhibited a consistent trend of inc
41 he Bromeae and Triticeae lineages within the Poaceae and identifies the Jekyll genes as lineage-speci
42   Rice is an important model species for the Poaceae and other monocotyledonous plants.
43                                              Poaceae and Quercus species pollen contribute to asthma
44 nstruct the history of AP1/FUL-like genes in Poaceae and to hypothesize a role for this gene duplicat
45 ly for Fraxinus, Betula, Carpinus, Platanus, Poaceae and Urticaceae for the whole pollen season, and
46  A complete plastome from Coix lacryma-jobi (Poaceae) and a draft plastome from Joinvillea plicata (J
47 duplications documented for ancestral grass (Poaceae) and core eudicot lineages.
48                                             (Poaceae) and the outgroups were used for maximum likelih
49 us species, Pinaceae (except Tsuga species), Poaceae, and Ambrosia species pollen concentrations and
50 omparative study of rhizomatousness in other Poaceae, and assessment of gene flow between cultivated
51 nt pollen exposure, two folds higher than to Poaceae, and greater than five folds higher than to Olea
52   These rearrangements are restricted to the Poaceae, and IR expansion into the small single-copy reg
53 yzed, primarily from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species, but also from represent
54 y enzymatic features of TPS-a enzymes in the Poaceae, and the development of more complex reactions o
55                                          The Poaceae appear to have evolved as separate lineages for
56                                          The Poaceae are characterized by a lack or reduction of hete
57              Plastid genomes of the grasses (Poaceae) are unusual in their organization and rates of
58  context of flowering time regulation in the Poaceae as well as elucidates the way humans have utiliz
59 odel grasses to study antiviral responses in Poaceae, aspects that have been relatively understudied,
60 ere we showcase analyses of a bamboo system (Poaceae: Bambusoideae) comprising a series of lineages f
61 ne copies has thus shaped the genomes of all Poaceae cereal, forage, and biomass crops.
62                                          The Poaceae constitute a taxon of flowering plants (grasses)
63                                              Poaceae contain three CBF subfamilies, two of which, HvC
64                            The grass family (Poaceae) contains major crop staples, including maize (Z
65                     Continued improvement of Poaceae crops is necessary in order to continue to feed
66 psis, Gironniera, Rutaceae, Helicia, Randia, Poaceae, Dicranopteris and Pteris always existed during
67 uch of the approximately 50-million years of Poaceae divergence.
68 ss of genes in plants is associated with the Poaceae divergence.
69 mapping has indicated that the grass family (Poaceae) exhibits extensive chromosomal collinearity.
70 atment of detached leaves from plants of the Poaceae, Fabaceae, Asteraceae, Brassicaceae, and Cucurbi
71 wn only in the legume (Fabaceae) and cereal (Poaceae) families, but peptides that mimic their trypsin
72 n evolutionarily distinct species within the Poaceae family and an additional screen for TE-related s
73 anitides L1-9, from the Panicum laxum of the Poaceae family and provide the first evidence of linear
74                                          The Poaceae family comprises over 12 000 wind-pollinated spe
75                                Moreover, the Poaceae family contains many important food crops, and o
76 e specificity, indicating that plants in the Poaceae family have the ability to synthesize fucogalact
77                                          The Poaceae family of plants provides cereal crops that are
78 Although several cyclotide-like genes in the Poaceae family were known from the data mining of the Na
79                                          The Poaceae family, also known as the grasses, includes agro
80 d animals, are not evenly distributed in the Poaceae family, but their presence or absence in flours
81 foxtail), a short life-cycle C4 plant in the Poaceae family, is the wild ancestor of Setaria italica
82 embers reside solely in the BEP clade of the Poaceae family, specifically, barley, rice (Oryza sativa
83 diversity and a highly valuable tool for the Poaceae family, that will advance plant biology research
84 studied 'model' crops, many of them from the Poaceae family.
85  cause disease on many species of the grass (Poaceae) family.
86 mictic species, including several members of Poaceae (Festuca, Poa and Stipa), Rosaceae (Potentilla)
87 ding genes for 47 angiosperms including nine Poaceae genera confirm that the branch leading to Poacea
88 identified between Nipponbare and four other Poaceae genomes.
89 ound in a multitude of species of the family Poaceae (Gramineae) and occur sporadically in single spe
90 the other major crop grasses from the family Poaceae (Gramineae) are mankind's most important source
91 s that corn genes, as well as genes of other Poaceae (Grass family), can be divided into two classes
92 ic breeding/engineering, particularly in the Poaceae (grass family), which includes the major food cr
93 representing the most economically important Poaceae (grass) clades have been published, and their ge
94  million years ago provided raw material for Poaceae (grass) diversification.
95  Pennisetum/Cenchrus species, members of the Poaceae (grass) family, reproduce by apospory.
96 osome evolution, across the diversity of the Poaceae (grass) plant family, and among 26 maize cultiva
97 oXyG with an XXXG core motif, whereas in the Poaceae (grasses and cereals), the structure of XyG is l
98 ns and the shifts in diversification rate of Poaceae (grasses) and Asteraceae (daisies), two exceptio
99       A set of 428 DNA probes from different Poaceae (grasses) detected 2460 loci in F1 progeny of th
100 second dimension, since it is not present in Poaceae (grasses), which also lack the developmental pro
101  crop species, including many members of the Poaceae (grasses).
102 ae genera confirm that the branch leading to Poaceae has significantly accelerated rates of change re
103                                              Poaceae have multiple structural rearrangements, includi
104 e, maize (Zea mays) and other members of the Poaceae have three paralogous genes, in contrast to only
105 ergent evolution of bract suppression in the Poaceae involved recruitment of a distinct genetic pathw
106                                              Poaceae is also one of the largest plant families, consi
107               Phyllostachys edulis Carriere (Poaceae) is a bamboo species that is part of the traditi
108                           (sugarcane, Family-Poaceae) is employed in Ibibio traditional medicine for
109  groups it regulates cell wall extension, in Poaceae its role is still unclear.
110 ion by seeds, present in some members of the Poaceae like Eragrostis curvula.
111  pattern of the rho-derived duplicates among Poaceae lineages and implications in adaptive evolution.
112  may benefit from using plant taxa of Pinus, Poaceae, Lonicera, Casuarina, Trema and Quercus.
113 bryogenesis in flowering plants by using the Poaceae maize and rice as monocot grass and crop models
114                                              Poaceae members shared a whole-genome duplication called
115 ted in the lignin from species in the family Poaceae (order Poales).
116 types from plant hosts (cereals and grasses, Poaceae) other than winter wheat and/or genotype-biased
117                        To better resolve the Poaceae phylogeny, we generated 342 transcriptomic and s
118 sed for coalescent analyses to reconstruct a Poaceae phylogeny.
119 orest cover within 200 m of each lake, using Poaceae phytoliths.
120    Leymus arenarius is a unique wild growing Poaceae plant exhibiting extreme tolerance to environmen
121 re known to infect either cultivated or wild Poaceae plant species, six have been identified on Reuni
122                                              Poaceae plants can locally accumulate iron to suppress p
123 isits per SD increase in Quercus species and Poaceae pollen and a 10% to 15% increased risk on days w
124                       Average total airborne Poaceae pollen count and standard deviation from January
125                                              Poaceae pollen is currently regarded as the leading airb
126 ime that the true morphological variation in Poaceae pollen micro-ornamentation becomes apparent thro
127                  Altered Quercus species and Poaceae pollen production caused by climate change could
128                                       Grass (Poaceae) pollen is the most important outdoor aeroallerg
129 ysis to quantify the morphometrics of grass (Poaceae) pollen micro-ornamentation from the Neotropics
130 ghly allergenic role of Fraxinus, Betula and Poaceae pollens but also showed a relatively unknown ass
131 d airborne pollen identified and classified: Poaceae, Polygonaceae, Amaranthaceae, Urticaceae, Cannab
132                                 The grasses (Poaceae) represent a monophyletic lineage that arose abo
133 ate lineages within the cereal/grass family (Poaceae) resulting in modern rice and maize.
134 s examined here help clarifying evolution in Poaceae, S. maritima being a part of the poorly-known Ch
135  fructosyltransferases and invertases in the Poaceae showed that the fructan biosynthetic genes may h
136 thin the Triticeae tribe of the grass family Poaceae, single major aluminum (Al) tolerance genes have
137 thologs in its distant cousins in the family Poaceae (Sorghum bicolor, Brachypodium distachyon), but
138                                              Poaceae species are classified into 12 subfamilies, with
139 ptomic datasets to provide sequences for 357 Poaceae species in 231 genera, representing 45 tribes an
140 ate physical distances among markers in many Poaceae species including rice and maize.
141 ments of the CPSGs with sequences from other Poaceae species show conservation across a putative doma
142 tic analysis revealed 2 chloroplastic GRs in Poaceae species, including rice, sorghum and brachypodiu
143     Here, we report HMAs in eleven different Poaceae species, including wheat.
144  of the putative homologs were obtained from Poaceae species, putative homologs were identified in di
145 ntergenic transcribed regions (ITRs) in four Poaceae species.
146 1S0.8 region' in various Triticeae and other Poaceae species.
147 LP markers by comparing 35 different maps of Poaceae species.
148 ly in perennial ryegrass and closely related Poaceae species.
149 dental calculus show that certain species of Poaceae (species of the genus Aegilops) were used since
150                    We show in various grass (Poaceae) species that MLG-specific antibody labeling is
151 eage-specific rice genes is termed conserved Poaceae-specific genes (CPSGs) to reflect the presence o
152                            We identified the Poaceae-specific rho whole-genome duplication as the ori
153                                  Focusing on Poaceae subfamilies Anomochlooideae, Pharoideae, Pueliod
154  of reproductive PHAS loci in the genomes of Poaceae subfamilies from Panicoideae to Oryzoideae and t
155 nt sequence similarity across three separate Poaceae subfamilies.
156 transcriptomes in species representing three Poaceae subgroups including the Pooideae (Brachypodium d
157 ommelinid monocotyledon families outside the Poaceae, such as the Arecaceae (the palms, order Arecale
158 jor clades (e.g., angiosperms, Brassicaceae, Poaceae), suggesting that polyploidy drives diversificat
159               By contrast, PT13 arose in the Poaceae, suggesting that grasses acquired a particular s
160 evalent in at least eight subfamilies of the Poaceae, suggesting that this duplication event preceded
161   Codons identified as having diverged among Poaceae taxa in response to positive selection were sign
162 f defense, in two species of Zea and several Poaceae taxa.
163 re present more broadly in the grass family (Poaceae) than previously known.
164 c grassland savanna, dominated by the Family Poaceae, that blankets most of the Central Highlands.
165      Only in Reykjavik, Madrid and Derby was Poaceae the dominant pollen, as was Oleaceae in Thessalo
166 iversification of the TPS-a subfamily in the Poaceae (the grass family), a plant family that contains
167                                              Poaceae (the grasses) includes rice, maize, wheat, and o
168                                  In grasses (Poaceae), the position of the AZ differs among species,
169                  Barley (Hordeum vulgare L.; Poaceae), the second most important grain after wheat, c
170 ar clock analyses estimated the crown age of Poaceae to be ~101 million years old.
171  genomic resources, and homeology within the Poaceae to identify candidate genes involved in the esse
172           Distinct catalytic features of the Poaceae TPS-a subfamily arose early in grass evolution a
173  clade shared with other monocot plants, the Poaceae TPS-a subfamily consists of five well-defined cl
174        This work lays a solid foundation for Poaceae translational genomics.
175 and other organs of Brachypodium distachyon (Poaceae) under 17 organ-condition combinations, includin
176 been used to reconstruct the biogeography of Poaceae, untangle crop domestication history and detect
177 ed plastochron), a phenotype shared with the Poaceae vascular plants TE1 and PLA2/LHD2 mutants.
178 e readily translated to other members of the Poaceae via integrated genomics approaches.
179 etween profilin and pollen count of Olea and Poaceae was observed (rho = 0.24; P < .001).
180  on the widespread and diverse grass family (Poaceae), we used data on species' climatic niches and g
181  with S. bicolor compared to other sequenced Poaceae, where 37.6% of the paired matching BESs are cor
182 pathway regulation operating in the grasses (Poaceae), which include plants of world-wide agronomic i
183                        This study presents a Poaceae whole-genome duplication profile with evidence f
184 nserved among six diverse species within the Poaceae yet lack significant sequence similarity with pl

 
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