ライフサイエンスコーパス: Poaceae

1 plast genome of members of the grass family (Poaceae).

2 and switchgrass (Panicum virgatum, monocot, Poaceae).

3 tems of 26 species, mainly European grasses (Poaceae).

4 the Pooideae sub-family of the grass family (Poaceae).

5 duplication event preceded evolution of the Poaceae.

6 in Brachypodium distachyon, a model plant of Poaceae.

7 e C4 crop and a model for research in family Poaceae.

8 that likewise enable discoveries outside the Poaceae.

9 umber to ZEP1 in rice, another member of the Poaceae.

10 plant miRNAs in general, particularly in the Poaceae.

11 as maize (Zea mays) and other grasses in the Poaceae.

12 angiosperm families outside the Fabaceae and Poaceae.

13 onservation for this set of genes within the Poaceae.

14 onserved within, as well as specific to, the Poaceae.

15 ce similarity with plant species outside the Poaceae.

16 sequence similarity in a species outside the Poaceae.

17 ly reported for core eudicots and members of Poaceae.

18 arrangements and nucleotide substitutions in Poaceae, a phenomenon that has been noted recently throu

19 In Poaceae, although species belonging to different subfami

20 Airborne Poaceae, Amaranthaceae, Cannabaceae, Uriticaceae.

21 were similar to that of the actual monocots (Poaceae and Asparagaceae).

22 rgenic pollen families Betulaceae, Oleaceae, Poaceae and Asteraceae across Europe.

23 ensity and duration of Betulaceae, Oleaceae, Poaceae and Asteraceae pollen seasons were examined.

24 class I gene activity between members of the Poaceae and Brassicaceae.

25 n diverse angiosperm lineages, including the Poaceae and Brassicaceae.

26 AP1/FUL-like genes duplicated at the base of Poaceae and codon substitutions occurred under relaxed s

27 Rice is an important model species for the Poaceae and other monocotyledonous plants.

28 Poaceae and Quercus species pollen contribute to asthma

29 nstruct the history of AP1/FUL-like genes in Poaceae and to hypothesize a role for this gene duplicat

30 ly for Fraxinus, Betula, Carpinus, Platanus, Poaceae and Urticaceae for the whole pollen season, and

31 A complete plastome from Coix lacryma-jobi (Poaceae) and a draft plastome from Joinvillea plicata (J

32 duplications documented for ancestral grass (Poaceae) and core eudicot lineages.

33 (Poaceae) and the outgroups were used for maximum likelih

34 us species, Pinaceae (except Tsuga species), Poaceae, and Ambrosia species pollen concentrations and

35 omparative study of rhizomatousness in other Poaceae, and assessment of gene flow between cultivated

36 nt pollen exposure, two folds higher than to Poaceae, and greater than five folds higher than to Olea

37 These rearrangements are restricted to the Poaceae, and IR expansion into the small single-copy reg

38 yzed, primarily from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species, but also from represent

39 The Poaceae appear to have evolved as separate lineages for

40 The Poaceae are characterized by a lack or reduction of hete

41 Plastid genomes of the grasses (Poaceae) are unusual in their organization and rates of

42 context of flowering time regulation in the Poaceae as well as elucidates the way humans have utiliz

43 odel grasses to study antiviral responses in Poaceae, aspects that have been relatively understudied,

44 ne copies has thus shaped the genomes of all Poaceae cereal, forage, and biomass crops.

45 Poaceae contain three CBF subfamilies, two of which, HvC

46 The grass family (Poaceae) contains major crop staples, including maize (Z

47 Continued improvement of Poaceae crops is necessary in order to continue to feed

48 psis, Gironniera, Rutaceae, Helicia, Randia, Poaceae, Dicranopteris and Pteris always existed during

49 ss of genes in plants is associated with the Poaceae divergence.

50 uch of the approximately 50-million years of Poaceae divergence.

51 mapping has indicated that the grass family (Poaceae) exhibits extensive chromosomal collinearity.

52 atment of detached leaves from plants of the Poaceae, Fabaceae, Asteraceae, Brassicaceae, and Cucurbi

53 wn only in the legume (Fabaceae) and cereal (Poaceae) families, but peptides that mimic their trypsin

54 n evolutionarily distinct species within the Poaceae family and an additional screen for TE-related s

55 anitides L1-9, from the Panicum laxum of the Poaceae family and provide the first evidence of linear

56 The Poaceae family comprises over 12 000 wind-pollinated spe

57 Moreover, the Poaceae family contains many important food crops, and o

58 e specificity, indicating that plants in the Poaceae family have the ability to synthesize fucogalact

59 Although several cyclotide-like genes in the Poaceae family were known from the data mining of the Na

60 The Poaceae family, also known as the grasses, includes agro

61 d animals, are not evenly distributed in the Poaceae family, but their presence or absence in flours

62 embers reside solely in the BEP clade of the Poaceae family, specifically, barley, rice (Oryza sativa

63 studied 'model' crops, many of them from the Poaceae family.

64 cause disease on many species of the grass (Poaceae) family.

65 ding genes for 47 angiosperms including nine Poaceae genera confirm that the branch leading to Poacea

66 ound in a multitude of species of the family Poaceae (Gramineae) and occur sporadically in single spe

67 the other major crop grasses from the family Poaceae (Gramineae) are mankind's most important source

68 s that corn genes, as well as genes of other Poaceae (Grass family), can be divided into two classes

69 ic breeding/engineering, particularly in the Poaceae (grass family), which includes the major food cr

70 representing the most economically important Poaceae (grass) clades have been published, and their ge

71 million years ago provided raw material for Poaceae (grass) diversification.

72 Pennisetum/Cenchrus species, members of the Poaceae (grass) family, reproduce by apospory.

73 oXyG with an XXXG core motif, whereas in the Poaceae (grasses and cereals), the structure of XyG is l

74 A set of 428 DNA probes from different Poaceae (grasses) detected 2460 loci in F1 progeny of th

75 second dimension, since it is not present in Poaceae (grasses), which also lack the developmental pro

76 crop species, including many members of the Poaceae (grasses).

77 ae genera confirm that the branch leading to Poaceae has significantly accelerated rates of change re

78 Poaceae have multiple structural rearrangements, includi

79 e, maize (Zea mays) and other members of the Poaceae have three paralogous genes, in contrast to only

80 ergent evolution of bract suppression in the Poaceae involved recruitment of a distinct genetic pathw

81 Phyllostachys edulis Carriere (Poaceae) is a bamboo species that is part of the traditi

82 may benefit from using plant taxa of Pinus, Poaceae, Lonicera, Casuarina, Trema and Quercus.

83 ted in the lignin from species in the family Poaceae (order Poales).

84 types from plant hosts (cereals and grasses, Poaceae) other than winter wheat and/or genotype-biased

85 Leymus arenarius is a unique wild growing Poaceae plant exhibiting extreme tolerance to environmen

86 isits per SD increase in Quercus species and Poaceae pollen and a 10% to 15% increased risk on days w

87 Average total airborne Poaceae pollen count and standard deviation from January

88 Poaceae pollen is currently regarded as the leading airb

89 Altered Quercus species and Poaceae pollen production caused by climate change could

90 ghly allergenic role of Fraxinus, Betula and Poaceae pollens but also showed a relatively unknown ass

91 d airborne pollen identified and classified: Poaceae, Polygonaceae, Amaranthaceae, Urticaceae, Cannab

92 The grasses (Poaceae) represent a monophyletic lineage that arose abo

93 ate lineages within the cereal/grass family (Poaceae) resulting in modern rice and maize.

94 s examined here help clarifying evolution in Poaceae, S. maritima being a part of the poorly-known Ch

95 fructosyltransferases and invertases in the Poaceae showed that the fructan biosynthetic genes may h

96 thin the Triticeae tribe of the grass family Poaceae, single major aluminum (Al) tolerance genes have

97 ate physical distances among markers in many Poaceae species including rice and maize.

98 ments of the CPSGs with sequences from other Poaceae species show conservation across a putative doma

99 tic analysis revealed 2 chloroplastic GRs in Poaceae species, including rice, sorghum and brachypodiu

100 of the putative homologs were obtained from Poaceae species, putative homologs were identified in di

101 1S0.8 region' in various Triticeae and other Poaceae species.

102 LP markers by comparing 35 different maps of Poaceae species.

103 ly in perennial ryegrass and closely related Poaceae species.

104 We show in various grass (Poaceae) species that MLG-specific antibody labeling is

105 eage-specific rice genes is termed conserved Poaceae-specific genes (CPSGs) to reflect the presence o

106 nt sequence similarity across three separate Poaceae subfamilies.

107 transcriptomes in species representing three Poaceae subgroups including the Pooideae (Brachypodium d

108 ommelinid monocotyledon families outside the Poaceae, such as the Arecaceae (the palms, order Arecale

109 jor clades (e.g., angiosperms, Brassicaceae, Poaceae), suggesting that polyploidy drives diversificat

110 By contrast, PT13 arose in the Poaceae, suggesting that grasses acquired a particular s

111 evalent in at least eight subfamilies of the Poaceae, suggesting that this duplication event preceded

112 Codons identified as having diverged among Poaceae taxa in response to positive selection were sign

113 f defense, in two species of Zea and several Poaceae taxa.

114 c grassland savanna, dominated by the Family Poaceae, that blankets most of the Central Highlands.

115 Only in Reykjavik, Madrid and Derby was Poaceae the dominant pollen, as was Oleaceae in Thessalo

116 genomic resources, and homeology within the Poaceae to identify candidate genes involved in the esse

117 This work lays a solid foundation for Poaceae translational genomics.

118 ed plastochron), a phenotype shared with the Poaceae vascular plants TE1 and PLA2/LHD2 mutants.

119 e readily translated to other members of the Poaceae via integrated genomics approaches.

120 with S. bicolor compared to other sequenced Poaceae, where 37.6% of the paired matching BESs are cor

121 pathway regulation operating in the grasses (Poaceae), which include plants of world-wide agronomic i

122 nserved among six diverse species within the Poaceae yet lack significant sequence similarity with pl