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1 ange within populations of black cottonwood (Populus trichocarpa).
2 aldoxime formation in western balsam poplar (Populus trichocarpa).
3  spruce, grape (Vitis vinifera), and poplar (Populus trichocarpa).
4 abidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa).
5 ous root formation in the model tree poplar (Populus trichocarpa).
6 acetylesterase (PAE1) from black cottonwood (Populus trichocarpa).
7 nd salirepin-7-sulfate, in black cottonwood (Populus trichocarpa).
8 ally expressed in developing wood of poplar (Populus trichocarpa).
9 Arabidopsis thaliana), and black cottonwood (Populus trichocarpa).
10 , from the dioecious tree, black cottonwood (Populus trichocarpa).
11 f leaf surface lipids from black cottonwood (Populus trichocarpa).
12 ion of D14 homologs in the model woody plant Populus trichocarpa.
13 evealed homology with a predicted protein of Populus trichocarpa.
14 iating xylem (SDX), in the model woody plant Populus trichocarpa.
15 wood-forming tissue of the model woody plant Populus trichocarpa.
16 two monolignol 4CLs, Ptr4CL3 and Ptr4CL5, in Populus trichocarpa.
17 ive of SND1 transcriptional network genes in Populus trichocarpa.
18 ly duplicated genes in the model forest tree Populus trichocarpa.
19 arCyc, from the recently sequenced genome of Populus trichocarpa.
20 ly contrasting populations of the model tree Populus trichocarpa.
21 he reference genome of the model woody plant Populus trichocarpa.
22 nsferases (COMTs) from the black cottonwood, Populus trichocarpa.
23 apaya, Medicago truncatula, Oryza sativa and Populus trichocarpa.
24 e draft genome of the black cottonwood tree, Populus trichocarpa.
25 e whose gene was cloned from the angiosperm, Populus trichocarpa.
26 f PA biosynthesis in Salvia miltiorrhiza and Populus trichocarpa.
27 t-specific TF in a TRN for wood formation in Populus trichocarpa.
28 (2)) mapping population from a cross between Populus trichocarpa (93-968) and P. deltoides Bart (ILL-
29 e investigated adaptive genetic variation in Populus trichocarpa, a potential biofuel feedstock crop,
30                                  In the tree Populus trichocarpa, a recent duplication event of a HOZ
31 AS) to link nucleotide variants to traits in Populus trichocarpa, a species with rapid linkage disequ
32 on-photochemical quenching parameters in 743 Populus trichocarpa accessions identified a nuclear-enco
33 studies of approximately 400 natural poplar (Populus trichocarpa) accessions phenotyped for 60 ecolog
34 omosome, was applied to the chromosome 19 of Populus trichocarpa, an incipient sex chromosome, deciph
35                                              Populus trichocarpa and Brachypodium distachyon are emer
36  We resequenced 16 genomes of the model tree Populus trichocarpa and genotyped 120 trees from 10 subp
37 eudo-backcross progeny of 154 individuals of Populus trichocarpa and P. deltoides analyzed with long-
38            The North American hybrid zone of Populus trichocarpa and Populus balsamifera represents a
39 bicolor influences abiotic cue perception by Populus trichocarpa and the ensuing signaling cascade.
40  Arabidopsis (Arabidopsis thaliana), poplar (Populus trichocarpa) and rice (Oryza sativa).
41 sphate synthase (DXS) enzyme was cloned from Populus trichocarpa, and the recombinant protein (PtDXS)
42 is thaliana, papaya [Carica papaya], poplar [Populus trichocarpa], and grape [Vitis vinifera]), we de
43        The number of F-box genes in Populus (Populus trichocarpa; approximately 320) is less than hal
44 ding SBEs in rice, Arabidopsis thaliana, and Populus trichocarpa are described.
45 tworks, using lignocellulose biosynthesis in Populus trichocarpa as a case study.
46 ncluding Arabidopsis thaliana, Oryza sativa, Populus trichocarpa, as well as a unicellular outgroup,
47 cies Populus tremula and Populus balsamifera/Populus trichocarpa at 5 Ma.
48        By functionally screening a subset of Populus trichocarpa BAHD/HXXXD acyltransferases, we iden
49 nscript and protein abundances in transgenic Populus trichocarpa based on targeted knockdowns of spec
50 reciprocal common gardens of the model tree, Populus trichocarpa (black cottonwood), to examine relat
51  of the known miRNAs from various tissues of Populus trichocarpa (black cottonwood).
52 sis using a population of 1204 wild trees of Populus trichocarpa (black cottonwood).
53 liana), guar (Cyamopsis tetragonolobus), and Populus trichocarpa catalyze beta-1,4-mannan and glucoma
54                   Using hydroponically grown Populus trichocarpa (clone Nisqually-1), we have establi
55           When the model bioenergy feedstock Populus trichocarpa (cottonwood), with predictable ligni
56 ation experiment using the black cottonwood (Populus trichocarpa) foliar microbiome, we manipulated h
57 s throughout the stem of the woody perennial Populus trichocarpa generating a high-resolution transcr
58  of floral development, we have isolated two Populus trichocarpa genes, PTAG1 and PTAG2, homologous t
59                    We identified and studied Populus trichocarpa genes, PtrHAB1 through PtrHAB15, bel
60                           Within the species Populus trichocarpa, genetic trade-offs show that for ea
61  insertion sites by reference to the nascent Populus trichocarpa genome sequence.
62                                    PTLF, the Populus trichocarpa homolog of LEAFY (LFY) and FLORICAUL
63 thropods within an association population of Populus trichocarpa in three common gardens to discover
64 bundance and distribution of foliar fungi of Populus trichocarpa in wild populations across its nativ
65 eductase (CCR) families in wood formation in Populus trichocarpa, including the regulatory effects of
66  this study, we show that transgenic poplar (Populus trichocarpa) lines can be solubilized without an
67 e changes during seasonal leaf senescence in Populus trichocarpa Nisqually-1, the Populus reference g
68 d from the genome of the model tree species (Populus trichocarpa), of which 11 are Populus specific.
69 urthermore, we demonstrated that the poplar (Populus trichocarpa) orthologs of SND2/3/4/5 also activa
70 ted traits in the F(2) generation-the female Populus trichocarpa parent is from Washington State (48
71 edon species Medicago truncatula (Medicago), Populus trichocarpa (poplar) and Arabidopsis thaliana (A
72                                              Populus trichocarpa (poplar) is distinguished from its h
73 lymorphism (SNP)-phenotype associations in a Populus trichocarpa population distributed from Californ
74 ory, the tree species western balsam poplar (Populus trichocarpa) produces a variety of Phe-derived m
75  small RNAs from abiotic stressed tissues of Populus trichocarpa (Ptc) and the identification of 68 p
76          Two nectary types that evolved with Populus trichocarpa (Ptr) and Populus tremula x Populus
77 detecting m6A from an independent dataset of Populus trichocarpa, RedNano achieves the highest AUC an
78   Interestingly, phylogenetic analysis using Populus trichocarpa revealed evidence for small RNA-medi
79 ice (Oryza sativa), Arabidopsis, and poplar (Populus trichocarpa) revealed a core binding site for Do
80 tuberosum), Medicago truncatula, and poplar (Populus trichocarpa) revealed conserved ratios of the AS
81 on a screen of natural accessions of poplar (Populus trichocarpa), revealing that the leaf cuticular
82 er 40% had up-regulated orthologs in poplar (Populus trichocarpa), rice (Oryza sativa), or Chlamydomo
83                      Using RNA sequencing of Populus trichocarpa roots in mutualistic symbiosis with
84  procedure for isolation and transfection of Populus trichocarpa stem differentiating xylem protoplas
85 ns peak in the developing phloem tissue of a Populus trichocarpa stem.
86 ated small RNAs from the developing xylem of Populus trichocarpa stems and cloned 22 miRNAs.
87 nstructed a genome-scale metabolic model for Populus trichocarpa, the first for a perennial woody tre
88 quence similarity of a KCS gene cluster from Populus trichocarpa to examine the evolution and molecul
89 h one finger) protein sequences from poplar (Populus trichocarpa) Torr.
90 hotspot, mapped using 390 leaf and 444 xylem Populus trichocarpa transcriptomes.
91 ence genome from the oldest branch of a wild Populus trichocarpa tree with two dominant stems which h
92 ection scans and association analyses of 544 Populus trichocarpa trees to reveal genomic bases of ada
93 representing 1,100 individual undomesticated Populus trichocarpa trees, 47 extreme phenotypes were se
94 parenchyma cells after embolism formation in Populus trichocarpa trees.
95 abidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa), two near-complete rosid genome seq
96       In stem differentiating xylem (SDX) of Populus trichocarpa, two cinnamic acid 4-hydroxylases (P
97 ) biosynthesis during stem wood formation in Populus trichocarpa, two enzymes, Ptr4CL3 and Ptr4CL5, c
98 tabolic pathways in Arabidopsis thaliana and Populus trichocarpa using high-throughput gene expressio
99 ce (Oryza sativa), Arabidopsis thaliana, and Populus trichocarpa using the Plant Cis-acting Regulator
100 ransient and CRISPR-mediated transgenesis in Populus trichocarpa, we unveiled in this adaptation a re
101 boring chromosome regions of A. thaliana and Populus trichocarpa; whereas, no pairs are mapped to the
102 unction endoglucanase from black cottonwood (Populus trichocarpa), which reveals a small, newly recog
103 two reference plant species, A. thaliana and Populus trichocarpa, with annotations based on UniProt,
104 rect evidence demonstrating that the poplar (Populus trichocarpa) wood-associated NAC domain transcri
105 sence of quantitative trait loci (QTLs) in a Populus trichocarpa x P. deltoides F(2) population.
106 nes spanning the natural hybrid zone between Populus trichocarpa x Populus balsamifera, we used whole

 
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