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1 e of stem defects in breeding populations of loblolly pine.
2 ocally misassembled contigs in assemblies of loblolly pine.
3 erage of 8.5 lethal equivalents reported for loblolly pine.
4 roups to represent the chromosomes n = 12 of loblolly pine.
5 thway associated with lignin biosynthesis in loblolly pine.
6  into 4CL mRNA in developing xylem tissue of loblolly pine.
7                           A near-full-length loblolly pine alpha-expansin sequence was obtained using
8        We also applied bcalm 2 to the 22 Gbp loblolly pine and 20 Gbp white spruce sequencing dataset
9  while slightly less accurate (OA of 92% for loblolly pine and 90% for longleaf pine), does not requi
10 accuracy (OA) of 98% and F1 score of 98% for loblolly pine and 95% and 94%, respectively, for longlea
11 nce tags (ESTs) from wood-forming tissues of loblolly pine and compared them to the gene sequences in
12 and used stimulated optical mapping data for loblolly pine and F.tularensis and used real optical map
13  for PtACO1 in compression wood formation in loblolly pine and the discovery of its NIP are discussed
14                              Pinus taeda L. (loblolly pine) and Arabidopsis thaliana differ greatly i
15 fferentially expressed in various tissues of loblolly pine, as well as in response to perturbations o
16 an reduce Na(+) accumulation of salt-exposed loblolly pine, but this effect depends on external K(+)
17       The transgenic tobacco plants carrying loblolly pine CCoAOMT promoter-GUS fusion localized the
18 l CoA ester O-methyltransferase (AEOMT) from loblolly pine differentiating xylem that was capable of
19        Changes in RNA transcript profiles of loblolly pine due to drought stress were correlated with
20 STRA, to predict eddy covariance data from a loblolly pine forest.
21 nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.
22 pply our method to various assemblies of the loblolly pine, Francisella tularensis, rice and budgerig
23 t CCoAOMT may exist as a single-copy gene in loblolly pine genome.
24  map QTL influencing wood property traits in loblolly pine has been completed.
25 ionally dominant fungal taxa associated with loblolly pine including Amphinema, Russula and Piloderma
26                      A cDNA clone (lp3) from loblolly pine induced by water deficit stress (WDS) has
27 tory to early-stage somatic embryo growth of loblolly pine (LP) was purified chromatographically from
28 conomically important plant species, such as loblolly pine (Pinus taeda L).
29             Ten homologous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudots
30 ssed under water deficit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characte
31 ssed sequence tag polymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.
32 ed in the long-lived, outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single n
33 the ECM fungus Paxillus ammoniavirescens and loblolly pine (Pinus taeda L.) in axenic and symbiotic c
34                  We have discovered a mutant loblolly pine (Pinus taeda L.) in which expression of th
35                                              Loblolly pine (Pinus taeda L.) is the most widely plante
36 ronartium quercuum f. sp fusiforme infecting loblolly pine (Pinus taeda L.) over much of this host's
37           Novel lignin is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinn
38 om longleaf pine (Pinus palustris Mill.) and loblolly pine (Pinus taeda L.) trees in Florida, USA, an
39                          A consensus map for loblolly pine (Pinus taeda L.) was constructed from the
40 rate:coenzyme A ligase (4CL; EC 6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned.
41 rotochlorophyllide oxidoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.
42                                For instance, loblolly pine (Pinus taeda L.), an ecologically and econ
43  a putative ACC synthase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial
44 lume, and aboveground biomass components for loblolly pine (Pinus taeda L.), the dominant tree specie
45 bryonic viability loci in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP mar
46 a clonally-replicated full-sibling family of loblolly pine (Pinus taeda L.).
47 ted with aridity across the natural range of loblolly pine (Pinus taeda L.).
48 opulations of zygotic and somatic embryos of loblolly pine (Pinus taeda L.).
49  AGP (PtaAGP6, accession number AF101785) in loblolly pine (Pinus taeda L.).
50  differentiating xylem and in mature wood of loblolly pine (Pinus taeda L.).
51 raits in a structured breeding population of loblolly pine (Pinus taeda L.).
52 s, ESTs were obtained from immature xylem of loblolly pine (Pinus taeda L.).
53 ession during adventitious root formation in loblolly pine (Pinus taeda) after treatment with the exo
54 ions of 292 metabolites measured in a single loblolly pine (Pinus taeda) association population.
55 of K(+), Cu(2+), and Cl(-) diffusing through loblolly pine (Pinus taeda) cell wall layers under 70%,
56 nstrated that transcripts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-sp
57              In experimental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentr
58 to carbon (C) and nitrogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated C
59 future productivity and water use of planted loblolly pine (Pinus taeda) growing across the southeast
60 e individuals from common gardens across the loblolly pine (Pinus taeda) natural range.
61                    Only two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce
62       In a glasshouse experiment, we exposed loblolly pine (Pinus taeda) saplings (n = 83) to drought
63 lation genomic approach to identify genes in loblolly pine (Pinus taeda) that are associated with res
64 essed genes within a pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated
65 ned the reproductive response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide
66 mprove our understanding of the responses of loblolly pine (Pinus taeda) to drought stress.
67 produced using mRNA from lignifying xylem of loblolly pine (Pinus taeda) trunk wood.
68        We report here the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multif
69 ript, PtNIP1;1, that is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos,
70                                              Loblolly pine (Pinus taeda), in contrast, possesses a si
71  and identified 26 miRNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conser
72 ea glauca), Norway spruce (Picea abies), and loblolly pine (Pinus taeda).
73  DNA microarrays containing 2,178 cDNAs from loblolly pine (Pinus taeda).
74                                              Loblolly pine, Pinus taeda L., is one of the most widely
75 bon budget estimate for a typical commercial loblolly pine plantation in North Carolina, USA, spannin
76 , based on 5 years of data from two adjacent loblolly pine plantations.
77 aining various amounts of water and roots of loblolly pine planted into similar sand.
78                        Application of SEM to loblolly pine QTL data provided support for biologically
79  identify additional ACC oxidase clones from loblolly pine root cDNA libraries characterized as part
80                                        While loblolly pine root growth and development decreased with
81                 The mycorrhizal influence on loblolly pine salinity response was strongly dependent o
82 onvertible forested area of the watershed to loblolly pine savannas at a greater cost efficiency (<$1
83 nitrogen that accompanied nearly 50 years of loblolly pine secondary forest development.
84  efficiently methylated in crude extracts of loblolly pine secondary xylem.
85                                    Images of loblolly pine seedling roots planted in identical sand s
86  in the base of hypocotyl stem cuttings from loblolly pine seedlings in response to indole-3-butyric
87 . are used, the effective population size of loblolly pine should be 5.6 x 10(5).
88                             Members of three loblolly pine-specific miRNA families target a large num
89 a), which belong to four conserved and seven loblolly pine-specific miRNA families.
90 expected for a large majority of the planted loblolly pine stands in the southeastern United States d
91                                             (loblolly pine) stands on the upper Coastal Plain of Sout
92 rms, a 1.3 kb CCoAOMT cDNA was isolated from loblolly pine that showed 79-82% amino acid sequence ide
93 tance properties, measured in a Pinus taeda (loblolly pine) training population of 951 individuals ge
94 luable addition to development of a complete loblolly pine transcriptome.
95                                           In loblolly pine, transient expression increased 10-fold ut
96                                              Loblolly pine trees (Pinus taeda L.) occupy more than 20
97 ntified in an outbred full-sibling family of loblolly pine, using single-nucleotide polymorphism mark
98         Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pesticide 2,4-dichl
99 mines resistance to fusiform rust disease in loblolly pine where no discrete, simply inherited resist
100  is significant genetic variation for RCN in loblolly pine, which can be exploited in breeding for el
101 ethylation pathway in lignin biosynthesis in loblolly pine xylem.
102 onstructed from differentiating Pinus taeda (loblolly pine) xylem RNA.

 
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