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1 way spruce (Picea abies), and loblolly pine (Pinus taeda).
2 s containing 2,178 cDNAs from loblolly pine (Pinus taeda).
3 dventitious root formation in loblolly pine (Pinus taeda) after treatment with the exogenous auxin in
4 abolites measured in a single loblolly pine (Pinus taeda) association population.
5 a silt loam soil and a biochar obtained from Pinus taeda at 500 degrees C.
6 15NH4Cl, 15N-Gln, and 15N-Glu) in lignifying Pinus taeda cell cultures was investigated, using a comb
7  profiling of the phenylpropanoid pathway in Pinus taeda cell suspension cultures was carried out usi
8 , and Cl(-) diffusing through loblolly pine (Pinus taeda) cell wall layers under 70%, 75%, or 80% rel
9 ranscripts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-specific expressi
10                                           In Pinus taeda, dwarf phenotypes originate from abnormal br
11  experimental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentrations, nearly
12 lization on EMM production and turnover in a Pinus taeda forest.
13 nd nitrogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated CO(2) by measuri
14 atural and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment
15 atural and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment
16 vity and water use of planted loblolly pine (Pinus taeda) growing across the southeastern United Stat
17                               Loblolly pine (Pinus taeda), in contrast, possesses a single 4CL protei
18 ee environments in a complex pedigree of 520 Pinus taeda individuals (CCLONES).
19 rigin of early 20th century introductions of Pinus taeda into Zimbabwe is possible given microsatelli
20 ortant plant species, such as loblolly pine (Pinus taeda L).
21 en and Cambage (Camden white gum) and native Pinus taeda L.
22                                              Pinus taeda L. (loblolly pine) and Arabidopsis thaliana
23                    Molecular dissection of a Pinus taeda L. selfed pedigree detected a chromosomal re
24  at a FACE site where leaf area index (L) of Pinus taeda L. was altered through nitrogen fertilizatio
25  homologous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudotsuga menziesii [
26 r deficit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characterized.
27 ag polymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.
28 lived, outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single nucleotide polym
29 Paxillus ammoniavirescens and loblolly pine (Pinus taeda L.) in axenic and symbiotic conditions at li
30   We have discovered a mutant loblolly pine (Pinus taeda L.) in which expression of the gene encoding
31                               Loblolly pine (Pinus taeda L.) is the most widely planted tree species
32                         Loblolly pine trees (Pinus taeda L.) occupy more than 20% of the forested are
33 uum f. sp fusiforme infecting loblolly pine (Pinus taeda L.) over much of this host's natural range.
34  lignin is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinnamyl alcohol de
35 e (Pinus palustris Mill.) and loblolly pine (Pinus taeda L.) trees in Florida, USA, and compared the
36           A consensus map for loblolly pine (Pinus taeda L.) was constructed from the integration of
37  ligase (4CL; EC 6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned.
38 ide oxidoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.
39                 For instance, loblolly pine (Pinus taeda L.), an ecologically and economically import
40  synthase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial forest tree spe
41 ground biomass components for loblolly pine (Pinus taeda L.), the dominant tree species, and broad-le
42 ty loci in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP markers from an es
43 icated full-sibling family of loblolly pine (Pinus taeda L.).
44 y across the natural range of loblolly pine (Pinus taeda L.).
45 ygotic and somatic embryos of loblolly pine (Pinus taeda L.).
46 accession number AF101785) in loblolly pine (Pinus taeda L.).
47 g xylem and in mature wood of loblolly pine (Pinus taeda L.).
48 tained from immature xylem of loblolly pine (Pinus taeda L.).
49 ctured breeding population of loblolly pine (Pinus taeda L.).
50 ndidate genes for drought-stress response in Pinus taeda L., an important tree crop.
51                               Loblolly pine, Pinus taeda L., is one of the most widely planted, comme
52  and 6 yr of nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.
53 disease-resistance properties, measured in a Pinus taeda (loblolly pine) training population of 951 i
54                      Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pestic
55 m a library constructed from differentiating Pinus taeda (loblolly pine) xylem RNA.
56                      This MYB family member, Pinus taeda MYB1 (PtMYB1), was most abundantly expressed
57                                    This MYB, Pinus taeda MYB4 (PtMYB4), is expressed in cells undergo
58 rom common gardens across the loblolly pine (Pinus taeda) natural range.
59 ee cohorts of selfed offspring from a single Pinus taeda parent were genotyped for nuclear microsatel
60 sis thaliana, is most closely related to the Pinus taeda phenylpropenal double bond reductase, involv
61       Analysis of full-length AAH cDNAs from Pinus taeda, Physcomitrella patens, and Chlamydomonas re
62 and assembled for Picea abies, Picea glauca, Pinus taeda, Pinus lambertiana, and Pseudotsuga menziesi
63 us, the response of understory vegetation in Pinus taeda plantation at the Duke Forest FACE site afte
64 luated the utility of genomic selection in a Pinus taeda population of c.
65     Only two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce (Picea sitchens
66  we show that range expansions of introduced Pinus taeda result from an interaction between genetic p
67 lore this, we performed a microcosm study on Pinus taeda roots inoculated with Suillus cothurnatus tr
68 shouse experiment, we exposed loblolly pine (Pinus taeda) saplings (n = 83) to drought-induced water
69 rus (P)) transfers and their ratios, between Pinus taeda seedlings and two ectomycorrhizal (EM) funga
70 owever, mCG-enriched genes in the gymnosperm Pinus taeda shared some similarities with gbM genes in A
71 approach to identify genes in loblolly pine (Pinus taeda) that are associated with resistance to pitc
72 hin a pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated at three sites
73 ctive response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide (CO2) enrichme
74 rstanding of the responses of loblolly pine (Pinus taeda) to drought stress.
75  endophytic fungi associated with needles of Pinus taeda trees across regional scales in the absence
76 mRNA from lignifying xylem of loblolly pine (Pinus taeda) trunk wood.
77 enzylic ether reductase from the gymnosperm, Pinus taeda, was cloned, with the recombinant protein he
78  26 miRNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conserved and seven l
79 t here the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multifunctional enzym
80  that is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetec