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1 ruce (Picea abies), and loblolly pine (Pinus taeda).
2 aining 2,178 cDNAs from loblolly pine (Pinus taeda).
3  the basis for stable dwarf phenotypes in P. taeda.
4    The results of this study show that in P. taeda, a small number of major QTL can provide effective
5 tious root formation in loblolly pine (Pinus taeda) after treatment with the exogenous auxin indole-3
6                                       The P. taeda and P. patens AAHs were specific for Phe, required
7 es measured in a single loblolly pine (Pinus taeda) association population.
8  loam soil and a biochar obtained from Pinus taeda at 500 degrees C.
9 l, 15N-Gln, and 15N-Glu) in lignifying Pinus taeda cell cultures was investigated, using a combinatio
10 ulation of their transcript levels in the P. taeda cell cultures; this in turn was accompanied by con
11 ling of the phenylpropanoid pathway in Pinus taeda cell suspension cultures was carried out using qua
12 Cl(-) diffusing through loblolly pine (Pinus taeda) cell wall layers under 70%, 75%, or 80% relative
13 ipts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-specific expression pat
14                                     In Pinus taeda, dwarf phenotypes originate from abnormal branches
15 imental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentrations, nearly half o
16 on on EMM production and turnover in a Pinus taeda forest.
17 rogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated CO(2) by measuring ext
18  and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment to inv
19  and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment to inv
20 nd water use of planted loblolly pine (Pinus taeda) growing across the southeastern United States.
21                         Loblolly pine (Pinus taeda), in contrast, possesses a single 4CL protein exhi
22 ironments in a complex pedigree of 520 Pinus taeda individuals (CCLONES).
23 of early 20th century introductions of Pinus taeda into Zimbabwe is possible given microsatellite mar
24 s study was designed to determine whether P. taeda introductions into Zimbabwe came from one U.S. reg
25                                       For P. taeda, it is concluded that eCO(2) affects allometries,
26  plant species, such as loblolly pine (Pinus taeda L).
27  Cambage (Camden white gum) and native Pinus taeda L.
28                                        Pinus taeda L. (loblolly pine) and Arabidopsis thaliana differ
29 enetic mechanism promoting outcrossing in P. taeda L. appears to have a balancing selection system du
30 omparative analysis of P. lambertiana and P. taeda L. reveals new insights on the conservation, age,
31              Molecular dissection of a Pinus taeda L. selfed pedigree detected a chromosomal region i
32 FACE site where leaf area index (L) of Pinus taeda L. was altered through nitrogen fertilization, ice
33 ogous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudotsuga menziesii [Mirb.]
34 cit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characterized.
35 ymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.
36  outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single nucleotide polymorphis
37 us ammoniavirescens and loblolly pine (Pinus taeda L.) in axenic and symbiotic conditions at limited
38 ave discovered a mutant loblolly pine (Pinus taeda L.) in which expression of the gene encoding cinna
39                         Loblolly pine (Pinus taeda L.) is the most widely planted tree species in the
40                   Loblolly pine trees (Pinus taeda L.) occupy more than 20% of the forested area in t
41  sp fusiforme infecting loblolly pine (Pinus taeda L.) over much of this host's natural range.
42 n is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinnamyl alcohol dehydrog
43 us palustris Mill.) and loblolly pine (Pinus taeda L.) trees in Florida, USA, and compared the perfor
44     A consensus map for loblolly pine (Pinus taeda L.) was constructed from the integration of linkag
45 e (4CL; EC 6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned.
46 idoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.
47           For instance, loblolly pine (Pinus taeda L.), an ecologically and economically important co
48 ase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial forest tree species.
49  biomass components for loblolly pine (Pinus taeda L.), the dominant tree species, and broad-leaved s
50 i in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP markers from an essentia
51  breeding population of loblolly pine (Pinus taeda L.).
52  full-sibling family of loblolly pine (Pinus taeda L.).
53 ss the natural range of loblolly pine (Pinus taeda L.).
54  and somatic embryos of loblolly pine (Pinus taeda L.).
55 ion number AF101785) in loblolly pine (Pinus taeda L.).
56 m and in mature wood of loblolly pine (Pinus taeda L.).
57  from immature xylem of loblolly pine (Pinus taeda L.).
58 e genes for drought-stress response in Pinus taeda L., an important tree crop.
59                         Loblolly pine, Pinus taeda L., is one of the most widely planted, commerciall
60  yr of nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.
61 e-resistance properties, measured in a Pinus taeda (loblolly pine) training population of 951 individ
62                Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pesticide 2,
63 brary constructed from differentiating Pinus taeda (loblolly pine) xylem RNA.
64                This MYB family member, Pinus taeda MYB1 (PtMYB1), was most abundantly expressed in di
65                              This MYB, Pinus taeda MYB4 (PtMYB4), is expressed in cells undergoing li
66 mmon gardens across the loblolly pine (Pinus taeda) natural range.
67 orts of selfed offspring from a single Pinus taeda parent were genotyped for nuclear microsatellites.
68 architecture of disease resistance in two P. taeda parents that showed high resistance across multipl
69 aliana, is most closely related to the Pinus taeda phenylpropenal double bond reductase, involved in,
70 Analysis of full-length AAH cDNAs from Pinus taeda, Physcomitrella patens, and Chlamydomonas reinhard
71 sembled for Picea abies, Picea glauca, Pinus taeda, Pinus lambertiana, and Pseudotsuga menziesii var.
72 e response of understory vegetation in Pinus taeda plantation at the Duke Forest FACE site after 15-1
73  the utility of genomic selection in a Pinus taeda population of c.
74 ly two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce (Picea sitchensis) Ps
75 ow that range expansions of introduced Pinus taeda result from an interaction between genetic provena
76 his, we performed a microcosm study on Pinus taeda roots inoculated with Suillus cothurnatus treated
77  experiment, we exposed loblolly pine (Pinus taeda) saplings (n = 83) to drought-induced water stress
78 )) transfers and their ratios, between Pinus taeda seedlings and two ectomycorrhizal (EM) fungal spec
79 , mCG-enriched genes in the gymnosperm Pinus taeda shared some similarities with gbM genes in Amborel
80 with over 98% of all probes designed from P. taeda that were efficient in sequence capture, were also
81 ch to identify genes in loblolly pine (Pinus taeda) that are associated with resistance to pitch cank
82 pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated at three sites in th
83 response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide (CO2) enrichment (am
84 ing of the responses of loblolly pine (Pinus taeda) to drought stress.
85 roximately 72,000 sequences in a collated P. taeda transcript assembly derived from >245,000 ESTs der
86 hytic fungi associated with needles of Pinus taeda trees across regional scales in the absence of str
87                            In particular, P. taeda trees at a given diameter were observed to be tall
88 rom lignifying xylem of loblolly pine (Pinus taeda) trunk wood.
89 c ether reductase from the gymnosperm, Pinus taeda, was cloned, with the recombinant protein heterolo
90 RNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conserved and seven lobloll
91  RCN quantitative trait loci (QTLs) in a (P. taeda x Pinus elliottii) x P. elliottii pseudo-backcross
92  the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multifunctional enzyme, SAM
93 is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetectable