ライフサイエンスコーパス: taeda

1 ruce (Picea abies), and loblolly pine (Pinus taeda).

2 aining 2,178 cDNAs from loblolly pine (Pinus taeda).

3 tious root formation in loblolly pine (Pinus taeda) after treatment with the exogenous auxin indole-3

4 The P. taeda and P. patens AAHs were specific for Phe, required

5 es measured in a single loblolly pine (Pinus taeda) association population.

6 l, 15N-Gln, and 15N-Glu) in lignifying Pinus taeda cell cultures was investigated, using a combinatio

7 ulation of their transcript levels in the P. taeda cell cultures; this in turn was accompanied by con

8 ling of the phenylpropanoid pathway in Pinus taeda cell suspension cultures was carried out using qua

9 ipts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-specific expression pat

10 imental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentrations, nearly half o

11 on on EMM production and turnover in a Pinus taeda forest.

12 rogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated CO(2) by measuring ext

13 and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment to inv

14 and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment to inv

15 nd water use of planted loblolly pine (Pinus taeda) growing across the southeastern United States.

16 Loblolly pine (Pinus taeda), in contrast, possesses a single 4CL protein exhi

17 ironments in a complex pedigree of 520 Pinus taeda individuals (CCLONES).

18 of early 20th century introductions of Pinus taeda into Zimbabwe is possible given microsatellite mar

19 s study was designed to determine whether P. taeda introductions into Zimbabwe came from one U.S. reg

20 plant species, such as loblolly pine (Pinus taeda L).

21 Pinus taeda L. (loblolly pine) and Arabidopsis thaliana differ

22 enetic mechanism promoting outcrossing in P. taeda L. appears to have a balancing selection system du

23 omparative analysis of P. lambertiana and P. taeda L. reveals new insights on the conservation, age,

24 Molecular dissection of a Pinus taeda L. selfed pedigree detected a chromosomal region i

25 FACE site where leaf area index (L) of Pinus taeda L. was altered through nitrogen fertilization, ice

26 ogous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudotsuga menziesii [Mirb.]

27 cit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characterized.

28 ymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.

29 outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single nucleotide polymorphis

30 ave discovered a mutant loblolly pine (Pinus taeda L.) in which expression of the gene encoding cinna

31 Loblolly pine (Pinus taeda L.) is the most widely planted tree species in the

32 Loblolly pine trees (Pinus taeda L.) occupy more than 20% of the forested area in t

33 sp fusiforme infecting loblolly pine (Pinus taeda L.) over much of this host's natural range.

34 n is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinnamyl alcohol dehydrog

35 A consensus map for loblolly pine (Pinus taeda L.) was constructed from the integration of linkag

36 e (4CL; EC 6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned.

37 idoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.

38 For instance, loblolly pine (Pinus taeda L.), an ecologically and economically important co

39 ase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial forest tree species.

40 i in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP markers from an essentia

41 breeding population of loblolly pine (Pinus taeda L.).

42 ss the natural range of loblolly pine (Pinus taeda L.).

43 and somatic embryos of loblolly pine (Pinus taeda L.).

44 ion number AF101785) in loblolly pine (Pinus taeda L.).

45 m and in mature wood of loblolly pine (Pinus taeda L.).

46 from immature xylem of loblolly pine (Pinus taeda L.).

47 full-sibling family of loblolly pine (Pinus taeda L.).

48 e genes for drought-stress response in Pinus taeda L., an important tree crop.

49 Loblolly pine, Pinus taeda L., is one of the most widely planted, commerciall

50 yr of nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.

51 e-resistance properties, measured in a Pinus taeda (loblolly pine) training population of 951 individ

52 Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pesticide 2,

53 brary constructed from differentiating Pinus taeda (loblolly pine) xylem RNA.

54 This MYB family member, Pinus taeda MYB1 (PtMYB1), was most abundantly expressed in di

55 This MYB, Pinus taeda MYB4 (PtMYB4), is expressed in cells undergoing li

56 orts of selfed offspring from a single Pinus taeda parent were genotyped for nuclear microsatellites.

57 aliana, is most closely related to the Pinus taeda phenylpropenal double bond reductase, involved in,

58 Analysis of full-length AAH cDNAs from Pinus taeda, Physcomitrella patens, and Chlamydomonas reinhard

59 e response of understory vegetation in Pinus taeda plantation at the Duke Forest FACE site after 15-1

60 the utility of genomic selection in a Pinus taeda population of c.

61 ly two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce (Picea sitchensis) Ps

62 ow that range expansions of introduced Pinus taeda result from an interaction between genetic provena

63 , mCG-enriched genes in the gymnosperm Pinus taeda shared some similarities with gbM genes in Amborel

64 with over 98% of all probes designed from P. taeda that were efficient in sequence capture, were also

65 ch to identify genes in loblolly pine (Pinus taeda) that are associated with resistance to pitch cank

66 pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated at three sites in th

67 response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide (CO2) enrichment (am

68 ing of the responses of loblolly pine (Pinus taeda) to drought stress.

69 roximately 72,000 sequences in a collated P. taeda transcript assembly derived from >245,000 ESTs der

70 hytic fungi associated with needles of Pinus taeda trees across regional scales in the absence of str

71 rom lignifying xylem of loblolly pine (Pinus taeda) trunk wood.

72 c ether reductase from the gymnosperm, Pinus taeda, was cloned, with the recombinant protein heterolo

73 RNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conserved and seven lobloll

74 RCN quantitative trait loci (QTLs) in a (P. taeda x Pinus elliottii) x P. elliottii pseudo-backcross

75 the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multifunctional enzyme, SAM

76 is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetectable