ライフサイエンスコーパス: Pinus taeda

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 15NH4Cl, 15N-Gln, and 15N-Glu) in lignifying Pinus taeda cell cultures was investigated, using a comb

6 profiling of the phenylpropanoid pathway in Pinus taeda cell suspension cultures was carried out usi

7 ranscripts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-specific expressi

8 experimental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentrations, nearly

9 lization on EMM production and turnover in a Pinus taeda forest.

10 nd nitrogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated CO(2) by measuri

11 atural and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment

12 atural and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment

13 vity and water use of planted loblolly pine (Pinus taeda) growing across the southeastern United Stat

14 Loblolly pine (Pinus taeda), in contrast, possesses a single 4CL protei

15 ee environments in a complex pedigree of 520 Pinus taeda individuals (CCLONES).

16 rigin of early 20th century introductions of Pinus taeda into Zimbabwe is possible given microsatelli

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

18 Pinus taeda L. (loblolly pine) and Arabidopsis thaliana

19 Molecular dissection of a Pinus taeda L. selfed pedigree detected a chromosomal re

20 at a FACE site where leaf area index (L) of Pinus taeda L. was altered through nitrogen fertilizatio

21 homologous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudotsuga menziesii [

22 r deficit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characterized.

23 ag polymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.

24 lived, outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single nucleotide polym

25 We have discovered a mutant loblolly pine (Pinus taeda L.) in which expression of the gene encoding

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

27 Loblolly pine trees (Pinus taeda L.) occupy more than 20% of the forested are

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

29 lignin is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinnamyl alcohol de

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

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

32 ide oxidoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.

33 For instance, loblolly pine (Pinus taeda L.), an ecologically and economically import

34 synthase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial forest tree spe

35 ty loci in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP markers from an es

36 y across the natural range of loblolly pine (Pinus taeda L.).

37 ctured breeding population of loblolly pine (Pinus taeda L.).

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

39 accession number AF101785) in loblolly pine (Pinus taeda L.).

40 g xylem and in mature wood of loblolly pine (Pinus taeda L.).

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

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

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

44 Loblolly pine, Pinus taeda L., is one of the most widely planted, comme

45 and 6 yr of nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.

46 disease-resistance properties, measured in a Pinus taeda (loblolly pine) training population of 951 i

47 Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pestic

48 m a library constructed from differentiating Pinus taeda (loblolly pine) xylem RNA.

49 This MYB family member, Pinus taeda MYB1 (PtMYB1), was most abundantly expressed

50 This MYB, Pinus taeda MYB4 (PtMYB4), is expressed in cells undergo

51 ee cohorts of selfed offspring from a single Pinus taeda parent were genotyped for nuclear microsatel

52 sis thaliana, is most closely related to the Pinus taeda phenylpropenal double bond reductase, involv

53 Analysis of full-length AAH cDNAs from Pinus taeda, Physcomitrella patens, and Chlamydomonas re

54 us, the response of understory vegetation in Pinus taeda plantation at the Duke Forest FACE site afte

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

56 Only two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce (Picea sitchens

57 we show that range expansions of introduced Pinus taeda result from an interaction between genetic p

58 owever, mCG-enriched genes in the gymnosperm Pinus taeda shared some similarities with gbM genes in A

59 approach to identify genes in loblolly pine (Pinus taeda) that are associated with resistance to pitc

60 hin a pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated at three sites

61 ctive response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide (CO2) enrichme

62 rstanding of the responses of loblolly pine (Pinus taeda) to drought stress.

63 endophytic fungi associated with needles of Pinus taeda trees across regional scales in the absence

64 mRNA from lignifying xylem of loblolly pine (Pinus taeda) trunk wood.

65 enzylic ether reductase from the gymnosperm, Pinus taeda, was cloned, with the recombinant protein he

66 26 miRNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conserved and seven l

67 t here the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multifunctional enzym

68 that is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetec