ライフサイエンスコーパス: loblolly pine

1 ocally misassembled contigs in assemblies of loblolly pine.

2 erage of 8.5 lethal equivalents reported for loblolly pine.

3 roups to represent the chromosomes n = 12 of loblolly pine.

4 thway associated with lignin biosynthesis in loblolly pine.

5 into 4CL mRNA in developing xylem tissue of loblolly pine.

6 e of stem defects in breeding populations 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 nce tags (ESTs) from wood-forming tissues of loblolly pine and compared them to the gene sequences in

10 and used stimulated optical mapping data for loblolly pine and F.tularensis and used real optical map

11 for PtACO1 in compression wood formation in loblolly pine and the discovery of its NIP are discussed

12 Pinus taeda L. (loblolly pine) and Arabidopsis thaliana differ greatly i

13 fferentially expressed in various tissues of loblolly pine, as well as in response to perturbations o

14 The transgenic tobacco plants carrying loblolly pine CCoAOMT promoter-GUS fusion localized the

15 l CoA ester O-methyltransferase (AEOMT) from loblolly pine differentiating xylem that was capable of

16 Changes in RNA transcript profiles of loblolly pine due to drought stress were correlated with

17 STRA, to predict eddy covariance data from a loblolly pine forest.

18 nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.

19 pply our method to various assemblies of the loblolly pine, Francisella tularensis, rice and budgerig

20 t CCoAOMT may exist as a single-copy gene in loblolly pine genome.

21 map QTL influencing wood property traits in loblolly pine has been completed.

22 ionally dominant fungal taxa associated with loblolly pine including Amphinema, Russula and Piloderma

23 A cDNA clone (lp3) from loblolly pine induced by water deficit stress (WDS) has

24 tory to early-stage somatic embryo growth of loblolly pine (LP) was purified chromatographically from

25 conomically important plant species, such as loblolly pine (Pinus taeda L).

26 Ten homologous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudots

27 ssed under water deficit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characte

28 ssed sequence tag polymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.

29 ed in the long-lived, outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single n

30 We have discovered a mutant loblolly pine (Pinus taeda L.) in which expression of th

31 Loblolly pine (Pinus taeda L.) is the most widely plante

32 ronartium quercuum f. sp fusiforme infecting loblolly pine (Pinus taeda L.) over much of this host's

33 Novel lignin is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinn

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

35 rate:coenzyme A ligase (4CL; EC 6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned.

36 rotochlorophyllide oxidoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.

37 For instance, loblolly pine (Pinus taeda L.), an ecologically and econ

38 a putative ACC synthase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial

39 bryonic viability loci in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP mar

40 raits in a structured breeding population of loblolly pine (Pinus taeda L.).

41 ted with aridity across the natural range of loblolly pine (Pinus taeda L.).

42 opulations of zygotic and somatic embryos of loblolly pine (Pinus taeda L.).

43 AGP (PtaAGP6, accession number AF101785) in loblolly pine (Pinus taeda L.).

44 differentiating xylem and in mature wood of loblolly pine (Pinus taeda L.).

45 s, ESTs were obtained from immature xylem of loblolly pine (Pinus taeda L.).

46 a clonally-replicated full-sibling family of loblolly pine (Pinus taeda L.).

47 ession during adventitious root formation in loblolly pine (Pinus taeda) after treatment with the exo

48 ions of 292 metabolites measured in a single loblolly pine (Pinus taeda) association population.

49 nstrated that transcripts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-sp

50 In experimental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentr

51 to carbon (C) and nitrogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated C

52 future productivity and water use of planted loblolly pine (Pinus taeda) growing across the southeast

53 Only two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce

54 lation genomic approach to identify genes in loblolly pine (Pinus taeda) that are associated with res

55 essed genes within a pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated

56 ned the reproductive response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide

57 mprove our understanding of the responses of loblolly pine (Pinus taeda) to drought stress.

58 produced using mRNA from lignifying xylem of loblolly pine (Pinus taeda) trunk wood.

59 We report here the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multif

60 ript, PtNIP1;1, that is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos,

61 Loblolly pine (Pinus taeda), in contrast, possesses a si

62 and identified 26 miRNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conser

63 ea glauca), Norway spruce (Picea abies), and loblolly pine (Pinus taeda).

64 DNA microarrays containing 2,178 cDNAs from loblolly pine (Pinus taeda).

65 Loblolly pine, Pinus taeda L., is one of the most widely

66 bon budget estimate for a typical commercial loblolly pine plantation in North Carolina, USA, spannin

67 , based on 5 years of data from two adjacent loblolly pine plantations.

68 aining various amounts of water and roots of loblolly pine planted into similar sand.

69 Application of SEM to loblolly pine QTL data provided support for biologically

70 identify additional ACC oxidase clones from loblolly pine root cDNA libraries characterized as part

71 nitrogen that accompanied nearly 50 years of loblolly pine secondary forest development.

72 efficiently methylated in crude extracts of loblolly pine secondary xylem.

73 Images of loblolly pine seedling roots planted in identical sand s

74 in the base of hypocotyl stem cuttings from loblolly pine seedlings in response to indole-3-butyric

75 . are used, the effective population size of loblolly pine should be 5.6 x 10(5).

76 Members of three loblolly pine-specific miRNA families target a large num

77 a), which belong to four conserved and seven loblolly pine-specific miRNA families.

78 expected for a large majority of the planted loblolly pine stands in the southeastern United States d

79 rms, a 1.3 kb CCoAOMT cDNA was isolated from loblolly pine that showed 79-82% amino acid sequence ide

80 tance properties, measured in a Pinus taeda (loblolly pine) training population of 951 individuals ge

81 luable addition to development of a complete loblolly pine transcriptome.

82 In loblolly pine, transient expression increased 10-fold ut

83 Loblolly pine trees (Pinus taeda L.) occupy more than 20

84 ntified in an outbred full-sibling family of loblolly pine, using single-nucleotide polymorphism mark

85 Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pesticide 2,4-dichl

86 mines resistance to fusiform rust disease in loblolly pine where no discrete, simply inherited resist

87 is significant genetic variation for RCN in loblolly pine, which can be exploited in breeding for el

88 ethylation pathway in lignin biosynthesis in loblolly pine xylem.

89 onstructed from differentiating Pinus taeda (loblolly pine) xylem RNA.