ライフサイエンスコーパス: radiata

1 control of torques in non-human primates (M. radiata).

2 nge of C. tramoserica) to 27.6 degrees C (C. radiata).

3 macaque monkeys (Macaca fascicularis and M. radiata).

4 H(+)-pyrophosphatase (EC 3.6.1.1) from Vigna radiata.

5 ontal gyrus white matter and anterior corona radiata.

6 minantly in the centrum semiovale and corona radiata.

7 ior limb of the internal capsule, and corona radiata.

8 otropy in the corpus callosum and the corona radiata.

9 thalamic radiation and right anterior corona radiata.

10 a ROI in the left hemisphere anterior corona radiata.

11 maternal and fetal organs in pregnant Macaca radiata.

12 erior longitudinal fasciculus and the corona radiata.

13 llucida matrix and had a disorganized corona radiata.

14 wed persistently lower FA in anterior corona radiata (ACR) (group, P = .04; group x age x sex, P = .0

15 Greater FA in the anterior corona radiata (ACR) was associated with better inhibition, ind

16 P = .02); MD, beta = -0.01 (P = .03)] corona radiata and external capsule [right FA, beta = 0.01 (P =

17 l anisotropy were evident only in the corona radiata and genu of the corpus callosum.

18 f the corpus callosum and beyond (eg, corona radiata and inferior longitudinal fasciculus) across all

19 onent of the motor system through the corona radiata and internal capsule are well described in non-h

20 han control subjects in the posterior corona radiata and the optic radiation (P < 0.002).

21 and alternative pathways in mung bean (Vigna radiata) and soybean (Glycine max) following growth at l

22 Parietal operculum, corona radiata, and internal capsule differences between cases

23 (in corpus callosum, cingulum bundle, corona radiata, and superior fronto-occipital fasciculus) and c

24 , fornix, stria terminalis, posterior corona radiata, and superior longitudinal fasciculus in remitte

25 rnix, and stria terminalis, posterior corona radiata, and superior longitudinal fasciculus.

26 callosum, the superior and posterior corona radiata, and the cingulum.

27 isotropy (optic radiations, posterior corona radiata, and the splenium region of the corpus callosum)

28 fronto-occipital fasciculus, superior corona radiata, and uncinate fasciculus.

29 rior longitudinal fasciculi, superior corona radiata, anterior thalamic radiations, and posterior lim

30 tor (M1) cortex of nonhuman primates (Macaca radiata) are modulated by reward expectation during reac

31 ferences also emerged in the anterior corona radiata as well as in white matter underlying the superi

32 ol and FA in left hemisphere anterior corona radiata, as well as the correlation between memory perfo

33 ernal capsule, superior and posterior corona radiata, bilateral external capsule and the right superi

34 ases in MD in the bilateral posterior corona radiata, bilateral superior longitudinal fasciculus, bil

35 nsferase (CCoAOMT) was isolated from a Pinus radiata cDNA library derived from differentiating xylem.

36 es) were isolated from a radiata pine (Pinus radiata) cDNA library prepared from immature female stro

37 lysis included anterior and posterior corona radiata, cortico-spinal tracts, cingulum fibre bundles,

38 of the corticofugal projection in the corona radiata (CR) and internal capsule (IC) can assist in eva

39 gulate (M4) motor regions through the corona radiata (CR), internal capsule (IC) and crus cerebri of

40 uperior longitudinal fasciculus (LF), corona radiata (CR), internal capsule (IC) and external capsule

41 obcone (Pinus attenuata Lemm.), Monterey (P. radiata D. Don), and bishop (P. muricata D. Don).

42 The anterior corona radiata (d=0.40) and corpus callosum (d=0.39), specifica

43 ole-brain FA in parts of the anterior corona radiata, external capsule, and cerebellum (P<0.05, famil

44 tween memory performance and anterior corona radiata FA.

45 nd archaeal communities on the kelp Ecklonia radiata from three biogeographical provinces spanning 10

46 f our study indicate that the exotic pine P. radiata has limited genetic constraints on the evolution

47 enced higher FA in the right superior corona radiata, higher FA and AD in bilateral corticospinal tra

48 traception of male nonhuman primates (Macaca radiata) immunized with Eppin, a testis/epididymis-speci

49 ocalizations by wild bonnet macaques (Macaca radiata) in southern India The bonnet macaques' flight a

50 red, socially-housed bonnet macaques (Macaca radiata) in three age groups: juvenile, adolescent, and

51 of interest in the centrum semiovale, corona radiata, internal capsule, corpus callosum, and subcorti

52 awn from a sample of the population of Pinus radiata introduced to Spain in the mid-19th century.

53 numbers of captive-reared A. gigantea and A. radiata is cost-effective and successful in the short te

54 Mungbean (Vigna radiata) is a fast-growing, warm-season legume crop that

55 lopmental gradients along a mung bean (Vigna radiata L.) hypocotyl of the growth rate, plasma membran

56 isolated from hypocotyls of mung bean (Vigna radiata L.), and pyrophosphate (PPi)- or ATP-dependent a

57 lated a 2022 bp cDNA (VrCDPK-1) from a Vigna radiata lambda gt11 library.

58 rrier genotypes in the left and right corona radiata, left uncinate fasciculus, left inferior fronto-

59 A pine (Pinus radiata) male cone-specific promoter, PrMC2, was used to

60 The pregnant M. radiata model allows the noninvasive measurement of radi

61 of this repeated element recovered from a P. radiata (Monterey pine) genomic DNA library was found to

62 eria is not likely to be the sister group of Radiata or Ctenophora, nor is it likely that Bilateria g

63 al capsule, callosal isthmus, and the corona radiata (p=0.04 for FIQ and p=0.01 for PIQ, corrected fo

64 Pinus radiata (Pinaceae) was found to exhibit ABA-driven stoma

65 1,4-glucanases (EGases) were isolated from a radiata pine (Pinus radiata) cDNA library prepared from

66 e presence of a family of EGase genes in the radiata pine genome, and that PrCel1 and PrCel2 are tran

67 We studied three species: Pinus radiata, Pinus sylvestris, and Cedrus libani.

68 sterior limb of the internal capsule, corona radiata, posterior frontal white matter, and parietal wh

69 e x-ray scattering study of mung bean (Vigna radiata) primary cell walls was combined with published

70 D in the right superior and posterior corona radiata, right superior longitudinal fasciculus, and in

71 , specifically within right posterior corona radiata, right tapetum, and bilateral corpus callosum, s

72 141 bp fragment of DNA from mungbeans (Vigna radiata Rwilcz cv. Berken).

73 ing phytic acid content in green gram (Vigna radiata) seeds was investigated by Fourier Transform Nea

74 yringyl units in softwood species such as P. radiata, suggesting that it might be possible to retain

75 orpus callosum, anterior and superior corona radiata, superior longitudinal and inferior fronto-occip

76 Pyrolysis-GC/MS and 2D-NMR analysis of P. radiata TE cultures transformed to express ferulate 5-hy

77 e cerebral peduncle, and the superior corona radiata than did the HC.

78 sis and from another plant, mung bean (Vigna radiata), to ascertain if this mechanism is commonly use

79 ises, Aldabrachelys gigantea and Astrochelys radiata, to two offshore Mauritian islands, and the cost

80 Using a transformable Pinus radiata tracheary element (TE) system as an experimental

81 e cinnamoyl-CoA reductase (CCR) in the Pinus radiata tracheary element (TE) system impacted both the

82 Suppression of PrCCoAOMT expression in P. radiata tracheary element cultures affected lignin conte

83 to the optic radiations and posterior corona radiata tracts (P < 0.05).

84 ients with NMO, mainly located in the corona radiata, uncinate fasciculus, corpus callosum, optic rad

85 on process in Arabidopsis thaliana and Pinus radiata under various feeding regimens.

86 d doses on leguminous plant mung bean (Vigna radiata) under laboratory condition.

87 The present assembly of V. radiata var. radiata will facilitate genome research and

88 ells in normal and compression wood of Pinus radiata, was examined to determine the relationships wit

89 Six pregnant M. radiata weighing 3.8-9.0 kg were anesthetized and MR ima

90 s and 3 pregnant nonhuman primates (Macaques radiata) weighing 4.5-7 kg were used for the imaging stu

91 ally immature A. gigantea and twelve male A. radiata were introduced to Round Island, Mauritius.

92 Australia (C. tramoserica) and Singapore (C. radiata), were compared across environments with differe

93 Tropical C. radiata, which lives in the least variable and most pred

94 The present assembly of V. radiata var. radiata will facilitate genome research and accelerate m

95 Seven bonnet macaques (Macaca radiata) with strong hand preferences in performing a co