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1  macaque monkeys (Macaca fascicularis and M. radiata).
2 cortex of awake monkeys (three female Macaca radiata).
3 control of torques in non-human primates (M. radiata).
4 nge of C. tramoserica) to 27.6 degrees C (C. radiata).
5 erior longitudinal fasciculus and the corona radiata.
6 llucida matrix and had a disorganized corona radiata.
7 o brain regions: the thalamus and the corona radiata.
8 e observed in the corpus callosum and corona radiata.
9 lthy seedlings of Pinus sylvestris and Pinus radiata.
10 anisotropy in the corpus callosum and corona radiata.
11 ased mean diffusivity of the anterior corona radiata.
12 minantly in the centrum semiovale and corona radiata.
13 H(+)-pyrophosphatase (EC 3.6.1.1) from Vigna radiata.
14 ontal gyrus white matter and anterior corona radiata.
15 ior limb of the internal capsule, and corona radiata.
16 otropy in the corpus callosum and the corona radiata.
17 thalamic radiation and right anterior corona radiata.
18 a ROI in the left hemisphere anterior corona radiata.
19 maternal and fetal organs in pregnant Macaca radiata.
20 s the bilateral anterior and superior corona radiatas.
21 tus; 200 Mb) and the Thorny Skate (Amblyraja radiata; 2650 Mb).
22 wed persistently lower FA in anterior corona radiata (ACR) (group, P = .04; group x age x sex, P = .0
23            Greater FA in the anterior corona radiata (ACR) was associated with better inhibition, ind
24 us, posterior thalamic radiation, and corona radiata (all p < 0.05).
25 ite matter microstructure at the left corona radiata and also associated with overall symptoms (all c
26                 Our findings suggest that V. radiata and B. diazoefficiens USDA110 may use NopE to op
27 h the highest lesion frequency in the corona radiata and between C2 and C4 vertebral levels.
28  the mPPases from Thermotoga maritima, Vigna radiata and Clostridium leptum and characterised by inte
29              We sampled beneath mature Pinus radiata and Eucalyptus racemosa in a pine-invaded eucaly
30 P = .02); MD, beta = -0.01 (P = .03)] corona radiata and external capsule [right FA, beta = 0.01 (P =
31 al anisotropy in the corpus callosum, corona radiata and external capsule, and increased mean diffusi
32 l anisotropy were evident only in the corona radiata and genu of the corpus callosum.
33 f the corpus callosum and beyond (eg, corona radiata and inferior longitudinal fasciculus) across all
34 onent of the motor system through the corona radiata and internal capsule are well described in non-h
35 pecific within the araphid 2 taxon Astrosyne radiata and radial 2 taxon Proboscia sp.
36  centered bilaterally in the superior corona radiata and subcortical gray and white matter (cluster p
37    The loading factor in the anterior corona radiata and temporo-parieto-frontal components were asso
38 han control subjects in the posterior corona radiata and the optic radiation (P < 0.002).
39 Seeds of Oryza sativa, Brassica nigra, Vigna radiata and V. aconitifolia were enclosed in Petri dishe
40 and alternative pathways in mung bean (Vigna radiata) and soybean (Glycine max) following growth at l
41 imb of the internal capsule, superior corona radiata, and cerebellar peduncles), the association betw
42  callosum (CC) and bilateral anterior corona radiata, and higher FW in the body of the CC compared wi
43                   Parietal operculum, corona radiata, and internal capsule differences between cases
44 mb of the internal capsule, posterior corona radiata, and partly in the left sagittal stratum.
45 (in corpus callosum, cingulum bundle, corona radiata, and superior fronto-occipital fasciculus) and c
46 , fornix, stria terminalis, posterior corona radiata, and superior longitudinal fasciculus in remitte
47 rnix, and stria terminalis, posterior corona radiata, and superior longitudinal fasciculus.
48  callosum, the superior and posterior corona radiata, and the cingulum.
49 isotropy (optic radiations, posterior corona radiata, and the splenium region of the corpus callosum)
50 fronto-occipital fasciculus, superior corona radiata, and uncinate fasciculus.
51 rior longitudinal fasciculi, superior corona radiata, anterior thalamic radiations, and posterior lim
52 tor (M1) cortex of nonhuman primates (Macaca radiata) are modulated by reward expectation during reac
53 ferences also emerged in the anterior corona radiata as well as in white matter underlying the superi
54     Here, using mungbean (Vigna radiata var. radiata) as a test case, we investigated the genomes of
55 gitudinal fasciculus, right posterior corona radiata, as well as the bilateral anterior and superior
56 ol and FA in left hemisphere anterior corona radiata, as well as the correlation between memory perfo
57 nown CI assembly intermediate CI* from Vigna radiata at 3.9 angstrom resolution.
58 ernal capsule, superior and posterior corona radiata, bilateral external capsule and the right superi
59 ases in MD in the bilateral posterior corona radiata, bilateral superior longitudinal fasciculus, bil
60 nsferase (CCoAOMT) was isolated from a Pinus radiata cDNA library derived from differentiating xylem.
61 es) were isolated from a radiata pine (Pinus radiata) cDNA library prepared from immature female stro
62 cts including the corpus callosum and corona radiata compared to mature-born adults.
63  longitudinal fasciculus and superior corona radiata) compared to controls (adjusted-p values < 0.05)
64 ical and cortico-thalamic fibers: the corona radiata, corpus callosum, superior longitudinal fascicul
65 lysis included anterior and posterior corona radiata, cortico-spinal tracts, cingulum fibre bundles,
66 of the corticofugal projection in the corona radiata (CR) and internal capsule (IC) can assist in eva
67 gulate (M4) motor regions through the corona radiata (CR), internal capsule (IC) and crus cerebri of
68 uperior longitudinal fasciculus (LF), corona radiata (CR), internal capsule (IC) and external capsule
69 ecifically triggered incompatibility with V. radiata cv. KPS2, but it promoted nodulation in other va
70 obcone (Pinus attenuata Lemm.), Monterey (P. radiata D. Don), and bishop (P. muricata D. Don).
71 ciculus (Cohen's d = 0.37), posterior corona radiata (d = 0.32), and superior fronto-occipital fascic
72                          The anterior corona radiata (d=0.40) and corpus callosum (d=0.39), specifica
73 of CIII(2), CIV, and SC III(2)+IV from Vigna radiata determined by single-particle cryoEM.
74 ps of the genus Ecklonia maxima and Ecklonia radiata, each associated with specific thermal niches, a
75 ole-brain FA in parts of the anterior corona radiata, external capsule, and cerebellum (P<0.05, famil
76 tween memory performance and anterior corona radiata FA.
77 no such relationships observed in the corona radiata for any of the metabolites examined.
78 nd archaeal communities on the kelp Ecklonia radiata from three biogeographical provinces spanning 10
79 nidae; Lampsilis siliquoidea (Barnes) and L. radiata (Gmelin)] that present intermediate forms in are
80                       Brown seaweed Ecklonia radiata harbors valuable polyphenols, notably phlorotann
81 f our study indicate that the exotic pine P. radiata has limited genetic constraints on the evolution
82 enced higher FA in the right superior corona radiata, higher FA and AD in bilateral corticospinal tra
83 traception of male nonhuman primates (Macaca radiata) immunized with Eppin, a testis/epididymis-speci
84 the corpus callosum and left anterior corona radiata in individuals with HUD correlated with a reduct
85 entation dispersion index in superior corona radiata in males.
86 ocalizations by wild bonnet macaques (Macaca radiata) in southern India The bonnet macaques' flight a
87 red, socially-housed bonnet macaques (Macaca radiata) in three age groups: juvenile, adolescent, and
88 promoted nodulation in other varieties of V. radiata, including KPS1.
89 5% CI, 5.5-13.4 mm3]), left posterior corona radiata (intensive treatment, 26.0 mm3 [95% CI, 12.9-39.
90 e matter regions of the left anterior corona radiata (intensive treatment, 30.3 mm3 [95% CI, 16.0-44.
91 of interest in the centrum semiovale, corona radiata, internal capsule, corpus callosum, and subcorti
92 and specific brain regions (including corona radiata, internal capsule, superior and inferior longitu
93 awn from a sample of the population of Pinus radiata introduced to Spain in the mid-19th century.
94 numbers of captive-reared A. gigantea and A. radiata is cost-effective and successful in the short te
95                              Mungbean (Vigna radiata) is a fast-growing, warm-season legume crop that
96                  The Thorny Skate (Amblyraja radiata) is a vulnerable species displaying a discrete s
97 lopmental gradients along a mung bean (Vigna radiata L.) hypocotyl of the growth rate, plasma membran
98                             Mung bean (Vigna radiata L.) is an edible legume seed which has attracted
99 isolated from hypocotyls of mung bean (Vigna radiata L.), and pyrophosphate (PPi)- or ATP-dependent a
100  and crop yield, including mung bean [(Vigna radiata (L.) R.
101 s, especially in crops like mung bean (Vigna radiata (L.) R.
102 nk] in response to different mungbean [Vigna radiata (L.) R.
103 lated a 2022 bp cDNA (VrCDPK-1) from a Vigna radiata lambda gt11 library.
104 rrier genotypes in the left and right corona radiata, left uncinate fasciculus, left inferior fronto-
105                                A pine (Pinus radiata) male cone-specific promoter, PrMC2, was used to
106 lly by axial diffusivity of the right corona radiata, (maximum indirect effect beta = -0.034 (CI: -0.
107                              The pregnant M. radiata model allows the noninvasive measurement of radi
108 of this repeated element recovered from a P. radiata (Monterey pine) genomic DNA library was found to
109  we demonstrated that the symbiosis of Vigna radiata (mung bean) with Bradyrhizobium diazoefficiens U
110 o non-human primates (NHPs), one male Macaca Radiata (NHP S) and one female Macaca Mulatta (NHP P), t
111 a 100 km range contraction of kelp (Ecklonia radiata) off Western Australia, but recently recovering
112 eria is not likely to be the sister group of Radiata or Ctenophora, nor is it likely that Bilateria g
113 anterior thalamic radiation, anterior corona radiata, or external capsule.
114 al capsule, callosal isthmus, and the corona radiata (p=0.04 for FIQ and p=0.01 for PIQ, corrected fo
115                                        Pinus radiata (Pinaceae) was found to exhibit ABA-driven stoma
116 1,4-glucanases (EGases) were isolated from a radiata pine (Pinus radiata) cDNA library prepared from
117 e presence of a family of EGase genes in the radiata pine genome, and that PrCel1 and PrCel2 are tran
118              We studied three species: Pinus radiata, Pinus sylvestris, and Cedrus libani.
119 chemical properties between non-native Pinus radiata plantations, and nearby native forests in a regi
120 sterior limb of the internal capsule, corona radiata, posterior frontal white matter, and parietal wh
121   This study illuminated the potential of E. radiata potential as a polyphenol source and offers opti
122  higher fractional anisotropy of left corona radiata, predicted fewer inhibitory deficits, suggesting
123 e x-ray scattering study of mung bean (Vigna radiata) primary cell walls was combined with published
124 r microstructure (e.g. genu, anterior corona radiata), rather than posterior (e.g. splenium, posterio
125 allosal and projection fibers (IC and corona radiata) relative to controls, but lower FA than control
126 D in the right superior and posterior corona radiata, right superior longitudinal fasciculus, and in
127 , specifically within right posterior corona radiata, right tapetum, and bilateral corpus callosum, s
128 141 bp fragment of DNA from mungbeans (Vigna radiata Rwilcz cv. Berken).
129 ing phytic acid content in green gram (Vigna radiata) seeds was investigated by Fourier Transform Nea
130                             Mung bean (Vigna radiata) stands as a crucial legume crop in Asia, contri
131 yringyl units in softwood species such as P. radiata, suggesting that it might be possible to retain
132 orpus callosum, anterior and superior corona radiata, superior longitudinal and inferior fronto-occip
133 ively, including the corpus callosum, corona radiata, superior longitudinal fasciculus, and corticosp
134    Pyrolysis-GC/MS and 2D-NMR analysis of P. radiata TE cultures transformed to express ferulate 5-hy
135 e cerebral peduncle, and the superior corona radiata than did the HC.
136 n posterior (e.g. splenium, posterior corona radiata)-the mediatory effect of anterior white matter s
137 matter microstructure of the anterior corona radiata, then cognition (working memory, focused attenti
138                                        In P. radiata, this distinction was possible even before the s
139 sis and from another plant, mung bean (Vigna radiata), to ascertain if this mechanism is commonly use
140 ises, Aldabrachelys gigantea and Astrochelys radiata, to two offshore Mauritian islands, and the cost
141                  Using a transformable Pinus radiata tracheary element (TE) system as an experimental
142 e cinnamoyl-CoA reductase (CCR) in the Pinus radiata tracheary element (TE) system impacted both the
143    Suppression of PrCCoAOMT expression in P. radiata tracheary element cultures affected lignin conte
144 to the optic radiations and posterior corona radiata tracts (P < 0.05).
145 ients with NMO, mainly located in the corona radiata, uncinate fasciculus, corpus callosum, optic rad
146 on process in Arabidopsis thaliana and Pinus radiata under various feeding regimens.
147 d doses on leguminous plant mung bean (Vigna radiata) under laboratory condition.
148                   The present assembly of V. radiata var. radiata will facilitate genome research and
149                  Here, using mungbean (Vigna radiata var. radiata) as a test case, we investigated th
150 ion ~ 70 km eastward, to sites where only E. radiata was previously reported.
151 ells in normal and compression wood of Pinus radiata, was examined to determine the relationships wit
152 ing native genotypes of Monterey pine (Pinus radiata), we performed a common garden experiment at a f
153                              Six pregnant M. radiata weighing 3.8-9.0 kg were anesthetized and MR ima
154 s and 3 pregnant nonhuman primates (Macaques radiata) weighing 4.5-7 kg were used for the imaging stu
155 callosum, longitudinal fasciculus and corona radiata were independent contributors to the Brief Visuo
156 ally immature A. gigantea and twelve male A. radiata were introduced to Round Island, Mauritius.
157 Australia (C. tramoserica) and Singapore (C. radiata), were compared across environments with differe
158                                  Tropical C. radiata, which lives in the least variable and most pred
159  cortex FC significantly mediated the corona radiata white matter effects on SICI (p = .007).
160      The present assembly of V. radiata var. radiata will facilitate genome research and accelerate m
161                Seven bonnet macaques (Macaca radiata) with strong hand preferences in performing a co

 
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