ライフサイエンスコーパス: cerebrum

1 52% (temporal cortical gray matter) and 76% (cerebrum).

2 te matter of the spinal cord, brainstem, and cerebrum.

3 tic rats still possessed more GLUT1 than the cerebrum.

4 subventricular zones (SVZs) of the embryonic cerebrum.

5 nmental and genetic insults to the postnatal cerebrum.

6 r spread outside the brainstem including the cerebrum.

7 ytes following transplantation into neonatal cerebrum.

8 t was recovered also from trachea, lung, and cerebrum.

9 D67, which is significantly less than in the cerebrum.

10 ses jointly affecting the cerebellum and the cerebrum.

11 te matter abnormalities involving the entire cerebrum.

12 utionary mechanisms culminating in the human cerebrum.

13 s observed throughout the frontal cortex and cerebrum.

14 as markedly decreased in Alzheimer's disease cerebrum.

15 ning the telencephalon, the precursor to the cerebrum.

16 eries from 112 regions comprising the entire cerebrum.

17 es optimized for both the cerebellum and the cerebrum.

18 the cortices of the mammalian cerebellum and cerebrum.

19 higher levels in the cerebellum than in the cerebrum.

20 al pressure into the deep gray matter of the cerebrum.

21 olume variation-lags far behind that for the cerebrum.

22 the neuron specific marker betaTUBIII in the cerebrum.

23 at confers this sensitivity in the adult rat cerebrum.

24 ular volumes were less prominent than in the cerebrum.

25 n of activity in the brainstem, thalamus and cerebrum.

26 to the epicardium (71%), endocardium (93%), cerebrum (183%), brain stem (177%), renal cortex (53%),

27 found between Sz and reduced volumes of the cerebrum (-.22 [-.30/-.14]) and white matter (-.17 [-.25

28 Slices of cerebrum, 300-500 microm thick, were made from P3 newbor

29 oxLDL may be present in parenchymal cells of cerebrum after infarction and that oxLDL may influence t

30 bnormal myelin compaction in spinal cord and cerebrum, an ultrastructural defect that we propose to b

31 sed as an approximately 3.3-kb transcript in cerebrum and as an approximately 4.4-kb transcript in th

32 in a serially sectioned C57BL/6 mouse brain (cerebrum and brainstem).

33 f the intranuclear inclusions throughout the cerebrum and brainstem, being most numerous in the hippo

34 disorders: evolutionary-driven expansion of cerebrum and cerebellar size; imbalance in the excitator

35 essing cells were randomly localized in Rett cerebrum and cerebellum and showed normal MeCP2 expressi

36 THGr measures demonstrated diaschisis in the cerebrum and cerebellum of patients with glioma.

37 THGr measures demonstrated diaschisis in the cerebrum and cerebellum of patients with glioma.

38 plicated in the expansion and folding of the cerebrum and cerebellum, respectively.

39 overactivations of the motor system in both cerebrum and cerebellum, with right cerebral dominance.

40 in the evolution of cortical folding of the cerebrum and cerebellum.

41 astic medulloblastomas and can occur in both cerebrum and cerebellum.

42 rmally unaffected brain regions, such as the cerebrum and cerebellum.

43 arily in developing limbic structures of the cerebrum and diencephalon, and in the medulla of the bra

44 tivation were observed in the contralesional cerebrum and ipsilesional cerebellum (P = .009).

45 ted (grey and white matter) volumes of total cerebrum and lobar regions.

46 d, with expression significantly high in the cerebrum and low in the cerebellum.

47 MeCP2(hi) neurons highest in layer IV of the cerebrum and MeCP2(lo )neurons highest in the granular l

48 Lesions that involved the cerebrum and posterior fossa accounted for 11.7% (218 of

49 Cortical thickness across the cerebrum and presence of DSM-IV-defined ADHD at follow-u

50 nts demonstrated white matter disease in the cerebrum and spinal cord.

51 Volumes of the total cerebrum and the hippocampus were measured.

52 in the parietal and occipital regions of the cerebrum and the suprapyramidal region of the medulla.

53 Volumes of the cerebrum and total and regional GM were obtained by usin

54 The cerebrums and ventricles were isolated and then parcella

55 (SCPN), which send projections away from the cerebrum, and callosal projection neurons (CPN), which s

56 n carbonyl derivatives in the liver, kidney, cerebrum, and cerebellum, respectively.

57 lls in the lung, in pyramidal neurons in the cerebrum, and in Purkinje cells in the cerebellum.

58 mage was observed in the outer layers of the cerebrum, and numerous condensed neuronal nuclei were pr

59 l precursors in the cerebellum, hippocampus, cerebrum, and olfactory bulb, where migration establishe

60 of GLUT1 and GLUT3 expression in the retina, cerebrum, and their respective microvessels by Western b

61 ntitative measurements were obtained for the cerebrum, anterior frontal region, lateral ventricles, t

62 The cerebrum appeared most severely affected, but the gross

63 nal tumors, which are often localized in the cerebrum, are both characterized by a neoplastic glial c

64 -soluble and insoluble Abeta by ELISA in the cerebrum, as compared with TLR4 wild-type mouse models.

65 Post-mortem material from the cerebrum, brainstem and spinal cord of 55 multiple scler

66 Quantitative CBF fell 6-8% in the cerebrum, brainstem, and cerebellum.

67 ed concentrations of these substances in the cerebrum, brainstem, and spinal cord.

68 eased markedly in the anterior and posterior cerebrum but increased in the brainstem of GAP43-/- mice

69 se paralysis or significant infection of the cerebrum but showed marked involvement of the cerebellum

70 cells of cerebellum and in neuronal cells of cerebrum, but at very high levels in testis.

71 Volumetric measures of the cerebrum, caudate nucleus, putamen, globus pallidus, amy

72 tally with a markedly enlarged and malformed cerebrum caused by reduced apoptosis during brain develo

73 cingulate and neocortex, and white matter of cerebrum, cerebellum, and corpus callosum).

74 om various regions of rat brain, namely, the cerebrum, cerebellum, and medulla.

75 The entire brain was segmented into cerebrum, cerebellum, brainstem and ventricles.

76 ated with severe, mutifocal apoptosis in the cerebrum, cerebellum, brainstem, spinal cord, and retina

77 and prospective age-related changes of total cerebrum, cerebellum, gray and white matter for the 4 ma

78 differences were observed for intracranial, cerebrum, cerebellum, or lateral ventricle volume or for

79 with message detected in mouse adult spleen, cerebrum, cerebellum/medulla, and thymus.

80 pression of GAT-1 and GAT-3 in the adult rat cerebrum changes after needle lesion and colchicine infu

81 sis before death, and viral infection of the cerebrum, characterized by inflammation and necrosis.

82 FC), as well as postcentral gyrus and global cerebrum control regions.

83 We measured volumes of total cerebrum, frontal lobes, caudate nucleus, globus pallidu

84 and the following hierarchy of mRNA levels: cerebrum > kidney > spleen congruent with lung congruent

85 he caudate, thalamus, cerebellar vermis, and cerebrum in 20 first-episode psychosis patients and 18 h

86 damage to the DHA-containing compartments in cerebrum in AD patients than controls, and suggest that

87 ortex and temporal and parietal lobes of the cerebrum in both groups.

88 not other GABAergic markers, throughout the cerebrum in PGC-1alpha +/- and -/- mice.

89 The cerebellum, like the cerebrum, includes a nuclear structure and an overlying

90 points toward a relevant role of cerebellum-cerebrum interaction in a sophisticated cognitive task r

91 These results suggest that the cerebrum is involved in adaptation of the timing, but no

92 Volumetric measurements of the cerebrum, lateral ventricles, third ventricle, and hippo

93 arousal regulation, the process by which the cerebrum mobilizes resources.

94 tem (i.e., cerebrum, plasma cholinesterases; cerebrum muscarinic, nicotinic receptors).

95 cerebral and cerebellar cortex of adults and cerebrum of fetuses.

96 njected transcranially to the frontoparietal cerebrum of mice.

97 Abeta peptide and plaque accumulation in the cerebrum of patients with AD.

98 as distribution (by immunohistology), in the cerebrum of rats with CRF 6 wk after 5/6 nephrectomy.

99 f tissue in the posterior, but not anterior, cerebrum of the BTBR mouse.

100 Here we show that in the cerebrums of mice expressing human familial mutant prese

101 l volumes for both prefrontal and the entire cerebrum on each specimen (n = 46).

102 ulted in no reduction in GLUT1 expression in cerebrum or its microvessels.

103 ion was found for each of morphine or M6G in cerebrums or epencephalons of acute morphine tolerance m

104 However, how these two "scales" of cerebrum organization are linked remains an open questio

105 The Drosophila cerebrum originates from about 100 neuroblasts per hemis

106 ive status, or the cholinergic system (i.e., cerebrum, plasma cholinesterases; cerebrum muscarinic, n

107 dered a subcortical disease of the posterior cerebrum, posterior reversible encephalopathy syndrome h

108 lt decerebrate mouse model (a mouse with the cerebrum removed) enables the study of sensory-motor int

109 id brain volumes, adjusted for age and total cerebrum size.

110 an induction of ODC activity in newborn rat cerebrum slices.

111 e neurocognitive function (NCF) of radiating cerebrum that appeared radiographically normal relative

112 ortical lobar hypo (hyper)-metabolism in the cerebrum that were 2 SDx from the mean were recorded as

113 The auditory center in the cerebrum, the auditory cortex, consists of multiple inte

114 aining peak thickness throughout most of the cerebrum: the median age by which 50% of the cortical po

115 acids were detected and visualized from rat cerebrum tissue using a MALDI MSI instrument operating i

116 eotide excision repair capacity in the mouse cerebrum to gain some insight into the optimal circadian

117 By linking the Visible Man cerebrum to the Talairach stereotaxic coordinate space,

118 The cerebrum was subdivided into cerebral cortex, cerebral w

119 For coated vesicles from bovine cerebrum, we examined the binding properties of [3H]musc

120 Borders of the amygdala, hippocampus, and cerebrum were defined, and their volumes were measured i

121 Cerebrums were removed 6h after trauma.

122 s pallidus, but not of the thalamus or total cerebrum, were significantly greater in the group of chi

123 ected in the choroid plexus, cerebellum, and cerebrum, where the percent engraftment between animals

124 of complexity of cortical growth across the cerebrum, which align closely with established architect

125 en considered of secondary importance to the cerebrum, which has typically been acknowledged as the m