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1 t of the molecular landscape during cortical parcellation.
2 esonance (MR) imaging enable regional volume parcellation.
3 ved a near-facsimile of the adult functional parcellation.
4 the network - this process is referred to as parcellation.
5 f a schizophrenia-related change in cortical parcellation.
6 ncluded grey-white segmentation and cortical parcellation.
7 anatomical and microscopic cytoarchitectural parcellations.
8 ly locate areas in individuals with atypical parcellations.
10 er studies on the consistency of HARDI based parcellation across subjects and comparison with indepen
11 n regions derived from an automated cortical parcellation algorithm by calculating the Risch lambda.
12 ion between tractography-based basal ganglia parcellation and anatomical data from previously reporte
13 ially powerful approach for in vivo amygdala parcellation and can serve as a guide in studies that ex
15 ny neurological diseases, few studies on the parcellation and extent of the human TPC are available t
16 s different contact sites on a limb; and the parcellation and separate representation of the static a
18 al basis for understanding the organization, parcellation, and anterior-posterior difference of human
19 connectivity, connectivity-based functional parcellation, and complex network models powered from da
20 areas in new subjects, replicated the group parcellation, and could correctly locate areas in indivi
21 the boundary-shift integral and atlas-based parcellation, and rates of regional grey matter atrophy
22 data using neurobiologically accurate brain parcellations; and (vii) share published data via user-f
25 ntially across regions, and that whole-brain parcellations based on those differences produce distrib
27 ects regardless of cortical and sub-cortical parcellations, but show significant, interpretable devia
28 From PND11 to PND16, thionin facilitates parcellation by extensive staining of dendritic processe
30 rithms may be applied in cases of atlas-free parcellation for a fully network-driven comparison of co
31 n network estimates can be derived from this parcellation if sufficient data are collected-considerab
33 in the vestibular nuclei, with intranuclear parcellation in the anterior octavus, magnocellularis, t
35 monstrates an unexpectedly complex molecular parcellation into a relatively coherent set of nine expr
36 the diencephalon, is characterized by their parcellation into distinct cell groups, or nuclei, that
37 ariation among grey matter regions to inform parcellation into distinct functional regions, and that
38 proposed to perform atlas-free random brain parcellation into nodes and align brains in the network
39 ent cluster solutions provided support for a parcellation into two parts as observed in monkeys, but
42 The present study, applying a new anatomical parcellation method, demonstrated a subregion-specific O
44 xtraction, tissue segmentation, and cortical parcellation methods were applied to obtain volume measu
45 ented temporal lobe subregions with reliable parcellation methods, relating volume with clinical and
47 ouse provides a subnuclear cytoarchitectonic parcellation (Nissl stain) of the NST into rostral, inte
48 a unique spatial signature of cortical macro-parcellation not predicted by classical cytoarchitectoni
49 study we revealed detailed organization and parcellation of all subfields of the hippocampal head an
52 d cortical mechanisms contribute to cortical parcellation of body map subdivisions in an NMDA recepto
53 hese results support the concept of temporal parcellation of brain activity, which reflects the diffe
54 The findings demonstrate distinct functional parcellation of core and noncore areas within human audi
57 rstanding of the mechanisms that control the parcellation of dTh and vTh and the differentiation of n
60 Neuron, Nelson and colleagues report a novel parcellation of human lateral parietal cortex based on t
62 This combined approach results in a 6-fold parcellation of LLPC based on the presence (or absence)
64 umans and may also have played a role in the parcellation of neocortex during mammalian evolution.
65 ntrol (HC) subjects, using a novel, reliable parcellation of OFC subregions and their association wit
67 nnections are consistent with our functional parcellation of PPC based on intracortical long-train mi
68 e identified a tripartite connectivity-based parcellation of SN with a limbic, cognitive, motor arran
69 rovides insights into the anatomo-functional parcellation of the anteroposterior OFC gradient observe
70 maps, (2) a hierarchical transcriptome-based parcellation of the brain and (3) a facility to retrieve
71 Here, we examine the precision of FreeSurfer parcellation of the cortex and introduce a method to ali
73 very limited data are available on detailed parcellation of the HF subfields, especially in the comp
74 y, we use resting state fMRI for the in vivo parcellation of the human LFC on a subjectwise and data-
75 urofilament suggests that this developmental parcellation of the lateral pallial complex is associate
78 One limitation in studies of the functional parcellation of the PFC has been the absence of tests th
79 We consider the anatomical and functional parcellation of the primate SN/VTA and find that its hom
82 w systematic investigation of the functional parcellation of the SN/VTA in animals, new developments
85 l grey matter volumes were generated using a parcellation of the volumetric T1-weighted magnetic reso
89 ebo group, we replicated previously observed parcellations of the OFC into two and six subregions bas
90 lex human cerebral cortex requires a map (or parcellation) of its major subdivisions, known as cortic
94 of cortical organization, and they suggest a parcellation scheme in which modality-specific cortical
95 of >50 expressed molecules confirms the BST parcellation scheme proposed by Swanson in 2004, with tw
96 e define regions within LLPC by developing a parcellation scheme that integrates data from resting-st
99 studies of callosal development tend to use parcellation schemes that may not capture the complex sp
100 gdala connectivity observed support previous parcellation schemes that segregate the LA into dorsal,
102 ical measures that rely on gray-white matter parcellation, since an indistinct transition zone could
103 antly changed the composition of the sixfold parcellation, suggesting a dopamine-dependent reconfigur
106 nternally valid subject-specific areal-level parcellation that corresponds with subject-specific task
107 sentation in the brainstem with well-defined parcellation that resembles the barrelettes found in rod
108 revious methods by using a data-driven brain parcellation to compare connectivity profiles of dyslexi
109 olume of significantly asymmetrical cortical parcellation units (leftward plus rightward), as well as
117 based on dominant connections with cortical parcellations, we observed a near-facsimile of the adult
118 cessing pipeline and a novel high-resolution parcellation were created to analyze brain scans of 1189
119 Voxel-based morphometry and atlas-based parcellation were used to compare patterns of grey matte
120 tion and a novel high-resolution gray matter parcellation were used to extract GMD, GMV, gray matter
121 ed to segment each subject's MR scan and the parcellations were applied to the coregistered PET scans
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