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1 gher visual areas, LM (lateromedial) and PM (posteromedial).
2 t the neuroepithelium, from anteroventral to posteromedial.
3             Within the agranular insula, the posteromedial agranular (Iapm), lateral agranular (Ial),
4 bed nucleus of the stria terminalis (BSTPM), posteromedial amygdala (MeP), lateral habenula (LHb), ve
5  enhances the fidelity of envelope coding in posteromedial and posterolateral auditory cortex.
6 a-cortical transition zone rostrally and the posteromedial and posterolateral nuclei caudally contain
7 itral annulus commissures [anterolateral and posteromedial] and z-axis directed toward the left ventr
8 e posterior cruciate ligament (anterolateral/posteromedial; aPCL/pPCL) were analyzed.
9                              In rodents, the posteromedial area (PM) mediates visual information betw
10 isual areas, AL (anterolateral area) and PM (posteromedial area), display distinct visual properties
11 area, rostrolateral area, anteromedial area, posteromedial area, laterointermediate area, posterior a
12       Furthermore, precuneus and surrounding posteromedial areas are amongst the brain structures dis
13 gastrulation into a spatial anterolateral-to-posteromedial arrangement.
14 mework in which magnified envelope coding in posteromedial auditory cortex disrupts the segregation o
15 , magnified cortical envelope coding in left posteromedial auditory cortex predict speech identificat
16 enhances the amplitude of envelope coding in posteromedial auditory cortex, whereas it enhances the f
17 cally organized and highly segregated in the posteromedial barrel subfield (PMBSF) of rat layer IV pr
18 ty of neurons in the different layers of the posteromedial barrel subfield (PMBSF) of the rat somatos
19 h existing data indicate that barrels in rat posteromedial barrel subfield are structurally and funct
20 e found that individual large barrels in the posteromedial barrel subfield encompass two or three dis
21                        Barrel hollows in the posteromedial barrel subfield of adult rat somatosensory
22 ed the pattern of retrograde labeling in the posteromedial barrel subfield of primary somatosensory c
23 sterior thalamic nucleus from P2, and in the posteromedial barrel subfield of somatosensory cortex (S
24 angential slices that isolate layer 4 in the posteromedial barrel subfield.
25 as increased in the medial preoptic area and posteromedial bed nucleus of the stria terminalis (BST)
26 eviously shown to express T-induced Fos: the posteromedial bed nucleus of the stria terminalis (BSTPM
27                            They involved the posteromedial border of the gastric fundus in eight pati
28 smooth, undulating, submucosal masses on the posteromedial border of the gastric fundus.
29  mRNA levels in the medial preoptic area and posteromedial BST of aged rats.
30 nt (aACL and pACL) and the anterolateral and posteromedial bundles of the posterior cruciate ligament
31 between markers 1 and 2 (seg12) began at the posteromedial commissure, and remaining segments were nu
32 s well as injuries of the posterolateral and posteromedial corners of the knee.
33 involving the medial temporal lobe (MTL) and posteromedial cortex (PMC) are related to early Alzheime
34  To probe the causal importance of the human posteromedial cortex (PMC) in processing the sense of se
35                                          The posteromedial cortex (PMC) including the posterior cingu
36                                          The posteromedial cortex (PMC) is a highly connected cortica
37                                          The posteromedial cortex (PMC) is a major hub of the brain's
38                                          The posteromedial cortex (PMC) is known to be a core node of
39 ng and Alzheimer's disease (AD) and that the posteromedial cortex (PMC) is particularly vulnerable to
40  we use intracranial recordings in the human posteromedial cortex (PMC), a core node within the DMN,
41 n, we recorded intracranially from the human posteromedial cortex (PMC), a core structure of the defa
42 ater life cognitive health via its effect on posteromedial cortex (PMC), a hub region within a brain
43 ding ventromedial prefrontal cortex (vmPFC), posteromedial cortex (PMC), hippocampus, and amygdala.
44 cortices constitute an ensemble known as the posteromedial cortex (PMC), which consists of Brodmann a
45 bolism and a major neural hub in the ventral posteromedial cortex (vPMC).
46 ct-word pairs, and posterior hippocampus and posteromedial cortex for scene-word pairs.
47 significantly lower medial prefrontal cortex-posteromedial cortex functional connectivity (area under
48 th ASD and highlights fundamental aspects of posteromedial cortex heterogeneity.
49 rogeneous profile of connectivity within the posteromedial cortex in both TD and ASD children was obs
50 he machine learning medial prefrontal cortex-posteromedial cortex multimodal classifier had a signifi
51 he functionally heterogeneous profile of the posteromedial cortex raises questions regarding how alte
52 ent with the selective hypometabolism in the posteromedial cortex reported in a wide range of altered
53                            However, areas in posteromedial cortex showed the opposite pattern across
54 arly localized rhythm in the homologous deep posteromedial cortex that was temporally correlated with
55 etwork (DMN), a brain system anchored in the posteromedial cortex, has been identified as underconnec
56 epressant effects, and a 3 Hz oscillation in posteromedial cortex, previously proposed as a mechanism
57 corded, and the analysis was targeted on the posteromedial cortex, the medial prefrontal cortex, and
58 amus, and additional volume reduction in the posteromedial cortex.
59 ter-hippocampal connectivity and activity in posteromedial cortex.
60 ortex, basal ganglia, and locally within the posteromedial cortex.
61 owed specific structural disturbances within posteromedial cortex.
62 me interval was more widespread and included posteromedial cortical areas, where tau accumulation rat
63 physiological properties of a conserved deep posteromedial cortical rhythm that underlies states of d
64 ith further reduced mediodorsal thalamic and posteromedial cortical volumes.
65 titute a region of cortex referred to as the posteromedial cortices (PMC).
66 iform gyri, and increasing activation in the posteromedial cortices (PMCs), primarily in the precuneu
67  a previously undescribed pattern within the posteromedial cortices (the ensemble of precuneus, poste
68  contribute insights on the functions of the posteromedial cortices and on the recruitment of the ant
69 erest (ROIs), including lateral parietal and posteromedial cortices, medial temporal lobe (MTL), hipp
70       Instead, patients demonstrated reduced posteromedial cortico-hippocampal and inter-hippocampal
71                       The precuneus (PCu), a posteromedial DMN hub, is thought to play a role in this
72  network shape the glucose metabolism of the posteromedial DMN in opposing directions.
73   We show that the glucose metabolism of the posteromedial DMN is dependent on the metabolic demands
74 f both metabolism and the BOLD signal in the posteromedial DMN, cognitive control during working memo
75 ted functional connectivity (FC) of alEC and posteromedial EC (pmEC), subregions of EC that differ in
76 teral EC showed stronger temporal drift than posteromedial EC.
77             End-systolic displacement of the posteromedial edge of the central scallop was 1.4+/-0.9
78 nts) and perirhinal cortices, but not in the posteromedial entorhinal and parahippocampal cortices.
79 anes (STPs), with peaks of activity at their posteromedial extents, in regions classically considered
80 overlapped greatly in the posterolateral and posteromedial glomerular layer, a finding one should pre
81 VI-to-II sequence and in an anterolateral to posteromedial gradient [the transverse neurogenetic grad
82 his approach has revealed a primary field in posteromedial Heschl's gyrus (HG) with pronounced induce
83 ency (F0) and were significantly enhanced in posteromedial HG during speaking compared with when subj
84             In contrast to primary cortex in posteromedial HG, a non-primary field in anterolateral H
85                                  Compared to posteromedial HG, responses from anterolateral HG-an aud
86                                    Cortex of posteromedial HG, the presumed core of human auditory co
87 was performed to harvest the FHL through the posteromedial hindfoot incision using a single minimally
88  (lateromedial), AL (anterolateral), and PM (posteromedial)) in mice of both sexes.
89                                     Cells in posteromedial lateral suprasylvian (PMLS) cortex display
90 o either visual cortical areas 17 and 18, or posteromedial lateral suprasylvian (PMLS) cortex in the
91 though no such change was documented for the posteromedial lateral suprasylvian area (PMLS), labeled
92 s of connectivity in the cat, identified the posteromedial lateral suprasylvian visual area (PMLS) as
93 hinal, lateral entorhinal, and anteromedial, posteromedial, lateroposterior, laterointermediate, and
94   These associations are not observed in the posteromedial network, specialized for context/spatial i
95 he neocortex and in the ventral anterior and posteromedial nuclei of the thalamus.
96  interface of the central medial and ventral posteromedial nucleus (parvicellular part) (CM-VPMpc).
97 these neurons are targeted by axons from the posteromedial nucleus (POm), a paralemniscal thalamic nu
98  with their whiskers, neurons in the ventral posteromedial nucleus (VPM) fired in response to touch a
99 tosensory barrel cortex (S1) and the ventral posteromedial nucleus (VPm) of the thalamus using silico
100 movement activated FS neurons in the ventral posteromedial nucleus (VPM) target layers, a subset of S
101 ceptive field (RF) properties of the ventral posteromedial nucleus (VPM), neurons of the ventral thal
102        The parvicellular part of the ventral posteromedial nucleus (VPMpc) of the thalamus, also know
103                         Here we identify the posteromedial nucleus of the cortical amygdala (COApm) a
104                        Here we show that the posteromedial nucleus of the cortical amygdala (COApm) s
105 gate the role of axonal projections from the posteromedial nucleus of the thalamus (POm) to the forep
106 modulators of ongoing spiking in the ventral posteromedial nucleus of the thalamus (VPm), either supp
107   First-order neurons located in the ventral posteromedial nucleus projected mainly to trigeminal are
108 igher visual areas LM (lateromedial) and PM (posteromedial) of mice.
109 or hair cells and neurons overlap within the posteromedial otic epithelium.
110 either the anterolateral papillary muscle or posteromedial papillary muscles of the left ventricle.
111  cortex anterior to E-row barrels and in the posteromedial parietal cortex in addition to S-II.
112 within which the levels of activity in right posteromedial parietal cortical foci [right posterior in
113 ) at an excitatory synapse, derived from the posteromedial part of the amygdalohippocampal area (AHiP
114 anosus tendon, the other originated from the posteromedial part of the capsule.
115  given fate very early; (2) in contrast, the posteromedial part of the ear harbors a population of co
116 in more anterolateral and the latter in more posteromedial parts, suggesting template matching to occ
117 Thirty-five PMs exhibited clinical VAs (N=29 posteromedial PM and N=6 anterolateral PM).
118                            Anterolateral and posteromedial PM areas were 19.9+/-7 cm(2) and 17.1+/-6
119              The number of anterolateral and posteromedial PM heads was 2.7+/-0.7 and 2.6+/-0.7, resp
120 (PV) and parietal rhinal (PR) areas, and the posteromedial (PM) region.
121 areas lateromedial (LM), anterolateral (AL), posteromedial (PM), and anteromedial (AM) have specializ
122  (lateromedial [LM], anterolateral [AL], and posteromedial [PM]) for perception of orientation and co
123 ctionally distinct anterolateral (alERC) and posteromedial (pmERC) subregions.
124 ted channelrhodopsin-2-expressing long-range posteromedial (POm) thalamic axon terminals in cortex an
125 ponsive sites in the superior colliculus and posteromedial (POm) thalamus, the labeled projections fr
126            Neural activity was recorded from posteromedial portion of Heschl's gyrus (HGPM) and anter
127 ing unexpected functional attributes for the posteromedial portion of the parietal lobe, the precuneu
128 between the infralimbic cortex (ILC) and the posteromedial portions of the ventral tegmental area (pm
129 ve functional connection between ILC and the posteromedial portions of the VTA (pmVTA) and the mNAc s
130 tions of the dorsolateral prefrontal cortex, posteromedial prefrontal cortex, lateral parietal cortex
131                (3) Activation at the site of posteromedial right atrial functional block can organize
132 rly and 0.9+/-0.6 mm laterally away from the posteromedial scallop, corresponding to anterior displac
133 l 4 showed calcifications affecting both the posteromedial sclero-choroid and adjacent medial rectus
134 th commissures (eg, 8.3 versus 6.2 mm on the posteromedial side) and increased z (ie, shifted toward
135 1) A functional line of block is seen at the posteromedial (sinus venosa region) right atrium during
136 ll patients, a line of block was seen in the posteromedial (sinus venosa) right atrium; this was mani
137                          We propose that the posteromedial STP generates sequenced auditory represent
138           In particular, MeP projects to the posteromedial subdivision of the bed nucleus of the stri
139 es of the total entorhinal cortex and of its posteromedial subdivision.
140 lex scenes relies on an extended hippocampal posteromedial system, we currently have limited insight
141 sensory-discriminative pain, such as ventral posteromedial thalamic nuclei.
142                                          The posteromedial thalamic nucleus (POm), the higher-order t
143 mus, the parvicellular region of the ventral posteromedial thalamic nucleus (VPMpc), dramatically red
144                                      Ventral posteromedial thalamic nucleus afferents in GC make syna
145  lCBF and lCMR(glc) responses in the ventral posteromedial thalamic nucleus and barrel cortex but not
146 es between the synapses of Po versus ventral posteromedial thalamic nucleus axons in the whisker sens
147 cipal sensory trigeminal nuclei, the ventral posteromedial thalamic nucleus, and the barrel region of
148  nucleus, and a portion of the right ventral posteromedial thalamic nucleus.
149  the rostral spinal trigeminal interpolaris, posteromedial thalamic, and ventral zona incerta nuclei,
150 ntral medial nucleus (VMpo) and a portion of posteromedial thalamus designated as the ventral caudal
151 tion between the superior colliculus and the posteromedial thalamus, we have uncovered a circuit that
152 ted to be mediated by A(2A) receptors in the posteromedial thalamus.
153 g pain and tenderness on palpation along the posteromedial tibia (shin splints) underwent clinical ex
154 originated from the posterior surface of the posteromedial tibia condyle, merged with fibers from the
155                            Five patients had posteromedial tibial plateau bruises: Two had bruises at
156                            Five patients had posteromedial tibial plateau fractures: Four had avulsio
157   There appears to be an association between posteromedial tibial plateau injuries and ACL tears.
158                                              Posteromedial tibial plateau injuries may be predictive
159 adiographs was performed in 10 patients with posteromedial tibial plateau injuries, including avulsio
160 s from separate regions of Pf as well as the posteromedial to anterolateral topographic gradient of i
161 an involvement of fibres running lateral and posteromedial to the STN in the pathogenesis of SID, ind
162  regions, with complexity increasing along a posteromedial-to-anterolateral direction in core and lat
163 y input and may correspond to an area on the posteromedial transverse gyrus of humans and the anterio
164 ed by thalamocortical axons from the ventral posteromedial (VPM) and posterior (Po) nuclei in the fir
165 d in 60 degrees of flexion, equaling 6.24 mm posteromedial, while the posterior horn remained relativ

 
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