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1  Catfish IgM(+)/IgD(+) B cells are small and agranular.
2                 Rats given unilateral medial agranular (AGm) cortex ablations show neglect for contra
3 of labeled neurons in layer VI of the medial agranular (Agm) zone, which corresponds to the MI whiske
4 anular cortex which in turn projected to the agranular (all layers) and granular cortices (layers I a
5 puts also receive significant innervation by agranular and dysgranular insula subdivisions that are t
6                                          The agranular and dysgranular insula, the parainsula, and ro
7 igh numbers of retrogradely labeled cells in agranular and dysgranular regions.
8                          This holds for both agranular and granular cortex.
9                                The anterior (agranular and rostral dysgranular) insula has significan
10               The ADE group also showed less agranular anterior insula activation during periods of b
11 tex projected to medial mediodorsal nucleus, agranular anterior insular and infralimbic cortices as w
12                                              Agranular anterior insular cortex projected to the dysgr
13 ly, however, than MO to the medial (frontal) agranular, anterior cingulate, sensorimotor, posterior p
14                                          The agranular architecture of motor cortex lacks a functiona
15 ification of primary motor cortex (M1) as an agranular area has been challenged recently when a funct
16 Primary motor cortex was coextensive with an agranular area of cortex marked by a distinct layer V of
17 tor cortex (M1) is classically considered an agranular area, lacking a distinct layer 4 (L4).
18 lesions of the dmPFC, centered on the medial agranular area, spared rats' ability to choose between a
19 anular area but only weak enhancement in the agranular area.
20  postsynaptic potentials of the granular and agranular areas displayed similar frequency sensitivity,
21 minimal model to study the microcircuitry of agranular areas of the frontal lobe involved in cognitiv
22 a molecular dissociation among the so-called agranular areas of the neocortex.
23  the adjacent anterior cingulate and lateral agranular areas overlap those of AGm but are concentrate
24  from the insular cortex, primarily from its agranular areas.
25 ar cells and a minor population of small and agranular cells here referred to as recycling stem cells
26 the axon remodeling process occurring in all agranular cerebella.
27                                       In the agranular cerebellar cortex of the weaver mutant mouse,
28            These included areas AGm, lateral agranular cortex (AGl), orbital cortex, posterior pariet
29                        These include lateral agranular cortex (AGl), posterior parietal cortex (PPC),
30 ate early gene c-fos after unilateral medial agranular cortex (AGm) ablation.
31 (DCS) is the major site of input from medial agranular cortex (AGm) and has been implicated as an ass
32                                       Medial agranular cortex (AGm) has a prominent bilateral project
33                      Although the rat medial agranular cortex (AGm) has been implicated in a variety
34 he rostral and caudal portions of rat medial agranular cortex (AGm) play different functional roles.
35                               The rat medial agranular cortex (AGm) projects bilaterally to the stria
36 egion in which axons from ipsilateral medial agranular cortex (AGm) terminate within the striatum.
37 neglect following cortical lesions of medial agranular cortex (AGm), an association area that is its
38 2) is known by other names, including medial agranular cortex (AGm), medial precentral cortex (PrCm),
39 from several cortical areas including medial agranular cortex (AGm), posterior parietal cortex (PPC),
40 e anterior cingulate cortex (ACC) and medial agranular cortex (AGm).
41 CS include visual association areas, lateral agranular cortex and orbital cortex.
42 nd the central medial nuclei; (2) the medial agranular cortex distributes strongly to the rostral int
43                 Here we recorded from medial agranular cortex neurons in rats while they freely behav
44 the anterior cingulate cortex and the medial agranular cortex projected bilaterally, with an ipsilate
45                       The data indicate that agranular cortex resembles sensory areas in certain resp
46 ral entorhinal cortex, and the retrosplenial agranular cortex.
47 ll layers of the supplementary eye field, an agranular cortical area, in monkeys performing a saccade
48  SFC occurs when traversing from granular to agranular cortical regions.
49 d "indirect" paths to the "limbic" striatum, agranular cortices formed a "foundational," broad projec
50 ic, prelimbic, anterior cingulate and medial agranular cortices, to the thalamus in the rat by using
51             Projections from the "classical" agranular, disgranular, and granular insular areas were
52  posterior insular cortex (PI-comprising the agranular, dysgranular and granular fields).
53 ntral orbitofrontal cortices (VMO, VLO), and agranular/dysgranular insular (AI/DI) cortex of rats.
54 tivation of two frontal regions in rats, the agranular/dysgranular insular cortex (AIC) and the ventr
55 cally by a neurochemical manipulation of the agranular/dysgranular region of gustatory insula (AI/DI)
56 anterior insular cortex projected to lateral agranular frontal cortex and granular and dysgranular po
57  development from the phylogenetically older agranular frontal cortex that lies above the anterior pa
58 recorded simultaneously across all layers of agranular frontal cortex using linear electrode arrays.
59  across the unimodal-transmodal and granular-agranular gradients; 2) increased myelination and lower
60  the posteromedial agranular (Iapm), lateral agranular (Ial), and posterolateral agranular (Iapl) sub
61  lateral agranular (Ial), and posterolateral agranular (Iapl) subdivisions have the strongest inputs.
62 thin the agranular insula, the posteromedial agranular (Iapm), lateral agranular (Ial), and posterola
63 atement, the PIc or the more anterior dorsal agranular IC (AId) was inactivated to determine their ro
64                                          The agranular insula (areas Iam, Iapm, Iai, and Ial) extends
65  project to two subdivisions of the OFC, the agranular insula and the lateral orbitofrontal cortex (A
66 network on the posterior orbital surface and agranular insula send only weak projections to the poste
67                                   Within the agranular insula, the posteromedial agranular (Iapm), la
68 L, area 25) cortices and the dorsal anterior agranular insular (AId) and regions of posterior insular
69                                      Orbital/agranular insular (ORB/AI) cortex has been implicated in
70 these neurons were more often present in the agranular insular and piriform cortices.
71 specificity of lidocaine inactivation of the agranular insular and prelimbic areas.
72  10m, rostral orbital areas 10o and 11m, and agranular insular area Iai in the posterior orbital cort
73 er lidocaine-induced inactivation within the agranular insular area of the prefrontal cortex (PFC) or
74  delayed win-shift task was dependent on the agranular insular area, whereas acquisition of the visua
75 ons that project to the PB were found in the agranular insular area; bed nuclei of terminal stria; an
76 iate with refeeding-activated neurons in the agranular insular area; bed nuclei of terminal stria; an
77 orbital area, dorsolateral orbital area, and agranular insular areas.
78                                  The rostral agranular insular cortex (RAIC) has recently been identi
79                                  The rostral agranular insular cortex (RAIC) is a relevant structure
80                                  The rostral agranular insular cortex (RAIC) of rats has opioid recep
81 efined opioid-responsive site in the rostral agranular insular cortex (RAIC) of the rat and character
82  activated by painful stimuli is the rostral agranular insular cortex (RAIC) where, as in other parts
83  reuptake inhibitor GBR-12935 in the rostral agranular insular cortex (RAIC), a cortical area that re
84 ocesses were distributed most densely in the agranular insular cortex and the paraventricular nuclei
85        Inactivation of the adjacent anterior agranular insular cortex had no effect.
86 luding the secondary somatosensory (SII) and agranular insular cortex ipsilaterally, as well as the h
87 ect oxytocinergic projections to the rostral agranular insular cortex on GABAergic and oxytocin recep
88 nsely labeled dendrite-like processes in the agranular insular cortex.
89 APC neurons, but not in the primary motor or agranular insular cortices in response to an IAA-deficie
90 e include the infralimbic, prelimbic, dorsal agranular insular, and entorhinal cortices, the ventral
91 iculum, and in the cerebral cortex including agranular insular, cingulate, entorhinal, orbital, parie
92 e orbital, ventral medial prefrontal (mPFC), agranular insular, piriform, retrosplenial, and parahipp
93                      Within the infralimbic, agranular insular, primary motor, parietal association,
94  ventral retrosplenial, dorsal and posterior agranular insular, visceral, temporal association, dorsa
95 ecording, we found that projections from the agranular insular/lateral orbital (AI/LO) cortex to the
96  were made in the anterior cingulate, medial agranular, lateral agranular, or somatosensory cortex.
97  in subregions approximating the dysgranular/agranular layers.
98                  The former includes several agranular limbic areas, and the latter includes the homo
99                CD34+/CD18- cells were small, agranular lymphocytes which contained the majority of pr
100 and include the agranular orbital cortex and agranular medial frontal cortex (areas 24, 32, and 25).
101 ytoarchitectonic types (i.e. periallocortex, agranular mesocortex, dysgranular mesocortex, eulaminate
102 in superficial and deep layers of the medial agranular motor cortex (M2) project directly to the audi
103 nduce experience-dependent plasticity in the agranular motor cortex and that this LC-driven plasticit
104 he granular somatosensory cortex but not the agranular motor cortex of rats.
105 thology were characterized by lesions in the agranular motor cortex, brainstem motor nuclei of crania
106 ilarly impacts neural representations in the agranular motor cortical regions that are responsible fo
107 nterior cingulate, medial agranular, lateral agranular, or somatosensory cortex.
108       These are limbic areas and include the agranular orbital cortex and agranular medial frontal co
109  resulted in heavy labeling of the subjacent agranular parietal insular cortex and strong labeling of
110                                              Agranular parts of the PFC emerged in early mammals, and
111 eeding disorder, thrombocytopenia, and large agranular platelets characteristic of GPS, while obligat
112 tomically, this projection is largest in the agranular portion of GC; however, its synaptic targets a
113                                              Agranular posterior insular cortex projected to medial m
114                                              Agranular projections were similar, although they includ
115 r) region of the IC and the anterior (dorsal agranular) region of the IC, respectively.
116        Within the granular, dysgranular, and agranular regions described in prior studies, we identif
117                          The dysgranular and agranular regions lying on the orbital and medial surfac
118 nted projections from MD to the more caudal, agranular regions of the frontal cortex, suggesting that
119 utrophil herniation of the nuclear lobes and agranular regions within the cytosol.
120 f particular subdivisions [granular (RSG) vs agranular retrosplenial area (RSA)] and the circuit mech
121 te activity, respectively, especially in the agranular retrosplenial cortex (aRSC).
122 by the same class also invading midbrain and agranular retrosplenial cortex; Cornu Ammonis receives i
123 e, sensorimotor, posterior parietal, lateral agranular retrosplenial, and temporal association cortic
124 prefrontal cortex is limited to this earlier agranular stage and is often referred to as the "medial
125                In contrast, the intermediate agranular subdivision (Iai) is relatively devoid of visc
126 predictions from higher-level deep layers to agranular (superficial and deep) lower-level layers.(7)(
127                                          The agranular temporal pole (TGa) is connected with several
128 les impinging on the MoG contain pleomorphic agranular vesicles and are immunoreactive to GABA and no
129 t as many other profiles that contain round, agranular vesicles and that are immunoreactive to glutam
130 y of the presynaptic terminals contain small agranular vesicles, are of large diameter, and are immun

 
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