ライフサイエンスコーパス: agranular

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 tex projected to medial mediodorsal nucleus, agranular anterior insular and infralimbic cortices as w

11 Agranular anterior insular cortex projected to the dysgr

12 ly, however, than MO to the medial (frontal) agranular, anterior cingulate, sensorimotor, posterior p

13 The agranular architecture of motor cortex lacks a functiona

14 ification of primary motor cortex (M1) as an agranular area has been challenged recently when a funct

15 Primary motor cortex was coextensive with an agranular area of cortex marked by a distinct layer V of

16 tor cortex (M1) is classically considered an agranular area, lacking a distinct layer 4 (L4).

17 lesions of the dmPFC, centered on the medial agranular area, spared rats' ability to choose between a

18 anular area but only weak enhancement in the agranular area.

19 postsynaptic potentials of the granular and agranular areas displayed similar frequency sensitivity,

20 a molecular dissociation among the so-called agranular areas of the neocortex.

21 the adjacent anterior cingulate and lateral agranular areas overlap those of AGm but are concentrate

22 from the insular cortex, primarily from its agranular areas.

23 ar cells and a minor population of small and agranular cells here referred to as recycling stem cells

24 the axon remodeling process occurring in all agranular cerebella.

25 In the agranular cerebellar cortex of the weaver mutant mouse,

26 These included areas AGm, lateral agranular cortex (AGl), orbital cortex, posterior pariet

27 These include lateral agranular cortex (AGl), posterior parietal cortex (PPC),

28 ate early gene c-fos after unilateral medial agranular cortex (AGm) ablation.

29 (DCS) is the major site of input from medial agranular cortex (AGm) and has been implicated as an ass

30 Medial agranular cortex (AGm) has a prominent bilateral project

31 Although the rat medial agranular cortex (AGm) has been implicated in a variety

32 he rostral and caudal portions of rat medial agranular cortex (AGm) play different functional roles.

33 The rat medial agranular cortex (AGm) projects bilaterally to the stria

34 egion in which axons from ipsilateral medial agranular cortex (AGm) terminate within the striatum.

35 neglect following cortical lesions of medial agranular cortex (AGm), an association area that is its

36 2) is known by other names, including medial agranular cortex (AGm), medial precentral cortex (PrCm),

37 from several cortical areas including medial agranular cortex (AGm), posterior parietal cortex (PPC),

38 e anterior cingulate cortex (ACC) and medial agranular cortex (AGm).

39 CS include visual association areas, lateral agranular cortex and orbital cortex.

40 nd the central medial nuclei; (2) the medial agranular cortex distributes strongly to the rostral int

41 Here we recorded from medial agranular cortex neurons in rats while they freely behav

42 the anterior cingulate cortex and the medial agranular cortex projected bilaterally, with an ipsilate

43 The data indicate that agranular cortex resembles sensory areas in certain resp

44 ral entorhinal cortex, and the retrosplenial agranular cortex.

45 ic, prelimbic, anterior cingulate and medial agranular cortices, to the thalamus in the rat by using

46 Projections from the "classical" agranular, disgranular, and granular insular areas were

47 posterior insular cortex (PI-comprising the agranular, dysgranular and granular fields).

48 tivation of two frontal regions in rats, the agranular/dysgranular insular cortex (AIC) and the ventr

49 anterior insular cortex projected to lateral agranular frontal cortex and granular and dysgranular po

50 recorded simultaneously across all layers of agranular frontal cortex using linear electrode arrays.

51 the posteromedial agranular (Iapm), lateral agranular (Ial), and posterolateral agranular (Iapl) sub

52 lateral agranular (Ial), and posterolateral agranular (Iapl) subdivisions have the strongest inputs.

53 thin the agranular insula, the posteromedial agranular (Iapm), lateral agranular (Ial), and posterola

54 atement, the PIc or the more anterior dorsal agranular IC (AId) was inactivated to determine their ro

55 The agranular insula (areas Iam, Iapm, Iai, and Ial) extends

56 project to two subdivisions of the OFC, the agranular insula and the lateral orbitofrontal cortex (A

57 network on the posterior orbital surface and agranular insula send only weak projections to the poste

58 Within the agranular insula, the posteromedial agranular (Iapm), la

59 L, area 25) cortices and the dorsal anterior agranular insular (AId) and regions of posterior insular

60 Orbital/agranular insular (ORB/AI) cortex has been implicated in

61 these neurons were more often present in the agranular insular and piriform cortices.

62 specificity of lidocaine inactivation of the agranular insular and prelimbic areas.

63 10m, rostral orbital areas 10o and 11m, and agranular insular area Iai in the posterior orbital cort

64 er lidocaine-induced inactivation within the agranular insular area of the prefrontal cortex (PFC) or

65 delayed win-shift task was dependent on the agranular insular area, whereas acquisition of the visua

66 iate with refeeding-activated neurons in the agranular insular area; bed nuclei of terminal stria; an

67 ons that project to the PB were found in the agranular insular area; bed nuclei of terminal stria; an

68 orbital area, dorsolateral orbital area, and agranular insular areas.

69 The rostral agranular insular cortex (RAIC) has recently been identi

70 The rostral agranular insular cortex (RAIC) of rats has opioid recep

71 efined opioid-responsive site in the rostral agranular insular cortex (RAIC) of the rat and character

72 activated by painful stimuli is the rostral agranular insular cortex (RAIC) where, as in other parts

73 reuptake inhibitor GBR-12935 in the rostral agranular insular cortex (RAIC), a cortical area that re

74 ocesses were distributed most densely in the agranular insular cortex and the paraventricular nuclei

75 luding the secondary somatosensory (SII) and agranular insular cortex ipsilaterally, as well as the h

76 nsely labeled dendrite-like processes in the agranular insular cortex.

77 APC neurons, but not in the primary motor or agranular insular cortices in response to an IAA-deficie

78 e include the infralimbic, prelimbic, dorsal agranular insular, and entorhinal cortices, the ventral

79 iculum, and in the cerebral cortex including agranular insular, cingulate, entorhinal, orbital, parie

80 e orbital, ventral medial prefrontal (mPFC), agranular insular, piriform, retrosplenial, and parahipp

81 Within the infralimbic, agranular insular, primary motor, parietal association,

82 ventral retrosplenial, dorsal and posterior agranular insular, visceral, temporal association, dorsa

83 were made in the anterior cingulate, medial agranular, lateral agranular, or somatosensory cortex.

84 in subregions approximating the dysgranular/agranular layers.

85 The former includes several agranular limbic areas, and the latter includes the homo

86 CD34+/CD18- cells were small, agranular lymphocytes which contained the majority of pr

87 in superficial and deep layers of the medial agranular motor cortex (M2) project directly to the audi

88 he granular somatosensory cortex but not the agranular motor cortex of rats.

89 thology were characterized by lesions in the agranular motor cortex, brainstem motor nuclei of crania

90 nterior cingulate, medial agranular, lateral agranular, or somatosensory cortex.

91 resulted in heavy labeling of the subjacent agranular parietal insular cortex and strong labeling of

92 eeding disorder, thrombocytopenia, and large agranular platelets characteristic of GPS, while obligat

93 tomically, this projection is largest in the agranular portion of GC; however, its synaptic targets a

94 Agranular posterior insular cortex projected to medial m

95 Agranular projections were similar, although they includ

96 r) region of the IC and the anterior (dorsal agranular) region of the IC, respectively.

97 Within the granular, dysgranular, and agranular regions described in prior studies, we identif

98 The dysgranular and agranular regions lying on the orbital and medial surfac

99 nted projections from MD to the more caudal, agranular regions of the frontal cortex, suggesting that

100 utrophil herniation of the nuclear lobes and agranular regions within the cytosol.

101 e, sensorimotor, posterior parietal, lateral agranular retrosplenial, and temporal association cortic

102 In contrast, the intermediate agranular subdivision (Iai) is relatively devoid of visc

103 The agranular temporal pole (TGa) is connected with several

104 les impinging on the MoG contain pleomorphic agranular vesicles and are immunoreactive to GABA and no

105 t as many other profiles that contain round, agranular vesicles and that are immunoreactive to glutam

106 y of the presynaptic terminals contain small agranular vesicles, are of large diameter, and are immun