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1 oduce matrix proteins and thicken the lamina reticularis.
2 cia is only seen in dermatopathia pigmentosa reticularis.
3 ially contribute to thickening of the lamina reticularis.
4 glomerulosa (ZG), zona fasciculata, and zona reticularis].
5 7.4%), venous thrombosis (25.7%), and livedo reticularis (31.4%).
6                     Thickening of the lamina reticularis, a feature of remodeling in the asthmatic ai
7 x, acute renal failure, gut ischemia, livedo reticularis and blue-toe syndrome.
8 the adrenal cortex, specifically in the zona reticularis and fasciculata that produce glucocorticoids
9 lective increases in the widths of the zonae reticularis and glomerulosa (p < 0.001).
10 eral tissues including the cells of the zona reticularis and the zona fasciculata of the adrenal cort
11 pses, excite neurons in the thalamic nucleus reticularis, and both excite and inhibit neurons within
12 a small family with dermatopathia pigmentosa reticularis, and our linkage data suggest that dermatopa
13 l nucleus of thalamus, substantia nigra pars reticularis, and ventral tegmental area) in a combined g
14 assohn syndrome and dermatopathia pigmentosa reticularis are autosomal dominant ectodermal dysplasias
15 (GABAB) inhibition generated by the thalamic reticularis cells.
16 gned to investigate a role of the subnucleus reticularis dorsalis (SRD) in the analgesia produced by
17 PA projects preferentially to the subnucleus reticularis dorsalis, commissural nucleus tractus solita
18 h varicosities in the ipsilateral subnucleus reticularis dorsalis, commissural subnucleus of the nucl
19 ular formation nuclei such as the subnucleus reticularis dorsalis, gigantocellular, dorsal paragigant
20 ys later in a limited portion of the nucleus reticularis gigantocellularis (Gi) and Gi pars alpha.
21 uding the nucleus raphe magnus (NRM), nuclei reticularis gigantocellularis (NGC) and gigantocellulari
22 ctrical stimulation of the medullary nucleus reticularis gigantocellularis (NRGc) evoked large amplit
23  swellings were also observed in the nucleus reticularis gigantocellularis and in the ventrolateral m
24 of non-5HT neurons, in the medullary nucleus reticularis gigantocellularis and magnocellularis, that
25 compasses the ventral portion of the nucleus reticularis gigantocellularis and the nucleus magnocellu
26  have recently demonstrated that the nucleus reticularis gigantocellularis pars alpha (GiA) is a majo
27 he nucleus raphe magnus (NRM) or the nucleus reticularis gigantocellularis pars alpha (NGCp alpha) of
28 ected in the nucleus raphe magnus or nucleus reticularis gigantocellularis pars alpha of rats pretrea
29 35348 in the nucleus raphe magnus or nucleus reticularis gigantocellularis pars alpha of saline-pretr
30 and/or dense axonal swellings in the nucleus reticularis gigantocellularis, nucleus reticularis magno
31 erone (DHEA) and DHEA sulfate in the adrenal reticularis is inversely correlated with the expression
32  area is an external portion of the formatio reticularis lateralis (FRLx).
33 cleus raphe magnus (RM) and adjacent nucleus reticularis magnocellularis (NRMC) project to the spinal
34 llary raphe magnus (RM) and adjacent nucleus reticularis magnocellularis (NRMC).
35 cleus reticularis gigantocellularis, nucleus reticularis magnocellularis, raphe magnus, and the ventr
36 raphe magnus and the ventral part of nucleus reticularis magnocellularis; and 2) serotonergic cells p
37 e data suggest that dermatopathia pigmentosa reticularis may map to the same chromosomal region.
38           In the thalamus, GABAergic nucleus reticularis neurons that regulate thalamocortical oscill
39 diated neurotransmission in thalamic nucleus reticularis (nRT) and ventrobasalis complex (VB) neurons
40 neurons acutely dissociated from the nucleus reticularis of thalamus (nRt) treated and untreated with
41 is protein, not only in the zona fasciculata/reticularis of the adrenal cortex, but also in the Leydi
42 genic cells in the zona fasciculata and zona reticularis of the adrenal gland and to the corpus lutea
43 striatum, and (2) DA innervation of the pars reticularis of the substantia nigra.
44  [125I]-alphaBTX binding include the nucleus reticularis of the thalamus, the lateral and medial geni
45 2D16 in microsomes from the inner zone (zona reticularis) of the adrenal cortex than from the outer z
46  magnus (NRM) but independent of the nucleus reticularis paragigantocellularis (NRPgc).
47 idus); 6) the ventrolateral medulla (nucleus reticularis parvocellularis and the rostral ventrolatera
48 ospinal neurons in the contralateral nucleus reticularis PnC and bilaterally in the lateral paragigan
49 n and vasculopathy (recurrent fevers, livedo reticularis, polyarteritis nodosa, lacunar ischemic stro
50 project, among other targets, to the nucleus reticularis pontis caudalis (PnC), a major component of
51 on (MRF) that in turn project to the nucleus reticularis pontis caudalis (PnC), an obligatory relay i
52 H; 0, 10, 20, 40 and 80 ng) into the nucleus reticularis pontis caudalis (PnC), an obligatory synapse
53 r the ventrolateral lemniscus (VLL), nucleus reticularis pontis caudalis (PnC), and spinal motoneuron
54 r Fluoro-Gold into the ventrolateral nucleus reticularis pontis caudalis labeled neurons in the deep
55 ing various methodologies have implicated n. reticularis pontis oralis (RPO) and n. subcoeruleus (Sub
56 edian raphe, raphe pontis, raphe magnus, and reticularis pontis oralis.
57 en reticular nuclei have spinal projections: reticularis (r.) dorsalis, r. ventralis pars alpha and b
58            Axonal projections to the nucleus reticularis tegmenti pontis (RTP) were studied in 11 mac
59  in programming of saccades, and the nucleus reticularis tegmenti pontis in saccade-vergence interact
60 ypoglossi, supragenual, Roller/intercalatus, reticularis tegmenti pontis, and pontine nuclei.
61 ar-response neurons exist within the nucleus reticularis tegmenti pontis, which receives input from t
62  in the ipsilateral basis pontis and nucleus reticularis tegmenti pontis.
63 Y mRNA and protein expression in the nucleus reticularis thalami (nRt) and hippocampus, but not in th
64 waves, both GABAergic neurons of the nucleus reticularis thalami (NRT) and thalamocortical (TC) neuro
65 shold calcium spikes from neurons of nucleus reticularis thalami (nRT) in brain slices from young rat
66 ained from GABAergic neurones of rat nucleus reticularis thalami (NRT) in vitro to assess pre- and po
67          In thalamocortical (TC) and nucleus reticularis thalami (NRT) neurones, and possibly in neoc
68 arising from T-type Ca2+ channels in nucleus reticularis thalami (nRT) play a critical role in genera
69  cells and inhibitory neurons of the nucleus reticularis thalami (nRt) to fire bursts of action poten
70 observed in GABAergic neurons of the nucleus reticularis thalami (NRT).
71 rents (T-currents) in neurons of the nucleus reticularis thalami (nRT).
72                                      Nucleus reticularis thalami neurons expressed only alpha3 as the
73 rons that express Cav3.1, whereas in nucleus reticularis thalami neurons that express Cav3.2 and Cav3
74 ession of inhibitory synapses in the nucleus reticularis thalami, a region where Nxph1 is normally ex
75 M cells were found to be mediated by nucleus reticularis thalamic (nRt) cells.
76                                     Thalamic reticularis, thalamocortical, and cortical cells partici
77 uded in the Sapporo criteria, such as livedo reticularis, thrombocytopenia, low-titer IgG or IgM anti
78 characterized by the association of a livedo reticularis with stroke.

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