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1 red the presence of the gap junction protein connexin 36.
2                          Our data shows that connexin 36, a gap junction protein specific to neurons,
3 ression of the neuronal gap junction protein connexin-36 among inhibitory interneurons and found a re
4         The selective delta cell knockout of connexin 36 confirmed the involvement of gap junctions.
5  which appear to be electrically coupled via connexin 36 containing gap junctions to the vertically o
6 on of heart rate and blood pressure involves connexin 36-containing gap junctions.
7 bility, and we here report that, indeed, the connexin-36-containing glutamatergic mossy fiber synapse
8       Gap-junction coupling of beta-cells by connexin-36 coordinates intracellular free calcium oscil
9 onal gap junction coupling and expression of connexin 36 (Cx36) (neuronal gap junction protein), and
10   During development, two connexin isoforms, connexin 36 (Cx36) and Cx45, are expressed in bipolar ce
11 channels formed by two homologs of mammalian connexin 36 (Cx36) and that, while Cx35 is restricted to
12                       We have found variable connexin 36 (cx36) expression in different types of ON c
13                               In the retina, connexin 36 (Cx36) gap junctions couple AII amacrine cel
14 at forms an electrically coupled network via connexin 36 (Cx36) gap junctions.
15 ce lacking the neuronal gap junction protein connexin 36 (Cx36) have nearly normal firing patterns at
16  In this study, we studied the expression of connexin 36 (Cx36) in the olfactory epithelium and olfac
17 nd in vitro is associated with a decrease in connexin 36 (Cx36) protein expression.
18 kade of gap junctions or genetic ablation of connexin 36 (Cx36) subunits eliminates the long-range co
19 gical blockade of GJs or genetic ablation of connexin 36 (Cx36) subunits, which are highly expressed
20 e contribution of the gap junctional protein connexin 36 (Cx36) to the regulation of sympathetic acti
21                                          For connexin 36 (Cx36), the major neuronal connexin, it has
22 ession of the neuronal gap junction protein, connexin 36 (Cx36), transiently increase during early po
23 OB) engage in strong electrical coupling via connexin 36 (Cx36)-mediated gap junctions.
24 ytosolic pores formed by the neuron-specific connexin 36 (Cx36).
25 s well as gap junctions that are mediated by connexin 36 (Cx36).
26 onal gap junction coupling and expression of connexin 36 (Cx36; neuronal gap junction protein) are re
27      beta-cells are electrically coupled via connexin-36 (Cx36) gap junction channels, which coordina
28                                              Connexin-36 (Cx36) gap junction permeability and associa
29 , hypothalamus, and thalamus of rats express connexin-36 (Cx36) gap junctions (GJs) and couple electr
30                                              Connexin-36 (Cx36) gap junctions also regulate islet ele
31 f stimulation intensities, primarily through connexin-36-dependent rod pathways.
32 pressed key intercellular junction proteins (connexin-36, E-cadherin, and occludin) at different leve
33 ell strains lacking the gap junction protein connexin-36 exhibited nonnegligible ice propagation rate
34 or incorporating the neuronal promoter human connexin 36 (hCx36) transduced ganglion cells within a d
35  show that, in rabbit retina, an antibody to connexin 36 heavily labels processes of AII amacrine cel
36  immunogold labeling revealed that 70-76% of connexin-36-immunolabeled particles were localized at fo
37                                Expression of connexin-36 immunoreactivity is widespread in the forebr
38 unctions be demonstrated in association with connexin-36 immunoreactivity.
39                                              Connexin-36 is a neuronally specific protein associated
40 ctron microscopy, and electrophysiology that Connexin-36 is necessary for functional gap junctions (G
41    It is known that the gap junction protein connexin-36 is widely expressed in the sexually dimorphi
42 ctional coupling, and was still prevalent in connexin 36 knock-out animals.
43                 The recent generation of the connexin-36 knock-out (Cx36 KO) mouse has offered a uniq
44 Utilizing islets from a gap junction protein connexin 36 knockout mouse model together with chemical
45                         We characterized the connexin-36 knockout (Cx36(-/-)) mouse phenotype and per
46 recordings in bulb slices from wild-type and connexin 36-knockout (KO) mice.
47 ssion between AII cells and OFF cone BCs and connexin 36-labeled gap junctions between AII cells and
48                                              Connexin-36 localization was studied in the mouse somato
49 direct OSN inputs are drastically shunted by connexin 36-mediated gap junctions on MCs, but not tufte
50 tial association between GluN2B subunits and connexin 36 on AII amacrines, suggesting that NMDA recep
51 expression of the electrical synapse-forming connexin-36 protein.
52 read distribution of focal concentrations of connexin-36 subunits could provide a basis for the elect
53 g among these interneurons and expression of connexin 36 suggested that they form electrically couple
54 cate an energetic failure; and (2) a loss of connexin 36, suggesting alterations in the AII coupling
55  with myopia is near the GJD2 gene, encoding connexin-36, which forms retinal gap junctions.