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1 ishevelled (Dsh - a protein operating in Wnt second messenger systems).
2 iated by CRH1 receptors and a cAMP-dependent second messenger system.
3  end may be made by the phosphatidylinositol second messenger system.
4 n activate KCa channels via an intracellular second messenger system.
5 ar to signal upstream of a G protein-coupled second messenger system.
6 nthesis may do so via modulation of the cAMP second messenger system.
7  D3 receptor has little or no effect on this second messenger system.
8 capable of producing a maximal effect on the second messenger system.
9 onist, was due to changes in the receptor or second messenger system.
10  the resulting activation of a cAMP-mediated second messenger system.
11 he membrane bilayer to a G-protein-activated second messenger system.
12 than indirect effects, such as activation of second messenger systems.
13 ed to both the MAP kinase and cAMP-dependent second messenger systems.
14 be dissociated and are mediated by different second messenger systems.
15 gulated by a number of neurotransmitters and second-messenger systems.
16 m, indicating the involvement of IP3-related second-messenger systems.
17 orhabditis elegans that affect components of second messenger systems, a G-protein subunit, phospholi
18 gly, NFATc4 is particularly sensitive to the second messenger systems activated by BDNF.
19                                          The second-messenger systems activated in the parietal cell
20 esia, because it was independent of the cAMP second messenger system and blocked by the guanylyl cycl
21 rate a novel regulation of CaMKII by another second messenger system and indicate its involvement in
22 fects of glutathione and redox modulation on second messenger systems and gene regulation.
23 f voltage-gated calcium channel activity via second messenger systems and ion channel subunit express
24 ors evokes distinct, but highly interacting, second messenger systems and multiple effectors.
25 n is dependent on the activation of neuronal second messenger systems and requires protein synthesis.
26 ns (G proteins) which, in turn, can activate second messenger systems and/or ion channels, such as G
27 clude hormonal regulation, calcium channels, second messenger systems, and glutamate signaling.
28 GE catalog were found for surface receptors, second-messenger systems, and cytoskeletal, apoptotic, a
29 tion mechanisms, involving G-protein-coupled second-messenger systems, and neural processing mechanis
30 fected genes implicated the adenylyl cyclase second-messenger system as key in learning and memory.
31  to interfere with the phosphoinositide (PI) second messenger system by inhibiting the activity of in
32                         Stimulating the cAMP second messenger system by PGE1 supplementation resulted
33 ite specifically responding to activation by second messenger system (Ca(2+) messenger system) in pla
34 ere have been notable surprises-conventional second messenger systems co-opted for intricate associat
35 imuli reported as salty or sour, whereas the second messenger systems cyclic AMP and inositol trispho
36 ether different cell types utilize different second-messenger systems for this purpose.
37  by Gq depend on the transient activation of second-messenger systems, Gq utilizes a hard-wired prote
38                                              Second messenger systems have been shown to modulate dop
39                Calcium plays a key role as a second messenger system in astrocytes, both in regulatio
40  the metabotropic glutamate receptor (mGluR) second messenger system in cerebellar Purkinje cells is
41 have implicated several neurotransmitter and second messenger systems in extinction learning, and rev
42 clase--cyclic adenosine monophosphate (cAMP) second-messenger system in the transduction of adenosine
43 ition enhancement, we tested the role of key second-messenger systems in maintaining such long-lastin
44            In addition, estrogens can affect second messenger systems including calcium mobilization
45                   In addition, E2 can affect second messenger systems including calcium mobilization
46 n of NARPPs should lead to identification of second messenger systems involved in NMDA receptor signa
47 ecific coupling of the receptor to different second messenger systems may be cell-specific, depending
48                                              Second messenger systems mediate neuronal responses to e
49 , we evaluated whether the same or different second messenger systems mediate the development of this
50 g events important in embryogenesis, but the second messenger systems modulated by Wnts have not been
51 receptor systems and intracellular ion flux, second messenger systems, new synaptic connections and a
52 t a weaker linkage of 5-HT(2) sites to their second-messenger system relative to 6J mice.
53 n to be agonists of the phosphatidylinositol second messenger system (serotonin, 2,4-dichlorophenoxya
54                  Perturbation of other major second messenger systems, such as cAMP and protein kinas
55 cytes in vitro causes activation of multiple second messenger systems that are very similar to growth
56 ferent, we are also studying the dorsal horn second messenger systems that underlie the development o
57 holinergic pathways coupled to intracellular second-messenger systems that determine the trafficking
58 ther than other transporters or conventional second-messenger systems that link to secretory pathways
59 the C-termini in specifying which of the two second messenger systems the receptors are able to activ
60 of ER are expressed in a form that activates second messenger systems, these findings support a testa
61  cross-talk between cAMP and tyrosine kinase second messenger systems, thus defining a new mode of ce
62 s to recruit specific components of the cAMP second-messenger system to nascent integrin adhesions an
63 dulatory influences, from soluble factors to second-messenger systems, to specific proteins in nerve
64 tor subtypes m1 and m3, which are coupled to second messenger systems via Gq/11, showed little agonis
65 block at-RA uncoupling effects indicating no second messenger systems were involved.
66     In studies on freshly excised rat aorta, second-messenger systems were pharmacologically modulate
67 cological coupling of OctyR99AB to different second messenger systems when expressed in Xenopus oocyt
68 tters can activate the phosphoinositide (PI) second-messenger system which has been investigated usin
69 pled activation of the phosphoinositide/Ca2+ second messenger system, which in turn leads to the open
70 re primarily linked to the adenylate cyclase second messenger system, which would help the intracellu
71 gests that moderate changes in RyR gating by second-messenger systems will principally alter the spat
72 ductive-related hypothalamic physiology, via second messenger systems with dopamine-induced cell sign

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