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1 B3 is an agonist of a Caenorhabditis elegans TRPV channel.
2 ecular mechanism underlying NA regulation of TRPV channels.
3 l borate (2-APB), a common agonist for these TRPV channels.
4 ation threshold of gating elements shared by TRPV channels.
5 ization may be conserved in the subfamily of TRPV channels.
6 t is known to be an effective blocker of all TRPV channels.
7 ructural features contribute to diversity of TRPV channels.
8 e by vanilloid transient receptor potential (TRPV) channels.
9 intraflagellar transport and the OCR-2/OSM-9 TRPV channel act in concert, regulating two layers of ac
12 s well as the orthologous Drosophila Nan-Iav TRPV channel, and we examine stoichiometry of subunit as
13 our understanding of ligand interaction with TRPV channels, and the availability of purified human TR
15 stinct mechanotransduction channels and that TRPV channels contribute to encoding and transmitting in
16 arbon polyunsaturated fatty acids (PUFAs) in TRPV channel-dependent olfactory and nociceptive behavio
20 , revealing modality-specific mechanisms for TRPV channel function in the regulation of C. elegans ch
21 o further understand the structural basis of TRPV channel function, we determined the structure of fu
23 ocr-2, since mutants lacking npr-1 and both TRPV channels had more severe defects in heat avoidance
26 the putative selectivity filter of OSM-9, a TRPV channel, in osmotic avoidance behaviour of Caenorha
28 d influx of Ca(2+) that was abolished by the TRPV channel inhibitor, ruthenium red, or in tubules iso
29 ve effects were blocked by co-injection of a TRPV channel inhibitor, which are thought to function as
31 of corresponding residues within two related TRPV channels leads to comparable effects on their activ
32 d support cells, that it is not required for TRPV channel localization, and that it is not essential
33 o acid point mutation in OCR-2 that disrupts TRPV channel-mediated gene expression, but does not decr
39 er show that p38/MAPK signals to AKT and the TRPV channel OSM-9, a sensory channel in ASH neurons.
41 neither of these genes, but does require the TRPV channel osm-9, which is dispensable for associative
43 the transient receptor potential vanilloid (TRPV) channels OSM-9 and OCR-2 selectively restore grk-2
45 nants, and specific functional properties of TRPV channel proteins may be selectively conserved acros
47 protein in the vanilloid receptor subfamily (TRPV) channel subunit, Nanchung (NAN), is localized to t
48 sults identify a specific set of heteromeric TRPV channels that redundantly regulate neuroendocrine f
50 (TRPV2) is an intracellular Ca(2+)-permeable TRPV channel upregulated by NGF via the mitogen-activate
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