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1 B3 is an agonist of a Caenorhabditis elegans TRPV channel.
2 modulating the activity of calcium-selective TRPV channels.
3 ructural features contribute to diversity of TRPV channels.
4 ecular mechanism underlying NA regulation of TRPV channels.
5 l borate (2-APB), a common agonist for these TRPV channels.
6 ation threshold of gating elements shared by TRPV channels.
7 ization may be conserved in the subfamily of TRPV channels.
8 t is known to be an effective blocker of all TRPV channels.
9 e by vanilloid transient receptor potential (TRPV) channels.
10 intraflagellar transport and the OCR-2/OSM-9 TRPV channel act in concert, regulating two layers of ac
11 iguing link between metabolic regulation and TRPV channel activity.
12 ans and Drosophila, serving as an agonist of TRPV channels affecting sensory neurons and mimicking th
13                        Our results show that TRPV channels and the FLP-21/NPR-1 neuropeptide signalin
14 s well as the orthologous Drosophila Nan-Iav TRPV channel, and we examine stoichiometry of subunit as
15 our understanding of ligand interaction with TRPV channels, and the availability of purified human TR
16 the role of the ankyrin repeats in different TRPV channels are discussed.
17                    NAM is thought to bind to TRPV channels causing overstimulation of sensory neurons
18 stinct mechanotransduction channels and that TRPV channels contribute to encoding and transmitting in
19 arbon polyunsaturated fatty acids (PUFAs) in TRPV channel-dependent olfactory and nociceptive behavio
20 ; however, the molecular mechanisms by which TRPV channels establish precise and robust temperature s
21          This current was independent of two TRPV channels expressed in ASH.
22           A requirement for IFT140 in stable TRPV channel expression also suggests that IFT-A protein
23      Third, the response to ascr#10 requires TRPV channel function in the ADL neurons and the daf-7 s
24 , revealing modality-specific mechanisms for TRPV channel function in the regulation of C. elegans ch
25 o further understand the structural basis of TRPV channel function, we determined the structure of fu
26                                   C. elegans TRPV channels function in olfaction, mechanosensation, o
27 s provide a foundation to further understand TRPV channel gating, their divergent physiological funct
28  ocr-2, since mutants lacking npr-1 and both TRPV channels had more severe defects in heat avoidance
29 the specific activation of each of the three TRPV channels in a single sample.
30                Here, we review evidence that TRPV channels in the central nervous system might contri
31 transient receptor potential vanilloid-type (TRPV) channels in insects, likely form a heteromeric cha
32  the putative selectivity filter of OSM-9, a TRPV channel, in osmotic avoidance behaviour of Caenorha
33                       Here, we report that a TRPV channel, Inactive (Iav), maintains presynaptic rest
34 d influx of Ca(2+) that was abolished by the TRPV channel inhibitor, ruthenium red, or in tubules iso
35 ve effects were blocked by co-injection of a TRPV channel inhibitor, which are thought to function as
36                       Although loss of these TRPV channels inhibits behavioral responses to noxious s
37 he Transient Receptor Potential Vanilloid 1 (TRPV) channel is activated by an array of stimuli, inclu
38 of corresponding residues within two related TRPV channels leads to comparable effects on their activ
39 d support cells, that it is not required for TRPV channel localization, and that it is not essential
40 o acid point mutation in OCR-2 that disrupts TRPV channel-mediated gene expression, but does not decr
41 ate that mechanosensory neurons expressing a TRPV channel nanchung, located in the antennae and chord
42                             In contrast, the TRPV channels Nanchung and Inactive are required for res
43                     Further, we identified a TRPV channel, Nanchung, and a specific Nanchung-expressi
44                 Furthermore, we found that a TRPV channel, Nanchung, and a specific Nanchung-expressi
45                                        Among TRPV channels, only the selective activation of TRPV2 ch
46                  These behaviors require the TRPV channel OSM-9 because osm-9 mutants do not avoid no
47 er show that p38/MAPK signals to AKT and the TRPV channel OSM-9, a sensory channel in ASH neurons.
48                                          The TRPV channel OSM-9, previously suggested to be an obliga
49 neither of these genes, but does require the TRPV channel osm-9, which is dispensable for associative
50      Transient receptor potential vanilloid (TRPV) channels OSM-9 and OCR-2 move in ciliary membranes
51  the transient receptor potential vanilloid (TRPV) channels OSM-9 and OCR-2 selectively restore grk-2
52                        C. elegans OSM-9 is a TRPV channel protein involved in sensory transduction an
53 nants, and specific functional properties of TRPV channel proteins may be selectively conserved acros
54 ealth of structures, many aspects concerning TRPV channels remain poorly understood, including the po
55  characterize the activity of BAA on certain TRPV channel subtypes.
56 protein in the vanilloid receptor subfamily (TRPV) channel subunit, Nanchung (NAN), is localized to t
57 sults identify a specific set of heteromeric TRPV channels that redundantly regulate neuroendocrine f
58            Though homologous to TRPV1, other TRPV channels (TRPV2-6) are insensitive to TRPV1 activat
59                                 Unlike other TRPV channels, TRPV5 and its close homolog, TRPV6, do no
60 (TRPV2) is an intracellular Ca(2+)-permeable TRPV channel upregulated by NGF via the mitogen-activate
61 vate transient receptor potential vanilloid (TRPV) channels when coupled with ferritin.
62      Transient receptor potential vanilloid (TRPV) channels, which include the thermosensitive TRPV1-