about
Structure of the TRPA1 ion channel suggests regulatory mechanismsInternational Union of Basic and Clinical Pharmacology. LXXVI. Current progress in the mammalian TRP ion channel familyThe cation channel TRPA1 tunes mosquito thermotaxis to host temperaturesThermotaxis, circadian rhythms, and TRP channels in DrosophilaSpecies-specific temperature sensitivity of TRPA1TRP ion channels in thermosensation, thermoregulation and metabolismHow the TRPA1 receptor transmits painful stimuli: Inner workings revealed by electron cryomicroscopyTRPA1 as a drug target--promise and challengesStructure of thermally activated TRP channelsTRP Channels in Skin Biology and PathophysiologySnake Genome Sequencing: Results and Future ProspectsWarmth suppresses and desensitizes damage-sensing ion channel TRPA1Evolutionary trajectories of snake genes and genomes revealed by comparative analyses of five-pacer viperMolecular mechanisms of temperature adaptationFrom the ultrasonic to the infrared: molecular evolution and the sensory biology of bats.A multi-organ transcriptome resource for the Burmese Python (Python molurus bivittatus)The role of proboscis of the malaria vector mosquito Anopheles stephensi in host-seeking behaviorTRP channel mediated neuronal activation and ablation in freely behaving zebrafishGenetic and neural mechanisms that inhibit Drosophila from mating with other species.Signaling by sensory receptorsSensory biology. Evolution of sweet taste perception in hummingbirds by transformation of the ancestral umami receptor.TRPA1 mediates sensation of the rate of temperature change in Drosophila larvae.Characterization of TRPA channels in the starfish Patiria pectinifera: involvement of thermally activated TRPA1 in thermotaxis in marine planktonic larvaeTRPA1 expression and its functional activation in rodent cortex.TRPV1 temperature activation is specifically sensitive to strong decreases in amino acid hydrophobicity.Single cell transcriptomics of hypothalamic warm sensitive neurons that control core body temperature and fever response Signaling asymmetry and an extension of chemical neuroanatomy.Coagulating Colubrids: Evolutionary, Pathophysiological and Biodiscovery Implications of Venom Variations between Boomslang (Dispholidus typus) and Twig Snake (Thelotornis mossambicanus).Thermogenetic neurostimulation with single-cell resolution.Evolution of vertebrate transient receptor potential vanilloid 3 channels: opposite temperature sensitivity between mammals and western clawed frogsTrpA1 regulates thermal nociception in DrosophilaMolecular evolution of the infrared sensory gene TRPA1 in snakes and implications for functional studies.The dynamic TRPA1 channel: a suitable pharmacological pain target?Ganglion-specific splicing of TRPV1 underlies infrared sensation in vampire batsConservation of tubulin-binding sequences in TRPV1 throughout evolution.Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl.Human TRPA1 is intrinsically cold- and chemosensitive with and without its N-terminal ankyrin repeat domainInfrared-sensitive pit organ and trigeminal ganglion in the crotaline snakes.Modular thermal sensors in temperature-gated transient receptor potential (TRP) channelsDiscovery of a novel accessory structure of the pitviper infrared receptor organ (serpentes: viperidae).Evolutionarily conserved, multitasking TRP channels: lessons from worms and flies
P2860
Q24336461-6ACDACC9-96A0-464F-A25E-4B3DD0188BE4Q24623493-9D3EC4CB-E1C0-4013-8D76-3C690D5CC85BQ24810555-FF04CBF8-0FAC-4651-86C5-4443015AB4EFQ26745807-F9176FE8-9B3E-4339-9C56-895700CE0672Q26745809-88710A03-A984-4AB0-8C89-B8A173291D8FQ26745816-4FBE5423-488F-4E14-9EB9-0A364883E56AQ26783066-A50EBA41-F807-4F63-BB74-F51066F62389Q26863458-0C6C09E5-2EEF-41B7-88E7-7929D5AF5543Q27011684-C71196FD-9048-4D87-A179-0C2F8171052CQ28066420-2BE19CA7-DA7A-4960-93B9-6A979BD86114Q28066516-6EC75F8F-7666-41A7-BFCA-F1530B760F07Q28580915-5D52F39F-3BEF-4416-921C-433563708C06Q28597729-32F797FF-86BE-4CD0-AD10-8928EE0D97D8Q28608015-B75ECCFB-61F2-4F02-86D0-A0767B3247F5Q28685283-EF01C5D6-66EC-4546-83B5-53CD31D7C946Q28740408-701A4B88-B024-4779-8127-AF58CE968777Q28742588-3675C673-0D19-4155-ADF4-69E08DF95FEBQ30381473-5B9F6420-E89F-4131-BB0A-214003258AE0Q30444806-F13DE264-EBAB-45BC-A9D8-4E213BEFADA8Q30445020-ACC4B641-D903-48DD-B93E-5928BAEC5762Q30617373-10806A17-300A-40AD-B196-AA8F9F001E58Q30833282-8FF13170-0357-4F71-A734-A249E8DE44A7Q30852080-6DDE21DA-6944-4283-BDA3-D7EFC60FB7DBQ33628837-EC89B5D3-9E66-4E95-8B40-95A924875DC3Q33674257-E862C5F3-2A55-4CAE-94B1-2FF0D8105489Q33726456-3005C21E-D317-49A2-8F9F-7360181713E2Q33744791-CA480450-BF75-4B83-9E9A-D5DF4B553675Q33860707-8BD07E32-F6A5-4735-9F60-EE54D96F183FQ33872246-2728FE9A-00B7-498C-BE6A-1BA0894A0AB8Q34016472-BD5FBC9B-2B00-4A5D-9588-8EC585CEC061Q34098293-1081760F-F692-4229-AC88-AC27927A94C5Q34175932-D0232FA2-1301-4B33-911D-3877E4A68A04Q34205845-3ECD628B-3FAE-41AB-A1D0-1F8687D1D24BQ34229765-1BA503A3-00D2-49A3-AE4A-FE86F70AA8CAQ34383771-4565B041-5BCD-4B75-AC15-F2365153BFE5Q34601695-6CE23CFF-788B-4366-A94B-A37A68FB8778Q34822287-F62DA1B7-E08E-4EF3-8BF9-B0B963DEB164Q35090957-5F4BB30A-B33A-421C-B7D5-189C4353DE6CQ35111038-A0148218-452D-459E-9A14-EB182EAB2DB0Q35122164-8289222F-C1F7-4055-8F0E-C538319DBFDD
P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Molecular basis of infrared detection by snakes
@ast
Molecular basis of infrared detection by snakes
@en
Molecular basis of infrared detection by snakes
@nl
type
label
Molecular basis of infrared detection by snakes
@ast
Molecular basis of infrared detection by snakes
@en
Molecular basis of infrared detection by snakes
@nl
prefLabel
Molecular basis of infrared detection by snakes
@ast
Molecular basis of infrared detection by snakes
@en
Molecular basis of infrared detection by snakes
@nl
P2093
P2860
P3181
P356
P1433
P1476
Molecular basis of infrared detection by snakes
@en
P2093
Alexander T Chesler
David Julius
Elda E Sánchez
Gunther Hollopeter
John C Perez
Julio F Cordero-Morales
Nicholas T Ingolia
Yvonne M Kelly
P2860
P2888
P304
P3181
P356
10.1038/NATURE08943
P407
P577
2010-03-14T00:00:00Z
P5875
P6179
1002291889