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pro vyhledávání: '"neurotoxin receptor site"'
Akademický článek
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Akademický článek
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Autor:
Shuijiao Peng, Minzhi Chen, Zhen Xiao, Xin Xiao, Sen Luo, Songping Liang, Xi Zhou, Zhonghua Liu
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Venomous animals have evolved to produce peptide toxins that modulate the activity of voltage-gated sodium (Nav) channels. These specific modulators are powerful probes for investigating the structural and functional features of Nav channels. Here, w
Externí odkaz:
https://doaj.org/article/e341bd26a3654491adce27c9cc9b85c2
Publikováno v:
Journal of neurochemistry. 65(3)
Reconstitution of purified sodium channels into phospholipid vesicles restores many aspects of sodium channel function including high-affinity neurotoxin binding and action at neurotoxin receptor sites 1-3 and 5, but neurotoxin binding and action at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f95c0c0ce1c494b10874ae6cf9fec2f
https://pubmed.ncbi.nlm.nih.gov/7643113
https://pubmed.ncbi.nlm.nih.gov/7643113
Autor:
Thomsen W; Department of Pharmacology, University of Washington Medical School, Seattle 98195, USA., Martin-Eauclaire MF, Rochat H, Catterall WA
Publikováno v:
Journal of neurochemistry [J Neurochem] 1995 Sep; Vol. 65 (3), pp. 1358-64.
Publikováno v:
Scopus-Elsevier
The peptide conotoxin TxVIA is selectively toxic to molluscs and slows sodium current inactivation in mollusc neurons. Here we show that TxVIA binds with high affinity to new sites on sodium channels in both mollusc and rat central nervous systems, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b177631cccf132584ae2ac4fa4eda7
https://pubmed.ncbi.nlm.nih.gov/8300586
https://pubmed.ncbi.nlm.nih.gov/8300586
Autor:
Peng, Shuijiao, Chen, Minzhi, Xiao, Zhen, Xiao, Xin, Luo, Sen, Liang, Songping, Zhou, Xi, Liu, Zhonghua
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Venomous animals have evolved to produce peptide toxins that modulate the activity of voltage-gated sodium (Nav) channels. These specific modulators are powerful probes for investigating the structural and functional features of Nav channels. Here, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c75e071c90ba648ede19fb4ca227b8
https://doi.org/10.3389/fphar.2021.778534
https://doi.org/10.3389/fphar.2021.778534
Publikováno v:
Toxicon; April 1994, Vol. 32 Issue: 4 p396-396, 1p
Autor:
Bauer, Marta1 (AUTHOR) marta.bauer@gumed.edu.pl, Glowacka, Magdalena2 (AUTHOR) magdalena.glowacka@wsei.pl, Kamysz, Wojciech3 (AUTHOR) wojciech.kamysz@gumed.edu.pl, Kleczkowska, Patrycja2,4 (AUTHOR) marta.bauer@gumed.edu.pl
Publikováno v:
International Journal of Molecular Sciences. Dec2024, Vol. 25 Issue 23, p12601. 17p.
Autor:
Peng, Shuijiao, Chen, Minzhi, Xiao, Zhen, Xiao, Xin, Luo, Sen, Liang, Songping, Zhou, Xi, Liu, Zhonghua
Publikováno v:
Frontiers in Pharmacology; 12/6/2021, Vol. 12, p1-13, 13p