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Year | Number of Results |
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qiu chu ying
(1 results)?
µ-TRTX-Ca1a: a novel neurotoxin from Cyriopagopus albostriatus with analgesic effects.
Acta Pharmacol Sin. 2019 Jul;40(7):859-866. doi: 10.1038/s41401-018-0181-9. Epub 2018 Oct 31.
Acta Pharmacol Sin. 2019.
PMID: 30382183
Free PMC article.
Engineering of highly potent and selective HNTX-III mutant against hNav1.7 sodium channel for treatment of pain.
Zhang Y, Wang L, Peng D, Zhang Q, Yang Q, Li J, Li D, Tang D, Chen M, Liang S, Liu Y, Wang S, Liu Z.
Zhang Y, et al. Among authors: yang q.
J Biol Chem. 2021 Jan-Jun;296:100326. doi: 10.1016/j.jbc.2021.100326. Epub 2021 Jan 23.
J Biol Chem. 2021.
PMID: 33493520
Free PMC article.
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Scorpion toxin inhibits the voltage-gated proton channel using a Zn2+ -like long-range conformational coupling mechanism.
Tang D, Yang Y, Xiao Z, Xu J, Yang Q, Dai H, Liang S, Tang C, Dong H, Liu Z.
Tang D, et al. Among authors: yang q.
Br J Pharmacol. 2020 May;177(10):2351-2364. doi: 10.1111/bph.14984. Epub 2020 Mar 3.
Br J Pharmacol. 2020.
PMID: 31975366
Free PMC article.
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Discovery of a Novel Nav1.7 Inhibitor From Cyriopagopus albostriatus Venom With Potent Analgesic Efficacy.
Zhang Y, Peng D, Huang B, Yang Q, Zhang Q, Chen M, Rong M, Liu Z.
Zhang Y, et al. Among authors: yang q.
Front Pharmacol. 2018 Oct 16;9:1158. doi: 10.3389/fphar.2018.01158. eCollection 2018.
Front Pharmacol. 2018.
PMID: 30386239
Free PMC article.
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Engineering Gain-of-Function Analogues of the Spider Venom Peptide HNTX-I, A Potent Blocker of the hNaV1.7 Sodium Channel.
Zhang Y, Yang Q, Zhang Q, Peng D, Chen M, Liang S, Zhou X, Liu Z.
Zhang Y, et al. Among authors: yang q.
Toxins (Basel). 2018 Sep 4;10(9):358. doi: 10.3390/toxins10090358.
Toxins (Basel). 2018.
PMID: 30181499
Free PMC article.
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