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Spider-venom Peptides that Target the Human NaV1.7 channel: Potential Analgesics for the Treatment of Chronic Pain
被引:0
|
作者
:
论文数:
引用数:
h-index:
机构:
Klint, Julie
[
1
]
Anangi, Raveendra
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
Anangi, Raveendra
[
1
]
论文数:
引用数:
h-index:
机构:
Mobli, Mehdi
[
1
]
Knapp, Oliver
论文数:
0
引用数:
0
h-index:
0
机构:
RMIT Univ, Hlth Innovat Res Inst, Melbourne, Vic, Australia
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
Knapp, Oliver
[
2
]
Adams, David J.
论文数:
0
引用数:
0
h-index:
0
机构:
RMIT Univ, Hlth Innovat Res Inst, Melbourne, Vic, Australia
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
Adams, David J.
[
2
]
King, Glenn F.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
King, Glenn F.
[
1
]
机构
:
[1]
Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
[2]
RMIT Univ, Hlth Innovat Res Inst, Melbourne, Vic, Australia
来源
:
TOXICON
|
2012年
/ 60卷
/ 02期
关键词
:
spider-venom peptides;
NaV1.7;
therapeutics;
analgesics;
structure-function relationships;
pharmacophore;
drug development;
D O I
:
10.1016/j.toxicon.2012.04.032
中图分类号
:
R9 [药学];
学科分类号
:
1007 ;
摘要
:
31
引用
收藏
页码:110 / 111
页数:2
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