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Engineering of highly potent and selective HNTX-III mutant against hNa(v)1.7 sodium channel for treatment of pain
Human voltage-gated sodium channel Na(v)1.7 (hNa(v)1.7) is involved in the generation and conduction of neuropathic and nociceptive pain signals. Compelling genetic and preclinical studies have validated that hNa(v)1.7 is a therapeutic target for the treatment of pain; however, there is a dearth of...
Tallennettuna:
| Julkaisussa: | J Biol Chem |
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| Päätekijät: | , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society for Biochemistry and Molecular Biology
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7988488/ https://ncbi.nlm.nih.gov/pubmed/33493520 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jbc.2021.100326 |
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