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  • Biophysics of voltage-activated sodium channels: A window into neuroscience

    Biophysics of voltage-activated sodium channels by de Oliveira Silva, Anita; de Moraes, Éder Ricardo;

    A window into neuroscience

      • GET 5% OFF

      • The discount is only available for 'Alert of Favourite Topics' newsletter recipients.
      • Publisher's listprice EUR 35.90
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        14 889 Ft (14 180 Ft + 5% VAT)
      • Discount 5% (cc. 744 Ft off)
      • Discounted price 14 145 Ft (13 471 Ft + 5% VAT)

    14 889 Ft

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    Availability

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    Product details:

    • Publisher Our Knowledge Publishing
    • Date of Publication 17 March 2025
    • Number of Volumes Großformatiges Paperback. Klappenbroschur

    • ISBN 9786208749668
    • Binding Paperback
    • No. of pages52 pages
    • Size 220x150 mm
    • Language English
    • 646

    Categories

    Long description:

    Voltage-activated sodium channels form a superfamily of transmembrane proteins that act in electrical signalling and ion homeostasis in electrically excitable cells. Given their importance and diversity, it is essential that studies are continually carried out to clarify the pathological processes involving voltage-activated sodium channels and the pharmacology of their ligands. Due to their specificity in certain tissues at different stages of life, in-depth studies, both in vitro and in vivo, of these channels using experimental models that are closer to human reality should be encouraged. For this reason, it is important to correlate the understanding of pathophysiology and pharmacokinetics in order to obtain more efficient therapies. In the case of sodium channels that are specifically expressed in certain tissues, the side effects of the drug can be minimised. Therefore, the current lack of specific ligands for certain subtypes of sodium channels that are also specific makes this line of research as fascinating as it is promising.

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