Zobrazeno 1 - 4
of 4
pro vyhledávání: '"László Béress"'
Autor:
Dongchen An, Ernesto Lopes Pinheiro-Junior, László Béress, Irina Gladkikh, Elena Leychenko, Eivind A. B. Undheim, Steve Peigneur, Jan Tytgat
Publikováno v:
Marine Drugs, Vol 20, Iss 2, p 140 (2022)
(1) Background: G protein-coupled inward-rectifier potassium (GIRK) channels, especially neuronal GIRK1/2 channels, have been the focus of intense research interest for developing drugs against brain diseases. In this context, venom peptides that sel
Externí odkaz:
https://doaj.org/article/c30e3f24ff8f44c7821bc2c20af3c4bc
Autor:
Beata Niklas, Milena Jankowska, Dalia Gordon, László Béress, Maria Stankiewicz, Wieslaw Nowak
Publikováno v:
Molecules, Vol 26, Iss 5, p 1302 (2021)
Animal venoms are considered as a promising source of new drugs. Sea anemones release polypeptides that affect electrical activity of neurons of their prey. Voltage dependent sodium (Nav) channels are the common targets of Av1, Av2, and Av3 toxins fr
Externí odkaz:
https://doaj.org/article/83bd9f8037ac491ba0e533246a0da44c
Autor:
Anne Béress, Otmar Wassermann, Thomas Bruhn, László Béress, Edmundo N. Kraiselburd, Luz Virginia Gonazalez, Gladys E. de Motta, Pedro J. Chavez
Publikováno v:
Journal of Natural Products. 59:552-552
Autor:
Lien Moreels, Steve Peigneur, Diogo T. Galan, Edwin De Pauw, Lászlo Béress, Etienne Waelkens, Luis A. Pardo, Loïc Quinton, Jan Tytgat
Publikováno v:
Marine Drugs, Vol 15, Iss 9, p 287 (2017)
The human ether-à-go-go channel (hEag1 or KV10.1) is a cancer-relevant voltage-gated potassium channel that is overexpressed in a majority of human tumors. Peptides that are able to selectively inhibit this channel can be lead compounds in the searc
Externí odkaz:
https://doaj.org/article/207d82e65fb645f0972d8d95a84aec72