Zobrazeno 1 - 7
of 7
pro vyhledávání: '"T R, Werkman"'
Publikováno v:
Neuropharmacology. 33:795-804
The effects of alaproclate on voltage-dependent K+ currents and N-methyl- d -aspartate (NMDA) and ψ -aminobutyric acidA (GABAA) receptor currents were investigated in cultured rat hippocampal neurons using whole-cell voltage clamp recording techniqu
Publikováno v:
Neuroscience. 50:935-946
The blocking actions of the K+ channel toxins charybdotoxin, dendrotoxin and mast cell degranulating peptide were studied in B82 mouse fibroblast cells transformed to express NGK1 (Kv1.2) K+ channels. All three toxins were potent blockers of the K+ c
Publikováno v:
Synapse (New York, N.Y.). 26(2)
Previously it was found that the amplitude of Ca currents in CA1 hippocampal neurons increases after adrenalectomy (ADX) of young adult rats. Preliminary data suggested that this effect of ADX is age-dependent. In the present study we therefore inves
Autor:
R S, Rogowski, J H, Collins, T J, O'Neill, T A, Gustafson, T R, Werkman, M A, Rogawski, T C, Tenenholz, D J, Weber, M P, Blaustein
Publikováno v:
Molecular pharmacology. 50(5)
Three 35-amino acid peptide K+ channel toxins (pandinotoxins) were purified from the venom of the scorpion Pandinus imperaton the toxins are designated pandinotoxin (PiTX)-K alpha, PiTX-K beta, and PiTX-K gamma. In an 86Rb tracer flux assay on rat br
Publikováno v:
Neuropharmacology. 33(6)
The effects of alaproclate on voltage-dependent K+ currents and N-methyl-D-aspartate (NMDA) and gamma-aminobutyric acidA (GABAA) receptor currents were investigated in cultured rat hippocampal neurons using whole-cell voltage clamp recording techniqu
Publikováno v:
Molecular pharmacology. 44(2)
The interaction between two nonhomologous K+ channel toxins, Tityus serrulatus (scorpion) toxin tityustoxin-K alpha (TsTX-K alpha) and Dendroaspis angusticeps (snake) toxin dendrotoxin (alpha-DTX), was investigated on K+ currents in B82 fibroblast ce
Publikováno v:
Neuroscience. 50(4)
The blocking actions of the K+ channel toxins charybdotoxin, dendrotoxin and mast cell degranulating peptide were studied in B82 mouse fibroblast cells transformed to express NGK1 (Kv1.2) K+ channels. All three toxins were potent blockers of the K+ c