| human | Q5 |
| P496 | ORCID iD | 0000-0001-6227-3301 |
| P1153 | Scopus author ID | 6603684531 |
| P166 | award received | EBSA Young Investigators’ Medal and Prize | Q106646588 |
| P108 | employer | University of Debrecen | Q903092 |
| P735 | given name | György | Q942625 |
| György | Q942625 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q114867299 | A Novel Insecticidal Spider Peptide that Affects the Mammalian Voltage-Gated Ion Channel hKv1.5 |
| Q104693657 | A disulfide-stabilised helical hairpin fold in acrorhagin I: an emerging structural motif in peptide toxins |
| Q41598401 | A new mechanism of voltage-dependent gating exposed by KV10.1 channels interrupted between voltage sensor and pore |
| Q39940935 | A selective blocker of Kv1.2 and Kv1.3 potassium channels from the venom of the scorpion Centruroides suffusus suffusus. |
| Q44637503 | Active and passive behaviour in the regulation of stiffness of the lateral wall in outer hair cells of the guinea-pig |
| Q38810149 | An engineered scorpion toxin analogue with improved Kv1.3 selectivity displays reduced conformational flexibility. |
| Q34047165 | C-type inactivation of a voltage-gated K+ channel occurs by a cooperative mechanism |
| Q41914490 | Closed-state inactivation involving an internal gate in Kv4.1 channels modulates pore blockade by intracellular quaternary ammonium ions |
| Q36295859 | Cross talk between activation and slow inactivation gates of Shaker potassium channels |
| Q111848919 | Cyclodextrins Exert a Ligand-like Current Inhibitory Effect on the KV1.3 Ion Channel Independent of Membrane Cholesterol Extraction |
| Q90557183 | Determining the target of membrane sterols on voltage-gated potassium channels |
| Q39800294 | Developmental switch of the expression of ion channels in human dendritic cells. |
| Q36890498 | Different expression of β subunits of the KCa1.1 channel by invasive and non-invasive human fibroblast-like synoviocytes |
| Q91563039 | Direct and indirect cholesterol effects on membrane proteins with special focus on potassium channels |
| Q42745192 | Erratum to: Different expression of β subunits of the KCa1.1 channel by invasive and non-invasive human fibroblast-like synoviocytes |
| Q118948554 | Genomic, functional and structural analyses elucidate evolutionary innovation within the sea anemone 8 toxin family |
| Q104566554 | Immunomagnetic separation is a suitable method for electrophysiology and ion channel pharmacology studies on T cells |
| Q37566472 | Ion channels and anti-cancer immunity. |
| Q37660620 | Ion channels in T lymphocytes: an update on facts, mechanisms and therapeutic targeting in autoimmune diseases |
| Q38790596 | Isolation, chemical and functional characterization of several new K(+)-channel blocking peptides from the venom of the scorpion Centruroides tecomanus |
| Q112719419 | KCNE4-dependent functional consequences of Kv1.3-related leukocyte physiology |
| Q38990025 | Margatoxin is a non-selective inhibitor of human Kv1.3 K+ channels |
| Q28353645 | Multiple binding sites for melatonin on Kv1.3 |
| Q92017020 | N-methyl-D-aspartate (NMDA) receptor expression and function is required for early chondrogenesis |
| Q40396290 | Novel alpha-KTx peptides from the venom of the scorpion Centruroides elegans selectively blockade Kv1.3 over IKCa1 K+ channels of T cells |
| Q50983811 | OcyKTx2, a new K⁺-channel toxin characterized from the venom of the scorpion Opisthacanthus cayaporum. |
| Q125975113 | Of Seven New K+ Channel Inhibitor Peptides of Centruroides bonito, α-KTx 2.24 Has a Picomolar Affinity for Kv1.2 |
| Q110902551 | Peptide Inhibitors of Kv1.5: An Option for the Treatment of Atrial Fibrillation |
| Q89920733 | Periodic Membrane Potential and Ca2+ Oscillations in T Cells Forming an Immune Synapse |
| Q35124232 | Pituitary adenylate cyclase activating polypeptide (PACAP) signalling exerts chondrogenesis promoting and protecting effects: implication of calcineurin as a downstream target. |
| Q92832010 | Pore-modulating toxins exploit inherent slow inactivation to block K+ channels |
| Q47897876 | Potassium channel expression in human CD4+ regulatory and naïve T cells from healthy subjects and multiple sclerosis patients |
| Q42187027 | Probing pattern and dynamics of disulfide bridges using synthesis and NMR of an ion channel blocker peptide toxin with multiple diselenide bonds |
| Q36299751 | Probing the cavity of the slow inactivated conformation of shaker potassium channels |
| Q58801118 | Selective Na1.1 activation rescues Dravet syndrome mice from seizures and premature death |
| Q38597528 | Sterol Regulation of Voltage-Gated K+ Channels |
| Q92278938 | Structural basis of the potency and selectivity of Urotoxin, a potent Kv1 blocker from scorpion venom |
| Q27678772 | Structure, function, and chemical synthesis of Vaejovis mexicanus peptide 24: a novel potent blocker of Kv1.3 potassium channels of human T lymphocytes |
| Q39005229 | Structure, molecular modeling, and function of the novel potassium channel blocker urotoxin isolated from the venom of the Australian scorpion Urodacus yaschenkoi. |
| Q28742417 | Switch of voltage-gated K+ channel expression in the plasma membrane of chondrogenic cells affects cytosolic Ca2+-oscillations and cartilage formation |
| Q57606156 | Synthesis, folding, structure and activity of a predicted peptide from the sea anemone Oulactis sp. with an ShKT fold |
| Q55312735 | The C-terminal HRET sequence of Kv1.3 regulates gating rather than targeting of Kv1.3 to the plasma membrane. |
| Q95649781 | The activation gate controls steady-state inactivation and recovery from inactivation in Shaker |
| Q52885404 | The anti-proliferative effect of cation channel blockers in T lymphocytes depends on the strength of mitogenic stimulation. |
| Q97551822 | The voltage-gated potassium channel KV1.3 as a therapeutic target for venom-derived peptides |
| Q94452292 | The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
| Q39842223 | Tst26, a novel peptide blocker of Kv1.2 and Kv1.3 channels from the venom of Tityus stigmurus |
| Q36174761 | Vm24, a natural immunosuppressive peptide, potently and selectively blocks Kv1.3 potassium channels of human T cells |
| Q84471166 | Voltage-gated sodium channel Nav1.7 maintains the membrane potential and regulates the activation and chemokine-induced migration of a monocyte-derived dendritic cell subset |
| Q92215408 | Weaponisation 'on the fly': Convergent recruitment of knottin and defensin peptide scaffolds into the venom of predatory assassin flies |
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