Varkevisser R, Houtman MJC, Linder T, de Git KCG, Beekman HDM, Tidwell RR et al. Structure-activity relationships of pentamidine-affected ion channel trafficking and dofetilide mediated rescue. British Journal of Pharmacology. 2013 Jul;169(6):1322-1334. doi: 10.1111/bph.12208

Garg V, Stary-Weinzinger A, Sanguinetti MC. ICA-105574 interacts with a common binding site to elicit opposite effects on inactivation gating of EAG and ERG potassium channels. Molecular Pharmacology. 2013 Apr;83(4):805-813. doi: 10.1124/mol.112.084384

Saxena P, Erker T, Bauer F, Weinzinger A, Linder T, Hering S et al. Drug Trapping in hERG Channels does not Require Closure of the Activation Gate. Biophysical Journal. 2013 Jan 29;104(2):266A-266A.

Linder T, de Groot BL, Stary-Weinzinger A. Probing the energy landscape of activation gating of the bacterial potassium channel KcsA. PLoS Computational Biology. 2013;9(5):e1003058. doi: 10.1371/journal.pcbi.1003058

Beyl S, Depil K, Hohaus A, Weinzinger A, Linder T, Timin E et al. Neutralisation of a single voltage sensor affects gating determinants in all four pore-forming S6 segments of Ca(V)1.2: a cooperative gating model. Pflügers Archiv: European Journal of Physiology. 2012 Oct;464(4):391-401. doi: 10.1007/s00424-012-1144-5

Ke S, Zangerl E-M, Weinzinger A. Distinct interactions of Na(+) and Ca(2+) ions with the selectivity filter of the bacterial sodium channel Na(V)Ab. Biochemical and Biophysical Research Communications. 2012;430(4):1272-1276. doi: 10.1016/j.bbrc.2012.12.055

Jansen SA, Kleerekooper I, Hofman ZLM, Kappen IFPM, Weinzinger A, van der Heyden MAG. Grayanotoxin Poisoning: 'Mad Honey Disease' and Beyond. Cardiovascular Toxicology. 2012;12(3):208-215. doi: 10.1007/s12012-012-9162-2

Phillips S, Brammer AE, Rodriguez L, Lim H-H, Weinzinger A, Matulef K. Surprises from an Unusual CLC Homolog. Biophysical Journal. 2012;103(9):44-46. doi: 10.1016/j.bpj.2012.08.063

Boukharta L, Keranen H, Weinzinger A, Wallin G, De Groot B, Aqvist J. Computer simulations of structure-activity relationships for HERG channel blockers. Biochemistry. 2011;50(27):6146-6156. doi: 10.1021/bi200173n

Knape K, Linder T, Wolschann KP, Beyer A, Weinzinger A. In silico Analysis of Conformational Changes Induced by Mutation of Aromatic Binding Residues: Consequences for Drug Binding in the hERG K+ Channel. PLoS ONE. 2011;6(12). doi: 10.1371/journal.pone.0028778

Garg V, Weinzinger A, Sachse F, Sanguinetti MC. Molecular Determinants for Activation of Human Ether-a-go-go-related Gene 1 Potassium Channels by 3-Nitro-N-(4-phenoxyphenyl) Benzamide. Molecular Pharmacology. 2011;80(4):630-637. doi: 10.1124/mol.111.073809

Suwattanasophon C, Faller R, Wolschann KP, Weinzinger A. Molecular dynamics simulations on the function of the transmembrane Cav1.2 channel in dependence of the content of cholesterol in the membrane. European Biophysics Journal. 2011;40(Suppl.1):118-118.

Beyl S, Depil K, Hohaus A, Weinzinger A, Timin E, Shabbir W et al. Physicochemical properties of pore residues predict activation gating of Ca(V)1.2: A correlation mutation analysis. Pflügers Archiv: European Journal of Physiology. 2011;461(1):53-63. doi: 10.1007/s00424-010-0885-2

Depil K, Beyl S, Weinzinger A, Hohaus A, Timin E, Hering S. Timothy mutation disrupts the link between activation and inactivation in Ca(V)1.2 protein. Journal of Biological Chemistry. 2011;286(36):31557-31564. doi: 10.1074/jbc.M111.255273

Karmazinova M, Beyl S, Weinzinger A, Suwattanasophon C, Klugbauer N, Hering S et al. Cysteines in the loop between IS5 and the pore helix of Ca(V)3.1 are essential for channel gating: Cysteines in the loop between IS5 and the pore helix of Ca(V)3.1 are essential for channel gating. Pflügers Archiv: European Journal of Physiology. 2010;460(6):1015-1028. doi: 10.1007/s00424-010-0874-5

de Boer T, Nalos L, Weinzinger A, Kok B, Houtman MJC, Antoons G et al. The anti-protozoal drug pentamidine blocks KIR2.x-mediated inward rectifier current by entering the cytoplasmic pore region of the channel. British Journal of Pharmacology. 2010;159(7):1532-1541. doi: 10.1111/j.1476-5381.2010.00658.x

Thai KM, Windisch A, Stork D, Weinzinger A, Schiesaro A, Guy HR et al. The hERG potassium channel and drug trapping: insights from docking studies with propafenone derivatives: The hERG potassium channel and drug trapping: insight from docking studies with propafenone derivatives. ChemMedChem: chemistry enabling drug discovery. 2010;5(3):436-442. doi: 10.1002/cmdc.200900374

Weinzinger A, Wacker SJ, Boukharta L, Zachariae U, Karimi-Nejad Y, Aqvist J et al. Toward a Consensus Model of the hERG Potassium Channel. ChemMedChem: chemistry enabling drug discovery. 2010;5(3):455-467. doi: 10.1002/cmdc.200900461

Kudrnac M, Beyl S, Hohaus A, Weinzinger A, Peterbauer T, Timin E et al. Coupled and independent contributions of residues in IS6 and IIS6 to activation gating of CaV1.2. Journal of Biological Chemistry. 2009;284(18):12276-12284.

Knape K, Beyer A, Weinzinger A, Buchbauer G, Wolschann KP. Evolutionary trace of human odorant receptors of chromosome 17. Flavour & Fragrance Journal. 2009;24(4):192-197. doi: 10.1002/ffj.1933