J. Mitterdorfer

发表

Synthesis and biological evaluation of 14-alkoxymorphinans. Part 7. 14,14′-dimethoxy analogues of norbinaltorphimine: Synthesis and determination of their χ opioid antagonist selectivity†

J. Rollinger, H. Schmidhammer, E. Ganglbauer, 1990 .

Calcium channels: The β‐subunit increases the affinity of dihydropyridine and Ca2+ binding sites of the α1‐subunit

H. Glossmann, J. Striessnig, M. Grabner, 1994 .

Conserved Ca2+-antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain.

T. Langer, H. Glossmann, J. Striessnig, 2000, The Biochemical journal.

Coordination of Ca2+ by the pore region glutamates is essential for high-affinity dihydropyridine binding to the cardiac Ca2+ channel alpha 1 subunit.

H. Glossmann, J. Striessnig, M. Grabner, 1995, Biochemistry.

Calcium channel block by (-)devapamil is affected by the sequence environment and composition of the phenylalkylamine receptor site.

F. Döring, D. Kimball, E. Timin, 1997, Biophysical journal.

Identification of the benzothiazepine-binding polypeptide of skeletal muscle calcium channels with (+)-cis-azidodiltiazem and anti-ligand antibodies.

H. Glossmann, J. Striessnig, J. Mitterdorfer, 1990, The Journal of biological chemistry.

Synthesis and Biological Evaluation of 14‐Alkoxymorphinans. Part 8. 14‐methoxymetopon, an extremely potent opioid agonist

H. Schmidhammer, J. Mitterdorfer, A. Schratz, 1990 .

Conserved Ca2+-antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain.

T. Langer, H. Glossmann, J. Striessnig, 2000, The Biochemical journal.

Structural basis of drug binding to L Ca2+ channels.

H. Glossmann, J. Striessnig, S. Hering, 1998, Trends in pharmacological sciences.

Mechanism of action of dexniguldipine-HCl (B8509-035), a new potent modulator of multidrug resistance.

S. Hofer, V. Gekeler, H. Glossmann, 1995, Biochemical pharmacology.

Subunit Composition of Brain Voltage-gated Potassium Channels Determined by Hongotoxin-1, a Novel Peptide Derived fromCentruroides limbatus Venom*

A. Koschak, G. Kaczorowski, H. Knaus, 1998, The Journal of Biological Chemistry.

Potassium Currents during the Action Potential of Hippocampal CA3 Neurons

B. Bean, Bruce P Bean, Jörg Mitterdorfer, 2002, The Journal of Neuroscience.

Cloning and functional expression of a neuronal calcium channel beta subunit from house fly (Musca domestica).

H. Glossmann, P. Charnet, S. Hering, 1994, The Journal of biological chemistry.

Differential Effects of Ca2+ Channel β1a and β2a Subunits on Complex Formation with α1S and on Current Expression in tsA201 Cells*

B. Flucher, H. Glossmann, B. Neuhuber, 1998, The Journal of Biological Chemistry.

Two Amino Acid Residues in the IIIS5 Segment of L-Type Calcium Channels Differentially Contribute to 1,4-Dihydropyridine Sensitivity*

H. Glossmann, S. Hering, M. Grabner, 1996, The Journal of Biological Chemistry.

Identification of PK-A phosphorylation sites in the carboxyl terminus of L-type calcium channel alpha 1 subunits.

H. Glossmann, F. F. Moebius, J. Striessnig, 1996, Biochemistry.

Molecular Basis of Drug Interaction with L-Type Ca2+ Channels

H. Prinz, R. Kraus, H. Glossmann, 1998, Journal of bioenergetics and biomembranes.

Nine L-type Amino Acid Residues Confer Full 1,4-Dihydropyridine Sensitivity to the Neuronal Calcium Channel α1ASubunit

H. Glossmann, J. Striessnig, S. Hering, 1997, The Journal of Biological Chemistry.

Transfer of High Sensitivity for Benzothiazepines from L-type to Class A (BI) Calcium Channels*

F. Döring, H. Glossmann, J. Striessnig, 1996, The Journal of Biological Chemistry.