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Arzneimittel-Forschung|January 1, 1982
[3H]-Nimodipine and [3H]-nitrendipine as tools to directly identify the sites of action of 1,4-dihydropyridine calcium antagonists in guinea-pig tissues. Tissue-specific effects of anions and ionic strengthP Bellemann, D Ferry, F Lübbecke, et al.
Trends in Endocrinology and Metabolism: TEM|March 9, 2000
Genetic defects in postsqualene cholesterol biosynthesisF F Moebius, B U Fitzky, H Glossmann
European Journal of Pharmacology|November 15, 1988
The mitochondrial high-capacity low-affinity (+/-)-[3H]nitrendipine binding site is regulated by nucleotidesG Zernig, T Moshammer, I Graziadei, et al.
European Journal of Pharmacology|October 14, 1991
Novel sites for phenylalkylamines: characterisation of a sodium-sensitive drug receptor with (-)-[3H]emopamilC Zech, R Staudinger, J Mühlbacher, et al.
The Journal of Biological Chemistry|March 30, 2001
Mechanism of dihydropyridine interaction with critical binding residues of L-type Ca2+ channel alpha 1 subunitsE Wappl, J Mitterdorfer, H Glossmann, et al.
Pflugers Archiv : European Journal of Physiology|March 1, 1992
The dihydropyridine niguldipine inhibits T-type Ca2+ currents in atrial myocytesC Romanin, K Seydl, H Glossmann, et al.
FEBS Letters|March 3, 1986
Purified calcium channels have three allosterically coupled drug receptorsJ Striessnig, A Goll, K Moosburger, et al.
Biomedica Biochimica Acta|January 1, 1987
Purified L-type calcium channels: only one single polypeptide (alpha 1-subunit) carries the drug receptor domains and is regulated by protein kinasesH Glossmann, J Striessnig, L Hymel, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Purified skeletal muscle 1,4-dihydropyridine receptor forms phosphorylation-dependent oligomeric calcium channels in planar bilayersL Hymel, J Striessnig, H Glossmann, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|December 27, 1978
Solubilization of a mammalian beta-adrenergic receptorJ Kleinstein, H Glossmann, L Braun, et al.
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