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Cav 1.3 (CACNA1D) L-type Ca2+ channel dysfunction in CNS disorders.
Pinggera A, Striessnig J. Pinggera A, et al. Among authors: striessnig j. J Physiol. 2016 Oct 15;594(20):5839-5849. doi: 10.1113/JP270672. Epub 2016 Feb 29. J Physiol. 2016. PMID: 26842699 Free PMC article. Review.
[35S]sadopine, a novel high affinity, high specific activity, L-type Ca2+ channel probe: characterization of two equipotent diastereomers with opposite allosteric properties.
Knaus HG, Striessnig J, Hering S, Marrer S, Schwenner E, Höltje HD, Glossmann H. Knaus HG, et al. Among authors: striessnig j. Mol Pharmacol. 1992 Feb;41(2):298-307. Mol Pharmacol. 1992. PMID: 1311409
Receptor sites for Ca2+ channel antagonists.
Catterall WA, Striessnig J. Catterall WA, et al. Among authors: striessnig j. Trends Pharmacol Sci. 1992 Jun;13(6):256-62. doi: 10.1016/0165-6147(92)90079-l. Trends Pharmacol Sci. 1992. PMID: 1321525 Review.
Very high affinity interaction of DPI 201-106 and BDF 8784 enantiomers with the phenylalkylamine-sensitive Ca2(+)-channel in Drosophila head membranes.
Glossmann H, Zech C, Striessnig J, Staudinger R, Hall L, Greenberg R, Armah BI. Glossmann H, et al. Among authors: striessnig j. Br J Pharmacol. 1991 Feb;102(2):446-52. doi: 10.1111/j.1476-5381.1991.tb12193.x. Br J Pharmacol. 1991. PMID: 1849770 Free PMC article.
Molecular properties of calcium channels.
Glossmann H, Striessnig J. Glossmann H, et al. Among authors: striessnig j. Rev Physiol Biochem Pharmacol. 1990;114:1-105. doi: 10.1007/BFb0031018. Rev Physiol Biochem Pharmacol. 1990. PMID: 2155469 Review. No abstract available.
Purification and reconstitution of calcium channel drug-receptor sites.
Glossmann H, Striessnig J, Hymel L, Schindler H. Glossmann H, et al. Among authors: striessnig j. Ann N Y Acad Sci. 1988;522:150-61. doi: 10.1111/j.1749-6632.1988.tb33351.x. Ann N Y Acad Sci. 1988. PMID: 2454049 No abstract available.
Coordination of Ca2+ by the pore region glutamates is essential for high-affinity dihydropyridine binding to the cardiac Ca2+ channel alpha 1 subunit.
Mitterdorfer J, Sinnegger MJ, Grabner M, Striessnig J, Glossmann H. Mitterdorfer J, et al. Among authors: striessnig j. Biochemistry. 1995 Jul 25;34(29):9350-5. doi: 10.1021/bi00029a010. Biochemistry. 1995. PMID: 7626604
Calcium channels: the beta-subunit increases the affinity of dihydropyridine and Ca2+ binding sites of the alpha 1-subunit.
Mitterdorfer J, Froschmayr M, Grabner M, Striessnig J, Glossmann H. Mitterdorfer J, et al. Among authors: striessnig j. FEBS Lett. 1994 Sep 26;352(2):141-5. doi: 10.1016/0014-5793(94)00938-4. FEBS Lett. 1994. PMID: 7925963
Heterogeneity of L-type calcium channel alpha 1 subunits: stereoselective discrimination of different populations by the novel 1,4-dihydropyridine B 874-67.
Lakitsch M, Knaus HG, Topar G, Romanin C, Boer R, Flockerzi D, Striessnig J, Schindler H, Hoeltje HD, Glossmann H. Lakitsch M, et al. Among authors: striessnig j. Mol Pharmacol. 1993 Feb;43(2):293-301. Mol Pharmacol. 1993. PMID: 8381514
Activation of L-type Ca2+ channels after purinoceptor stimulation by ATP in an alveolar epithelial cell (L2).
Dietl P, Haller T, Wirleitner B, Völkl H, Friedrich F, Striessnig J. Dietl P, et al. Among authors: striessnig j. Am J Physiol. 1995 Dec;269(6 Pt 1):L873-83. doi: 10.1152/ajplung.1995.269.6.L873. Am J Physiol. 1995. PMID: 8572250
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