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Journal Abstract Search

88 related items for PubMed ID: 9266826

  • 1. Expression of dihydropyridine binding sites in renal epithelial cells.
    O'Neil RG, Reid JM, Williams RL, Karin NJ.
    Biochem Biophys Res Commun; 1997 Aug 08; 237(1):41-5. PubMed ID: 9266826
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  • 2. Conserved Ca2+-antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain.
    Huber I, Wappl E, Herzog A, Mitterdorfer J, Glossmann H, Langer T, Striessnig J.
    Biochem J; 2000 May 01; 347 Pt 3(Pt 3):829-36. PubMed ID: 10769189
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  • 6. Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel.
    Mikami A, Imoto K, Tanabe T, Niidome T, Mori Y, Takeshima H, Narumiya S, Numa S.
    Nature; 1989 Jul 20; 340(6230):230-3. PubMed ID: 2474130
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  • 8. Fluorescent probing with felodipine of the dihydropyridine receptor and its interaction with the ryanodine receptor calcium release channel.
    Minarovic I, Mészáros LG.
    Biochem Biophys Res Commun; 1998 Mar 17; 244(2):519-24. PubMed ID: 9514900
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  • 10. High-affinity binding of DTZ323, a novel derivative of diltiazem, to rabbit skeletal muscle L-type Ca++ channels.
    Hagiwara M, Adachi-Akahane S, Nagao T.
    J Pharmacol Exp Ther; 1997 Apr 17; 281(1):173-9. PubMed ID: 9103495
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  • 13. Are dihydropyridine receptors downregulated in the ischemic myocardium?
    Zucchi R, Ronca-Testoni S, Yu G, Galbani P, Ronca G, Mariani M.
    Cardiovasc Res; 1995 Nov 17; 30(5):769-74. PubMed ID: 8595625
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  • 14. Chlorotrifluoroethylcysteine interaction with rabbit proximal tubule cell basolateral membrane organic anion transport and apical membrane amino acid transport.
    Groves CE, Morales MN.
    J Pharmacol Exp Ther; 1999 Nov 17; 291(2):555-61. PubMed ID: 10525071
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  • 17. Distinctions in the molecular determinants of charged and neutral dihydropyridine block of L-type calcium channels.
    Lacinová L, An RH, Xia J, Ito H, Klugbauer N, Triggle D, Hofmann F, Kass RS.
    J Pharmacol Exp Ther; 1999 Jun 17; 289(3):1472-9. PubMed ID: 10336541
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  • 19. Key roles of Phe1112 and Ser1115 in the pore-forming IIIS5-S6 linker of L-type Ca2+ channel alpha1C subunit (CaV 1.2) in binding of dihydropyridines and action of Ca2+ channel agonists.
    Yamaguchi S, Zhorov BS, Yoshioka K, Nagao T, Ichijo H, Adachi-Akahane S.
    Mol Pharmacol; 2003 Aug 17; 64(2):235-48. PubMed ID: 12869628
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