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Summary Expression Phenotypes Gene Literature (15) GO Terms (8) Nucleotides (100) Proteins (44) Interactants (15) Wiki
XB-GENEPAGE-1000801

Papers associated with dpyd



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Changes of gamma-tubulin expression and distribution in the zebrafish (Danio rerio) ovary, oocyte and embryo., Liu J, Lessman CA., Gene Expr Patterns. April 1, 2008; 8 (4): 237-47.    


DHP-insensitive L-type-like Ca channel of ascidian acquires sensitivity to DHP with single amino acid change in domain III P-region., Izumi-Nakaseko H, Yamaguchi S, Ohtsuka Y, Ebihara T, Adachi-Akahane S, Okamura Y., FEBS Lett. August 14, 2003; 549 (1-3): 67-71.


Ca2+ channel sensitivity towards the blocker isradipine is affected by alternative splicing of the human alpha1C subunit gene., Zühlke RD, Bouron A, Soldatov NM, Reuter H., FEBS Lett. May 8, 1998; 427 (2): 220-4.


Molecular studies on the voltage dependence of dihydropyridine action on L-type Ca2+ channels. Critical involvement of tyrosine residues in motif IIIS6 and IVS6., Bodi I, Yamaguchi H, Hara M, He M, Schwartz A, Varadi G., J Biol Chem. October 3, 1997; 272 (40): 24952-60.


Dihydropyridine action on voltage-dependent potassium channels expressed in Xenopus oocytes., Avdonin V, Shibata EF, Hoshi T., J Gen Physiol. February 1, 1997; 109 (2): 169-80.                            


Motif III S5 of L-type calcium channels is involved in the dihydropyridine binding site. A combined radioligand binding and electrophysiological study., He M, Bodi I, Mikala G, Schwartz A., J Biol Chem. January 31, 1997; 272 (5): 2629-33.


Functional expression of GABA rho 3 receptors in Xenopus oocytes., Shingai R, Yanagi K, Fukushima T, Sakata K, Ogurusu T., Neurosci Res. December 1, 1996; 26 (4): 387-90.


Two amino acid residues in the IIIS5 segment of L-type calcium channels differentially contribute to 1,4-dihydropyridine sensitivity., Mitterdorfer J, Wang Z, Sinnegger MJ, Hering S, Striessnig J, Grabner M, Glossmann H., J Biol Chem. November 29, 1996; 271 (48): 30330-5.


The beta 1-subunit is essential for modulation by protein kinase C of an human and a non-human L-type Ca2+ channel., Bouron A, Soldatov NM, Reuter H., FEBS Lett. December 18, 1995; 377 (2): 159-62.


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., Biochemistry. July 25, 1995; 34 (29): 9350-5.


Cyclic AMP-dependent modulation of cardiac Ca channels expressed in Xenopus laevis oocytes., Lory P, Nargeot J., Biochem Biophys Res Commun. February 14, 1992; 182 (3): 1059-65.


Native-type DHP-sensitive calcium channel currents are produced by cloned rat aortic smooth muscle and cardiac alpha 1 subunits expressed in Xenopus laevis oocytes and are regulated by alpha 2- and beta-subunits., Itagaki K, Koch WJ, Bodi I, Klöckner U, Slish DF, Schwartz A., FEBS Lett. February 10, 1992; 297 (3): 221-5.


Effects of steroids on gamma-aminobutyric acid receptors expressed in Xenopus oocytes by poly(A)+ RNA from mammalian brain and retina., Woodward RM, Polenzani L, Miledi R., Mol Pharmacol. January 1, 1992; 41 (1): 89-103.


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. July 20, 1989; 340 (6230): 230-3.


Specific block of calcium channel expression by a fragment of dihydropyridine receptor cDNA., Lotan I, Goelet P, Gigi A, Dascal N., Science. February 3, 1989; 243 (4891): 666-9.

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