Papers associated with dpys

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	Dihydropyrimidinase protects from DNA replication stress caused by cytotoxic metabolites., Basbous J, Aze A, Chaloin L, Lebdy R, Hodroj D, Ribeyre C, Larroque M, Shepard C, Kim B, Pruvost A, Moreaux J, Maiorano D, Mechali M, Constantinou A., Nucleic Acids Res. February 28, 2020; 48 (4): 1886-1904.
	Induction of ovulation in Xenopus without hCG injection: the effect of adding steroids into the aquatic environment., Ogawa A, Dake J, Iwashina YK, Tokumoto T., Reprod Biol Endocrinol. January 21, 2011; 9 11.
	Amino acid derivatives are substrates or non-transported inhibitors of the amino acid transporter PAT2 (slc36a2)., Edwards N, Anderson CM, Gatfield KM, Jevons MP, Ganapathy V, Thwaites DT., Biochim Biophys Acta. January 1, 2011; 1808 (1): 260-70.
	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T, Washiyama K, Ikeda K., PLoS One. July 21, 2009; 4 (7): e6311.
	Five different profiles of dihydropyridines in blocking T-type Ca(2+) channel subtypes (Ca(v)3.1 (alpha(1G)), Ca(v)3.2 (alpha(1H)), and Ca(v)3.3 (alpha(1I))) expressed in Xenopus oocytes., Furukawa T, Nukada T, Namiki Y, Miyashita Y, Hatsuno K, Ueno Y, Yamakawa T, Isshiki T., Eur J Pharmacol. June 24, 2009; 613 (1-3): 100-7.
	FGF-activated calcium channels control neural gene expression in Xenopus., Lee KW, Moreau M, Néant I, Bibonne A, Leclerc C., Biochim Biophys Acta. June 1, 2009; 1793 (6): 1033-40.
	Calcium transients and calcium signalling during early neurogenesis in the amphibian embryo Xenopus laevis., Leclerc C, Néant I, Webb SE, Miller AL, Moreau M., Biochim Biophys Acta. November 1, 2006; 1763 (11): 1184-91.
	Insight into the mechanism of action of neuroactive steroids., Morris KD, Amin J., Mol Pharmacol. July 1, 2004; 66 (1): 56-69.
	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.
	Cilnidipine is a novel slow-acting blocker of vascular L-type calcium channels that does not target protein kinase C., Löhn M, Muzzulini U, Essin K, Tsang SY, Kirsch T, Litteral J, Waldron P, Conrad H, Klugbauer N, Hofmann F, Haller H, Luft FC, Huang Y, Gollasch M., J Hypertens. May 1, 2002; 20 (5): 885-93.
	Calcium mediates dorsoventral patterning of mesoderm in Xenopus., Palma V, Kukuljan M, Mayor R., Curr Biol. October 16, 2001; 11 (20): 1606-10.
	Voltage-dependent acceleration of Ca(v)1.2 channel current decay by (+)- and (-)-isradipine., Berjukow S, Hering S., Br J Pharmacol. August 1, 2001; 133 (7): 959-66.
	Calcium channel isoforms underlying synaptic transmission at embryonic Xenopus neuromuscular junctions., Thaler C, Li W, Brehm P., J Neurosci. January 15, 2001; 21 (2): 412-22.
	A novel positive allosteric modulator of the GABA(A) receptor: the action of (+)-ROD188., Thomet U, Baur R, Razet R, Dodd RH, Furtmüller R, Sieghart W, Sigel E., Br J Pharmacol. October 1, 2000; 131 (4): 843-50.
	COOH-terminal truncated alpha(1S) subunits conduct current better than full-length dihydropyridine receptors., Morrill JA, Cannon SC., J Gen Physiol. September 1, 2000; 116 (3): 341-8.
	Molecular mechanism of calcium channel block by isradipine. Role of a drug-induced inactivated channel conformation., Berjukow S, Marksteiner R, Gapp F, Sinnegger MJ, Hering S., J Biol Chem. July 21, 2000; 275 (29): 22114-20.
	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.
	Effect of bay K 8644 (-) and the beta2a subunit on Ca2+-dependent inactivation in alpha1C Ca2+ channels., Noceti F, Olcese R, Qin N, Zhou J, Stefani E., J Gen Physiol. March 1, 1998; 111 (3): 463-75.
	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.
	Okadaic acid enhances prepulse facilitation of cardiac alpha 1-subunit but not endogenous calcium channel currents in Xenopus laevis oocytes., Chahine M, Bibikova A, Sculptoreanu A., Can J Physiol Pharmacol. October 1, 1996; 74 (10): 1149-56.
	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.
	Modulation of ionic currents through GABAA receptor subtypes by endogenous steroids., Shingai R, Fukushima T, Ogurusu T., Jpn J Physiol. January 1, 1994; 44 Suppl 2 S137-40.
	Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action., Tang S, Yatani A, Bahinski A, Mori Y, Schwartz A., Neuron. December 1, 1993; 11 (6): 1013-21.
	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.
	Effect of benzodiazepine ligands on Ca2+ channel currents in Xenopus oocytes injected with rat heart RNA., Gershon E., J Basic Clin Physiol Pharmacol. January 1, 1992; 3 (1): 81-97.
	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.
	Characterization of voltage-dependent calcium channels expressed in Xenopus oocytes injected with mRNA from rat heart., Lory P, Rassendren FA, Richard S, Tiaho F, Nargeot J., J Physiol. October 1, 1990; 429 95-112.
	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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