Papers associated with multicellular anatomical structure (and kcne1)

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	Isolation and characterization of TGF-beta 2 and TGF-beta 5 from medium conditioned by Xenopus XTC cells., Roberts AB., Growth Factors. January 1, 1990; 2 (2-3): 135-47.
	Immunohistochemical study of a rat membrane protein which induces a selective potassium permeation: its localization in the apical membrane portion of epithelial cells., Sugimoto T., J Membr Biol. January 1, 1990; 113 (1): 39-47.
	Receptor-mediated regulation of IsK, a very slowly activating, voltage-dependent K+ channel in Xenopus oocytes., Honore E., Biochem Biophys Res Commun. May 15, 1992; 184 (3): 1135-41.
	Transforming growth factor beta (TGF beta) is produced by and influences the proliferative response of Xenopus laevis lymphocytes., Haynes L., Dev Immunol. January 1, 1993; 3 (3): 223-30.
	Are Xenopus oocytes unique in displaying functional IsK channel heterologous expression?, Lesage F., Recept Channels. January 1, 1993; 1 (2): 143-52.
	Species variants of the IsK protein: differences in kinetics, voltage dependence, and La3+ block of the currents expressed in Xenopus oocytes., Hice RE., Pflugers Arch. January 1, 1994; 426 (1-2): 139-45.
	Differential expression of Isk mRNAs in mouse tissue during development and pregnancy., Felipe A., Am J Physiol. September 1, 1994; 267 (3 Pt 1): C700-5.
	A corticosteroid-induced gene expressing an "IsK-like" K+ channel activity in Xenopus oocytes., Attali B., Proc Natl Acad Sci U S A. June 20, 1995; 92 (13): 6092-6.
	Coexpression and stimulation of parathyroid hormone receptor positively regulates slowly activating IsK channels expressed in Xenopus oocytes., Waldegger S., Kidney Int. January 1, 1996; 49 (1): 112-6.
	Cellular localization and regulation of CHIF in kidney and colon., Capurro C., Am J Physiol. September 1, 1996; 271 (3 Pt 1): C753-62.
	Inhibition of IKs in guinea pig cardiac myocytes and guinea pig IsK channels by the chromanol 293B., Busch AE., Pflugers Arch. October 1, 1996; 432 (6): 1094-6.
	cAMP increases apical IsK channel current and K+ secretion in vestibular dark cells., Sunose H., J Membr Biol. March 1, 1997; 156 (1): 25-35.
	Properties and regulation of the minK potassium channel protein., Kaczmarek LK., Physiol Rev. July 1, 1997; 77 (3): 627-41.
	Block by propofol and thiopentone of the min K current (IsK) expressed in Xenopus oocytes., Heath BM., Naunyn Schmiedebergs Arch Pharmacol. September 1, 1997; 356 (3): 404-9.
	TGF-beta receptor-mediated signalling through Smad2, Smad3 and Smad4., Nakao A., EMBO J. September 1, 1997; 16 (17): 5353-62.
	KQT2, a new putative potassium channel family produced by alternative splicing. Isolation, genomic structure, and alternative splicing of the putative potassium channels., Nakamura M., Recept Channels. January 1, 1998; 5 (5): 255-71.
	Axolotl (Ambystoma mexicanum) lymphocytes produce and are growth-inhibited by transforming growth factor-beta., Koniski A., Dev Comp Immunol. January 1, 1998; 22 (1): 91-102.
	Blockade of HERG channels by the class III antiarrhythmic azimilide: mode of action., Busch AE., Br J Pharmacol. January 1, 1998; 123 (1): 23-30.
	Voltage-dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits., Tristani-Firouzi M., J Physiol. July 1, 1998; 510 ( Pt 1) 37-45.
	Activation and inactivation of homomeric KvLQT1 potassium channels., Pusch M., Biophys J. August 1, 1998; 75 (2): 785-92.
	Divalent cations inhibit IsK/KvLQT1 channels in excised membrane patches of strial marginal cells., Shen Z., Hear Res. September 1, 1998; 123 (1-2): 157-67.
	Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome., Sesti F., J Gen Physiol. December 1, 1998; 112 (6): 651-63.
	Increase of the single-channel conductance of KvLQT1 potassium channels induced by the association with minK., Pusch M., Pflugers Arch. December 1, 1998; 437 (1): 172-4.
	Norpropoxyphene-induced cardiotoxicity is associated with changes in ion-selectivity and gating of HERG currents., Ulens C., Cardiovasc Res. December 1, 1999; 44 (3): 568-78.
	Gating and flickery block differentially affected by rubidium in homomeric KCNQ1 and heteromeric KCNQ1/KCNE1 potassium channels., Pusch M., Biophys J. January 1, 2000; 78 (1): 211-26.
	Molecular basis for differential sensitivity of KCNQ and I(Ks) channels to the cognitive enhancer XE991., Wang HS., Mol Pharmacol. June 1, 2000; 57 (6): 1218-23.
	MinK subdomains that mediate modulation of and association with KvLQT1., Tapper AR., J Gen Physiol. September 1, 2000; 116 (3): 379-90.
	Identification and characterization of constitutively active Smad2 mutants: evaluation of formation of Smad complex and subcellular distribution., Funaba M., Mol Endocrinol. October 1, 2000; 14 (10): 1583-91.
	Inhibition of IKs channels by HMR 1556., Gögelein H., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2000; 362 (6): 480-8.
	MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis., Abbott GW., Cell. January 26, 2001; 104 (2): 217-31.
	Blocking effects of the antiarrhythmic drug propafenone on the HERG potassium channel., Mergenthaler J., Naunyn Schmiedebergs Arch Pharmacol. April 1, 2001; 363 (4): 472-80.
	Chromanol 293B, a blocker of the slow delayed rectifier K+ current (IKs), inhibits the CFTR Cl- current., Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. June 1, 2001; 363 (6): 590-6.
	Regulation and properties of KCNQ1 (K(V)LQT1) and impact of the cystic fibrosis transmembrane conductance regulator., Boucherot A., J Membr Biol. July 1, 2001; 182 (1): 39-47.
	Xe991 reveals differences in K(+) channels regulating chloride secretion in murine airway and colonic epithelium., MacVinish LJ., Mol Pharmacol. October 1, 2001; 60 (4): 753-60.
	Synthesis and activity of novel and selective I(Ks)-channel blockers., Gerlach U., J Med Chem. November 8, 2001; 44 (23): 3831-7.
	The oxidant thimerosal modulates gating behavior of KCNQ1 by interaction with the channel outer shell., Kerst G., J Membr Biol. March 15, 2002; 186 (2): 89-100.
	A truncated splice variant of KCNQ1 cloned from rat heart., Yamada Y., Biochem Biophys Res Commun. June 7, 2002; 294 (2): 199-204.
	Inhibitory effects of volatile anesthetics on currents produced on heterologous expression of KvLQT1 and minK in Xenopus oocytes., Chen X., Vascul Pharmacol. July 1, 2002; 39 (1-2): 33-8.
	KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current., Angelo K., Biophys J. October 1, 2002; 83 (4): 1997-2006.
	Regulation of KCNE1-dependent K(+) current by the serum and glucocorticoid-inducible kinase (SGK) isoforms., Embark HM., Pflugers Arch. February 1, 2003; 445 (5): 601-6.
	Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome., Yamaguchi M., Clin Sci (Lond). April 1, 2003; 104 (4): 377-82.
	Novel gene hKCNE4 slows the activation of the KCNQ1 channel., Teng S., Biochem Biophys Res Commun. April 11, 2003; 303 (3): 808-13.
	KCNE2 modulates current amplitudes and activation kinetics of HCN4: influence of KCNE family members on HCN4 currents., Decher N., Pflugers Arch. September 1, 2003; 446 (6): 633-40.
	Tight coupling of rubidium conductance and inactivation in human KCNQ1 potassium channels., Seebohm G., J Physiol. October 15, 2003; 552 (Pt 2): 369-78.
	Acute effects of dronedarone on both components of the cardiac delayed rectifier K+ current, HERG and KvLQT1/minK potassium channels., Thomas D., Br J Pharmacol. November 1, 2003; 140 (5): 996-1002.
	Association of the serum and glucocorticoid regulated kinase (sgk1) gene with QT interval., Busjahn A., Cell Physiol Biochem. January 1, 2004; 14 (3): 135-42.
	The MinK-related peptides., McCrossan ZA., Neuropharmacology. November 1, 2004; 47 (6): 787-821.
	KCNE3 truncation mutants reveal a bipartite modulation of KCNQ1 K+ channels., Gage SD., J Gen Physiol. December 1, 2004; 124 (6): 759-71.
	Interaction of KCNE subunits with the KCNQ1 K+ channel pore., Panaghie G., J Physiol. February 1, 2006; 570 (Pt 3): 455-67.
	Ancillary subunits and stimulation frequency determine the potency of chromanol 293B block of the KCNQ1 potassium channel., Bett GC., J Physiol. November 1, 2006; 576 (Pt 3): 755-67.

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