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Summary Anatomy Item Literature (7318) Expression Attributions Wiki
XB-ANAT-489

Papers associated with trunk (and ikzf1)

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Facilitation of IKr current by some hERG channel blockers suppresses early afterdepolarizations., Furutani K., J Gen Physiol. February 4, 2019; 151 (2): 214-230.                      


Inhibition of inwardly rectifying Kir2.x channels by the novel anti-cancer agent gambogic acid depends on both pore block and PIP2 interference., Scherer D., Naunyn Schmiedebergs Arch Pharmacol. July 1, 2017; 390 (7): 701-710.


Dual Mechanism for Inhibition of Inwardly Rectifying Kir2.x Channels by Quinidine Involving Direct Pore Block and PIP2-interference., Koepple C., J Pharmacol Exp Ther. May 1, 2017; 361 (2): 209-218.


Class III antiarrhythmic drug dronedarone inhibits cardiac inwardly rectifying Kir2.1 channels through binding at residue E224., Xynogalos P., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2014; 387 (12): 1153-61.


VEGFA-dependent and -independent pathways synergise to drive Scl expression and initiate programming of the blood stem cell lineage in Xenopus., Ciau-Uitz A., Development. June 1, 2013; 140 (12): 2632-42.                                                                                                                            


Puerarin: a novel antagonist to inward rectifier potassium channel (IK1)., Zhang H., Mol Cell Biochem. June 1, 2011; 352 (1-2): 117-23.


HoxA3 is an apical regulator of haemogenic endothelium., Iacovino M., Nat Cell Biol. January 1, 2011; 13 (1): 72-8.        


Integrative genomic analyses on Ikaros and its expression related to solid cancer prognosis., Yang L., Oncol Rep. August 1, 2010; 24 (2): 571-7.


Novel, potent inhibitors of human Kv1.5 K+ channels and ultrarapidly activating delayed rectifier potassium current., Lagrutta A., J Pharmacol Exp Ther. June 1, 2006; 317 (3): 1054-63.


Human cardiac inwardly rectifying current IKir2.2 is upregulated by activation of protein kinase A., Zitron E., Cardiovasc Res. August 15, 2004; 63 (3): 520-7.


Human cardiac inwardly-rectifying K+ channel Kir(2.1b) is inhibited by direct protein kinase C-dependent regulation in human isolated cardiomyocytes and in an expression system., Karle CA., Circulation. September 17, 2002; 106 (12): 1493-9.


Identification and expression of Helios, a member of the Ikaros family, in the Mexican axolotl: implications for the embryonic origin of lymphocyte progenitors., Durand C., Eur J Immunol. June 1, 2002; 32 (6): 1748-52.


Role of the thrombopoietin (TPO)/Mpl system: c-Mpl-like molecule/TPO signaling enhances early hematopoiesis in Xenopus laevis., Kakeda M., Dev Growth Differ. February 1, 2002; 44 (1): 63-75.                


FLRF, a novel evolutionarily conserved RING finger gene, is differentially expressed in mouse fetal and adult hematopoietic stem cells and progenitors., Abdullah JM., Blood Cells Mol Dis. January 1, 2001; 27 (1): 320-33.


Inhibition of IKs channels by HMR 1556., Gögelein H., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2000; 362 (6): 480-8.


Lymphocyte development in fish and amphibians., Hansen JD., Immunol Rev. December 1, 1998; 166 199-220.


Unitary current through the inward rectifier K+ channel cloned from rabbit heart--comparison with the native K+ channel., Nagashima M., J Mol Cell Cardiol. May 1, 1996; 28 (5): 957-65.


Cloning and functional expression of a human gene, hIRK1, encoding the heart inward rectifier K+-channel., Wood LS., Gene. October 3, 1995; 163 (2): 313-7.


Cloning and functional expression of an inwardly rectifying K+ channel from human atrium., Wible BA., Circ Res. March 1, 1995; 76 (3): 343-50.

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