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Activation of calcium- and voltage-gated potassium channels of large conductance by leukotriene B4., Bukiya AN., J Biol Chem. December 19, 2014; 289 (51): 35314-25.
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Cerebrovascular dilation via selective targeting of the cholane steroid-recognition site in the BK channel β1-subunit by a novel nonsteroidal agent., Bukiya AN., Mol Pharmacol. May 1, 2013; 83 (5): 1030-44.
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Antagonism of NMDA receptors by butanesulfonyl-homospermine guanidine and neuroprotective effects in in vitro and in vivo., Masuko T., Neurosci Lett. January 11, 2012; 506 (2): 251-5.
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Na(+)-K (+)-2Cl (-) cotransport inhibitor attenuates cerebral edema following experimental stroke via the perivascular pool of aquaporin-4., Migliati ER., Neurocrit Care. August 1, 2010; 13 (1): 123-31.
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Channel beta2-4 subunits fail to substitute for beta1 in sensitizing BK channels to lithocholate., Bukiya AN., Biochem Biophys Res Commun. December 18, 2009; 390 (3): 995-1000.
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The BK channel accessory beta1 subunit determines alcohol-induced cerebrovascular constriction., Bukiya AN., FEBS Lett. September 3, 2009; 583 (17): 2779-84.
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Direct regulation of BK channels by phosphatidylinositol 4,5-bisphosphate as a novel signaling pathway., Vaithianathan T., J Gen Physiol. July 1, 2008; 132 (1): 13-28. 
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Synthesis and structure-activity relationships of 3-aryloxindoles: a new class of calcium-dependent, large conductance potassium (maxi-K) channel openers with neuroprotective properties., Hewawasam P., J Med Chem. March 28, 2002; 45 (7): 1487-99.
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