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Journal of Medicinal Chemistry|March 29, 2000
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 1. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivityJ A Butera, M M Antane, S A Antane, et al.
Journal of Medicinal Chemistry|March 29, 2000
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenedionesA M Gilbert, M M Antane, T M Argentieri, et al.
BMC Immunology|August 24, 2010
Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseasesPaolo G V Martini, Lynette C Cook, Scott Alderucci, et al.
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