2015

High blood pressure as a driver of structural and biomechanical changes in mesenteric resistance arteries in chronic kidney disease

oaladhami, 719, Journal Article, , High blood pressure as a driver of structural and biomechanical changes in mesenteric resistance arteries in chronic kidney disease. (2015). United States: Lippincott Williams & Wilkins, 2015.

2015

Design and evaluation of 3-(benzylthio) benzamide derivatives as potent and selective SIRT2 inhibitors

mkhanfar, 645, Journal Article, , Design and evaluation of 3-(benzylthio) benzamide derivatives as potent and selective SIRT2 inhibitors. (2015). ACS Medicinal Chemistry Letters 6 (5), 607-611, 2015, 6, 607–611.

2014

Development and characterization of 3-(benzylsulfonamido) benzamides as potent and selective SIRT2 inhibitors

mkhanfar, 645, Journal Article, , Development and characterization of 3-(benzylsulfonamido) benzamides as potent and selective SIRT2 inhibitors. (2014). European Journal of Medicinal Chemistry 76, 414-426, 2014, 76, 414–426.

2014

Opposing changes in thoracic and abdominal aortic biomechanical properties in rodent models of vascular calcification and hypertension

oaladhami, 719, Journal Article, , Opposing changes in thoracic and abdominal aortic biomechanical properties in rodent models of vascular calcification and hypertension. (2014). American Journal of Physiology-Heart and Circulatory Physiology, 307, H143–H151.

2014

Development and characterization of 3-(benzylsulfonamido) benzamides as potent and selective SIRT2 inhibitors

mkhanfar, 645, Journal Article, , Development and characterization of 3-(benzylsulfonamido) benzamides as potent and selective SIRT2 inhibitors. (2014). European Journal of Medicinal Chemistry, 76, 414–426.

2014

Sympathetic overactivity prevails over the vascular amplifier phenomena in a chronic kidney disease rat model of hypertension

oaladhami, 719, Journal Article, , Sympathetic overactivity prevails over the vascular amplifier phenomena in a chronic kidney disease rat model of hypertension. (2014). Physiological Reports, 2, e12205.

2014

Articles in PresS. Am J Physiol Heart Circ Physiol (May 16, 2014). doi: 10.1152/ajpheart. 00139.2014

isalman, 854, Journal Article, , Articles in PresS. Am J Physiol Heart Circ Physiol (May 16, 2014). doi: 10.1152/ajpheart. 00139.2014. (2014).

2014

The use of docking-based comparative intermolecular contacts analysis to identify optimal docking conditions within glucokinase and to discover of new GK activators

mkhanfar, 645, Journal Article, , The use of docking-based comparative intermolecular contacts analysis to identify optimal docking conditions within glucokinase and to discover of new GK activators. (2014). Journal of Computer-Aided Molecular Design 28 (5), 509-547, 2014, 28, 509–547.

2014

Quantification of in situ granulation-induced changes in pre-compression, solubility, dose distribution and intrinsic in vitro release characteristics of ibuprofen–cationic …

amustapha, 990, Journal Article, , Quantification of in situ granulation-induced changes in pre-compression, solubility, dose distribution and intrinsic in vitro release characteristics of ibuprofen–cationic …. (2014). International Journal of Pharmaceutics 471 (1-2), 453-477, 2014.

2014

The use of docking-based comparative intermolecular contacts analysis to identify optimal docking conditions within glucokinase and to discover of new GK activators

mkhanfar, 645, Journal Article, , The use of docking-based comparative intermolecular contacts analysis to identify optimal docking conditions within glucokinase and to discover of new GK activators. (2014). Journal of Computer-Aided Molecular Design, 28, 509–547.