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JMIR Formative Research|December 20, 2022
Preferences of Older Adult Veterans With Heart Failure for Engaging With Mobile Health Technology to Support Self-care: Qualitative Interview Study Among Patients With Heart Failure and Content AnalysisMarva Foster, Wei Xiong, Lisa Quintiliani, et al.
Chemmedchem|September 29, 2016
Discovery and Biophysical Evaluation of First Low Nanomolar Hits Targeting CYP125 of M. tuberculosisChristian Brengel, Andreas Thomann, Alexander Schifrin, et al.
Advances in Skin & Wound Care|April 19, 2016
Contextual Facilitators of and Barriers to Nursing Home Pressure Ulcer PreventionChristine W Hartmann, Jeffrey Solomon, Jennifer A Palmer, et al.
Andrologia|May 1, 1986
Shape and position of the haploid peak in flow cytometric sperm histograms for the assessment of andrological diseasesH Hettwer, N Hofmann, B Ehle, et al.
Archiv Der Pharmazie|July 9, 2004
Synthesis of amidinohydrazones and evaluation of their inhibitory effect towards aldosterone synthase (CYP11B2) and the formation of selected steroidsMarieke Voets, Ursula Müller-Vieira, Sandrine Marchais-Oberwinkler, et al.
Planta Medica|April 1, 1997
Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium speciesB Ducrey, A Marston, S Göhring, et al.
Archiv Der Pharmazie|January 9, 1999
Spectrofluorimetric quantification of malondialdehyde for evaluation of cyclooxygenase-1/thromboxane synthase inhibitionG Dannhardt, L Flemmer, R W Hartmann, et al.
Scandinavian Journal of Gastroenterology|January 1, 1980
Immunoreactive secretin release following taurocholate perfusions of the cat duodenumL E Hanssen, J Hotz, W Hartmann, et al.
Bioorganic & Medicinal Chemistry Letters|July 22, 2008
Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitorsMarie-Pierre Lézé, Anja Palusczak, Rolf W Hartmann, et al.
Journal of Medicinal Chemistry|March 10, 2011
Fine-tuning the selectivity of aldosterone synthase inhibitors: structure-activity and structure-selectivity insights from studies of heteroaryl substituted 1,2,5,6-tetrahydropyrrolo[3,2,1-ij]quinolin-4-one derivativesSimon Lucas, Matthias Negri, Ralf Heim, et al.
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