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Tissue Engineering. Part C, Methods|March 30, 2010
Identification of the chondrocyte lineage using microfibril-associated glycoprotein-2, a novel marker that distinguishes chondrocytes from synovial cellsStephen Rapko, Mindy Zhang, Brenda Richards, et al.
Critical Care Nurse|June 3, 2017
Decreasing Catheter-Associated Urinary Tract Infections in the Neurological Intensive Care Unit: One Unit's SuccessBrenda Richards, Bindhu Sebastian, Hillary Sullivan, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|January 31, 2025
Transcriptomic analysis in liver spheroids identifies a dog-specific mechanism of hepatotoxicity for amcenestrantPiyush Bajaj, Richard J Brennan, Sébastien Laurent, et al.
PDA Journal of Pharmaceutical Science and Technology|December 6, 2014
Detection of adventitious agents using next-generation sequencingBrenda Richards, Sherry Cao, Mark Plavsic, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 3, 2025
AAV delivery of artificial miRNA targeting MAPT for the reduction of tau pathology in Alzheimer's diseaseJessica M Hogestyn, Erik Wischhof, Yao Chen, et al.
Molecular Cancer Therapeutics|January 22, 2011
sFLT01: a novel fusion protein with antiangiogenic activityRebecca G Bagley, Leslie Kurtzberg, William Weber, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 14, 2025
Artificial miRNA-mediated reduction of SNCA for the treatment of α-synucleinopathiesBradford Elmer, Erik Wischhof, Tiffany Chan, et al.
Genomics|October 23, 2004
New insights into ADPKD molecular pathways using combination of SAGE and microarray technologiesHervé Husson, Partha Manavalan, Viatcheslav R Akmaev, et al.
Human Molecular Genetics|July 5, 2020
Correction of cilia structure and function alleviates multi-organ pathology in Bardet-Biedl syndrome miceHervé Husson, Nikolay O Bukanov, Sarah Moreno, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 4, 2025
Development of an AAV-delivered microRNA gene therapy for Myotonic Dystrophy Type 1Giulio S Tomassy, Wei Fan, Shuwen Cao, et al.
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