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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 21, 2019
Targeting PD-L1 Initiates Effective Antitumor Immunity in a Murine Model of Cushing DiseaseHanna R Kemeny, Aladine A Elsamadicy, S Harrison Farber, et al.
Oncoimmunology|June 7, 2018
Temozolomide lymphodepletion enhances CAR abundance and correlates with antitumor efficacy against established glioblastomaCarter M Suryadevara, Rupen Desai, Melissa L Abel, et al.
Science (New York, N.Y.)|April 23, 2021
Preventing Engrailed-1 activation in fibroblasts yields wound regeneration without scarringShamik Mascharak, Heather E desJardins-Park, Michael F Davitt, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 3, 2025
Endothelium- and Fibroblast-Derived C-Type Natriuretic Peptide Prevents the Development and Progression of Aortic AneurysmsAisah A Aubdool, Amie J Moyes, Cristina Pérez-Ternero, et al.
Bioorganic & Medicinal Chemistry|November 14, 2007
Benzenesulfonamide indole inhibitors of cytosolic phospholipase A2alpha: optimization of in vitro potency and rat pharmacokinetics for oral efficacyKatherine L Lee, Mark L Behnke, Megan A Foley, et al.
Obesity Surgery|June 13, 2020
Correlation between Obstructive Sleep Apnea and Non-Alcoholic Fatty Liver Disease before and after Metabolic Bariatric SurgeryY X Zhang, L Yang, C C Yang, et al.
Circulation|December 31, 2019
Critical Role of Cytosolic DNA and Its Sensing Adaptor STING in Aortic Degeneration, Dissection, and RuptureWei Luo, Yidan Wang, Lin Zhang, et al.
Journal of Medicinal Chemistry|February 20, 2007
Discovery of Ecopladib, an indole inhibitor of cytosolic phospholipase A2alphaKatherine L Lee, Megan A Foley, Lihren Chen, et al.
Eukaryotic Cell|July 26, 2015
Transcriptome Analysis of Aspergillus flavus Reveals veA-Dependent Regulation of Secondary Metabolite Gene Clusters, Including the Novel Aflavarin ClusterJ W Cary, Z Han, Y Yin, et al.
Leukemia|February 3, 2012
Newly diagnosed acute lymphoblastic leukemia in China (II): prognosis related to genetic abnormalities in a series of 1091 casesJ-Q Mi, X Wang, Y Yao, et al.
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