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JAMA Cardiology|January 9, 2020
Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish CommunityDavid J Tester, Hannah M Bombei, Kristi K Fitzgerald, et al.
Elife|September 25, 2015
Perforin-2 is essential for intracellular defense of parenchymal cells and phagocytes against pathogenic bacteriaRyan M McCormack, Lesley R de Armas, Motoaki Shiratsuchi, et al.
Aging|May 8, 2023
<i>In vitro</i> and <i>in vivo</i> effects of zoledronic acid on senescence and senescence-associated secretory phenotype markersParinya Samakkarnthai, Dominik Saul, Lei Zhang, et al.
Pharmacogenetics|October 23, 2001
The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variantsJ Zhang, P Kuehl, E D Green, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 27, 2022
Incident dementia and long-term exposure to constituents of fine particle air pollution: A national cohort study in the United StatesLiuhua Shi, Qiao Zhu, Yifan Wang, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
<i>In vitro</i> and <i>in vivo</i> effects of zoledronate on senescence and senescence-associated secretory phenotype markersParinya Samakkarnthai, Dominik Saul, Lei Zhang, et al.
Endocrinology|October 25, 2003
A transgenic mouse with a deletion in the collagenous domain of adiponectin displays elevated circulating adiponectin and improved insulin sensitivityTerry P Combs, Utpal B Pajvani, Anders H Berg, et al.
Nature|December 16, 2005
The earliest record of human activity in northern EuropeSimon A Parfitt, René W Barendregt, Marzia Breda, et al.
Journal of Medicinal Chemistry|June 23, 1999
Fluorination of 3-(3-(piperidin-1-yl)propyl)indoles and 3-(3-(piperazin-1-yl)propyl)indoles gives selective human 5-HT1D receptor ligands with improved pharmacokinetic profilesM B van Niel, I Collins, M S Beer, et al.
Blood|May 21, 2013
Defects in neutrophil granule mobilization and bactericidal activity in familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) syndrome caused by STXBP2/Munc18-2 mutationsXi Wen Zhao, Roel P Gazendam, Agata Drewniak, et al.
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