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Cell|May 20, 2025
Arrestin-biased allosteric modulator of neurotensin receptor 1 alleviates acute and chronic painRan Guo, Ouyang Chen, Yang Zhou, et al.
Journal of Cardiology|January 25, 2022
COVID-19 and arrhythmia: An overviewJoseph A Varney, Vinh S Dong, Tiffany Tsao, et al.
International Journal of Cardiology|February 13, 2021
Investigation of current models of care for genetic heart disease in Australia: A national clinical auditRachel Austin, Michael C J Quinn, Clifford Afoakwah, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 8, 2023
A promoterless AAV6.2FF-based lung gene editing platform for the correction of surfactant protein B deficiencySylvia P Thomas, Jakob M Domm, Jacob P van Vloten, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 19, 2020
Quantifying infection risks in incompatible living donor kidney transplant recipientsRobin K Avery, Jennifer D Motter, Kyle R Jackson, et al.
The Journal of Infection|October 20, 2023
Analysis of blood and nasal epithelial transcriptomes to identify mechanisms associated with control of SARS-CoV-2 viral load in the upper respiratory tractMahdi Moradi Marjaneh, Joseph D Challenger, Antonio Salas, et al.
MMWR. Morbidity and Mortality Weekly Report|July 31, 2015
Large Outbreak of Botulism Associated with a Church Potluck Meal--Ohio, 2015Carolyn L McCarty, Kristina Angelo, Karlyn D Beer, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|June 3, 2021
Treatment Practices for Adults With Candidemia at 9 Active Surveillance Sites-United States, 2017-2018Jeremy A W Gold, Emma E Seagle, Joelle Nadle, et al.
Pacing and Clinical Electrophysiology : PACE|September 24, 2019
Predicting atrial fibrillation recurrence after ablation in patients with heart failure: Validity of the APPLE and CAAP-AF risk scoring systemsEric Black-Maier, Alice Parish, Benjamin A Steinberg, et al.
Human Molecular Genetics|June 25, 2021
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disordersEthiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira, et al.
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