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Frontiers in Immunology|December 26, 2022
Case report: Persistent shedding of a live vaccine-derived rubella virus in a young man with severe combined immunodeficiency and cutaneous granulomaKimberly E Bonner, Ellie Sukerman, Juventila Liko, et al.Vaccine|August 8, 2022
Employer requirements and COVID-19 vaccination and attitudes among healthcare personnel in the U.S.: Findings from National Immunization Survey Adult COVID Module, August - September 2021James T Lee, S Sean Hu, Tianyi Zhou, et al.Cancer Research Communications|March 16, 2023
S100A8/S100A9 Promote Progression of Multiple Myeloma via Expansion of MegakaryocytesCindy Lin, Laura Garcia-Gerique, Erin E Bonner, et al.Cancer Research|September 7, 2022
A Novel Selective Inhibitor JBI-589 Targets PAD4-Mediated Neutrophil Migration to Suppress Tumor ProgressionHui Deng, Cindy Lin, Laura Garcia-Gerique, et al.Journal of Medical Internet Research|April 10, 2026
Child Vaccination Status and Behavioral and Social Drivers of Vaccination Among Their Caregivers in the Philippines: Cross-Sectional Survey Study Comparison of Household, Mobile, and Online ModesKimberly E Bonner, Mikka Hipol, Dominique Sy, et al.ACR Open Rheumatology|July 3, 2026
DNASE1L3 Deficiency With Novel Missense Variant: Enzymatic and Plasma Fragmentomic Evidence of Pathogenicity and Partial Response to JAK BlockadeAnnel Andrea Leon Tenorio, Takeshi Sugio, Jordan Cheng, et al.Vaccine|January 24, 2024
Strengthening COVID-19 vaccine confidence & demand during the US COVID-19 emergency responseNeetu Abad, Kimberly E Bonner, Jessica Kolis, et al.Medrxiv : the Preprint Server for Health Sciences|September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.American Journal of Preventive Medicine|February 12, 2023
Behavioral and Social Drivers of COVID-19 Vaccination in the United States, August-November 2021Kimberly E Bonner, Kushagra Vashist, Neetu S Abad, et al.Annals of Clinical and Translational Neurology|February 4, 2024
Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathySandra Donkervoort, Payam Mohassel, Melanie O'Leary, et al.Pageof 15