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Infection and Immunity|April 23, 2004
Human leukocyte antigen class II alleles influence levels of antibodies to the Plasmodium falciparum asexual-stage apical membrane antigen 1 but not to merozoite surface antigen 2 and merozoite surface protein 1Armead H Johnson, Rose G F Leke, Nancy R Mendell, et al.
Annals of Neurology|August 4, 2023
Delandistrogene Moxeparvovec Gene Therapy in Ambulatory Patients (Aged ≥4 to <8 Years) with Duchenne Muscular Dystrophy: 1-Year Interim Results from Study SRP-9001-103 (ENDEAVOR)Craig M Zaidman, Crystal M Proud, Craig M McDonald, et al.
Annals of Neurology|October 3, 2009
Limb-girdle muscular dystrophy type 2D gene therapy restores alpha-sarcoglycan and associated proteinsJerry R Mendell, Louise R Rodino-Klapac, Xiomara Rosales-Quintero, et al.
Science Translational Medicine|April 7, 2010
Follistatin gene delivery enhances muscle growth and strength in nonhuman primatesJanaiah Kota, Chalonda R Handy, Amanda M Haidet, et al.
The American Journal of Tropical Medicine and Hygiene|June 17, 2025
Survey of Fleas and Ticks for Rickettsia rickettsii and Rickettsia typhi in the El Paso Community and Other Areas in Texas, New Mexico, and Ciudad Juarez, MexicoKaren R Valdez, Nicole L Mendell, Angélica María Escárcega-Ávila, et al.
Nature Immunology|January 8, 2025
A multi-kinase inhibitor screen identifies inhibitors preserving stem-cell-like chimeric antigen receptor T cellsFeifei Song, Ourania Tsahouridis, Simone Stucchi, et al.
CPT: Pharmacometrics & Systems Pharmacology|March 17, 2025
Comparison of Model-Predicted and Observed Evinacumab Pharmacokinetics and Efficacy in Children Aged < 5 Years With Homozygous Familial HypercholesterolemiaSébastien Bihorel, Robert Dingman, Jeanne Mendell, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2025
Lymphatic dysfunction is linked to disease pathogenesis in Duchenne muscular dystrophy animal modelsBhuvaneshwaran Subramanian, Shedreanna Johnson, Akshaya Narayanan, et al.
American Journal of Medical Genetics|August 15, 2001
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophyC A Brown, R W Lanning, K Q McKinney, et al.
Pediatrics|August 27, 2020
Gene Therapy for Spinal Muscular Atrophy: Safety and Early OutcomesMegan A Waldrop, Cassandra Karingada, Mike A Storey, et al.
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