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Msystems|June 21, 2024
Genomic insights into the evolution of secondary metabolism of Escovopsis and its allies, specialized fungal symbionts of fungus-farming antsAileen Berasategui, Hassan Salem, Abraham G Moller, et al.
Emerging Infectious Diseases|September 21, 2019
Localized Outbreaks of Epidemic Polyarthritis among Military Personnel Caused by Different Sublineages of Ross River Virus, Northeastern Australia, 2016-2017Wenjun Liu, Joanne R Kizu, Luke R Le Grand, et al.
The American Surgeon|November 4, 2021
Surgical and Oncologic Outcomes With Intraoperative Radiation Therapy for Early Breast CancerOrli Friedman-Eldar, Christina Layton, Iago De Castro Silva, et al.
Annals of Surgical Oncology|March 18, 2022
Axillary Response to Neoadjuvant Therapy in Node-Positive, Estrogen Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Breast Cancer Patients: Predictors and Oncologic OutcomesOrli Friedman-Eldar, Tolga Ozmen, Salah James El Haddi, et al.
Emerging Infectious Diseases|November 21, 2020
Circulation of 2 Barmah Forest Virus Lineages in Military Training Areas, AustraliaWenjun Liu, Joanne R Kizu, David R Matley, et al.
Nature Communications|February 28, 2025
Transcriptional diversification in a human-adapting zoonotic pathogen drives niche-specific evolutionSoma Ghosh, Chao-Jung Wu, Abraham G Moller, et al.
Peerj|March 25, 2025
Comparative genomic analysis of emerging non-typeable Haemophilus influenzae (NTHi) causing emerging septic arthritis in AtlantaBrianna J Bixler, Charlotte J Royer, Robert A Petit Iii, et al.
Microbiology Resource Announcements|January 29, 2019
Whole-Genome Sequences of Staphylococcus aureus Isolates from Cystic Fibrosis Lung InfectionsEryn E Bernardy, Robert A Petit, Abraham G Moller, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|September 17, 1999
The use of dexamethasone in women with preterm premature rupture of membranes--a multicentre, double-blind, placebo-controlled, randomised trial. Dexiprom Study GroupR C Pattinson, J D Makin, M Funk, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
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