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Genes & Development|July 4, 2020
A role for alternative splicing in circadian control of exocytosis and glucose homeostasisBiliana Marcheva, Mark Perelis, Benjamin J Weidemann, et al.Journal of Medicinal Chemistry|January 5, 1996
Diarylspiro[2.4]heptenes as orally active, highly selective cyclooxygenase-2 inhibitors: synthesis and structure-activity relationshipsH C Huang, J J Li, D J Garland, et al.Integrated Environmental Assessment and Management|November 1, 2017
A refined ecological risk assessment for California red-legged frog, Delta smelt, and California tiger salamander exposed to malathionYvonne H Clemow, Gillian E Manning, Roger L Breton, et al.Lancet (London, England)|June 15, 2020
Safety and immunogenicity of a mosquito saliva peptide-based vaccine: a randomised, placebo-controlled, double-blind, phase 1 trialJessica E Manning, Fabiano Oliveira, Iliano V Coutinho-Abreu, et al.Circulation Research|October 18, 2008
Role of kinin B2 receptor signaling in the recruitment of circulating progenitor cells with neovascularization potentialNicolle Kränkel, Rajesh G Katare, Mauro Siragusa, et al.The American Journal of Tropical Medicine and Hygiene|May 13, 2020
Prevalence of CYP2D6 Genotypes and Predicted Phenotypes in a Cohort of Cambodians at High Risk for Infections with <i>Plasmodium vivax</i>Michele D Spring, Chanthap Lon, Somethy Sok, et al.Annals of Biomedical Engineering|August 29, 2025
Locally Reprogramming Tumor-Associated Macrophages with Cytokine-Loaded Injectable Cryogels for Breast CancerSydney R Henriques, Evan B Glass, Kristen L Hoek, et al.The Journal of Allergy and Clinical Immunology. in Practice|February 3, 2018
Health-Related Quality of Life with Subcutaneous C1-Inhibitor for Prevention of Attacks of Hereditary AngioedemaWilliam R Lumry, Timothy Craig, Bruce Zuraw, et al.Journal of Asthma and Allergy|March 2, 2026
Donidalorsen for Long-Term Prophylaxis of Hereditary Angioedema Attacks: Results from the OASISplus Open-Label Extension Cohort at Year 1William R Lumry, Raffi Tachdjian, Timothy Craig, et al.Journal of Medical Genetics|January 31, 2024
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndromeKerry A Miller, David A Cruz Walma, Daniel M Pinkas, et al.Pageof 42