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Nature Medicine|July 9, 2003
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouseQi Long Lu, Christopher J Mann, Fang Lou, et al.Nature Medicine|November 12, 2021
Deaths in children and young people in England after SARS-CoV-2 infection during the first pandemic yearClare Smith, David Odd, Rachel Harwood, et al.Nature Medicine|March 16, 2021
A perfusable, multifunctional epicardial device improves cardiac function and tissue repairShixing Huang, Dong Lei, Qi Yang, et al.Nature Medicine|March 16, 2021
Toward universal health coverage in the post-COVID-19 eraStéphane Verguet, Alemayehu Hailu, Getachew Teshome Eregata, et al.Nature Medicine|March 19, 2021
Fetal cranial growth trajectories are associated with growth and neurodevelopment at 2 years of age: INTERBIO-21st Fetal StudyJosé Villar, Robert B Gunier, Chrystelle O O Tshivuila-Matala, et al.Nature Medicine|November 16, 2021
Dexamethasone modulates immature neutrophils and interferon programming in severe COVID-19Sarthak Sinha, Nicole L Rosin, Rohit Arora, et al.Nature Medicine|November 18, 2021
Reporting guidelines for human microbiome research: the STORMS checklistChloe Mirzayi, Audrey Renson, , et al.Nature Medicine|November 21, 2018
Dynamic molecular monitoring reveals that SWI-SNF mutations mediate resistance to ibrutinib plus venetoclax in mantle cell lymphomaRishu Agarwal, Yih-Chih Chan, Constantine S Tam, et al.Nature Medicine|February 20, 2019
Development of a CRISPR/Cas9-based therapy for Hutchinson-Gilford progeria syndromeOlaya Santiago-Fernández, Fernando G Osorio, Víctor Quesada, et al.Nature Medicine|February 20, 2019
Single-dose CRISPR-Cas9 therapy extends lifespan of mice with Hutchinson-Gilford progeria syndromeErgin Beyret, Hsin-Kai Liao, Mako Yamamoto, et al.Pageof 619