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The Journal of Experimental Medicine|May 6, 2015
STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and functionRobert P Wilson, Megan L Ives, Geetha Rao, et al.Nature|January 1, 2025
Monoallelic expression can govern penetrance of inborn errors of immunityO'Jay Stewart, Conor Gruber, Haley E Randolph, et al.Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.Immunity|November 27, 2024
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signalingMasato Ogishi, Koji Kitaoka, Kim L Good-Jacobson, et al.The Journal of Clinical Investigation|March 13, 2020
Inherited human IFN-γ deficiency underlies mycobacterial diseaseGaspard Kerner, Jérémie Rosain, Antoine Guérin, et al.Science Immunology|March 1, 2020
PAX1 is essential for development and function of the human thymusYasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.JAMA|August 30, 2024
Continuation vs Discontinuation of Renin-Angiotensin System Inhibitors Before Major Noncardiac Surgery: The Stop-or-Not Randomized Clinical TrialMatthieu Legrand, Jérémy Falcone, Bernard Cholley, et al.Heart Rhythm|November 16, 2025
Prominent U-waves without QT prolongation in X-linked creatine transporter deficiency caused by SLC6A8 variantsAntoine Delinière, Chloé Mulatier, David Cheillan, et al.Science Immunology|September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signalingCassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.Journal of Clinical Microbiology|March 28, 2008
Genotypic diversity of coagulase-negative staphylococci causing endocarditis: a global perspectiveCathy A Petti, Keith E Simmon, Jose M Miro, et al.Pageof 96