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Biophysical Journal|July 13, 2017
Assessing the Collective Dynamics of Motile Cilia in Cultures of Human Airway Cells by Multiscale DDMLuigi Feriani, Maya Juenet, Cedar J Fowler, et al.Neurology|November 10, 2022
Clinical, Imaging, and Laboratory Findings in Patients With GATA2 Deficiency Presenting With Early-Onset Ischemic StrokeShaia Bierman-Chow, Steven M Holland, Amy P Hsu, et al.Journal of Translational Autoimmunity|May 27, 2021
Bortezomib treatment for refractory nontuberculous mycobacterial infection in the setting of interferon gamma autoantibodiesJoseph M Rocco, Lindsey B Rosen, Gloria H Hong, et al.Journal of Immunology (Baltimore, Md. : 1950)|February 24, 2009
Analysis of adhesion molecules, target cells, and role of IL-2 in human FOXP3+ regulatory T cell suppressor functionDat Q Tran, Deborah D Glass, Gulbu Uzel, et al.Journal of Virology|August 23, 2013
Signal transducer and activator of transcription 3 limits Epstein-Barr virus lytic activation in B lymphocytesErik R Hill, Siva Koganti, Jizu Zhi, et al.Transfusion|February 2, 2021
Daratumumab for delayed RBC engraftment following major ABO mismatched haploidentical bone marrow transplantationBonnie Yates, Eoghan Molloy, Alina Dulau-Florea, et al.Pathogens (Basel, Switzerland)|June 8, 2017
Molecular Typing of Staphylococcus aureus Isolated from Patients with Autosomal Dominant Hyper IgE SyndromeInka Sastalla, Kelli W Williams, Erik D Anderson, et al.International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|April 10, 2023
Disseminated mycobacterial infections after tumor necrosis factor inhibitor use, revealing inborn errors of immunityJacqueline D Squire, Claudia R Libertin, Harry Powers, et al.The Journal of Allergy and Clinical Immunology|March 29, 2013
Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndromeGulbu Uzel, Elizabeth P Sampaio, Monica G Lawrence, et al.The Journal of Allergy and Clinical Immunology|March 5, 2014
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairmentYu Zhang, Xiaomin Yu, Mie Ichikawa, et al.Pageof 68