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Journal of Innate Immunity|July 1, 2010
Rapid neutrophil destruction following phagocytosis of Staphylococcus aureusScott D Kobayashi, Kevin R Braughton, Amy M Palazzolo-Ballance, et al.
Hepatology (Baltimore, Md.)|February 28, 2007
Hepatic abnormalities in patients with chronic granulomatous diseaseNadeem Hussain, Jordan J Feld, David E Kleiner, et al.
Blood|August 19, 2010
Anti-cytokine autoantibodies are associated with opportunistic infection in patients with thymic neoplasiaPeter D Burbelo, Sarah K Browne, Elizabeth P Sampaio, et al.
Clinical Immunology (Orlando, Fla.)|June 19, 2013
B-cell activating factor (BAFF) is elevated in chronic granulomatous diseaseKabir Matharu, Kol A Zarember, Beatriz E Marciano, et al.
The Journal of Allergy and Clinical Immunology|September 2, 2017
Novel signal transducer and activator of transcription 1 mutation disrupts small ubiquitin-related modifier conjugation causing gain of functionElizabeth P Sampaio, Li Ding, Stacey R Rose, et al.
The Journal of Allergy and Clinical Immunology. in Practice|January 16, 2023
Gastrointestinal and Hepatic Manifestations of Chronic Granulomatous DiseaseAlexander H Yang, Brigit Sullivan, Christa S Zerbe, et al.
American Journal of Human Genetics|March 5, 2016
A Clinical Service to Support the Return of Secondary Genomic Findings in Human ResearchAndrew J Darnell, Howard Austin, David A Bluemke, et al.
The Journal of Infectious Diseases|July 12, 2012
Serologic reactivity to the emerging pathogen Granulibacter bethesdensisDavid E Greenberg, Adam R Shoffner, Kimberly R Marshall-Batty, et al.
Frontiers in Immunology|September 11, 2025
Reliable genetic diagnosis of NCF1 (p47phox)-deficient chronic granulomatous disease using high-throughput sequencingAmy P Hsu, Eric Karlins, Justin Lack, et al.
The Journal of Experimental Medicine|August 1, 2020
Constructing and deconstructing GATA2-regulated cell fate programs to establish developmental trajectoriesKirby D Johnson, Daniel J Conn, Evgenia Shishkova, et al.
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