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BMC Medical Genetics|July 4, 2007
Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type IbLilia L Bi, George Pan, T Prescott Atkinson, et al.Blood|April 3, 2010
Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndromeKennichi C Dowdell, Julie E Niemela, Susan Price, et al.Pediatrics|November 18, 2015
Newborn Screening for Cystic Fibrosis in CaliforniaMartin Kharrazi, Juan Yang, Tracey Bishop, et al.The Journal of Experimental Medicine|January 20, 2016
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70Alice Y Chan, Divya Punwani, Theresa A Kadlecek, et al.Frontiers in Immunology|March 3, 2025
Disruption of the moonlighting function of CTF18 in a patient with T-lymphopeniaRobert Sertori, Billy Truong, Manoj K Singh, et al.Journal of Clinical Immunology|January 10, 2014
Bone density and fractures in autosomal dominant hyper IgE syndromeKathryn J Sowerwine, Pamela A Shaw, Wenjuan Gu, et al.Human Genetics|February 1, 2006
Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndromeShigui Zhu, Amy P Hsu, Marla M Vacek, et al.Evolutionary Applications|January 25, 2013
Natural selection in utero induced by mass layoffs: the hCG evidenceRalph Catalano, Claire Margerison-Zilko, Sidra Goldman-Mellor, et al.American Journal of Hematology|January 25, 2006
Fluorodeoxyglucose positron emission tomography (FDG-PET) for monitoring lymphadenopathy in the autoimmune lymphoproliferative syndrome (ALPS)V Koneti Rao, Jorge A Carrasquillo, Janet K Dale, et al.The Journal of Experimental Medicine|July 16, 2008
Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylationGuillaume Vogt, Jacinta Bustamante, Ariane Chapgier, et al.Pageof 17