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Proceedings of the National Academy of Sciences of the United States of America|May 23, 2007
NRAS mutation causes a human autoimmune lymphoproliferative syndromeJoão B Oliveira, Nicolas Bidère, Julie E Niemela, et al.
Blood|March 21, 2007
Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiencyJavier Chinen, Joie Davis, Suk See De Ravin, et al.
Nature Biotechnology|December 11, 2019
Polymer-stabilized Cas9 nanoparticles and modified repair templates increase genome editing efficiencyDavid N Nguyen, Theodore L Roth, P Jonathan Li, et al.
Pediatric Transplantation|September 3, 2011
Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCIDGrace P Yu, Kari C Nadeau, David R Berk, et al.
The New England Journal of Medicine|December 14, 2016
Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11BDivya Punwani, Yong Zhang, Jason Yu, et al.
The Journal of Allergy and Clinical Immunology|August 13, 2021
Poor T-cell receptor β repertoire diversity early posttransplant for severe combined immunodeficiency predicts failure of immune reconstitutionOttavia M Delmonte, Riccardo Castagnoli, Jason Yu, et al.
The Journal of Allergy and Clinical Immunology|April 30, 2013
Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicismAmy P Hsu, Kathryn J Sowerwine, Monica G Lawrence, et al.
Immunity|August 1, 2025
Innate-like memory T cells rapidly emerge in humans after gene therapy for SCID-X1Anoop Babu Vasandan, Hossam A Abdelsamed, Shannon K Boi, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2013
Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experienceWilliam T Shearer, Elizabeth Dunn, Luigi D Notarangelo, et al.
Nature Immunology|October 7, 2008
The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiencyLawrence R Shiow, David W Roadcap, Kenneth Paris, et al.
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