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Journal of Clinical Immunology|November 13, 2014
Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS geneKoichi Oshima, Kohsuke Imai, Michael H Albert, et al.Proceedings of the National Academy of Sciences of the United States of America|January 11, 2007
WIP is a chaperone for Wiskott-Aldrich syndrome protein (WASP)Miguel A de la Fuente, Yoji Sasahara, Marco Calamito, et al.Clinical Immunology (Orlando, Fla.)|August 2, 2011
Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndromeKeisuke Otsubo, Hirokazu Kanegane, Yoshiro Kamachi, et al.Nature Communications|June 2, 2015
Platelet actin nodules are podosome-like structures dependent on Wiskott-Aldrich syndrome protein and ARP2/3 complexNatalie S Poulter, Alice Y Pollitt, Amy Davies, et al.Current Biology : CB|July 15, 2014
Cellular control of cortical actin nucleationMiia Bovellan, Yves Romeo, Maté Biro, et al.The Journal of Allergy and Clinical Immunology|December 17, 2009
Primary immunodeficiencies: 2009 update, Luigi D Notarangelo, Alain Fischer, et al.The Journal of Allergy and Clinical Immunology|August 18, 2009
Comèl-Netherton syndrome defined as primary immunodeficiencyEllen D Renner, Dominik Hartl, Stacey Rylaarsdam, et al.Journal of Clinical Immunology|July 25, 2024
Discordant Phenotypes of Nephritis in Patients with X-linked AgammaglobulinemiaToru Kanamori, Tomohiro Udagawa, Takayuki Fujii, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|December 20, 2014
Perforin gene transfer into hematopoietic stem cells improves immune dysregulation in murine models of perforin deficiencyMarlene Carmo, Kimberly A Risma, Paritha Arumugam, et al.Blood|October 16, 2015
N-WASP is required for B-cell-mediated autoimmunity in Wiskott-Aldrich syndromeStefano Volpi, Elettra Santori, Katrina Abernethy, et al.Pageof 52