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The Journal of Experimental Medicine|November 1, 1980
Production of predominantly polymeric IgA by human peripheral blood lymphocytes stimulated in vitro with mitogensW H Kutteh, W J Koopman, M E Conley, et al.
Human Genetics|December 1, 1991
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineagesL D Notarangelo, O Parolini, A Albertini, et al.
The Journal of Allergy and Clinical Immunology|July 1, 1991
Retrospective analysis of the incidence of pulmonary disease in hypogammaglobulinemiaS K Sweinberg, R A Wodell, M P Grodofsky, et al.
Blood|May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiencyM E Conley, N B Spinner, B S Emanuel, et al.
Transfusion|March 1, 1988
Direct quantitation of IgG subclasses 1, 2, and 3 bound to red cells by Rh1 (D) antibodiesD R Shaw, M E Conley, F J Knox, et al.
Blood|November 15, 1995
High prevalence of nonsense, frame shift, and splice-site mutations in 16 patients with full-blown Wiskott-Aldrich syndromeG S Wengler, L D Notarangelo, S Berardelli, et al.
The Journal of Experimental Medicine|January 31, 1998
Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemiaY Minegishi, E Coustan-Smith, Y H Wang, et al.
American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
Scientific Reports|October 21, 2025
Distinct roles of amniotic membrane epithelial (hAEC) and mesenchymal stromal cells (hAMSC) in amniotic membrane-driven wound healingM Alcaraz, I Hernández-Mármol, J M Puente-Cuadrado, et al.
Blood|June 15, 1990
Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivationJ M Puck, K A Siminovitch, M Poncz, et al.
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