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Cancer Cell|October 26, 2002
Slug, a highly conserved zinc finger transcriptional repressor, protects hematopoietic progenitor cells from radiation-induced apoptosis in vivoAkira Inoue, Markus G Seidel, Wenshu Wu, et al.Frontiers in Immunology|January 9, 2019
Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Working GroupSimon Bomken, Jutte van der Werff Ten Bosch, Andishe Attarbaschi, et al.The Journal of Allergy and Clinical Immunology|December 25, 2019
Treatment with rapamycin can restore regulatory T-cell function in IPEX patientsLaura Passerini, Federica Barzaghi, Rosalia Curto, et al.The Journal of Allergy and Clinical Immunology|January 16, 2016
The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiencyLaura Gámez-Díaz, Dietrich August, Polina Stepensky, et al.Haematologica|August 16, 2023
Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndromeMiriam Erlacher, Felicia Andresen, Martina Sukova, et al.Blood|June 5, 2014
Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiencyAnne Rensing-Ehl, Simon Völkl, Carsten Speckmann, et al.Journal of Clinical Immunology|January 17, 2024
Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple CentersPriya K Patel, Michell Lozano Chinga, Melis Yilmaz, et al.The Journal of Allergy and Clinical Immunology|April 7, 2015
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiencyOmar K Alkhairy, Ruy Perez-Becker, Gertjan J Driessen, et al.Blood|April 22, 2016
The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosisBernd Hartz, Rebecca Marsh, Kanchan Rao, et al.Clinical Immunology (Orlando, Fla.)|September 14, 2010
Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiencyA Rensing-Ehl, K Warnatz, S Fuchs, et al.Pageof 24