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Immunobiology|July 25, 2009
Wiskott-Aldrich Syndrome: Immunodeficiency resulting from defective cell migration and impaired immunostimulatory activationGerben Bouma, Siobhan O Burns, Adrian J ThrasherGenes & Diseases|March 18, 2020
Gene therapy and genome editing for primary immunodeficiency diseasesZhi-Yong Zhang, Adrian J Thrasher, Fang ZhangExpert Reviews in Molecular Medicine|July 9, 2004
Gene therapy for severe combined immune deficiencyWaseem Qasim, H Bobby Gaspar, Adrian J ThrasherMolecular Therapy : the Journal of the American Society of Gene Therapy|April 22, 2010
Hybrid lentiviral vectorsWaseem Qasim, Conrad A Vink, Adrian J ThrasherCurrent Opinion in Hematology|October 18, 2016
Primary immunodeficiencies due to abnormalities of the actin cytoskeletonSiobhan O Burns, Anton Zarafov, Adrian J ThrasherImmunologic Research|October 6, 2007
IPEX, FOXP3 and regulatory T-cells: a model for autoimmunityHans D Ochs, Eleonora Gambineri, Troy R TorgersonClinical Immunology (Orlando, Fla.)|May 27, 2008
Restricted immunoglobulin constant heavy G chain genes in primary immunodeficienciesVivi-Anne Oxelius, Hans D Ochs, Lennart HammarströmThe Journal of Allergy and Clinical Immunology|May 5, 2009
TH17 cells and regulatory T cells in primary immunodeficiency diseasesHans D Ochs, Mohamed Oukka, Troy R TorgersonJournal of Immunology (Baltimore, Md. : 1950)|June 5, 2009
Wiskott-Aldrich syndrome protein is required for homeostasis and function of invariant NKT cellsAlexander Astrakhan, Hans D Ochs, David J RawlingsCurrent Opinion in Rheumatology|June 24, 2003
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasisEleonora Gambineri, Troy R Torgerson, Hans D OchsPageof 51