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Journal of Immunology (Baltimore, Md. : 1950)|July 4, 2012
Transcription factor zinc finger and BTB domain 1 is essential for lymphocyte developmentDivya Punwani, Karen Simon, Youngnim Choi, et al.Immunogenetics|November 15, 2007
The hyper-IgE syndrome is not caused by a microdeletion syndromeDietmar Pfeifer, Cristina Woellner, Astrid Petersen, et al.Blood|June 19, 2002
Retroviral transduction of IL2RG into CD34(+) cells from X-linked severe combined immunodeficiency patients permits human T- and B-cell development in sheep chimerasEmily J Tsai, Harry L Malech, Martha R Kirby, et al.The Journal of Allergy and Clinical Immunology|June 6, 2016
Primary Immune Deficiency Treatment Consortium (PIDTC) updateLinda M Griffith, Morton J Cowan, Luigi D Notarangelo, et al.Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 17, 2019
Low Exposure Busulfan Conditioning to Achieve Sufficient Multilineage Chimerism in Patients with Severe Combined ImmunodeficiencyChristopher C Dvorak, Janel Long-Boyle, Jasmeen Dara, et al.International Journal of Neonatal Screening|August 18, 2020
Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future SequencingAashish N Adhikari, Robert J Currier, Hao Tang, et al.Journal of Clinical Immunology|January 7, 2021
When Screening for Severe Combined Immunodeficiency (SCID) with T Cell Receptor Excision Circles Is Not SCID: a Case-Based ReviewDavid Buchbinder, Jolan E Walter, Manish J Butte, et al.The Journal of Allergy and Clinical Immunology|October 24, 2007
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification CommitteeRaif S Geha, Luigi D Notarangelo, Jean-Laurent Casanova, et al.Journal of Clinical Immunology|January 29, 2015
Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantationDivya Punwani, Haopeng Wang, Alice Y Chan, et al.Blood|April 3, 2010
Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndromeKennichi C Dowdell, Julie E Niemela, Susan Price, et al.Pageof 20