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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.BMC Medical Genetics|July 4, 2007
Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type IbLilia L Bi, George Pan, T Prescott Atkinson, et al.Transplantation|December 16, 2004
Engraftment potential of human amnion and chorion cells derived from term placentaMarco Bailo, Maddalena Soncini, Elsa Vertua, 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.The Journal of Experimental Medicine|January 20, 2016
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70Alice Y Chan, Divya Punwani, Theresa A Kadlecek, et al.Nature|September 22, 2006
Gene therapy: X-SCID transgene leukaemogenicityAdrian J Thrasher, H Bobby Gaspar, Christopher Baum, et al.Frontiers in Immunology|March 3, 2025
Disruption of the moonlighting function of CTF18 in a patient with T-lymphopeniaRobert Sertori, Billy Truong, Manoj K Singh, et al.Journal of Clinical Immunology|January 10, 2014
Bone density and fractures in autosomal dominant hyper IgE syndromeKathryn J Sowerwine, Pamela A Shaw, Wenjuan Gu, et al.Human Genetics|February 1, 2006
Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndromeShigui Zhu, Amy P Hsu, Marla M Vacek, et al.Blood|July 5, 2011
Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiencyRobert Sokolic, Irina Maric, Chimene Kesserwan, et al.Pageof 28