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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1991
[Bone marrow transplantation in congenital defects of immunity]F Porta, L D Notarangelo, F Candotti, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1988
Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiencyM E Conley, A Lavoie, C Briggs, et al.The Journal of Experimental Medicine|August 1, 1980
Role of Ia-positive cells in induction of secondary human immune responses to haptens in vitroR R Rich, S L Abramson, M F Seldin, et al.Blood|August 15, 2000
Lentiviral-mediated gene transfer into human lymphocytes: role of HIV-1 accessory proteinsD Chinnasamy, N Chinnasamy, M J Enriquez, et al.Blood|April 1, 1987
The regulatory role of interleukin 2-responsive T lymphocytes on human marrow granulopoiesisZ Estrov, C Roifman, G Mills, et al.DNA and Cell Biology|September 1, 1993
Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS)L D Notarangelo, F Candotti, O Parolini, et al.The Journal of Pediatrics|June 1, 1990
Heterogeneity of clinical severity and molecular lesions in Aicardi syndromeJ A Neidich, R L Nussbaum, R J Packer, et al.Clinical Immunology (Orlando, Fla.)|May 4, 2000
Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiencyJ E Niemela, J M Puck, R E Fischer, et al.Gene Therapy|August 24, 1999
Retrovirus-mediated WASP gene transfer corrects defective actin polymerization in B cell lines from Wiskott-Aldrich syndrome patients carrying 'null' mutationsF Candotti, F Facchetti, L Blanzuoli, et al.Journal of Clinical Immunology|January 1, 1997
Maternal mosaicism for a novel interleukin-2 receptor gamma-chain mutation causing X-linked severe combined immunodeficiency in a Navajo kindredA S O'Marcaigh, J M Puck, A E Pepper, et al.Pageof 14