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Gene therapy for adenosine deaminase deficiency.
Parkman R, Weinberg K, Crooks G, Nolta J, Kapoor N, Kohn D. Parkman R, et al. Among authors: weinberg k. Annu Rev Med. 2000;51:33-47. doi: 10.1146/annurev.med.51.1.33. Annu Rev Med. 2000. PMID: 10774451 Review.
T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates.
Kohn DB, Hershfield MS, Carbonaro D, Shigeoka A, Brooks J, Smogorzewska EM, Barsky LW, Chan R, Burotto F, Annett G, Nolta JA, Crooks G, Kapoor N, Elder M, Wara D, Bowen T, Madsen E, Snyder FF, Bastian J, Muul L, Blaese RM, Weinberg K, Parkman R. Kohn DB, et al. Among authors: weinberg k. Nat Med. 1998 Jul;4(7):775-80. doi: 10.1038/nm0798-775. Nat Med. 1998. PMID: 9662367 Free PMC article.
Amendment to Clinical Research Project. Project 90-C-195. April 1, 1993. Treatment of severe combined immunodeficiency disease (SCID) due to adenosine deaminase deficiency with autologous lymphocytes transduced with a human ADA gene.
Dunbar C, Chang L, Mullen C, Ramsey WJ, Carter C, Kohn D, Parkman R, Lenarsky C, Weinberg K, Wara D, Culver KW, Anderson WF, Leitman S, Fleisher T, Klein H, Shearer G, Clerici M, McGarrity G, Bastian J, Hershfield MS. Dunbar C, et al. Among authors: weinberg k. Hum Gene Ther. 1999 Feb 10;10(3):477-88. doi: 10.1089/10430349950018913. Hum Gene Ther. 1999. PMID: 10048399 No abstract available.
203 results