Kahl CA, Tarantal AF, Lee CI, Jimenez DF, Choi C, Pepper K, Petersen D, Fletcher MD, Leapley AC, Fisher J, Burns TS, Ultsch MN, Dorey FJ, Kohn DB. (2006) Effects of busulfan dose escalation on engraftment of infant rhesus monkey hematopoietic stem cells after gene marking by a lentiviral vector. Exp Hematol. Volume 34, Issue 3, pgs. 369-81
Podsakoff GM, Engel BC, Carbonaro DA, Choi C, Smogorzewska EM, Bauer G, Selander D, Csik S, Wilson K, Betts MR, Koup RA, Nabel GJ, Bishop K, King S, Schmidt M, von Kalle C, Church JA, Kohn DB. (2005) Selective survival of peripheral blood lymphocytes in children with HIV-1 following delivery of an anti-HIV gene to bone marrow CD34(+) cells. Mol Therapy Volume 12, Issue 1, pgs. 77-86
Yu A, Olosz F, Choi C, and Malek TR. (2000) Efficient Internalization of IL-2 Depends on the Distal Portion of the Cytoplasmic Tail of the IL-2R Common 
-Chain and a Lymphoid Cell Environment. J Immunol Volume 165, pgs. 2556-2562.
Abstracts:
Shaw KL, Sokolic R and Choi C et al. (2009) Immune reconstitution after gene therapy for adenosine deaminase deficient severe combined immune deficiency (ADA-SCID), Presented at the 12th Annual Meeting of the American Society of Gene Therapy. San Diego, California, May 27- 30.
Choi C,Cudahy D, Cabonaro D, Li S, Nikoli V, Cotoi D, Crooks G, Kohn DB. (2008) Inhibition of GSK3β in human CD34+ cells activates β-catenin and induces limited cell proliferation, improves survival and promotes maintenance of homing and engraftment. Presented at the 2008 Saban Research Institute 13th Annual Poster Session.
Kahl CA, Tarantal AF, Lee CI, Jimenez DF,Choi C, Pepper K, Petersen D, Fletcher MD, Leapley AC, Kohn DB. (2005) Busulfan Dose Escalation to Increase Gene Marking of Hematopoietic Stem Cells by Lentiviral Vectors in Infant Rhesus Monkeys. Mol Therapy, 11, Supplement 1:179
Candotti F, Podsakoff G, Schurman SH, Muul LM, Engel BC, Carbonaro DC, Jagadeesh GJ, Hematti P, Tuschong LM, Carter CS, Ramsey WJ, Choi C, Smogorzewska M, Hershfield MS, Read EJ, Tisdale JF, Dunbar CE and Kohn DB. (2003) Corrective gene transfer into hematopoietic stem/progenitor cells for adenosine deaminase (ADA) deficiency: results in four patients after one year of follow-up. Mol Therapy, 7, 5, Supplement 1: 1163
