X. Yu

发表

Multiple modifications in cis elements of the long terminal repeat of retroviral vectors lead to increased expression and decreased DNA methylation in embryonic carcinoma cells

K. Weinberg, A. El-Khoueiry, D. Kohn, 1995, Journal of virology.

Increased levels of spliced RNA account for augmented expression from the MFG retroviral vector in hematopoietic cells.

R. Mulligan, D. Kohn, D. Skelton, 1996, Gene therapy.

Consistent, persistent expression from modified retroviral vectors in murine hematopoietic stem cells.

D. Kohn, D. Skelton, S. Halene, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Comparison of trans-dominant inhibitory mutant human immunodeficiency virus type 1 genes expressed by retroviral vectors in human T lymphocytes

C. Zhou, D. Kohn, J. Guatelli, 1993, Journal of virology.

Human fetal mesenchymal stem cells differentiating towards chondrocytes display a similar gene expression profile as growth plate cartilage

Rappold, J. Goeman, J. Wit, 2010 .

Retroviral-mediated gene expression in human myelomonocytic cells: a comparison of hematopoietic cell promoters to viral promoters.

C. Zhou, P. Malik, D. Kohn, 1995, Blood.

Recombinant adeno-associated virus mediates a high level of gene transfer but less efficient integration in the K562 human hematopoietic cell line

P. Malik, D. Kohn, G. Kurtzman, 1997, Journal of virology.

Retroviral-mediated transfer of the human glucocerebrosidase gene into cultured Gaucher bone marrow.

D. Kohn, J. Nolta, I. Bahner, 1992, The Journal of clinical investigation.

Retrovirus-mediated transfer of the human α- L-iduronidase cDNA into human hematopoietic progenitor cells leads to correction in trans of Hurler fibroblasts

D. Kohn, X. Yu, E. Kakkis, 1997, Gene Therapy.

Toward gene therapy for Gaucher disease.

G. Crooks, D. Kohn, J. Nolta, 1991, Human gene therapy.

Increased probability of expression from modified retroviral vectors in embryonal stem cells and embryonal carcinoma cells

D. Kohn, Xiao-Jin Yu, P. Robbins, 1997, Journal of virology.

Lentiviral vectors for efficient delivery of CD80 and granulocyte-macrophage- colony-stimulating factor in human acute lymphoblastic leukemia and acute myeloid leukemia cells to induce antileukemic immune responses.

K. Weinberg, L. Nadler, A. Cardoso, 2000, Blood.

Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors.

L. Naldini, D. Haas, S. S. Case, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Intrakines--evidence for a trans-cellular mechanism of action.

S. Chen, D. Kohn, G. Bauer, 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

Clonal diversity of primitive human hematopoietic progenitors following retroviral marking and long-term engraftment in immune-deficient mice.

J. Nolta, M. Dao, X. Yu, 1997, Experimental hematology.

Expression of human glucocerebrosidase following retroviral vector-mediated transduction of murine hematopoietic stem cells.

D. Kohn, J. Nolta, L. Uribe, 1991, Bone marrow transplantation.