Xiao-Jin Yu

发表

of enzyme-replacement therapy and cytoreduction Gene therapy / bone marrow transplantation in ADA-deficient mice : roles

Michael L Kaufman, D. Gjertson, D. Kohn, 2012 .

Stable gene transfer to human CD34(+) hematopoietic cells using the Sleeping Beauty transposon.

Xiuli Wang, L. Barsky, G. Crooks, 2006, Experimental hematology.

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

P. Malik, D. Kohn, Xiao-Jin Yu, 2010 .

Specific and stable gene transfer to human embryonic stem cells using pseudotyped lentiviral vectors.

C. Lutzko, D. Kohn, Jungeun Jang, 2006, Stem cells and development.

Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans.

Aaron R Cooper, O. Yang, D. Gjertson, 2012, Blood.

Gene therapy/bone marrow transplantation in ADA-deficient mice: roles of enzyme-replacement therapy and cytoreduction.

Michael L Kaufman, D. Gjertson, D. Kohn, 2012, Blood.

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 .

Transient gene expression by nonintegrating lentiviral vectors.

Xiao-Jin Yu, Donald B Kohn, D. Kohn, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

Expression from second-generation feline immunodeficiency virus vectors is impaired in human hematopoietic cells.

G. Nolan, J. Abkowitz, S. S. Case, 2002, Molecular therapy : the journal of the American Society of Gene Therapy.

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

K. Weinberg, L. Nadler, A. Cardoso, 2013 .

Neonatal bone marrow transplantation of ADA-deficient SCID mice results in immunologic reconstitution despite low levels of engraftment and an absence of selective donor T lymphoid expansion.

D. Kohn, D. Skelton, Tiejuan Mi, 2008, Blood.

immunologic reconstitution despite low levels of engraftment Neonatal bone marrow transplantation of ADA-deficient SCID mice

D. Kohn, D. Skelton, Tiejuan Mi, 2008 .

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.

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.

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.

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.

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.

Expression of human Wiskott–Aldrich syndrome protein in patients’ cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins

S. Tsuboi, U. Francke, J. Derry, 2000, Gene Therapy.