Resultados de procura - Jin, Xiangyang
- Mostrando 1 - 8 Resultados de 8
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1
Gene delivery using AAV8 in vivo for disease stabilization in a bimodal gene therapy approach for the treatment of ADA-deficient SCID por Carbonaro-Sarracino, Denise A., Chun, Krista, Clark, Danielle N., Kaufman, Michael L., Jin, Xiangyang, Wang, Xiaoyan, Kohn, Donald B.
Publicado 2021Text -
2
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... por Carbonaro, Denise A., Jin, Xiangyang, Cotoi, Daniel, Mi, Tiejuan, Yu, Xiao-Jin, Skelton, Dianne C., Dorey, Frederick, Kellems, Rodney E., Blackburn, Michael R., Kohn, Donald B.
Publicado 2008Text -
3
Gene therapy/bone marrow transplantation in ADA-deficient mice: roles of enzyme-replacement therapy and cytoreduction por Carbonaro, Denise A., Jin, Xiangyang, Wang, Xingchao, Yu, Xiao-Jin, Rozengurt, Nora, Kaufman, Michael L., Wang, Xiaoyan, Gjertson, David, Zhou, Yang, Blackburn, Michael R., Kohn, Donald B.
Publicado 2012Text -
4
Effects of Vector Backbone and Pseudotype on Lentiviral Vector-mediated Gene Transfer: Studies in Infant ADA-Deficient Mice and Rhesus Monkeys por Carbonaro Sarracino, Denise, Tarantal, Alice F, Lee, C Chang I., Martinez, Michele, Jin, Xiangyang, Wang, Xiaoyan, Hardee, Cinnamon L, Geiger, Sabine, Kahl, Christoph A, Kohn, Donald B
Publicado 2014Text -
5
Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing por Smith, Laura J., Wright, Jason, Clark, Gabriella, Ul-Hasan, Taihra, Jin, Xiangyang, Fong, Abigail, Chandra, Manasa, St Martin, Thia, Rubin, Hillard, Knowlton, David, Ellsworth, Jeff L., Fong, Yuman, Wong, Kamehameha K., Chatterjee, Saswati
Publicado 2018Text -
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Dosing and Re-Administration of Lentiviral Vector for In Vivo Gene Therapy in Rhesus Monkeys and ADA-Deficient Mice por Carbonaro-Sarracino, Denise A., Tarantal, Alice F., Lee, C. Chang I., Kaufman, Michael L., Wandro, Stephen, Jin, Xiangyang, Martinez, Michele, Clark, Danielle N., Chun, Krista, Koziol, Colin, Hardee, Cinnamon L., Wang, Xiaoyan, Kohn, Donald B.
Publicado 2019Text -
7
Preclinical Demonstration of Lentiviral Vector-mediated Correction of Immunological and Metabolic Abnormalities in Models of Adenosine Deaminase Deficiency por Carbonaro, Denise A, Zhang, Lin, Jin, Xiangyang, Montiel-Equihua, Claudia, Geiger, Sabine, Carmo, Marlene, Cooper, Aaron, Fairbanks, Lynette, Kaufman, Michael L, Sebire, Neil J, Hollis, Roger P, Blundell, Michael P, Senadheera, Shantha, Fu, Pei-Yu, Sahaghian, Arineh, Chan, Rebecca Y, Wang, Xiaoyan, Cornetta, Kenneth, Thrasher, Adrian J, Kohn, Donald B, Gaspar, H Bobby
Publicado 2014Text -
8
β-globin gene transfer to human bone marrow for sickle cell disease por Romero, Zulema, Urbinati, Fabrizia, Geiger, Sabine, Cooper, Aaron R., Wherley, Jennifer, Kaufman, Michael L., Hollis, Roger P., Ruiz de Assin, Rafael, Senadheera, Shantha, Sahagian, Arineh, Jin, Xiangyang, Gellis, Alyse, Wang, Xiaoyan, Gjertson, David, DeOliveira, Satiro, Kempert, Pamela, Shupien, Sally, Abdel-Azim, Hisham, Walters, Mark C., Meiselman, Herbert J., Wenby, Rosalinda B., Gruber, Theresa, Marder, Victor, Coates, Thomas D., Kohn, Donald B.
Publicado 2013Text