检索结果 - Shaw, Kit

Foamy Virus Envelope Glycoprotein Is Sufficient for Particle Budding and Release 由 Shaw, Kit L., Lindemann, Dirk, Mulligan, Mark J., Goepfert, Paul A.

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Characterization of the R572T Point Mutant of a Putative Cleavage Site in Human Foamy Virus Env 由 Bansal, Anju, Shaw, Kit L., Edwards, Bradley H., Goepfert, Paul A., Mulligan, Mark J.

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An Endoplasmic Reticulum Retrieval Signal Partitions Human Foamy Virus Maturation to Intracytoplasmic Membranes 由 Goepfert, Paul A., Shaw, Kit, Wang, George, Bansal, Anju, Edwards, Bradley H., Mulligan, Mark J.

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Lentiviral Vectors with Amplified Beta Cell-Specific Gene Expression 由 Shaw, Kit L., Pais, Eszter, Ge, Shundi, Hardee, Cinnamon, Skelton, Dianne, Hollis, Roger, Crooks, Gay M., Kohn, Donald B.

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Cytoreductive conditioning intensity predicts clonal diversity in ADA-SCID retroviral gene therapy patients 由 Cooper, Aaron R., Lill, Georgia R., Shaw, Kit, Carbonaro-Sarracino, Denise A., Davila, Alejandra, Sokolic, Robert, Candotti, Fabio, Pellegrini, Matteo, Kohn, Donald B.

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Busulfan Pharmacokinetics in ADA SCID Gene Therapy 由 Bradford, Kathryn L., Liu, Siyu, Krajinovic, Maja, Ansari, Marc, Garabedian, Elizabeth, Tse, John, Wang, Xiaoyan, Shaw, Kit L., Gaspar, H. Bobby, Candotti, Fabio, Kohn, Donald B.

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Regulated Expansion of Human Pancreatic β-Cells 由 Pais, Eszter, Park, Jean, Alexy, Tamas, Nikolian, Vahagn, Ge, Shundi, Shaw, Kit, Senadheera, Shantha, Hardee, Cinnamon L, Skelton, Dianne, Hollis, Roger, Crooks, Gay M, Kohn, Donald B

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Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency 由 Sokolic, Robert, Maric, Irina, Kesserwan, Chimene, Garabedian, Elizabeth, Hanson, I. Celine, Dodds, Margaret, Buckley, Rebecca, Issekutz, Andrew C., Kamani, Naynesh, Shaw, Kit, Tan, Ben, Bali, Pawan, Hershfield, Michael S., Kohn, Donald B., Wayne, Alan S., Candotti, Fabio

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Post-Transcriptional Genetic Silencing of BCL11A to Treat Sickle Cell Disease 由 Esrick, Erica B., Lehmann, Leslie E., Biffi, Alessandra, Achebe, Maureen, Brendel, Christian, Ciuculescu, Marioara F., Daley, Heather, MacKinnon, Brenda, Morris, Emily, Federico, Amy, Abriss, Daniela, Boardman, Kari, Khelladi, Radia, Shaw, Kit, Negre, Helene, Negre, Olivier, Nikiforow, Sarah, Ritz, Jerome, Pai, Sung-Yun, London, Wendy B., Dansereau, Colleen, Heeney, Matthew M., Armant, Myriam, Manis, John P, Williams, David A.

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Gene therapy for adenosine deaminase–deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans 由 Candotti, Fabio, Shaw, Kit L., Muul, Linda, Carbonaro, Denise, Sokolic, Robert, Choi, Christopher, Schurman, Shepherd H., Garabedian, Elizabeth, Kesserwan, Chimene, Jagadeesh, G. Jayashree, Fu, Pei-Yu, Gschweng, Eric, Cooper, Aaron, Tisdale, John F., Weinberg, Kenneth I., Crooks, Gay M., Kapoor, Neena, Shah, Ami, Abdel-Azim, Hisham, Yu, Xiao-Jin, Smogorzewska, Monika, Wayne, Alan S., Rosenblatt, Howard M., Davis, Carla M., Hanson, Celine, Rishi, Radha G., Wang, Xiaoyan, Gjertson, David, Yang, Otto O., Balamurugan, Arumugam, Bauer, Gerhard, Ireland, Joanna A., Engel, Barbara C., Podsakoff, Gregory M., Hershfield, Michael S., Blaese, R. Michael, Parkman, Robertson, Kohn, Donald B.

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Long-term outcomes after gene therapy for adenosine deaminase severe combined immune deficiency 由 Reinhardt, Bryanna, Habib, Omar, Shaw, Kit L., Garabedian, Elizabeth, Carbonaro-Sarracino, Denise A., Terrazas, Dayna, Fernandez, Beatriz Campo, De Oliveira, Satiro, Moore, Theodore B., Ikeda, Alan K., Engel, Barbara C., Podsakoff, Gregory M., Hollis, Roger P., Fernandes, Augustine, Jackson, Connie, Shupien, Sally, Mishra, Suparna, Davila, Alejandra, Mottahedeh, Jack, Vitomirov, Andrej, Meng, Wenzhao, Rosenfeld, Aaron M., Roche, Aoife M., Hokama, Pascha, Reddy, Shantan, Everett, John, Wang, Xiaoyan, Luning Prak, Eline T., Cornetta, Kenneth, Hershfield, Michael S., Sokolic, Robert, De Ravin, Suk See, Malech, Harry L., Bushman, Frederic D., Candotti, Fabio, Kohn, Donald B.

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Clinical efficacy of gene-modified stem cells in adenosine deaminase–deficient immunodeficiency 由 Shaw, Kit L., Garabedian, Elizabeth, Mishra, Suparna, Barman, Provaboti, Davila, Alejandra, Carbonaro, Denise, Shupien, Sally, Silvin, Christopher, Geiger, Sabine, Nowicki, Barbara, Smogorzewska, E. Monika, Brown, Berkley, Wang, Xiaoyan, de Oliveira, Satiro, Choi, Yeong, Ikeda, Alan, Terrazas, Dayna, Fu, Pei-Yu, Yu, Allen, Fernandez, Beatriz Campo, Cooper, Aaron R., Engel, Barbara, Podsakoff, Greg, Balamurugan, Arumugam, Anderson, Stacie, Muul, Linda, Jagadeesh, G. Jayashree, Kapoor, Neena, Tse, John, Moore, Theodore B., Purdy, Ken, Rishi, Radha, Mohan, Kathey, Skoda-Smith, Suzanne, Buchbinder, David, Abraham, Roshini S., Scharenberg, Andrew, Yang, Otto O., Cornetta, Kenneth, Gjertson, David, Hershfield, Michael, Sokolic, Rob, Candotti, Fabio, Kohn, Donald B.

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Lentiviral gene therapy for X-linked chronic granulomatous disease 由 Kohn, Donald B., Booth, Claire, Kang, Elizabeth M., Pai, Sung-Yun, Shaw, Kit L., Santilli, Giorgia, Armant, Myriam, Buckland, Karen F., Choi, Uimook, De Ravin, Suk See, Dorsey, Morna J., Kuo, Caroline Y., Leon-Rico, Diego, Rivat, Christine, Izotova, Natalia, Gilmour, Kimberly, Snell, Katie, Dip, Jinhua Xu-Bayford, Darwish, Jinan, Morris, Emma C., Terrazas, Dayna RN, Wang, Leo D., Bauser, Christopher A., Paprotka, Tobias, Kuhns, Douglas B., Gregg, John, Raymond, Hayley E., Everett, John K., Honnet, Geraldine, Biasco, Luca, Newburger, Peter E., Bushman, Frederic D., Grez, Manuel, Gaspar, H. Bobby, Williams, David A., Malech, Harry L., Galy, Anne, Thrasher, Adrian J.

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