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Dan Wang
Dan Wang
Assistant Professor, RNA Therapeutics Institute & Gene Therapy Center, University of Massachusetts
Verified email at umassmed.edu - Homepage
Title
Cited by
Cited by
Year
Adeno-associated virus vector as a platform for gene therapy delivery
D Wang, PWL Tai, G Gao
Nature Reviews Drug Discovery 18 (5), 358-378, 2019
16642019
Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses
D Wang, H Mou, S Li, Y Li, S Hough, K Tran, J Li, H Yin, DG Anderson, ...
Human gene therapy 26 (7), 432-442, 2015
3832015
CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors
D Wang, F Zhang, G Gao
Cell 181 (1), 136-150, 2020
3442020
AMH/MIS as a contraceptive that protects the ovarian reserve during chemotherapy
M Kano, AE Sosulski, LH Zhang, HD Saatcioglu, D Wang, N Nagykery, ...
Proceedings of the National Academy of Sciences 114 (9), E1688-E1697, 2017
1902017
AMH/MIS as a contraceptive that protects the ovarian reserve during chemotherapy
M Kano, AE Sosulski, LH Zhang, HD Saatcioglu, D Wang, N Nagykery, ...
Proceedings of the National Academy of Sciences 114 (9), E1688-E1697, 2017
1902017
State-of-the-art human gene therapy: part Ii. gene therapy strategies and applications
D Wang, G Gao
Discovery medicine 18 (98), 151, 2014
1272014
The potential of adeno-associated viral vectors for gene delivery to muscle tissue
D Wang, L Zhong, MA Nahid, G Gao
Expert opinion on drug delivery 11 (3), 345-364, 2014
1232014
Suppression of premature termination codons as a therapeutic approach
KM Keeling, D Wang, SE Conard, DM Bedwell
Critical reviews in biochemistry and molecular biology 47 (5), 444-463, 2012
1232012
State-of-the-art human gene therapy: part I. Gene delivery technologies
D Wang, G Gao
Discovery medicine 18 (97), 67, 2014
1182014
Short DNA hairpins compromise recombinant adeno-associated virus genome homogeneity
J Xie, Q Mao, PWL Tai, R He, J Ai, Q Su, Y Zhu, H Ma, J Li, S Gong, ...
Molecular Therapy 25 (6), 1363-1374, 2017
1112017
Attenuation of nonsense-mediated mRNA decay enhances in vivo nonsense suppression
KM Keeling, D Wang, Y Dai, S Murugesan, B Chenna, J Clark, ...
PloS one 8 (4), e60478, 2013
1092013
The designer aminoglycoside NB84 significantly reduces glycosaminoglycan accumulation associated with MPS I-H in the Idua-W392X mouse
D Wang, V Belakhov, J Kandasamy, T Baasov, SC Li, YT Li, DM Bedwell, ...
Molecular genetics and metabolism 105 (1), 116-125, 2012
932012
Streamlined ex vivo and in vivo genome editing in mouse embryos using recombinant adeno-associated viruses
Y Yoon, D Wang, PWL Tai, J Riley, G Gao, JA Rivera-Pérez
Nature Communications 9 (1), 412, 2018
832018
Bone-targeting AAV-mediated silencing of Schnurri-3 prevents bone loss in osteoporosis
YS Yang, J Xie, D Wang, JM Kim, PWL Tai, E Gravallese, G Gao, JH Shim
Nature Communications 10 (1), 2958, 2019
782019
In Vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT Deficiency
CQ Song, D Wang, T Jiang, K O'Connor, Q Tang, L Cai, X Li, Z Weng, ...
Human gene therapy 29 (8), 853-860, 2018
752018
CNS-restricted transduction and CRISPR/Cas9-mediated gene deletion with an engineered AAV vector
G Murlidharan, K Sakamoto, L Rao, T Corriher, D Wang, G Gao, ...
Molecular Therapy-Nucleic Acids 5, 2016
752016
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation
D Wang, C Shukla, X Liu, TR Schoeb, LA Clarke, DM Bedwell, ...
Molecular genetics and metabolism 99 (1), 62-71, 2010
742010
Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo
R Ibraheim, PWL Tai, A Mir, N Javeed, J Wang, TC Rodríguez, ...
Nature communications 12 (1), 6267, 2021
612021
AAV9 delivering a modified human Mullerian inhibiting substance as a gene therapy in patient-derived xenografts of ovarian cancer
D Pépin, A Sosulski, L Zhang, D Wang, V Vathipadiekal, K Hendren, ...
Proceedings of the National Academy of Sciences 112 (32), E4418-E4427, 2015
612015
AAV-delivered suppressor tRNA overcomes a nonsense mutation in mice
J Wang, Y Zhang, CA Mendonca, O Yukselen, K Muneeruddin, L Ren, ...
Nature 604 (7905), 343-348, 2022
552022
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