David T. Curiel
Affiliations: | 1993-2011 | Medicine | University of Alabama, Birmingham, Birmingham, AL, United States |
| 2011- | Washington University, Saint Louis, St. Louis, MO |
Area:
vector development, gene therapy vaccine and virotherapy interventions.Website:
http://ocf.wustl.edu/research/cancerbio/curiel/people.aspxGoogle:
"David Terry Curiel" OR "David T Curiel"Bio:
http://btc.wustl.edu/people.html
https://radonc.wustl.edu/people/david-t-curiel-md-phd/
http://hdl.handle.net/11370/dcd8ddf3-011e-413e-8255-228db4f8108a
Mean distance: 20.95 (cluster 59)
Parents
Sign in to add mentor| Hidde J Haisma | grad student | 2002 | RUG (Cell Biology Tree) | |
| (Genetic capsid modification for adenovirus retargeting) | ||||
| Herbert Michael Pinedo | grad student | 2002 | RUG (Chemistry Tree) | |
Children
Sign in to add trainee| C. Ryan Miller | grad student | 1999 | UAB |
| Bryan W. Tillman | grad student | 2000 | UAB |
| Shannon D. Barker | grad student | 2002 | UAB |
| Joshua J. Short | grad student | 2004 | UAB |
| Vaibhav Saini | grad student | 2008 | UAB |
| Yizhe Tang | grad student | 2005-2009 | UAB |
| Lena J. Gamble | grad student | 2010 | UAB |
| Miho Murakami | grad student | 2010 | UAB |
| Matthew S. Beatty | grad student | 2013 | UAB |
BETA: Related publications
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Publications
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| Rice-Boucher PJ, Mendonça SA, Alvarez AB, et al. (2023) Adenoviral vectors infect B lymphocytes in vivo. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Lorincz R, Alvarez AB, Walkey CJ, et al. (2022) In vivo editing of the pan-endothelium by immunity evading simian adenoviral vector. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 158: 114189 |
| Lu ZH, Li J, Dmitriev IP, et al. (2022) Efficient Genome Editing Achieved via Plug-and-Play Adenovirus Piggyback Transport of Cas9/gRNA Complex on Viral Capsid Surface. Acs Nano |
| Collins LT, Curiel DT. (2021) Synthetic Biology Approaches for Engineering Next-Generation Adenoviral Gene Therapies. Acs Nano |
| Lee M, Lu ZH, Shoemaker CB, et al. (2021) Advanced genetic engineering to achieve in vivo targeting of adenovirus utilizing camelid single domain antibody. Journal of Controlled Release : Official Journal of the Controlled Release Society. 334: 106-113 |
| Gonzalez-Pastor R, Goedegebuure PS, Curiel DT. (2020) Understanding and addressing barriers to successful adenovirus-based virotherapy for ovarian cancer. Cancer Gene Therapy |
| Hassan AO, Kafai NM, Dmitriev IP, et al. (2020) A Single-Dose Intranasal ChAd Vaccine Protects Upper and Lower Respiratory Tracts against SARS-CoV-2. Cell |
| Boucher P, Cui X, Curiel DT. (2020) Adenoviral vectors for in vivo delivery of CRISPR-Cas gene editors. Journal of Controlled Release : Official Journal of the Controlled Release Society |
| Lorincz R, Curiel DT. (2020) Advances in Alpha-1 Antitrypsin Gene Therapy. American Journal of Respiratory Cell and Molecular Biology |
| Mooney R, Majid AA, Batalla-Covello J, et al. (2020) Erratum: Enhanced Delivery of Oncolytic Adenovirus by Neural Stem Cells for Treatment of Metastatic Ovarian Cancer. Molecular Therapy Oncolytics. 17: 508 |