David T. Curiel

Medicine University of Alabama, Birmingham, Birmingham, AL, United States 
"David Curiel"
Mean distance: 20.95 (cluster 59)


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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
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Lu ZH, Dmitriev IP, Brough DE, et al. (2020) A new gorilla adenoviral vector with natural lung tropism avoids liver toxicity and is amenable for capsid engineering and vector retargeting. Journal of Virology
Lee M, Lu ZH, Li J, et al. (2020) Targeting tumor neoangiogenesis via targeted adenoviral vector to achieve effective cancer gene therapy for disseminated neoplastic disease. Molecular Cancer Therapeutics
Broeckel RM, Haese N, Ando T, et al. (2019) Vaccine-Induced Skewing of T Cell Responses Protects Against Chikungunya Virus Disease. Frontiers in Immunology. 10: 2563
Hassan AO, Dmitriev IP, Kashentseva EA, et al. (2019) A Gorilla Adenovirus-Based Vaccine against Zika Virus Induces Durable Immunity and Confers Protection in Pregnancy. Cell Reports. 28: 2634-2646.e4
Stephens CJ, Lauron EJ, Kashentseva E, et al. (2019) Long-term correction of hemophilia B using adenoviral delivery of CRISPR/Cas9. Journal of Controlled Release : Official Journal of the Controlled Release Society
González-Pastor R, Ashshi AM, El-Shemi AG, et al. (2019) Defining a murine ovarian cancer model for the evaluation of conditionally-replicative adenovirus (CRAd) virotherapy agents. Journal of Ovarian Research. 12: 18
Chondronasiou D, Eisden TTHD, Stam AGM, et al. (2018) Improved Induction of Anti-Melanoma T Cells by Adenovirus-5/3 Fiber Modification to Target Human DCs. Vaccines. 6
Fonseca JA, McCaffery JN, Caceres J, et al. (2018) Inclusion of the murine IgGκ signal peptide increases the cellular immunogenicity of a simian adenoviral vectored Plasmodium vivax multistage vaccine. Vaccine
Stephens CJ, Kashentseva E, Everett W, et al. (2018) Targeted in vivo knock-in of human alpha-1-antitrypsin cDNA using adenoviral delivery of CRISPR/Cas9. Gene Therapy
Kuroki LM, Jin X, Dmitriev IP, et al. (2017) Adenovirus platform enhances transduction efficiency of human mesenchymal stem cells: An opportunity for cellular carriers of targeted TRAIL-based TR3 biologics in ovarian cancer. Plos One. 12: e0190125
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