Search Results - "KASHENTSEVA, Elena"

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    Efficient Genome Editing Achieved via Plug-and-Play Adenovirus Piggyback Transport of Cas9/gRNA Complex on Viral Capsid Surface by Lu, Zhi Hong, Li, Jie, Dmitriev, Igor P., Kashentseva, Elena A., Curiel, David T.

    Published in ACS nano (26-07-2022)
    “…The capacity to efficiently deliver the gene-editing enzyme complex to target cells is favored over other forms of gene delivery as it offers one-time…”
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    Journal Article
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    Long-term correction of hemophilia B using adenoviral delivery of CRISPR/Cas9 by Stephens, Calvin J., Lauron, Elvin J., Kashentseva, Elena, Lu, Zhi Hong, Yokoyama, Wayne M., Curiel, David T.

    Published in Journal of controlled release (28-03-2019)
    “…Hemophilia B (HB) is a life-threatening inherited disease caused by mutations in the FIX gene, leading to reduced protein function and abnormal blood clotting…”
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    Targeted in vivo knock-in of human alpha-1-antitrypsin cDNA using adenoviral delivery of CRISPR/Cas9 by Stephens, Calvin J., Kashentseva, Elena, Everett, William, Kaliberova, Lyudmila, Curiel, David T.

    Published in Gene therapy (01-04-2018)
    “…Serum deficiency diseases such as alpha-1-antitrypsin deficiency are characterized by reduced function of serum proteins, caused by deleterious genetic…”
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    Prolonged prophylactic protection from botulism with a single adenovirus treatment promoting serum expression of a VHH-based antitoxin protein by Mukherjee, Jean, Dmitriev, Igor, Debatis, Michelle, Tremblay, Jacqueline M, Beamer, Gillian, Kashentseva, Elena A, Curiel, David T, Shoemaker, Charles B

    Published in PloS one (29-08-2014)
    “…Current therapies for most acute toxin exposures are limited to administration of polyclonal antitoxin serum. We have shown that VHH-based neutralizing agents…”
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    Adenoviral vectors infect B lymphocytes in vivo by Rice-Boucher, Paul J., Mendonça, Samir Andrade, Alvarez, Aluet Borrego, Sturtz, Alexandria J., Lorincz, Reka, Dmitriev, Igor P., Kashentseva, Elena A., Lu, Zhi Hong, Romano, Rosa, Selby, Mark, Pingale, Kunal, Curiel, David T.

    Published in Molecular therapy (06-09-2023)
    “…B cells are the antibody-producing arm of the adaptive immune system and play a critical role in controlling pathogens. Several groups have now demonstrated…”
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    A Gorilla Adenovirus-Based Vaccine against Zika Virus Induces Durable Immunity and Confers Protection in Pregnancy by Hassan, Ahmed O., Dmitriev, Igor P., Kashentseva, Elena A., Zhao, Haiyan, Brough, Douglas E., Fremont, Daved H., Curiel, David T., Diamond, Michael S.

    Published in Cell reports (Cambridge) (03-09-2019)
    “…The teratogenic potential of Zika virus (ZIKV) has made the development of an effective vaccine a global health priority. Here, we generate two gorilla…”
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    A New Gorilla Adenoviral Vector with Natural Lung Tropism Avoids Liver Toxicity and Is Amenable to Capsid Engineering and Vector Retargeting by Lu, Zhi Hong, Dmitriev, Igor P, Brough, Douglas E, Kashentseva, Elena A, Li, Jie, Curiel, David T

    Published in Journal of virology (04-05-2020)
    “…Human adenoviruses have many attractive features for gene therapy applications. However, the high prevalence of preexisting immunity against these viruses in…”
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    Journal Article
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    Engineering a Novel Modular Adenoviral mRNA Delivery Platform Based on Tag/Catcher Bioconjugation by Geng, Kexin, Rice-Boucher, Paul J, Kashentseva, Elena A, Dmitriev, Igor P, Lu, Zhi Hong, Goedegebuure, S Peter, Gillanders, William E, Curiel, David T

    Published in Viruses (01-11-2023)
    “…mRNA vaccines have attracted widespread research attention with clear advantages in terms of molecular flexibility, rapid development, and potential for…”
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    Targeting Tumor Neoangiogenesis via Targeted Adenoviral Vector to Achieve Effective Cancer Gene Therapy for Disseminated Neoplastic Disease by Lee, Myungeun, Lu, Zhi Hong, Li, Jie, Kashentseva, Elena A, Dmitriev, Igor P, Mendonca, Samir A, Curiel, David T

    Published in Molecular cancer therapeutics (01-03-2020)
    “…The application of cancer gene therapy has heretofore been restricted to local, or locoregional, neoplastic disease contexts. This is owing to the lack of gene…”
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    A Plasmodium Promiscuous T Cell Epitope Delivered within the Ad5 Hexon Protein Enhances the Protective Efficacy of a Protein Based Malaria Vaccine by Fonseca, Jairo Andres, Cabrera-Mora, Monica, Kashentseva, Elena A, Villegas, John Paul, Fernandez, Alejandra, Van Pelt, Amelia, Dmitriev, Igor P, Curiel, David T, Moreno, Alberto

    Published in PloS one (29-04-2016)
    “…A malaria vaccine is a public health priority. In order to produce an effective vaccine, a multistage approach targeting both the blood and the liver stage…”
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    Advanced genetic engineering to achieve in vivo targeting of adenovirus utilizing camelid single domain antibody by Lee, Myungeun, Lu, Zhi Hong, Shoemaker, Charles B., Tremblay, Jacqueline M., St. Croix, Bradley, Seaman, Steven, Gonzalez-Pastor, Rebeca, Kashentseva, Elena A., Dmitriev, Igor P., Curiel, David T.

    Published in Journal of controlled release (10-06-2021)
    “…For the developing field of gene therapy the successful address of the basic requirement effective gene delivery has remained a critical barrier. In this…”
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    Development of an adenovirus vector vaccine platform for targeting dendritic cells by Sharma, Piyush K., Dmitriev, Igor P., Kashentseva, Elena A., Raes, Geert, Li, Lijin, Kim, Samuel W., Lu, Zhi-Hong, Arbeit, Jeffrey M., Fleming, Timothy P., Kaliberov, Sergey A., Goedegebuure, S. Peter, Curiel, David T., Gillanders, William E.

    Published in Cancer gene therapy (01-02-2018)
    “…Adenoviral (Ad) vector vaccines represent one of the most promising modern vaccine platforms, and Ad vector vaccines are currently being investigated in human…”
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