Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Snehal Rane"'
Publikováno v:
International Research Journal of Multidisciplinary Scope. 1:1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4c3cf20ddbd7407cfe56f795e1e2861
https://doi.org/10.47857/irjms.2020.v01i03.013
https://doi.org/10.47857/irjms.2020.v01i03.013
Autor:
Akhila Gollakota, Snehal Rane, Charles H. Jones, Tai-Chun Chung, Blaine A. Pfeifer, Guojian Zhang, Mahmoud Kamal Ahmadi
Publikováno v:
Mol Pharm
Bactofection offers a gene delivery option particularly useful in the context of immune modulation. The bacterial host naturally attracts recognition and cellular uptake by antigen presenting cells (APCs) as the initial step in triggering an immune r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00011a551a57af8374b725a5c02dcba3
https://doi.org/10.1021/acs.molpharmaceut.5b00172
https://doi.org/10.1021/acs.molpharmaceut.5b00172
Autor:
Snehal Rane, Mingfu Chen, Charles H. Jones, Anders Håkansson, Anitha Ravikrishnan, Mahmoud Kamal Ahmadi, Blaine A. Pfeifer, Ryan M. Reddinger
Publikováno v:
Proceedings of the National Academy of Sciences. 111:12360-12365
Genetic vaccines offer a treatment opportunity based upon successful gene delivery to specific immune cell modulators. Driving the process is the vector chosen for gene cargo packaging and subsequent delivery to antigen-presenting cells (APCs) capabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4071f319469157b21686270f4c780937
https://doi.org/10.1073/pnas.1411355111
https://doi.org/10.1073/pnas.1411355111
Publikováno v:
Molecular Pharmaceutics. 10:4082-4098
A key end goal of gene delivery research is to develop clinically-relevant vectors that can be used to combat elusive diseases such as AIDS. Despite promising engineering strategies, efficiency and ultimately gene modulation efficacy of nonviral vect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10ef4e4648cfd3347bfb170055b4367a
https://doi.org/10.1021/mp400467x
https://doi.org/10.1021/mp400467x
Autor:
Charles H. Jones, Snehal Rane, Chih-Kuang Chen, Anitha Ravikrishnan, Emily Patt, Blaine A. Pfeifer, Chong Cheng
Improvements to bacterial vectors have resulted in non-viral gene therapy vehicles that are easily prepared and can achieve high levels of transfection efficacy. However, these vectors are plagued by potential cytotoxicity and immunogenicity, prompti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cbc6c19fc45581d4ee94220fdf488c9
https://europepmc.org/articles/PMC5232419/
https://europepmc.org/articles/PMC5232419/
