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Your search keyword '"Saljoughian, Noushin"' showing total 8 results
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8 results on '"Saljoughian, Noushin"'

2. Pseudomonas aeruginosa pulmonary infection results in S100A8/A9-dependent cardiac dysfunction

Author

Kumar, Naresh, primary, Pestrak, Matthew J., additional, Wu, Qian, additional, Ahumada, Omar Santiagonunez, additional, Dellos-Nolan, Sheri, additional, Saljoughian, Noushin, additional, Shukla, Rajni Kant, additional, Mitchem, Cortney F., additional, Nagareddy, Prabhakara R., additional, Ganesan, Latha P., additional, William, Lafuse P., additional, Wozniak, Daniel J., additional, and Rajaram, Murugesan V. S., additional

Published
2023
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4. Pseudomonas aeruginosapulmonary infection results in S100A8/9-dependent cardiac dysfunction

Author

Rajaram, Murugesan, primary, Kumar, Naresh, additional, Pestrak, Matthew, additional, Wu, Qian, additional, Ahumada, Omar, additional, Saljoughian, Noushin, additional, Shukla, Rajnikant, additional, Mitchem, Cortney, additional, Nagareddy, Prabhakara, additional, William, Lafuse, additional, Ganesan, Latha, additional, and Wozniak, Daniel J, additional

Published
2023
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6. Pseudomonas aeruginosa pulmonary infection results in S100A8/A9-dependent cardiac dysfunction

Author

Rajaram, Murugesan, primary, Kumar, Naresh, additional, Pestrak, Matthew, additional, Wu, Qian, additional, Ahumada, Omar Santiagonunez, additional, Dellos-Nolan, Sheri, additional, Saljoughian, Noushin, additional, Shukla, Rajnikant, additional, Mitchem, Cortney, additional, Nagareddy, Prabhakara, additional, Ganesan, Latha Prabha, additional, Lafuse, William, additional, and Wozniak, Daniel, additional

Published
2022
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8. CRISPR Gene Editing of Human Primary NK and T Cells for Cancer Immunotherapy

Author

Elmas, Ezgi, Saljoughian, Noushin, de Souza Fernandes Pereira, Marcelo, Tullius, Brian P., Sorathia, Kinnari, Nakkula, Robin J., Lee, Dean A., and Naeimi Kararoudi, Meisam

Subjects
Cancer Research, Oncology
Abstract

Antitumor activity of immune cells such as T cells and NK cells has made them auspicious therapeutic regimens for adaptive cancer immunotherapy. Enhancing their cytotoxic effects against malignancies and overcoming their suppression in tumor microenvironment (TME) may improve their efficacy to treat cancers. Clustered, regularly interspaced short palindromic repeats (CRISPR) genome editing has become one of the most popular tools to enhance immune cell antitumor activity. In this review we highlight applications and practicability of CRISPR/Cas9 gene editing and engineering strategies for cancer immunotherapy. In addition, we have reviewed several approaches to study CRISPR off-target effects.

Published
2021

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