Andrea L. Kasinski, Ph.D.
Affiliations: | 2009 | Biological and Biomedical Sciences | Emory University, Atlanta, GA |
Area:
Oncology, Pharmacology, GeneticsGoogle:
"Andrea Kasinski"Mean distance: (not calculated yet)
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| Puckett MC, Goldman EH, Cockrell LM, et al. (2022) Correction for Puckett et al., "Integration of Apoptosis Signal-Regulating Kinase 1-Mediated Stress Signaling with the Akt/Protein Kinase B-IκB Kinase Cascade". Molecular and Cellular Biology. e0028222 |
| Pal AS, Bains M, Agredo A, et al. (2020) Identification of microRNAs that promote erlotinib resistance in non-small cell lung cancer. Biochemical Pharmacology. 114154 |
| Orellana EA, Li C, Lisevick A, et al. (2019) Identification and validation of microRNAs that synergize with miR-34a - a basis for combinatorial microRNA therapeutics. Cell Cycle (Georgetown, Tex.). 1-14 |
| Zhou W, Pal AS, Hsu AY, et al. (2018) MicroRNA-223 Suppresses the Canonical NF-κB Pathway in Basal Keratinocytes to Dampen Neutrophilic Inflammation. Cell Reports. 22: 1810-1823 |
| Pal AS, Kasinski AL. (2017) Animal Models to Study MicroRNA Function. Advances in Cancer Research. 135: 53-118 |
| Orellana EA, Tenneti S, Rangasamy L, et al. (2017) FolamiRs: Ligand-targeted, vehicle-free delivery of microRNAs for the treatment of cancer. Science Translational Medicine. 9 |
| Gilbert-Ross M, Konen J, Koo J, et al. (2017) Targeting adhesion signaling in KRAS, LKB1 mutant lung adenocarcinoma. Jci Insight. 2: e90487 |
| Pal AS, Agredo A, Kasinski AL. (2017) Abstract 3142: Aberrantly expressed microRNAs drive the development of acquired Erlotinib resistance in non-small cell lung cancer Cancer Research. 77: 3142-3142 |
| Kasinski AL, Kelnar K, Stahlhut C, et al. (2015) A combinatorial microRNA therapeutics approach to suppressing non-small cell lung cancer. Oncogene. 34: 3547-55 |
| Adams BD, Kasinski AL, Slack FJ. (2014) Aberrant regulation and function of microRNAs in cancer. Current Biology : Cb. 24: R762-76 |