Gina L. Razidlo, Ph.D.
Affiliations: | 2005 | University of Nebraska Medical Center, Omaha, NE, United States |
Area:
Molecular BiologyGoogle:
"Gina Razidlo"Parents
Sign in to add mentor| Robert E. Lewis | grad student | 2005 | University of Nebraska Medical Center | |
| (Proliferative control by KSR1 in response to growth factors and DNA damage.) | ||||
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Publications
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| Gutierrez-Ruiz OL, Johnson KM, Krueger EW, et al. (2023) Ectopic expression of DOCK8 regulates lysosome-mediated pancreatic tumor cell invasion. Cell Reports. 42: 113042 |
| Rozeveld CN, Johnson KM, Zhang L, et al. (2020) KRAS controls pancreatic cancer cell lipid metabolism and invasive potential through the lipase HSL. Cancer Research |
| Burton KM, Cao H, Chen J, et al. (2020) Dynamin 2 interacts with alpha-actinin 4 to drive tumor cell invasion. Molecular Biology of the Cell. mbcE19070395 |
| Rozeveld C, Schulze R, Zhang L, et al. (2019) Abstract PR09: KRas modulates pancreatic cancer cell metabolism and invasive potential through the lipase HSL Cancer Research. 79 |
| Razidlo GL, Johnson HJ, Stoeger SM, et al. (2018) Correction: KSR1 is required for cell cycle reinitiation following DNA damage. The Journal of Biological Chemistry. 293: 19136 |
| Qiang L, Cao H, Chen J, et al. (2018) Pancreatic tumor cell metastasis is restricted by MT1-MMP binding protein MTCBP-1. The Journal of Cell Biology |
| Razidlo GL, Burton KM, McNiven MA. (2018) Interleukin-6 promotes pancreatic cancer cell migration by rapidly activating the small GTPase CDC42. The Journal of Biological Chemistry |
| Boddicker RL, Razidlo GL, Feldman AL. (2016) Genetic alterations affecting GTPases and T-cell receptor signaling in peripheral T-cell lymphomas. Small Gtpases. 0 |
| Boddicker RL, Razidlo GL, Dasari S, et al. (2016) Integrated mate-pair and RNA sequencing identifies novel, targetable gene fusions in peripheral T-cell lymphoma. Blood |
| Cao H, Eppinga RD, Razidlo GL, et al. (2015) Stromal fibroblasts facilitate cancer cell invasion by a novel invadopodia-independent matrix degradation process. Oncogene |