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Timothy L. Ratliff

Researcher at Purdue University

Publications -  312
Citations -  20541

Timothy L. Ratliff is an academic researcher from Purdue University. The author has contributed to research in topics: Prostate cancer & Cancer. The author has an hindex of 69, co-authored 306 publications receiving 19092 citations. Previous affiliations of Timothy L. Ratliff include University of Iowa Hospitals and Clinics & Beth Israel Deaconess Medical Center.

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Folate Receptor Beta Designates Immunosuppressive Tumor-Associated Myeloid Cells that Can Be Reprogrammed with Folate-Targeted Drugs.

TL;DR: The data reveal a broadly applicable strategy across tumor types for reprogramming MDSCs and TAMs into antitumorigenic immune cells using a drug that would otherwise be too toxic to administer systemically and establish FRβ as the first marker that distinguishes immunosuppressive from nonimmunosuppression subsets of M DSCs and AMs.
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Strategy for improving therapy of superficial bladder cancer

TL;DR: It is believed that BCG is the current "gold standard" for the treatment of superficial bladder cancer; as such, improvements in BCG therapy would constitute improvement in the treatment and/or developing alternative therapeutic approaches.
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1α, 25 Dihydroxyvitamin D (1,25(OH)2D) inhibits the T cell suppressive function of myeloid derived suppressor cells (MDSC)

TL;DR: The data suggest that activation of vitamin D signaling could be used to suppress MDSC function and release a constraint on T-cell mediated clearance of TU cells.
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Cell-intrinsic abrogation of TGF-β signaling delays but does not prevent dysfunction of self/tumor-specific CD8 T cells in a murine model of autochthonous prostate cancer

TL;DR: It is found that persistence and antitumor activity of adoptively transferred effector T cells deficient in TGF-β signaling were significantly improved in the cancerous prostate, however, over time, despite persistence in peripheral lymphoid organs, the numbers of transferred cells in the prostate decreased and the residual prostate-infiltrating T cells were no longer functional.
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Evaluation of gene transfer efficiency by viral vectors to murine bladder epithelium

TL;DR: Significant differences in gene expression are achieved by varying physical parameters during intravesical instillation, and increased gene expression associated with larger volume instillation may be responsible for some reported variability of gene transfer to the bladder.