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Adegboyega K. Oyelere grad student 2013 Georgia Tech
 (New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists)
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Publications

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Garzón-Porras AM, Chory E, Gryder BE. (2022) Dynamic Opposition of Histone Modifications. Acs Chemical Biology
Ohguchi H, Park PMC, Wang T, et al. (2021) Lysine Demethylase 5A is Required for MYC Driven Transcription in Multiple Myeloma. Blood Cancer Discovery. 2: 370-387
Adelaiye-Ogala R, Gryder BE, Nguyen YTM, et al. (2020) Targeting the PI3K/AKT pathway overcomes enzalutamide resistance by inhibiting induction of the glucocorticoid receptor. Molecular Cancer Therapeutics
Gryder BE, Wu L, Woldemichael GM, et al. (2019) Chemical genomics reveals histone deacetylases are required for core regulatory transcription. Nature Communications. 10: 3004
Gryder BE, Akbashev MJ, Rood MK, et al. (2013) Selectively targeting prostate cancer with antiandrogen equipped histone deacetylase inhibitors. Acs Chemical Biology. 8: 2550-60
Gryder BE, Rood MK, Johnson KA, et al. (2013) Histone deacetylase inhibitors equipped with estrogen receptor modulation activity. Journal of Medicinal Chemistry. 56: 5782-96
Dreaden EC, Gryder BE, Austin LA, et al. (2012) Antiandrogen gold nanoparticles dual-target and overcome treatment resistance in hormone-insensitive prostate cancer cells. Bioconjugate Chemistry. 23: 1507-12
Gryder BE, Sodji QH, Oyelere AK. (2012) Targeted cancer therapy: giving histone deacetylase inhibitors all they need to succeed. Future Medicinal Chemistry. 4: 505-24
Patil V, Guerrant W, Chen PC, et al. (2010) Antimalarial and antileishmanial activities of histone deacetylase inhibitors with triazole-linked cap group. Bioorganic & Medicinal Chemistry. 18: 415-25
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