Y. Zhu

发表

Anti-Hepatitis B Virus Activity and Metabolism of 2′,3′-Dideoxy-2′,3′-Didehydro-β-l(−)-5-Fluorocytidine

Shwu-Huey Liu, E. Bridges, G. Dutschman, 1998, Antimicrobial Agents and Chemotherapy.

Anti-human immunodeficiency and anti-hepatitis B virus activities of β-l-2′,3′-dideoxy purine nucleosides

R. Schinazi, C. K. Chu, Ju-sheng Lin, 1996 .

Design and Synthesis of 2‘,3‘-Dideoxy- 2‘,3‘-didehydro-β-l-cytidine (β-l-d4C) and 2‘,3‘-Dideoxy-2‘,3‘-didehydro-β-l-5- fluorocytidine (β-l-Fd4C), Two Exceptionally Potent Inhibitors of Human Hepatitis B Virus (HBV) and Potent Inhibitors of Human Immunodeficiency Virus (HIV) in Vitro

E. Gullen, G. Dutschman, Tai-shun Lin, 1996 .

Antitumor sulfonylhydrazines: design, structure-activity relationships, resistance mechanisms, and strategies for improving therapeutic utility.

A. Sartorelli, R. Finch, R. Baumann, 2015, Journal of medicinal chemistry.

Studies of the Pharmacokinetics and Toxicology of 2′,3′-Dideoxy-β-L-5-fluorocytidine (β-L-FddC) and 2′,3′-Dideoxy-β-L-cytidine (β-L-ddC) In Vivo; and Synthesis and Antiviral Evaluations of 2′,3′-Dideoxy-β-L-5-azacytidine

G. Dutschman, S. Pai, M. Luo, 1995 .

Dioxolane cytosine nucleosides as anti-hepatitis B agents

M. Chun, C. K. Chu, S. Pai, 1995 .

Quantitative relationship between guanine O6-alkyl lesions produced by OnriginTM and tumor resistance by O6-alkylguanine- DNA alkyltransferase

A. Sartorelli, P. Penketh, K. Shyam, 2010 .

Triapine potentiates platinum-based combination therapy by disruption of homologous recombination repair

E. Ratner, A. Sartorelli, Z. Lin, 2016, British Journal of Cancer.

Distinct mechanisms of cell-kill by triapine and its terminally dimethylated derivative Dp44mT due to a loss or gain of activity of their copper(II) complexes.

E. Ratner, A. Sartorelli, T. Rutherford, 2014, Biochemical pharmacology.

In silico screening identifies a novel small molecule inhibitor that counteracts PARP inhibitor resistance in ovarian cancer

E. Ratner, Z. Lin, Nicole E. Bowen, 2021, Scientific Reports.

Cataloging antineoplastic agents according to their effectiveness against platinum-resistant and platinum-sensitive ovarian carcinoma cell lines.

E. Ratner, A. Sartorelli, T. Rutherford, 2016, Journal of translational science.

Prolonged retention after aggregation into secretory granules of human R183H-growth hormone (GH), a mutant that causes autosomal dominant GH deficiency type II.

M. Waters, B. Conway-Campbell, P. Dannies, 2002, Endocrinology.

Acquisition of Lubrol Insolubility, a Common Step for Growth Hormone and Prolactin in the Secretory Pathway of Neuroendocrine Cells*

P. Dannies, J. E. Chang, Y. Zhu, 2001, The Journal of Biological Chemistry.

Combination of triapine, olaparib, and cediranib suppresses progression of BRCA-wild type and PARP inhibitor-resistant epithelial ovarian cancer

P. LoRusso, E. Ratner, Z. Lin, 2018, PloS one.

Disruption of cAMP and Prostaglandin E2 Transport by Multidrug Resistance Protein 4 Deficiency Alters cAMP-Mediated Signaling and Nociceptive Response

S. Waxman, B. C. Hains, A. Sartorelli, 2007, Molecular Pharmacology.

Disruption of cAMP and PGE 2 Transport by Mrp4 Deficiency Alters cAMP-mediated Signaling and Nociceptive Response Fast

S. Waxman, A. Sartorelli, Z. Lin, 2007 .

Aggregation and lack of secretion of most newly synthesized proinsulin in non-beta-cell lines.

J. Gesmonde, W. Zawalich, K. Zawalich, 2004, Endocrinology.

Accumulation of synaptosomal-associated protein of 25 kDa (SNAP-25) and other proteins associated with the secretory pathway in GH4C1 cells upon treatment with estradiol, insulin, and epidermal growth factor.

A. Jeromin, P. Dannies, H. Rhee, 2000, Endocrinology.

Antitumor sulfonylhydrazines: design, structure-activity relationships, resistance mechanisms, and strategies for improving therapeutic utility.

A. Sartorelli, R. Finch, R. Baumann, 2015, Journal of medicinal chemistry.

Aggregation of Human Wild-Type and H27A-Prolactin in Cells and in Solution: Roles of Zn 2 (cid:1) , Cu 2 (cid:1) , and pH

M. Hodsdon, E. Lolis, P. Dannies, 2002 .