Research Faculty
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Henderson MC, Shaw YJ, Wang H, Han H, Hurley LH, Flynn G, Dorr RT, Von Hoff DD.
UA62784, a novel inhibitor of centromere protein E kinesin-like protein
Mol Cancer Ther, Jan;8(1):36-44. 2009.
Wang H, Stephens B, Von Hoff DD, Han H.
Identification and characterization of a novel anticancer agent with selectivity against deleted in pancreatic cancer locus 4 (DPC4)-deficient pancreatic and colon cancer cells
Pancreas, Jul;38(5):551-7. 2009.
Stephens B, Han H, Hostetter G, Demeure MJ, Von Hoff DD.
Small interfering RNA-mediated knockdown of PRL phosphatases results in altered Akt phosphorylation and reduced clonogenicity of pancreatic cancer cells
Mol Cancer Ther, Jan;7(1):202-10. 2008.
Baker AF, Koh MY, Williams RR, James B, Wang H, Tate WR, Gallegos A, Von Hoff DD, Han H, Powis G.
Identification of thioredoxin-interacting protein 1 as a hypoxia-inducible factor 1alpha-induced gene in pancreatic cancer
Pancreas, Mar;36(2):178-86. 2008.
Balagurunathan Y, Morse DL, Hostetter G, Shanmugam V, Stafford P, Shack S, Pearson J, Trissal M, Demeure MJ, Von Hoff DD, Hruby VJ, Gillies RJ, Han H.
Gene expression profiling-based identification of cell-surface targets for developing multimeric ligands in pancreatic cancer
Mol Cancer Ther., Sep;7(9):3071-80. 2008.
Warner SL, Muñoz RM, Bearss DJ, Grippo P, Han H, Von Hoff DD.
Pdx-1-driven overexpression of aurora a kinase induces mild ductal dysplasia of pancreatic ducts near islets in transgenic mice
Pancreas, Oct;37(3):e39-44.. 2008.
Chen S, Auletta T, Dovirak O, Hutter C, Kuntz K, El-Ftesi S, Kendall J, Han H, Von Hoff DD, Ashfaq R, Maitra A, Iacobuzio-Donahue CA, Hruban RH, Lucito R.
Copy number alterations in pancreatic cancer identify recurrent PAK4 amplification
Cancer Biol Ther, Nov 21;7(11). 2008.
Zhu M, Gokhale VM, Szabo L, Munoz RM, Baek H, Bashyam S, Hurley LH, Von Hoff DD, Han H.
Identification of a novel inhibitor of urokinase-type plasminogen activator
Mol Cancer Ther, Apr;6(4):1348-56. 2007.
Wang H, Han H, Mousses S, Von Hoff DD.
Targeting loss-of-function mutations in tumor-suppressor genes as a strategy for development of cancer therapeutic agents
Semin Oncol, Aug;33(4):513-20. 2006.
Warner SL, Bashyam S, Vankayalapati H, Bearss DJ, Han H, Mahadevan D, Von Hoff DD, Hurley LH.
Identification of a lead small-molecule inhibitor of the Aurora kinases using a structure-assisted, fragment-based approach
Mol Cancer Ther, Jul;5(7):1764-73.. 2006.
Han H, Von Hoff DD.
Aurora sheds light on head and neck squamous cell carcinoma
Clin Cancer Res, Sep 1;12(17):5003-4. 2006.
Wang H, Han H, Von Hoff DD.
Identification of an agent selectively targeting DPC4 (deleted in pancreatic cancer locus 4)-deficient pancreatic cancer cells
Cancer Res, Oct 1;66(19):9722-30. 2006.
Warner SL, Munoz RM, Stafford P, Koller E, Hurley LH, Von Hoff DD, Han H.
Comparing Aurora A and Aurora B as molecular targets for growth inhibition of pancreatic cancer cells
Mol Cancer Ther, Oct;5(10):2450-8. 2006.
Stephens BJ, Han H, Gokhale V, Von Hoff DD.
PRL phosphatases as potential molecular targets in cancer
Mol Cancer Ther, Nov;4(11):1653-61. 2005.
J. P. Gray, Jr, D. J. Bearss, H. Han, R. Nagle, M. Tsao, N. Dean, and D. D. Von Hoff.
Identification of Human Polo-like Kinase 1 as a Potential Therapeutic Target in Pancreatic Cancer.
Mol Cancer Ther, 3: 641-646. 2004.
S. Rojanala, H. Han, R. M. Munoz, W. Browne, R. Nagle and D. D. Von Hoff, D. J. Bearss.
The Mitotic Serine Threonine Kinase, Aurora-2, is a Potential Target for Drug Development in Human Pancreatic Cancer.
Mol. Cancer Ther., 3, 451-457. 2004.
S. L. Warner, D. J. Bearss, H. Han, D. D. Von Hoff.
Targeting aurora-2 kinase in cancer.
Mol. Cancer Ther., 2, 589-595. 2003.
H. Han, D. J. Bearss and L. W. Browne, R. Calaluce, R. B. Nagle, D. D. Von Hoff.
Identification of Genes Differentially Expressed in Pancreatic Cancer Cells Using cDNA Microarray.
Cancer Res., 62, 2890-2896. 2002.
C. L. Grand, H. Han, R. M. Munoz, S. Weitman, D. D. Von Hoff, L. H. Hurley, and D. J. Bearss.
The Cationic Porphyrin TMPyP4 Downregulates c-MYC and hTERT Expression and Inhibits Tumor Growth in vivo.
Mol. Cancer Ther., 1, 565-573. 2002.
H. Han, D. R. Langley, A. Rangan, L. H. Hurley.
Selective Interaction of Cationic Porphyrins with Different Types of G-Quadruplex Structures.
J. Am. Chem. Soc., 123, 8902-8913. 2001.
Duan W, Rangan A, Vankayalapati H, Kim MY, Zeng Q, Sun D, Han H, Fedoroff OY, Nishioka D, Rha SY, Izbicka E, Von Hoff DD, Hurley LH.
Design and synthesis of fluoroquinophenoxazines that interact with human telomeric G-quadruplexes and their biological effects
Mol Cancer Ther, Dec;1(2):103-20. 2001.
H. Han, L. H. Hurley.
G-quadruplex: a Potential Target for Anticancer Drug Design.
Trends Pharmacol. Sci., 21, 136-142. 2000.
Han H, Bennett RJ, Hurley LH.
Inhibition of unwinding of G-quadruplex structures by Sgs1 helicase in the presence of N,N'-bis[2-(1-piperidino)ethyl]-3,4,9,10-perylenetetracarboxylic diimide, a G-quadruplex-interactive ligand
Biochemistry, Aug 8;39(31):9311-6. 2000.
Hurley LH, Wheelhouse RT, Sun D, Kerwin SM, Salazar M, Fedoroff OY, Han FX, Han H, Izbicka E, Von Hoff DD.
G-quadruplexes as targets for drug design
Pharmacol Ther, Mar;85(3):141-58. 2000.
Han H, Hurley LH, Salazar M.
A DNA polymerase stop assay for G-quadruplex-interactive compounds
Nucleic Acids Res, Jan 15;27(2):537-42. 1999.
Han H, Cliff CL, Hurley LH.
Accelerated assembly of G-quadruplex structures by a small molecule
Biochemistry, Jun 1;38(22):6981-6. 1999.
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