Todd W Miller, PhD
Title(s)
Adjunct Professor of Molecular and Systems Biology
Additional Titles/Positions/Affiliations
Co-Director, Cancer Signaling, Genomes & Networks Research Program, Dartmouth Cancer Center
Scientific Director, Comprehensive Breast Program, Dartmouth Cancer Center
Co-Director, Molecular Tumor Board, Dartmouth Cancer Center
Department(s)
Molecular and Systems Biology
Education
University of Connecticut (Storrs, CT), B.S., Physiology & Neurobiology, 1998
University at Albany (Albany, NY), Ph.D. in Biomedical Sciences, 2004
Vanderbilt University (Nashville, TN), Post-doctoral Fellowship in Breast Cancer, 2004-2009
Programs
Molecular and Cellular Biology Graduate Programs
Dartmouth Cancer Center
Websites
Lab website:
https:
Publications:
http:
Academic Analytics
View Profile
Contact Information
1 Medical Center Drive
Rubin Bldg, HB 7936
Lebanon NH 03756
Office: Rubin 604
Phone: 603-646-5507
Email: Todd.W.Miller@Dartmouth.edu
Professional Interests
Breast cancer, targeted therapeutics, signaling pathways, drug resistance, biomarker development
Biography
Dr. Miller received his B.S. in Physiology and Neurobiology at the University of Connecticut in 1998, and his Ph.D. in Biomedical Sciences at the State University of New York at Albany in 2004 (thesis: Immunization and single-chain Fv intrabody gene therapies for Huntington’s Disease). He did his postdoctoral training at Vanderbilt University (2004-2009), and served as a Research Faculty member 2009-2012. Dr. Miller joined the Geisel School of Medicine at Dartmouth in 2012.
Pharmacological induction of chromatin remodeling drives chemosensitization in triple-negative breast cancer. TRIM33 Is a Co-Regulator of Estrogen Receptor Alpha. Alteration of DNA methyltransferases by eribulin elicits broad DNA methylation changes with potential therapeutic implications for triple-negative breast cancer. Estrogen Therapy Induces Receptor-Dependent DNA Damage Enhanced by PARP Inhibition in ER+ Breast Cancer. Alteration of DNMT1/DNMT3A by eribulin elicits global DNA methylation changes with potential therapeutic implications for triple-negative breast cancer. Alternating 17β-Estradiol and Aromatase Inhibitor Therapies Is Efficacious in Postmenopausal Women with Advanced Endocrine-Resistant ER+ Breast Cancer. Pharmacological Induction of mesenchymal-epithelial transition chemosensitizes breast cancer cells and prevents metastatic progression. The role of cancer cell bioenergetics in dormancy and drug resistance. Alpelisib Efficacy without Cherry-PI3King Mutations. Tumour, whole-blood, plasma and tissue concentrations of metformin in lung cancer patients. |
|