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James H. Doroshow

Researcher Next ID · RN-022452

Researcher · Biochemistry, Genetics and Molecular Biology

United States Department of Health and Human Services

Washington, Malaysia

Not currently recruitingFunding unknown
Works count
1,467
Citation count
38,953
H-index
97
i10-index
429

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Cancer Genomics and Diagnostics
Radiomics and Machine Learning in Medical Imaging
Cancer therapeutics and mechanisms
Lung Cancer Treatments and Mutations
PARP inhibition in cancer therapy

Publications

  • Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

    Nature Genetics · 2021 · https://doi.org/10.1038/s41588-020-00750-6

  • TPM, FPKM, or Normalized Counts? A Comparative Study of Quantification Measures for the Analysis of RNA-seq Data from the NCI Patient-Derived Models Repository

    Journal of Translational Medicine · 2021 · https://doi.org/10.1186/s12967-021-02936-w

  • Abeloff's Clinical Oncology

    Elsevier eBooks · 2020 · 10.1016/c2015-0-05400-4

  • The National Cancer Institute ALMANAC: A Comprehensive Screening Resource for the Detection of Anticancer Drug Pairs with Enhanced Therapeutic Activity

    Cancer Research · 2017 · 10.1158/0008-5472.can-17-0489

  • Phase I Study of Single-Agent AZD1775 (MK-1775), a Wee1 Kinase Inhibitor, in Patients With Refractory Solid Tumors

    Journal of Clinical Oncology · 2015 · 10.1200/jco.2014.60.4009

  • Rationale for Poly(ADP-ribose) Polymerase (PARP) Inhibitors in Combination Therapy with Camptothecins or Temozolomide Based on PARP Trapping versus Catalytic Inhibition

    Journal of Pharmacology and Experimental Therapeutics · 2014 · 10.1124/jpet.113.210146

  • Phase I/Ib Study of Olaparib and Carboplatin in BRCA1 or BRCA2 Mutation-Associated Breast or Ovarian Cancer With Biomarker Analyses

    JNCI Journal of the National Cancer Institute · 2014 · https://doi.org/10.1093/jnci/dju089

  • The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology

    Cancer Research · 2013 · 10.1158/0008-5472.can-12-3342

  • Criteria for the use of omics-based predictors in clinical trials

    Nature · 2013 · https://doi.org/10.1038/nature12564

  • Molecular mechanisms underlying chronic inflammation-associated cancers

    Cancer Letters · 2013 · 10.1016/j.canlet.2013.08.014

  • Stereospecific PARP Trapping by BMN 673 and Comparison with Olaparib and Rucaparib

    Molecular Cancer Therapeutics · 2013 · https://doi.org/10.1158/1535-7163.mct-13-0803

  • Loss of 53BP1 Causes PARP Inhibitor Resistance in Brca1 -Mutated Mouse Mammary Tumors

    Cancer Discovery · 2012 · 10.1158/2159-8290.cd-12-0049

  • Trapping of PARP1 and PARP2 by Clinical PARP Inhibitors

    Cancer Research · 2012 · https://doi.org/10.1158/0008-5472.can-12-2753

  • CellMiner: A Web-Based Suite of Genomic and Pharmacologic Tools to Explore Transcript and Drug Patterns in the NCI-60 Cell Line Set

    Cancer Research · 2012 · https://doi.org/10.1158/0008-5472.can-12-1370

  • Putative DNA/RNA helicase Schlafen-11 (SLFN11) sensitizes cancer cells to DNA-damaging agents

    Proceedings of the National Academy of Sciences · 2012 · 10.1073/pnas.1205943109

  • Analysis of Food and Drug Administration–Approved Anticancer Agents in the NCI60 Panel of Human Tumor Cell Lines

    Molecular Cancer Therapeutics · 2010 · 10.1158/1535-7163.mct-10-0106

  • Phase 0 Clinical Trial of the Poly (ADP-Ribose) Polymerase Inhibitor ABT-888 in Patients With Advanced Malignancies

    Journal of Clinical Oncology · 2009 · 10.1200/jco.2008.19.7681

  • Bacteria-Induced Intestinal Cancer in Mice with DisruptedGpx1andGpx2Genes

    Cancer Research · 2004 · 10.1158/0008-5472.can-03-2272

  • Benefit of cyclosporine modulation of drug resistance in patients with poor-risk acute myeloid leukemia: a Southwest Oncology Group study

    Blood · 2001 · https://doi.org/10.1182/blood.v98.12.3212

  • Mice with combined disruption of Gpx1 and Gpx2 genes have colitis

    American Journal of Physiology-Gastrointestinal and Liver Physiology · 2001 · 10.1152/ajpgi.2001.281.3.g848

  • Phase II study of fluorouracil and its modulation in advanced colorectal cancer: a Southwest Oncology Group study.

    Journal of Clinical Oncology · 1995 · 10.1200/jco.1995.13.6.1303

  • Expression, characterization, and tissue distribution of a new cellular selenium-dependent glutathione peroxidase, GSHPx-GI.

    Journal of Biological Chemistry · 1993 · 10.1016/s0021-9258(18)53812-6

  • Prospective randomized comparison of fluorouracil versus fluorouracil and high-dose continuous infusion leucovorin calcium for the treatment of advanced measurable colorectal cancer in patients previously unexposed to chemotherapy.

    Journal of Clinical Oncology · 1990 · https://doi.org/10.1200/jco.1990.8.3.491

  • Interleukin-2 and lymphokine-activated killer cell therapy of solid tumors: analysis of toxicity and management guidelines.

    Journal of Clinical Oncology · 1989 · 10.1200/jco.1989.7.4.486

  • Redox cycling of anthracyclines by cardiac mitochondria. II. Formation of superoxide anion, hydrogen peroxide, and hydroxyl radical.

    Journal of Biological Chemistry · 1986 · 10.1016/s0021-9258(17)35747-2

  • Redox cycling of anthracyclines by cardiac mitochondria. I. Anthracycline radical formation by NADH dehydrogenase.

    Journal of Biological Chemistry · 1986 · 10.1016/s0021-9258(17)35746-0

  • Anthracycline antibiotic-stimulated superoxide, hydrogen peroxide, and hydroxyl radical production by NADH dehydrogenase.

    PubMed · 1983

  • Effect of anthracycline antibiotics on oxygen radical formation in rat heart.

    PubMed · 1983

  • Enzymatic Defenses of the Mouse Heart Against Reactive Oxygen Metabolites

    Journal of Clinical Investigation · 1980 · 10.1172/jci109642

Current projects

    No projects listed.