Search Results - "RALSTON, Sherry"
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Characterization of ABBV-221, a Tumor-Selective EGFR-Targeting Antibody Drug Conjugate
Published in Molecular cancer therapeutics (01-04-2018)“…Depatuxizumab mafodotin (depatux-m, ABT-414) is a tumor-selective antibody drug conjugate (ADC) comprised of the anti-EGFR antibody ABT-806 and the monomethyl…”
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ABT-165, a Dual Variable Domain Immunoglobulin (DVD-Ig) Targeting DLL4 and VEGF, Demonstrates Superior Efficacy and Favorable Safety Profiles in Preclinical Models
Published in Molecular cancer therapeutics (01-05-2018)“…Antiangiogenic therapy is a clinically validated modality in cancer treatment. To date, all approved antiangiogenic drugs primarily inhibit the VEGF pathway…”
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Towards in vitro models for reducing or replacing the use of animals in drug testing
Published in Nature biomedical engineering (01-08-2024)“…Pharmaceutical companies continue to advocate for the use of in vitro models towards the reduction of animal use in drug discovery and development while…”
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Pharmaceutical industry perspective on combination toxicity studies: Results from an intra-industry survey conducted by IQ DruSafe Leadership Group
Published in Regulatory toxicology and pharmacology (01-03-2019)“…Interest in developing combination products to overcome drug resistance and treat complex diseases is growing. However, ambiguity remains around the value of…”
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BCL-XL-targeting antibody-drug conjugates are active in preclinical models and mitigate on-mechanism toxicity of small-molecule inhibitors
Published in Science advances (04-10-2024)“…Overexpression of the antiapoptotic protein B-cell lymphoma-extra large (BCL-XL) is associated with drug resistance and disease progression in numerous…”
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BCL-X L -targeting antibody-drug conjugates are active in preclinical models and mitigate on-mechanism toxicity of small-molecule inhibitors
Published in Science advances (04-10-2024)“…Overexpression of the antiapoptotic protein B-cell lymphoma-extra large (BCL-X ) is associated with drug resistance and disease progression in numerous…”
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Towards in vitro models for reducing or replacing the use of animals in drug testing
Published in Nature biomedical engineering (01-08-2024)Get full text
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Antiangiogenic and antitumor activity of a selective PDGFR tyrosine kinase inhibitor, CP-673,451
Published in Cancer research (Chicago, Ill.) (01-02-2005)“…CP-673,451 is a potent inhibitor of platelet-derived growth factor beta-receptor (PDGFR-beta) kinase- and PDGF-BB-stimulated autophosphorylation of PDGFR-beta…”
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Stereoselective Activation of Dibenzo[a,l]pyrene and Its trans-11,12-Dihydrodiol to Fjord Region 11,12-Diol 13,14-Epoxides in a Human Mammary Carcinoma MCF-7 Cell-Mediated V79 Cell Mutation Assay
Published in Chemical research in toxicology (01-06-1997)“…Dibenzo[a,l]pyrene (DB[a,l]P) represents the most potent carcinogenic polycyclic aromatic hydrocarbon (PAH) yet discovered. Like other PAHs, DB[a,l]P requires…”
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The potent carcinogen dibenzo[a,l]pyrene is metabolically activated to fjord-region 11,12-diol 13,14-epoxides in human mammary carcinoma MCF-7 cell cultures
Published in Cancer research (Chicago, Ill.) (15-02-1994)“…Dibenzo[a,l]pyrene (DB[a,l]P), an environmental hydrocarbon and very potent carcinogen in rodent bioassays, could be activated to DNA-binding intermediates in…”
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Abstract 867: ABT-165 is a first-in-class therapeutic Dual Variable Domain Immunoglobulin (DVD-IgTM) that targets DLL4 and VEGF for the treatment of cancer
Published in Cancer research (Chicago, Ill.) (15-07-2016)“…The first generation anti-angiogenic drugs designed to block the VEGF/VEGFR pathway lend modest clinical benefit for cancer patients. Other than VEGF, DLL4 is…”
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Discovery and pharmacologic characterization of CP-724,714, a selective ErbB2 tyrosine kinase inhibitor
Published in Cancer research (Chicago, Ill.) (15-10-2007)“…Amplification and overexpression of erbB2 (Her-2/neu) proto-oncogene has been linked to human malignancies including tumors of the breast, ovary, and stomach…”
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Development of a multi-organ rat model for evaluating chemopreventive agents: efficacy of indole-3-carbinol
Published in Carcinogenesis (New York) (01-02-2002)“…Indole-3-carbinol (I-3-C) is among the most widely and popularly known antiestrogens. Due to its putative chemopreventive action, I-3-C is being marketed to…”
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Stereoselective activation of dibenzo[a,l]pyrene to (-)-anti (11R,12S,13S,14R)- and (+)-syn(11S,12R,13S,14R)-11,12-diol-13,14-epoxides which bind extensively to deoxyadenosine residues of DNA in the human mammary carcinoma cell line MCF-7
Published in Carcinogenesis (New York) (01-12-1995)“…Dibenzo[a,l]pyrene (DB[a,l]P) is an environmental contaminant and a very potent carcinogen. DB[a,l]P exceeds the carcinogenic potency of both benzo[a]pyrene…”
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Development of a multi-organ rat model for evaluating chemopreventive agents: efficacy of indole-3-carbinol
Published in Carcinogenesis (New York) (01-10-2002)Get full text
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The mechanism of metabolic activation of the very potent carcinogen dibenzo(a,l)pyrene
Published 01-01-1996“…Dibenzo (a,l) pyrene (DB (a,l) P) is an environmental polycyclic aromatic hydrocarbon (PAH) and the most potent carcinogen tested in rodent bioassays. As with…”
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Dissertation -
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Expression of Cell Cycle Proteins in 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone-Induced Mouse Lung Tumors
Published in Experimental lung research (1998)“…Cyclin D1 dysregulation and differential inactivation of p16INK4a and Rb have been observed in human lung cancer. In chemically induced mouse lung tumors, the…”
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Professional Assessment and Development
Published 1978“…It is proposed that in considering teachers' professional development, emphasis should be placed on teacher assessment as an intergral part of the…”
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