Search Results - "Aujay, Monette A."
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A DLL3-targeted antibody-drug conjugate eradicates high-grade pulmonary neuroendocrine tumor-initiating cells in vivo
Published in Science translational medicine (26-08-2015)“…The high-grade pulmonary neuroendocrine tumors, small cell lung cancer (SCLC) and large cell neuroendocrine carcinoma (LCNEC), remain among the most deadly…”
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A selective inhibitor of the immunoproteasome subunit LMP7 blocks cytokine production and attenuates progression of experimental arthritis
Published in Nature medicine (01-07-2009)“…Christopher Kirk and his colleagues have developed the first specific inhibitor of the immunoproteasome. They find that the immunoproteasome has a major role…”
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Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome
Published in Cancer research (Chicago, Ill.) (01-07-2007)“…Clinical studies with bortezomib have validated the proteasome as a therapeutic target for the treatment of multiple myeloma and non-Hodgkin's lymphoma…”
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Design and Synthesis of an Orally Bioavailable and Selective Peptide Epoxyketone Proteasome Inhibitor (PR-047)
Published in Journal of medicinal chemistry (14-05-2009)“…Proteasome inhibition has been validated as a therapeutic modality in the treatment of multiple myeloma and Non-Hodgkin’s lymphoma. Carfilzomib, an epoxyketone…”
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PR‐924, a selective inhibitor of the immunoproteasome subunit LMP‐7, blocks multiple myeloma cell growth both in vitro and in vivo
Published in British journal of haematology (01-01-2011)“…Summary PR‐924 is an LMP‐7‐selective tripeptide epoxyketone proteasome inhibitor that covalently modifies proteasomal N‐terminal threonine active sites. In the…”
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Evaluation of PNU-159682 antibody drug conjugates (ADCs)
Published in Bioorganic & medicinal chemistry letters (15-12-2020)“…[Display omitted] PNU-159682 is a highly potent secondary metabolite of nemorubicin belonging to the anthracycline class of natural products. Due to its…”
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Elvn-001, a Next Generation ATP-Competitive ABL1 Tyrosine Kinase Inhibitor for the Treatment of Chronic Myeloid Leukemia
Published in Blood (15-11-2022)Get full text
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Abstract NT-113: SC-003, AN ANTIBODY-DRUG CONJUGATE TARGETING DIPEPTIDASE 3, EXHIBITS POTENT ANTI-TUMOR ACTIVITY IN PATIENT-DERIVED XENOGRAFT MODELS OF HIGH GRADE SEROUS OVARIAN CANCER
Published in Clinical cancer research (15-11-2019)“…Disclosures: All authors are employees of AbbVie. The design, study conduct, and financial support for this research were provided by AbbVie. AbbVie…”
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Erratum: A selective inhibitor of the immunoproteasome subunit LMP7 blocks cytokine production and attenuates progression of experimental arthritis
Published in Nature medicine (01-11-2009)“…Nat. Med. 15, 781–787 (2009); published online 14 June 2009; corrected after print 5 November 2009 In the version of this article initially published, the…”
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Immunoproteasome-Selective Keto-Epoxide Inhibitors: Potential Therapeutic Agents for the Treatment of Hematological Disorders
Published in Blood (16-11-2006)“…The clinical development of the dipeptide boronate bortezomib (Velcade™) has validated proteasome inhibition as a treatment for multiple myeloma and…”
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Pharmacologic Evaluation of Orally Bioavailable Inhibitors of the 20S Proteasome
Published in Blood (16-11-2006)“…Clinical application of proteasome inhibitors in the treatment of hematologic malignancies such as myeloma and lymphoma is restricted in part by the necessity…”
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Identification of Peptide Epoxy-Ketone Proteasome Inhibitors with Differential Active Site Selectivity
Published in Blood (16-11-2006)“…The proteasome is a multi-subunit structure responsible for degrading the majority of proteins in the cell. The three catalytic subunits in the 20S core of the…”
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A Proteasome Specific Binding Assay for Quantitation of Constitutive and Immunoproteasome Active Sites
Published in Blood (16-11-2005)“…The ubiquitin-proteasome pathway constitutes a major intracellular system for protein degradation. Substrates for this pathway include misfolded or unassembled…”
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