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Subject Areas on Research
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Aggresome disruption: a novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells.
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Cardio-oncology care in the era of the coronavirus disease 2019 (COVID-19) pandemic: An International Cardio-Oncology Society (ICOS) statement.
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Design and synthesis of naphthoquinone derivatives as antiproliferative agents and 20S proteasome inhibitors.
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Final Results of a Phase 1 Study of Vorinostat, Pegylated Liposomal Doxorubicin, and Bortezomib in Relapsed or Refractory Multiple Myeloma.
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HSP70 chaperones RNA-free TDP-43 into anisotropic intranuclear liquid spherical shells.
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Immunotherapy Gone Viral: Bortezomib and oHSV Enhance Antitumor NK-Cell Activity.
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Marizomib activity as a single agent in malignant gliomas: ability to cross the blood-brain barrier.
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New betulinic acid derivatives as potent proteasome inhibitors.
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Novel therapies for pancreatic adenocarcinoma.
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Oncogenic RAS-induced CK1α drives nuclear FOXO proteolysis.
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Outcomes of Maintenance Therapy with Bortezomib after Autologous Stem Cell Transplantation for Patients with Multiple Myeloma.
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Outcomes of patients with multiple myeloma refractory to CD38-targeted monoclonal antibody therapy.
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Phase 1 study of ixazomib, an investigational proteasome inhibitor, in advanced non-hematologic malignancies.
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Phase I study of opaganib, an oral sphingosine kinase 2-specific inhibitor, in relapsed and/or refractory multiple myeloma.
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Phase I/II study of the novel proteasome inhibitor delanzomib (CEP-18770) for relapsed and refractory multiple myeloma.
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Pretransplant Desensitization with Costimulation Blockade and Proteasome Inhibitor Reduces DSA and Delays Antibody-Mediated Rejection in Highly Sensitized Nonhuman Primate Kidney Transplant Recipients.
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Prevalence of bortezomib-resistant constitutive NF-kappaB activity in mantle cell lymphoma.
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Proteasome inhibition with bortezomib induces cell death in GBM stem-like cells and temozolomide-resistant glioma cell lines, but stimulates GBM stem-like cells' VEGF production and angiogenesis.
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Proteasome inhibitor attenuates skeletal muscle reperfusion injury by blocking the pathway of nuclear factor-kappaB activation.
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Proteasome regulators: activators and inhibitors.
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Regulation of RIPK3- and RHIM-dependent Necroptosis by the Proteasome.
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Requirement of dendritic Akt degradation by the ubiquitin-proteasome system for neuronal polarity.
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Reversible mislocalization of a disease-associated MRE11 splice variant product.
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SECTM1 produced by tumor cells attracts human monocytes via CD7-mediated activation of the PI3K pathway.
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Specific chemopreventive agents trigger proteasomal degradation of G1 cyclins: implications for combination therapy.
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Synthesis and biological evaluation of novel spin labeled 18β-glycyrrhetinic acid derivatives.
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Synthesis and proteasome inhibition of glycyrrhetinic acid derivatives.
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Synthesis and proteasome inhibition of lithocholic acid derivatives.
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The cyclophilin-like domain of Ran-binding protein-2 modulates selectively the activity of the ubiquitin-proteasome system and protein biogenesis.
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The impact of bone marrow fibrosis and JAK2 expression on clinical outcomes in patients with newly diagnosed multiple myeloma treated with immunomodulatory agents and/or proteasome inhibitors.
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Treatment Journeys of Patients With Newly Diagnosed Multiple Myeloma (NDMM): Results From The Connect MM Registry.
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Truncated ErbB2 expressed in tumor cell nuclei contributes to acquired therapeutic resistance to ErbB2 kinase inhibitors.
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Venetoclax or placebo in combination with bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma (BELLINI): a randomised, double-blind, multicentre, phase 3 trial.