Search Results - "Wolff, Karen"
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Synthesis and Structure-Activity relationship of covalent inhibitors of SARS-CoV-2 papain-like protease with antiviral potency
Published in Bioorganic & medicinal chemistry letters (21-11-2024)“…The papain-like protease (PLpro) is a highly conserved domain encoded by the coronavirus (CoV) genome and it plays an essential role in the replication and…”
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RNA adenosine deaminase ADAR1 deficiency leads to increased activation of protein kinase PKR and reduced vesicular stomatitis virus growth following interferon treatment
Published in Virology (New York, N.Y.) (20-01-2010)“…Abstract Two size forms of ADAR1 adenosine deaminase are known, one constitutively expressed (p110) and the other interferon (IFN)-induced (p150). To test the…”
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Discovery of CMX990: A Potent SARS-CoV‑2 3CL Protease Inhibitor Bearing a Novel Warhead
Published in Journal of medicinal chemistry (22-02-2024)“…There remains a need to develop novel SARS-CoV-2 therapeutic options that improve upon existing therapies by an increased robustness of response, fewer safety…”
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Correction to “Discovery of CMX990: A Potent SARS-CoV‑2 3CL Protease Inhibitor Bearing a Novel Warhead”
Published in Journal of medicinal chemistry (27-06-2024)Get full text
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Dexamethasone inhibits respiratory syncytial virus-driven mucus production while increasing viral replication without altering antiviral interferon signaling
Published in Virology (New York, N.Y.) (15-01-2020)“…Respiratory syncytial virus (RSV) infection can cause mucus overproduction and bronchiolitis in infants leading to severe disease and hospitalization. As a…”
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Design, synthesis and biological evaluations of novel oxindoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. Part I
Published in Bioorganic & medicinal chemistry letters (15-04-2006)“…A novel oxindole was discovered as an HIV non-nucleoside reverse transcriptase inhibitor via HTS using a cell-based assay. Systematic structural modifications…”
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Drug repurposing screens identify chemical entities for the development of COVID-19 interventions
Published in Nature communications (03-06-2021)“…The ongoing pandemic caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), necessitates strategies to identify prophylactic and…”
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Design, synthesis, and biological evaluations of novel oxindoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. Part 2
Published in Bioorganic & medicinal chemistry letters (15-04-2006)“…A series of heterocycle-containing oxindoles was synthesized and their HIV antiviral activities were assessed. Some of these analogs exhibited potent…”
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Identification of broad-spectrum antiviral compounds and assessment of the druggability of their target for efficacy against respiratory syncytial virus (RSV)
Published in Proceedings of the National Academy of Sciences - PNAS (26-04-2011)“…The search for novel therapeutic interventions for viral disease is a challenging pursuit, hallmarked by the paucity of antiviral agents currently prescribed…”
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Antiviral drug screen identifies DNA-damage response inhibitor as potent blocker of SARS-CoV-2 replication
Published in Cell reports (Cambridge) (06-04-2021)“…SARS-CoV-2 has currently precipitated the COVID-19 global health crisis. We developed a medium-throughput drug-screening system and identified a small-molecule…”
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“UnPAKing” Human Immunodeficiency Virus (HIV) Replication: Using Small Interfering RNA Screening To Identify Novel Cofactors and Elucidate the Role of Group I PAKs in HIV Infection
Published in Journal of Virology (01-01-2006)“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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An oral non-covalent non-peptidic inhibitor of SARS-CoV-2 Mpro ameliorates viral replication and pathogenesis in vivo
Published in Cell reports (Cambridge) (01-11-2024)“…Safe, effective, and low-cost oral antiviral therapies are needed to treat those at high risk for developing severe COVID-19. To that end, we performed a…”
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Identification of novel therapeutic targets for HIV infection through functional genomic cDNA screening
Published in Virology (New York, N.Y.) (25-05-2007)“…Abstract Despite decades of research, HIV remains a global health threat. Issues of multi-drug resistance and lack of an effective vaccine have recently led to…”
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Mutations in an Auxin Receptor Homolog AFB5 and in SGT1b Confer Resistance to Synthetic Picolinate Auxins and Not to 2,4-Dichlorophenoxyacetic Acid or Indole-3-Acetic Acid in Arabidopsis
Published in Plant physiology (Bethesda) (01-10-2006)“…Although a wide range of structurally diverse small molecules can act as auxins, it is unclear whether all of these compounds act via the same mechanisms that…”
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Design, synthesis, and biological evaluations of novel quinolones as HIV-1 non-nucleoside reverse transcriptase inhibitors
Published in Bioorganic & medicinal chemistry letters (15-08-2006)“…A novel series of quinolones was discovered as HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) using a structure-based approach. The lead…”
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The Music Marketplace And The Music Teacher: A Modern Dilemma
Published in The American Music Teacher (01-08-1992)“…The music educator of the 20th century is faced with a problem of combining the teaching of the classics in an environment that is predominantly influenced by…”
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Chemical Genetic Identification of Glutamine Phosphoribosylpyrophosphate Amidotransferase as the Target for a Novel Bleaching Herbicide in Arabidopsis
Published in Plant physiology (Bethesda) (01-07-2007)“…A novel phenyltriazole acetic acid compound (DAS734) produced bleaching of new growth on a variety of dicotyledonous weeds and was a potent inhibitor of…”
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The Nonmusical Outcomes of Music Education: A Review of the Literature
Published in Bulletin of the Council for Research in Music Education (01-07-1978)Get full text
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Synthesis and evaluation of N-aryl pyrrolidinones as novel anti-HIV-1 agents. Part 1
Published in Bioorganic & medicinal chemistry letters (01-07-2006)“…N-Aryl pyrrolidinones as novel anti-HIV-1 agents is reported. The synthesis and preliminary structure–activity relationship of a series of pyrrolidinones are…”
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Vaccinia Virus E3L Interferon Resistance Protein Inhibits the Interferon-Induced Adenosine Deaminase A-to-I Editing Activity
Published in Virology (New York, N.Y.) (25-10-2001)“…The RNA-specific adenosine deaminase (ADAR1) is an interferon-inducible editing enzyme that converts adenosine to inosine. ADAR1 contains three distinct…”
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