Search Results - "Wong, Lu Min"
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1
Discovery of Highly Selective and Potent p38 Inhibitors Based on a Phthalazine Scaffold
Published in Journal of medicinal chemistry (23-10-2008)“…Investigations into the structure−activity relationships (SAR) of a series of phthalazine-based inhibitors of p38 are described. These efforts originated from…”
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2
Reversible inhibition of tomato fruit senescence by antisense RNA
Published in Science (American Association for the Advancement of Science) (18-10-1991)“…Ethylene controls fruit ripening. Expression of antisense RNA to the rate-limiting enzyme in the biosynthetic pathway of ethylene,…”
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3
Identification of the auxin-responsive element, AuxRE, in the primary indoleacetic acid-inducible gene, PS-IAA4/5, of pea (Pisum sativum)
Published in Journal of molecular biology (20-10-1993)“…The plant hormone auxin transcriptionally activates early genes in pea. We have developed a transient assay system using protoplasts of auxin-responsive pea…”
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4
Signal Transduction and Ligand Specificity of the Human Monocyte Chemoattractant Protein-1 Receptor in Transfected Embryonic Kidney Cells (∗)
Published in The Journal of biological chemistry (17-03-1995)“…We have examined the ligand specificity and signal transduction pathways of a recently cloned receptor for monocyte chemoattractant protein-1 (MCP-1). In human…”
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5
NOT gated T cells that selectively target EGFR and other widely expressed tumor antigens
Published in iScience (21-06-2024)“…Here, we show that a NOT gated cell therapy (Tmod) can exploit antigens such as epidermal growth factor receptor (EGFR) and human leukocyte antigen-E (HLA-E)…”
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6
Differential cytokine modulation and T cell activation by two distinct classes of thalidomide analogues that are potent inhibitors of TNF-alpha
Published in The Journal of immunology (1950) (01-07-1999)“…TNF-alpha mediates both protective and detrimental manifestations of the host immune response. Our previous work has shown thalidomide to be a relatively…”
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7
DNA elements responsive to auxin
Published in BioEssays (01-08-1996)“…Genes induced by the plant hormone auxin are probably involved in the execution of vital cellular functions and developmental processes. Experimental…”
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8
Discovery of (S)-N-{2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methanesulfonylethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}acetamide (Apremilast), a Potent and Orally Active Phosphodiesterase 4 and Tumor Necrosis Factor-a Inhibitor
Published in Journal of medicinal chemistry (26-03-2009)Get full text
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9
Discovery of Pyridazinopyridinones as Potent and Selective p38 Mitogen-Activated Protein Kinase Inhibitors
Published in Journal of medicinal chemistry (09-09-2010)“…The p38 mitogen-activated protein kinase (MAPK) plays an important role in the production of proinflammatory cytokines, making it an attractive target for the…”
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10
3-Amino-7-phthalazinylbenzoisoxazoles as a Novel Class of Potent, Selective, and Orally Available Inhibitors of p38α Mitogen-Activated Protein Kinase
Published in Journal of medicinal chemistry (23-10-2008)“…The p38 mitogen-activated protein kinase (MAPK) is a central signaling molecule in many proinflammatory pathways, regulating the cellular response to a…”
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11
Organization and differential expression of the human monocyte chemoattractant protein 1 receptor gene. Evidence for the role of the carboxyl-terminal tail in receptor trafficking
Published in The Journal of biological chemistry (10-01-1997)“…Two forms of the monocyte chemoattractant protein-1 receptors (the type A monocyte chemoattractant protein 1 (MCP-1) receptor CCR-2A and the type B MCP-1…”
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12
Amino-substituted thalidomide analogs: Potent inhibitors of TNF-α production
Published in Bioorganic & medicinal chemistry letters (07-06-1999)“…Thalidomide, ( 1), is a known inhibitor of TNF-α release in LPS stimulated human PBMC. Herein we describe the TNF-α inhibitory activity of amino substituted…”
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Part 2: Structure–activity relationship (SAR) investigations of fused pyrazoles as potent, selective and orally available inhibitors of p38α mitogen-activated protein kinase
Published in Bioorganic & medicinal chemistry letters (01-03-2010)“…A novel class of pyrazolopyridazine p38α mitogen-activated protein kinase (MAPK) inhibitors is disclosed. A structure activity relationship (SAR) investigation…”
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14
Transcriptional regulation of PS-IAA4/5 and PS-IAA6 early gene expression by indoleacetic acid and protein synthesis inhibitors in pea (Pisum sativum)
Published in Journal of molecular biology (27-10-1995)“…The transcription of two genes, PS-IAA4/5 and PS-IAA6, in pea is induced by indoleacetic acid (IAA) and protein synthesis inhibitors such as cycloheximide…”
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15
Part 1: Structure–Activity Relationship (SAR) investigations of fused pyrazoles as potent, selective and orally available inhibitors of p38α mitogen-activated protein kinase
Published in Bioorganic & medicinal chemistry letters (15-08-2009)“…A novel class of fused pyrazole-derived inhibitors of p38α mitogen-activated protein kinase (MAPK) is disclosed. These inhibitors were evaluated for their…”
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16
Design and synthesis of potent pyridazine inhibitors of p38 MAP kinase
Published in Bioorganic & medicinal chemistry letters (02-05-2005)“…Novel potent trisubstituted pyridazine inhibitors of p38 MAP (mitogen activated protein) kinase are described that have activity in both cell-based assays of…”
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17
Identification of triazolopyridazinones as potent p38α inhibitors
Published in Bioorganic & medicinal chemistry letters (15-01-2012)“…Structure–activity relationship (SAR) investigations of a novel class of triazolopyridazinone p38α mitogen activated protein kinase (MAPK) inhibitors are…”
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18
Two Auxin-Responsive Domains Interact Positively to Induce Expression of the Early Indoleacetic Acid-Inducible Gene PS-IAA4/5
Published in Proceedings of the National Academy of Sciences - PNAS (11-04-1995)“…The plant growth hormone indole-3-acetic acid (IAA) transcriptionally activates expression of several genes in plants. We have previously identified a 164-bp…”
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19
A rational approach to assess off-target reactivity of a dual-signal integrator for T cell therapy
Published in Toxicology and applied pharmacology (15-02-2022)“…Cell therapy is an emerging therapeutic modality with the power to exploit new cancer targets and potentially achieve positive outcomes for patients with few…”
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20
Differential activation of the primary auxin response genes, PS‐IAA4/5 and PS‐IAA6, during early plant development
Published in The Plant journal : for cell and molecular biology (01-05-1996)“…Summary The plant growth hormone auxin typified by indoleacetic acid (IAA) transcriptionally activates early genes in pea, PS‐IAA4/5 and PS‐IAA6, that are…”
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