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A new family of covalent inhibitors block nucleotide binding to the active site of pyruvate kinase.
- Published in:
- Biochemical Journal, 2012, v. 448, n. 1, p. 67, doi. 10.1042/BJ20121014
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- Article
Erratum: Quantitative high throughput screening using a primary human three-dimensional organotypic culture predicts in vivo efficacy.
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- Nature Communications, 2016, v. 7, n. 2, p. 10649, doi. 10.1038/ncomms10649
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- Article
Quantitative high throughput screening using a primary human three-dimensional organotypic culture predicts in vivo efficacy.
- Published in:
- Nature Communications, 2015, v. 6, n. 2, p. 6220, doi. 10.1038/ncomms7220
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- Article
Discovery of novel inhibitors of human galactokinase by virtual screening.
- Published in:
- Journal of Computer-Aided Molecular Design, 2019, v. 33, n. 4, p. 405, doi. 10.1007/s10822-019-00190-3
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- Article
Drug-based modulation of endogenous stem cells promotes functional remyelination in vivo.
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- Nature, 2015, v. 522, n. 7555, p. 216, doi. 10.1038/nature14335
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- Article
The HIV protease inhibitor, ritonavir, corrects diverse brain phenotypes across development in mouse model of DYT-TOR1A dystonia.
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- Science Translational Medicine, 2021, v. 13, n. 607, p. 1, doi. 10.1126/scitranslmed.abd3904
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- Article
A Highly Potent and Selective Caspase 1 Inhibitor that Utilizes a Key 3-Cyanopropanoic Acid Moiety.
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- ChemMedChem, 2010, v. 5, n. 5, p. 730, doi. 10.1002/cmdc.200900531
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- Article
Inside Cover: A Highly Potent and Selective Caspase 1 Inhibitor that Utilizes a Key 3-Cyanopropanoic Acid Moiety (ChemMedChem 5/2010).
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- ChemMedChem, 2010, v. 5, n. 5, p. 634, doi. 10.1002/cmdc.201090016
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- Article
Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis.
- Published in:
- Nature Chemical Biology, 2012, v. 8, n. 12, p. 1008, doi. 10.1038/nchembio1212-1008b
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- Article
Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis.
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- Nature Chemical Biology, 2012, v. 8, n. 10, p. 839, doi. 10.1038/nchembio.1060
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- Article