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Large-scale integration of small molecule-induced genome-wide transcriptional responses, Kinome-wide binding affinities and cell-growth inhibition profiles reveal global trends characterizing systems-level drug action.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00342
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- Article
Connecting omics signatures and revealing biological mechanisms with iLINCS.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32205-3
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- Article
Drug target ontology to classify and integrate drug discovery data.
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- Journal of Biomedical Semantics, 2017, v. 8, p. 1, doi. 10.1186/s13326-017-0161-x
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- Article
LINCS Data Portal 2.0: next generation access point for perturbation-response signatures.
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- Nucleic Acids Research, 2020, v. 48, n. D1, p. D431, doi. 10.1093/nar/gkz1023
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- Article
Data Portal for the Library of Integrated Network-based Cellular Signatures (LINCS) program: integrated access to diverse large-scale cellular perturbation response data.
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- Nucleic Acids Research, 2018, v. 46, n. D1, p. D558, doi. 10.1093/nar/gkx1063
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- Publication type:
- Article
GPCR ontology: development and application of a G protein-coupled receptor pharmacology knowledge framework.
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- Bioinformatics, 2013, v. 29, n. 24, p. 3211, doi. 10.1093/bioinformatics/btt565
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- Article