Drug Discovery Today: Technologies
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Combination of ligand- and structure-based methods in virtual screening
Drug Discovery Today: Technologies - Tập 10 - Trang e395-e401 - 2013
Affinity assays for decrypting protein targets of unknown function
Drug Discovery Today: Technologies - Tập 2 - Trang 267-273 - 2005
Automation and robotics in ADME screening
Drug Discovery Today: Technologies - Tập 1 - Trang 373-380 - 2004
Kinase profiling in early stage drug discovery: sorting things out
Drug Discovery Today: Technologies - Tập 18 - Trang 52 - 2015
Protein kinases represent one of the largest superfamilies of drugable targets and a major research area for both the pharmaceutical industry and academic groups. This has resulted in the emergence of numerous screening technologies and services dedicated to kinase profiling. In spite of this plentiful offering, the field is not without its own pitfalls, as the profusion of reported conditions and...... hiện toàn bộ
‘Fuzziness’ in pharmacophore-based virtual screening and de novo design
Drug Discovery Today: Technologies - Tập 7 - Trang e237-e244 - 2010
Mycobacterial genetics in target validation
Drug Discovery Today: Technologies - Tập 1 - Trang 93-98 - 2004
Using Drosophila as a tool to identify pharmacological therapies for fragile X syndrome
Drug Discovery Today: Technologies - Tập 10 - Trang e129-e136 - 2013
Very large virtual compound spaces: construction, storage and utility in drug discovery
Drug Discovery Today: Technologies - Tập 10 - Trang e387-e394 - 2013
Challenges in profiling and lead optimization of drug discovery for methyltransferases
Drug Discovery Today: Technologies - Tập 18 - Trang 62-68 - 2015
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