The DOI matches its Crossref record; 87 of the 87 references it cites were found in a registry or an index.
Pharmacological inhibitors of glycogen synthase kinase 3
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In Vivo Activation of the p53 Pathway by Small-Molecule Antagonists of MDM2
Vassilev, L. T., Vu, B. T., Graves, B., Carvajal, D., Podlaski, F., Filipovic, Z., Kong, N., Kammlott, U., Lukacs, C., Klein, C., et al. (2004) · Science · doi:10.1126/science.1092472 · Cited by 4,661
Specificity and mechanism of action of some commonly used protein kinase inhibitors
DAVIES, S. P., REDDY, H., CAIVANO, M., & COHEN, P. (2000) · Biochemical Journal · doi:10.1042/bj3510095 · Cited by 3,132
A molecular mechanism for the effect of lithium on development.
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Protein kinases — the major drug targets of the twenty-first century?
Cohen, P. (2002) · Nature Reviews Drug Discovery · doi:10.1038/nrd773 · Cited by 2,186
Sato, N., Meijer, L., Skaltsounis, L., Greengard, P., & Brivanlou, A. H. (2004) · Nature Medicine · doi:10.1038/nm979 · Cited by 2,109
Self-citationGSK-3: tricks of the trade for a multi-tasking kinase
Doble, B. W., & Woodgett, J. R. (2003) · Journal of Cell Science · doi:10.1242/jcs.00384 · Cited by 2,084
The glamour and gloom of glycogen synthase kinase-3
Jope, R. S., & Johnson, G. V. W. (2004) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2003.12.004 · Cited by 1,517
GSK3 takes centre stage more than 20 years after its discovery
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The specificities of protein kinase inhibitors: an update
BAIN, J., McLAUCHLAN, H., ELLIOTT, M., & COHEN, P. (2003) · Biochemical Journal · doi:10.1042/bj20021535 · Cited by 1,369 · cited 6×
“However, because many GSK-3 inhibitors also affect CDKs (Table 1) [33], control experiments should be carried out using CDK inhibitors that do not target GSK-3 (such as roscovitine and purvalanol)[ 29 ].Insomecircumstances,CDK5‐GSK-3 dual specificity could be an advantage, as illustrated later.”
BackgroundInfluentialProtein Kinase Inhibitors: Insights into Drug Design from Structure
Noble, M. E. M., Endicott, J. A., & Johnson, L. N. (2004) · Science · doi:10.1126/science.1095920 · Cited by 1,198
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Rada, P., Rojo, A. I., Chowdhry, S., McMahon, M., Hayes, J. D., & Cuadrado, A. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01204-10 · Cited by 759
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Zhou, X., Yu, S., Zhao, D.-M., Harty, J. T., Badovinac, V. P., & Xue, H.-H. (2010) · Immunity · doi:10.1016/j.immuni.2010.08.002 · Cited by 688
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Metadata
- Authors
- MEIJER, L., FLAJOLET, M., & GREENGARD, P.
- Venue
- Trends in Pharmacological Sciences
- Publisher
- Elsevier BV
- Published
- 2004-09
- Volume
- 25
- Issue
- 9
- Pages
- 471-480
- ISSN
- 0165-6147 (ISSN-L)
- OpenAlex
- W2034595626
- Cited by
- 584
- References
- 87
- FWCI
- 12.36
- Type
- journal article
- Language
- en
- Open access
- green
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- MEIJER, L., FLAJOLET, M., & GREENGARD, P. (2004). Pharmacological inhibitors of glycogen synthase kinase 3. Trends in Pharmacological Sciences. https://doi.org/10.1016/j.tips.2004.07.006
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
