User profiles for Laurent Meijer

Laurent Meijer

Verified email at manros-therapeutics.com
Cited by 41713

Pharmacological inhibitors of glycogen synthase kinase 3

L Meijer, M Flajolet, P Greengard - Trends in pharmacological sciences, 2004 - cell.com
Three closely related forms of glycogen synthase kinase 3 (GSK-3α, GSK-3β and GSK-3β2)
have a major role in Wnt and Hedgehog signaling pathways and regulate the cell-division …

Pharmacological inhibitors of cyclin-dependent kinases

M Knockaert, P Greengard, L Meijer - Trends in pharmacological sciences, 2002 - cell.com
Cyclin-dependent kinases (CDKs) regulate the cell division cycle, apoptosis, transcription
and differentiation in addition to functions in the nervous system. Deregulation of CDKs in …

Roscovitine and other purines as kinase inhibitors. From starfish oocytes to clinical trials

L Meijer, E Raymond - Accounts of chemical research, 2003 - ACS Publications
This article reviews the steps that have led us from very fundamental research on the cell
division cycle, investigated with the starfish oocyte model, to the identification of drugs now …

Maintenance of pluripotency in human and mouse embryonic stem cells through activation of Wnt signaling by a pharmacological GSK-3-specific inhibitor

N Sato, L Meijer, L Skaltsounis, P Greengard… - Nature medicine, 2004 - nature.com
Human and mouse embryonic stem cells (HESCs and MESCs, respectively) self-renew
indefinitely while maintaining the ability to generate all three germ-layer derivatives. Despite the …

Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin‐dependent kinases cdc2, cdk2 and cdk5

L Meijer, A Borgne, O Mulner… - European journal of …, 1997 - Wiley Online Library
Cyclin‐dependent kinases (cdk) play an essential role in the intracellular control of the cell
division cycle (cdc). These kinases and their regulators are frequently deregulated in human …

Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors

…, DO Morgan, G Barnes, S LeClerc, L Meijer… - Science, 1998 - science.org
Selective protein kinase inhibitors were developed on the basis of the unexpected binding
mode of 2,6,9-trisubstituted purines to the adenosine triphosphate–binding site of the human …

Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases

…, E Niederberger, W Tang, G Eisenbrand, L Meijer - Nature cell …, 1999 - nature.com
Indirubin is the active ingredient of Danggui Longhui Wan, a mixture of plants that is used in
traditional Chinese medicine to treat chronic diseases. Here we identify indirubin and its …

[PDF][PDF] GSK-3-selective inhibitors derived from Tyrian purple indirubins

L Meijer, AL Skaltsounis, P Magiatis… - Chemistry & biology, 2003 - cell.com
Gastropod mollusks have been used for over 2500 years to produce the "Tyrian purple" dye
made famous by the Phoenicians. This dye is constituted of mixed bromine-substituted …

Inhibition of cyclin‐dependent kinases by purine analogues: crystal structure of human cdk2 complexed with roscovitine

WF De Azevedo, S Leclerc, L Meijer… - European journal of …, 1997 - Wiley Online Library
Cyclin‐dependent kinases (cdk) control the cell division cycle (cdc). These kinases and
their regulators are frequently deregulated in human tumours. A potent inhibitor of cdks, …

[HTML][HTML] Indirubins Inhibit Glycogen Synthase Kinase-3β and CDK5/P25, Two Protein Kinases Involved in Abnormal Tau Phosphorylation in Alzheimer's Disease: A …

…, YZ Wu, EM Mandelkow, G Eisenbrand, L Meijer - Journal of Biological …, 2001 - ASBMB
The bis-indole indirubin is an active ingredient of Danggui Longhui Wan, a traditional
Chinese medicine recipe used in the treatment of chronic diseases such as leukemias. The …