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Francine Acher

Researcher at Paris Descartes University

Publications -  139
Citations -  4691

Francine Acher is an academic researcher from Paris Descartes University. The author has contributed to research in topics: Metabotropic glutamate receptor & Agonist. The author has an hindex of 37, co-authored 135 publications receiving 4327 citations. Previous affiliations of Francine Acher include University of Paris & University of Montpellier.

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The metabotropic glutamate receptors: structure, activation mechanism and pharmacology.

TL;DR: The present review article focuses on the specific structural features of these receptors and highlights the various possibilities these offer for drug development.
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The Heptahelical Domain of GABAB2 Is Activated Directly by CGP7930, a Positive Allosteric Modulator of the GABAB Receptor *

TL;DR: The mechanism of action of CGP7930, a compound described as a positive allosteric regulator of the GABAB receptor, was explored and it was demonstrated that the HD of GABAB2 behaves similar to a rhodopsin-like receptor, because it can reach the cell surface alone, can couple to G-protein, and be activated by agonists.
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Heptahelical domain of metabotropic glutamate receptor 5 behaves like rhodopsin-like receptors

TL;DR: It is shown that the HD of metabotropic glutamate receptor 5 (mGlu5) displays the same agonist-independent constitutive activity as the wild-type receptor, and illustrates that, like rhodopsin-like receptors, theHD of mGluRs can constitutively couple to G proteins and be negatively and positively regulated by ligands.
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New perspectives for the development of selective metabotropic glutamate receptor ligands

TL;DR: The metabotropic glutamate receptors are GTP-binding-protein (G-protein) coupled receptors that play important roles in regulating the activity of many synapses in the central nervous system.
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Comparative effect of l-CCG-I, DCG-IV and γ-carboxy-l-glutamate on all cloned metabotropic glutamate receptor subtypes

TL;DR: It is shown here that L-CCG-I is a general mGlu receptor agonist activating all cloned receptors, and it is confirmed that DCG-IV, which corresponds to L- CCG- I with an additional carboxylic group, is a selective group-II agonist.