scispace - formally typeset
I

Isabelle Brabet

Researcher at Centre national de la recherche scientifique

Publications -  31
Citations -  2451

Isabelle Brabet is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Metabotropic glutamate receptor & Metabotropic receptor. The author has an hindex of 23, co-authored 31 publications receiving 2368 citations. Previous affiliations of Isabelle Brabet include University of Montpellier & French Institute of Health and Medical Research.

Papers
More filters
Journal ArticleDOI

Molecular, functional, and pharmacological characterization of the metabotropic glutamate receptor type 5 splice variants: comparison with mGluR1

TL;DR: A splice variant of mGluR5 is characterized which contains a 32 amino acid fragment inserted in the cytoplasmic tail, 50 residues after the 7th transmembrane domain, which indicates that the long C-terminal intracellular domain present only in mGlam glutamate receptors, although not well conserved, is likely to be involved in the specific functional properties of these receptors.
Journal ArticleDOI

Phenylglycine derivatives discriminate between mGluR1- and mGluR5-mediated responses

TL;DR: It is suggested that the apparent potency of phenylglycine antagonists depends on the agonist used to activate these receptors and the compound was found to potently and competitively antagonize the effect of 1S,3R-ACPD.
Journal ArticleDOI

BAY36-7620: a potent non-competitive mGlu1 receptor antagonist with inverse agonist activity.

TL;DR: BAY36-7620 will be useful to further delineate the functional importance of the mGlu1 receptor, including its putative agonist-independent activity, andTransmembrane helices 4 to 7 are shown to play a critical role in the selectivity of BAY36- 7620.
Journal ArticleDOI

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.