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Catherine Marquer

Showing results (11-20 of 23) with videos related to

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The Journal of Biological Chemistry|June 21, 2011
Structural model of ligand-G protein-coupled receptor (GPCR) complex based on experimental double mutant cycle data: MT7 snake toxin bound to dimeric hM1 muscarinic receptorCatherine Marquer, Carole Fruchart-Gaillard, Guillaume Letellier, et al.
The European Journal of Neuroscience|April 8, 2015
Inhibiting cholesterol degradation induces neuronal sclerosis and epileptic activity in mouse hippocampusFarah Chali, Fathia Djelti, Emmanuel Eugene, et al.
Nature Communications|June 24, 2016
Arf6 controls retromer traffic and intracellular cholesterol distribution via a phosphoinositide-based mechanismCatherine Marquer, Huasong Tian, Julie Yi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 25, 2011
Local cholesterol increase triggers amyloid precursor protein-Bace1 clustering in lipid rafts and rapid endocytosisCatherine Marquer, Viviane Devauges, Jack-Christophe Cossec, et al.
Biochimica Et Biophysica Acta|June 29, 2010
Clathrin-dependent APP endocytosis and Abeta secretion are highly sensitive to the level of plasma membrane cholesterolJack-Christophe Cossec, Anne Simon, Catherine Marquer, et al.
Current Biology : CB|January 2, 2018
Cell Size and Growth Rate Are Modulated by TORC2-Dependent SignalsRafael Lucena, Maria Alcaide-Gavilán, Katherine Schubert, et al.
Acta Neuropathologica|September 8, 2012
Time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging reveals cholesterol overload in the cerebral cortex of Alzheimer disease patientsAdina N Lazar, Claudia Bich, Maï Panchal, et al.
Communications Biology|February 24, 2023
Lysosomal phospholipase A2 contributes to the biosynthesis of the atypical late endosome lipid bis(monoacylglycero)phosphateJacinda Chen, Amaury Cazenave-Gassiot, Yimeng Xu, et al.
Ebiomedicine|May 28, 2023
Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C diseaseJacinda Chen, Rajesh Kumar Soni, Yimeng Xu, et al.
Molecular Neurobiology|September 8, 2022
Specific Mutations in the Cholesterol-Binding Site of APP Alter Its Processing and Favor the Production of Shorter, Less Toxic Aβ PeptidesLinda Hanbouch, Béatrice Schaack, Amal Kasri, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|June 21, 2011
Structural model of ligand-G protein-coupled receptor (GPCR) complex based on experimental double mutant cycle data: MT7 snake toxin bound to dimeric hM1 muscarinic receptorCatherine Marquer, Carole Fruchart-Gaillard, Guillaume Letellier, et al.
The European Journal of Neuroscience|April 8, 2015
Inhibiting cholesterol degradation induces neuronal sclerosis and epileptic activity in mouse hippocampusFarah Chali, Fathia Djelti, Emmanuel Eugene, et al.
Nature Communications|June 24, 2016
Arf6 controls retromer traffic and intracellular cholesterol distribution via a phosphoinositide-based mechanismCatherine Marquer, Huasong Tian, Julie Yi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 25, 2011
Local cholesterol increase triggers amyloid precursor protein-Bace1 clustering in lipid rafts and rapid endocytosisCatherine Marquer, Viviane Devauges, Jack-Christophe Cossec, et al.
Biochimica Et Biophysica Acta|June 29, 2010
Clathrin-dependent APP endocytosis and Abeta secretion are highly sensitive to the level of plasma membrane cholesterolJack-Christophe Cossec, Anne Simon, Catherine Marquer, et al.
Current Biology : CB|January 2, 2018
Cell Size and Growth Rate Are Modulated by TORC2-Dependent SignalsRafael Lucena, Maria Alcaide-Gavilán, Katherine Schubert, et al.
Acta Neuropathologica|September 8, 2012
Time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging reveals cholesterol overload in the cerebral cortex of Alzheimer disease patientsAdina N Lazar, Claudia Bich, Maï Panchal, et al.
Communications Biology|February 24, 2023
Lysosomal phospholipase A2 contributes to the biosynthesis of the atypical late endosome lipid bis(monoacylglycero)phosphateJacinda Chen, Amaury Cazenave-Gassiot, Yimeng Xu, et al.
Ebiomedicine|May 28, 2023
Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C diseaseJacinda Chen, Rajesh Kumar Soni, Yimeng Xu, et al.
Molecular Neurobiology|September 8, 2022
Specific Mutations in the Cholesterol-Binding Site of APP Alter Its Processing and Favor the Production of Shorter, Less Toxic Aβ PeptidesLinda Hanbouch, Béatrice Schaack, Amal Kasri, et al.
Pageof 3