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Methods in Molecular Biology (Clifton, N.J.)
|
March 29, 2019
β-Arrestins: Multitask Scaffolds Orchestrating the Where and When in Cell Signalling
Stéphane A Laporte, Mark G H Scott
Medecine Et Maladies Infectieuses
|
April 1, 2011
[Louse-borne infections in humans]
J-C Desenclos, A Laporte, P Brouqui
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
May 9, 1977
[Hypertensive encephalopathy. Clinical and physiopathologic developments]
J M Orgogozo, A Laporte, P Loiseau
Invasion & Metastasis
|
January 1, 1997
Differential responsiveness of murine T lymphomas to local growth and invasion factors may determine metastasis formation in the ovaries
C Schmidt, A Laporte, P De Baetselier
Frontiers in Endocrinology
|
May 22, 2014
Allosteric and biased g protein-coupled receptor signaling regulation: potentials for new therapeutics
Etienne Khoury, Stéphanie Clément, Stéphane A Laporte
Methods in Molecular Biology (Clifton, N.J.)
|
March 29, 2019
Methods to Monitor the Trafficking of β-Arrestin/G Protein-Coupled Receptor Complexes Using Enhanced Bystander BRET
Yubo Cao, Yoon Namkung, Stéphane A Laporte
Methods in Molecular Biology (Clifton, N.J.)
|
August 27, 2011
Study of G protein-coupled receptor/β-arrestin interactions within endosomes using FRAP
Benjamin Aguila, May Simaan, Stéphane A Laporte
Molecular Endocrinology (Baltimore, Md.)
|
October 23, 2004
c-Src regulates clathrin adapter protein 2 interaction with beta-arrestin and the angiotensin II type 1 receptor during clathrin- mediated internalization
Delphine Fessart, May Simaan, Stéphane A Laporte
British Journal of Pharmacology
|
November 6, 2012
GPCR heterodimers: asymmetries in ligand binding and signalling output offer new targets for drug discovery
Eugénie Goupil, Stéphane A Laporte, Terence E Hébert
The Journal of Clinical Investigation
|
May 1, 1994
Processing of urushiol (poison ivy) hapten by both endogenous and exogenous pathways for presentation to T cells in vitro
R S Kalish, J A Wood, A LaPorte
Page
of 15
Search research articles
Search
Showing results (11-20 of 150) with videos related to
Sort By:
Page
of 15
Methods in Molecular Biology (Clifton, N.J.)
|
March 29, 2019
β-Arrestins: Multitask Scaffolds Orchestrating the Where and When in Cell Signalling
Stéphane A Laporte, Mark G H Scott
Medecine Et Maladies Infectieuses
|
April 1, 2011
[Louse-borne infections in humans]
J-C Desenclos, A Laporte, P Brouqui
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
May 9, 1977
[Hypertensive encephalopathy. Clinical and physiopathologic developments]
J M Orgogozo, A Laporte, P Loiseau
Invasion & Metastasis
|
January 1, 1997
Differential responsiveness of murine T lymphomas to local growth and invasion factors may determine metastasis formation in the ovaries
C Schmidt, A Laporte, P De Baetselier
Frontiers in Endocrinology
|
May 22, 2014
Allosteric and biased g protein-coupled receptor signaling regulation: potentials for new therapeutics
Etienne Khoury, Stéphanie Clément, Stéphane A Laporte
Methods in Molecular Biology (Clifton, N.J.)
|
March 29, 2019
Methods to Monitor the Trafficking of β-Arrestin/G Protein-Coupled Receptor Complexes Using Enhanced Bystander BRET
Yubo Cao, Yoon Namkung, Stéphane A Laporte
Methods in Molecular Biology (Clifton, N.J.)
|
August 27, 2011
Study of G protein-coupled receptor/β-arrestin interactions within endosomes using FRAP
Benjamin Aguila, May Simaan, Stéphane A Laporte
Molecular Endocrinology (Baltimore, Md.)
|
October 23, 2004
c-Src regulates clathrin adapter protein 2 interaction with beta-arrestin and the angiotensin II type 1 receptor during clathrin- mediated internalization
Delphine Fessart, May Simaan, Stéphane A Laporte
British Journal of Pharmacology
|
November 6, 2012
GPCR heterodimers: asymmetries in ligand binding and signalling output offer new targets for drug discovery
Eugénie Goupil, Stéphane A Laporte, Terence E Hébert
The Journal of Clinical Investigation
|
May 1, 1994
Processing of urushiol (poison ivy) hapten by both endogenous and exogenous pathways for presentation to T cells in vitro
R S Kalish, J A Wood, A LaPorte
Page
of 15