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Alexandre Benmerah

Showing results (51-60 of 82) with videos related to

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Developmental Cell|November 17, 2012
The NF-κB signaling protein Bcl10 regulates actin dynamics by controlling AP1 and OCRL-bearing vesiclesSabrina Marion, Julie Mazzolini, Floriane Herit, et al.
Cellular Signalling|August 26, 2014
Ligand stimulation induces clathrin- and Rab5-dependent downregulation of the kinase-dead EphB6 receptor preceded by the disruption of EphB6-Hsp90 interactionOdette Allonby, Amr M El Zawily, Tanya Freywald, et al.
Traffic (Copenhagen, Denmark)|June 6, 2007
The conserved isoleucine-valine-phenylalanine motif couples activation state and endocytic functions of beta-arrestinsAnne Burtey, Eva M Schmid, Marijn G J Ford, et al.
Journal of Cell Science|January 23, 2021
EFA6A, an exchange factor for Arf6, regulates early steps in ciliogenesisMariagrazia Partisani, Carole L Baron, Rania Ghossoub, et al.
Journal of Cell Science|October 29, 2010
The AP-1 clathrin adaptor facilitates cilium formation and functions with RAB-8 in C. elegans ciliary membrane transportOktay I Kaplan, Anahi Molla-Herman, Sebiha Cevik, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2007
beta-arrestin 2 oligomerization controls the Mdm2-dependent inhibition of p53Cédric Boularan, Mark G H Scott, Karima Bourougaa, et al.
Journal of Cell Science|April 30, 2010
The ciliary pocket: an endocytic membrane domain at the base of primary and motile ciliaAnahi Molla-Herman, Rania Ghossoub, Thierry Blisnick, et al.
The Journal of Biological Chemistry|October 4, 2005
Homo- and hetero-oligomerization of beta-arrestins in living cellsHélène Storez, Mark G H Scott, Hassan Issafras, et al.
Cilia|May 15, 2015
The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathiesAlexandre Benmerah, Bénédicte Durand, Rachel H Giles, et al.
American Journal of Human Genetics|January 22, 2019
TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking PathwaysGuillaume Dorval, Valeryia Kuzmuk, Olivier Gribouval, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Developmental Cell|November 17, 2012
The NF-κB signaling protein Bcl10 regulates actin dynamics by controlling AP1 and OCRL-bearing vesiclesSabrina Marion, Julie Mazzolini, Floriane Herit, et al.
Cellular Signalling|August 26, 2014
Ligand stimulation induces clathrin- and Rab5-dependent downregulation of the kinase-dead EphB6 receptor preceded by the disruption of EphB6-Hsp90 interactionOdette Allonby, Amr M El Zawily, Tanya Freywald, et al.
Traffic (Copenhagen, Denmark)|June 6, 2007
The conserved isoleucine-valine-phenylalanine motif couples activation state and endocytic functions of beta-arrestinsAnne Burtey, Eva M Schmid, Marijn G J Ford, et al.
Journal of Cell Science|January 23, 2021
EFA6A, an exchange factor for Arf6, regulates early steps in ciliogenesisMariagrazia Partisani, Carole L Baron, Rania Ghossoub, et al.
Journal of Cell Science|October 29, 2010
The AP-1 clathrin adaptor facilitates cilium formation and functions with RAB-8 in C. elegans ciliary membrane transportOktay I Kaplan, Anahi Molla-Herman, Sebiha Cevik, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2007
beta-arrestin 2 oligomerization controls the Mdm2-dependent inhibition of p53Cédric Boularan, Mark G H Scott, Karima Bourougaa, et al.
Journal of Cell Science|April 30, 2010
The ciliary pocket: an endocytic membrane domain at the base of primary and motile ciliaAnahi Molla-Herman, Rania Ghossoub, Thierry Blisnick, et al.
The Journal of Biological Chemistry|October 4, 2005
Homo- and hetero-oligomerization of beta-arrestins in living cellsHélène Storez, Mark G H Scott, Hassan Issafras, et al.
Cilia|May 15, 2015
The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathiesAlexandre Benmerah, Bénédicte Durand, Rachel H Giles, et al.
American Journal of Human Genetics|January 22, 2019
TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking PathwaysGuillaume Dorval, Valeryia Kuzmuk, Olivier Gribouval, et al.
Pageof 9