Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Albane A Bizet

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Journal of Cellular Biochemistry|September 8, 2011
CD109-mediated degradation of TGF-β receptors and inhibition of TGF-β responses involve regulation of SMAD7 and Smurf2 localization and functionAlbane A Bizet, Nicolas Tran-Khanh, Anshuman Saksena, et al.
Experimental Dermatology|May 5, 2011
CD109 release from the cell surface in human keratinocytes regulates TGF-β receptor expression, TGF-β signalling and STAT3 activation: relevance to psoriasisIvan V Litvinov, Albane A Bizet, Yousef Binamer, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 7, 2006
Identification of CD109 as part of the TGF-beta receptor system in human keratinocytesKenneth W Finnson, Betty Y Y Tam, Kai Liu, et al.
Biochimica Et Biophysica Acta|February 8, 2011
The TGF-β co-receptor, CD109, promotes internalization and degradation of TGF-β receptorsAlbane A Bizet, Kai Liu, Nicolas Tran-Khanh, et al.
The Journal of Investigative Dermatology|November 22, 2016
Overexpression of CD109 in the Epidermis Differentially Regulates ALK1 Versus ALK5 Signaling and Modulates Extracellular Matrix Synthesis in the SkinJoshua Vorstenbosch, Christopher M Nguyen, Shufeng Zhou, et al.
Nature Communications|January 31, 2017
KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signallingKenneth B Schou, Johanne B Mogensen, Stine K Morthorst, et al.
Human Mutation|June 21, 2016
DCDC2 Mutations Cause Neonatal Sclerosing CholangitisMuriel Girard, Albane A Bizet, Alain Lachaux, et al.
Journal of the American Society of Nephrology : JASN|May 31, 2014
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGSEvelyne Huynh Cong, Albane A Bizet, Olivia Boyer, et al.
American Journal of Human Genetics|April 17, 2012
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutationsIsabelle Perrault, Sophie Saunier, Sylvain Hanein, et al.
Human Mutation|February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseMiriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Cellular Biochemistry|September 8, 2011
CD109-mediated degradation of TGF-β receptors and inhibition of TGF-β responses involve regulation of SMAD7 and Smurf2 localization and functionAlbane A Bizet, Nicolas Tran-Khanh, Anshuman Saksena, et al.
Experimental Dermatology|May 5, 2011
CD109 release from the cell surface in human keratinocytes regulates TGF-β receptor expression, TGF-β signalling and STAT3 activation: relevance to psoriasisIvan V Litvinov, Albane A Bizet, Yousef Binamer, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 7, 2006
Identification of CD109 as part of the TGF-beta receptor system in human keratinocytesKenneth W Finnson, Betty Y Y Tam, Kai Liu, et al.
Biochimica Et Biophysica Acta|February 8, 2011
The TGF-β co-receptor, CD109, promotes internalization and degradation of TGF-β receptorsAlbane A Bizet, Kai Liu, Nicolas Tran-Khanh, et al.
The Journal of Investigative Dermatology|November 22, 2016
Overexpression of CD109 in the Epidermis Differentially Regulates ALK1 Versus ALK5 Signaling and Modulates Extracellular Matrix Synthesis in the SkinJoshua Vorstenbosch, Christopher M Nguyen, Shufeng Zhou, et al.
Nature Communications|January 31, 2017
KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signallingKenneth B Schou, Johanne B Mogensen, Stine K Morthorst, et al.
Human Mutation|June 21, 2016
DCDC2 Mutations Cause Neonatal Sclerosing CholangitisMuriel Girard, Albane A Bizet, Alain Lachaux, et al.
Journal of the American Society of Nephrology : JASN|May 31, 2014
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGSEvelyne Huynh Cong, Albane A Bizet, Olivia Boyer, et al.
American Journal of Human Genetics|April 17, 2012
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutationsIsabelle Perrault, Sophie Saunier, Sylvain Hanein, et al.
Human Mutation|February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseMiriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Pageof 2