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

M Berthoud

Showing results (91-100 of 102) with videos related to

Pageof 11
Sort By:
Biochemical and Biophysical Research Communications|June 28, 2005
Connexin43 with a cytoplasmic loop deletion inhibits the function of several connexinsMin Wang, Agustín D Martínez, Viviana M Berthoud, et al.
Experimental Eye Research|November 3, 2012
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataractG Senthil Kumar, John W Kyle, Peter J Minogue, et al.
Molecular Vision|September 17, 2009
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutationJochen Graw, Werner Schmidt, Peter J Minogue, et al.
Journal of Proteome Research|December 17, 2010
Identification of CaMKII phosphorylation sites in Connexin43 by high-resolution mass spectrometryRichard Y-C Huang, James G Laing, Evelyn M Kanter, et al.
Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Molecular Biosystems|January 6, 2012
Modulation of gap junction channels and hemichannels by growth factorsKurt A Schalper, Manuel A Riquelme, María C Brañes, et al.
Biological Research|May 23, 2024
Connexin channels and hemichannels are modulated differently by charge reversal at residues forming the intracellular pocketFelipe Villanelo, Peter J Minogue, Jaime Maripillán, et al.
Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.
Molecular Biology of the Cell|July 13, 2012
Critical role of the first transmembrane domain of Cx26 in regulating oligomerization and functionOscar Jara, Rodrigo Acuña, Isaac E García, et al.
Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Biochemical and Biophysical Research Communications|June 28, 2005
Connexin43 with a cytoplasmic loop deletion inhibits the function of several connexinsMin Wang, Agustín D Martínez, Viviana M Berthoud, et al.
Experimental Eye Research|November 3, 2012
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataractG Senthil Kumar, John W Kyle, Peter J Minogue, et al.
Molecular Vision|September 17, 2009
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutationJochen Graw, Werner Schmidt, Peter J Minogue, et al.
Journal of Proteome Research|December 17, 2010
Identification of CaMKII phosphorylation sites in Connexin43 by high-resolution mass spectrometryRichard Y-C Huang, James G Laing, Evelyn M Kanter, et al.
Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Molecular Biosystems|January 6, 2012
Modulation of gap junction channels and hemichannels by growth factorsKurt A Schalper, Manuel A Riquelme, María C Brañes, et al.
Biological Research|May 23, 2024
Connexin channels and hemichannels are modulated differently by charge reversal at residues forming the intracellular pocketFelipe Villanelo, Peter J Minogue, Jaime Maripillán, et al.
Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.
Molecular Biology of the Cell|July 13, 2012
Critical role of the first transmembrane domain of Cx26 in regulating oligomerization and functionOscar Jara, Rodrigo Acuña, Isaac E García, et al.
Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.
Pageof 11