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

Miles D Houslay

Showing results (41-50 of 137) with videos related to

Pageof 14
Sort By:
The Biochemical Journal|December 21, 2016
Identification of a multifunctional docking site on the catalytic unit of phosphodiesterase-4 (PDE4) that is utilised by multiple interaction partnersKirsty F Houslay, Frank Christian, Ruth MacLeod, et al.
Cellular Signalling|September 16, 2006
Oxidative stress employs phosphatidyl inositol 3-kinase and ERK signalling pathways to activate cAMP phosphodiesterase-4D3 (PDE4D3) through multi-site phosphorylation at Ser239 and Ser579Elaine V Hill, Catherine L Sheppard, York-Fong Cheung, et al.
Molecular and Cellular Biology|October 26, 2011
Eukaryotic translation initiation factor 3, subunit a, regulates the extracellular signal-regulated kinase pathwayTian-Rui Xu, Rui-Fang Lu, David Romano, et al.
The Journal of Biological Chemistry|September 15, 2007
Dynamic regulation, desensitization, and cross-talk in discrete subcellular microdomains during beta2-adrenoceptor and prostanoid receptor cAMP signalingDebbie Willoughby, George S Baillie, Martin J Lynch, et al.
FEBS Letters|July 11, 2006
Reduced PDE4 expression and activity contributes to enhanced catecholamine-induced cAMP accumulation in adipocytes from FOXC2 transgenic miceLine M Grønning, George S Baillie, Anna Cederberg, et al.
Cellular Signalling|March 8, 2002
In addition to the SH3 binding region, multiple regions within the N-terminal noncatalytic portion of the cAMP-specific phosphodiesterase, PDE4A5, contribute to its intracellular targetingMatthew B Beard, Elaine Huston, Lachlan Campbell, et al.
Cancer Research|June 5, 2007
Chemoresistant KM12C colon cancer cells are addicted to low cyclic AMP levels in a phosphodiesterase 4-regulated compartment via effects on phosphoinositide 3-kinaseDavid G McEwan, Valerie G Brunton, George S Baillie, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|March 30, 2004
Differential expression of PDE4 cAMP phosphodiesterase isoforms in inflammatory cells of smokers with COPD, smokers without COPD, and nonsmokersRachael Barber, George S Baillie, Reinhard Bergmann, et al.
The Journal of Biological Chemistry|September 23, 2003
The unique amino-terminal region of the PDE4D5 cAMP phosphodiesterase isoform confers preferential interaction with beta-arrestinsGraeme B Bolger, Angela McCahill, Elaine Huston, et al.
The Biochemical Journal|August 31, 2007
Structures of the four subfamilies of phosphodiesterase-4 provide insight into the selectivity of their inhibitorsHuanchen Wang, Ming-Sheng Peng, Yi Chen, et al.
Pageof 14

Showing results (41-50 of 137) with videos related to

Sort By:
Pageof 14
The Biochemical Journal|December 21, 2016
Identification of a multifunctional docking site on the catalytic unit of phosphodiesterase-4 (PDE4) that is utilised by multiple interaction partnersKirsty F Houslay, Frank Christian, Ruth MacLeod, et al.
Cellular Signalling|September 16, 2006
Oxidative stress employs phosphatidyl inositol 3-kinase and ERK signalling pathways to activate cAMP phosphodiesterase-4D3 (PDE4D3) through multi-site phosphorylation at Ser239 and Ser579Elaine V Hill, Catherine L Sheppard, York-Fong Cheung, et al.
Molecular and Cellular Biology|October 26, 2011
Eukaryotic translation initiation factor 3, subunit a, regulates the extracellular signal-regulated kinase pathwayTian-Rui Xu, Rui-Fang Lu, David Romano, et al.
The Journal of Biological Chemistry|September 15, 2007
Dynamic regulation, desensitization, and cross-talk in discrete subcellular microdomains during beta2-adrenoceptor and prostanoid receptor cAMP signalingDebbie Willoughby, George S Baillie, Martin J Lynch, et al.
FEBS Letters|July 11, 2006
Reduced PDE4 expression and activity contributes to enhanced catecholamine-induced cAMP accumulation in adipocytes from FOXC2 transgenic miceLine M Grønning, George S Baillie, Anna Cederberg, et al.
Cellular Signalling|March 8, 2002
In addition to the SH3 binding region, multiple regions within the N-terminal noncatalytic portion of the cAMP-specific phosphodiesterase, PDE4A5, contribute to its intracellular targetingMatthew B Beard, Elaine Huston, Lachlan Campbell, et al.
Cancer Research|June 5, 2007
Chemoresistant KM12C colon cancer cells are addicted to low cyclic AMP levels in a phosphodiesterase 4-regulated compartment via effects on phosphoinositide 3-kinaseDavid G McEwan, Valerie G Brunton, George S Baillie, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|March 30, 2004
Differential expression of PDE4 cAMP phosphodiesterase isoforms in inflammatory cells of smokers with COPD, smokers without COPD, and nonsmokersRachael Barber, George S Baillie, Reinhard Bergmann, et al.
The Journal of Biological Chemistry|September 23, 2003
The unique amino-terminal region of the PDE4D5 cAMP phosphodiesterase isoform confers preferential interaction with beta-arrestinsGraeme B Bolger, Angela McCahill, Elaine Huston, et al.
The Biochemical Journal|August 31, 2007
Structures of the four subfamilies of phosphodiesterase-4 provide insight into the selectivity of their inhibitorsHuanchen Wang, Ming-Sheng Peng, Yi Chen, et al.
Pageof 14