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

C Shore

Showing results (501-510 of 520) with videos related to

Pageof 52
Sort By:
Nature Cell Biology|September 20, 2011
Bcl-xL regulates metabolic efficiency of neurons through interaction with the mitochondrial F1FO ATP synthaseKambiz N Alavian, Hongmei Li, Leon Collis, et al.
Plos One|April 16, 2011
A field guide to pandemic, epidemic and sporadic clones of methicillin-resistant Staphylococcus aureusStefan Monecke, Geoffrey Coombs, Anna C Shore, et al.
Hypertension (Dallas, Tex. : 1979)|March 21, 2018
Development and Validation of a Path Length Calculation for Carotid-Femoral Pulse Wave Velocity Measurement: A TASCFORCE, SUMMIT, and Caerphilly Collaborative VentureJonathan R Weir-McCall, Liam Brown, Jennifer Summersgill, et al.
Journal of Hypertension|September 9, 2024
Aortic reservoir-excess pressure parameters are associated with worse cognitive function in people with untreated stage II/III hypertensionKunihiko Aizawa, Andrew N Jordan, Kim M Gooding, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.
American Journal of Human Genetics|October 4, 2016
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis ImperfectaDavid A Parry, Claire E L Smith, Walid El-Sayed, et al.
Molecular and Cellular Biology|August 26, 2009
The small molecule GMX1778 is a potent inhibitor of NAD+ biosynthesis: strategy for enhanced therapy in nicotinic acid phosphoribosyltransferase 1-deficient tumorsMark Watson, Anne Roulston, Laurent Bélec, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 9, 2015
Elevated Plasma Levels of MMP-12 Are Associated With Atherosclerotic Burden and Symptomatic Cardiovascular Disease in Subjects With Type 2 DiabetesIsabel Goncalves, Eva Bengtsson, Helen M Colhoun, et al.
BMC Cardiovascular Disorders|September 7, 2016
Association between renin and atherosclerotic burden in subjects with and without type 2 diabetesIsabel Gonçalves, Andreas Edsfeldt, Helen M Colhoun, et al.
American Journal of Human Genetics|August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.
Pageof 52

Showing results (501-510 of 520) with videos related to

Sort By:
Pageof 52
Nature Cell Biology|September 20, 2011
Bcl-xL regulates metabolic efficiency of neurons through interaction with the mitochondrial F1FO ATP synthaseKambiz N Alavian, Hongmei Li, Leon Collis, et al.
Plos One|April 16, 2011
A field guide to pandemic, epidemic and sporadic clones of methicillin-resistant Staphylococcus aureusStefan Monecke, Geoffrey Coombs, Anna C Shore, et al.
Hypertension (Dallas, Tex. : 1979)|March 21, 2018
Development and Validation of a Path Length Calculation for Carotid-Femoral Pulse Wave Velocity Measurement: A TASCFORCE, SUMMIT, and Caerphilly Collaborative VentureJonathan R Weir-McCall, Liam Brown, Jennifer Summersgill, et al.
Journal of Hypertension|September 9, 2024
Aortic reservoir-excess pressure parameters are associated with worse cognitive function in people with untreated stage II/III hypertensionKunihiko Aizawa, Andrew N Jordan, Kim M Gooding, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.
American Journal of Human Genetics|October 4, 2016
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis ImperfectaDavid A Parry, Claire E L Smith, Walid El-Sayed, et al.
Molecular and Cellular Biology|August 26, 2009
The small molecule GMX1778 is a potent inhibitor of NAD+ biosynthesis: strategy for enhanced therapy in nicotinic acid phosphoribosyltransferase 1-deficient tumorsMark Watson, Anne Roulston, Laurent Bélec, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 9, 2015
Elevated Plasma Levels of MMP-12 Are Associated With Atherosclerotic Burden and Symptomatic Cardiovascular Disease in Subjects With Type 2 DiabetesIsabel Goncalves, Eva Bengtsson, Helen M Colhoun, et al.
BMC Cardiovascular Disorders|September 7, 2016
Association between renin and atherosclerotic burden in subjects with and without type 2 diabetesIsabel Gonçalves, Andreas Edsfeldt, Helen M Colhoun, et al.
American Journal of Human Genetics|August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.
Pageof 52