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

David L Gasser

Showing results (1-10 of 14) with videos related to

Pageof 2
Sort By:
Molecular Genetics and Metabolism|December 1, 2009
Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapyZhe Zhang, David L Gasser, Eric F Rappaport, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 10, 2003
Cutting Edge: Multiple autoimmune pathways in kd/kd miceWayne W Hancock, Tsai-Lung Tsai, Michael P Madaio, et al.
Journal of the American Society of Nephrology : JASN|August 27, 2005
The kd/kd mouse is a model of collapsing glomerulopathyLaura Barisoni, Michael P Madaio, Maria Eraso, et al.
Journal of Autoimmunity|December 13, 2005
The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditionsTroy M Hallman, Min Peng, Ray Meade, et al.
American Journal of Physiology. Renal Physiology|September 12, 2008
Coenzyme Q10 supplementation rescues renal disease in Pdss2kd/kd mice with mutations in prenyl diphosphate synthase subunit 2Ryoichi Saiki, Adam L Lunceford, Yuchen Shi, et al.
Kidney International|June 18, 2004
Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd miceMin Peng, Leonard Jarett, Ray Meade, et al.
Mitochondrion|October 11, 2011
Parkinson's disease-like neuromuscular defects occur in prenyl diphosphate synthase subunit 2 (Pdss2) mutant miceCarly G K Ziegler, Min Peng, Marni J Falk, et al.
American Journal of Nephrology|November 12, 2005
Glomerular and tubular epithelial defects in kd/kd mice lead to progressive renal failureMichael P Madaio, Rexford S Ahima, Ray Meade, et al.
American Journal of Physiology. Renal Physiology|August 9, 2013
Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10David L Gasser, Cheryl A Winkler, Min Peng, et al.
Human Molecular Genetics|June 5, 2015
Inhibiting cytosolic translation and autophagy improves health in mitochondrial diseaseMin Peng, Julian Ostrovsky, Young Joon Kwon, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Molecular Genetics and Metabolism|December 1, 2009
Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapyZhe Zhang, David L Gasser, Eric F Rappaport, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 10, 2003
Cutting Edge: Multiple autoimmune pathways in kd/kd miceWayne W Hancock, Tsai-Lung Tsai, Michael P Madaio, et al.
Journal of the American Society of Nephrology : JASN|August 27, 2005
The kd/kd mouse is a model of collapsing glomerulopathyLaura Barisoni, Michael P Madaio, Maria Eraso, et al.
Journal of Autoimmunity|December 13, 2005
The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditionsTroy M Hallman, Min Peng, Ray Meade, et al.
American Journal of Physiology. Renal Physiology|September 12, 2008
Coenzyme Q10 supplementation rescues renal disease in Pdss2kd/kd mice with mutations in prenyl diphosphate synthase subunit 2Ryoichi Saiki, Adam L Lunceford, Yuchen Shi, et al.
Kidney International|June 18, 2004
Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd miceMin Peng, Leonard Jarett, Ray Meade, et al.
Mitochondrion|October 11, 2011
Parkinson's disease-like neuromuscular defects occur in prenyl diphosphate synthase subunit 2 (Pdss2) mutant miceCarly G K Ziegler, Min Peng, Marni J Falk, et al.
American Journal of Nephrology|November 12, 2005
Glomerular and tubular epithelial defects in kd/kd mice lead to progressive renal failureMichael P Madaio, Rexford S Ahima, Ray Meade, et al.
American Journal of Physiology. Renal Physiology|August 9, 2013
Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10David L Gasser, Cheryl A Winkler, Min Peng, et al.
Human Molecular Genetics|June 5, 2015
Inhibiting cytosolic translation and autophagy improves health in mitochondrial diseaseMin Peng, Julian Ostrovsky, Young Joon Kwon, et al.
Pageof 2