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

Ruth Belostotsky

Showing results (11-20 of 20) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
International Journal of Oncology|June 9, 2005
Utilizing a GnRH-based chimeric protein for the detection of adenocarcinomaMichal Lichtenstein, Ahmi Ben-Yehudah, Ruth Belostotsky, et al.
Pediatric Nephrology (Berlin, Germany)|January 9, 2022
Association of post-transplantation anellovirus viral load with kidney transplant rejection in childrenYifat Eldar-Yedidia, Efrat Ben-Shalom, Miriam Hillel, et al.
Pediatric Nephrology (Berlin, Germany)|October 7, 2009
Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?Yaacov Frishberg, Dganit Dinour, Ruth Belostotsky, et al.
American Journal of Human Genetics|January 25, 2011
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndromeRuth Belostotsky, Efrat Ben-Shalom, Choni Rinat, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 20, 2018
Translation inhibition corrects aberrant localization of mutant alanine-glyoxylate aminotransferase: possible therapeutic approach for hyperoxaluriaRuth Belostotsky, Roman Lyakhovetsky, Michael Y Sherman, et al.
The Journal of Urology|December 22, 2020
Mutations in <i>HOGA1</i> do Not Confer a Dominant Phenotype Manifesting as Kidney Stone DiseaseRoi Bar, Efrat Ben-Shalom, Mordechai Duvdevani, et al.
American Journal of Human Genetics|December 27, 2008
Mutations in DDR2 gene cause SMED with short limbs and abnormal calcificationsRuth Bargal, Valerie Cormier-Daire, Ziva Ben-Neriah, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in DHDPSL are responsible for primary hyperoxaluria type IIIRuth Belostotsky, Eric Seboun, Gregory H Idelson, et al.
Journal of Cell Science|November 12, 2020
A piggybacking mechanism enables peroxisomal localization of the glyoxylate cycle enzyme Mdh2 in yeastShiran Gabay-Maskit, Luis Daniel Cruz-Zaragoza, Nadav Shai, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 8, 2011
Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasisCarla G Monico, Sandro Rossetti, Ruth Belostotsky, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
International Journal of Oncology|June 9, 2005
Utilizing a GnRH-based chimeric protein for the detection of adenocarcinomaMichal Lichtenstein, Ahmi Ben-Yehudah, Ruth Belostotsky, et al.
Pediatric Nephrology (Berlin, Germany)|January 9, 2022
Association of post-transplantation anellovirus viral load with kidney transplant rejection in childrenYifat Eldar-Yedidia, Efrat Ben-Shalom, Miriam Hillel, et al.
Pediatric Nephrology (Berlin, Germany)|October 7, 2009
Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?Yaacov Frishberg, Dganit Dinour, Ruth Belostotsky, et al.
American Journal of Human Genetics|January 25, 2011
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndromeRuth Belostotsky, Efrat Ben-Shalom, Choni Rinat, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 20, 2018
Translation inhibition corrects aberrant localization of mutant alanine-glyoxylate aminotransferase: possible therapeutic approach for hyperoxaluriaRuth Belostotsky, Roman Lyakhovetsky, Michael Y Sherman, et al.
The Journal of Urology|December 22, 2020
Mutations in <i>HOGA1</i> do Not Confer a Dominant Phenotype Manifesting as Kidney Stone DiseaseRoi Bar, Efrat Ben-Shalom, Mordechai Duvdevani, et al.
American Journal of Human Genetics|December 27, 2008
Mutations in DDR2 gene cause SMED with short limbs and abnormal calcificationsRuth Bargal, Valerie Cormier-Daire, Ziva Ben-Neriah, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in DHDPSL are responsible for primary hyperoxaluria type IIIRuth Belostotsky, Eric Seboun, Gregory H Idelson, et al.
Journal of Cell Science|November 12, 2020
A piggybacking mechanism enables peroxisomal localization of the glyoxylate cycle enzyme Mdh2 in yeastShiran Gabay-Maskit, Luis Daniel Cruz-Zaragoza, Nadav Shai, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 8, 2011
Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasisCarla G Monico, Sandro Rossetti, Ruth Belostotsky, et al.
Pageof 2