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Pediatric Nephrology (Berlin, Germany)
|
November 6, 2020
Novel therapeutic approaches for the primary hyperoxalurias
Ruth Belostotsky, Yaacov Frishberg
International Journal of Molecular Sciences
|
January 21, 2022
Catabolism of Hydroxyproline in Vertebrates: Physiology, Evolution, Genetic Diseases and New siRNA Approach for Treatment
Ruth Belostotsky, Yaacov Frishberg
Clinical Immunology (Orlando, Fla.)
|
February 14, 2004
Utilizing Fcepsilon-Bak chimeric protein for studying IgE-FcepsilonRI interactions
Ruth Belostotsky, Haya Lorberboum-Galski
RNA Biology
|
January 20, 2012
Human mitochondrial tRNA quality control in health and disease: a channelling mechanism?
Ruth Belostotsky, Yaacov Frishberg, Nina Entelis
Journal of Molecular Medicine (Berlin, Germany)
|
June 26, 2012
Primary hyperoxaluria type III--a model for studying perturbations in glyoxylate metabolism
Ruth Belostotsky, James Jonathon Pitt, Yaacov Frishberg
Journal of Medical Genetics
|
July 6, 2014
Mutations in HAO1 encoding glycolate oxidase cause isolated glycolic aciduria
Yaacov Frishberg, Avraham Zeharia, Roman Lyakhovetsky, et al.
JIMD Reports
|
February 25, 2014
4-hydroxyglutamate is a biomarker for primary hyperoxaluria type 3
James J Pitt, Frank Willis, Nicholas Tzanakos, et al.
Biochemical and Biophysical Research Communications
|
January 10, 2002
Utilizing chimeric proteins for exploring the cellular fate of endogenous proteins
Ahmi Ben-Yehudah, Rami Aqeilan, Ruth Belostotsky, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 16, 2008
Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge
Rachel Becker-Cohen, Ruth Belostotsky, Efrat Ben-Shalom, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 30, 2018
Metabolite diagnosis of primary hyperoxaluria type 3
Lawrence Greed, Frank Willis, Lilian Johnstone, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Pediatric Nephrology (Berlin, Germany)
|
November 6, 2020
Novel therapeutic approaches for the primary hyperoxalurias
Ruth Belostotsky, Yaacov Frishberg
International Journal of Molecular Sciences
|
January 21, 2022
Catabolism of Hydroxyproline in Vertebrates: Physiology, Evolution, Genetic Diseases and New siRNA Approach for Treatment
Ruth Belostotsky, Yaacov Frishberg
Clinical Immunology (Orlando, Fla.)
|
February 14, 2004
Utilizing Fcepsilon-Bak chimeric protein for studying IgE-FcepsilonRI interactions
Ruth Belostotsky, Haya Lorberboum-Galski
RNA Biology
|
January 20, 2012
Human mitochondrial tRNA quality control in health and disease: a channelling mechanism?
Ruth Belostotsky, Yaacov Frishberg, Nina Entelis
Journal of Molecular Medicine (Berlin, Germany)
|
June 26, 2012
Primary hyperoxaluria type III--a model for studying perturbations in glyoxylate metabolism
Ruth Belostotsky, James Jonathon Pitt, Yaacov Frishberg
Journal of Medical Genetics
|
July 6, 2014
Mutations in HAO1 encoding glycolate oxidase cause isolated glycolic aciduria
Yaacov Frishberg, Avraham Zeharia, Roman Lyakhovetsky, et al.
JIMD Reports
|
February 25, 2014
4-hydroxyglutamate is a biomarker for primary hyperoxaluria type 3
James J Pitt, Frank Willis, Nicholas Tzanakos, et al.
Biochemical and Biophysical Research Communications
|
January 10, 2002
Utilizing chimeric proteins for exploring the cellular fate of endogenous proteins
Ahmi Ben-Yehudah, Rami Aqeilan, Ruth Belostotsky, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 16, 2008
Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge
Rachel Becker-Cohen, Ruth Belostotsky, Efrat Ben-Shalom, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 30, 2018
Metabolite diagnosis of primary hyperoxaluria type 3
Lawrence Greed, Frank Willis, Lilian Johnstone, et al.
Page
of 2