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Current Opinion in Nephrology and Hypertension
|
April 11, 2024
A molecular journey on the pathogenesis of primary hyperoxaluria
Barbara Cellini
The FEBS Journal
|
September 15, 2017
Electrostatic interactions drive native-like aggregation of human alanine:glyoxylate aminostransferase
Mirco Dindo, Carolina Conter, Barbara Cellini
Biochimica Et Biophysica Acta
|
January 27, 2015
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview
Elisa Oppici, Riccardo Montioli, Barbara Cellini
FEBS Letters
|
November 19, 2003
Treponema denticola cystalysin catalyzes beta-desulfination of L-cysteine sulfinic acid and beta-decarboxylation of L-aspartate and oxalacetate
Barbara Cellini, Mariarita Bertoldi, Carla Borri Voltattorni
Journal of Inherited Metabolic Disease
|
May 5, 2011
Molecular insights into the pathogenicity of variants associated with the aromatic amino acid decarboxylase deficiency
Riccardo Montioli, Barbara Cellini, Carla Borri Voltattorni
Biochimica Et Biophysica Acta
|
December 24, 2010
Human liver peroxisomal alanine:glyoxylate aminotransferase: characterization of the two allelic forms and their pathogenic variants
Barbara Cellini, Riccardo Montioli, Carla Borri Voltattorni
Current Opinion in Nephrology and Hypertension
|
December 6, 2024
Effect of the allelic background on the phenotype of primary hyperoxaluria type I
Giorgia Mandrile, Barbara Cellini, Pietro Manuel Ferraro
Current Drug Targets
|
March 3, 2016
Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type I
Elisa Oppici, Riccardo Montioli, Mirco Dindo, et al.
Frontiers in Bioscience (Landmark Edition)
|
December 29, 2011
Molecular insights into primary hyperoxaluria type 1 pathogenesis
Barbara Cellini, Elisa Oppici, Alessandro Paiardini, et al.
The Open Biochemistry Journal
|
December 25, 2012
Biochemical and computational approaches to improve the clinical treatment of dopa decarboxylase-related diseases: an overview
Barbara Cellini, Riccardo Montioli, Elisa Oppici, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 104) with videos related to
Sort By:
Page
of 11
Current Opinion in Nephrology and Hypertension
|
April 11, 2024
A molecular journey on the pathogenesis of primary hyperoxaluria
Barbara Cellini
The FEBS Journal
|
September 15, 2017
Electrostatic interactions drive native-like aggregation of human alanine:glyoxylate aminostransferase
Mirco Dindo, Carolina Conter, Barbara Cellini
Biochimica Et Biophysica Acta
|
January 27, 2015
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview
Elisa Oppici, Riccardo Montioli, Barbara Cellini
FEBS Letters
|
November 19, 2003
Treponema denticola cystalysin catalyzes beta-desulfination of L-cysteine sulfinic acid and beta-decarboxylation of L-aspartate and oxalacetate
Barbara Cellini, Mariarita Bertoldi, Carla Borri Voltattorni
Journal of Inherited Metabolic Disease
|
May 5, 2011
Molecular insights into the pathogenicity of variants associated with the aromatic amino acid decarboxylase deficiency
Riccardo Montioli, Barbara Cellini, Carla Borri Voltattorni
Biochimica Et Biophysica Acta
|
December 24, 2010
Human liver peroxisomal alanine:glyoxylate aminotransferase: characterization of the two allelic forms and their pathogenic variants
Barbara Cellini, Riccardo Montioli, Carla Borri Voltattorni
Current Opinion in Nephrology and Hypertension
|
December 6, 2024
Effect of the allelic background on the phenotype of primary hyperoxaluria type I
Giorgia Mandrile, Barbara Cellini, Pietro Manuel Ferraro
Current Drug Targets
|
March 3, 2016
Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type I
Elisa Oppici, Riccardo Montioli, Mirco Dindo, et al.
Frontiers in Bioscience (Landmark Edition)
|
December 29, 2011
Molecular insights into primary hyperoxaluria type 1 pathogenesis
Barbara Cellini, Elisa Oppici, Alessandro Paiardini, et al.
The Open Biochemistry Journal
|
December 25, 2012
Biochemical and computational approaches to improve the clinical treatment of dopa decarboxylase-related diseases: an overview
Barbara Cellini, Riccardo Montioli, Elisa Oppici, et al.
Page
of 11