Carla B. Voltattorni

Verona, Italy

Last Updated: 09/26/2026

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Found 15 publications

Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina.

Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina.

Journal: Frontiers in molecular biosciences

Published: April 14, 2021

New variants of AADC deficiency expand the knowledge of enzymatic phenotypes.

New variants of AADC deficiency expand the knowledge of enzymatic phenotypes.

Journal: Archives of biochemistry and biophysics

Published: November 15, 2019

Phosphorylation of pyridoxal 5'-phosphate enzymes: an intriguing and neglected topic.

Phosphorylation of pyridoxal 5'-phosphate enzymes: an intriguing and neglected topic.

Journal: Amino acids

Published: September 16, 2017

Radiation damage at the active site of human alanine:glyoxylate aminotransferase reveals that the cofactor position is finely tuned during catalysis.

Radiation damage at the active site of human alanine:glyoxylate aminotransferase reveals that the cofactor position is finely tuned during catalysis.

Journal: Scientific reports

Published: May 12, 2017

Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I.

Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I.

Journal: Nanomedicine : nanotechnology, biology, and medicine

Published: August 12, 2016

New Insights Emerging from Recent Investigations on Human Group II Pyridoxal 5'-Phosphate Decarboxylases.

New Insights Emerging from Recent Investigations on Human Group II Pyridoxal 5'-Phosphate Decarboxylases.

Journal: Current medicinal chemistry

Published: July 20, 2016

Parkinson's Disease: Recent Updates in the Identification of Human Dopa Decarboxylase Inhibitors.

Parkinson's Disease: Recent Updates in the Identification of Human Dopa Decarboxylase Inhibitors.

Journal: Current drug metabolism

Published: December 11, 2015

The novel R347g pathogenic mutation of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency.

The novel R347g pathogenic mutation of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency.

Journal: Biochimica et biophysica acta

Published: November 09, 2015

The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I.

The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I.

Journal: ACS chemical biology

Published: July 11, 2015

The chaperone role of the pyridoxal 5'-phosphate and its implications for rare diseases involving B6-dependent enzymes.

The chaperone role of the pyridoxal 5'-phosphate and its implications for rare diseases involving B6-dependent enzymes.

Journal: Clinical biochemistry

Published: September 18, 2013

Interaction of human Dopa decarboxylase with L-Dopa: spectroscopic and kinetic studies as a function of pH.

Interaction of human Dopa decarboxylase with L-Dopa: spectroscopic and kinetic studies as a function of pH.

Journal: BioMed research international

Published: April 18, 2013

S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine.

S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine.

Journal: Human molecular genetics

Published: January 17, 2013

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Last Updated: 09/26/2026