Alessandro Roncador

Via Sommarive 9
Trento, 38123, Italy

Last Updated: 09/26/2026

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Found 11 publications

Functionalization of TiO2 sol-gel derived films for cell confinement.

Functionalization of TiO2 sol-gel derived films for cell confinement.

Journal: Colloids and surfaces. B, Biointerfaces
Published: February 09, 2021

Increased transcription of transglutaminase 1 mediates neuronal death in in vitro models of neuronal stress and Aβ1-42-mediated toxicity.

Increased transcription of transglutaminase 1 mediates neuronal death in in vitro models of neuronal stress and Aβ1-42-mediated toxicity.

Journal: Neurobiology of disease
Published: December 20, 2019

Prototyping a memristive-based device to analyze neuronal excitability.

Prototyping a memristive-based device to analyze neuronal excitability.

Journal: Biophysical chemistry
Published: May 22, 2019

Ankyrin-G induces nucleoporin Nup358 to associate with the axon initial segment of neurons.

Ankyrin-G induces nucleoporin Nup358 to associate with the axon initial segment of neurons.

Journal: Journal of cell science
Published: July 17, 2018

Primary cortical neurons on PMCS TiO2 films towards bio-hybrid memristive device: A morpho-functional study.

Primary cortical neurons on PMCS TiO2 films towards bio-hybrid memristive device: A morpho-functional study.

Journal: Biophysical chemistry
Published: April 07, 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

Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine.

Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine.

Journal: Biochimica et biophysica acta
Published: June 03, 2015

S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation.

S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation.

Journal: Human molecular genetics
Published: July 04, 2014

Allele-specific characterization of alanine: glyoxylate aminotransferase variants associated with primary hyperoxaluria.

Allele-specific characterization of alanine: glyoxylate aminotransferase variants associated with primary hyperoxaluria.

Journal: PloS one
Published: January 07, 2014

Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.

Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.

Journal: Biochimica et biophysica acta
Published: July 25, 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