Pablo Rozas

Santiago, RM, Chile

Last Updated: 09/26/2026

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Found 14 publications

Expression of amyotrophic lateral sclerosis associated protein disulfide isomerase A3 D217N variant recapitulates early morphological alterations at the neuromuscular junction.

Expression of amyotrophic lateral sclerosis associated protein disulfide isomerase A3 D217N variant recapitulates early morphological alterations at the neuromuscular junction.

Journal: Neurobiology of disease
Published: May 27, 2025

Expression of protein disulfide isomerase A3Q481K variant associated with amyotrophic lateral sclerosis triggers disease features in mice.

Expression of protein disulfide isomerase A3Q481K variant associated with amyotrophic lateral sclerosis triggers disease features in mice.

Journal: Neurobiology of disease
Published: March 18, 2025

Genetically modified organisms: adapting regulatory frameworks for evolving genome editing technologies.

Genetically modified organisms: adapting regulatory frameworks for evolving genome editing technologies.

Journal: Biological research
Published: May 03, 2022

Critical roles of protein disulfide isomerases in balancing proteostasis in the nervous system.

Critical roles of protein disulfide isomerases in balancing proteostasis in the nervous system.

Journal: The Journal of biological chemistry
Published: November 07, 2021

Protein disulfide isomerase ERp57 protects early muscle denervation in experimental ALS.

Protein disulfide isomerase ERp57 protects early muscle denervation in experimental ALS.

Journal: Acta neuropathologica communications
Published: September 24, 2020

Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis.

Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis.

Journal: The EMBO journal
Published: May 05, 2020

Endoplasmic reticulum stress leads to accumulation of wild-type SOD1 aggregates associated with sporadic amyotrophic lateral sclerosis.

Endoplasmic reticulum stress leads to accumulation of wild-type SOD1 aggregates associated with sporadic amyotrophic lateral sclerosis.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 25, 2018

Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.

Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.

Journal: Scientific reports
Published: May 25, 2017

ERp57 as a novel cellular factor controlling prion protein biosynthesis: Therapeutic potential of protein disulfide isomerases.

ERp57 as a novel cellular factor controlling prion protein biosynthesis: Therapeutic potential of protein disulfide isomerases.

Journal: Prion
Published: February 12, 2016

The ER proteostasis network in ALS: Determining the differential motoneuron vulnerability.

The ER proteostasis network in ALS: Determining the differential motoneuron vulnerability.

Journal: Neuroscience letters
Published: February 04, 2016

Correction: Functional Role of the Disulfide Isomerase ERp57 in Axonal Regeneration.

Correction: Functional Role of the Disulfide Isomerase ERp57 in Axonal Regeneration.

Journal: PloS one
Published: October 03, 2015

ALS-linked protein disulfide isomerase variants cause motor dysfunction.

ALS-linked protein disulfide isomerase variants cause motor dysfunction.

Journal: The EMBO journal
Published: June 06, 2015
Showing 1-12 of 14

Last Updated: 09/26/2026