Laura Contreras

Madrid, MD 28049, Spain

Last Updated: 09/26/2026

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Found 20 publications

Exogenous aralar/slc25a12 can replace citrin/slc25a13 as malate aspartate shuttle component in liver.

Exogenous aralar/slc25a12 can replace citrin/slc25a13 as malate aspartate shuttle component in liver.

Journal: Molecular genetics and metabolism reports
Published: March 09, 2023

Regulation of neuronal energy metabolism by calcium: Role of MCU and Aralar/malate-aspartate shuttle.

Regulation of neuronal energy metabolism by calcium: Role of MCU and Aralar/malate-aspartate shuttle.

Journal: Biochimica et biophysica acta. Molecular cell research
Published: February 13, 2023

AGC1 Deficiency: Pathology and Molecular and Cellular Mechanisms of the Disease.

AGC1 Deficiency: Pathology and Molecular and Cellular Mechanisms of the Disease.

Journal: International journal of molecular sciences
Published: November 22, 2021

Chronic inhibition of the mitochondrial ATP synthase in skeletal muscle triggers sarcoplasmic reticulum distress and tubular aggregates.

Chronic inhibition of the mitochondrial ATP synthase in skeletal muscle triggers sarcoplasmic reticulum distress and tubular aggregates.

Journal: Cell death & disease
Published: October 13, 2021

βOHB Protective Pathways in Aralar-KO Neurons and Brain: An Alternative to Ketogenic Diet.

βOHB Protective Pathways in Aralar-KO Neurons and Brain: An Alternative to Ketogenic Diet.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: March 27, 2020

The Response to Stimulation in Neurons and Astrocytes.

The Response to Stimulation in Neurons and Astrocytes.

Journal: Neurochemical research
Published: March 07, 2019

Mitochondrial movement in Aralar/Slc25a12/AGC1 deficient cortical neurons.

Mitochondrial movement in Aralar/Slc25a12/AGC1 deficient cortical neurons.

Journal: Neurochemistry international
Published: January 31, 2019

De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.

De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.

Journal: American journal of human genetics
Published: May 19, 2017

Uncoupling Protein 2 (UCP2) Function in the Brain as Revealed by the Cerebral Metabolism of (1-13C)-Glucose.

Uncoupling Protein 2 (UCP2) Function in the Brain as Revealed by the Cerebral Metabolism of (1-13C)-Glucose.

Journal: Neurochemical research
Published: May 31, 2016

Deficient glucose and glutamine metabolism in Aralar/AGC1/Slc25a12 knockout mice contributes to altered visual function.

Deficient glucose and glutamine metabolism in Aralar/AGC1/Slc25a12 knockout mice contributes to altered visual function.

Journal: Molecular vision
Published: January 27, 2016

Calcium regulation of mitochondrial carriers.

Calcium regulation of mitochondrial carriers.

Journal: Biochimica et biophysica acta
Published: January 25, 2016

Glutamate excitotoxicity and Ca2+-regulation of respiration: Role of the Ca2+ activated mitochondrial transporters (CaMCs).

Glutamate excitotoxicity and Ca2+-regulation of respiration: Role of the Ca2+ activated mitochondrial transporters (CaMCs).

Journal: Biochimica et biophysica acta
Published: January 15, 2016
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Last Updated: 09/26/2026