ARALAR/AGC1 deficiency, a neurodevelopmental disorder with severe impairment of neuronal mitochondrial respiration, does not produce a primary increase in brain lactate.

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ARALAR/AGC1 deficiency, a neurodevelopmental disorder with severe impairment of neuronal mitochondrial respiration, does not produce a primary increase in brain lactate.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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ARALAR/AGC1 deficiency, a neur ...... ary increase in brain lactate.

@en

ARALAR/AGC1 deficiency, a neur ...... ary increase in brain lactate.

@nl

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Item

label

ARALAR/AGC1 deficiency, a neur ...... ary increase in brain lactate.

@en

ARALAR/AGC1 deficiency, a neur ...... ary increase in brain lactate.

@nl

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ARALAR/AGC1 deficiency, a neur ...... ary increase in brain lactate.

@en

ARALAR/AGC1 deficiency, a neur ...... ary increase in brain lactate.

@nl

P1476

ARALAR/AGC1 deficiency, a neur ...... mary increase in brain lactate

@en

P2093

Irene Llorente-Folch

http://www.w3.org/2001/XMLSchema#string

Tiago B Rodrigues

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P2860

Citrin and aralar1 are Ca(2+)-stimulated aspartate/glutamate transporters in mitochondria

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

Molecular cloning of Aralar, a new member of the mitochondrial carrier superfamily that binds calcium and is present in human muscle and brain

Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome

Mouse lacking NAD+-linked glycerol phosphate dehydrogenase has normal pancreatic beta cell function but abnormal metabolite pattern in skeletal muscle

A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function

Evidence supporting a role for N-acetyl-l-aspartate as a molecular water pump in myelinated neurons in the central nervous system

Calcium signaling in brain mitochondria: interplay of malate aspartate NADH shuttle and calcium uniporter/mitochondrial dehydrogenase pathways.

Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies.

The in-depth evaluation of suspected mitochondrial disease

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132-139

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scholarly article

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10.1111/JNC.14047

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English

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142

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María Luisa García-Martín

Inés Juaristi

J Satrústegui

Beatriz Pardo

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2017-05-22T00:00:00Z

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P698

28429368

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neurodevelopmental disorders