(Q34199388)

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Developmental changes in the Ca2+-regulated mitochondrial aspartate-glutamate carrier aralar1 in brain and prominent expression in the spinal cord.

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3 November 2019

Developmental changes in the Ca2+-regulated mitochondrial aspartate-glutamate carrier aralar1 in brain and prominent expression in the spinal cord (English)

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3 November 2019

Araceli del Arco

2

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3 November 2019

Juan R Martínez-Morales

5

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3 November 2019

Jorgina Satrustegui Gil Delgado

11

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3 November 2019

Paola Bovolenta

9

object named as

Paola Bovolenta

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3 November 2019

author name string

Milagros Ramos

1

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3 November 2019

Beatriz Pardo

3

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3 November 2019

Alberto Martínez-Serrano

4

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3 November 2019

Keiko Kobayashi

6

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3 November 2019

Tomotsugu Yasuda

7

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3 November 2019

Elena Bogónez

8

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3 November 2019

Takeyori Saheki

10

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3 November 2019

publication date

1 June 2003

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3 November 2019

number of pages

14

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Developmental Brain Research

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3 November 2019

143

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3 November 2019

33-46

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3 November 2019

1

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3 November 2019

Expression of three mitochondrial solute carriers, citrin, aralar1 and ornithine transporter, in relation to urea cycle in mice.

1 reference

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Characterization of the cellular reduction of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT): subcellular localization, substrate dependence, and involvement of mitochondrial electron transport in MTT reduction

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Survival and growth of hippocampal neurons in defined medium at low density: advantages of a sandwich culture technique or low oxygen

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Influence of the Malate-Aspartate Shuttle on Oxidative Metabolism in Synaptosomes

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Emergence of excitotoxicity in cultured forebrain neurons coincides with larger glutamate-stimulated [Ca(2+)](i) increases and NMDA receptor mRNA levels

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Mitochondrial maturation during neuronal differentiation in vivo and in vitro

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7 January 2021

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Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24

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Pathogenesis of adult-onset type II citrullinemia caused by deficiency of citrin, a mitochondrial solute carrier protein: tissue and subcellular localization of citrin

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Changing patterns of transcriptional and post-transcriptional control of beta-F1-ATPase gene expression during mitochondrial biogenesis in liver.

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Aminooxyacetic acid inhibits the malate-aspartate shuttle in isolated nerve terminals and prevents the mitochondria from utilizing glycolytic substrates

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The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

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Mechanism of cellular 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction.

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7 January 2021

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Maturation of vulnerability to excitotoxicity: intracellular mechanisms in cultured postnatal hippocampal neurons.

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7 January 2021

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Regulation of cytosolic free calcium concentration by intrasynaptic mitochondria

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Relationship between synaptogenesis and cytochrome oxidase activity in Purkinje cells of the developing rat cerebellum

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7 January 2021

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Assignment of the calcium-binding mitochondrial carrier Aralar1 gene (SLC25A12) to human chromosome band 2q31 by in situ hybridization

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Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia

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Identifiers

10.1016/S0165-3806(03)00097-X

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3 November 2019

1 reference

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3 November 2019

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