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| 3 | 10702666 | Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24. | Cytogenet Cell Genet | 1999 |
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| 4 | 10965105 | Assignment of the calcium-binding mitochondrial carrier Aralar1 gene (SLC25A12) to human chromosome band 2q31 by in situ hybridization. | Cytogenet Cell Genet | 2000 |
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| 7 | 17693006 | Association study of polymorphisms in the mitochondrial aspartate/glutamate carrier SLC25A12 (aralar) gene with schizophrenia. | Prog Neuropsychopharmacol Biol Psychiatry | 2007 Oct 1 |
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| 8 | 17894412 | Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism. | Am J Med Genet B Neuropsychiatr Genet | 2008 Apr 5 |
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| 9 | 18180767 | SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects. | Mol Psychiatry | 2008 Apr |
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| 10 | 18607376 | Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1. | Mol Psychiatry | 2010 Jan |
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| 11 | 19360665 | Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism. | Autism Res | 2008 Jun |
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| 12 | 19641205 | AGC1 deficiency associated with global cerebral hypomyelination. | N Engl J Med | 2009 Jul 30 |
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| 13 | 20736955 | Brain glutamine synthesis requires neuronal-born aspartate as amino donor for glial glutamate formation. | J Cereb Blood Flow Metab | 2011 Jan |
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| 14 | 21691713 | The mitochondrial aspartate/glutamate carrier AGC1 and calcium homeostasis: physiological links and abnormalities in autism. | Mol Neurobiol | 2011 Aug |
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| 15 | 23216354 | AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway. | J Neurochem | 2013 Feb |
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| 16 | 24007662 | Quantitative clinical proteomic study of autopsied human infarcted brain specimens to elucidate the deregulated pathways in ischemic stroke pathology. | J Proteomics | 2013 Oct 8 |
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| 17 | 24515575 | AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate. | JIMD Rep | 2014 |
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| 18 | 24679184 | Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome. | Mol Autism | 2014 Mar 31 |
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| 19 | 24820519 | Ca(2+) regulation of mitochondrial function in neurons. | Biochim Biophys Acta | 2014 Oct |
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| 20 | 25313047 | Pyruvate kinase and aspartate-glutamate carrier distributions reveal key metabolic links between neurons and glia in retina. | Proc Natl Acad Sci U S A | 2014 Oct 28 |
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| 21 | 25663199 | Mitochondrial Aspartate/Glutamate Carrier SLC25A12 and Autism Spectrum Disorder: a Meta-Analysis. | Mol Neurobiol | 2016 Apr |
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| 22 | 25809592 | The regulation of neuronal mitochondrial metabolism by calcium. | J Physiol | 2015 Aug 15 |
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| 23 | 25921325 | Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis. | Am J Med Genet B Neuropsychiatr Genet | 2015 Jun |
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| 24 | 26330901 | Aralar plays a significant role in maintaining the survival and mitochondrial membrane potential of BV2 microglia. | Int J Physiol Pathophysiol Pharmacol | 2015 |
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| 25 | 27401256 | Uncoupling Protein 2 (UCP2) Function in the Brain as Revealed by the Cerebral Metabolism of (1-<sup>13</sup>C)-Glucose. | Neurochem Res | 2017 Jan |
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| 26 | 28235644 | Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells. | Biochim Biophys Acta Mol Basis Dis | 2017 Jun |
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| 27 | 28429368 | ARALAR/AGC1 deficiency, a neurodevelopmental disorder with severe impairment of neuronal mitochondrial respiration, does not produce a primary increase in brain lactate. | J Neurochem | 2017 Jul |
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| 28 | 30122555 | Cytosolic Aspartate Availability Determines Cell Survival When Glutamine Is Limiting. | Cell Metab | 2018 Nov 6 |
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| 29 | 30321589 | Epigenetic upregulation and functional role of the mitochondrial aspartate/glutamate carrier isoform 1 in hepatocellular carcinoma. | Biochim Biophys Acta Mol Basis Dis | 2019 Jan |
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| 30 | 31403263 | Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification. | Am J Med Genet A | 2019 Nov |
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| 31 | 31472174 | Mitochondrial movement in Aralar/Slc25a12/AGC1 deficient cortical neurons. | Neurochem Int | 2019 Dec |
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| 32 | 31514314 | Deficiency of Mitochondrial Aspartate-Glutamate Carrier 1 Leads to Oligodendrocyte Precursor Cell Proliferation Defects Both In Vitro and In Vivo. | Int J Mol Sci | 2019 Sep 11 |
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| 33 | 31766059 | Expanding Phenotypic Spectrum of Cerebral Aspartate-Glutamate Carrier Isoform 1 (AGC1) Deficiency. | Neuropediatrics | 2020 Apr |
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| 34 | 33292758 | Deficiency of malate-aspartate shuttle component SLC25A12 induces pulmonary metastasis. | Cancer Metab | 2020 Nov 26 |
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| 35 | 35008954 | AGC1 Deficiency: Pathology and Molecular and Cellular Mechanisms of the Disease. | Int J Mol Sci | 2022 Jan 4 |
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