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35008954 | AGC1 Deficiency: Pathology and Molecular and Cellular Mechanisms of the Disease. | 2022 Jan 4 |
3 |
| 2 |
33292758 | Deficiency of malate-aspartate shuttle component SLC25A12 induces pulmonary metastasis. | 2020 Nov 26 |
2 |
| 3 |
31403263 | Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification. | 2019 Nov |
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| 4 |
31472174 | Mitochondrial movement in Aralar/Slc25a12/AGC1 deficient cortical neurons. | 2019 Dec |
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| 5 |
31514314 | Deficiency of Mitochondrial Aspartate-Glutamate Carrier 1 Leads to Oligodendrocyte Precursor Cell Proliferation Defects Both In Vitro and In Vivo. | 2019 Sep 11 |
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| 6 |
28235644 | Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells. | 2017 Jun |
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| 7 |
28429368 | ARALAR/AGC1 deficiency, a neurodevelopmental disorder with severe impairment of neuronal mitochondrial respiration, does not produce a primary increase in brain lactate. | 2017 Jul |
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| 8 |
25809592 | The regulation of neuronal mitochondrial metabolism by calcium. | 2015 Aug 15 |
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| 9 |
24515575 | AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate. | 2014 |
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| 10 |
24820519 | Ca(2+) regulation of mitochondrial function in neurons. | 2014 Oct |
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| 11 |
25313047 | Pyruvate kinase and aspartate-glutamate carrier distributions reveal key metabolic links between neurons and glia in retina. | 2014 Oct 28 |
2 |
| 12 |
23216354 | AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway. | 2013 Feb |
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| 13 |
24007662 | Quantitative clinical proteomic study of autopsied human infarcted brain specimens to elucidate the deregulated pathways in ischemic stroke pathology. | 2013 Oct 8 |
1 |
| 14 |
21691713 | The mitochondrial aspartate/glutamate carrier AGC1 and calcium homeostasis: physiological links and abnormalities in autism. | 2011 Aug |
1 |
| 15 |
19641205 | AGC1 deficiency associated with global cerebral hypomyelination. | 2009 Jul 30 |
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