169 related articles for article (PubMed ID: 28235644)
1. Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells.
Profilo E; Peña-Altamira LE; Corricelli M; Castegna A; Danese A; Agrimi G; Petralla S; Giannuzzi G; Porcelli V; Sbano L; Viscomi C; Massenzio F; Palmieri EM; Giorgi C; Fiermonte G; Virgili M; Palmieri L; Zeviani M; Pinton P; Monti B; Palmieri F; Lasorsa FM
Biochim Biophys Acta Mol Basis Dis; 2017 Jun; 1863(6):1422-1435. PubMed ID: 28235644
[TBL] [Abstract][Full Text] [Related]
2. AGC1 Deficiency: Pathology and Molecular and Cellular Mechanisms of the Disease.
Pardo B; Herrada-Soler E; Satrústegui J; Contreras L; Del Arco A
Int J Mol Sci; 2022 Jan; 23(1):. PubMed ID: 35008954
[TBL] [Abstract][Full Text] [Related]
3. Transcriptional and metabolic effects of aspartate-glutamate carrier isoform 1 (AGC1) downregulation in mouse oligodendrocyte precursor cells (OPCs).
Balboni N; Babini G; Poeta E; Protti M; Mercolini L; Magnifico MC; Barile SN; Massenzio F; Pignataro A; Giorgi FM; Lasorsa FM; Monti B
Cell Mol Biol Lett; 2024 Mar; 29(1):44. PubMed ID: 38553684
[TBL] [Abstract][Full Text] [Related]
4. ARALAR/AGC1 deficiency, a neurodevelopmental disorder with severe impairment of neuronal mitochondrial respiration, does not produce a primary increase in brain lactate.
Juaristi I; García-Martín ML; Rodrigues TB; Satrústegui J; Llorente-Folch I; Pardo B
J Neurochem; 2017 Jul; 142(1):132-139. PubMed ID: 28429368
[TBL] [Abstract][Full Text] [Related]
5. Deficiency of Mitochondrial Aspartate-Glutamate Carrier 1 Leads to Oligodendrocyte Precursor Cell Proliferation Defects Both In Vitro and In Vivo.
Petralla S; Peña-Altamira LE; Poeta E; Massenzio F; Virgili M; Barile SN; Sbano L; Profilo E; Corricelli M; Danese A; Giorgi C; Ostan R; Capri M; Pinton P; Palmieri F; Lasorsa FM; Monti B
Int J Mol Sci; 2019 Sep; 20(18):. PubMed ID: 31514314
[TBL] [Abstract][Full Text] [Related]
6. The ketogenic diet compensates for AGC1 deficiency and improves myelination.
Dahlin M; Martin DA; Hedlund Z; Jonsson M; von Döbeln U; Wedell A
Epilepsia; 2015 Nov; 56(11):e176-81. PubMed ID: 26401995
[TBL] [Abstract][Full Text] [Related]
7. AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway.
Llorente-Folch I; Sahún I; Contreras L; Casarejos MJ; Grau JM; Saheki T; Mena MA; Satrústegui J; Dierssen M; Pardo B
J Neurochem; 2013 Feb; 124(3):347-62. PubMed ID: 23216354
[TBL] [Abstract][Full Text] [Related]
8. AGC1 deficiency associated with global cerebral hypomyelination.
Wibom R; Lasorsa FM; Töhönen V; Barbaro M; Sterky FH; Kucinski T; Naess K; Jonsson M; Pierri CL; Palmieri F; Wedell A
N Engl J Med; 2009 Jul; 361(5):489-95. PubMed ID: 19641205
[TBL] [Abstract][Full Text] [Related]
9. Expanding Phenotypic Spectrum of Cerebral Aspartate-Glutamate Carrier Isoform 1 (AGC1) Deficiency.
Pfeiffer B; Sen K; Kaur S; Pappas K
Neuropediatrics; 2020 Apr; 51(2):160-163. PubMed ID: 31766059
[TBL] [Abstract][Full Text] [Related]
10. Loss of Wwox Causes Defective Development of Cerebral Cortex with Hypomyelination in a Rat Model of Lethal Dwarfism with Epilepsy.
Tochigi Y; Takamatsu Y; Nakane J; Nakai R; Katayama K; Suzuki H
Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31340538
[TBL] [Abstract][Full Text] [Related]
11. Neurochemistry in shiverer mouse depicted on MR spectroscopy.
Takanashi J; Nitta N; Iwasaki N; Saito S; Tanaka R; Barkovich AJ; Aoki I
J Magn Reson Imaging; 2014 Jun; 39(6):1550-7. PubMed ID: 24243812
[TBL] [Abstract][Full Text] [Related]
12. Deficient glucose and glutamine metabolism in
Contreras L; Ramirez L; Du J; Hurley JB; Satrústegui J; de la Villa P
Mol Vis; 2016; 22():1198-1212. PubMed ID: 27746674
[TBL] [Abstract][Full Text] [Related]
13. βOHB Protective Pathways in Aralar-KO Neurons and Brain: An Alternative to Ketogenic Diet.
Pérez-Liébana I; Casarejos MJ; Alcaide A; Herrada-Soler E; Llorente-Folch I; Contreras L; Satrústegui J; Pardo B
J Neurosci; 2020 Nov; 40(48):9293-9305. PubMed ID: 33087477
[TBL] [Abstract][Full Text] [Related]
14. Kif14 mutation causes severe brain malformation and hypomyelination.
Fujikura K; Setsu T; Tanigaki K; Abe T; Kiyonari H; Terashima T; Sakisaka T
PLoS One; 2013; 8(1):e53490. PubMed ID: 23308235
[TBL] [Abstract][Full Text] [Related]
15. Low-prevalence mosaicism of chromosome 18q distal deletion identified by exome-based copy number profiling in a child with cerebral hypomyelination.
Shiohama T; Nakashima M; Ikehara H; Kato M; Saitsu H
Congenit Anom (Kyoto); 2020 May; 60(3):94-96. PubMed ID: 31328296
[No Abstract] [Full Text] [Related]
16. 5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy, and cerebral hypomyelination.
Rodan LH; Qi W; Ducker GS; Demirbas D; Laine R; Yang E; Walker MA; Eichler F; Rabinowitz JD; Anselm I; Berry GT;
Mol Genet Metab; 2018 Sep; 125(1-2):118-126. PubMed ID: 30031689
[TBL] [Abstract][Full Text] [Related]
17. Cytosolic Aspartate Availability Determines Cell Survival When Glutamine Is Limiting.
Alkan HF; Walter KE; Luengo A; Madreiter-Sokolowski CT; Stryeck S; Lau AN; Al-Zoughbi W; Lewis CA; Thomas CJ; Hoefler G; Graier WF; Madl T; Vander Heiden MG; Bogner-Strauss JG
Cell Metab; 2018 Nov; 28(5):706-720.e6. PubMed ID: 30122555
[TBL] [Abstract][Full Text] [Related]
18. Silencing of the mitochondrial NADH shuttle component aspartate-glutamate carrier AGC1/Aralar1 in INS-1E cells and rat islets.
Casimir M; Rubi B; Frigerio F; Chaffard G; Maechler P
Biochem J; 2009 Dec; 424(3):459-66. PubMed ID: 19764902
[TBL] [Abstract][Full Text] [Related]
19. AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.
Falk MJ; Li D; Gai X; McCormick E; Place E; Lasorsa FM; Otieno FG; Hou C; Kim CE; Abdel-Magid N; Vazquez L; Mentch FD; Chiavacci R; Liang J; Liu X; Jiang H; Giannuzzi G; Marsh ED; Yiran G; Tian L; Palmieri F; Hakonarson H
JIMD Rep; 2014; 14():77-85. PubMed ID: 24515575
[TBL] [Abstract][Full Text] [Related]
20. The mitochondrial aspartate/glutamate carrier AGC1 and calcium homeostasis: physiological links and abnormalities in autism.
Napolioni V; Persico AM; Porcelli V; Palmieri L
Mol Neurobiol; 2011 Aug; 44(1):83-92. PubMed ID: 21691713
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
