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5. Secondary NAD+ deficiency in the inherited defect of glutamine synthetase. Hu L; Ibrahim K; Stucki M; Frapolli M; Shahbeck N; Chaudhry FA; Görg B; Häussinger D; Penberthy WT; Ben-Omran T; Häberle J J Inherit Metab Dis; 2015 Nov; 38(6):1075-83. PubMed ID: 25896882 [TBL] [Abstract][Full Text] [Related]
6. Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetase. Jones AG; Aquilino M; Tinker RJ; Duncan L; Jenkins Z; Carvill GL; DeWard SJ; Grange DK; Hajianpour MJ; Halliday BJ; Holder-Espinasse M; Horvath J; Maitz S; Nigro V; Morleo M; Paul V; Spencer C; Esterhuizen AI; Polster T; Spano A; Gómez-Lozano I; Kumar A; Poke G; Phillips JA; Underhill HR; Gimenez G; Namba T; Robertson SP Am J Hum Genet; 2024 Apr; 111(4):729-741. PubMed ID: 38579670 [TBL] [Abstract][Full Text] [Related]
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9. Glutamine synthetase deficiency in murine astrocytes results in neonatal death. He Y; Hakvoort TB; Vermeulen JL; Labruyère WT; De Waart DR; Van Der Hel WS; Ruijter JM; Uylings HB; Lamers WH Glia; 2010 Apr; 58(6):741-54. PubMed ID: 20140959 [TBL] [Abstract][Full Text] [Related]
10. Selective deletion of glutamine synthetase in the mouse cerebral cortex induces glial dysfunction and vascular impairment that precede epilepsy and neurodegeneration. Zhou Y; Dhaher R; Parent M; Hu QX; Hassel B; Yee SP; Hyder F; Gruenbaum SE; Eid T; Danbolt NC Neurochem Int; 2019 Feb; 123():22-33. PubMed ID: 30053506 [TBL] [Abstract][Full Text] [Related]
11. Congenital glutamine deficiency with glutamine synthetase mutations. Rose C; Jalan R N Engl J Med; 2006 Mar; 354(10):1093-4; author reply 1093-4. PubMed ID: 16528811 [No Abstract] [Full Text] [Related]
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20. MicroRNA-140-5p suppresses invasion and proliferation of glioma cells by targeting glutamate-ammonia ligase (GLUL). Zhang R; Zhu JC; Hu H; Lin QY; Shao W; Ji TH Neoplasma; 2020 Mar; 67(2):371-378. PubMed ID: 31986891 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]