human glutathione synthetase kda

human glutathione synthetase kda Inborn errors in the metabolism of | Orphanet Journal of Rare Diseases RCSB PDB - 2HGS: HUMAN

Name: human glutathione synthetase kda Inborn errors in the metabolism of | Orphanet Journal of Rare Diseases RCSB PDB - 2HGS: HUMAN
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SKU: 52253942377
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RCSB PDB 2HGS: HUMAN GLUTATHIONE SYNTHETASE Controlling glutathione entry into mitochondria: potential roles for SLC25A39 in health and (treatment of) disease Signal Transduction and Targeted Therapy Cellular Compartmentalization, Glutathione Transport and Its Relevance in Some Pathologies Human GSS (Glutathione Synthetase) knockout HEK 293T cell line (ab266342) Abcam Impaired Glutathione Synthesis in Neurodegeneration

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Arbour KC, Riely GJ

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