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2. Glutathione synthetase deficient human fibroblasts in culture. Larsson A, Mattsson B, Hagenfeldt L, Moldéus P. Clin Chim Acta; 1983 Nov 30; 135(1):57-64. PubMed ID: 6652919 [Abstract] [Full Text] [Related]
3. Survival curves of glutathione synthetase deficient human fibroblasts: correlation between radiosensitivity in hypoxia and glutathione synthetase activity. Debieu D, Deschavanne PJ, Midander J, Larsson A, Malaise EP. Int J Radiat Biol Relat Stud Phys Chem Med; 1985 Oct 30; 48(4):525-43. PubMed ID: 3876305 [Abstract] [Full Text] [Related]
4. Glutathione synthetase deficiency: is gamma-glutamylcysteine accumulation a way to cope with oxidative stress in cells with insufficient levels of glutathione? Ristoff E, Hebert C, Njålsson R, Norgren S, Rooyackers O, Larsson A. J Inherit Metab Dis; 2002 Nov 30; 25(7):577-84. PubMed ID: 12638941 [Abstract] [Full Text] [Related]
5. Enhancement of glutathione content in glutathione synthetase-deficient fibroblasts from a patient with 5-oxoprolinuria via metabolic cooperation with normal fibroblasts. Kavanagh TJ, Raghu G, White CC, Martin GM, Rabinovitch PS, Eaton DL. Exp Cell Res; 1994 May 30; 212(1):69-76. PubMed ID: 7909755 [Abstract] [Full Text] [Related]
6. Erythrocyte glutathione synthetase in 5-oxoprolinuria: kinetic studies of the mutant enzyme and detection of heterozygotes. Larsson A, Zetterström R, Hörnell H, Porath U. Clin Chim Acta; 1976 Nov 15; 73(1):19-23. PubMed ID: 11905 [Abstract] [Full Text] [Related]
7. Treatment of glutathione synthetase deficient fibroblasts by inhibiting gamma-glutamyl transpeptidase activity with serine and borate. Spielberg SP, Butler JD, MacDermot K, Schulman JD. Biochem Biophys Res Commun; 1979 Jul 27; 89(2):504-11. PubMed ID: 39559 [No Abstract] [Full Text] [Related]
15. Genotype, enzyme activity, glutathione level, and clinical phenotype in patients with glutathione synthetase deficiency. Njålsson R, Ristoff E, Carlsson K, Winkler A, Larsson A, Norgren S. Hum Genet; 2005 Apr 27; 116(5):384-9. PubMed ID: 15717202 [Abstract] [Full Text] [Related]
16. Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiency. Beutler E, Gelbart T, Pegelow C. J Clin Invest; 1986 Jan 27; 77(1):38-41. PubMed ID: 3944259 [Abstract] [Full Text] [Related]
17. Sulphur amino-acid degradation in subjects with hereditary glutathione synthetase deficiency (5-oxoprolinuria). Mårtensson J, Kågedal B, Larsson A. Eur J Clin Invest; 1985 Dec 27; 15(6):371-4. PubMed ID: 3938407 [Abstract] [Full Text] [Related]
18. Hemolytic anemia, recurrent metabolic acidosis, and incomplete albinism associated with glutathione synthetase deficiency. Prchal JT, Crist WM, Roper M, Wellner VP. Blood; 1983 Oct 27; 62(4):754-7. PubMed ID: 6882923 [Abstract] [Full Text] [Related]
19. Patients with genetic defects in the gamma-glutamyl cycle. Ristoff E, Larsson A. Chem Biol Interact; 1998 Apr 24; 111-112():113-21. PubMed ID: 9679548 [Abstract] [Full Text] [Related]
20. Reduced oxygen enhancement of the radiosensitivity of glutathione-deficient fibroblasts. Malaise EP. Radiat Res; 1983 Sep 24; 95(3):486-94. PubMed ID: 6611861 [Abstract] [Full Text] [Related] Page: [Next] [New Search]