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197 related items for PubMed ID: 26836257
1. Molecular Mechanisms of Glutamine Synthetase Mutations that Lead to Clinically Relevant Pathologies. Frieg B, Görg B, Homeyer N, Keitel V, Häussinger D, Gohlke H. PLoS Comput Biol; 2016 Feb; 12(2):e1004693. PubMed ID: 26836257 [Abstract] [Full Text] [Related]
2. Congenital glutamine deficiency with glutamine synthetase mutations. Häberle J, Görg B, Rutsch F, Schmidt E, Toutain A, Benoist JF, Gelot A, Suc AL, Höhne W, Schliess F, Häussinger D, Koch HG. N Engl J Med; 2005 Nov 03; 353(18):1926-33. PubMed ID: 16267323 [Abstract] [Full Text] [Related]
3. The Molecular Basis of TnrA Control by Glutamine Synthetase in Bacillus subtilis. Hauf K, Kayumov A, Gloge F, Forchhammer K. J Biol Chem; 2016 Feb 12; 291(7):3483-95. PubMed ID: 26635369 [Abstract] [Full Text] [Related]
4. Inborn error of amino acid synthesis: human glutamine synthetase deficiency. Häberle J, Görg B, Toutain A, Rutsch F, Benoist JF, Gelot A, Suc AL, Koch HG, Schliess F, Häussinger D. J Inherit Metab Dis; 2006 Feb 12; 29(2-3):352-8. PubMed ID: 16763901 [Abstract] [Full Text] [Related]
5. Discovery of the ammonium substrate site on glutamine synthetase, a third cation binding site. Liaw SH, Kuo I, Eisenberg D. Protein Sci; 1995 Nov 12; 4(11):2358-65. PubMed ID: 8563633 [Abstract] [Full Text] [Related]
6. Crystal structures of mammalian glutamine synthetases illustrate substrate-induced conformational changes and provide opportunities for drug and herbicide design. Krajewski WW, Collins R, Holmberg-Schiavone L, Jones TA, Karlberg T, Mowbray SL. J Mol Biol; 2008 Jan 04; 375(1):217-28. PubMed ID: 18005987 [Abstract] [Full Text] [Related]
7. Congenital glutamine deficiency with glutamine synthetase mutations. Rose C, Jalan R. N Engl J Med; 2006 Mar 09; 354(10):1093-4; author reply 1093-4. PubMed ID: 16528811 [No Abstract] [Full Text] [Related]
8. Mechanism of Fully Reversible, pH-Sensitive Inhibition of Human Glutamine Synthetase by Tyrosine Nitration. Frieg B, Görg B, Qvartskhava N, Jeitner T, Homeyer N, Häussinger D, Gohlke H. J Chem Theory Comput; 2020 Jul 14; 16(7):4694-4705. PubMed ID: 32551588 [Abstract] [Full Text] [Related]
9. Attenuated glutamine synthetase as a selection marker in CHO cells to efficiently isolate highly productive stable cells for the production of antibodies and other biologics. Lin PC, Chan KF, Kiess IA, Tan J, Shahreel W, Wong SY, Song Z. MAbs; 2019 Jul 14; 11(5):965-976. PubMed ID: 31043114 [Abstract] [Full Text] [Related]
15. The isolated, twenty-three-residue-long, N-terminal region of the glutamine synthetase inactivating factor binds to its target. Neira JL, Florencio FJ, Muro-Pastor MI. Biophys Chem; 2017 Sep 14; 228():1-9. PubMed ID: 28601005 [Abstract] [Full Text] [Related]
16. A Very Rare Etiology of Hypotonia and Seizures: Congenital Glutamine Synthetase Deficiency. Ünal Ö, Ceylaner S, Akın R. Neuropediatrics; 2019 Feb 14; 50(1):51-53. PubMed ID: 30440076 [Abstract] [Full Text] [Related]
17. The three-dimensional structure of an eukaryotic glutamine synthetase: functional implications of its oligomeric structure. Llorca O, Betti M, González JM, Valencia A, Márquez AJ, Valpuesta JM. J Struct Biol; 2006 Dec 14; 156(3):469-79. PubMed ID: 16884924 [Abstract] [Full Text] [Related]
19. Interaction of substrates with glutamine synthetase after limited proteolysis. Monroe DM, Noyes CM, Lundblad RL, Kingdon HS, Griffith MJ. Biochemistry; 1984 Sep 25; 23(20):4565-72. PubMed ID: 6149764 [Abstract] [Full Text] [Related]
20. Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency. Roifman M, Niles KM, MacNeil L, Blaser S, Noor A, Godoy R, van Mieghem T, Ryan G, Seaward G, Sondheimer N, Mercimek-Andrews S, Schulze A, Hewson S, Ovadia A, Chitayat D, Morgen EK, Hojilla C, Kolomietz E, Watkins N, Häberle J, Shannon P. Clin Genet; 2020 Dec 25; 98(6):613-619. PubMed ID: 32888207 [Abstract] [Full Text] [Related] Page: [Next] [New Search]