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Journal Abstract Search

208 related items for PubMed ID: 16528811

  • 1.
    ; . PubMed ID:
    [No 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. Congenital glutamine deficiency with glutamine synthetase mutations.
    Kölker S, Hoffmann GF, Okun JG.
    N Engl J Med; 2006 Mar 09; 354(10):1093-4; author reply 1093-4. PubMed ID: 16525152
    [No Abstract] [Full Text] [Related]

  • 4. Metabolic disorders in the center of genetic medicine.
    Levy HL.
    N Engl J Med; 2005 Nov 03; 353(18):1968-70. PubMed ID: 16267330
    [No Abstract] [Full Text] [Related]

  • 5. 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 Nov 03; 29(2-3):352-8. PubMed ID: 16763901
    [Abstract] [Full Text] [Related]

  • 6. Direct molecular and spectroscopic evidence for increased ammonia removal capacity of skeletal muscle in acute liver failure.
    Chatauret N, Desjardins P, Zwingmann C, Rose C, Rao KV, Butterworth RF.
    J Hepatol; 2006 Jun 03; 44(6):1083-8. PubMed ID: 16530878
    [Abstract] [Full Text] [Related]

  • 7. 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 03; 12(2):e1004693. PubMed ID: 26836257
    [Abstract] [Full Text] [Related]

  • 8. [Studies on regulation of glutamine synthetase activity from Streptomyces lincolnensis].
    Jin Z, Jiao R, Mao Y.
    Wei Sheng Wu Xue Bao; 2001 Aug 03; 41(4):481-8. PubMed ID: 12552916
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. The role of multiple molecular forms of glutamine synthetase in the regulation of glutamine metabolism in Escherichia coli.
    Stadtman ER.
    Harvey Lect; 1971 Aug 03; 65():97-125. PubMed ID: 4399373
    [No Abstract] [Full Text] [Related]

  • 11. 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 03; 98(6):613-619. PubMed ID: 32888207
    [Abstract] [Full Text] [Related]

  • 12. 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 03; 38(6):1075-83. PubMed ID: 25896882
    [Abstract] [Full Text] [Related]

  • 13. A Very Rare Etiology of Hypotonia and Seizures: Congenital Glutamine Synthetase Deficiency.
    Ünal Ö, Ceylaner S, Akın R.
    Neuropediatrics; 2019 Feb 03; 50(1):51-53. PubMed ID: 30440076
    [Abstract] [Full Text] [Related]

  • 14. Natural course of glutamine synthetase deficiency in a 3 year old patient.
    Häberle J, Shahbeck N, Ibrahim K, Hoffmann GF, Ben-Omran T.
    Mol Genet Metab; 2011 May 03; 103(1):89-91. PubMed ID: 21353613
    [Abstract] [Full Text] [Related]

  • 15. The loach Misgurnus anguillicaudatus reduces amino acid catabolism and accumulates alanine and glutamine during aerial exposure.
    Chew SF, Jin Y, Ip YK.
    Physiol Biochem Zool; 2001 May 03; 74(2):226-37. PubMed ID: 11247742
    [Abstract] [Full Text] [Related]

  • 16. The glutamine paradox in a neonate with propionic acidaemia and severe hyperammonaemia.
    Ierardi-Curto L, Kaplan P, Saitta S, Mazur A, Berry GT.
    J Inherit Metab Dis; 2000 Feb 03; 23(1):85-6. PubMed ID: 10682312
    [No Abstract] [Full Text] [Related]

  • 17. Developmental study of hepatic glutamine synthetase in a mouse model of congenital hyperammonemia.
    Skarpetas A, Mawal Y, Qureshi IA.
    Biochem Mol Biol Int; 1997 Sep 03; 43(1):133-9. PubMed ID: 9315291
    [Abstract] [Full Text] [Related]

  • 18. Rapid determination of L-glutamine using engineered Escherichia coli overexpressing glutamine synthetase.
    Hong NN, Yang G, Li J, Zhang YP, Li JL.
    Appl Biochem Biotechnol; 2009 Aug 03; 158(2):398-407. PubMed ID: 18712288
    [Abstract] [Full Text] [Related]

  • 19. Glutamine synthesis is essential for growth of Streptococcus thermophilus in milk and is linked to urea catabolism.
    Monnet C, Mora D, Corrieu G.
    Appl Environ Microbiol; 2005 Jun 03; 71(6):3376-8. PubMed ID: 15933046
    [Abstract] [Full Text] [Related]

  • 20. Mutation of the adenylylated tyrosine of glutamine synthetase alters its catalytic properties.
    Luo S, Kim G, Levine RL.
    Biochemistry; 2005 Jul 12; 44(27):9441-6. PubMed ID: 15996098
    [Abstract] [Full Text] [Related]

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