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PUBMED FOR HANDHELDS

Journal Abstract Search


263 related items for PubMed ID: 8424807

  • 21. On the mechanism of inhibition of gluconeogenesis and ureagenesis by sodium benzoate.
    Cyr DM, Egan SG, Brini CM, Tremblay GC.
    Biochem Pharmacol; 1991 Jul 15; 42(3):645-54. PubMed ID: 1677573
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  • 22. Progressive decrease of cerebral cytochrome C oxidase activity in sparse-fur mice: role of acetyl-L-carnitine in restoring the ammonia-induced cerebral energy depletion.
    Rao KV, Mawal YR, Qureshi IA.
    Neurosci Lett; 1997 Mar 14; 224(2):83-6. PubMed ID: 9086462
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  • 23. Comprehensive characterization of ureagenesis in the spfash mouse, a model of human ornithine transcarbamylase deficiency, reveals age-dependency of ammonia detoxification.
    Allegri G, Deplazes S, Rimann N, Causton B, Scherer T, Leff JW, Diez-Fernandez C, Klimovskaia A, Fingerhut R, Krijt J, Kožich V, Nuoffer JM, Grisch-Chan HM, Thöny B, Häberle J.
    J Inherit Metab Dis; 2019 Nov 14; 42(6):1064-1076. PubMed ID: 30714172
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  • 24. Regional amino acid neurotransmitter changes in brains of spf/Y mice with congenital ornithine transcarbamylase deficiency.
    Ratnakumari L, Qureshi IA, Butterworth RF.
    Metab Brain Dis; 1994 Mar 14; 9(1):43-51. PubMed ID: 7914668
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  • 25. Differential inhibition by hyperammonemia of the electron transport chain enzymes in synaptosomes and non-synaptic mitochondria in ornithine transcarbamylase-deficient spf-mice: restoration by acetyl-L-carnitine.
    Qureshi K, Rao KV, Qureshi IA.
    Neurochem Res; 1998 Jun 14; 23(6):855-61. PubMed ID: 9572674
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  • 27. Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.
    Marini JC, Erez A, Castillo L, Lee B.
    Am J Physiol Endocrinol Metab; 2007 Dec 14; 293(6):E1764-71. PubMed ID: 17925451
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  • 29. Evidence for a central cholinergic deficit in congenital ornithine transcarbamylase deficiency.
    Butterworth RF.
    Dev Neurosci; 1998 Dec 14; 20(4-5):478-84. PubMed ID: 9778587
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  • 34. Ornithine transcarbamylase deficiency: pathogenesis of the cerebral disorder and new prospects for therapy.
    Michalak A, Butterworth RF.
    Metab Brain Dis; 1997 Sep 14; 12(3):171-82. PubMed ID: 9346466
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  • 36. The effects of various inhibitors on the regulation of orotic acid excretion in sparse-fur mutant mice (spf/Y) deficient in ornithine transcarbamylase.
    Nelson J, Qureshi IA, Vasudevan S, Sarma DS.
    Chem Biol Interact; 1993 Oct 14; 89(1):35-47. PubMed ID: 8221965
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  • 39. Decompensation of hepatic and cerebral acyl-CoA metabolism in BALB/cByJ mice by chronic riboflavin deficiency: restoration by acetyl-L-carnitine.
    Rao KV, Qureshi IA.
    Can J Physiol Pharmacol; 1997 May 14; 75(5):423-30. PubMed ID: 9250376
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