Mitchell GA - Search Results

1

Hereditary and acquired diseases of acyl-coenzyme A metabolism.

Mitchell GA, Gauthier N, Lesimple A, Wang SP, Mamer O, Qureshi I. Mitchell GA, et al. Mol Genet Metab. 2008 May;94(1):4-15. doi: 10.1016/j.ymgme.2007.12.005. Epub 2008 Mar 11. Mol Genet Metab. 2008. PMID: 18337138 Review.

2

A liver-specific defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia and a distinct hepatic Acyl-CoA pattern.

Gauthier N, Wu JW, Wang SP, Allard P, Mamer OA, Sweetman L, Moser AB, Kratz L, Alvarez F, Robitaille Y, Lépine F, Mitchell GA. Gauthier N, et al. Among authors: mitchell ga. PLoS One. 2013 Jul 5;8(7):e60581. doi: 10.1371/journal.pone.0060581. Print 2013. PLoS One. 2013. PMID: 23861731 Free PMC article.

3

Hereditary diseases of coenzyme A thioester metabolism.

Yang H, Zhao C, Wang Y, Wang SP, Mitchell GA. Yang H, et al. Among authors: mitchell ga. Biochem Soc Trans. 2019 Feb 28;47(1):149-155. doi: 10.1042/BST20180423. Epub 2019 Jan 9. Biochem Soc Trans. 2019. PMID: 30626707 Review.

4

Inborn errors of mitochondrial acyl-coenzyme a metabolism: acyl-CoA biology meets the clinic.

Yang H, Zhao C, Tang MC, Wang Y, Wang SP, Allard P, Furtos A, Mitchell GA. Yang H, et al. Among authors: mitchell ga. Mol Genet Metab. 2019 Sep-Oct;128(1-2):30-44. doi: 10.1016/j.ymgme.2019.05.002. Epub 2019 May 9. Mol Genet Metab. 2019. PMID: 31186158 Review.

5

A heterozygote phenotype is present in the jvs +/- mutant mouse livers.

Lahjouji K, Elimrani I, Wu J, Mitchell GA, Qureshi IA. Lahjouji K, et al. Among authors: mitchell ga. Mol Genet Metab. 2002 May;76(1):76-80. doi: 10.1016/s1096-7192(02)00017-3. Mol Genet Metab. 2002. PMID: 12175785

6

Metabolism as a tool for understanding human brain evolution: lipid energy metabolism as an example.

Wang SP, Yang H, Wu JW, Gauthier N, Fukao T, Mitchell GA. Wang SP, et al. Among authors: mitchell ga. J Hum Evol. 2014 Dec;77:41-9. doi: 10.1016/j.jhevol.2014.06.013. Epub 2014 Dec 6. J Hum Evol. 2014. PMID: 25488255 Review.

7

Inborn errors of cytoplasmic triglyceride metabolism.

Wu JW, Yang H, Wang SP, Soni KG, Brunel-Guitton C, Mitchell GA. Wu JW, et al. Among authors: mitchell ga. J Inherit Metab Dis. 2015 Jan;38(1):85-98. doi: 10.1007/s10545-014-9767-7. Epub 2014 Oct 10. J Inherit Metab Dis. 2015. PMID: 25300978 Review.

8

Mildly elevated succinylacetone and normal liver function in compound heterozygotes with pathogenic and pseudodeficient FAH alleles.

Yang H, Rossignol F, Cyr D, Laframboise R, Wang SP, Soucy JF, Berthier MT, Giguère Y, Waters PJ, Mitchell GA; Québec NTBC Study Group. Yang H, et al. Among authors: mitchell ga. Mol Genet Metab Rep. 2017 Dec 27;14:55-58. doi: 10.1016/j.ymgmr.2017.12.002. eCollection 2018 Mar. Mol Genet Metab Rep. 2017. PMID: 29326876 Free PMC article.

9

Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal.

Feoli-Fonseca JC, Lambert M, Mitchell G, Melançon SB, Dallaire L, Millington DS, Qureshi IA. Feoli-Fonseca JC, et al. Biochem Mol Med. 1996 Feb;57(1):31-6. doi: 10.1006/bmme.1996.0006. Biochem Mol Med. 1996. PMID: 8812724 Clinical Trial.

10

Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: testing the biochemical phenotype of double-mutant mice as a model for ammonia: fatty acyl CoA synergism.

Qureshi IA, Leblanc D, Cyr D, Giguère R, Mitchell G. Qureshi IA, et al. Biochem Biophys Res Commun. 1993 Mar 15;191(2):744-9. doi: 10.1006/bbrc.1993.1280. Biochem Biophys Res Commun. 1993. PMID: 8461026

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