Wang S - Search Results

1

The multiple facets of acetyl-CoA metabolism: Energetics, biosynthesis, regulation, acylation and inborn errors.

Wang Y, Yang H, Geerts C, Furtos A, Waters P, Cyr D, Wang S, Mitchell GA. Wang Y, et al. Among authors: wang s. Mol Genet Metab. 2023 Jan;138(1):106966. doi: 10.1016/j.ymgme.2022.106966. Epub 2022 Nov 30. Mol Genet Metab. 2023. PMID: 36528988 Review.

2

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. 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.

3

Propionic acidemia in mice: Liver acyl-CoA levels and clinical course.

Zhao C, Wang Y, Yang H, Wang S, Tang MC, Cyr D, Parente F, Allard P, Waters P, Furtos A, Yang G, Mitchell GA. Zhao C, et al. Among authors: wang y, wang s. Mol Genet Metab. 2022 Jan;135(1):47-55. doi: 10.1016/j.ymgme.2021.11.011. Epub 2021 Nov 27. Mol Genet Metab. 2022. PMID: 34896004

4

Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers.

Yang H, Wang Y, Tang MC, Waters P, Wang S, Allard P, Ryan RO, Nuyt AM, Paradis P, Schiffrin EL, Furtos A, Mitchell GA. Yang H, et al. Among authors: wang y, wang s. Mol Genet Metab. 2022 Nov;137(3):257-264. doi: 10.1016/j.ymgme.2022.09.008. Epub 2022 Sep 30. Mol Genet Metab. 2022. PMID: 36228350

5

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.

6

Lipolysis and the integrated physiology of lipid energy metabolism.

Wang S, Soni KG, Semache M, Casavant S, Fortier M, Pan L, Mitchell GA. Wang S, et al. Mol Genet Metab. 2008 Nov;95(3):117-26. doi: 10.1016/j.ymgme.2008.06.012. Epub 2008 Aug 31. Mol Genet Metab. 2008. PMID: 18762440 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. 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

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. 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.

9

Hypersuccinylacetonaemia and normal liver function in maleylacetoacetate isomerase deficiency.

Yang H, Al-Hertani W, Cyr D, Laframboise R, Parizeault G, Wang SP, Rossignol F, Berthier MT, Giguère Y, Waters PJ, Mitchell GA; Québec NTBC Study Group. Yang H, et al. J Med Genet. 2017 Apr;54(4):241-247. doi: 10.1136/jmedgenet-2016-104289. Epub 2016 Nov 22. J Med Genet. 2017. PMID: 27876694

10

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. 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.

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