Yu H - Search Results

1

Hepatic SRC-1 activity orchestrates transcriptional circuitries of amino acid pathways with potential relevance for human metabolic pathogenesis.

Tannour-Louet M, York B, Tang K, Stashi E, Bouguerra H, Zhou S, Yu H, Wong LJ, Stevens RD, Xu J, Newgard CB, O'Malley BW, Louet JF. Tannour-Louet M, et al. Among authors: yu h. Mol Endocrinol. 2014 Oct;28(10):1707-18. doi: 10.1210/me.2014-1083. Epub 2014 Aug 22. Mol Endocrinol. 2014. PMID: 25148457 Free PMC article.

2

Ablation of steroid receptor coactivator-3 resembles the human CACT metabolic myopathy.

York B, Reineke EL, Sagen JV, Nikolai BC, Zhou S, Louet JF, Chopra AR, Chen X, Reed G, Noebels J, Adesina AM, Yu H, Wong LJ, Tsimelzon A, Hilsenbeck S, Stevens RD, Wenner BR, Ilkayeva O, Xu J, Newgard CB, O'Malley BW. York B, et al. Among authors: yu h. Cell Metab. 2012 May 2;15(5):752-63. doi: 10.1016/j.cmet.2012.03.020. Cell Metab. 2012. PMID: 22560224 Free PMC article.

3

Evaluation of gene therapy for citrullinaemia using murine and bovine models.

Patejunas G, Lee B, Dennis JA, Healy PJ, Reeds PJ, Yu H, Frazer M, Mull B, Warman AW, Beaudet AL, O'Brien WE. Patejunas G, et al. Among authors: yu h. J Inherit Metab Dis. 1998;21 Suppl 1:138-50. doi: 10.1023/a:1005322010854. J Inherit Metab Dis. 1998. PMID: 9686351

4

Hepatocyte gene therapy in a large animal: a neonatal bovine model of citrullinemia.

Lee B, Dennis JA, Healy PJ, Mull B, Pastore L, Yu H, Aguilar-Cordova E, O'Brien W, Reeds P, Beaudet AL. Lee B, et al. Among authors: yu h. Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3981-6. doi: 10.1073/pnas.96.7.3981. Proc Natl Acad Sci U S A. 1999. PMID: 10097149 Free PMC article.

5

Detection of a novel intragenic rearrangement in the creatine transporter gene by next generation sequencing.

Yu H, van Karnebeek C, Sinclair G, Hill A, Cui H, Zhang VW, Wong LJ. Yu H, et al. Mol Genet Metab. 2013 Dec;110(4):465-71. doi: 10.1016/j.ymgme.2013.09.018. Epub 2013 Oct 4. Mol Genet Metab. 2013. PMID: 24140398

6

Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

Yu H, Zhang VW. Yu H, et al. Biomed Res Int. 2015;2015:745043. doi: 10.1155/2015/745043. Epub 2015 Jun 7. Biomed Res Int. 2015. PMID: 26137492 Free PMC article. Review.

7

Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing.

Qin L, Wang J, Tian X, Yu H, Truong C, Mitchell JJ, Wierenga KJ, Craigen WJ, Zhang VW, Wong LC. Qin L, et al. Among authors: yu h. J Mol Diagn. 2016 May;18(3):446-453. doi: 10.1016/j.jmoldx.2016.01.002. Epub 2016 Mar 2. J Mol Diagn. 2016. PMID: 26944031 Free article.

8

In vivo urea cycle flux distinguishes and correlates with phenotypic severity in disorders of the urea cycle.

Lee B, Yu H, Jahoor F, O'Brien W, Beaudet AL, Reeds P. Lee B, et al. Among authors: yu h. Proc Natl Acad Sci U S A. 2000 Jul 5;97(14):8021-6. doi: 10.1073/pnas.140082197. Proc Natl Acad Sci U S A. 2000. PMID: 10869432 Free PMC article.

9

Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types.

Wang J, Yu H, Zhang VW, Tian X, Feng Y, Wang G, Gorman E, Wang H, Lutz RE, Schmitt ES, Peacock S, Wong LJ. Wang J, et al. Among authors: yu h. Genet Med. 2016 May;18(5):513-21. doi: 10.1038/gim.2015.121. Epub 2015 Sep 24. Genet Med. 2016. PMID: 26402642 Free article.

10

Dietary amino acids are the preferential source of hepatic protein synthesis in piglets.

Stoll B, Burrin DG, Henry J, Yu H, Jahoor F, Reeds PJ. Stoll B, et al. Among authors: yu h. J Nutr. 1998 Sep;128(9):1517-24. doi: 10.1093/jn/128.9.1517. J Nutr. 1998. PMID: 9732313

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