Lee YC - Search Results

1

GLUT10 maintains the integrity of major arteries through regulation of redox homeostasis and mitochondrial function.

Syu YW, Lai HW, Jiang CL, Tsai HY, Lin CC, Lee YC. Syu YW, et al. Among authors: lee yc. Hum Mol Genet. 2018 Jan 15;27(2):307-321. doi: 10.1093/hmg/ddx401. Hum Mol Genet. 2018. PMID: 29149261

2

Mutations in the SLC2A10 gene cause arterial abnormalities in mice.

Cheng CH, Kikuchi T, Chen YH, Sabbagha NG, Lee YC, Pan HJ, Chang C, Chen YT. Cheng CH, et al. Among authors: lee yc. Cardiovasc Res. 2009 Feb 1;81(2):381-8. doi: 10.1093/cvr/cvn319. Epub 2008 Nov 21. Cardiovasc Res. 2009. PMID: 19028722

3

Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.

Lee YC, Huang HY, Chang CJ, Cheng CH, Chen YT. Lee YC, et al. Hum Mol Genet. 2010 Oct 1;19(19):3721-33. doi: 10.1093/hmg/ddq286. Epub 2010 Jul 16. Hum Mol Genet. 2010. PMID: 20639396

4

Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV.

Lee YC, Chang CJ, Bali D, Chen YT, Yan YT. Lee YC, et al. Hum Mol Genet. 2011 Feb 1;20(3):455-65. doi: 10.1093/hmg/ddq492. Epub 2010 Nov 12. Hum Mol Genet. 2011. PMID: 21075835

5

Glucose transporter 10 modulates adipogenesis via an ascorbic acid-mediated pathway to protect mice against diet-induced metabolic dysregulation.

Jiang CL, Jen WP, Tsao CY, Chang LC, Chen CH, Lee YC. Jiang CL, et al. Among authors: lee yc. PLoS Genet. 2020 May 26;16(5):e1008823. doi: 10.1371/journal.pgen.1008823. eCollection 2020 May. PLoS Genet. 2020. PMID: 32453789 Free PMC article.

6

Association of an IGHV3-66 gene variant with Kawasaki disease.

Johnson TA, Mashimo Y, Wu JY, Yoon D, Hata A, Kubo M, Takahashi A, Tsunoda T, Ozaki K, Tanaka T, Ito K, Suzuki H, Hamada H, Kobayashi T, Hara T, Chen CH, Lee YC, Liu YM, Chang LC, Chang CP, Hong YM, Jang GY, Yun SW, Yu JJ, Lee KY, Kim JJ, Park T; Korean Kawasaki Disease Genetics Consortium, Taiwan Kawasaki Disease Genetics Consortium, Taiwan Pediatric ID Alliance, Japan Kawasaki Disease Genome Consortium; Lee JK, Chen YT, Onouchi Y. Johnson TA, et al. Among authors: lee yc, lee ky, lee jk. J Hum Genet. 2021 May;66(5):475-489. doi: 10.1038/s10038-020-00864-z. Epub 2020 Oct 26. J Hum Genet. 2021. PMID: 33106546 Free PMC article.

7

Vitamin C attenuates predisposition to high-fat diet-induced metabolic dysregulation in GLUT10-deficient mouse model.

Jiang CL, Tsao CY, Lee YC. Jiang CL, et al. Among authors: lee yc. Genes Nutr. 2022 Jul 16;17(1):10. doi: 10.1186/s12263-022-00713-y. Genes Nutr. 2022. PMID: 35842612 Free PMC article.

8

Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.

Lee YC, Kuo HC, Chang JS, Chang LY, Huang LM, Chen MR, Liang CD, Chi H, Huang FY, Lee ML, Huang YC, Hwang B, Chiu NC, Hwang KP, Lee PC, Chang LC, Liu YM, Chen YJ, Chen CH; Taiwan Pediatric ID Alliance; Chen YT, Tsai FJ, Wu JY. Lee YC, et al. Among authors: lee ml, lee pc. Nat Genet. 2012 Mar 25;44(5):522-5. doi: 10.1038/ng.2227. Nat Genet. 2012. PMID: 22446961

9

Twist1 Plays an Anti-apoptotic Role in Mutant Huntingtin Expression Striatal Progenitor Cells.

Jen WP, Chen HM, Lin YS, Chern Y, Lee YC. Jen WP, et al. Among authors: lee yc. Mol Neurobiol. 2020 Mar;57(3):1688-1703. doi: 10.1007/s12035-019-01836-x. Epub 2019 Dec 7. Mol Neurobiol. 2020. PMID: 31813126

10

Knock-in human FGFR3 achondroplasia mutation as a mouse model for human skeletal dysplasia.

Lee YC, Song IW, Pai YJ, Chen SD, Chen YT. Lee YC, et al. Sci Rep. 2017 Feb 23;7:43220. doi: 10.1038/srep43220. Sci Rep. 2017. PMID: 28230213 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

5,506 results

Search Page