Chen YT - Search Results

1

A large kindred of early-onset osteoarthritis of the knee and hip: excluding the link to COL2A1 gene.

Mu SC, Liu HC, Wu JY, Lee MT, Chuang HP, Chen LK, Chen YT. Mu SC, et al. Among authors: chen lk, chen yt. Rheumatology (Oxford). 2009 Apr;48(4):371-4. doi: 10.1093/rheumatology/kep010. Epub 2009 Feb 17. Rheumatology (Oxford). 2009. PMID: 19223283

2

ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease.

Wu JY, Kao HJ, Li SC, Stevens R, Hillman S, Millington D, Chen YT. Wu JY, et al. Among authors: chen yt. J Clin Invest. 2004 Feb;113(3):434-40. doi: 10.1172/JCI19574. J Clin Invest. 2004. PMID: 14755340 Free PMC article.

3

Medical genetics: a marker for Stevens-Johnson syndrome.

Chung WH, Hung SI, Hong HS, Hsih MS, Yang LC, Ho HC, Wu JY, Chen YT. Chung WH, et al. Among authors: chen yt. Nature. 2004 Apr 1;428(6982):486. doi: 10.1038/428486a. Nature. 2004. PMID: 15057820

4

HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol.

Hung SI, Chung WH, Liou LB, Chu CC, Lin M, Huang HP, Lin YL, Lan JL, Yang LC, Hong HS, Chen MJ, Lai PC, Wu MS, Chu CY, Wang KH, Chen CH, Fann CS, Wu JY, Chen YT. Hung SI, et al. Among authors: chen ch, chen mj, chen yt. Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4134-9. doi: 10.1073/pnas.0409500102. Epub 2005 Mar 2. Proc Natl Acad Sci U S A. 2005. PMID: 15743917 Free PMC article.

5

A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity.

Yuan HY, Chen JJ, Lee MT, Wung JC, Chen YF, Charng MJ, Lu MJ, Hung CR, Wei CY, Chen CH, Wu JY, Chen YT. Yuan HY, et al. Among authors: chen jj, chen ch, chen yf, chen yt. Hum Mol Genet. 2005 Jul 1;14(13):1745-51. doi: 10.1093/hmg/ddi180. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888487

6

Type II collagen gene variants and inherited osteonecrosis of the femoral head.

Liu YF, Chen WM, Lin YF, Yang RC, Lin MW, Li LH, Chang YH, Jou YS, Lin PY, Su JS, Huang SF, Hsiao KJ, Fann CS, Hwang HW, Chen YT, Tsai SF. Liu YF, et al. Among authors: chen wm, chen yt. N Engl J Med. 2005 Jun 2;352(22):2294-301. doi: 10.1056/NEJMoa042480. N Engl J Med. 2005. PMID: 15930420 Free article.

7

A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect.

Niu DM, Hwang B, Hwang HW, Wang NH, Wu JY, Lee PC, Chien JC, Shieh RC, Chen YT. Niu DM, et al. Among authors: chen yt. J Med Genet. 2006 Oct;43(10):817-21. doi: 10.1136/jmg.2006.042192. Epub 2006 May 17. J Med Genet. 2006. PMID: 16707561 Free PMC article.

8

Long contiguous stretches of homozygosity in the human genome.

Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT. Li LH, et al. Among authors: chen ch, chen yt. Hum Mutat. 2006 Nov;27(11):1115-21. doi: 10.1002/humu.20399. Hum Mutat. 2006. PMID: 16955415

9

ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunit.

Kao HJ, Cheng CF, Chen YH, Hung SI, Huang CC, Millington D, Kikuchi T, Wu JY, Chen YT. Kao HJ, et al. Among authors: chen yh, chen yt. Hum Mol Genet. 2006 Dec 15;15(24):3569-77. doi: 10.1093/hmg/ddl433. Epub 2006 Nov 20. Hum Mol Genet. 2006. PMID: 17116638

10

Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease.

Chiang MC, Chen HM, Lee YH, Chang HH, Wu YC, Soong BW, Chen CM, Wu YR, Liu CS, Niu DM, Wu JY, Chen YT, Chern Y. Chiang MC, et al. Among authors: chen hm, chen cm, chen yt. Hum Mol Genet. 2007 Mar 1;16(5):483-98. doi: 10.1093/hmg/ddl481. Epub 2007 Jan 9. Hum Mol Genet. 2007. PMID: 17213233

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