Pan CJ - Search Results

1

Increased scavenger receptor class B type I-mediated cellular cholesterol efflux and antioxidant capacity in the sera of glycogen storage disease type Ia patients.

Nguyen AD, Pan CJ, Weinstein DA, Chou JY. Nguyen AD, et al. Among authors: pan cj. Mol Genet Metab. 2006 Nov;89(3):233-8. doi: 10.1016/j.ymgme.2006.05.002. Epub 2006 Jun 14. Mol Genet Metab. 2006. PMID: 16777453

2

Sustained hepatic and renal glucose-6-phosphatase expression corrects glycogen storage disease type Ia in mice.

Sun MS, Pan CJ, Shieh JJ, Ghosh A, Chen LY, Mansfield BC, Ward JM, Byrne BJ, Chou JY. Sun MS, et al. Among authors: pan cj. Hum Mol Genet. 2002 Sep 1;11(18):2155-64. doi: 10.1093/hmg/11.18.2155. Hum Mol Genet. 2002. PMID: 12189168

3

Adenovirus-mediated gene therapy in a mouse model of glycogen storage disease type 1a.

Chou JY, Zingone A, Pan CJ. Chou JY, et al. Among authors: pan cj. Eur J Pediatr. 2002 Oct;161 Suppl 1:S56-61. doi: 10.1007/s00431-002-1005-x. Epub 2002 Jul 19. Eur J Pediatr. 2002. PMID: 12373573 Review.

4

Structure-function analysis of the glucose-6-phosphate transporter deficient in glycogen storage disease type Ib.

Chen LY, Pan CJ, Shieh JJ, Chou JY. Chen LY, et al. Among authors: pan cj. Hum Mol Genet. 2002 Dec 1;11(25):3199-207. doi: 10.1093/hmg/11.25.3199. Hum Mol Genet. 2002. PMID: 12444104

5

Increased cellular cholesterol efflux in glycogen storage disease type Ia mice: a potential mechanism that protects against premature atherosclerosis.

Nguyen AD, Pan CJ, Shieh JJ, Chou JY. Nguyen AD, et al. Among authors: pan cj. FEBS Lett. 2005 Aug 29;579(21):4713-8. doi: 10.1016/j.febslet.2005.07.042. FEBS Lett. 2005. PMID: 16098970 Free article.

6

Functional analysis of mutations in the glucose-6-phosphate transporter that cause glycogen storage disease type Ib.

Chen SY, Pan CJ, Lee S, Peng W, Chou JY. Chen SY, et al. Among authors: pan cj. Mol Genet Metab. 2008 Dec;95(4):220-3. doi: 10.1016/j.ymgme.2008.08.005. Epub 2008 Oct 2. Mol Genet Metab. 2008. PMID: 18835800 Free PMC article.

7

Structure-function study of the glucose-6-phosphate transporter, an eukaryotic antiporter deficient in glycogen storage disease type Ib.

Pan CJ, Chen SY, Lee S, Chou JY. Pan CJ, et al. Mol Genet Metab. 2009 Jan;96(1):32-7. doi: 10.1016/j.ymgme.2008.10.005. Epub 2008 Nov 12. Mol Genet Metab. 2009. PMID: 19008136 Free PMC article.

8

Complete normalization of hepatic G6PC deficiency in murine glycogen storage disease type Ia using gene therapy.

Yiu WH, Lee YM, Peng WT, Pan CJ, Mead PA, Mansfield BC, Chou JY. Yiu WH, et al. Among authors: pan cj. Mol Ther. 2010 Jun;18(6):1076-84. doi: 10.1038/mt.2010.64. Epub 2010 Apr 13. Mol Ther. 2010. PMID: 20389290 Free PMC article.

9

Prevention of hepatocellular adenoma and correction of metabolic abnormalities in murine glycogen storage disease type Ia by gene therapy.

Lee YM, Jun HS, Pan CJ, Lin SR, Wilson LH, Mansfield BC, Chou JY. Lee YM, et al. Among authors: pan cj. Hepatology. 2012 Nov;56(5):1719-29. doi: 10.1002/hep.25717. Epub 2012 Aug 27. Hepatology. 2012. PMID: 22422504 Free PMC article.

10

The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia.

Lee YM, Pan CJ, Koeberl DD, Mansfield BC, Chou JY. Lee YM, et al. Among authors: pan cj. Mol Genet Metab. 2013 Nov;110(3):275-80. doi: 10.1016/j.ymgme.2013.06.014. Epub 2013 Jun 25. Mol Genet Metab. 2013. PMID: 23856420 Free PMC article.

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