Chen YT - Search Results

1

Liquid chromatographic assay for a glucose tetrasaccharide, a putative biomarker for the diagnosis of Pompe disease.

An Y, Young SP, Hillman SL, Van Hove JL, Chen YT, Millington DS. An Y, et al. Among authors: chen yt. Anal Biochem. 2000 Dec 1;287(1):136-43. doi: 10.1006/abio.2000.4838. Anal Biochem. 2000. PMID: 11078593

2

Purification of recombinant human precursor acid alpha-glucosidase.

Van Hove JL, Yang HW, Oliver LM, Pennybacker MF, Chen YT. Van Hove JL, et al. Among authors: chen yt. Biochem Mol Biol Int. 1997 Oct;43(3):613-23. doi: 10.1080/15216549700204421. Biochem Mol Biol Int. 1997. PMID: 9352080

3

Renal involvement in type I glycogen storage disease.

Chen YT, Van Hove JL. Chen YT, et al. Adv Nephrol Necker Hosp. 1995;24:357-65. Adv Nephrol Necker Hosp. 1995. PMID: 7572419 Review. No abstract available.

4

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.

Van Hove JL, Zhang W, Kahler SG, Roe CR, Chen YT, Terada N, Chace DH, Iafolla AK, Ding JH, Millington DS. Van Hove JL, et al. Among authors: chen yt. Am J Hum Genet. 1993 May;52(5):958-66. Am J Hum Genet. 1993. PMID: 8488845 Free PMC article.

5

High-level production of recombinant human lysosomal acid alpha-glucosidase in Chinese hamster ovary cells which targets to heart muscle and corrects glycogen accumulation in fibroblasts from patients with Pompe disease.

Van Hove JL, Yang HW, Wu JY, Brady RO, Chen YT. Van Hove JL, et al. Among authors: chen yt. Proc Natl Acad Sci U S A. 1996 Jan 9;93(1):65-70. doi: 10.1073/pnas.93.1.65. Proc Natl Acad Sci U S A. 1996. PMID: 8552676 Free PMC article.

6

Expression of catalytically active human multifunctional glycogen-debranching enzyme and lysosomal acid alpha-glucosidase in insect cells.

Wu JY, Van Hove JL, Huang YS, Chen YT. Wu JY, et al. Among authors: chen yt. Biochem Mol Biol Int. 1996 Jul;39(4):755-64. doi: 10.1080/15216549600201841. Biochem Mol Biol Int. 1996. PMID: 8843344

7

Recombinant human acid alpha-glucosidase corrects acid alpha-glucosidase-deficient human fibroblasts, quail fibroblasts, and quail myoblasts.

Yang HW, Kikuchi T, Hagiwara Y, Mizutani M, Chen YT, Van Hove JL. Yang HW, et al. Among authors: chen yt. Pediatr Res. 1998 Mar;43(3):374-80. doi: 10.1203/00006450-199803000-00011. Pediatr Res. 1998. PMID: 9505277

8

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

Shen JJ, Matern D, Millington DS, Hillman S, Feezor MD, Bennett MJ, Qumsiyeh M, Kahler SG, Chen YT, Van Hove JL. Shen JJ, et al. Among authors: chen yt. J Inherit Metab Dis. 2000 Feb;23(1):27-44. doi: 10.1023/a:1005694712583. J Inherit Metab Dis. 2000. PMID: 10682306

9

Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus.

Lei KJ, Chen YT, Chen H, Wong LJ, Liu JL, McConkie-Rosell A, Van Hove JL, Ou HC, Yeh NJ, Pan LY, et al. Lei KJ, et al. Among authors: chen h, chen yt. Am J Hum Genet. 1995 Oct;57(4):766-71. Am J Hum Genet. 1995. PMID: 7573034 Free PMC article.

10

Early, sustained efficacy of adeno-associated virus vector-mediated gene therapy in glycogen storage disease type Ia.

Koeberl DD, Sun BD, Damodaran TV, Brown T, Millington DS, Benjamin DK Jr, Bird A, Schneider A, Hillman S, Jackson M, Beaty RM, Chen YT. Koeberl DD, et al. Among authors: chen yt. Gene Ther. 2006 Sep;13(17):1281-9. doi: 10.1038/sj.gt.3302774. Epub 2006 May 4. Gene Ther. 2006. PMID: 16672983

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