Chen YT - Search Results

1

Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.

Chen YT, He JK, Ding JH, Brown BI. Chen YT, et al. Am J Hum Genet. 1987 Dec;41(6):1002-15. Am J Hum Genet. 1987. PMID: 2961257 Free PMC article.

2

Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme.

Yang BZ, Ding JH, Enghild JJ, Bao Y, Chen YT. Yang BZ, et al. Among authors: chen yt. J Biol Chem. 1992 May 5;267(13):9294-9. J Biol Chem. 1992. PMID: 1374391 Free article.

3

Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

Ding JH, Yang BZ, Bao Y, Roe CR, Chen YT. Ding JH, et al. Among authors: chen yt. Am J Hum Genet. 1992 Jan;50(1):229-33. Am J Hum Genet. 1992. PMID: 1729890 Free PMC article.

4

Type III glycogen storage disease: an adult case with mild disease but complete absence of debrancher protein.

Yang BZ, Stewart C, Ding JH, Chen YT. Yang BZ, et al. Among authors: chen yt. Neuromuscul Disord. 1991;1(3):173-6. doi: 10.1016/0960-8966(91)90021-j. Neuromuscul Disord. 1991. PMID: 1822791

5

Definitive prenatal diagnosis for type III glycogen storage disease.

Yang BZ, Ding JH, Brown BI, Chen YT. Yang BZ, et al. Among authors: chen yt. Am J Hum Genet. 1990 Oct;47(4):735-9. Am J Hum Genet. 1990. PMID: 2220811 Free PMC article.

6

Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III.

Ding JH, de Barsy T, Brown BI, Coleman RA, Chen YT. Ding JH, et al. Among authors: chen yt. J Pediatr. 1990 Jan;116(1):95-100. doi: 10.1016/s0022-3476(05)81652-x. J Pediatr. 1990. PMID: 2295969

7

Glycogen storage disease in adults.

Talente GM, Coleman RA, Alter C, Baker L, Brown BI, Cannon RA, Chen YT, Crigler JF Jr, Ferreira P, Haworth JC, Herman GE, Issenman RM, Keating JP, Linde R, Roe TF, Senior B, Wolfsdorf JI. Talente GM, et al. Among authors: chen yt. Ann Intern Med. 1994 Feb 1;120(3):218-26. doi: 10.7326/0003-4819-120-3-199402010-00008. Ann Intern Med. 1994. PMID: 8273986 Review.

8

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.

9

Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage disease.

McConkie-Rosell A, Wilson C, Piccoli DA, Boyle J, DeClue T, Kishnani P, Shen JJ, Boney A, Brown B, Chen YT. McConkie-Rosell A, et al. Among authors: chen yt. J Inherit Metab Dis. 1996;19(1):51-8. doi: 10.1007/BF01799348. J Inherit Metab Dis. 1996. PMID: 8830177

10

Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene.

Andresen BS, Jensen TG, Bross P, Knudsen I, Winter V, Kølvraa S, Bolund L, Ding JH, Chen YT, Van Hove JL, et al. Andresen BS, et al. Among authors: chen yt. Am J Hum Genet. 1994 Jun;54(6):975-88. Am J Hum Genet. 1994. PMID: 8198141 Free PMC article.

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