Chen YT - Search Results

1

Isolation and nucleotide sequence of canine glucose-6-phosphatase mRNA: identification of mutation in puppies with glycogen storage disease type Ia.

Kishnani PS, Bao Y, Wu JY, Brix AE, Lin JL, Chen YT. Kishnani PS, et al. Among authors: chen yt. Biochem Mol Med. 1997 Aug;61(2):168-77. doi: 10.1006/bmme.1997.2600. Biochem Mol Med. 1997. PMID: 9259982

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

Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.

Bao Y, Kishnani P, Wu JY, Chen YT. Bao Y, et al. Among authors: chen yt. J Clin Invest. 1996 Feb 15;97(4):941-8. doi: 10.1172/JCI118517. J Clin Invest. 1996. PMID: 8613547 Free PMC article.

4

Pulmonary hypertension in glycogen storage disease type I.

Kishnani P, Bengur AR, Chen YT. Kishnani P, et al. Among authors: chen yt. J Inherit Metab Dis. 1996;19(2):213-6. doi: 10.1007/BF01799432. J Inherit Metab Dis. 1996. PMID: 8739968 No abstract available.

5

A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.

Shen J, Bao Y, Chen YT. Shen J, et al. Among authors: chen yt. Hum Mutat. 1997;9(1):37-40. doi: 10.1002/(SICI)1098-1004(1997)9:1<37::AID-HUMU6>3.0.CO;2-M. Hum Mutat. 1997. PMID: 8990006

6

Isolation and nucleotide sequence of human liver glycogen debranching enzyme mRNA: identification of multiple tissue-specific isoforms.

Bao Y, Yang BZ, Dawson TL Jr, Chen YT. Bao Y, et al. Among authors: chen yt. Gene. 1997 Sep 15;197(1-2):389-98. doi: 10.1016/s0378-1119(97)00291-6. Gene. 1997. PMID: 9332391

7

Nutritional deficiencies in a patient with glycogen storage disease type Ib.

Kishnani PS, Boney A, Chen YT. Kishnani PS, et al. Among authors: chen yt. J Inherit Metab Dis. 1999 Oct;22(7):795-801. doi: 10.1023/a:1005549823146. J Inherit Metab Dis. 1999. PMID: 10518279

8

Genotype-phenotype correlation in two frequent mutations and mutation update in type III glycogen storage disease.

Shaiu WL, Kishnani PS, Shen J, Liu HM, Chen YT. Shaiu WL, et al. Among authors: chen yt. Mol Genet Metab. 2000 Jan;69(1):16-23. doi: 10.1006/mgme.1999.2953. Mol Genet Metab. 2000. PMID: 10655153

9

Canine model and genomic structural organization of glycogen storage disease type Ia (GSD Ia).

Kishnani PS, Faulkner E, VanCamp S, Jackson M, Brown T, Boney A, Koeberl D, Chen YT. Kishnani PS, et al. Among authors: chen yt. Vet Pathol. 2001 Jan;38(1):83-91. doi: 10.1354/vp.38-1-83. Vet Pathol. 2001. PMID: 11199168

10

Delivery of glucose-6-phosphatase in a canine model for glycogen storage disease, type Ia, with adeno-associated virus (AAV) vectors.

Beaty RM, Jackson M, Peterson D, Bird A, Brown T, Benjamin DK Jr, Juopperi T, Kishnani P, Boney A, Chen YT, Koeberl DD. Beaty RM, et al. Among authors: chen yt. Gene Ther. 2002 Aug;9(15):1015-22. doi: 10.1038/sj.gt.3301728. Gene Ther. 2002. PMID: 12101432

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