Zhang Z - Search Results

1

In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene.

Habara Y, Takeshima Y, Awano H, Okizuka Y, Zhang Z, Saiki K, Yagi M, Matsuo M. Habara Y, et al. Among authors: zhang z. J Med Genet. 2009 Aug;46(8):542-7. doi: 10.1136/jmg.2008.061259. Epub 2008 Nov 10. J Med Genet. 2009. PMID: 19001018

2

Dystrophin nonsense mutations can generate alternative rescue transcripts in lymphocytes.

Nishiyama A, Takeshima Y, Zhang Z, Habara Y, Tran TH, Yagi M, Matsuo M. Nishiyama A, et al. Among authors: zhang z. Ann Hum Genet. 2008 Nov;72(Pt 6):717-24. doi: 10.1111/j.1469-1809.2008.00468.x. Epub 2008 Jul 24. Ann Hum Genet. 2008. PMID: 18652600

3

A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene.

Tran VK, Zhang Z, Yagi M, Nishiyama A, Habara Y, Takeshima Y, Matsuo M. Tran VK, et al. Among authors: zhang z. J Hum Genet. 2005;50(8):425-433. doi: 10.1007/s10038-005-0272-6. Epub 2005 Aug 30. J Hum Genet. 2005. PMID: 16133659

4

Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophy.

Katayama Y, Tran VK, Hoan NT, Zhang Z, Goji K, Yagi M, Takeshima Y, Saiki K, Nhan NT, Matsuo M. Katayama Y, et al. Among authors: zhang z. Hum Genet. 2006 Jun;119(5):516-9. doi: 10.1007/s00439-006-0159-4. Epub 2006 Mar 10. Hum Genet. 2006. PMID: 16528518

5

Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four-nucleotide deletion in the dystrophin gene.

Tran VK, Takeshima Y, Zhang Z, Yagi M, Nishiyama A, Habara Y, Matsuo M. Tran VK, et al. Among authors: zhang z. J Med Genet. 2006 Dec;43(12):924-30. doi: 10.1136/jmg.2006.042317. Epub 2006 May 31. J Med Genet. 2006. PMID: 16738009 Free PMC article.

6

A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient.

Tran VK, Takeshima Y, Zhang Z, Habara Y, Haginoya K, Nishiyama A, Yagi M, Matsuo M. Tran VK, et al. Among authors: zhang z. Hum Genet. 2007 Jan;120(5):737-42. doi: 10.1007/s00439-006-0241-y. Epub 2006 Sep 26. Hum Genet. 2007. PMID: 17024373

7

Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons.

Zhang Z, Habara Y, Nishiyama A, Oyazato Y, Yagi M, Takeshima Y, Matsuo M. Zhang Z, et al. J Hum Genet. 2007;52(7):607-617. doi: 10.1007/s10038-007-0163-0. Epub 2007 Jun 20. J Hum Genet. 2007. PMID: 17579806

8

Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy.

Zhang Z, Takeshima Y, Awano H, Nishiyama A, Okizuka Y, Yagi M, Matsuo M. Zhang Z, et al. J Hum Genet. 2008;53(3):215-219. doi: 10.1007/s10038-007-0235-1. Epub 2007 Dec 27. J Hum Genet. 2008. PMID: 18160999

9

Small mutations detected by multiplex ligation-dependent probe amplification of the dystrophin gene.

Okizuka Y, Takeshima Y, Awano H, Zhang Z, Yagi M, Matsuo M. Okizuka Y, et al. Among authors: zhang z. Genet Test Mol Biomarkers. 2009 Jun;13(3):427-31. doi: 10.1089/gtmb.2009.0002. Genet Test Mol Biomarkers. 2009. PMID: 19473085

10

Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene.

Zhang Z, Yagi M, Okizuka Y, Awano H, Takeshima Y, Matsuo M. Zhang Z, et al. J Hum Genet. 2009 Aug;54(8):466-73. doi: 10.1038/jhg.2009.63. Epub 2009 Jul 17. J Hum Genet. 2009. PMID: 19609279

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