Awano H - Search Results

1

A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old.

Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M. Nakagawa T, et al. Among authors: awano h. Clin Chim Acta. 2013 Aug 23;423:10-4. doi: 10.1016/j.cca.2013.03.031. Epub 2013 Apr 19. Clin Chim Acta. 2013. PMID: 23603101

2

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. Among authors: awano h. 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

3

Wide ranges of serum myostatin concentrations in Duchenne muscular dystrophy patients.

Awano H, Takeshima Y, Okizuka Y, Saiki K, Yagi M, Matsuo M. Awano H, et al. Clin Chim Acta. 2008 May;391(1-2):115-7. doi: 10.1016/j.cca.2008.01.024. Epub 2008 Feb 1. Clin Chim Acta. 2008. PMID: 18284920 No abstract available.

4

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: awano h. 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

5

High incidence of electrocardiogram abnormalities in young patients with duchenne muscular dystrophy.

Takami Y, Takeshima Y, Awano H, Okizuka Y, Yagi M, Matsuo M. Takami Y, et al. Among authors: awano h. Pediatr Neurol. 2008 Dec;39(6):399-403. doi: 10.1016/j.pediatrneurol.2008.08.006. Pediatr Neurol. 2008. PMID: 19027585

6

Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations.

Nishiyama A, Yagi M, Awano H, Okizuka Y, Maeda T, Yoshida S, Takeshima Y, Matsuo M. Nishiyama A, et al. Among authors: awano h. Pediatr Int. 2009 Dec;51(6):775-9. doi: 10.1111/j.1442-200X.2009.02863.x. Epub 2009 Mar 31. Pediatr Int. 2009. PMID: 19438831

7

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: awano h. Genet Test Mol Biomarkers. 2009 Jun;13(3):427-31. doi: 10.1089/gtmb.2009.0002. Genet Test Mol Biomarkers. 2009. PMID: 19473085

8

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. Among authors: awano h. 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

9

Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD.

Okizuka Y, Takeshima Y, Itoh K, Zhang Z, Awano H, Maruyama K, Kumagai T, Yagi M, Matsuo M. Okizuka Y, et al. Among authors: awano h. BMC Med Genet. 2010 Mar 30;11:49. doi: 10.1186/1471-2350-11-49. BMC Med Genet. 2010. PMID: 20350330 Free PMC article.

10

Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.

Takeshima Y, Yagi M, Okizuka Y, Awano H, Zhang Z, Yamauchi Y, Nishio H, Matsuo M. Takeshima Y, et al. Among authors: awano h. J Hum Genet. 2010 Jun;55(6):379-88. doi: 10.1038/jhg.2010.49. Epub 2010 May 20. J Hum Genet. 2010. PMID: 20485447

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