Hirano A - Search Results

1

A type of familial cleft of the soft palate maps to 2p24.2-p24.1 or 2p21-p12.

Tsuda M, Yamada T, Mikoya T, Sogabe I, Nakashima M, Minakami H, Kishino T, Kinoshita A, Niikawa N, Hirano A, Yoshiura K. Tsuda M, et al. Among authors: hirano a. J Hum Genet. 2010 Feb;55(2):124-6. doi: 10.1038/jhg.2009.131. Epub 2010 Jan 15. J Hum Genet. 2010. PMID: 20075946 Free article.

2

A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene.

Nakano M, Miwa N, Hirano A, Yoshiura K, Niikawa N. Nakano M, et al. Among authors: hirano a. BMC Genet. 2009 Aug 4;10:42. doi: 10.1186/1471-2156-10-42. BMC Genet. 2009. PMID: 19650936 Free PMC article.

3

Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.

Nakashima M, Nakano M, Hirano A, Kishino T, Kondoh S, Miwa N, Niikawa N, Yoshiura KI. Nakashima M, et al. Among authors: hirano a. J Hum Genet. 2008;53(1):34-41. doi: 10.1007/s10038-007-0214-6. Epub 2007 Nov 7. J Hum Genet. 2008. PMID: 17987257

4

PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses.

Ichikawa E, Watanabe A, Nakano Y, Akita S, Hirano A, Kinoshita A, Kondo S, Kishino T, Uchiyama T, Niikawa N, Yoshiura KI. Ichikawa E, et al. Among authors: hirano a. J Hum Genet. 2006;51(1):38-46. doi: 10.1007/s10038-005-0319-8. Epub 2005 Oct 25. J Hum Genet. 2006. PMID: 16247549

5

Two missense mutations of the IRF6 gene in two Japanese families with popliteal pterygium syndrome.

Matsuzawa N, Kondo S, Shimozato K, Nagao T, Nakano M, Tsuda M, Hirano A, Niikawa N, Yoshiura K. Matsuzawa N, et al. Among authors: hirano a. Am J Med Genet A. 2010 Sep;152A(9):2262-7. doi: 10.1002/ajmg.a.33338. Am J Med Genet A. 2010. PMID: 20803643

6

No evidence of association between 8q24 and susceptibility to nonsyndromic cleft lip with or without palate in Japanese population.

Hikida M, Tsuda M, Watanabe A, Kinoshita A, Akita S, Hirano A, Uchiyama T, Yoshiura K. Hikida M, et al. Among authors: hirano a. Cleft Palate Craniofac J. 2012 Nov;49(6):714-7. doi: 10.1597/10-242. Epub 2011 Oct 7. Cleft Palate Craniofac J. 2012. PMID: 21981552

7

Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.

Kashiyama K, Nakazawa Y, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Yamashita S, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Takahashi Y, Nagayama Y, Mitsutake N, Lehmann AR, Ogi T. Kashiyama K, et al. Among authors: hirano a. Am J Hum Genet. 2013 May 2;92(5):807-19. doi: 10.1016/j.ajhg.2013.04.007. Epub 2013 Apr 25. Am J Hum Genet. 2013. PMID: 23623389 Free PMC article.

8

The split fracture of mandibular symphysis.

Yano H, Hirata R, Nakashima M, Hirano A. Yano H, et al. Among authors: hirano a. J Trauma. 2007 Aug;63(2):E55-8. doi: 10.1097/01.ta.0000246894.84637.d3. J Trauma. 2007. PMID: 17308487 No abstract available.

9

Cranioplasty with auto-purified bone flap after infection.

Yano H, Tanaka K, Matsuo T, Tsuda M, Akita S, Hirano A. Yano H, et al. Among authors: hirano a. J Craniofac Surg. 2006 Nov;17(6):1076-9. doi: 10.1097/01.scs.0000244916.84511.b6. J Craniofac Surg. 2006. PMID: 17119408

10

The usefulness of basic fibroblast growth factor for radiation-exposed tissue.

Kinoshita N, Tsuda M, Hamuy R, Nakashima M, Nakamura-Kurashige T, Matsuu-Matsuyama M, Hirano A, Akita S. Kinoshita N, et al. Among authors: hirano a. Wound Repair Regen. 2012 Jan-Feb;20(1):91-102. doi: 10.1111/j.1524-475X.2011.00758.x. Wound Repair Regen. 2012. PMID: 22276588

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