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Did you mean kumiko matsuoka (2 results)?
Molecular Analysis of Long-Term Cultured Cardiac Stem Cells for Cardiac Regeneration.
Kawaguchi N, Takagaki Y, Matsuoka R, Nakanishi T. Kawaguchi N, et al. Among authors: matsuoka r. 2016 Jun 25. In: Nakanishi T, Markwald RR, Baldwin HS, Keller BB, Srivastava D, Yamagishi H, editors. Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology [Internet]. Tokyo: Springer; 2016. Chapter 49. 2016 Jun 25. In: Nakanishi T, Markwald RR, Baldwin HS, Keller BB, Srivastava D, Yamagishi H, editors. Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology [Internet]. Tokyo: Springer; 2016. Chapter 49. PMID: 29787151 Free Books & Documents. Review.
RAF1 mutations in childhood-onset dilated cardiomyopathy.
Dhandapany PS, Razzaque MA, Muthusami U, Kunnoth S, Edwards JJ, Mulero-Navarro S, Riess I, Pardo S, Sheng J, Rani DS, Rani B, Govindaraj P, Flex E, Yokota T, Furutani M, Nishizawa T, Nakanishi T, Robbins J, Limongelli G, Hajjar RJ, Lebeche D, Bahl A, Khullar M, Rathinavel A, Sadler KC, Tartaglia M, Matsuoka R, Thangaraj K, Gelb BD. Dhandapany PS, et al. Among authors: matsuoka r. Nat Genet. 2014 Jun;46(6):635-639. doi: 10.1038/ng.2963. Epub 2014 Apr 28. Nat Genet. 2014. PMID: 24777450 Free PMC article.
The genetics of tethered cord syndrome.
Bassuk AG, Craig D, Jalali A, Mukhopadhyay A, Kim F, Charrow J, Gulbu U, Epstein LG, Bowman R, McLone D, Yagi H, Matsuoka R, Stephan DA, Kessler JA. Bassuk AG, et al. Among authors: matsuoka r. Am J Med Genet A. 2005 Feb 1;132A(4):450-3. doi: 10.1002/ajmg.a.30439. Am J Med Genet A. 2005. PMID: 15558749 No abstract available.
Characterization of a novel KRAS mutation identified in Noonan syndrome.
Razzaque MA, Komoike Y, Nishizawa T, Inai K, Furutani M, Higashinakagawa T, Matsuoka R. Razzaque MA, et al. Among authors: matsuoka r. Am J Med Genet A. 2012 Mar;158A(3):524-32. doi: 10.1002/ajmg.a.34419. Epub 2012 Feb 2. Am J Med Genet A. 2012. PMID: 22302539
Role of TBX1 in human del22q11.2 syndrome.
Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, Ichida F, Joo K, Kimura M, Imamura S, Kamatani N, Momma K, Takao A, Nakazawa M, Shimizu N, Matsuoka R. Yagi H, et al. Among authors: matsuoka r. Lancet. 2003 Oct 25;362(9393):1366-73. doi: 10.1016/s0140-6736(03)14632-6. Lancet. 2003. PMID: 14585638
Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.
Chida A, Inai K, Sato H, Shimada E, Nishizawa T, Shimada M, Furutani M, Furutani Y, Kawamura Y, Sugimoto M, Ishihara J, Fujiwara M, Soga T, Kawana M, Fuji S, Tateno S, Kuraishi K, Kogaki S, Nishimura M, Ayusawa M, Ichida F, Yamazawa H, Matsuoka R, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: matsuoka r. Heart Vessels. 2017 Jun;32(6):700-707. doi: 10.1007/s00380-016-0920-0. Epub 2016 Nov 24. Heart Vessels. 2017. PMID: 27885498
72 results