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Tailor-made RNAi knockdown against triplet repeat disease-causing alleles.
Takahashi M, Watanabe S, Murata M, Furuya H, Kanazawa I, Wada K, Hohjoh H. Takahashi M, et al. Among authors: furuya h. Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21731-6. doi: 10.1073/pnas.1012153107. Epub 2010 Nov 22. Proc Natl Acad Sci U S A. 2010. PMID: 21098280 Free PMC article.
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.
Ishiura H, Takahashi Y, Hayashi T, Saito K, Furuya H, Watanabe M, Murata M, Suzuki M, Sugiura A, Sawai S, Shibuya K, Ueda N, Ichikawa Y, Kanazawa I, Goto J, Tsuji S. Ishiura H, et al. Among authors: furuya h. J Hum Genet. 2014 Mar;59(3):163-72. doi: 10.1038/jhg.2013.139. Epub 2014 Jan 23. J Hum Genet. 2014. PMID: 24451228
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.
Ishiura H, Takahashi Y, Hayashi T, Saito K, Furuya H, Watanabe M, Murata M, Suzuki M, Sugiura A, Sawai S, Shibuya K, Ueda N, Ichikawa Y, Kanazawa I, Goto J, Tsuji S. Ishiura H, et al. Among authors: furuya h. J Hum Genet. 2016 Apr;61(4):363-4. doi: 10.1038/jhg.2015.159. J Hum Genet. 2016. PMID: 27108959 No abstract available.
[Triplet repeat disease and dementia].
Furuya H. Furuya H. Nihon Rinsho. 2004 Apr;62 Suppl 4:224-8. Nihon Rinsho. 2004. PMID: 15174675 Review. Japanese. No abstract available.
900 results