Masuda A - Search Results

1

Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8.

Kaneko H, Kitoh H, Matsuura T, Masuda A, Ito M, Mottes M, Rauch F, Ishiguro N, Ohno K. Kaneko H, et al. Among authors: masuda a. Hum Genet. 2011 Nov;130(5):671-83. doi: 10.1007/s00439-011-1006-9. Epub 2011 May 19. Hum Genet. 2011. PMID: 21594610

2

Essential role of GATA transcriptional factors in the activation of mast cells.

Masuda A, Hashimoto K, Yokoi T, Doi T, Kodama T, Kume H, Ohno K, Matsuguchi T. Masuda A, et al. J Immunol. 2007 Jan 1;178(1):360-8. doi: 10.4049/jimmunol.178.1.360. J Immunol. 2007. PMID: 17182574

3

In vitro and in silico analysis reveals an efficient algorithm to predict the splicing consequences of mutations at the 5' splice sites.

Sahashi K, Masuda A, Matsuura T, Shinmi J, Zhang Z, Takeshima Y, Matsuo M, Sobue G, Ohno K. Sahashi K, et al. Among authors: masuda a. Nucleic Acids Res. 2007;35(18):5995-6003. doi: 10.1093/nar/gkm647. Epub 2007 Aug 28. Nucleic Acids Res. 2007. PMID: 17726045 Free PMC article.

4

Human branch point consensus sequence is yUnAy.

Gao K, Masuda A, Matsuura T, Ohno K. Gao K, et al. Among authors: masuda a. Nucleic Acids Res. 2008 Apr;36(7):2257-67. doi: 10.1093/nar/gkn073. Epub 2008 Feb 19. Nucleic Acids Res. 2008. PMID: 18285363 Free PMC article.

5

Viral vector-mediated [corrected] expression of human collagen Q in cultured cells.

Ito M, Masuda A, Jinno S, Katagiri T, Krejci E, Ohno K. Ito M, et al. Among authors: masuda a. Chem Biol Interact. 2008 Sep 25;175(1-3):346-8. doi: 10.1016/j.cbi.2008.02.003. Epub 2008 Feb 14. Chem Biol Interact. 2008. PMID: 18374322

6

hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome.

Masuda A, Shen XM, Ito M, Matsuura T, Engel AG, Ohno K. Masuda A, et al. Hum Mol Genet. 2008 Dec 15;17(24):4022-35. doi: 10.1093/hmg/ddn305. Epub 2008 Sep 20. Hum Mol Genet. 2008. PMID: 18806275 Free PMC article.

7

Tannic acid facilitates expression of the polypyrimidine tract binding protein and alleviates deleterious inclusion of CHRNA1 exon P3A due to an hnRNP H-disrupting mutation in congenital myasthenic syndrome.

Bian Y, Masuda A, Matsuura T, Ito M, Okushin K, Engel AG, Ohno K. Bian Y, et al. Among authors: masuda a. Hum Mol Genet. 2009 Apr 1;18(7):1229-37. doi: 10.1093/hmg/ddp023. Epub 2009 Jan 15. Hum Mol Genet. 2009. PMID: 19147685 Free PMC article.

8

Molecular hydrogen is protective against 6-hydroxydopamine-induced nigrostriatal degeneration in a rat model of Parkinson's disease.

Fu Y, Ito M, Fujita Y, Ito M, Ichihara M, Masuda A, Suzuki Y, Maesawa S, Kajita Y, Hirayama M, Ohsawa I, Ohta S, Ohno K. Fu Y, et al. Among authors: masuda a. Neurosci Lett. 2009 Apr 3;453(2):81-5. doi: 10.1016/j.neulet.2009.02.016. Epub 2009 Feb 12. Neurosci Lett. 2009. PMID: 19356598

9

[Molecular bases and therapeutic strategies in defective neuromuscular transmissions: lessons learned from a prototypical synapse].

Ohno K, Ito M, Masuda A. Ohno K, et al. Among authors: masuda a. Nihon Shinkei Seishin Yakurigaku Zasshi. 2009 Aug;29(4):145-51. Nihon Shinkei Seishin Yakurigaku Zasshi. 2009. PMID: 19764481 Review. Japanese.

10

Molecular hydrogen suppresses FcepsilonRI-mediated signal transduction and prevents degranulation of mast cells.

Itoh T, Fujita Y, Ito M, Masuda A, Ohno K, Ichihara M, Kojima T, Nozawa Y, Ito M. Itoh T, et al. Among authors: masuda a. Biochem Biophys Res Commun. 2009 Nov 27;389(4):651-6. doi: 10.1016/j.bbrc.2009.09.047. Epub 2009 Sep 17. Biochem Biophys Res Commun. 2009. PMID: 19766097

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