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The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.
Ishiura H, Sako W, Yoshida M, Kawarai T, Tanabe O, Goto J, Takahashi Y, Date H, Mitsui J, Ahsan B, Ichikawa Y, Iwata A, Yoshino H, Izumi Y, Fujita K, Maeda K, Goto S, Koizumi H, Morigaki R, Ikemura M, Yamauchi N, Murayama S, Nicholson GA, Ito H, Sobue G, Nakagawa M, Kaji R, Tsuji S. Ishiura H, et al. Among authors: morigaki r. Am J Hum Genet. 2012 Aug 10;91(2):320-9. doi: 10.1016/j.ajhg.2012.07.014. Am J Hum Genet. 2012. PMID: 22883144 Free PMC article.
[Pathomechanisms of motor neuron death by mutant TFG].
Kawarai T, Morita M, Morigaki R, Fujita K, Nodera H, Izumi Y, Goto S, Nakano I, Kaji R. Kawarai T, et al. Among authors: morigaki r. Rinsho Shinkeigaku. 2013;23(11):1199. doi: 10.5692/clinicalneurol.53.1199. Rinsho Shinkeigaku. 2013. PMID: 24291928 Japanese.
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease.
Kawarai T, Miyamoto R, Nakagawa E, Koichihara R, Sakamoto T, Mure H, Morigaki R, Koizumi H, Oki R, Montecchiani C, Caltagirone C, Orlacchio A, Hattori A, Mashimo H, Izumi Y, Mezaki T, Kumada S, Taniguchi M, Yokochi F, Saitoh S, Goto S, Kaji R. Kawarai T, et al. Among authors: morigaki r. Parkinsonism Relat Disord. 2018 Jul;52:55-61. doi: 10.1016/j.parkreldis.2018.03.022. Epub 2018 Apr 5. Parkinsonism Relat Disord. 2018. PMID: 29653907
Basic research and surgical techniques for brain arteriovenous malformations.
Takagi Y, Kanematsu Y, Mizobuchi Y, Mure H, Shimada K, Tada Y, Morigaki R, Sogabe S, Fujihara T, Miyamoto T, Miyake K. Takagi Y, et al. Among authors: morigaki r. J Med Invest. 2020;67(3.4):222-228. doi: 10.2152/jmi.67.222. J Med Invest. 2020. PMID: 33148892 Free article. Review.
51 results