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Infrequent RAS mutation is not associated with specific histological phenotype in gliomas.
Makino Y, Arakawa Y, Yoshioka E, Shofuda T, Minamiguchi S, Kawauchi T, Tanji M, Kanematsu D, Nonaka M, Okita Y, Kodama Y, Mano M, Hirose T, Mineharu Y, Miyamoto S, Kanemura Y. Makino Y, et al. Among authors: shofuda t. BMC Cancer. 2021 Sep 15;21(1):1025. doi: 10.1186/s12885-021-08733-4. BMC Cancer. 2021. PMID: 34525976 Free PMC article.
Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus).
Yamasaki M, Nonaka M, Suzumori N, Nakamura H, Fujita H, Namba A, Kamei Y, Yamada T, Pooh RK, Tanemura M, Sudo N, Nagasaka M, Yoshioka E, Shofuda T, Kanemura Y. Yamasaki M, et al. Among authors: shofuda t. J Neurosurg Pediatr. 2011 Oct;8(4):411-6. doi: 10.3171/2011.7.PEDS10531. J Neurosurg Pediatr. 2011. PMID: 21961551
Differentiation, polarization, and migration of human induced pluripotent stem cell-derived neural progenitor cells co-cultured with a human glial cell line with radial glial-like characteristics.
Bamba Y, Shofuda T, Kanematsu D, Nonaka M, Yamasaki M, Okano H, Kanemura Y. Bamba Y, et al. Among authors: shofuda t. Biochem Biophys Res Commun. 2014 May 16;447(4):683-8. doi: 10.1016/j.bbrc.2014.04.070. Epub 2014 Apr 19. Biochem Biophys Res Commun. 2014. PMID: 24755070
65 results