Funayama R - Search Results

1

Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations.

Mitsuzawa S, Suzuki N, Akiyama T, Ishikawa M, Sone T, Kawada J, Funayama R, Shirota M, Mitsuhashi H, Morimoto S, Ikeda K, Shijo T, Ohno A, Nakamura N, Ono H, Ono R, Osana S, Nakagawa T, Nishiyama A, Izumi R, Kaneda S, Ikeuchi Y, Nakayama K, Fujii T, Warita H, Okano H, Aoki M. Mitsuzawa S, et al. Among authors: funayama r. Stem Cell Reports. 2021 Jun 8;16(6):1527-1541. doi: 10.1016/j.stemcr.2021.04.021. Epub 2021 May 27. Stem Cell Reports. 2021. PMID: 34048688 Free PMC article.

2

Bach1 is critical for the transformation of mouse embryonic fibroblasts by Ras(V12) and maintains ERK signaling.

Nakanome A, Brydun A, Matsumoto M, Ota K, Funayama R, Nakayama K, Ono M, Shiga K, Kobayashi T, Igarashi K. Nakanome A, et al. Among authors: funayama r. Oncogene. 2013 Jul 4;32(27):3231-45. doi: 10.1038/onc.2012.336. Epub 2012 Jul 30. Oncogene. 2013. PMID: 22847612

3

Nrf2-MafG heterodimers contribute globally to antioxidant and metabolic networks.

Hirotsu Y, Katsuoka F, Funayama R, Nagashima T, Nishida Y, Nakayama K, Engel JD, Yamamoto M. Hirotsu Y, et al. Among authors: funayama r. Nucleic Acids Res. 2012 Nov 1;40(20):10228-39. doi: 10.1093/nar/gks827. Epub 2012 Sep 10. Nucleic Acids Res. 2012. PMID: 22965115 Free PMC article.

4

Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure.

Izumi R, Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y. Izumi R, et al. Among authors: funayama r. J Hum Genet. 2013 May;58(5):259-66. doi: 10.1038/jhg.2013.9. Epub 2013 Feb 28. J Hum Genet. 2013. PMID: 23446887

5

Y chromosome-linked B and NK cell deficiency in mice.

Sun SL, Horino S, Itoh-Nakadai A, Kawabe T, Asao A, Takahashi T, So T, Funayama R, Kondo M, Saitsu H, Matsumoto N, Nakayama K, Ishii N. Sun SL, et al. Among authors: funayama r. J Immunol. 2013 Jun 15;190(12):6209-20. doi: 10.4049/jimmunol.1300303. Epub 2013 May 20. J Immunol. 2013. PMID: 23690476

6

Distinct microRNAs expression profile in primary biliary cirrhosis and evaluation of miR 505-3p and miR197-3p as novel biomarkers.

Ninomiya M, Kondo Y, Funayama R, Nagashima T, Kogure T, Kakazu E, Kimura O, Ueno Y, Nakayama K, Shimosegawa T. Ninomiya M, et al. Among authors: funayama r. PLoS One. 2013 Jun 12;8(6):e66086. doi: 10.1371/journal.pone.0066086. Print 2013. PLoS One. 2013. PMID: 23776611 Free PMC article.

7

Ras-induced changes in H3K27me3 occur after those in transcriptional activity.

Hosogane M, Funayama R, Nishida Y, Nagashima T, Nakayama K. Hosogane M, et al. Among authors: funayama r. PLoS Genet. 2013 Aug;9(8):e1003698. doi: 10.1371/journal.pgen.1003698. Epub 2013 Aug 29. PLoS Genet. 2013. PMID: 24009517 Free PMC article.

8

TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.

Ogata T, Niihori T, Tanaka N, Kawai M, Nagashima T, Funayama R, Nakayama K, Nakashima S, Kato F, Fukami M, Aoki Y, Matsubara Y. Ogata T, et al. Among authors: funayama r. PLoS One. 2014 Mar 17;9(3):e91598. doi: 10.1371/journal.pone.0091598. eCollection 2014. PLoS One. 2014. PMID: 24637876 Free PMC article.

9

Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemia.

Fujiwara T, Fukuhara N, Funayama R, Nariai N, Kamata M, Nagashima T, Kojima K, Onishi Y, Sasahara Y, Ishizawa K, Nagasaki M, Nakayama K, Harigae H. Fujiwara T, et al. Among authors: funayama r. Ann Hematol. 2014 Sep;93(9):1515-22. doi: 10.1007/s00277-014-2090-4. Epub 2014 Apr 30. Ann Hematol. 2014. PMID: 24782121 Free PMC article.

10

GNE myopathy associated with congenital thrombocytopenia: a report of two siblings.

Izumi R, Niihori T, Suzuki N, Sasahara Y, Rikiishi T, Nishiyama A, Nishiyama S, Endo K, Kato M, Warita H, Konno H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Nakayama K, Kure S, Matsubara Y, Aoki Y, Aoki M. Izumi R, et al. Among authors: funayama r. Neuromuscul Disord. 2014 Dec;24(12):1068-72. doi: 10.1016/j.nmd.2014.07.008. Epub 2014 Aug 8. Neuromuscul Disord. 2014. PMID: 25257349

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