Kanemura Y - Search Results

1

Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis.

Shigemizu D, Miya F, Akiyama S, Okuda S, Boroevich KA, Fujimoto A, Nakagawa H, Ozaki K, Niida S, Kanemura Y, Okamoto N, Saitoh S, Kato M, Yamasaki M, Matsunaga T, Mutai H, Kosaki K, Tsunoda T. Shigemizu D, et al. Among authors: kanemura y. Sci Rep. 2018 Jul 4;8(1):10367. doi: 10.1038/s41598-018-28698-y. Sci Rep. 2018. PMID: 29970886 Free PMC article.

2

Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM.

Okamoto N, Del Maestro R, Valero R, Monros E, Poo P, Kanemura Y, Yamasaki M. Okamoto N, et al. Among authors: kanemura y. J Hum Genet. 2004;49(6):334-337. doi: 10.1007/s10038-004-0153-4. Epub 2004 May 18. J Hum Genet. 2004. PMID: 15148591

3

Human neural stem/progenitor cells, expanded in long-term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils.

Ishibashi S, Sakaguchi M, Kuroiwa T, Yamasaki M, Kanemura Y, Shizuko I, Shimazaki T, Onodera M, Okano H, Mizusawa H. Ishibashi S, et al. Among authors: kanemura y. J Neurosci Res. 2004 Oct 15;78(2):215-23. doi: 10.1002/jnr.20246. J Neurosci Res. 2004. PMID: 15378509

4

First case of L1CAM gene mutation identified in MASA syndrome in Asia.

Kanemura Y, Takuma Y, Kamiguchi H, Yamasaki M. Kanemura Y, et al. Congenit Anom (Kyoto). 2005 Jun;45(2):67-9. doi: 10.1111/j.1741-4520.2005.00067.x. Congenit Anom (Kyoto). 2005. PMID: 15904436

5

Inhibition of glioma cell proliferation by neural stem cell factor.

Suzuki T, Izumoto S, Wada K, Fujimoto Y, Maruno M, Yamasaki M, Kanemura Y, Shimazaki T, Okano H, Yoshimine T. Suzuki T, et al. Among authors: kanemura y. J Neurooncol. 2005 Sep;74(3):233-9. doi: 10.1007/s11060-004-7118-5. J Neurooncol. 2005. PMID: 16187020

6

Effect of neurosphere size on the growth rate of human neural stem/progenitor cells.

Mori H, Ninomiya K, Kino-oka M, Shofuda T, Islam MO, Yamasaki M, Okano H, Taya M, Kanemura Y. Mori H, et al. Among authors: kanemura y. J Neurosci Res. 2006 Dec;84(8):1682-91. doi: 10.1002/jnr.21082. J Neurosci Res. 2006. PMID: 17044035

7

Molecular mechanisms and neuroimaging criteria for severe L1 syndrome with X-linked hydrocephalus.

Kanemura Y, Okamoto N, Sakamoto H, Shofuda T, Kamiguchi H, Yamasaki M. Kanemura Y, et al. J Neurosurg. 2006 Nov;105(5 Suppl):403-12. doi: 10.3171/ped.2006.105.5.403. J Neurosurg. 2006. PMID: 17328266

8

Image cytometry for analyzing regional distribution of cells inside human neurospheres.

Mori H, Ninomiya K, Kanemura Y, Yamasaki M, Kino-Oka M, Taya M. Mori H, et al. Among authors: kanemura y. J Biosci Bioeng. 2007 Apr;103(4):384-7. doi: 10.1263/jbb.103.384. J Biosci Bioeng. 2007. PMID: 17502283

9

Recombination rates of genes expressed in human tissues.

Kato M, Miya F, Kanemura Y, Tanaka T, Nakamura Y, Tsunoda T. Kato M, et al. Among authors: kanemura y. Hum Mol Genet. 2008 Feb 15;17(4):577-86. doi: 10.1093/hmg/ddm332. Epub 2007 Nov 13. Hum Mol Genet. 2008. PMID: 18000027

10

Two new cases of pure 1q terminal deletion presenting with brain malformations.

Hiraki Y, Okamoto N, Ida T, Nakata Y, Kamada M, Kanemura Y, Yamasaki M, Fujita H, Nishimura G, Kato M, Harada N, Matsumoto N. Hiraki Y, et al. Among authors: kanemura y. Am J Med Genet A. 2008 May 15;146A(10):1241-7. doi: 10.1002/ajmg.a.32275. Am J Med Genet A. 2008. PMID: 18384145

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