Kuramoto T - Search Results

1

Oligodendroglial pathology in the development of myelin breakdown in the dmy mutant rat.

Kuwamura M, Inumaki K, Tanaka M, Shirai M, Izawa T, Yamate J, Franklin RJ, Kuramoto T, Serikawa T. Kuwamura M, et al. Among authors: kuramoto t. Brain Res. 2011 May 10;1389:161-8. doi: 10.1016/j.brainres.2011.03.009. Epub 2011 Mar 9. Brain Res. 2011. PMID: 21396920

2

The myelin vacuolation (mv) rat with a null mutation in the attractin gene.

Kuwamura M, Maeda M, Kuramoto T, Kitada K, Kanehara T, Moriyama M, Nakane Y, Yamate J, Ushijima T, Kotani T, Serikawa T. Kuwamura M, et al. Among authors: kuramoto t. Lab Invest. 2002 Oct;82(10):1279-86. doi: 10.1097/01.lab.0000032375.70196.26. Lab Invest. 2002. PMID: 12379762 Free article.

3

Immunohistochemical and morphometrical studies on myelin breakdown in the demyelination (dmy) mutant rat.

Kuwamura M, Kanehara T, Tokuda S, Kumagai D, Yamate J, Kotani T, Nakane Y, Kuramoto T, Serikawa T. Kuwamura M, et al. Among authors: kuramoto t. Brain Res. 2004 Oct 1;1022(1-2):110-6. doi: 10.1016/j.brainres.2004.07.007. Brain Res. 2004. PMID: 15353220

4

Mutation at the Lmx1a locus provokes aberrant brain development in the rat.

Kuwamura M, Muraguchi T, Matsui T, Ueno M, Takenaka S, Yamate J, Kotani T, Kuramoto T, Guénet JL, Kitada K, Serikawa T. Kuwamura M, et al. Among authors: kuramoto t. Brain Res Dev Brain Res. 2005 Mar 31;155(2):99-106. doi: 10.1016/j.devbrainres.2004.12.009. Brain Res Dev Brain Res. 2005. PMID: 15804398

5

Abnormal myelinogenesis in the central nervous system of the VF mutant rat with recoverable tremor.

Tanaka M, Soma K, Izawa T, Yamate J, Franklin RJ, Kuramoto T, Serikawa T, Kuwamura M. Tanaka M, et al. Among authors: kuramoto t. Brain Res. 2012 Dec 7;1488:104-12. doi: 10.1016/j.brainres.2012.09.037. Epub 2012 Oct 1. Brain Res. 2012. PMID: 23036276

6

The VF rat with abnormal myelinogenesis has a mutation in Dopey1.

Tanaka M, Izawa T, Yamate J, Franklin RJ, Kuramoto T, Serikawa T, Kuwamura M. Tanaka M, et al. Among authors: kuramoto t. Glia. 2014 Sep;62(9):1530-42. doi: 10.1002/glia.22698. Epub 2014 May 24. Glia. 2014. PMID: 24863653

7

Downregulation of aspartoacylase during the progression of myelin breakdown in the dmy mutant rat with mitochondrial magnesium channel MRS2 defect.

Kuwamura M, Tanimura S, Hasegawa Y, Hoshiai R, Moriyama Y, Tanaka M, Takenaka S, Nagayoshi H, Izawa T, Yamate J, Kuramoto T, Serikawa T. Kuwamura M, et al. Among authors: kuramoto t. Brain Res. 2019 Sep 1;1718:169-175. doi: 10.1016/j.brainres.2019.05.017. Epub 2019 May 14. Brain Res. 2019. PMID: 31100216

8

Rat neurological mutations cerebellar vermis defect and hobble are caused by mutations in the netrin-1 receptor gene Unc5h3.

Kuramoto T, Kuwamura M, Serikawa T. Kuramoto T, et al. Brain Res Mol Brain Res. 2004 Mar 30;122(2):103-8. doi: 10.1016/j.molbrainres.2003.12.003. Brain Res Mol Brain Res. 2004. PMID: 15010202

9

A mutation in the gene encoding mitochondrial Mg²+ channel MRS2 results in demyelination in the rat.

Kuramoto T, Kuwamura M, Tokuda S, Izawa T, Nakane Y, Kitada K, Akao M, Guénet JL, Serikawa T. Kuramoto T, et al. PLoS Genet. 2011 Jan 6;7(1):e1001262. doi: 10.1371/journal.pgen.1001262. PLoS Genet. 2011. PMID: 21253565 Free PMC article.

10

Tremor dominant Kyoto (Trdk) rats carry a missense mutation in the gene encoding the SK2 subunit of small-conductance Ca²⁺-activated K⁺ channel.

Kuramoto T, Yokoe M, Kunisawa N, Ohashi K, Miyake T, Higuchi Y, Yoshimi K, Mashimo T, Tanaka M, Kuwamura M, Kaneko S, Shimizu S, Serikawa T, Ohno Y. Kuramoto T, et al. Brain Res. 2017 Dec 1;1676:38-45. doi: 10.1016/j.brainres.2017.09.012. Epub 2017 Sep 13. Brain Res. 2017. PMID: 28917524

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