Yamamoto T - Search Results

1

MCP-1/CCR2 signaling-mediated astrocytosis is accelerated in a transgenic mouse model of SOD1-mutated familial ALS.

Kawaguchi-Niida M, Yamamoto T, Kato Y, Inose Y, Shibata N. Kawaguchi-Niida M, et al. Among authors: yamamoto t. Acta Neuropathol Commun. 2013 Jun 4;1:21. doi: 10.1186/2051-5960-1-21. Acta Neuropathol Commun. 2013. PMID: 24252211 Free PMC article.

2

Oxidative stress in the human fetal brain: an immunohistochemical study.

Yamamoto T, Shibata N, Muramatsu F, Sakayori N, Kobayashi M. Yamamoto T, et al. Pediatr Neurol. 2002 Feb;26(2):116-22. doi: 10.1016/s0887-8994(01)00369-1. Pediatr Neurol. 2002. PMID: 11897475

3

Selective formation of certain advanced glycation end products in spinal cord astrocytes of humans and mice with superoxide dismutase-1 mutation.

Shibata N, Hirano A, Hedley-Whyte ET, Dal Canto MC, Nagai R, Uchida K, Horiuchi S, Kawaguchi M, Yamamoto T, Kobayashi M. Shibata N, et al. Among authors: yamamoto t. Acta Neuropathol. 2002 Aug;104(2):171-8. doi: 10.1007/s00401-002-0537-5. Epub 2002 Apr 18. Acta Neuropathol. 2002. PMID: 12111360

4

Fukutin expression in glial cells and neurons: implication in the brain lesions of Fukuyama congenital muscular dystrophy.

Yamamoto T, Kato Y, Karita M, Takeiri H, Muramatsu F, Kobayashi M, Saito K, Osawa M. Yamamoto T, et al. Acta Neuropathol. 2002 Sep;104(3):217-24. doi: 10.1007/s00401-002-0542-8. Epub 2002 Jun 21. Acta Neuropathol. 2002. PMID: 12172906

5

Oxidative stress in the brain of Fukuyama type congenital muscular dystrophy: immunohistochemical study on astrocytes.

Yamamoto T, Shibata N, Kobayashi M, Saito K, Osawa M. Yamamoto T, et al. J Child Neurol. 2002 Nov;17(11):793-9. doi: 10.1177/08830738020170110701. J Child Neurol. 2002. PMID: 12585716

6

Accumulation of protein-bound 4-hydroxy-2-hexenal in spinal cords from patients with sporadic amyotrophic lateral sclerosis.

Shibata N, Yamada S, Uchida K, Hirano A, Sakoda S, Fujimura H, Sasaki S, Iwata M, Toi S, Kawaguchi M, Yamamoto T, Kobayashi M. Shibata N, et al. Among authors: yamamoto t. Brain Res. 2004 Sep 3;1019(1-2):170-7. doi: 10.1016/j.brainres.2004.05.110. Brain Res. 2004. PMID: 15306251

7

Expression of genes related to muscular dystrophy with lissencephaly.

Yamamoto T, Kato Y, Karita M, Kawaguchi M, Shibata N, Kobayashi M. Yamamoto T, et al. Pediatr Neurol. 2004 Sep;31(3):183-90. doi: 10.1016/j.pediatrneurol.2004.03.020. Pediatr Neurol. 2004. PMID: 15351017

8

Fukutin expression in mouse non-muscle somatic organs: its relationship to the hypoglycosylation of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

Saito Y, Yamamoto T, Ohtsuka-Tsurumi E, Oka A, Mizuguchi M, Itoh M, Voit T, Kato Y, Kobayashi M, Saito K, Osawa M. Saito Y, et al. Among authors: yamamoto t. Brain Dev. 2004 Oct;26(7):469-79. doi: 10.1016/j.braindev.2004.01.004. Brain Dev. 2004. PMID: 15351084

9

Expression and localization of fukutin, POMGnT1, and POMT1 in the central nervous system: consideration for functions of fukutin.

Yamamoto T, Kato Y, Kawaguchi M, Shibata N, Kobayashi M. Yamamoto T, et al. Med Electron Microsc. 2004 Dec;37(4):200-7. doi: 10.1007/s00795-004-0260-5. Med Electron Microsc. 2004. PMID: 15614444 Review.

10

Crotonaldehyde accumulates in glial cells of Alzheimer's disease brain.

Kawaguchi-Niida M, Shibata N, Morikawa S, Uchida K, Yamamoto T, Sawada T, Kobayashi M. Kawaguchi-Niida M, et al. Among authors: yamamoto t. Acta Neuropathol. 2006 May;111(5):422-9. doi: 10.1007/s00401-006-0044-1. Epub 2006 Mar 15. Acta Neuropathol. 2006. PMID: 16538519

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