Morishima A - Search Results

1

Apolipoprotein E and Reelin ligands modulate tau phosphorylation through an apolipoprotein E receptor/disabled-1/glycogen synthase kinase-3beta cascade.

Ohkubo N, Lee YD, Morishima A, Terashima T, Kikkawa S, Tohyama M, Sakanaka M, Tanaka J, Maeda N, Vitek MP, Mitsuda N. Ohkubo N, et al. Among authors: morishima a. FASEB J. 2003 Feb;17(2):295-7. doi: 10.1096/fj.02-0434fje. Epub 2002 Dec 18. FASEB J. 2003. PMID: 12490540

2

Reelin signals survival through Src-family kinases that inactivate BAD activity.

Ohkubo N, Vitek MP, Morishima A, Suzuki Y, Miki T, Maeda N, Mitsuda N. Ohkubo N, et al. Among authors: morishima a. J Neurochem. 2007 Oct;103(2):820-30. doi: 10.1111/j.1471-4159.2007.04804.x. Epub 2007 Aug 13. J Neurochem. 2007. PMID: 17696989 Free article.

3

NFkappaB regulates plasma apolipoprotein A-I and high density lipoprotein cholesterol through inhibition of peroxisome proliferator-activated receptor alpha.

Morishima A, Ohkubo N, Maeda N, Miki T, Mitsuda N. Morishima A, et al. J Biol Chem. 2003 Oct 3;278(40):38188-93. doi: 10.1074/jbc.M306336200. Epub 2003 Jul 25. J Biol Chem. 2003. PMID: 12882972 Free article.

4

The 4,752 C/T polymorphism in the presenilin 1 gene increases the risk of Alzheimer's disease in apolipoprotein E4 carriers.

Matsubara-Tsutsui M, Yamagata H, Morishima A, Nakura J, Mitsuda N, Kamino K, Kondo I, Miki T. Matsubara-Tsutsui M, et al. Among authors: morishima a. Intern Med. 2002 Oct;41(10):823-8. doi: 10.2169/internalmedicine.41.823. Intern Med. 2002. PMID: 12413003 Free article.

5

Molecular and epidemiological studies of Werner syndrome in the Japanese population.

Miki T, Nakura J, Ye L, Mitsuda N, Morishima A, Sato N, Kamino K, Ogihara T. Miki T, et al. Among authors: morishima a. Mech Ageing Dev. 1997 Dec;98(3):255-65. doi: 10.1016/s0047-6374(97)00112-7. Mech Ageing Dev. 1997. PMID: 9352494

6

[Genetic analysis of Werner syndrome in a family].

Morishima A, Mitsuda N, Nakura J, Kamino K, Sato N, Miki T, Ogihara T. Morishima A, et al. Nihon Ronen Igakkai Zasshi. 1995 Dec;32(12):817-21. doi: 10.3143/geriatrics.32.817. Nihon Ronen Igakkai Zasshi. 1995. PMID: 8865743 Free article. Japanese.

7

The genes responsible for human progeroid syndromes.

Miki T, Morishima A, Nakura J. Miki T, et al. Among authors: morishima a. Intern Med. 2000 Apr;39(4):327-8. doi: 10.2169/internalmedicine.39.327. Intern Med. 2000. PMID: 10801150 Free article. Review. No abstract available.

8

Helicases and aging.

Nakura J, Ye L, Morishima A, Kohara K, Miki T. Nakura J, et al. Among authors: morishima a. Cell Mol Life Sci. 2000 May;57(5):716-30. doi: 10.1007/s000180050036. Cell Mol Life Sci. 2000. PMID: 10892338 Free PMC article. Review.

9

17-year follow-up study of a patient with obstructive hypertrophic cardiomyopathy with a deletion mutation in the cardiac myosin binding protein C gene.

Ogimoto A, Hamada M, Nakura J, Shigematsu Y, Hara Y, Ohtsuka T, Morishima A, Kimura A, Miki T, Hiwada K. Ogimoto A, et al. Among authors: morishima a. Circ J. 2004 Feb;68(2):174-7. doi: 10.1253/circj.68.174. Circ J. 2004. PMID: 14745156 Free article.

10

[A case of mild-type myotonic dystrophy with dementia and severe arteriosclerosis obliterans].

Horiki M, Morishima A, Yamagata H, Rakugi H, Ikegami H, Miki T, Ogihara T. Horiki M, et al. Among authors: morishima a. Nihon Ronen Igakkai Zasshi. 1998 Feb;35(2):136-8. doi: 10.3143/geriatrics.35.136. Nihon Ronen Igakkai Zasshi. 1998. PMID: 9584492 Free article. Japanese.

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