Sato N - Search Results

1

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: sato n. Mech Ageing Dev. 1997 Dec;98(3):255-65. doi: 10.1016/s0047-6374(97)00112-7. Mech Ageing Dev. 1997. PMID: 9352494

2

[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. Among authors: sato n. 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.

3

T/G polymorphism at intron 9 of presenilin 1 gene is associated with, but not responsible for sporadic late-onset Alzheimer's disease in Japanese population.

Nishiwaki Y, Kamino K, Yoshiiwa A, Sato N, Tateishi K, Takeda M, Kobayashi T, Yamamoto H, Nonomura Y, Yoneda H, Sakai T, Imagawa M, Miki T, Ogihara T. Nishiwaki Y, et al. Among authors: sato n. Neurosci Lett. 1997 May 16;227(2):123-6. doi: 10.1016/s0304-3940(97)00317-0. Neurosci Lett. 1997. PMID: 9180219

4

alpha 1-Antichymotrypsin as a risk modifier for late-onset Alzheimer's disease in Japanese apolipoprotein E epsilon 4 allele carriers.

Yoshiiwa A, Kamino K, Yamamoto H, Kobayashi T, Imagawa M, Nonomura Y, Yoneda H, Sakai T, Nishiwaki Y, Sato N, Rakugi H, Miki T, Ogihara T. Yoshiiwa A, et al. Among authors: sato n. Ann Neurol. 1997 Jul;42(1):115-7. doi: 10.1002/ana.410420118. Ann Neurol. 1997. PMID: 9225693

5

Low density lipoprotein receptor-related protein gene polymorphisms and risk for late-onset Alzheimer's disease in a Japanese population.

Hatanaka Y, Kamino K, Fukuo K, Mitsuda N, Nishiwaki-Ueda Y, Sato N, Satoh T, Yamamoto H, Yoneda H, Imagawa M, Miki T, Ohta S, Ogihara T. Hatanaka Y, et al. Among authors: sato n. Clin Genet. 2000 Oct;58(4):319-23. doi: 10.1034/j.1399-0004.2000.580410.x. Clin Genet. 2000. PMID: 11076057

6

Elevated amyloid beta protein(1-40) level induces CREB phosphorylation at serine-133 via p44/42 MAP kinase (Erk1/2)-dependent pathway in rat pheochromocytoma PC12 cells.

Sato N, Kamino K, Tateishi K, Satoh T, Nishiwaki Y, Yoshiiwa A, Miki T, Ogihara T. Sato N, et al. Biochem Biophys Res Commun. 1997 Mar 27;232(3):637-42. doi: 10.1006/bbrc.1997.6341. Biochem Biophys Res Commun. 1997. PMID: 9126327

7

Association of variants in critical core promoter element of angiotensinogen gene with increased risk of essential hypertension in Japanese.

Sato N, Katsuya T, Rakugi H, Takami S, Nakata Y, Miki T, Higaki J, Ogihara T. Sato N, et al. Hypertension. 1997 Sep;30(3 Pt 1):321-5. doi: 10.1161/01.hyp.30.3.321. Hypertension. 1997. PMID: 9314411

8

Polymorphism of angiotensin converting enzyme, angiotensinogen, and apolipoprotein E genes in a Japanese population with cerebrovascular disease.

Nakata Y, Katsuya T, Rakugi H, Takami S, Sato N, Kamide K, Ohishi M, Miki T, Higaki J, Ogihara T. Nakata Y, et al. Among authors: sato n. Am J Hypertens. 1997 Dec;10(12 Pt 1):1391-5. doi: 10.1016/s0895-7061(97)00315-4. Am J Hypertens. 1997. PMID: 9443775

9

Angiotensin II type 1 receptor gene polymorphism is associated with increase of left ventricular mass but not with hypertension.

Takami S, Katsuya T, Rakugi H, Sato N, Nakata Y, Kamitani A, Miki T, Higaki J, Ogihara T. Takami S, et al. Among authors: sato n. Am J Hypertens. 1998 Mar;11(3 Pt 1):316-21. doi: 10.1016/s0895-7061(97)00457-3. Am J Hypertens. 1998. PMID: 9544872

10

No association between alpha-adducin 460 polymorphism and essential hypertension in a Japanese population.

Ishikawa K, Katsuya T, Sato N, Nakata Y, Takami S, Takiuchi S, Fu Y, Higaki J, Ogihara T. Ishikawa K, et al. Among authors: sato n. Am J Hypertens. 1998 Apr;11(4 Pt 1):502-6. doi: 10.1016/s0895-7061(97)00486-x. Am J Hypertens. 1998. PMID: 9607391

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