Ogihara T - Search Results

1

Splicing mutation of presenilin-1 gene for early-onset familial Alzheimer's disease.

Sato S, Kamino K, Miki T, Doi A, Ii K, St George-Hyslop PH, Ogihara T, Sakaki Y. Sato S, et al. Among authors: ogihara t. Hum Mutat. 1998;Suppl 1:S91-4. doi: 10.1002/humu.1380110131. Hum Mutat. 1998. PMID: 9452052 No abstract available.

2

Three different mutations of presenilin 1 gene in early-onset Alzheimer's disease families.

Kamino K, Sato S, Sakaki Y, Yoshiiwa A, Nishiwaki Y, Takeda M, Tanabe H, Nishimura T, Ii K, St George-Hyslop PH, Miki T, Ogihara T. Kamino K, et al. Among authors: ogihara t. Neurosci Lett. 1996 Apr 26;208(3):195-8. doi: 10.1016/0304-3940(96)12587-8. Neurosci Lett. 1996. PMID: 8733303

3

[Genetic analysis of familial Alzheimer's disease].

Miki T, Katsuya T, Ogihara T. Miki T, et al. Among authors: ogihara t. Tanpakushitsu Kakusan Koso. 1991 Jan;36(1):21-9. Tanpakushitsu Kakusan Koso. 1991. PMID: 1672464 Japanese. No abstract available.

4

The 717Val----Ile substitution in amyloid precursor protein is associated with familial Alzheimer's disease regardless of ethnic groups.

Yoshioka K, Miki T, Katsuya T, Ogihara T, Sakaki Y. Yoshioka K, et al. Among authors: ogihara t. Biochem Biophys Res Commun. 1991 Aug 15;178(3):1141-6. doi: 10.1016/0006-291x(91)91011-z. Biochem Biophys Res Commun. 1991. PMID: 1908231

5

[Werner's syndrome and familial Alzheimer's disease].

Miki T, Nakura J, Kamino K, Ogihara T. Miki T, et al. Among authors: ogihara t. Tanpakushitsu Kakusan Koso. 1993 Feb;38(3):366-73. Tanpakushitsu Kakusan Koso. 1993. PMID: 8098160 Review. Japanese. No abstract available.

6

Mutational screening of APP gene in patients with early-onset Alzheimer disease utilizing mismatched PCR-RFLP.

Nishiwaki Y, Kamino K, Yoshiiwa A, Nagano K, Takeda M, Tanabe H, Nishimura T, Kobayashi T, Yamamoto H, Nonomura Y, Yoneda H, Sakai T, Imagawa M, Miki T, Ogihara T. Nishiwaki Y, et al. Among authors: ogihara t. Clin Genet. 1996 Mar;49(3):119-23. doi: 10.1111/j.1399-0004.1996.tb03269.x. Clin Genet. 1996. PMID: 8737975

7

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: ogihara t. Neurosci Lett. 1997 May 16;227(2):123-6. doi: 10.1016/s0304-3940(97)00317-0. Neurosci Lett. 1997. PMID: 9180219

8

Identification of a single base polymorphism in intron 2 of the c-fos gene and its detection by mismatched PCR-RFLP.

Kamino K, Miki T, Ogihara T. Kamino K, et al. Among authors: ogihara t. Jpn J Hum Genet. 1994 Dec;39(4):439-40. doi: 10.1007/BF01892390. Jpn J Hum Genet. 1994. PMID: 7873757

9

Genetic association study between senile dementia of Alzheimer's type and APOE/C1/C2 gene cluster.

Kamino K, Yoshiiwa A, Nishiwaki Y, Nagano K, Yamamoto H, Kobayashi T, Nonomura Y, Yoneda H, Sakai T, Imagawa M, Miki T, Ogihara T. Kamino K, et al. Among authors: ogihara t. Gerontology. 1996;42 Suppl 1:12-9. doi: 10.1159/000213820. Gerontology. 1996. PMID: 8804993

10

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: ogihara t. Ann Neurol. 1997 Jul;42(1):115-7. doi: 10.1002/ana.410420118. Ann Neurol. 1997. PMID: 9225693

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