Výsledky vyhledávání - "Miho Matsubara-Tsutsui"

Molecular evidence of presenilin 1 mutation in familial early onset dementia

Autor: Keiko Taguchi, Tetsuro Miki, Minoru Yasuda, Hidehisa Yamagata, Takuo Nomura, Katsuhiko Kohara, Koho Miyoshi, Miho Matsubara-Tsutsui

Publikováno v: American Journal of Medical Genetics. 114:292-298

Early onset familial Alzheimer disease (FAD) has been associated with mutations in three genes, of which presenilin 1 (PSEN1) mutations are the most frequent. We reported previously a variant form of FAD, due to deletion of exon 9 of PSEN1, with spas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f95457e696cc74a2d3c19ea862e46c8
https://doi.org/10.1002/ajmg.10250

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The -4,752 C/T Polymorphism in the Presenilin 1 Gene Increases the Risk of Alzheimer's Disease in Apolipoprotein E4 Carriers

Autor: Hidehisa Yamagata, Noriaki Mitsuda, Kouzin Kamino, Jun Nakura, Miho Matsubara-Tsutsui, Ikuko Kondo, Tetsuro Miki, Atsuyuki Morishima

Publikováno v: Internal Medicine. 41:823-828

Objective We sought to establish an association between sporadic Alzheimer's disease (AD) and presenilin 1 (PSEN1) gene polymorphisms in the Japanese population.Methods A 5 kb fragment containing the putative promoter of the PSENl gene for randomly s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba973502edabd0e47c549550534f0194
https://doi.org/10.2169/internalmedicine.41.823

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