Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism

por Kuroda, Y, Mitsui, T, Akaike, M, Azuma, H, Matsumoto, T
Publicado 2001

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.

por Kawai, H, Akaike, M, Endo, T, Adachi, K, Inui, T, Mitsui, T, Kashiwagi, S, Fujiwara, T, Okuno, S, Shin, S
Publicado 1995

Prognostic significance of CD44 variant 2 upregulation in colorectal cancer

por Ozawa, M, Ichikawa, Y, Zheng, Y-W, Oshima, T, Miyata, H, Nakazawa, K, Guan, H-B, Shiozawa, M, Akaike, M, Watanabe, K, Ota, M, Fujii, S, Kunisaki, C, Ishikawa, T, Tanaka, K, Akiyama, H, Endo, I, Taniguchi, H
Publicado 2014