Suzuki, Yasuyuki

Developmental immunohistochemistry of catalase in the human brain

Houdou, S., Kuruta, H., Hasegawa, M., Konomi, H., Takashima, S., Suzuki, Y., & Hashimoto, T. (1991) · Brain Research

Neurogenesis and neuroplasticity mechanismsRedox biology and oxidative stress

Cited by 59

Peroxisomal acyl CoA oxidase deficiency

Suzuki, Y., Iai, M., Kamei, A., Tanabe, Y., Chida, S., Yamaguchi, S., Zhang, Z., Takemoto, Y., Shimozawa, N., & Kondo, N. (2002) · The Journal of Pediatrics

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 43

Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes

Matsukawa, T., Asheuer, M., Takahashi, Y., Goto, J., Suzuki, Y., Shimozawa, N., Takano, H., Onodera, O., Nishizawa, M., Aubourg, P., et al. (2011) · neurogenetics

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 36

Adrenoleukodystrophy: Subcellular localization and degradation of adrenoleukodystrophy protein (ALDP/ABCD1) with naturally occurring missense mutations

Takahashi, N., Morita, M., Maeda, T., Harayama, Y., Shimozawa, N., Suzuki, Y., Furuya, H., Sato, R., Kashiwayama, Y., & Imanaka, T. (2007) · Journal of Neurochemistry

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 28

Molecular Mechanism of a Temperature-Sensitive Phenotype in Peroxisomal Biogenesis Disorder

Hashimoto, K., Kato, Z., Nagase, T., Shimozawa, N., Kuwata, K., Omoya, K., Li, A., Matsukuma, E., Yamamoto, Y., Ohnishi, H., et al. (2005) · Pediatric Research

Metabolism and Genetic DisordersProtein Structure and Dynamics

Cited by 16