Shimozawa, Nobuyuki

Proteomic Analysis of Rat Liver Peroxisome

Kikuchi, M., Hatano, N., Yokota, S., Shimozawa, N., Imanaka, T., & Taniguchi, H. (2004) · Journal of Biological Chemistry

Advanced Proteomics Techniques and ApplicationsRedox biology and oxidative stress

Cited by 258

Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders

Takemoto, Y., Suzuki, Y., Horibe, R., Shimozawa, N., Wanders, R. J. A., & Kondo, N. (2003) · Brain and Development

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 101

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

Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

Iwasa, M., Yamagata, T., Mizuguchi, M., Itoh, M., Matsumoto, A., Hironaka, M., Honda, A., Momoi, M. Y., & Shimozawa, N. (2013) · Neuropathology

Metabolism and Genetic DisordersGenomic variations and chromosomal abnormalities

Cited by 30

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

Hexacosenoyl-CoA is the most abundant very long-chain acyl-CoA in ATP binding cassette transporter D1-deficient cells

Hama, K., Fujiwara, Y., Takashima, S., Hayashi, Y., Yamashita, A., Shimozawa, N., & Yokoyama, K. (2020) · Journal of Lipid Research

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 16