Shigehiko Tamura

Human <i>PEX19</i> : cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

Yuji Matsuzono, Naohiko Kinoshita, Shigehiko Tamura et al. · Proceedings of the National Academy of Sciences · 1999 · 222 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

The pathogenic peroxin Pex26p recruits the Pex1p–Pex6p AAA ATPase complexes to peroxisomes

Naomi Matsumoto, Shigehiko Tamura, Yukio Fujiki · Nature Cell Biology · 2003 · 195 citations

Life Sciences, Biochemistry, Molecular Biology +12

Mutation in Is Causal in the Peroxisome-Deficient Zellweger Syndrome of Complementation Group D

Masanori Honsho, Shigehiko Tamura, Nobuyuki Shimozawa et al. · The American Journal of Human Genetics · 1998 · 169 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

The Peroxin Pex3p Initiates Membrane Assembly in Peroxisome Biogenesis

Kamran Ghaedi, Shigehiko Tamura, Kanji Okumoto et al. · Molecular Biology of the Cell · 2000 · 126 citations

Life Sciences, Genetics, Molecular Biology +13

Human gastric (H+ + K+)-ATPase gene. Similarity to (Na+ + K+)-ATPase genes in exon/intron organization but difference in control region.

Masatomo Maeda, Ko Ichi Oshiman, Shigehiko Tamura et al. · Journal of Biological Chemistry · 1990 · 123 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +14