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, +7

Proceedings of the National Academy of Sciences

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

Naomi Matsumoto, Shigehiko Tamura, Yukio Fujiki

Nature Cell Biology

Redox SignalingBiochemistryMitochondrial FunctionNatural SciencesMolecular Biology +6

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

Masanori Honsho, Shigehiko Tamura, Nobuyuki Shimozawa, +3

The American Journal of Human Genetics

Complementation Group DComplement SystemMendelian DisorderGenetic DisorderGenetics +9

The Peroxin Pex3p Initiates Membrane Assembly in Peroxisome Biogenesis

Kamran Ghaedi, Shigehiko Tamura, Kanji Okumoto, +2

Molecular Biology of the Cell

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, +1

Journal of Biological Chemistry

GastroenterologyMolecular BiologyMolecular GeneticsSixth ExonHuman Enzyme +19

Gastric DNA-binding proteins recognize upstream sequence motifs of parietal cell-specific genes.

Shigehiko Tamura, Xiaohong Wang, Masatomo Maeda, +1

Proceedings of the National Academy of Sciences

GeneticsGene CharacterizationMolecular GeneticsUpstream Sequence MotifsTranscriptional Regulation +23

<i>PEX12</i> , the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

Kanji Okumoto, Nobuyuki Shimozawa, Atsusi Kawai, +8

Molecular and Cellular Biology

Human <i>PEX1</i> cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

Shigehiko Tamura, Kanji Okumoto, Ryusuke Toyama, +6

Proceedings of the National Academy of Sciences

GeneticsMolecular GeneticsDisease Gene IdentificationMendelian DisorderBiochemical Genetics +17

Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation

Naomi Matsumoto, Shigehiko Tamura, Satomi Furuki, +7

The American Journal of Human Genetics

Complement SystemAllelic VariantDevelopmental BiologyMendelian DisorderGenetic Disorder +10

A Cytoplasmic AAA Family Peroxin, Pex1p, Interacts with Pex6p

Shigehiko Tamura, Nobuyuki Shimozawa, Yasuyuki Suzuki, +3

Biochemical and Biophysical Research Communications

Natural SciencesMolecular BiologyRedox BiologyCellular StructureCellular Biochemistry +3