T. Kamijo

发表

Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients.

T. Aoyama, K. Tanaka, T. Hashimoto, 1995, American journal of human genetics.

Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients.

William, T. Aoyama, K. Tanaka, 1995, The Journal of clinical investigation.

Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.

R. Wanders, T. Hashimoto, A. Komiyama, 1994, The Journal of clinical investigation.

Peroxisomal acyl-coenzyme A oxidase is a rate-limiting enzyme in a very-long-chain fatty acid beta-oxidation system.

T. Hashimoto, T. Aoyama, M. Souri, 1994, Biochemical and biophysical research communications.

Structural analysis of cDNAs for subunits of human mitochondrial fatty acid beta-oxidation trifunctional protein.

T. Aoyama, T. Hashimoto, A. Komiyama, 1994, Biochemical and biophysical research communications.

Molecular cloning of the cDNAs for the subunits of rat mitochondrial fatty acid beta-oxidation multienzyme complex. Structural and functional relationships to other mitochondrial and peroxisomal beta-oxidation enzymes.

T. Hashimoto, T. Aoyama, T. Kamijo, 1993, The Journal of biological chemistry.

Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunits.

T. Aoyama, R. Wanders, J. Vockley, 1996, American journal of human genetics.

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein.

R. Wanders, R. Wanders, T. Hashimoto, 1994, Biochimica et biophysica acta.

Medium Chain 3-Ketoacyl-Coenzyme A Thiolase Deficiency: A New Disorder of Mitochondrial Fatty Acid β-Oxidation

T. Hashimoto, A. Komiyama, T. Aoyama, 1997, Pediatric Research.

Nucleotide sequence of the human 70 kDa peroxisomal membrane protein: a member of ATP-binding cassette transporters.

K. Kamijo, T. Osumi, I. Ueno, 1992, Biochimica et biophysica acta.

The 70-kDa Peroxisomal Membrane Protein

T. Hashimoto, K. Kamijo, T. Osumi, 1992 .

Rat very-long-chain acyl-CoA dehydrogenase, a novel mitochondrial acyl-CoA dehydrogenase gene product, is a rate-limiting enzyme in long-chain fatty acid beta-oxidation system. cDNA and deduced amino acid sequence and distinct specificities of the cDNA-expressed protein.

T. Hashimoto, T. Aoyama, I. Ueno, 1994, The Journal of biological chemistry.

Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase.

T. Hashimoto, T. Aoyama, Y. Suzuki, 1994, Biochemical and biophysical research communications.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype

R. Wanders, T. Hashimoto, L. Ijlst, 1995, Journal of Inherited Metabolic Disease.