The scientist’s investigation covers issues in Biochemistry, Molecular biology, Mucopolysaccharidosis, Genetics and Mucopolysaccharidosis Type IVA. The various areas that Tadao Orii examines in his Molecular biology study include Gene expression, Thiolase, 3-Hydroxyacyl-CoA Dehydrogenase, Gene mutation and Complementary DNA. His Complementary DNA research includes elements of Peroxisomal disorder, Open reading frame and Mutant.
His research in Mucopolysaccharidosis intersects with topics in Immunology, Bone marrow, Sulfatase and Enzyme replacement therapy. His research integrates issues of Endocrinology, Urinary system and Surgery, Family history in his study of Enzyme replacement therapy. He interconnects Lysosomal storage disease, Natural history, Allele, Genetic heterogeneity and Elosulfase alfa in the investigation of issues within Mucopolysaccharidosis Type IVA.
Molecular biology, Internal medicine, Biochemistry, Genetics and Endocrinology are his primary areas of study. The concepts of his Molecular biology study are interwoven with issues in Thiolase, Mutation, Point mutation, Mucopolysaccharidosis and Complementary DNA. His Mucopolysaccharidosis study incorporates themes from Keratan sulfate and Sulfatase, Mucopolysaccharidosis Type IVA, Enzyme replacement therapy.
Tadao Orii has researched Internal medicine in several fields, including Gastroenterology and Immunology. His work on Biochemistry deals in particular with Peroxisome, Enzyme, Zellweger syndrome, Mitochondrion and Glycoprotein. His is involved in several facets of Genetics study, as is seen by his studies on Gene, Exon, Missense mutation, Allele and Restriction fragment length polymorphism.
Tadao Orii mainly focuses on Mucopolysaccharidosis, Enzyme replacement therapy, Keratan sulfate, Internal medicine and Hematopoietic stem cell transplantation. His Mucopolysaccharidosis research includes themes of Mucopolysaccharidosis Type IVA and Bone marrow. His work deals with themes such as Stage, Surgery, Newborn screening and Dysplasia, which intersect with Enzyme replacement therapy.
His Keratan sulfate research is multidisciplinary, incorporating elements of Heparan sulfate, Dermatan sulfate, Immunology, Urine and Biomarker. Tadao Orii combines subjects such as Gastroenterology and Physical therapy with his study of Internal medicine. His biological study spans a wide range of topics, including Molecular biology, Endocrinology and Lysosomal storage disorders.
His scientific interests lie mostly in Mucopolysaccharidosis, Enzyme replacement therapy, Surgery, Dysplasia and Internal medicine. He has included themes like Immunology, Bone marrow, Mucopolysaccharidosis Type IVA and Cartilage in his Mucopolysaccharidosis study. His Immunology research focuses on subjects like Keratan sulfate, which are linked to Phenotype, Genotype, Sulfatase, Missense mutation and Allelic heterogeneity.
His Enzyme replacement therapy study integrates concerns from other disciplines, such as Stage, Hematopoietic stem cell transplantation, Bone disease and Newborn screening. In his study, Transplantation is strongly linked to Urinary system, which falls under the umbrella field of Dysplasia. His Internal medicine research is multidisciplinary, relying on both Gastroenterology and Endocrinology.
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Epidemiology of mucopolysaccharidoses
Shaukat A. Khan;Hira Peracha;Diana Ballhausen;Alfred Wiesbauer.
Molecular Genetics and Metabolism (2017)
A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
Nobuyuki Shimozawa;Toshiro Tsukamoto;Yasuyuki Suzuki;Tadao Orii.
Science (1992)
Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein.
Y Uchida;K Izai;T Orii;T Hashimoto.
Journal of Biological Chemistry (1992)
International Morquio A Registry: Clinical manifestation and natural course of Morquio A disease
A. M. Montaño;S. Tomatsu;G. S. Gottesman;M. Smith.
Journal of Inherited Metabolic Disease (2007)
Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase.
K Izai;Y Uchida;T Orii;S Yamamoto.
Journal of Biological Chemistry (1992)
MOLECULAR CLONING OF CDNA ENCODING RAT VERY LONG-CHAIN ACYL-COA SYNTHETASE
Atsushi Uchiyama;Toshifumi Aoyama;Keiju Kamijo;Yasushi Uchida.
Journal of Biological Chemistry (1996)
Japan Elaprase Treatment (JET) study: idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (Mucopolysaccharidosis II, MPS II).
Torayuki Okuyama;Akemi Tanaka;Yasuyuki Suzuki;Hiroyuki Ida.
Molecular Genetics and Metabolism (2010)
Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases.
Fukao T;Song Xq;Mitchell Ga;Yamaguchi S.
Pediatric Research (1997)
Review of clinical presentation and diagnosis of mucopolysaccharidosis IVA
C.J. Hendriksz;P. Harmatz;M. Beck;S. Jones.
Molecular Genetics and Metabolism (2013)
Cord blood lymphocyte responses to food antigens for the prediction of allergic disorders.
N Kondo;Y Kobayashi;S Shinoda;K Kasahara.
Archives of Disease in Childhood (1992)
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