His main research concerns Zellweger syndrome, Peroxisome, Biochemistry, Peroxisomal disorder and Molecular biology. Zellweger syndrome is closely attributed to Complementation in his study. His research integrates issues of Beta oxidation, Mutant and Chinese hamster ovary cell in his study of Peroxisome.
Peroxisomal disorder is the subject of his research, which falls under Genetics. In his study, Missense mutation is inextricably linked to Point mutation, which falls within the broad field of Molecular biology. Yasuyuki Suzuki works mostly in the field of Heparan sulfate, limiting it down to topics relating to Urinary system and, in certain cases, Enzyme replacement therapy and Mucopolysaccharidosis.
Yasuyuki Suzuki mainly investigates Internal medicine, Peroxisome, Zellweger syndrome, Biochemistry and Genetics. His Internal medicine research includes themes of Gastroenterology and Endocrinology. His Peroxisome study incorporates themes from Complementation, Chinese hamster ovary cell and Enzyme.
Yasuyuki Suzuki combines topics linked to Peroxisomal disorder with his work on Zellweger syndrome. His research in Genetics focuses on subjects like Molecular biology, which are connected to Point mutation and Complementary DNA. His work focuses on many connections between Enzyme replacement therapy and other disciplines, such as Surgery, that overlap with his field of interest in Dysplasia.
His primary areas of investigation include Enzyme replacement therapy, Medical education, Hematopoietic stem cell transplantation, Internal medicine and Keratan sulfate. His biological study spans a wide range of topics, including Molecular biology, Adverse effect, Dysplasia and Newborn screening. His study looks at the intersection of Dysplasia and topics like Cartilage with Mucopolysaccharidosis.
His Hematopoietic stem cell transplantation research incorporates themes from Lysosomal storage disorders and Mucopolysaccharidosis type II. His Internal medicine study combines topics in areas such as Gastroenterology and Surgery. His Keratan sulfate research is multidisciplinary, incorporating perspectives in Mucopolysaccharidosis IV, Heparan sulfate, Dermatan sulfate, Immunology and Urine.
His scientific interests lie mostly in Keratan sulfate, Enzyme replacement therapy, Internal medicine, Dysplasia and Mucopolysaccharidosis. His Keratan sulfate research is multidisciplinary, relying on both Mucopolysaccharidosis IV, Dermatan sulfate, Heparan sulfate, Immunology and Biomarker. His research in Mucopolysaccharidosis IV intersects with topics in Molecular biology and Sulfation.
His Internal medicine research focuses on Hunter syndrome and Hematopoietic stem cell transplantation. His research investigates the link between Dysplasia and topics such as Surgery that cross with problems in Gastroenterology and Respiratory function. His Mucopolysaccharidosis research is multidisciplinary, incorporating elements of Cartilage and Anatomy.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Epidemiology of mucopolysaccharidoses
Shaukat A. Khan;Hira Peracha;Diana Ballhausen;Alfred Wiesbauer.
Molecular Genetics and Metabolism (2017)
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.
Norio Niikawa;Yoshikazu Kuroki;Tadashi Kajii;Nobuo Matsuura.
American Journal of Medical Genetics (1988)
A new malformation syndrome of long palpebralfissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation
Yoshikazu Kuroki;Yasuyuki Suzuki;Hiroyuki Chyo;Akira Hata.
The Journal of Pediatrics (1981)
A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
Nobuyuki Shimozawa;Toshiro Tsukamoto;Yasuyuki Suzuki;Tadao Orii.
Science (1992)
Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment
S Tomatsu;A M Montaño;H Oikawa;M Smith.
Current Pharmaceutical Biotechnology (2011)
Degradation of amyotrophic lateral sclerosis-linked mutant Cu,Zn-superoxide dismutase proteins by macroautophagy and the proteasome.
Tomohiro Kabuta;Yasuyuki Suzuki;Keiji Wada.
Journal of Biological Chemistry (2006)
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)
Long-term efficacy of hematopoietic stem cell transplantation on brain involvement in patients with mucopolysaccharidosis type II: a nationwide survey in Japan.
Akemi Tanaka;Torayuki Okuyama;Yasuyuki Suzuki;Norio Sakai.
Molecular Genetics and Metabolism (2012)
Newborn screening and diagnosis of mucopolysaccharidoses
Shunji Tomatsu;Tadashi Fujii;Masaru Fukushi;Toshihiro Oguma.
Molecular Genetics and Metabolism (2013)
Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.
N. Shimozawa;Y. Suzuki;T. Orii;A. Moser.
American Journal of Human Genetics (1993)
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