H. Sato

发表

Isolation and sequencing of rat liver bilirubin UDP-glucuronosyltransferase cDNA: possible alternate splicing of a common primary transcript.

S. Kashiwamata, O. Koiwai, K. Tanabe, 1990, Biochemical and biophysical research communications.

A solid phase radioimmunoassay for the detection of anti-insulin antibodies.

S. Kashiwamata, K. Miura, S. Sakata, 1983, Endocrinologia japonica.

Comparative Study of Glial Marker Proteins in the Hypoplastic Cerebellum of Jaundiced Gunn Rats

L. Eng, R. Semba, Kanefusa Kato, 1988, Journal of neurochemistry.

Studies on a Cerebellar 50,000‐Dalton Protein Associated with Cerebellar Hypoplasia in Jaundiced Gunn Rats: Its Identity with Glial Fibrillary Acidic Protein as Evidenced by the Improved Immunoblotting Method

L. Eng, R. Semba, S. Kashiwamata, 1985, Journal of neurochemistry.

A simple method for preparation of molecular weight marker proteins for sodium dodecyl sulfate‐polyacrylamide gel electrophoresis by photopolymerizations of hemoglobin subunits

R. Semba, S. Kashiwamata, S. Aono, 1988, Electrophoresis.

[A solid phase radioimmunoassay using 125I-protein A for the detection of anti-human thyroglobulin antibodies].

S. Kashiwamata, K. Miura, O. Tarutani, 1983, Nihon Naibunpi Gakkai zasshi.

Thyroid hormone metabolism and nuclear binding in Gunn rats

H. Keino, S. Kashiwamata, K. Miura, 1991, Journal of endocrinological investigation.

Interaction of bilirubin with human erythrocyte membranes. Bilirubin binding to neuraminidase- and phospholipase-treated membranes.

R. Semba, S. Kashiwamata, S. Aono, 1987, Biochemical Journal.

Interaction of bilirubin with human erythrocyte membranes.

S. Kashiwamata, H. Sato, 1983, Biochemical Journal.

Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait.

Y. Adachi, O. Koiwai, T. Kamisako, 1996, Human molecular genetics.

Danger of bucolome in infants with hyperbilirubinaemia. Experimental evidence.

R. Semba, H. Sato, H. Yamamura, 1978, Archives of disease in childhood.

Genetic defect of bilirubin UDP-glucuronosyltransferase in the hyperbilirubinemic Gunn rat.

S. Kashiwamata, O. Koiwai, S. Aono, 1991, Biochemical and biophysical research communications.

Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome

H. Keino, E. Uyama, E. Uyama, 1995, The Lancet.

Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II.

H. Keino, O. Koiwai, N. Hanada, 1993, Biochemical and biophysical research communications.

Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.

Hiroshi Sato, Y. Maruo, M. Shimada, 1998, The Journal of pediatrics.

Different Behaviors Among Lysosomal Enzymes in the Cerebellum of Jaundiced Gunn Rats with Cerebellar Hypoplasia

H. Sato, Hiroomi Keino, Sachiko Aono, 1987, Journal of neurochemistry.

Cyclic Nucleotides and the Activity of Glia Maturation Factor in the Hypoplastic Cerebellum of Developing Jaundiced Gunn Rats

R. Semba, Taiji Kato, S. Aono, 1988, Journal of neurochemistry.

Distribution of acid phosphatase and β-glucuronidase in the hypoplastic cerebellum of jaundiced Gunn rats

H. Sato, Hiroomi Keino, Shigeo Kashiwamata, 1990, Cell and Tissue Research.

Effect of milk on plasma unbound-bilirubin concentration in homozygous Gunn rat sucklings

R. Semba, H. Sato, 1977, Experientia.

Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.

Y. Adachi, O. Koiwai, O Koiwai, 1995, Human molecular genetics.

Mode of bilirubin deposition in the cerebellum of developing jaundiced Gunn rats.

R. Semba, S. Kashiwamata, S. Aono, 1989, Biology of the neonate.

Mode of prevention by phototherapy of cerebellar hypoplasia in a new Sprague-Dawley strain of jaundiced Gunn rats.

R. Semba, E. Aoki, H. Keino, 1985, Pediatric neuroscience.

[Bilirubin encephalopathy--bilirubin metabolism and Gunn rat as an experimental model].

S. Kashiwamata, R. Katoh‐Semba, H. Sato, 1984, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

Relationship between plasma unbound-bilirubin concentration and cerebellar bilirubin content in homozygnous Gunn rat sucklings

R. Semba, H. Sato, 1978, Experientia.

A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene

K. Yamamoto, Y. Maruo, T. Yamano, 1999, European Journal of Pediatrics.

Co‐occurrence of three different mutations in the bilirubin UDP‐glucuronosyltransferase gene in a Chinese family with Crigler–Najjar syndrome type I and Gilbert's syndrome

A. Mori, Y. Maruo, M. Iwai, 2003, Clinical genetics.

Mapping of rat bilirubin UDP-glucuronosyl-transferase gene (Ugt1a1) to chromosome region 9q35-->q36.

H. Satoh, H. Homma, O. Koiwai, 1995, Cytogenetics and cell genetics.

Transfer of 125I-albumin from blood to brain in newborn rats and the effect of hyperbilirubinemia on the transfer.

H. Sato, H. Yamamura, M. Ohsugi, 1992, Biology of the Neonate.