S. Fujibayashi

发表

Prostaglandin E2 production by glomeruli and collecting tubules isolated from rat kidney.

J. Uemasu, K. Kurokawa, S. Fujibayashi, 1987, The Japanese journal of physiology.

Somatostatin-like immunoreactivity in the glomerulus of rat kidney.

K. Kurokawa, T. Yamada, G. Aponte, 1983, Kidney international.

Molecular cloning of the sphingolipid activator protein-1 (SAP-1), the sulfatide sulfatase activator.

J. O'brien, D. Wenger, F. Esch, 1986, Biochemical and biophysical research communications.

Prenatal diagnosis of Hurler's syndrome—Biochemical studies on the affected fetus

K. Abo, T. Nakao, S. Tsugawa, 2004, Human Genetics.

Biosynthesis of the sulfatide/GM1 activator protein (SAP-1) in control and mutant cultured skin fibroblasts.

D. Wenger, S. Fujibayashi, 1986, Biochimica et biophysica acta.

Activator protein-deficient metachromatic leukodystrophy: diagnosis in leukocytes using immunologic methods.

D. Wenger, K. Inui, S. Fujibayashi, 1984, Jornal de Pediatria.

The gene coding for a sphingolipid activator protein, SAP-1, is on human chromosome 10

C. Jones, D. Wenger, K. Inui, 2004, Human Genetics.

Assignment of the gene for human sphingolipid activator protein-2 (SAP-2) to chromosome 10.

C. Jones, D. Wenger, F. Kao, 1985, American journal of human genetics.

Studies on a sphingolipid activator protein (SAP-2) in fibroblasts from patients with lysosomal storage diseases, including Niemann-Pick disease Type C.

D. Wenger, S. Fujibayashi, 1985, Clinica chimica acta; international journal of clinical chemistry.

Synthesis and processing of sphingolipid activator protein-2 (SAP-2) in cultured human fibroblasts.

D. Wenger, S. Fujibayashi, 1986, The Journal of biological chemistry.

Heparan sulfate and dermatan sulfate from the liver of a patient with Hurler syndrome: high performance liquid chromatography of their degradation products after incubation with alpha-L-iduronidase-deficient fibroblasts.

Y. Ishikawa, C. Igarashi, T. Nakao, 1984, Clinica chimica acta; international journal of clinical chemistry.

Activities of sulfatases for the degradation of acidic glycosaminoglycans in cultured skin fibroblasts from two siblings with multiple sulfatase deficiency.

N. Tachi, T. Orii, T. Nakao, 1983, Clinica chimica acta; international journal of clinical chemistry.

Properties of α-l-iduronidase in cultured skin fibroblasts from α-l-iduronidase-deficient patients

Y. Ishikawa, T. Nakao, S. Tsugawa, 2004, Human Genetics.

Clinical and Molecular Characteristics of Human Rotavirus G8P[8] Outbreak Strain, Japan, 2014

H. Tsutsumi, K. Katayama, Y. Yoto, 2017, Emerging infectious diseases.

Studies of SAP-1 and SAP-2 in Cultured Skin Fibroblasts

D. Wenger, S. Fujibayashi, 1986 .

Immunocytochemical localization of sphingolipid activator protein-1, the sulfatide/GM1 ganglioside activator, to lysosomes in human liver and colon

W. Brown, D. Wenger, S. Fujibayashi, 2004, Histochemistry.