スポンサーリンク
Department Of Clinical Genetics The Tokyo Metropolitan Institute Of Medical Science Tokyo Metropolit | 論文
- Differential distribution of ganglioside GM1 and sulfatide during the development of Xenoqus
- Evidence for Direct Binding of Intracellularly Distributed Ganglioside GM2 to Isolated Vimentin Intermediate Filaments in Normal and Tay-Sachs Disease Human Fibroblasts
- Inefficiency in GM2 Ganglioside Elimination by Human Lysosomal β-Hexosaminidase β-Subunit Gene Transfer to Fibroblastic Cell Line Derived from Sandhoff Disease Model Mice(Biochemistry)
- Establishment of immortalized Schwann cells from Sandhoff mice and corrective effect of recombinant human β-hexosaminidase A on the accumulated GM2 ganglioside
- Expression of Sialylparagloboside in a Case of Liposarcoma: Aberrant Glycosylation in Tumors Arising in Adipose Tissues
- Polysialogangliosides Expressed by Amelanotic Melanoma : A Possible Explanation for the Poor Response to Anti-monosialoganglioside Antibody 202 in a Patient with Melanoma
- Production of a Recombinant Single-Chain Variable-Fragment (scFv) Antibody against Sulfoglycolipid
- EFFECTS OF p-TERT-BUTYLPHENYL TRANS-4-GUANIDINOMETHYLCYCLOHEXANE CARBOXYLATE HYDROCHLORIDE (NCO-650) AND ITS METABOLITE, p-TERT-BUTYLPHENOL(BP) ON DRUG-METABOLIZING ENZYMES AND FINE STRUCTURE IN RAT LIVER
- Differential Distribution of Glycosphingolipid Antigens in the Central Nervous System (Recent Progresses in Carbohydrate Histochemistry)
- Significant Decrease in Tropoelastin Gene Expression in Fibroblasts from a Japanese Costello Syndrome Patient with Impaired Elastogenesis and Enhanced Proliferation
- Actin-Actin Contact: Chemical Cross-Linking between Actin and the 2.6-kDa Peptide from Subdomain 4 of Actin
- Biochemical and structural study on a S529V mutant acid α-glucosidase responsive to pharmacological chaperones
- Structural modeling of mutant α-glucosidases resulting in a processing/transport defect in Pompe disease
- High-throughput screening identified disease-causing-mutants and functional variants of α-galactosidase A gene in Japanese male hemodialysis patients
- Japanese-type adult galactosialidosis. A unique and common splice junction mutation causing exon skipping in the protective protein/carboxypeptidase gene.:A Unique and Common Splice Junction Mutation Causing Exon Skipping in the Protective Protein/Carboxy
- Immunohistochemical Localization of Major Gangliosides in Rat Cerebellum.
- Effect of chronic treatment of propranolol on lipid metabolism in spontaneously hypertensive rats (SHR).