440 results on '"Shimozawa, N."'
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2. Baicalein 5,6,7-trimethyl ether activates peroxisomal but not mitochondrial fatty acid β-oxidation
3. Molecular and clinical aspects of peroxisomal diseases
4. Comparison of methods to stimulate ovarian follicular growth in cynomolgus and African green monkeys for collection of mature oocytes
5. Epidemiology of X-linked adrenoleukodystrophy in Japan
6. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders
7. Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy
8. Disorders of peroxisome biogenesis: Complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)
9. Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
10. Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase : 3-hydroxyacyl-CoA dehydrogenase cDNA
11. Retinitis pigmentosa and mucopolysaccharidosis type II: An extremely attenuated phenotype
12. Zellweger Syndrome Caused by PEX13 Deficiency: Report of Two Novel Mutations
13. Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations
14. Molecular analysis by Southern blot for theN-acetylgalactosamine-6-sulphate sulphatase gene causing mucopolysaccharidosis IVA in the Japanese population
15. Peroxisomal 3-ketoacyl-CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata
16. An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem
17. Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders
18. Development of genotyping method for functionally relevant variants of cytochromes P450 in cynomolgus macaques
19. The common phospholipid-binding activity of the N-terminal domains of PEX1 and VCP/p97
20. Biosynthesis of peroxisomal membrane polypeptides in infants with Zellweger syndrome
21. Association between drusen and blood test results in a colony of 1,174 monkeys
22. [A case of rectal lues]
23. Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan
24. The common phospholipid-binding activity of the N-terminal domains of PEX1 and VCP/p97
25. PEROXISOMAL ASSEMBLY DEFECTS - CLINICAL, PATHOLOGICAL, AND BIOCHEMICAL FINDINGS IN 2 PATIENTS IN A NEWLY IDENTIFIED COMPLEMENTATION GROUP
26. Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
27. Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect
28. 378 INTRACYTOPLASMIC SPERM INJECTION AND ESTABLISHMENT OF EMBRYONIC STEM CELLS IN AFRICAN GREEN MONKEYS (CERCOPITHECUS AETHIOPS)
29. 322 DIFFERENTIAL DEVELOPMENT OF RABBIT EMBRYOS FOLLOWING MICROINSEMINATION USING SPERM AND SPERMATIDS
30. Disruption of imprinting in cloned mouse fetuses from embryonic stem cells
31. Production of cloned mice from embryonic stem cells arrested at metaphase
32. The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6
33. Lethal form of chondrodysplasia punctata with normal plasmalogen and cholesterol biosynthesis
34. Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures
35. Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders
36. Isolation, Characterization and Mutation Analysis of PEX13-Defective Chinese Hamster Ovary Cell Mutants
37. Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders
38. A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata
39. Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisome
40. Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations
41. Adrenoleukodystrophy: The Restoration of Peroxisomal β-Oxidaton by Transfection of Normal cDNA
42. Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient
43. High-Intensity Proton and T2-Weighted MRI Signals in the Globus Pallidus in Juvenile-Type of Dentatorubral and Pallidoluysian Atrophy
44. Molecular analysis by Southern blot for the N ‐acetylgalactosamine‐6‐sulphate sulphatase gene causing mucopolysaccharidosis IVA in the Japanese population
45. Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis.
46. Intravenous Immunoglobulins Suppress Immunoglobulin Productions by Suppressing Ca2+ -Dependent Signal Transduction Through Fc gamma Receptors in B Lymphocytes
47. A WILD‐TYPE μs C‐TERMINAL GENE IS EXPRESSED IN BLOOM'S SYNDROME CELLS
48. Molecular Cloning and Functional Expression of a Human Peroxisomal Acyl-Coenzyme A Oxidase
49. Identification of a Nonsense Mutation in ALD Protein cDNA from a Patient with Adrenoleukodystrophy
50. Expression of Secreted Immunoglobulin Heavy Chain Genes and Immunoglobulin‐Secreting Cells in Human Lymphocytes
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