65 results on '"Matsuda, I."'
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2. Rice stripe virus 23.9 K protein aggregates and forms inclusion bodies in cultured insect cells and virus-infected plant cells
3. Surface Soil Effects Study Using Short-period Microtremor Observations in Almería City, Southern Spain
4. Molecular and cellular analyses of HLA class II-associated susceptibility to autoimmune diseases in the Japanese population
5. Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families
6. The Holocene development of Kushu Lake on Rebun Island in Hokkaido, Japan
7. Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan
8. Predominance of large low density lipoprotein particles and lower fractional esterification rate of cholesterol in high density lipoprotein in children with insulin-dependent diabetes mellitus
9. Depressed natural killer cell activity due to decreased natural killer cell population in a vitamin E-deficient patient with Shwachman syndrome: reversible natural killer cell abnormality by α-tocopherol supplementation
10. Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency
11. Urinary propionylcarnitine analysis for monitoring carnitine supplementation in inherited disorders of propionate metabolism
12. Measurement of blood holoceruloplasmin by EIA using a mouse monoclonal antibody directed to holoceruloplasmin. Implication for mass screening of Wilson disease
13. A family of selective immunodeficiency with normal immunoglobulins: possible autosomal dominant inheritance
14. Characterization of a point mutation in the pyruvate dehydrogenase E1α gene from two boys with primary lactic acidaemia
15. Follow up study on children with dyslipidaemia detected by mass screening at 18 months of age: effect of 12 months dietary treatment
16. Specificity of PCR-SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency
17. Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis
18. Molecular diagnosis of maple syrup urine disease: Screening and identification of gene mutations in the branched-chain α-ketoacid dehydrogenase multienzyme complex
19. Gene analysis of mennonite maple syrup urine disease kindred using primer-specified restriction map modification
20. Tyrosinaemia type III: Immunochemical studies on 4-hydroxyphenylpyruvic acid dioxygenase and molecular cloning of cDNA for the enzyme
21. Maple syrup urine disease: Clinical and biochemical significance of gene analysis
22. Abnormal mRNA and inactive polypeptide in a patient with prolidase deficiency
23. Anti-neutrophil antibodies in patients with nutritional copper deficiency
24. The human prolidase gene: Structure and restriction fragment length polymorphisms
25. In/Si(111): Self-Assembled One and Two-Dimensional Electron Gases
26. Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: A murine model for hereditary tyrosinaemia type III
27. A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiency
28. A fluorescent microscopy study of biopsied muscles from infantile neuromuscular disorders
29. Aarskog syndrome with isolated growth hormone deficiency
30. Delayed cutaneous hypersensitivity in children with severe multiple handicaps treated with phenytoin
31. Biochemical nature of pyruvate dehydrogenase complex in the patient with primary lactic acidaemia
32. Mutation of the 97-197-197-1subunit of the pyruvate dehydrogenase complex, in relation to heterogeneity
33. Deduced amino acid sequence of human prolidase and molecular analyses of prolidase deficiency
34. Agenesis of an internal carotid artery: Angiographic, tomographic and computed tomographic correlation
35. Extravascular iodine in contrast enhancement with computed tomography
36. Restriction fragment length polymorphisms in the 5′ end region of the human argininosuccinate synthetase gene
37. Pathology of skeletal muscle and intramuscular nerves in infantile neuroaxonal dystrophy
38. Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblings
39. Study on established lymphoid cells in maple syrup urine disease. Correlation with clinical heterogeneity
40. Structural organization of the human ornithine transcarbamylase gene
41. Immunochemical evidence of pyruvate dehydrogenase (E1) deficiency
42. Kinetic analysis of argininosuccinate synthetase in a variant form of citrullinaemia
43. Decreased bone density in severely handicapped children and adults, with reference to the influence of limited mobility and anticonvulsant medication
44. Laurence-Moon-Biedl syndrome (?) and Prader-Willi syndrome (?) in a single family
45. Follow-up study of a nation-wide neonatal metabolic screening program in Japan: A collaborative study group of neonatal screening for inborn errors of metabolism in Japan
46. Effect of low-content zinc and copper formula on infant nutrition
47. Plasma concentrations of vitamin K1 and PIVKA-II in bottle-fed and breast-fed infants with and without vitamin K prophylaxis at birth
48. Study of a female patient with ornithine transcarbamylase deficiency: Detection of a nonsense mutation
49. British Diabetic Association Medical and Scientific Section, Autumn Meeting Abstracts: London, 30th September and 1st October, 1966
50. Immunochemical analysis of prolidase deficiency and molecular cloning of cDNA for prolidase of human liver
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