82 results on '"Tada, K."'
Search Results
2. Association of the G-protein β3 subunit gene polymorphism with the incidence of cardiovascular disease independent of hypertension: the Funagata study
3. Electron-Spin-Based Phenomena Arising from Pore Edges of Graphene Nanomeshes
4. Stenotrophomonas maltophilia infection in hematopoietic SCT recipients: high mortality due to pulmonary hemorrhage
5. Development and characterization of an efficient bio-white polymer light-emitting diode with red and green phosphorescent dyes as dopants
6. Effects of Substrate Materials on Self-Formation of Ti-Rich Interface Layers in Cu(Ti) Alloy Films
7. RUNX3 protein is overexpressed in human basal cell carcinomas
8. Multicentre prospective study of perinatal depression in Japan: incidence and correlates of antenatal and postnatal depression
9. Experimental investigation of geologically produced antineutrinos with KamLAND
10. A shaking bioreactor equipped with twin ceramic membranes for acetic acid production using Acetobacter pasteurianus
11. Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene ( ψ GLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia
12. Structire, Properties, and Process Characteristics of Low-K Materials Prepared by PECVD
13. Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics
14. Optical characterization of MEH–PPV/Alq3 composite films
15. πNN Dynamics in pp → pp, pp →πd and πd →πd Processes Below 1 GeV
16. Influence of ageing on onset of mitochondrial disease
17. Prenatal diagnosis in a new peroxisomal disease by the W-particle separation method
18. Clinical and biochemical phenotype of the MELAS mutation
19. Propionic acidaemia: Sequence analysis of mutant mRNAs from Japanese β subunit-deficient patients
20. Quantitative evaluation of electron transport system proteins in mitochondrial encephalomyopathy
21. Non-ketotic hyperglycinaemia: Molecular lesion, diagnosis and pathophysiology
22. Defects of mitochondrial respiratory enzymes in cloned cells from MELAS fibroblasts
23. Medium-chain acyl-CoA dehydrogenase deficiency: Molecular aspects
24. A new type of mitochondrial DNA deletion in patients with encephalomyopathy
25. A four-nucleotide insertion at the E1 α gene in a patient with pyruvate dehydrogenase deficiency
26. Type 4 renal tubular acidosis (subtype 2) in a patient with methylmalonic acidaemia
27. Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase
28. Molecular analysis of dihydropteridine reductase deficiency and restoration of the enzyme activity by gene transfer
29. Genomic analysis of non-ketotic hyperglycinaemia: A partial deletion of P-protein gene
30. Simple and rapid detection of phenylketonuria mutation tightly linked to haplotype 2 by modified polymerase chain reaction
31. Aged-onset Kienböck's disease
32. Laparoscopic resection of large leiomyomas of the gastric fundus
33. Acute autonomic and sensory neuropathy: a case report
34. An 84bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNA
35. Chronic pancreatitis in a child with glycogen storage disease type 1
36. Secondary amyloidosis in glycogen storage disease type Ib
37. Minocycline-related lupus in childhood
38. Mammary tumorigenic effect of a new nitrosourea, 1,3-dibutyl-l-nitrosourea (B-BNU), in female Donryu rats
39. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy
40. Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy
41. Arthropathy of the wrist in leprosy —What changes are caused by long-standing peripheral nerve palsy?
42. Cloning of a defective gene encoding the pyruvate dehydrogenase E1α subunit from a patient with its deficiency
43. Immunochemical study in three patients with cytochromec oxidase deficiency presenting leigh's encephalomyelopathy
44. A new variant of glycogen storage disease type 1: Probably due to a defect in the glucose-6-phosphate transport system
45. Development of spinal motoneuron innervation of the upper limb muscle in the rat
46. Successful transplantation of soy bean agglutinin-fractionated, histoincompatible, maternal marrow in a patient with severe combined immunodeficiency and BCG infection
47. Serum bile acids and their conjugates in breast-fed infants with prolonged jaundice
48. Biosynthesis of peroxisomal membrane polypeptides in infants with Zellweger syndrome
49. Dietary therapy in two patients with vitamin B12-unresponsive methylmalonic acidemia
50. Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis
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