32 results on '"Ohse, Morimasa"'
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2. Prenatal diagnosis of methylmalonic aciduria by measuring methylmalonic acid in dried amniotic fluid on filter paper using gas chromatography-mass spectrometry
3. A GC/MS-based metabolomic approach for diagnosing citrin deficiency
4. Urinary 2-hydroxy-5-oxoproline, the lactam form of α-ketoglutaramate, is markedly increased in urea cycle disorders
5. Prenatal diagnosis of propionic acidemia by measuring methylcitric acid in dried amniotic fluid on filter paper using GC/MS
6. Changes in urinary level and configuration ratio of d-lactic acid in patients with short bowel syndrome
7. Simple and quantitative analysis of urinary sulfated tauro- and glycodihydroxycholic acids in infant with cholestasis by electrospray ionization mass spectrometry
8. Application of optical isomer analysis by diastereomer derivatization GC/MS to determine the condition of patients with short bowel syndrome
9. Identification of new biomarkers of pyridoxine-dependent epilepsy by GC/MS-based urine metabolomics
10. Stability of 5-aminolevulinic acid on dried urine filter paper for a diagnostic marker of tyrosinemia type I
11. Differential chemical diagnosis of primary hyperoxaluria type II: Highly sensitive analysis of optical isomers of glyceric acid by GC/MS as diastereoisomeric derivatives
12. Rapid gas chromatographic–mass spectrometric diagnosis of dihydropyrimidine dehydrogenase deficiency and dihydropyrimidinase deficiency
13. A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis
14. Rapid and sensitive detection of urinary 4-hydroxybutyric acid and its related compounds by gas chromatography–mass spectrometry in a patient with succinic semialdehyde dehydrogenase deficiency
15. Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography–mass spectrometry
16. Pilot study of gas chromatographic–mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease
17. Erratum to: A GC/MS-based metabolomic approach for diagnosing citrin deficiency
18. A Japanese case of β-ureidopropionase deficiency with dysmorphic features
19. Application of Electroporation for Transformation in A Thermophilic Bacterium, Bacillus stearothermophilus
20. Gene Tranfer into Some Species of Bacillus by Electroporation
21. A Simple and Rapid Method for DNA Transformation of Intact Cells of Bacillus by Electroporation
22. A Biomarker Found in Cadmium Exposed Residents of Thailand by Metabolome Analysis
23. Metabolomic analysis reveals hepatic metabolite perturbations in citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mice, a model of human citrin deficiency
24. Urinary metabolic profile of phenylketonuria in patients receiving total parenteral nutrition and medication
25. Screening and diagnosis of β‐ureidopropionase deficiency by gas chromatographic/mass spectrometric analysis of urine
26. Simple gas chromatographic–mass spectrometric procedure for diagnosing pyrimidine degradation defects for prevention of severe anticancer side effects
27. Effects of DNA Topology on Transformation Efficiency ofBacillus subtilisISW1214 by Electroporation
28. A New and Efficient Method for Gene Transfer into Mouse FM3A Cells Using Metaphase Chromosomes by Electroporation
29. Effects of Plasmid DNA Sizes and Several Other Factors on Transformation ofBacillus subtilisISW1214 with Plasmid DNA by Electroporation
30. Effects of DNA Topology on Transformation Efficiency of Bacillus subtilisISW1214 by Electroporation
31. Screening and diagnosis of beta-ureidopropionase deficiency by gas chromatographic/mass spectrometric analysis of urine.
32. A study on alpha-ketoadipic aciduria by gas chromatographic-mass spectrometry.
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