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Division Of Human Genetics Medical Research Institute Kanazawa Medical University | 論文
- Inherited metabolic disorders in Thai infants identified by Gas-Liquid Chromatography and Mass spectrometry (GC/MS)
- Incidence of Diffuse Large B-Cell Lymphoma of Germinal Center B-Cell Origin in Whole Diffuse Large B-Cell Lymphoma : Tissue Fluorescence In Situ Hybridization Using t(14 ; 18) Compared with Immunohistochemistry
- Neonatal ketosis is not rare : experience of neonatal screening using gas chromatography-mass spectrometry
- Changes in urinary level and configuration ratio of D-lactic acid in patients with short bowel syndrome
- Simple and quantitative analysis of urinary sulfated tauro- and glycodihydroxycholic acids in infant with cholestasis by electrospray ionization mass spectrometry
- Application of optical isomer analysis by diastereomer derivatization GC/MS to determine the condition of patients with short bowel syndrome
- Stability of 5-aminolevulinic acid on dried urine filter paper for a diagnostic marker of tyrosinemia type I
- Differential chemical diagnosis of primary hyperoxaluria type II : Highly sensitive analysis of optical isomers of glyceric acid by GC/MS as diastereoisomeric derivatives
- Quantification of urinary 5-aminolevulinic acid by gas chromatography-mass spectrometry
- In Memory of Professor Isamu Matsumoto, the Founder of JSBMS and Pioneer in Human Metabolome Science
- Simple gas chromatographic-mass spectrometric procedure for diagnosing pyrimidine degradation defects for prevention of severe anticancer side effects
- Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography-mass spectrometry
- Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography-mass spectrometry
- Diagnosis and monitoring of inborn errors of metabolism using urease-pretreatment of urine, isotope dilution, and gas chromatography-mass spectrometry
- Noninvasive human metabolome analysis for differential diagnosis of inborn errors of metabolism
- Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas chromatography - mass spectrometry
- Low-grade malignant soft-tissue perineurioma : Interphase fluorescence in situ hybridization
- Fluorescence In Situ Hybridization Detection of Chromosome IGH/BCL2 Translocations from Paraffin-Embedded Tissue : Evaluation in Follicular Lymphoma
- Lectin Binding in Meth-A Cells Polyploidized by Different Mechanisms
- Different Responses of Polyploidized V79 Cells after Removal of Two Drugs, Demecolcine and K-252a