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Department Of Legal Medicine Osaka Medical College | 論文
- OE-103 Human Amniotic Membrane-derived Stem Cell with no HLA-DR Expression can be a Promising Cellular Source for Cardiac Stem Cell Therapy(Regeneration (angiogenesis/myocardial regeneration)-1, The 71st Annual Scientific Meeting of the Japanese Circulati
- Possible involvement of calcineurin, protein kinase C, and Src-family kinases in angiotensin II-induced tyrosine phosphorylation of p130^ in rat cardiac muscle
- Postmortem Molecular Screening for Cardiac Ryanodine Receptor Type 2 Mutations in Sudden Unexplained Death : R420W Mutated Case With Characteristics of Status Thymico-Lymphaticus
- Fatality due to acute fluoride poisoning in the workplace
- Analysis of two types of novel alleles in the DXS10011 locus
- Sequence analysis of two de novo mutation alleles at the DXS10011 locus
- Sibling incest and formulation of paternity probability : case report
- Haplotype analysis of a de novo allele at a vWF STR locus using flanking STR loci
- Estimation of Age from the Femur of Japanese Cadavers
- Plasmid Maintenance Renders Bacteria More Susceptible to Heat Stress
- Radiotherapy to pulmonary metastases of a malignant phyllodes tumor of the breast
- A study of monoamine neuronal systems of schizophrenic patients : Using forensic autopsy brains
- Radiofrequency Ablation for WPW Syndrome with Monitoring the Local Electrogram at the Ablation Site
- Altered Expression of Both β-Carotene 15,15'Monooxygenase and Lecithin : Retinol Acyltransferase in Obese Zucker Rats
- Co-expression of vascular endothelial growth factor and its receptor, neuropilin-1, in a B cell lymphoma cell line (OHK) with primary effusion lymphoima immunophenotype
- Clinical improvement of membranous nephropathy after endoscopic resection of double early gastrointestinal cancers
- Expression of Toll-like Receptors in the Pancreas of Recent-onset Fulminant Type 1 Diabetes
- ABO blood group alleles and genetic recombination
- Postmortem genetic analysis for a sudden death case complicated with Marfan syndrome