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名古屋大学 医学系研究科皮膚病態学 | 論文
- Immunohistochemical Discrimination of Plasmacytoid Dendritic Cells from Myeloid Dendritic Cells in Human Pathological Tissues
- Genotyping of Candida albicans by Fragment Analysis of Microsatellites Combined with 25S rDNA and RPS-based Strategies
- Granulocyte Colony-Stimulating Factor and Lineage-Independent Modulation of VLA-4 Expression on Circulating CD34^+ Cells
- Trisomy 12 and t(14;18) in B-cell chronic lymphocytic leukemia
- G-CSF-induced mobilization of peripheral blood stem cells for allografting: comparative study of daily single versus divided dose of G-CSF
- The effect of adding rituximab to CHOP-based therapy on clinical outcomes for Japanese patients with diffuse large B-cell lymphoma : a propensity score matching analysis
- Induction of lung adenocarcinoma in transgenic mice expressing activated EGFR driven by the SP-C promoter
- p27^ is Detected on Most Gastric MALT Lymphomas, but not Large Cell Lymphomas
- Expression of Heat Shock Protein 60 in Normal and Neoplastic Human Lymphoid Tissues
- Severe Bleeding Tendency Caused by Leukemic Infiltration and Destruction of Vascular Walls in Chronic Neutrophilic Leukemia
- Epidemiological study of Candida species in cutaneous candidiasis based on PCR using a primer mix specific for the DNA topoisomerase II gene
- PCR and PCR-RFLP techniques targeting the DNA topoisomerase II gene for rapid clinical diagnosis of the etiologic agent of dermatophytosis
- Phase I/II study of tandem high-dose chemotherapy with autologous peripheral blood stem cell transplantation for advanced multiple myeloma
- Use of micafungin versus fluconazole for antifungal prophylaxis in neutropenic patients receiving hematopoietic stem cell transplantation
- Myositis as a Manifestation of Chronic Graft-Versus-Host Disease
- Malignant fibrous histiocytoma of the right ventricle of the heart
- Dyschromatosis symmetrica hereditaria associated with neurological disorders
- Patients with localized primary non-tonsillar oral diffuse large B-cell lymphoma exhibit favorable prognosis despite a non-germinal center B-cell-like phenotype
- Investigation of the IVS5 +5G → A splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome
- Characterization of the human RAB38 and RAB7 genes : exclusion of new major pathological loci for Japanese OCA