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Department of Molecular Biology, Institute of Gerontology, Nippon Medical School | 論文
- Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1-cM Intervals on Genomic Contigs at 6q21 and 6q25.3
- Diaphragmatic repair of two cases of hepatic hydrothorax using video-assisted thoracoscopic surgery
- Hereditary Factors in Multiple Primary Malignancies Associated with Lung Cancer
- P1-IS-19 PR, ssDNA and Ki67 antigen, the better immunohistochemical predictors of hormonal response in the biopsy specimens of endometrial adenocarcinoma during the high dose progestin therapy?
- Somatic Mutations of the PTEN/MMAC1 Gene in Fifteen Japanese Endometrial Cancers : Evidence for Inactivation of Both Alleles
- Surgical Treatment of Superior Sulcus Tumors
- Localization of a Target Region of Allelic Loss to a 1-cM Interval on Chromosome 16p.13.13 in Hepatocellular Carcinoma
- Two single nucleotide polymorphisms of the hSNF5/INI1 gene
- Binding Affinity of Bunazosin, Dorzolamide, and Timolol to Synthetic Melanin
- Human Growth Hormone Induces SOCS3 and CIS mRNA Increase in the Hypothalamic Neurons Hypophysectomized Rats
- A Histochemical Study of the Effect of 6-OHDA on the Adrenergic Nerves in the Rabbit Bladder Base After Local Administration
- A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene
- Long-term Survival of Askin Tumor for 10 Years with 2 Relapses
- Successful Thoracoscopic Sympathectomy for Primary Erythromelalgia in the Upper Extremities
- Comparison of Changes in Hemodynamics between Unilateral and Bilateral Lung Volume Reduction for Pulmonary Emphysema
- Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients : four germline mutations, but no evidence of somatic mutation
- Isolation and characterization of antibodies against three consecutive Tn-antigen clusters from a phage library displaying human single-chain variable fragments
- A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene
- Association of amino acid variation (Trp64Arg) in the beta3-adrenergic receptor gene with bone mineral density
- Ethnic difference in contribution of alleles of the interleukin-1 receptor antagonist gene to predisposition to osteoporosis