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Department of Molecular Biology, Institute of Gerontology, Nippon Medical School | 論文
- Genomic Structure and Mapping of Human Orphan Receptor LXR Alpha : Upregulation of LXRa mRNA During Monocyte to Macrophage Differentiation
- Genetic Association between Aldehyde Dehydrogenase 2 (ALDH2) Variation and High-Density Lipoprotein Cholesterol (HDL-C) Among Non-Drinkers in Two Large Population Samples in Japan
- Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations
- Resection of Sternal Tumors and Reconstruction of the Thorax : A Review of 15 Patients
- Prolactin secretion in response to prolactin-releasing peptide and the expression of the prolactin-releasing peptide gene in the medulla oblongata are estrogen dependent in rats
- Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients
- Correlation of Allelic Losses and Clinicopathological Factors in 504 Primary Breast Cancers
- Association of Allelic Losses at 3p25.1, 13q12, or 17p13.3 with Poor Prognosis in Breast Cancers with Lymph Node Metastasis
- Allelic Loss at 1p34-36 Predicts Poor Prognosis in Node-negative Breast Cancer
- DNA alterations during multi-step development of human hepatocellular carcinomas revealed by laser capture microdissection
- Obstructive Ileus Caused by Blood Clot After Emergency Total Gastrectomy in a Patient with Hemophilia A : Report of a Case
- Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase : comparison of exon/intron organization of sterol-sensing domains among four related genes
- Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene
- Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population
- Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers
- Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line
- Two Target Regions of Allelic Loss on Chromosome 9 in Urinary-bladder Cancer
- Mapping of a New Target Region of Allelic Loss to a 6-cM Interval at 21q21 in Primary Breast Cancers
- A Case of Extracranial Atypical Meningioma Involving Maxillofacial Region
- Hypermethylation associated with inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human hepatoblastomas