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Yamagata Univ. School Of Medicine Yamagata | 論文
- Prevention of tracheal high-dose tolerance induction by granulocyte-macrophage colony stimulating factor-dependent restoration of antigen-presenting cell function
- CD44 on blood eosinophils as a novel marker of bronchial asthma management
- Haploid allele mapping of Y-chromosome minisatellite, MSY1 (DYF155S1), to a Japanese population
- Sudden Death of a Cocaine Abuser
- MAD-related Genes on 18q21.1, Smad2 and Smad4, Are Altered Infrequently in Esophageal Squamous Cell Carcinoma
- Epithelial-cadherin Gene Is Not Mutated in Ductal Carcinomas of the Breast
- Absence of BAT-26 instability in gastric intestinal metaplasia
- Microsatellite instability in esophageal squamous cell carcinoma is not associated with hMLH1 promoter hypermethylation
- De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
- Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
- Promoter hypermethylation of tumor suppressor and tumor-related genes in non-small cell lung cancers
- Esophageal adenocarcinoma that probably originated in the esophageal gland duct : A case report
- Frequent Epigenetic Silencing of the p16 Gene in Non-small Cell Lung Cancers of Tobacco Smokers
- Flow Cytometric DNA Analysis of Abnormal Endometrium
- Analysis of the DPC4 Gene in Gastric Carcinoma
- Inactivation of the E-Cadherin Gene in Primary Gastric Carcinomas and Gastric Carcinoma Cell Lines
- Loss of Heterozygosity on the Short Arm of Chromosome 9 without p16 Gene Mutation in Gastric Carcinomas
- Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
- ITIH1^* Q0_, A NULL ALLELE OF INTER-ALPHA-TRYPSIN INHIBITOR H1 CAUSED BY DELETION/FRAMESHIFT MUTATION
- 東アジア4集団におけるalpha-2-HS-glycoprotein型の分布〔英文〕