Emi Mitsuru | 日本医科大学第2生化

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著作論文

Down-regulation of members of glycolipid-enriched membrane raft gene family, MAL and BENE, in cervical squamous cell cancers
Genetic Association of Low-Density Lipoprotein Receptor-Related Protein 2 (LRP2) with Plasma Lipid Levels
Association of nucleotide variations in the apolipoprotein B48 receptor gene (APOB48R) with hypercholesterolemia
A promoter SNP (-1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia
Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 gene
G-substrate gene promoter SNP (-1323T>C) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia : Intra-familial association study in an eight-generation hyperlipidemic kindred
Characterization of liver-cirrhosis nodules by analysis of gene-expression profiles and patterns of allelic loss
Common null variant, Arg192Stop, in a G-protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activity
Genetic mapping of allelic loss on chromosome 6q within heterogeneous prostate carcinoma
Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population : the Takahata study
Expression profiling to predict postoperative prognosis for estrogen receptor-negative breast cancers by analysis of 25,344 genes on a cDNA microarray
Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancers
Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers
Upregulation and Overexpression of Human X-box Binding Protein 1 (hXBP-1) Gene in Primary Breast Cancers
Amplification, up-regulation and over-expression of DVL-1, the human counterpart of the Drosophila disheveled gene, in primary breast cancers
Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer
Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis
Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis
Genomic Structure and Mapping of Human Orphan Receptor LXR Alpha : Upregulation of LXRa mRNA During Monocyte to Macrophage Differentiation
DNA alterations during multi-step development of human hepatocellular carcinomas revealed by laser capture microdissection
Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia : A Molecular Study in an Eight-generation Hyperlipidemic Family
A family with spinal anaplastic ependymoma : evidence of loss of chromosome 22q in tumor
Overestimated frequency of a possible emphysema-susceptibility allele when microsomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method
Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene
Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability
Frameshift Mutations and a Length Polymorphism in the hMSH3 Gene and the Spectrum of Microsatellite Instability in Sporadic Colon Cancer
A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus
Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locus
Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus
A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFAα) locus
Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human matrix Gla protein (MGP) locus
Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locus
The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population : the Takahata study

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