Emi Mitsuru | Research Institute Of Geriatric Medicine Nippon Medical University

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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
Hypercholesterolemia associated with splice-junction variation of inter-α-trypsin inhibitor heavy chain 4 (ITIH4) 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
Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia : intrafamilial 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
Clinical variant of Tangier disease in Japan : mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis
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
Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer
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
Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients
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
Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women
Association of a single-nucleotide polymorphism in the promoter region of leukemia inhibitory factor receptor gene with low bone mineral density in adult women
Association of a single-nucleotide polymorphism in low-density lipoprotein receptor-related protein 5 gene with bone mineral density
Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene
Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene
Association of bone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locus
Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women
The important role for βVLDLs binding at the fourth cysteine of first ligand-binding domain in the low-density lipoprotein receptor
Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japa
Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene
Familial Hypercholesterolemia with Cholesteryl Ester Traansfer Protein Deficiency
Association of estrogen receptor β (ESR2) gene polymorphism with blood pressure
Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities
A novel LDLR mutation, H190Y, in a Utah kindred with familial Hypercholesterolemia
A family with spinal anaplastic ependymoma : evidence of loss of chromosome 22q in tumor
Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) gene
Human calcitonin receptor-like receptor for adrenomedullin : genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis
Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenoposal Japanese women

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