Association of estrogen receptor β (ESR2) gene polymorphism with blood pressure

スポンサーリンク

概要

• 論文の詳細を見る
• Springer-Verlag Tokyoの論文
• 2000-11-01

著者

• HOSOI Takayuki

  Department of Advanced Medicine, National Center for Geriatrics and Gerontology

• Emi Mitsuru

  Department of Molecular Biology, Institute of Gerontology, Nippon Medical School

• Inoue Satoshi

  Department of Geriatric Medicine, University of Tokyo

• OUCHI Yasuyoshi

  Department of Geriatric Medicine, University of Tokyo

• Emi Mitsuru

  東京都老人医療センター

• OGAWA Sumito

  Department of Geriatric Medicine, Graduate School of Medicine, University of Tokyo

• SHIRAKI Masataka

  Research Institute and Practice for Involutional Diseases

• Ogawa Sumito

  東京大学 医学系研究科老年病学

• Ogawa Sumito

  Department Of Geriatric Medicine Graduate School Of Medicine The University Of Tokyo

• Inoue S

  Department Of Geriatric Medicine The University Of Tokyo

• Inoue Satoshi

  Department Of Geriatric Medicine The University Of Tokyo

• Hosoi Takayuki

  Department Of Advanced Medicine National Center For Geriatrics And Gerontology

• Hosoi Takayuki

  Endocrinology Section

• Emi Mitsuru

  Department Of Biochemistry Cancer Institute

• Ouchi Yasuyoshi

  Department Of Geriatric Medicine Faculty Of Medicine The University Of Tokyo

• Shintani Masafumi

  Department Of Obstetrics And Gynecology Narakenritsu Mimuro Hospital

• Hosoi Takayuki

  Department Of Internal Medicine Tokyo Metropolitan Geriatric Hospital

• Emi Mitsuru

  Research Institute Of Geriatric Medicine Nippon Medical University

• Emi Mitsuru

  Department Of Neurology Hematology Metabolism Endocrinology And Diabetes Yamagata University School

• Shiraki Masataka

  Department Of Internal Medicine Research Institute And Practice For Involutional Diseases

• Shiraki Masataka

  Research Institute And Practice For Involutional Disease

• Inoue Satoshi

  Department Of Chemistry And Materials Engineering Faculty Of Chemistry Materials And Bioengineering

• Emi Mitsuru

  Department Of Neurology Hematology Metabolism Endocrinology And Diabetes Yamagata University School

• Ouchi Yasuyoshi

  Department Of Biostatistics Epidemiology And Preventive Health Sciences The University Of Tokyo

• OGAWA Sumito

  Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo

• Inoue Satoshi

  Department of Applied Chemistry, Graduate School of Engineering, Osaka University

関連論文

• Smoking Confers a MTHFR 677C>T Genotype-Dependent Risk for Systemic Atherosclerosis : Results from a Large Number of Elderly Autopsy Cases that Died in a Community-Based General Geriatric Hospital
• Overrepresentation of the EBAG9 Gene at 8q23 Associated with Early-Stage Breast Cancers
• 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
• 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
• Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia : intrafamilial association study in an eight-generation hyperlipidemic kindred
• Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter : molecular study in a 1135-member familial hypercholesterolemia 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
• Nutritional Effects of γ-Glutamyl Carboxylase Gene Polymorphism on the Correlation between the Vitamin K Status and γ-Carboxylation of Osteocalcin in Young Males
• Three Distinct Commonly Deleted Regions of Chromosome Arm 16q in Human Primary and Metastatic Prostate Cancers
• Localization of a Tumor Suppressor Gene Associated With Progression of Human Prostate Cancer Within a 1.2 Mb Region of 8p22-p21.3
• A 3-Mb Physical Map of the Chromosome Region 8p21.3-p22,Including a 600-kb Region Commonly Deleted in Human Hepatocellular Carcinoma, Colorectal Cancer, and Non-Small Cell Lung Cancer
• Clinical variant of Tangier disease in Japan : mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis
• Allelic Losses of Loci at 3p25.1,8p22,13q12,17p13.3,and 22q13 Correlate with Postoperative Recurrence in Breast Cancer
• Segmental Copy Number Loss of SFMBT1 Gene in Elderly Individuals with Ventriculomegaly: A Community-Based Study
• Genetic mapping of allelic loss on chromosome 6q within heterogeneous prostate carcinoma
• Identification of a 1-Mb Common Region at 16q24.1-24.2 Deleted in Hepatocellular Carcinoma
• Allelic Loss at 1p34,13q12,17p13.3,and 17q21.1 Correlates With Poor Postoperative Prognosis in Breast Cancer
• Identification of a 1-cM Region of Common Deletion on 4q35 Associated With Progression of Hepatocellular Carcinoma
• Correlation of Allelic Loss with Poor Postoperative Survival in Breast Cancer
• PTEN/MMAC1 Mutations in Hepatocellular Carcinomas: Somatic Inactivation of Both Alleles in Tumors
• Frequent Allelic Loss at 6q26-27 in Breast Carcinomas of the Solid-tubular Histologic Type
• Detailed Deletion Mapping of Chromosome Arm 3p in Breast Cancers : A 2-cM Region on 3p 14.3-21.1 and a 5-cM Region on 3p 24.3-25.1 Commonly Deleted in Tumors
• Correlation of Allelic Losses and Clinicopathological Factors in Primary Breast Cancers
• Mapping of a Breast Cancer Tumor Suppressor Gene Locus to a 4-cM Interval on Chromosome 18q21
• 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
• Ret/PTC3 is the most frequent form of gene rearrangement in papillary thyroid carcinomas in Japan
• Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
• Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer
• Association of common missense changes in ELAC2 (HPC2) with prostate cancer in a Japanese case-control series
• 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
• 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
• 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
• 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
• 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
• Polymorphism of cytochrome P450 2B6 and prostate cancer risk : A significant association in a Japanese population
• Role of DNA repair systems in malignant tumor development in the elderly
• Reviewing the definition of "elderly"
• Impaired gamma carboxylation of osteocalcin in elderly women with type II diabetes mellitus : relationship between increase in undercarboxylated osteocalcin levels and low bone mineral density
• Association of a single nucleotide polymorphism in the secreted frizzled-related protein 4 (sFRP4) gene with bone mineral density
• Hypermethylation associated with inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human hepatoblastomas
• Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
• 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
• Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) gene
• Association of a single-nucleotide polymorphism in low-density lipoprotein receptor-related protein 5 gene with bone mineral density
• Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women
• Association of natural tooth loss with genetic variation at the human matrix Gla protein locus in elderly women
• Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss
• Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals
• 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
• Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus
• The sample size required for intervention studies on fracture prevention can be decreased by using a bone resorption marker in the inclusion criteria : prospective study of a subset of the Nagano Cohort, on behalf of the Adequate Treatment of Osteoporosis
• Absolute height reduction and percent height ratio of the vertebral body in incident fracture in Japanese women
• A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density
• Diagnostic criteria for primary osteoporosis: year 2000 revision
• Association of bone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locus
• Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis
• Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women
• Identification of a novel polymorphism of estrogen receptor-α gene that is associated with calcium excretion in urine
• Trends in the incidence of hip fracture in Japan,1987-1997:The third nationwide survey
• Guidelines on the use of biochemical markers of bone turnover in osteoporosis (2001)
• Association of estrogen receptor β (ESR2) gene polymorphism with blood pressure
• Nationwide incidence survey of femoral neck fracture in Japan, 1992
• Case of bone Paget's disease with cheek pain, hearing loss and tremor whose histological findings showed peculiar calcified structures
• The Val158Met polymorphism of the catechol-O-methyltransferase gene is not associated with the risk of sporadic or latent prostate cancer in Japanese men
• Association of HTRA1 promoter polymorphism with spinal disc degeneration in Japanese women
• Cooperative effect of serum 25-hydroxyvitamin D concentration and a polymorphism of transforming growth factor-β1 gene on the prevalence of vertebral fractures in postmenopausal osteoporosis
• Association of a Single Nucleotide Polymorphism in the Insulin-Like Growth Factor-1 Receptor Gene With Spinal Disc Degeneration in Postmenopausal Japanese Women
• Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenoposal Japanese women
• High level of serum undercarboxylated osteocalcin in patients with incident fractures during bisphosphonate treatment
• Postprandial Reactive Hypoglycemia in an Oldest-old Patient Effectively Treated with Low-dose Acarbose
• A Case of Type 2 Diabetes Mellitus in an Elderly Patient with Rapid Attenuation of Insulin Secretion that Resembled Fulminant Type 1 DM but with Incomplete Beta Cell Damage
• 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
• Association between a promoter polymorphism of the paraoxonase PON1 gene and pathologically verified idiopathic Parkinson's disease
• Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human estrogen receptor βlocus
• ASSOCIATION OF ESTROGEN RECEPTOR DINUCLEOTIDE REPEAT POLYMORPHISM WITH OSTEOPOROSIS
• Design of a pragmatic approach to evaluate the effectiveness of concurrent treatment for the prevention of osteoporotic fractures

もっと見る 閉じる

スポンサーリンク