Collagen type Iα1 gene polymorphism may be associated with the rate of bone mineral density decrease in female hemodialyzed patients
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-12-01
著者
-
Marumo Fumiaki
Department of Internal Medicine, Kitasato University School of Medicine
-
Akiba Takashi
Department Of Medicine Kidney Center Tokyo Women's Medical University
-
Kuwahara Michio
東京医科歯科大学 血液浄化療法
-
Kuwahara M
Division Of Nephrology Shuwa General Hospital
-
KUWAHARA Michio
Division of Nephrology, Shuwa General Hospital
-
TERADA Yoshio
Department of Nephrology, Tokyo Medical and Dental University Graduate School
-
KUWAHARA Michio
Department of Homeostasis Medicine and Nephrology, Tokyo Medical and Dental University Graduate Scho
-
ASAI Tomoki
Department of Homeostasis Medicine and Nephrology, Tokyo Medical and Dental University Graduate Scho
-
SATO Kazunori
Department of Homeostasis Medicine and Nephrology, Graduate School, Tokyo Medical and Dental Univers
-
KURIHARA Satoshi
Internal Medicine, Kasukabe Shuuwa Hospital
-
YONESHIMA Hideo
Internal Medicine, Kasukabe Shuuwa Hospital
-
Asai Takashi
Department Of Cardiovascular Medicine Wakayama Medical University
-
Akashi Takumi
Department Of Clinical Pathology Graduate School Of Medicine Tokyo Medical And Dental University
-
Akiba T
Kowa Co. Ltd. Shizuoka Jpn
-
Akiba Takashi
Department Of Blood Purification Kidney Center Tokyo Women's Medical University
-
Akiba Takashi
Department Of Blood Purification Tokyo Women's Medical University
-
Akiba Takashi
Kidney Center Tokyo Medical And Dental University
-
Akiba Takashi
Patient Registration Committee Japanese Society For Dialysis Therapy
-
Akiba Tomohide
Dept. Of Toxicology Fuji Research Laboratoris Kowa Co. Ltd.
-
Marumo F
Tokyo Medical And Dental Univ. Tokyo Jpn
-
Marumo Fumiaki
Department Of Clinical And Molecular Endocrinology Graduate School Tokyo Medical And Dental Universi
-
Marumo Fumiaki
Department Of Blood Purification Tokyo Medical And Dental University
-
Marumo Fumiaki
Kidney Center Tokyo Medical And Dental University
-
Terada Yoshio
Department Of Nephrology Graduate School Of Medicine Tokyo Medical And Dental University
-
Terada Yoshio
Department Of Endocrinology Metabolism And Nephrology Kochi Medical School Kochi University
-
Akiba Takashi
The Second Department Of Internal Medicine Tokyo Medical And Dental University School Of Medicine
-
Yoneshima Hideo
Internal Medicine Kasukabe Shuuwa Hospital
-
Akizawa Tadao
Center Of Blood Purification Therapy Wakayama Medical School
-
Takeshita Akira
From Reseach Institute Of Angiocardiology And Cardiovascular Clinic Faculty Of Medicine Kyushu Unive
-
Asai Tomoki
Department Of Homeostasis Medicine And Nephrology Tokyo Medical And Dental University Graduate Schoo
-
Akiba Takashi
Department Of Blood Purification And Department Of Urology Tokyo Medical And Dental University
-
Takeshita Akira
The Research Institute Of Angiocardiology And Cardiovascular Clinic Faculty Of Medicine Kyushu Unive
-
Sato Kazunori
Department Of Homeostasis Medicine And Nephrology Graduate School Tokyo Medical And Dental Universit
-
Sato Kazunori
Department Of Computational Nanomaterials Design Nanoscience And Nanotechnology Center The Institute
-
Kurihara Satoshi
Internal Medicine Kasukabe Shuuwa Hospital
-
Takeshita Akira
The Research Institute Of Angiocardiology And Cardiovascular Clinic Faculty Of Medicine Kyushu Unive
-
KUWAHARA Michio
Department of Electronics, Toyama University
-
SATO Kazunori
Department of Biology, Faculty of Science, Kyushu University
関連論文
- OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
- OE-009 Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Socie
- -445- CLINICAL EVALUATION ON THE RESPONSE OF PLASMA ATRIAL NATRIURETIC PEPTIDE TO EXERCISE IN PATIENTS WITH HYPERTROPHIC CARDIOMYOPATHY
- A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
- A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
- Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
- PJ-438 Identification of Proteins that Bind Galectin-2, Encoded by a Gene Associated with Myocardial Infarction Using Tandem Affinity Purification Method(Acute myocardial infarction, basic-4 (IHD) PJ74,Poster Session (Japanese),The 70th Anniversary Annual
- The characteristics of relapse in adult-onset minimal-change nephrotic syndrome
- Anti-Glomerular Basement Membrane Antibody Disease with Granulomatous Lesions on Renal Biopsy
- Wegeners Granulomatosis Complicated by Intestinal Ulcer due to Cytomegalovirus Infection and by Thrombotic Thrombocytopenic Purpura
- Association of a single-nucleotide polymorphism in the immunoglobulin μ-binding protein 2 gene with immunoglobulin A nephropathy
- Left Ventricular Hypertrophy Is Associated with Arterial Stiffness and Vascular Calcification in Hemodialysis Patients
- Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients
- Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy
- A high-throughput SNP typing system for genome-wide association studies
- PJ-152 A functional SNP in the Proteasome Subunit Alpha Type 6 Gene confers Risk of Myocardial Infarction in Japanese Population(Acute myocardial infarction, basic-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-212 Identification of a Novel non-coding RNA, MIAT, that Confers Risk of Myocardial Infarction(Genetics/Genetically engineered models/Gene therapy-2(H/M), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-340 Large-Scale Genetic Association Study of 30 Inflammation-Related Genes for Myocardial Infarction Using Tag SNPs from HapMap Data(Genetics/Genetically engineered models/Gene therapy-1 (M) OJ57,Oral Presentation (Japanese),The 70th Anniversary Annual
- Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene
- Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21
- Genome-wide association study to identify genes related to myocardial infarction
- A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction
- SNP projects in Japan
- High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2
- A case of Mikulicz's disease complicated with severe interstitial nephritis associated with IgG4
- Arterial Stiffness in Patients with Non-Diabetic Chronic Kidney Disease (CKD)
- Low-Dose Losartan Therapy Reduces Proteinuria in Normotensive Patients with Immunoglobulin A Nephropathy
- Clinical assessment of low-dose steroid therapy for patients with IgA nephropathy : a prospective study in a single center
- PJ-224 Primal role of intracellular zinc in PKC-dependent monocyte signalling and adhesive interaction(Atherosclerosis, basic(06)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- Patterns in the prevalence of hepatitis C virus infection at the start of hemodialysis in Japan
- Assessment of Coronary Artery Calcification in Hemodialysis Patients Using Multi-Detector Spiral CT Scan
- PJ-363 Functional Impacts of Selectin Haplotypes on Leukocyte-endothelial Interaction(Molecular Biology, Vascular 2 (H) : PJ61)(Poster Session (Japanese))
- Expression of bone type 1 PTH receptor in rats with chronic renal failure
- Renal expression of metallothionein in rats treated with cadmium
- Collagen type Iα1 gene polymorphism may be associated with the rate of bone mineral density decrease in female hemodialyzed patients
- Aquaporins in the body
- Isolation of a Novel Gene Showing Reduced Expression in Metastatic Colorectal Carcinoma Cell Lines and Carcinomas
- Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus
- Use of automated image registration to generate mean brain SPECT image of Alzheimer's patients
- Significance of methicillin-resistant Staphylococcus aureus (MRSA) survey in a university teaching hospital
- Membrane Localization of Protein-Tyrosine Phosphatase 1B is Essential for its Activation of Sterol Regulatory Element-Binding Protein-1 Gene Expression and Consequent Hypertriglyceridaemia
- Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
- Differential Effects of Hyperosmolality on Na-K-ATPase and Vasopressin-Dependent cAMP Generation in the Medullary Thick Ascending Limb and Outer Medullary Collecting Duct
- ORTHOSTATIC HYPERTENSION DUE TO COEXISTENCE OF RENAL FIBROMUSCULAR DYSPLASIA AND NEPHROPTOSIS
- Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
- Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels
- Genetic variations in five genes involved in the excitement of cardiomyocytes
- Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome
- High-density SNP map of human ITR, a gene associated with vascular remodeling
- Gene-based SNP discovery as part of the Japanese Millennium Genome Project : identification of 190 562 genetic variations in the human genome
- A familial case of mitochondrial disease resembling Alport syndrome
- IgA Nephropathy with Complement Deficiency
- A comparison of Tc-99m HMPAO brain SPECT images of young and aged normal individuals
- A method for the quantification of benzodiazepine receptors by using ^I-iomazenil and SPECT with one scan and one blood sampling
- Thymic Hyperplasia as a Source of Ectopic ACTH Production
- Kinetics of anticoagulant binding to continuous hemofilter membranes
- Mitogen-Activated Protein Kinase Cascade and Cell Cycle-Related Genes in the Kidney
- LONG-TERM, LOW-DOSE, CADMIUM-INDUCED NEPHROPATHY WITH RENAL OSTEOPATHY IN OVARIECTOMIZED RATS
- EVALUATION OF MYOCARDIAL CONTRACTILITY BY THE NON-INVASIVE METHOD
- OPTIMAL STATE OF BLOOD PRESSURE DEPRESSION AND RENAL CIRCULATION
- ATF3 Inhibits Doxorubicin-induced Apoptosis in Cardiac Myocytes
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- Hormonal Regulation of Glycolytic Enzyme Gene and Pyruvate Dehydrogenase Kinase/Phosphatase Gene Transcription
- Plasma Adiponectin Levels are Increased Despite Insulin Resistance in Corticotropin-releasing Hormone Transgenic Mice, an Animal Model of Cushing Syndrome
- Theoretical Prediction of Curie Temperature in (Zn, Cr)S, (Zn, Cr)Se and (Zn, Cr)Te by First Principles Calculations
- Perinephric angiomyolipoma : A unique development pattern surrounding the kidney
- Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10
- Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population
- High Glucose Induces Transactivation of the α2-HS Glycoprotein Gene Through the ERK1/2 Signaling Pathway
- Exchange Interaction and T_c in Alkaline-Earth-Metal-Oxide-Based DMS without Magnetic Impurities : First Principle Pseudo-SIC and Monte Carlo Calculation(Condensed matter: electronic structure and electrical, magnetic, and optical properties)
- Database of normal human cerebral blood flow measured by SPECT : II. Quantification of I-123-IMP studies with ARG method and effects of partial volume correction
- Database of normal human cerebral blood flow measured by SPECT : I. Comparison between I-123-IMP, Tc-99m-HMPAO, and Tc-99m-ECD as referred with O-15 labeled water PET and voxel-based morphometry
- Apparent CBF decrease with normal aging due to partial volume effects : MR-based partial volume correction on CBF SPECT
- Effects of tissue heterogeneity on cerebral vascular response to acetazolamide stress measured by an I-123-IMP autoradiographic method with single-photon emission computed tomography
- Error analysis of measured cerebral vascular response to acetazolamide stress by I-123-IMP autoradiographic method with single photon emission computed tomography : Errors due to distribution volume of I-123-IMP
- Overall Water Splitting by RuO_2-dispersed Divalent-ion-doped GaN Photocatalysts with d^ Electronic Configuration
- Expression profiles of two types of human knee-joint cartilage
- evidence-based practice guideline for the treatment of chronic kidney disease
- A CASE OF FANCONI SYNDROME WITH TYPE 1 RENAL TUBULAR ACIDOSIS
- A CASE OF RENAL TRANSPLANT RECIPIENT COMPLICATED WITH CRYPTOCOCCOSIS AND AMPHOTERICIN B INDUCED ACUTE TUBULAR NECROSIS
- Activation of an estrogen/estrogen receptor signaling by BIG3 through its inhibitory effect on nuclear transport of PHB2/REA in breast cancer
- Characterization of Thermal Annealing Effects on the Evolution of Coke Carbon Structure Using Raman Spectroscopy and X-ray Diffraction
- Successional Dynamical Models on the 2-Dimensional Lattice Space
- Herpes Simplex Encephalitis
- Generalization of Ramo's Theorem and Its Application to Semiconducting Materials
- Influence of Spatially Exponential Carrier Generation on Shot Noise in Linearly Graded Junctions
- Deposition of Copper Fine Particle by Cold Spray Process
- Shot Noise in Back-Biased Step Junctions with Exponential Carrier Generation Rate
- Effect of anemia on cardiac disorders in pre-dialysis patients immediately before starting hemodialysis
- Material Design of GaN-Based Ferromagnetic Diluted Magnetic Semiconductors
- Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
- Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
- SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
- Induction of remission following a single dose of rituximab alone in a patient with minimal change nephrotic syndrome
- Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
- Long-term beneficial effects of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker therapy for patients with advanced immunoglobulin A nephropathy and impaired renal function
- Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility
- A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1
- Comparison of inhibitors of renin-angiotensin-aldosterone system (RAS) and combination therapy of steroids plus RAS inhibitors for patients with advanced immunoglobulin A nephropathy and impaired renal function