Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2001-01-01
著者
-
Muto Tetsuichiro
Department Of Surgical Oncology The University Of Tokyo
-
Nagawa Hirokazu
Department Of Surgery Faculty Of Medicine University Of Tokyo
-
Nakamura Yusuke
Laboratory For Molecular Medicine Human Genome Center The Institute Of Medical Science University Of
-
Muto Tetsuichiro
Department Of Gastroenterological Surgery Cancer Institute Hospital
-
Kyo Kennoki
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
-
Lathrop G.
Centre National De Genotypage
-
Nagawa Hirokazu
Department Of Surgery Division Of Surgical Oncology University Of Tokyo
-
Nakamura Yusuke
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
-
Nakamura Yusuke
Laboratory For Genotyping Riken Snp Research Center C/o Riken Yokohama Institute
-
Muto Tetsuichiro
Department Of First Surgery Faculty Of Medicine University Of Tokyo
関連論文
- OE-071 A Genom-Wide Association Study of SNPs in the risk of Atherosclerosis Obliterans(Heart failure, clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
- A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
- Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
- High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the 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
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- Japanese single nucleotide polymorphism database for 267 possible drug-related genes
- 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
- 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
- Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferases
- Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin
- EphA4 receptor, overexpressed in pancreatic ductal adenocarcinoma, promotes cancer cell growth
- Novel tumor marker REG4 detected in serum of patients with resectable pancreatic cancer and feasibility for antibody therapy targeting REG4
- High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis
- Identification of C2orf18, termed ANT2BP (ANT2-binding protein), as one of the key molecules involved in pancreatic carcinogenesis
- Over-expression of cysteine proteinase inhibitor cystatin 6 promotes pancreatic cancer growth
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
- Variations in the FTO gene are associated with severe obesity in the Japanese
- 1P-044 DNAメチル化維持を仲介するSRAドメインのヘミメチル化DNA認識について熱力学的解析(蛋白質・構造機能相関(1),第46回日本生物物理学会年会)
- Targeting Id1 and Id3 inhibits peritoneal metastasis of gastric cancer
- Cholesterol Granuloma of the Breast Mimicking Carcinoma : Report of a Case
- Decreased Synthesis of Matrix Metalloproteinase-7 and Adhesion to the Extracellular Matrix Proteins of Human Colon Cancer Cells Treated with Troglitazone
- FISH MAPPING OF A TRANSLOCATION BREAKPOINT AT 6q21 (OR q22) IN A PATIENT WITH HETEROTAXIA
- Prediction of Sensitivity to STI571 among Chronic Myeloid Leukemia Patients by Genome-wide cDNA Microarray Analysis
- Microarray Analysis of Gene-expression Profiles in Diffuse Large B-cell Lymphoma : Identification of Genes Related to Disease Progression
- Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines
- Isolation of a Novel Gene Showing Reduced Expression in Metastatic Colorectal Carcinoma Cell Lines and Carcinomas
- Distinct pattern of gene expression in pyothorax-associated lymphoma (PAL), a lymphoma developing in long-standing inflammation
- Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1
- Correlation of Allelic Loss with Poor Postoperative Survival in Breast Cancer
- 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
- Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
- Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP)
- A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
- U-shaped Effect of Drinking and Linear Effect of Smoking on Risk for Stomach Cancer in Japan
- Effect of Age on the Relationship between Gastric Cancer and Helicobacter pylori
- Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
- Critical roles of T-LAK cell-originated protein kinase in cytokinesis
- Involvement of kinesin family member 2C/mitotic centromere-associated kinesin overexpression in mammary carcinogenesis
- Enhanced SMYD3 expression is essential for the growth of breast cancer cells
- Identification of Rad51 alteration in patients with bilateral breast cancer
- Multiplex Mutation Screening of the BRCA1 Gene in 1000 Japanese Breast Cancers
- Infrequent Mutation of the H-Cadherin Gene on Chromosome 16q24 in Human Breast Cancers
- Non-transmissible Sendai virus encoding granulocyte macrophage colony-stimulating factor is a novel and potent vector system for producing autologous tumor vaccines
- 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
- Pouchitis atlas for objective endoscopic diagnosis
- 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
- Guidelines for genetic testing
- Identification of candidate predictive markers of anticancer drug sensitivity using a panel of human cancer cell lines
- Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genes
- Significance of Thymidine Phosphorylase/Platelet-derived Endothelial Cell Growth Factor in Carcinoma of the Papilla of Vater
- Giant Solid Cystic Tumor of the Pancreas with a Fibrous Septum Caused by Extracapsular Growth in Middle-Aged Woman : Report of a Case
- A scoring system for the assessment of the risk of mortality after partial hepatectomy in patients with chronic liver dysfunction
- A new scoring system to classify patients with colorectal liver metastases : proposal of criteria to select candidates for hepatic resection
- Not Infrequent K-ras Mutations in Depressed-type Early Colorectal Carinomas Larger than 10 mm
- Histogenesis and morphogenesis of depressed-type early colorectal carcinoma
- Effect of a selective thromboxane A_2 synthetase inhibitor on the systemic changes induced by circulating pancreatic phospholipase A_2
- Bcl-X_L Antisense Sensitizes Human Colon Cancer Cell Line to 5-Fluorouracil
- Primary malignant melanoma of the esophagus treated by esophagectomy and adjuvant dendritic-cell therapy
- Vaccination with autologous endothelium inhibits angiogenesis and metastasis of colon cancer through autoimmunity
- Expression of platelet-derived endothelial cell growth factor in inflammatory bowel disease
- Chronic Active Disease Reflects Cancer Risk in Ulcerative Colitis
- Preoperative Grading System for Predicting Operative Conditions in Laparoscopic Cholecystectomy
- Minilaparotomy Approach to Colon Cancer
- Impact of a Clinical Pathway and Standardization of Treatment for Acute Appendicitis
- Chemoradiotherapy for rectal cancer : current status and perspectives
- Inhibitory Effect of ATF3 Antisense Oligonucleotide on Ectopic Growth of HT29 Human Colon Cancer Cells
- Analysis of Novel Metastasis-associated Gene TI-227
- Intraperitoneal administration of paclitaxel solubilized with poly(2-methacryloxyethyl phosphorylcholine-co n-butyl methacrylate) for peritoneal dissemination of gastric cancer
- Crohn's disease with life-threatening hemorrhage from terminal ileum : successful control by superselective arterial embolization
- Solitary Splenic Metastasis from Early Gastric Cancer : Report of a Case
- Solitary Nodal Recurrence in the Dorsal Area of the Thoracic Aorta After a Curative Resection of Esophageal Cancer : Report of Two Cases
- Massive postoperative polyuria following total gastrectomy for gastric cancer
- Successfully treated idiopathic rectosigmoid perforation 7 years after renal transplantation
- Microsatellite Instability of Colorectal Cancer and Adenoma in Synchronous Multiple Colorectal Cancer Patients with Associated Extracolonic Malignancies
- Superficial depressed early carcinoma that developed into protuberant advanced carcinoma in the transverse colon
- Functional expression of β1 and β2 integrins on tumor infiltrating lymphocytes (TILs) in colorectal cancer
- Correlation of the Therapeutic Effect of Activated Tumor - Draining Lymph Node Cells with Specific Interferon-γ Production In Vitro
- Early appendiceal adenocarcinoma. A review of the literature with special reference to optimal surgical procedures
- Adiponectin receptors are downregulated in human gastric cancer
- Exposure and Dissection of the Root of the Right Gastric Artery During Gastric Surgery
- Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease
- SURVEILLANCE COLONOSCOPY FOR COLITIC CANCER IN INFLAMMATORY BOWEL DISEASE
- Intratumoral injection of interleukin-2 augments the local and abscopal effects of radiotherapy in murine rectal cancer