The human caspase-activated DNase gene (hCAD) : genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 1999-11-01
著者
-
INAZAWA Johji
Department of Molecular Cytogenetics, Medical Research Institute and School of Biomedical Science, T
-
SUGIMOTO Nana
Department of Molecular Cytogenetics, Division of Genetics, Medical Research Institute, Tokyo Medica
-
FUKUDA Yoji
Department of Molecular Cytogenetics, Division of Genetics, Medical Research Institute, Tokyo Medica
-
KAMIYAMA Ryuichi
School of Allied Health Science, Faculty of Medicine, Tokyo Medical and Dental University
-
Inazawa J
Department Of Molecular Cytogenetics Medical Research Institute Tokyo Medical And Dental University
-
Inazawa Johji
Department Of Molecular Cytogenetics Medical Research Institute And School Of Biomedical Science Tok
-
Inazawa Johji
Department Of Hygiene Kyoto Prefectural University Of Medicine
-
Inazawa Johji
Department Of Molecular Cytogenetics Medical Research Institute And School Of Biomedical Science
-
Nakagawara Akira
Division Of Biochemistry Chiba Cancer Center Research Institute
-
SAITO-OHARA Fumiko
Department of Cytogenetics Medical Research Institute, Tokyo medical and Detal University
-
NAGATA Shigekazu
Department of Genetics, Osaka University Medical School
-
Nagata Shigekazu
Department Of Genetics Osaka University Medical School
-
Saito-ohara Fumiko
Department Of Cytogenetics Medical Research Institute Tokyo Medical And Dental University
-
Saito-ohara Fumiko
Department Of Molecular Cytogenetics Division Of Genetics Medical Research Institute Tokyo Medical A
-
Fukuda Yohji
Department Of Molecular Cytogenetics Medical Research Institute Tokyo Medical And Dental University
-
Fukuda Yoji
Human Genome Center Institute Of Medical Science The University Of Tokyo
-
Sugimoto N
Department Of Molecular Cytogenetics Division Of Genetics Medical Research Institute Tokyo Medical A
-
MUKAE Naomi
Department of Genetics, Osaka University Medical School
-
Mukae Naomi
Department Of Genetics Osaka University Medical School
-
Inoue Jun
Department Of Molecular Cytogenetics Medical Research Institute And School Of Biomedical Science Tok
-
Fukuda Yoji
Department Of Molecular Cytogenetics Medical Research Institute Tokyo Medical And Dental University
-
Kamiyama Ryuichi
School Of Allied Health Science Faculty Of Medicine Tokyo Medical And Dental University
-
Fukuda Yoji
Department Of Molecular Cytogenetics Division Of Genetics Medical Research Institute Tokyo Medical A
-
Nakagawara Akira
Division Of Biochemistry Chiba Cancer Center
-
Inazawa Johji
Department Of Molecular Cytogenetics Tokyo Medical And Dental University
-
Nakagawara Akira
Division Of Biochemistry And Innovative Cancer Therapeutics Chiba Cancer Center Research Institute
関連論文
- Overexpressed Skp2 within 5p amplification detected by array-based comparative genomic hybridization is associated with poor prognosis of glioblastomas
- Array-based comparative genomic hybridization analysis of high-grade neuroendocrine tumors of the lung
- Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines
- IQGAP1, a negative regulator of cell-cell adhesion, is upregulated by gene amplification at 15q26 in gastric cancer cell lines HSC39 and 40A
- Genome-wide array-based comparative genomic hybridization analysis of pancreatic adenocarcinoma : Identification of genetic indicators that predict patient outcome
- Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization
- Oxidation Resistance of Cr-N-O Thin Films Prepared by Pulsed Laser Deposition
- Increased Apoptosis Rate by Hyperthermochemoradiotherapy for Advanced Rectal Cancers
- Cloning and Sequencing of Mouse Complementary DNA for Heme Oxygenase-2
- Philadelphia chromosome-negative cells with trisomy 8 after busulfan and interferon treatment of Ph^1-positive chronic myelogenous leukemia
- Genomic Structure and Mapping of Human Orphan Receptor LXR Alpha : Upregulation of LXRa mRNA During Monocyte to Macrophage Differentiation
- Induction of cell death by chimeric L-selectin-Fas receptors
- ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array-based comparative genomic hybridization
- Determination of a Common Clonal Origin of Gastric and Pulmonary Mucosa-Associated Lymphoid Tissue Lymphomas Presenting Five Years Apart
- Multiple Primary Cancers with Microsatellite Instability: Report of a Case
- Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous-cell carcinoma
- PIK3CA mutation is an oncogenic aberration at advanced stages of oral squamous cell carcinoma
- Detection of Numerical alterations of Chromosomes 3,7,17 and X in Low-grade Intracystic Papillary Tumors of the Breast by Multi-color Fluorescence In Situ Hybridization
- Human N-Acetylglucosamine-6-O-Sulfotransferase Involved in the Biosynthesis of 6-Sulfo Sialy Lewis X : Molecular Cioning, Chromosomal Mapping, and Expreeion in Various Organs and Tumor Cells
- Skp2 overexpression is a p27^-independent predictor of poor prognosis in patients with biliary tract cancers
- Therapeutic effect of an anti-Fas ligand mAb on lethal graft-versus-host disease
- 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
- Oxidation Resistance of Cr-N-O Thin Films Prepared by Pulsed Laser Deposition
- Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
- Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
- Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene
- Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1 ; 19)(q23 ; p13)
- MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas
- Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines : Possible Involvement of the ATF3 and CENPF Genes in the 1q32 Amplicon
- Identification of brain-specific splicing variants of the hDLG1 gene and altered splicing in neuroblastoma cell lines
- SOCS-1 suppresses TNF-α-induced apoptosis through the regulation of Jak activation
- Successful Imatinib Treatment of Cardiac Involvement of FIP1L1-PDGFRA-Positive Chronic Eosinophilic Leukemia Followed by Severe Hepatotoxicity
- Activation of B-Myb by E2F1 in hepatocellular carcinoma
- Association of over-expressed TFDP1 with progression of hepatocellular carcinomas
- Multi-color FISH : Application to the Simultaneous Detection of Chromosome Aberrations in Neuro-epithelial Tumor Cell Lines
- Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta
- Allelic Loss of the Region of Chromosome 1p35-pter Is Associated with Progression of Human Gastric Carcinoma
- A novel human gene whose product shares significant homology with the bovine brain-specific protein p25 on chromosome 5p15.3
- Isolation, tissue expression, and chromosomal assignment of a novel human gene which encodes a protein with RING finger motif
- Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)
- Isolation, tissue expression, and chromosomal assignment of human RGS5, a novel G-protein signaling regulator gene
- P73 : Structure and function
- The c-Jun NH_2-terminal kinase3 (JNK3) gene : genomic structure, chromosomal assignment, and loss of expression in brain tumors
- Plasma midkine level is a prognostic factor for human neuroblastoma
- Genomic structure and chromosomal localization of the gene encoding TRAX, a Translin-associated factor X
- A Novel Amplicon at 9p23-24 in Squamous Cell Carcinoma of the Esophagus That Lies Proximal to GASC1 and Harbors NFIB
- Induction of mcl1/EAT, Bcl-2 Related Gene, by Retinoic Acid or Heat Shock in the Human Embryonal Carcinoma Cells, NCR-G3
- Clinicopathological relevance of UbcH10 in breast cancer
- Molecular Cytogenetic Analysis of 17 Renal Cancer Cell Lines: Increased Copy Number at 5q31-33 in Cell Lines from Nonpapillary Carcinomas
- Genetic or epigenetic silencing of low density lipoprotein receptor-related protein 1B expression in oral squamous cell carcinoma
- Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes
- CARCINOEMBRYONIC ANTIGEN (CEA) FAMILY GENES ARE LOCATED ON HUMAN CHROMOSOME 19 AT BAND q13.2 (In situ Hybridization III. : Application for Medical Investigation)
- Human arylhydrocarbon receptor repressor (AHRR) gene : genomic structure and analysis of polymorphism in endometriosis
- The human caspase-activated DNase gene (hCAD) : genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus
- Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hubridzation
- Molecular Cloning and Genomic Analysis of Mouse Glucuronyltransferase Involved in Biosynthesis of the HNK-1 Epitope
- Identification of novel cancer-related genes through genomic and epigenomic analyses of gastrointestinal cancer
- Translocation (1 ; 22)(p36 ; q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor
- Identification of PAK4 as a putative target gene for amplification within 19q13.12-q13.2 in oral squamous-cell carcinoma
- Identification of the breakpoint of inv(X) with severe mental, neural and muscle disease
- Genome-wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage
- Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes
- GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines
- REEXAMINATION OF CHROMOSOMAL LOCI OF HUMAN MUSCLE ACTIN GENES BY FLUORESCENCE IN SITU HYBRIDIZATION
- Human Gene for β-Microseminoprotein: Its Promoter Structure and Chromosomal Localization^1
- Polycomb group molecule PHC3 regulates polycomb complex composition and prognosis of osteosarcoma
- Thoracic paravertebral ganglioneuroma with high immunohistochemical expression of TrkA
- Overexpression of DA41 in v-Ha-ras-3Y1 Cells Causes Growth Suppression
- Molecular cloning and expression analysis of the human DA41 gene and its mapping to chromosome 9q21.2-q21.3
- Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
- ASSIGNMENT OF THE HUMAN GENE FOR KBF2/RBP-Jk TO CHROMOSOME 9p12-13 AND 9q13 BY FLUORESCENCE IN SITU HYBRIDIZATION
- HIGH-RESOLUTION CHROMOSOME R-BANDING IN LYMPHOBLASTOID CELL LINES BY THE COMBINED USE OF CELL SYNCHRONIZATION AND ETHIDIUM BROMIDE TREATMENT
- Reconfirmation of a previously reported de novo case of partial 7q trisomy by means of whole chromosome painting
- Down-regulation of SKP2 induces apoptosis in lunq-cancer cells
- Molecular mechanism of apoptotic cell death
- Fas-induced Apoptosis
- Dermokine as a novel biomarker for early-stage colorectal cancer
- Human autoimmune lymphoproliferative syndrome, a defect in the apoptosis-inducing Fas receptor : A lesson from the mouse model
- Identification of charcoal in Quaternary sediments and estimation of the charred temperature by reflectance measurements and H / C ratio analysis and observation through reflectance and scanning electron microscopy
- p73, a sophisticated p53 family member in the cancer world
- Bmi1 regulates cell fate via tumor suppressor WWOX repression in small-cell lung cancer cells
- Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation
- Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
- HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome
- Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
- Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation
- Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia
- Molecular and genetic bases of neuroblastoma
- Molecular Cloning and Genomic Analysis of Mouse Glucuronyltransferase Involved in Biosynthesis of the HNK-1 Epitope.
- Human N-Acetylglucosamine-6-O-Sulfotransferase Involved in the Biosynthesis of 6-Sulfo Sialyl Lewis X: Molecular Cloning, Chromosomal Mapping, and Expression in Various Organs and Tumor Cells.