A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilm's Tumors^1
スポンサーリンク
概要
- 論文の詳細を見る
- Japanese Biochemical Societyの論文
- 2000-11-01
著者
-
KANEKO Yasuhiko
Departments of Cancer Chemotherapy and Medicine, Saitama Cancer Center Hospital
-
SOEJIMA Hidenobu
Department of Pathology, University of Otago Medical School
-
HATA Jun-ichi
Department of Pathology, School of Medicine, Keio University
-
JINNO Yoshihiro
Department of Molecular Biology, Ryukyu University School of Medicine
-
HIGASHIMOTO Ken
Department of Biomolecular Sciences, Division of Molecular Biology and Genetics, Faculty of Medicine
-
MUKAI Tsunehiro
Department of Biomolecular Sciences, Division of Molecular Biology and Genetics, Faculty of Medicine
-
Mukai Tsunehiro
Saga University The Administration Office
-
Mukai T
Saga Medical School Saga
-
Mukai Tsunehiro
Department Of Biomolecular Sciences Saga Medical School
-
Higashimoto Ken
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
-
Soejima H
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
-
Soejima Hidenobu
Department Of Pathology University Of Otago Medical School
-
Ishino F
東海大学 健康科学部
-
Kaneko Yasuhiko
Department Of Cancer Chemotherapy Saitama Cancer Center Hospital
-
ZHU Xike
Department of Biomedical Research, University of Texas Health Center at Tyler
-
Zhu Xike
Department Of Biochemistry Saga Medical School
-
Hata Jun-ichi
Department Of Chemical Science And Engineering Graduate School Of Engineering Science Osaka Universi
-
YATSUKI Hitomi
Department of Biochemistry, Saga Medical School
-
MASAKI Zenjiro
Division of Urology Department of Surgery Saga Medical School
-
SATOH Yuji
Division of Molecular Biology and Genetics, Department of Biomolecular Sciences
-
XIN Zhenghan
Department of Biochemistry, Saga Medical School
-
SATOR Yuji
Department of Biochemistry, Saga Medical School
-
FUKUZAWA Ryuji
Department of Pathology, Keio University School of Medicine
-
Sator Yuji
Division Of Molecular Biology And Genetics Department Of Biomolecular Sciences
-
Yatsuki H
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
-
Yatsuki Hitomi
Department Of Biochemistry Saga Medical School
-
Jinno Y
Department Of Molecular Biology Ryukyu University School Of Medicine
-
Jinno Yoshihiro
Department Of Human Genetics Nagasaki University School Of Medicine
-
Fukuzawa Ryuji
Department Of Pathology Keio University School Of Medicine
-
Xin Zhenghan
Department Of Biochemistry Saga Medical School
-
Soejima Hidenobu
Department Of Biomolecular Sciences Faculty Of Medicine Saga University
-
MASAKI Zenjiro
Division of Urology, Department of Surgery, Saga Medical School
-
Hata Jun-ichi
Department of Chemical Engineering, Faculty of Engineering Science, Osaka University
-
Mukai Tsunehiro
Department of Biochemistry and Department of Surgery, Saga Medical School
関連論文
- Frequent Increase of DNA Copy Number in the 2q24 Chromosomal Region and Its Association with a Poor Clinical Outcome in Hepatoblastoma : Cytogenetic and Comparative Genomic Hybridization Analysis
- In situ detection of insulin-like growth factor II (IGF2) and H19 gene expression in hepatocellular carcinoma
- Altered cellular immunity in transgenic mice with T cell-specific expression of human D4-guanine diphosphate-dissociation inhibitor (D4-GDI)
- DIOXINS IN BILE IN RELATION TO THOSE IN THE HUMAN LIVER AND BLOOD
- Malignant fibrous histiocytoma of the cecum : Report of a case and review of the literature
- Gastric Carcinoma with Lymphoid Stroma : Clinicopathological Studies of Four Cases
- Tissue specificity of methylation and expression of human genes coding for neuropeptides and their receptors, and of a human endogenous retrovirus K family
- Isolation and localization of an IDDMK1,2-22-related human endogenous retroviral gene, and identification of a CA repeat marker at its locus
- THE GROWTH HORMONE RECEPTOR GENE MUTATION OF A JAPANESE PATIENT WITH LARON SYNDROME
- TWO POLYMORPHIC AvaI AND HhaI SITES IN A DIFFERENTIALLY METHYLATED REGION OF THE HUMAN H19 GENE
- Expression of bone marrow stromal cell specific antigen during murine development : Its expression in embryonic hematopoietic tissues as well as in other developing tissues
- Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers
- Clinical and Genetic Characterisitics of Japanese Burkitt Lymphomas with or without Leukemic Presentation
- Elevated Level of Plasma Basic Fibroblast Growth Factor in Multiple Myeloma Correlates with Increased Disease Activity
- Expression of MEF2 Genes during Human Cardiac Development
- A 35-year-old Man with Cerebral Hemorrhage and Pheochromocytoma : The Second Brain-dead Organ Donor in Japan
- Establishment of a Human Cell Line Secreting Neuron-specific Enolase from a Primitive Neuroectodermal Tumor of the Retroperitoneal Cavity
- Lipoma of the Stomach : A case report
- "Cloacogenic Carcinoma" of the Anorectal Junction : Light and Electron Microscopic Study of a Case
- Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1 ; 19)(q23 ; p13)
- Mouse Mef2b Gene: Unique Member of MEF2 Gene Family
- Expression and Imprinting Status of Human PEG8/IGF2AS, a Paternally Expressed Antisense Transcript from the IGF2 Locus, in Wilms'Tumors^1
- Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta
- Growth and Functional Behavior Neuroblastomas in Man and Nude Mice
- A case of generalized Hailey-Hailey disease with fatal liver injury
- A SacII polymorphism in the human ASCL2 (HASH2) gene region
- A Case of Aortoduodenal Fistula Occurring after Surgery and Radiation for Pancreatic Cancer
- Primary carcinoid tumor in a polycystic kidney
- The aged thymus shows normal recruitment of lymphohematopoietic progenitors but has defects in thymic epithelial cells
- An HIV Autopsy : Characterization of Zidovudine-resistant Subtype E HIV-1 from Autopsy Tissue Suggests the Route of Infection and an Alternative Protocol of Therapy
- Induction of mcl1/EAT, Bcl-2 Related Gene, by Retinoic Acid or Heat Shock in the Human Embryonal Carcinoma Cells, NCR-G3
- MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products
- The Essential Role of Histone H3 Lys9 Di-Methylation and MeCP2 Binding in MGMT Silencing with Poor DNA Methylation of the Promoter CpG Island
- The First Exon of the Rat Aldolase C Gene Is Essential for Restoring the Chromatin Structure in Transgenic Mice
- Copy-Dependent and Position-Independent Expression of Rat Aldolase A Gene^1
- Reduction in Carbon Dioxide Emission, and Enhancement of Cell Yield by Control of Light Intensity in Photomixotrophic Batch Culture of Marchantia polymorpha
- Photoautotrophic Cultures of the Host and Transformed Cells of Marchantia polymorpha under Controlled Incident Light Intensity
- Evaluation of Carbohydrate Utilization and Photosynthetic Carbon Dioxide Fixation in Photomixotrophic Culture of Marchantia polymorpha
- Elastofibroma : A Case Report and Review of the Literature
- Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes
- IS038 New mutations of FBN1 gene found in Japanese patients with Marfan syndrome
- Structures of cDNAs Encoding the Muscle-Type and Non-Muscle-Type Isozymes of Lamprey Fructose Bisphosphate Aldolases and the Evolution of Aldolase Genes
- Responsiveness of chemotherapy based on the histological type and Wilms' tumor suppressor gene mutation in bilateral Wilms' tumor
- Apoptosis of Human Embryonal Carcinoma Cells with in vitro Differentiation
- Molecular Analysis of Ewing's Sarcoma: Another Fusion Gene, EWS-E1AF, Available for Diagnosis
- Expression of EAT, an anti-apoptotic gene, in murine embryogenesis and human development
- EAT/mcl-1, a Member of the bcl-2 Related Genes, Confers Resistance to Apoptosis Induced by cis-Diammine Dichloroplatinum (II) via a p53-Independent Pathway
- B-36 Localization of EAT, a Differentiation and Apoptosis-Related Gene, in Adult and Fetal Tissue : A Study using a Newly Established Monoclonal Antibody
- Fibromuscular Dysplasia : A Histopathological Study
- Significance of hematoma size for evaluating the grade of blunt renal trauma
- Significant Reduction of WT1 Gene Expression, Possibly Due to Epigenetic Alteration in Wilms' Tumor
- A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilm's Tumors^1
- IN SITU PERFUSION BY RETROGRADE CANNULATION OF A TUMOR ARTERY FOR NEPHRON-SPARING SURGERY
- A Hhal/BstUl polymorphism in a novel gene at human chromosome 11p15.5
- Search for active endogenous retroviruses: identification and characterization of a HERV-E gene that is expressed in the pancreas and thyroid
- Primary carcinosarcoma of the vagina
- Antisense Transcription Occurs at the Promoter of a Mouse Imprinted Gene, Commd1, on the Repressed Paternal Allele
- An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)
- Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene
- Identification of a novel isoform of Murr1 transcript, U2mu, which is transcribed from the portions of two closely located but oppositely oriented genes
- A Case of Poorly Differentiated Hilar Lung Adenocarcinoma of an Unidentified Histological Type
- Identification of nonsynonymous polymorphisms in the superantigen-coding region of IDDMK_ 22 and a pilot study on the association between IDDMK_ 22 and type 1 diabetes
- Evaluation of Spirulina platensis Growth Considering Light Intensity Distribution in Photoautotrophic Batch Culture
- Simple and Rapid Method for Detection of Apoptotic Cells by Flow Cytometry
- Expression of Gap-Junctional Protein (Connexin 43 or α1 Gap Junction) is Down-Regulated at the Transcriptional Level during Adipocyte Differentiation of H-1/A Marrow Stromal Cells
- Abnormalities of the FHIT Transcripts in Osteosarcoma and Ewing Sarcoma
- Organotypic culture of human bone marrow adipose tissue
- Expression and Imprinting Status of Human PEG8/IGF2AS, a Patemally Expressed Antisense Transcript from the IGF2 Locus, in Wilms' Tumors.
- A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors.
- Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15 : Few clinical features suggestive of Beckwith-Wiedemann syndrome
- Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders