POLYMORPHIC AND TISSUE-SPECIFIC IMPRINTING OF THE HUMAN WILMS TUMOR GENE, WT1

スポンサーリンク

概要

• 論文の詳細を見る
• Japan Society of Human Geneticsの論文
• 1997-03-31

著者

• NIIKAWA Norio

  Department of Human Genetics, Nagasaki University School of Medicine

• ISHIKAWA Mutsuo

  Department of Obstetrics and Gynecology, Asahikawa Medical College

• Niikawa Norio

  Department Of Human Genetics Graduate School Of Biomedical Sciences Nagasaki University

• NISHIWAKI Kunihiko

  Department of Obstetrics and Gynecology, Asahikawa Medical College

• Ishikawa Mutsuo

  Department Of Obstetrics And Gynecology Asahikawa Medical College

• Ishikawa Mutsuo

  Department Of Laboratory Medicine Shinshu University Hospital

• Nishiwaki Kunihiko

  Department Of Obstetrics And Gynecology Asahikawa Medical College

• Ishikawa Mutsuo

  Department of Advanced Applied Electronics, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, Yokohama 226-8503, Japan

関連論文

• FISH MAPPING OF A TRANSLOCATION BREAKPOINT AT 6q21 (OR q22) IN A PATIENT WITH HETEROTAXIA
• PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese : population-based and family-based candidate gene analyses
• The IHPK1 gene is disrupted at the 3p21. 31 breakpoint of t(3 ; 9) in a family with type 2 diabetes mellitus
• A catalog of 106 single-nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-β1 (TGF-β1) and its signaling pathway
• Expression of the Snurf-Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domain
• A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome
• Phenotype-genotype correlation in two patients with 12q proximal deletion
• On the conflicting reports of imprinting status of mouse ATPIOa in the adult brain : strain-background-dependent imprinting?
• 127 Assessment of fallopian patency by transvaginal ultrasound.
• GENOMIC IMPRINTING AND ITS RELEVANCE TO GENETIC DISEASES
• Monozygotic Twins with Discordant Sexual Phenotypes due to Different Rations of Mosaicism of 47, X, idic(Y), idic(Y)/46, X, idic(Y)/45, X
• ASSIGNMENT OF THE HUMAN CONNEXIN43 GENE, GJA1, TO CHROMOSOME 6q22.3
• Contiguous Gene Syndromes as Multiple Anomalies Syndromes : Molecular Basis and Approach to Gene Cloning
• 4 Chromosome Aberration-based Positional Cloning of Cardiovascular Disease Genes(Perspectives of Genome-wide Study to Identify Genes Underlying Cardiovascular Diseases,Roundtable Discussion 10 (RT10) (M),The 70th Anniversary Annual Scientific Meeting of t
• Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest
• Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid
• Analysis of the NSD1 promoter region in patients with a Sotos syndrome phenotype
• Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family
• A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet
• Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE)
• 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
• Do monochorionic dizygotic twins increase after pregnancy by assisted reproductive technology?
• TWO POLYMORPHIC AvaI AND HhaI SITES IN A DIFFERENTIALLY METHYLATED REGION OF THE HUMAN H19 GENE
• Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation
• Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome
• POLYMORPHIC AND TISSUE-SPECIFIC IMPRINTING OF THE HUMAN WILMS TUMOR GENE, WT1
• Genetic Counseling System in Nagasaki University Hospital and Genetic Services in Nagasaki Prefecture-Now and Future
• Special Report A Genetic Counseling System in Nagasaki Prefecture: The Course and Current Status of the Genetic Counseling Unit in Nagasaki University Hospital
• Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression
• The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
• Core fucosylation of E-cadherin enhances cell-cell adhesion in human colon carcinoma WiDr cells
• The Role of Superoxide Dismutase in the Human Ovary and Fallopian Tube
• PHYSICAL MAP OF A YAC CONTIG CONTAINING THE REGION OF THE HUMAN GENE (HYRC) COMPLEMENTING HYPER-RADIOSENSITIVITY OF THE SCID MOUSE MUTATION
• Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta
• The human transcript induced in spermatogenesis 50
• IS-56 Heparin-binding Epidermal Growth Factor-like growth Factor Is an Autocrine Growth Factor Essential for the Survival of Human Luteinized Granulosa Cells
• A SacII polymorphism in the human ASCL2 (HASH2) gene region
• 207 Fundamental study of energy metabolism by P-NMR spectroscopy in perfused rabbit ovaries
• A Hhal/BstUl polymorphism in a novel gene at human chromosome 11p15.5
• Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis : Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies
• Intracrania1 Malignant Teratoma Diagnosed in a Fetus : Case Report
• Landry-Guillain-Barre-Strohl Syndrome in Pregnancy
• Growth of Epitaxial {100}-Oriented KNbO3--NaNbO3 Solid Solution Films on (100)\text{cSrRuO3$\varparallel$(100)SrTiO3 by Hydrothermal Method and Their Characterization
• Pregnancy, Labor and Delivery in a Woman with a Damaged Spinal Cord
• Growth of Epitaxial KNbO3 Thick Films by Hydrothermal Method and Their Characterization
• Fundamental Study on One-Dimensional-Array Medical Ultrasound Probe with Piezoelectric Polycrystalline Film by Hydrothermal Method: Experimental Fabrication of One-Dimensional-Array Ultrasound Probe
• Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome
• Synthesis of Nondoped Potassium Niobate Ceramics by Ultrasonic Assisted Hydrothermal Method
• Crystal Structure and Electrical Properties of {100}-Oriented Epitaxial BiCoO3–BiFeO3 Films Grown by Metalorganic Chemical Vapor Deposition
• Identification and Characterization of a Gene Encoding an ABC Transporter Expressed in the Dicarboxylic Acid-Producing Yeast Candida maltosa
• A 15-Year-Old Girl with Pubertal Masculinization due to Bilateral Gonadoblastoma and 45,X/46,X,+Mar Karyotype.

もっと見る 閉じる

スポンサーリンク