Search Results1-7 of  7

  • HIGASHIMOTO Ken ID: 1000030346887

    Articles in CiNii:7

    • ゲノムインプリンティングと疾患発症機序の解明-Beckwith-Wiedemann 症候群 (2000)
    • Genomic Imprinting and Beckwith-Wiedemann Syndrome (2008)
    • Beckwith-Wiedemann症候群の分子遺伝学 (特集 ウイルムス腫瘍と奇形症候群--形態形成と腫瘍化の接点) (2004)
  • HIGASHIMOTO Ken ID: 9000000412083

    Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University (2009 from CiNii)

    Articles in CiNii:7

    • A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilm's Tumors^1 (2000)
    • Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene (2000)
    • An NsiI RFLP in the human long QT intronic transcript 1 (LIT1) (2000)
  • HIGASHIMOTO Ken ID: 9000256644031

    Division of Molecular Genetics & Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University (2008 from CiNii)

    Articles in CiNii:1

    • Genomic Imprinting and Beckwith-Wiedemann Syndrome (2008)
  • HIGASHIMOTO Ken ID: 9000259322403

    Division of Molecular Genetics and Epigenetics, Department of Biumolecular Sciences, Saga University (2013 from CiNii)

    Articles in CiNii:1

    • Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15 : Few clinical features suggestive of Beckwith-Wiedemann syndrome (2013)
  • HIGASHIMOTO Ken ID: 9000262363541

    Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University (2013 from CiNii)

    Articles in CiNii:1

    • Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders (2013)
  • HIGASHIMOTO Ken ID: 9000370747255

    Division of Molecular Genetics & Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University (2017 from CiNii)

    Articles in CiNii:1

    • Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan (2017)
  • Higashimoto Ken ID: 9000253180385

    Department of Biochemistry and Department of Surgery, Saga Medical School (2000 from CiNii)

    Articles in CiNii:1

    • A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors. (2000)
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