Search Results1-8 of  8

  • ISEKI Hiroyoshi ID: 9000329426692

    Articles in CiNii:1

    • Generation of CRISPR/Cas9-mediated bicistronic knock-in ins1-cre driver mice (2016)
  • Iseki Hiroyoshi ID: 9000403879486

    Articles in CiNii:1

    • Generation of CRISPR/Cas9-mediated bicistronic knock-in ins1-cre driver mice (2016)
  • ISEKI Hiroyoshi ID: 9000000343759

    西宮中央市民病院耳鼻咽喉科 (1998 from CiNii)

    Articles in CiNii:2

    • A Case of Bilateral Agenesis of the Internal Carotid Artery Associated with Dizziness (1997)
    • A Clinical study of Lipo-Prostaglandin E_1(Palux^<【○!R】>)for Sudden Deafness (1998)
  • ISEKI Hiroyoshi ID: 9000000775354

    Department of Otolaryngology, Osaka University Medical School (1996 from CiNii)

    Articles in CiNii:2

    • Analysis of Equilibrium Function in Cochlear Implant Patients (1995)
    • Results of Handicap Inventory in Vestibular Neurectomy Cases (1996)
  • ISEKI Hiroyoshi ID: 9000001808463

    Laboratory Animal Resource Center, University of Tsukuba (2006 from CiNii)

    Articles in CiNii:1

    • Development of ELISA Using Recombinant Antigens for Specific Detection of Mouse Parvovirus Infection (2006)
  • ISEKI Hiroyoshi ID: 9000017478809

    Department of Digestive Surgery, Research Center for Genomic Medicine, Saitama Medical University (2010 from CiNii)

    Articles in CiNii:1

    • Human Arm protein lost in epithelial cancers, on chromosome X 1 (ALEX1) gene is transcriptionally regulated by CREB and Wnt/β-catenin signaling (2010)
  • Iseki Hiroyoshi ID: 9000391659676

    Laborarory Animal Resource Center, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan|International Institute for Integrative Sleep Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan (2016 from CiNii)

    Articles in CiNii:1

    • Generation of CRISPR/Cas9-mediated bicistronic knock-in <i>ins1-cre</i> driver mice (2016)
  • Iseki Hiroyoshi ID: 9000403316305

    Articles in CiNii:1

    • Exome sequencing of senescence-accelerated mice (SAM) reveals deleterious mutations in degenerative disease-causing genes (2013)
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