Search Results1-20 of  44

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  • Eiji Nanba ID: 9000006881240

    Articles in CiNii:1

    • Variations in Clinical Findings of Patients with Identical Tuberous Sclerosis Gene Mutations (2009)
  • Eiji Nanba ID: 9000403952879

    Articles in CiNii:1

    • Oxytocin for Male Subjects with Autism Spectrum Disorder and Comorbid Intellectual Disabilities: A Randomized Pilot Study (2016)
  • NANBA EIJI ID: 9000001974336

    Gene Research Center, Tottori University (2007 from CiNii)

    Articles in CiNii:1

    • Variation analysis of β_3-adrenergic receptor and melanocortin-4 receptor genes in childhood obesity (2007)
  • NANBA Eiji ID: 9000000380069

    the Gene Research Center,Tottri University (1999 from CiNii)

    Articles in CiNii:1

    • Analysis of the CAG Repeat Number in a patient with Huntington's Disease (1999)
  • NANBA Eiji ID: 9000000450214

    the Division of Child Neurology, Institute of Neurological Sciences (1995 from CiNii)

    Articles in CiNii:1

    • Hereditary Non-Progressive Torsion Dystonia with Intellectual disturbance (1995)
  • NANBA Eiji ID: 9000000605564

    Gene Reserch Center, Tottori University (2000 from CiNii)

    Articles in CiNii:1

    • Serum-Soluble c-Kit Levels During Mobilization of Peripheral Blood Stem Cells Correlate With Stem Cell Yield (2000)
  • NANBA Eiji ID: 9000000607716

    Gene Research Center, Tottori University (2001 from CiNii)

    Articles in CiNii:2

    • Increased expression of β-hexosaminidase α chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I (1998)
    • Galactonojirimycin derivatives restore mutant human β-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouse (2001)
  • NANBA Eiji ID: 9000000928938

    Gene Research Center, Tottori University (2000 from CiNii)

    Articles in CiNii:1

    • Congenital myotonic dystrophy : report of paternal transmission (2000)
  • NANBA Eiji ID: 9000001077732

    Gene Research Center, Tottori University (2000 from CiNii)

    Articles in CiNii:1

    • Two deletion mutations in the hydroxymethylbilane synthase gene in two unrelated Japanese patients with acute intermittent porphyria (2000)
  • NANBA Eiji ID: 9000001153089

    Gene Research Center, Tottori University (2001 from CiNii)

    Articles in CiNii:1

    • Absence of mutations in the β-catenin and adenomatous polyposis coli genes in papillary and follicular thyroid carcinomas (2001)
  • NANBA Eiji ID: 9000001879776

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2006 from CiNii)

    Articles in CiNii:1

    • Characteristic findings of auditory brainstem response and otoacoustic emission in the Bronx waltzer mouse (2006)
  • NANBA Eiji ID: 9000001891234

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2006 from CiNii)

    Articles in CiNii:1

    • Fibroblast screening for chaperone therapy in β-galactosidosis (2006)
  • NANBA Eiji ID: 9000001964798

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2010 from CiNii)

    Articles in CiNii:6

    • No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population (2005)
    • No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population (2007)
    • Serotonin transporter gene promoter polymorphism and autism : A family-based genetic association study in Japanese population (2006)
  • NANBA Eiji ID: 9000014170252

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2007 from CiNii)

    Articles in CiNii:1

    • Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome (2007)
  • NANBA Eiji ID: 9000016400147

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2008 from CiNii)

    Articles in CiNii:1

    • A case of galactosialidosis with a homozygous Q49R point mutation (2008)
  • NANBA Eiji ID: 9000017385222

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2009 from CiNii)

    Articles in CiNii:1

    • Intracerebral cell transplantation therapy for murine GM1 gangliosidosis (2009)
  • NANBA Eiji ID: 9000018485067

    Articles in CiNii:1

    • Angiotensinogen Gene Variation and Hypertension in a Cohort Study in Japanese (2001)
  • NANBA Eiji ID: 9000021686928

    Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University (2009 from CiNii)

    Articles in CiNii:1

    • Aberrant promoter methylation and expression of the imprinted PEG3 gene in glioma (2009)
  • NANBA Eiji ID: 9000252900259

    Division of Inherited Metabolic Disease, National Institute of Neuroscience, National Center of Neurology and Psychiatry (1987 from CiNii)

    Articles in CiNii:1

    • Galactosialidosis:Studies on Residual Enzymes in Early and Late Onset Clinical Phenotypes (1987)
  • NANBA Eiji ID: 9000410489133

    Research Strategy Division, Organization for Research Initiative and Promotion, Tottori University (2020 from CiNii)

    Articles in CiNii:1

    • Autophagy induction on impaired spermatogenesis of xeroderma pigmentosum group A gene-deficient mice (2020)
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