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Myelination in cultured rat peripheral nerve inducted mutant Po c DNA.

Research Project

Project/Area Number 11670773
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionSchool of Health Sciences, Sapporo Medical University

Principal Investigator

TACHI Nobutada  School of Health Sciences, Sapporo Medical University., 保健医療学部, 助教授 (80136944)

Co-Investigator(Kenkyū-buntansha) KOZUKA Naoki  School of Health Sciences, Sapporo Medical University, 保健医療学部, 助教授 (90225459)
NINOMIYA Tahafumi  Department of Anatomy, Schhol of Medicine, Sapporo Medical University, 医学部, 講師 (80156140)
YAMASITA Tosihara  Department of Dermatology, School of Medicine, Sapporo Medical University., 医学部, 講師 (50167706)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1999: ¥2,500,000 (Direct Cost: ¥2,500,000)
KeywordsMutated Po cDNA / constructed adenovirus vector / myelination / 変異Po cDNA / ラツト末梢神経
Research Abstract

We identified new mutations of Po genes, including 433A-G, 543G-C, GGCA insertion between 603 to 604, in patients with Charcot-Marie-Tooth disease. We constructed Po cDNA clones containing these mutations by site-directed mutagenesis. These cDNA clones were inserted into expression adenovirus vector by Graham's method. Cultured rat peripheral nerve was peformed using dorsal root ganglions of fetal rat. Now constructed adenovirus vector containg mutated Po cDNA is infected in cultured rat peripheral nerve.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (27 results)

All Other

All Publications (27 results)

  • [Publications] Tachi N,Ohya K,Chiba S.: "Expression of DM locus-associated homeodomain nprotein in"Journal of Child Neurology. 14. 471-473 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N,Kozuka N,Ohya K: "Charcot-Marie-Tooth disease type 1A duplication"Pediatric Neurology. 20. 360-363 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N,Kozuka N,Ohya K: "A small direct tandem duplication of the myelin protein"Journal of Neurological Sciences. 156. 167-171 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Lopes J,Ravise N,Tachi N et al.: "Fine mapping of de novo CMT1A and HNPP rearrangements"Human Molecular Genetics. 7. 141-148 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Suzuki Y,Wada T,Tachi N et al.: "Phenotypic variability in a family with a mitochondrial DNA"Pediatric Neurology. 19. 283-286 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Iinuma K,Minami T,Tachi N et al.: "Long-term effects of zonisamide in the treatment of epilepsy"Journal of Intellectual Disease Research. 42. 68-73 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "A new mutation of the Po gene in patients with charcot-Marie-Tooth disease type 1 B : screening of the Po gene by heteroduplex analysis."Neurosci Lett. 204. 173-176 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin."Neurology. 49. 579-583 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "Congenital muscular dystrophy with partial deficiency of merosin."J Neurol Sci. 151. 25-27 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "De novo mutation of Charcot-Marie-Tooth disease type 1A."Pediatr Neurol. 17. 67-69 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "Tomaculous neuropathy in Charcot-Marie-Tooth disease with Po mutation."J Neurol Sci. 153. 106-109 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "A small direct tandem duplication of the myelin protein zero gene in a patient with Dejerine-Sottas disease phenotype."J Neurol Sci. 156. 167-171 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "Expression of DM locus-Associated homeodomain protein in congenital myotonic dystropjy."J Cild Neurol. 14. 471-473 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "Charcot-Marie-Tooth disease type 1A duplication by PCR analysis."Pediatr Neurol. 20. 360-363 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tachi N et al.: "Hereditary cerebellar ataxia with peripheral neuropathy and mental retardation."Eur Neurol. 43. 82-87 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Moreira MC,Tachi N,Koenig M: "Homozygosity mapping of Portuguese and Japanese forms of ataxia-oculomotor apraxia (AOA1) to 9p13 and evidence for genetic heterogeneity"American Journal of Human Genetics. (In press). (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tachi N,Kozuka N,Ohya K: "Expression of peripheral myelin protein zero in sural nerve of patients with Charcot-Marie-Tooth disease 1B"Pediatric Neurology. (In press). (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tachi N,Kozuka N,Miyaji M: "A double mutation in a patient with X-linked myotubular myopathy"Pediatric Neurology. (In press). (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tachi N,Kozuka N,Ohya K: "Fukuyama-type congenital muscular dystrophy associated with a lack of C-terminal domain of dystrophin"Pediatric Neurology. (In press). (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tachi N,Kozuka N,Ohya K: "Hereditary cerebellar ataxia with peripheral neuropathy and mental retardation"European Neurology. 43. 82-87 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tachi N,Ohya K,Chiba S: "Expression of DM locus-associated homeodomain protein in congenital myotonic dystropjy"Journal of Child Neurology. 14. 471-473 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tachi N, Ohya K, Chiba S.: "Expression of DM locus-associated homeodomain nprotein in"Journal of Child Neurology. 14. 471-473 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Tachi N, Kozuka N, Ohya K: "Charcot-Marie-Tooth disease type 1A duplication"Pediatric Neurology. 20. 360-363 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Tachi N, Kozuka N, Ohya K: "A small direct tandem duplication of the myelin protein"Journal of Neurological Sciences. 156. 167-171 (1998)

    • Related Report
      1999 Annual Research Report
  • [Publications] Lopes J, Ravise N, Tachi N et al: "Fine mapping of de novo CMT1A and HNPP reattangements"Human Molecular Genetics. 7. 141-148 (1998)

    • Related Report
      1999 Annual Research Report
  • [Publications] Suzuki Y, Wada T, Tachi N et al: "Phenotypic variability in a family with a mitochondrial DNA"Pediatric Neurology. 19. 283-286 (1998)

    • Related Report
      1999 Annual Research Report
  • [Publications] Iinuma K, Minami T, Tachi N et al: "Long-term effects of zonisamide in the treatment of epilepsy"Journal of Intellectual Disease Research. 42. 68-73 (1998)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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