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HPS1 GENE : ITS MUTATION AND FUNCTION

Research Project

Project/Area Number 11670846
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Dermatology
Research InstitutionOSAKA CITY UNIVERSITY

Principal Investigator

FUKAI Kazuyoshi (2000)  OSAKA CITY UNIVERSITY MEDICAL SCHOOL, DEPARTMENT OF DERMATOLOGY, ASSOCIATE PROFESSOR, 医学部, 助教授 (20244642)

深井 和吉 (1999)  大阪市立大学, 医学部, 助教授 (00702953)

Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1999: ¥2,000,000 (Direct Cost: ¥2,000,000)
Keywordsoculocutaneous albinism / mutation analysis / polymorphism / 多型
Research Abstract

We were able to perform mutation analysis of six cases with Hermansky-Pudlak syndrome in Japan. The first case was a 2-year-old girl with oculocutaneous albnism, and pulmonary hemorrhage when delivery. Mutation analysis of tyrosinase and P revealed normal. She has heterozygous frameshift muation in exon 11 in the mutation hotspot. The second case was 18-year-old boy with OCA and bleeding tendency. He was compound heterozygous for IVS5 +5 G>A and 962-963insG.Giant melanosomes were shown in the epidermal melanocytes by electronmicroscopy. The third case was 49-year-old woman with OCA and pulmonary fibrosis. She was homozygous for IVS5 +5 G>A, splice site mutation. The fourth case was 35-year-old man with OCA and renal dysfunction. He was homozygous for IVS1-9C>T, but this turned out to be non-pathological by studying 50 normal controls. The fifth case was 70-year-old man withOCA and pulmonary fibrosis. He was all normal for HPS1. The sixth case was OCA and pulmonary fibrosis, and was homozygous for IVS5 +5G>A, splice site mutation. For those in which we cannot detect mutations in HPS1 gene, we are collaborating with Professor Richard Spritz in the University of Colorado, who recently cloned two new Hermansky-Pudlak syndrome genes (HPS3 and HPS4), to see whether these cases might fall into these new categories.

Report

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

    (14 results)

All Other

All Publications (14 results)

  • [Publications] Horikawa T,ARakik,Fukaik et al.: "Heterozygous HPSI mutations in a case of Hermansky-Pudlak syndrome with giant melanosomes"British Journal of Dermatology. 143. 635-640 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] KARichards,KFukai,Noiso AS Paller: "A novel KIT mutation results in piebaldism with progressive depigmentation"Journal of American Academy of Dermatology.. 44. 288-292 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] N.Oiso,KFuRai,MIshin: "Interleukin-4 receptor αchain polymorphism Gln551Arg is associated with adult atopic dermatitis in Japan"British Journal of dermatology. 142. 1003-1006 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] S Saito,Noiso et al.: "Oculocutaneous albinism type2 with a P gene miusce mutation in a patient with Angelman syndrome"Journal of Medical Genetics.. 37. 392-394 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Horikawa T.et al.: "Heterozygous HPS1 muation in a case of Hermansky-Pudlak syndrome with giant melanosomes"Br J Dermatol. 143. 635-40 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Richards KA et al.: "A novel KIT mutation results in piebaldism with progressive depigmentation"J Am Acad Dermatol. 44. 288-92 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Oiso N.et al.: "Interleukin-4 receptor alpha chain polymorphism Glu551Arg is associated with adult atopic dermatitis in Japan"Br J Dermatol. 142. 1003-6 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Saito S.et al.: "Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome"J Med Genet. 37. 392-4 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Horkawa T,Arakik,Fukaik et al.: "Heterozygous HPS1 mutations in a case of Hermansky-Pudlak syndrome with giant melanosomes"British Journal of Dermatology. 143. 635-640 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] KA Richasds.K Fukai,Noiso AS Paller: "A novel KIT mutation results in piebaldism with progressive depigmentation."Journal of Ammerican Academy of Dermatology.. 44. 288-292 (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] N.Oiso.K FuRai,Mishi: "Interleukin 4 receptor α chain polymorphism Gln551Arg is associated with adult atopic dermatitis in Japan"British Journal of Dermatology. 142. 1003-1006 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] S Saito,Noiso et al.: "Oculocutameous albinism type2 with a Pglue miscue mutation in a patient Augelar Tyalsome."Journal of Medical Genetics.. 37. 392-394 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] S. Saito, N. Oiso, T. Wada O Narazaki, K Fukai: "Angelman syndrome plus oculocataneous albinism type2 associated with a Pgene missence mutation"J Med Genet. (in press). (2000)

    • Related Report
      1999 Annual Research Report
  • [Publications] N Oiso, K Fukai, M Ishii: "Interleukin 4-receptor alpha chain polymorphisms in adult atopic dernatitis in Japan"Br J Dermatol. (in press). (2000)

    • Related Report
      1999 Annual Research Report

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

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