Anthropological and genetic studies on uveitis in Mongoloids

蒙古人种葡萄膜炎的人类学和遗传学研究

基本信息

  • 批准号:
    07041166
  • 负责人:
  • 金额:
    $ 9.92万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for international Scientific Research
  • 财政年份:
    1995
  • 资助国家:
    日本
  • 起止时间:
    1995 至 1997
  • 项目状态:
    已结题

项目摘要

Anthropological and molecular genetic studies on intractable uveitis syndromes which are frequently seen in the Mongoloid population were performed in Syria, Jordan, Mongol and Portugal in the fiscal year of 1997.In Syria and Jordan, there were many patients with Behcet's disease, and most of the patients in the Ophthalmology Department as well as the Rheumatology Department were those with Behcet's disease, quite similar to Japan. However, Vogt-Koyanagi-Harada's disease was rarely seen in these countries. In Syria, uveitis survey clinic was not yet established, and we advised them how to establish this for our future cooperative studies. In Jordan, however, a speciality clinic for Behcet's disease was already established, and we could see more than 50 typical cases of Behcet's disease. We could also get blood samples from these patients for the HLA-DNA typing. Molecular genetic analyzes on these samples are now in progress in our laboratory.In Mongolia, there were many patients with i … More ntractable uveitis syndromes, and typical cases with Behcet's disease or Vogt-Koyanagi-Harada's disease were seen. On the other hand, no patients were diagnosed as sarcoidosis in Mongolia. Clinical festures of uveitis in Mongolia was generally similar to Japan, as had been expected. In this investigation, we could establish a scientific basis for future cooperative studies.Portugal is located in the west end of the so-called Silk-Route, and similar to Japan and other Mediterranean countries, there were many Portuguese patients with Behcet's disease. However, Vogt-Koyanagi-Harada's disease or sarcoidosis was not as frequent as in Japan. In the next study, association of HLA-B^<**>5101 is to be studied in Portuguese patients with Behcet's disease.Blood samples collected before from Saudi Arabia or Greece were also HLA-DNA typed in our laboratory this year, and the same HLA class I association with Japanese patients was found in these patients.We can conclude from these results that certain types of intractable uveitis frequently seen in the Mongoloid population are also seen along with the Silk-Route, and these uveitis may have been spread along with the migration of the old Nomadic Tibes. Less
1997财政年度,对蒙古族人群中常见的顽固性葡萄膜炎综合征进行了人类学和分子遗传学研究,在叙利亚、约旦、蒙古和葡萄牙进行了研究。在叙利亚和约旦,白塞氏病患者较多,而且大多数人患有白塞氏病。眼科和风湿科的病人都是白塞氏病,和日本很相似。 Vogt-Koyanagi-Harada 病在这些国家很少见。在叙利亚,葡萄膜炎调查诊所尚未建立,我们建议他们如何为我们未来的合作研究建立这一诊所,但在约旦,已经建立了白塞氏病的专业诊所。已经建立了,我们可以看到50多个白塞氏病的典型病例,我们还可以从这些患者身上获取血液样本,对这些样本进行分子遗传拼接。在我们的实验室,有很多患有顽固性葡萄膜炎综合征的患者,并没有看到典型的白塞氏病或沃格特-小柳-原田氏病的病例。另一方面,蒙古国临床上没有诊断出结节病的患者。正如我们所预料的那样,蒙古的葡萄膜炎症状与日本大致相似。 葡萄牙位于葡萄牙。在所谓丝绸之路的西端,与日本和其他地中海国家类似,葡萄牙也有很多白塞氏病患者,但沃格特-小柳-原田氏病或结节病并不像日本那样频繁。下一项研究将在患有白塞氏病的葡萄牙患者中研究 HLA-B^<**>5101 的关联性。之前从沙特阿拉伯或希腊采集的血液样本也进行了研究今年我们实验室进行了HLA-DNA分型,在这些患者中也发现了与日本患者相同的HLA I类关联。从这些结果我们可以得出结论,蒙古族人群中常见的某些类型的顽固性葡萄膜炎也与这些患者一起出现。丝绸之路,这些葡萄膜炎可能是随着古老的游牧民族的迁徙而传播的。

项目成果

期刊论文数量(87)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Asako M.: "A juvenile case of Vogt-Koyanagi-Harada's disease with calcific band keratopathy" Jpn J Clin Ophthalmol. 51 : 3. 395-398 (1997)
Asako M.:“伴有钙化带状角膜病的 Vogt-Koyanagi-Harada 病青少年病例”Jpn J Clin Ophthalmol。
  • DOI:
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    0
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  • 通讯作者:
中村 聡: "ぶどう膜炎とoral tolerance" 医学のあゆみ. 177. 411-413 (1996)
Satoshi Nakamura:“葡萄膜炎和口腔耐受性”医学史 177. 411-413 (1996)。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Shindo Y,et al: "Clinical and immunogenetic investigation of a laotian patient with Vogt-Koyanagi-Harada's disease" Ophthalmologica. 210. 112-114 (1996)
Shindo Y 等人:“一名患有 Vogt-Koyanagi-Harada 病的老挝患者的临床和免疫遗传学研究”眼科。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Ishihara M.: "Genetic polymorphisms of the TNFB and HSP70 genes located in the human major histocompatibility complex in sarcoidosis" Tissue Antigens. 46. 59-62 (1995)
Ishihara M.:“位于结节病人类主要组织相容性复合体中的 TNFB 和 HSP70 基因的遗传多态性”组织抗原。
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  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Uchio E.: "Suppression of actively induced experimental autoimmune uveoretinitis by CD4+T cells" Graefe's Arch Clin Exp Ophthalmol. 235. 97-102 (1997)
Uchio E.:“CD4 T 细胞对主动诱导的实验性自身免疫性葡萄膜视网膜炎的抑制”Graefe 的 Arch Clin Exp Ophamol。
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    0
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OHNO Shigeaki其他文献

OHNO Shigeaki的其他文献

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{{ truncateString('OHNO Shigeaki', 18)}}的其他基金

Comprhensive examination for serum autoantigens in endogenous uveitis patients
内源性葡萄膜炎患者血清自身抗原的综合检查
  • 批准号:
    23592602
  • 财政年份:
    2011
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Investigation of disease susceptibility genes associated with intractable intraocular inflammation with racial differences and development of new antioxidant therapy
具有种族差异的顽固性眼内炎症相关疾病易感基因的研究及新型抗氧化疗法的开发
  • 批准号:
    19406028
  • 财政年份:
    2007
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Molecular genetics and molecular epidemiology of intractable intraocular inflammation frequently found in Mongoloids for prevention of blindness.
蒙古人种中常见的难治性眼内炎症的分子遗传学和分子流行病学,用于预防失明。
  • 批准号:
    16406032
  • 财政年份:
    2004
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
New development in molecular genetic and molecular pharmacological studies on intractable intraocular inflammation.
难治性眼内炎症的分子遗传学和分子药理学研究新进展。
  • 批准号:
    16209051
  • 财政年份:
    2004
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Molecule genetic and molecule immunologic investigations on the mechanisms of viral ocular inflammation
病毒性眼部炎症机制的分子遗传学和分子免疫学研究
  • 批准号:
    14370550
  • 财政年份:
    2002
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
ANTHROPOLOGICAL AND MOLECULAR GENETIC STUDIES ON THE EPIDEMIOLOGY OF INTRACTABLE OCULAR DISEASES
难治性眼病流行病学的人类学和分子遗传学研究
  • 批准号:
    12576022
  • 财政年份:
    2000
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Studies on molecular genetic mechanism of intractable immune-mediated inflammatory diseases of the eye by genomic analyses
通过基因组分析研究难治性免疫介导的眼部炎症性疾病的分子遗传机制
  • 批准号:
    12307038
  • 财政年份:
    2000
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Anthhropological and genetic studies on ocular inflammatory diseases in Mongoloids
蒙古人种眼部炎症疾病的人类学和遗传学研究
  • 批准号:
    10041203
  • 财政年份:
    1998
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A).
Molecular mechanism of intractable ocular diseases
眼部难治性疾病的分子机制
  • 批准号:
    10671650
  • 财政年份:
    1998
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Molecular genetic studies on Behcet's disease
白塞病的分子遗传学研究
  • 批准号:
    08457466
  • 财政年份:
    1996
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)

相似海外基金

Establishment of facial reconstruction method for unknown human mongoloid skeletal remains
未知人类蒙古人种骨骼遗骸面部重建方法的建立
  • 批准号:
    18K06447
  • 财政年份:
    2018
  • 资助金额:
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  • 项目类别:
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Immuno-genetics on Mongoloid in Pan-Pacific and Northland Areas
泛太平洋和北陆地区蒙古人种的免疫遗传学
  • 批准号:
    18406006
  • 财政年份:
    2006
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Immunogenetic study on Mongoloids in Asian-Pacific and Polar areas
亚太和极地地区蒙古人种的免疫遗传学研究
  • 批准号:
    15256002
  • 财政年份:
    2003
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Anthro-genetics on Paleomongoloid in Pan-Pacific and Northland Areas
泛太平洋和北陆地区古蒙古人种的人类遗传学
  • 批准号:
    11691226
  • 财政年份:
    1999
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Studies on Heads and Faces between Sundadonty and Sinodonty
Sundadonty与Sinodonty的头面研究
  • 批准号:
    10671713
  • 财政年份:
    1998
  • 资助金额:
    $ 9.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
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