Molecular genetic analysis of recurrence of endogenous uveitis
| Project/Area Number |
19592003
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Ophthalmology
|
|---|
| Research Institution | Hokkaido University |
|---|
Principal Investigator |
KITAICHI Nobuyoshi Hokkaido University, 大学院・医学研究科, 客員准教授 (40431366)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
OHNO Shigeaki 北海道大学, 大学院・医学研究科, 特任教授 (50002382)
NAMBA Kenichi 北海道大学, 北海道大学病院, 講師 (70333599)
YOSHIDA Kazuhiko 北海道大学, 北海道大学病院, 講師 (90281807)
OHGAMI Kazuhiro 北海道大学, 大学院・医学研究科, 客員研究員 (80443977)
|
|---|
| Project Period (FY) |
2007 – 2010
|
| Project Status |
Completed (Fiscal Year 2010)
|
| Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2010: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2009: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2008: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2007: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
|
|---|
| Keywords | 遺伝子 / 免疫学 / 臨床遺伝子 / 分子遺伝学 / 臨床 / ベーチェット病 / Vogt-小柳-原田病 |
|---|
| Research Abstract |
Disease susceptibility genes and prognostic factors of endogenous uveitis were examined in this project. First, descriptive questionnaires were collected from 25 eye centers in 14 countries. Behcet disease is still a common cause of blindness in Asia. It was less common in children than in adults in East/South Asian countries. Second, DNA samples were collected to analyze molecular genetic factors associated with clinical characteristics and prognostic factors of uveitic diseases. Some gene polymorphisms were associated with the diseases : Behcet disease, sarcoidosis, Vogt-Koyanagi-Harada disease, and vitiligo vulgaris. Polymorphisms expected to the recurrence of uveitis was analyzed in Behcet disease compared with Vogt-Koyanagi-Harada disease.
|
Report
(6 results)
Research Products
(151 results)
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
[Journal Article] Association of TLR4 polymorphism with Behcet disease in Korean population.2009
Author(s)
Horie Y, Meguro A, Ota M, Kitaichi N, Katsuyama Y, Takemoto Y, Namba K, Yoshida K, Song YW, Park KS, Lee, EB, Inoko H, Mizuki N, Ohno S.
-
Journal Title
Rheumatology 48
Pages: 638-642
Related Report
-
[Journal Article] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.2009
Author(s)
Horie Y, Kitaichi N, Yoshida K, Katsuyama Y, Yoshida K, Miura T, Ota M, Asukata Y, Inoko H, Mizuki N, Ishida S, Ohno S.
-
Journal Title
Mol Vis 15
Pages: 1115-1119
NAID
Related Report
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
[Presentation] Epidemiology of EKC in Japan2011
Author(s)
Kitaichi N
Organizer
Working Group for Human Adenovirus Genome, Taxonomy, and Nomenclature Standards, NCBI Virus Genome Annotation Workshop
Place of Presentation
NIH (Bethesda, USA)
Year and Date
2011-02-03
Related Report
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
