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Research projects supported by The Peking University Center For Human Disease Genomics |
| 编号 |
项目名称
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| 2001-1 | 中国人IL-4及其受体α亚单位的单核苷酸多态性与过敏性哮喘关系的的研究Single nucleotide polymorphism（SNP）of IL-4 andα subunite of its receptor in Chinese with allergic asthma |
| 2001-2 | 核基因突变所致Leigh综合征的临床与基因研究Clinical and Genetic Studies on Chromosomal Mutation Induced Leigh Syndrome |
| 2001-3 | 骨质疏松症后选基因在预测及综合防治骨质疏松症中作用的研究The study of candidate genes for osteoporosis |
| 2001-4 | 一个肺鳞癌差异表达新基因全长cDNA的克隆及功能初步研究Molecular Cloning and Functional Study of a Novel Gene Differentially Expressed in Lung Squamous Cell Carcinoma |
| 2001-5 | IL-4和IL-13信号通路基因SNP与变应性鼻炎及哮喘易感性的相关性研究The research of the association of SNP in IL-4 and IL-13 signaling gene with the susceptibility to developing allergic rhinitis and asthma |
| 2001-6 | 肝癌患者肝癌组织及外周血中HCA基因表达的研究The expression of HCA genes in the tumor tissues and the peripheral blood of the patients with hepatocellular carcinoma |
| 2001-7 | 已知MODY基因在中国北方"早发性的2型糖尿病"人群中致病作用的研究The study on the role of the identified MODY gene in the pathogenesis of early onset type 2 diabetes in northern Chinese population |
| 2001-8 | 侵袭性牙周炎致病相关基因的研究Pathogenic related gene study of aggressive periodontitis |
| 2001-9 | 外胚层发育不良致先天缺牙病的临床及分子遗传学研究Clinical & molecular genetics research of hypodontia caused by ectodermal dysphasia |
| 2001-10 | 牙源性角化囊肿中PTCH基因突变的分子生物学研究Molecular analysis of PTCH gene mutation in odontogenic keratocyst |
| 2001-11 | 多巴胺系统功能基因与注意缺陷多动障碍关系的研究A study of dopamine candidate gene and attention deficit hyperactivity disorder |
| 2001-12 | 关于人类自身免役病相关T细胞受体基因使用情况的分析Analysis of TCRs expressed by autoreactive T lymphocytes from patients with SLE |
| 2001-13 | 叶酸、VB12及其相关基因多态性与先天性心脏病发生的关系Study on folic acid，vitamin B12 and their correlated gene polymorphisms in the risk of congenital heart disease |