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人類致病基因定位的策略與方法

授課年級:基醫所及臨醫所研究生
時間:星期三,3-4節 (10:10AM - 12:00 PM)
地點:醫學院 302D
教科書:Approaches to gene mapping in complex human disease (Haines & Pericak -Vance, 1998, WILEY-LISS)
課程目的:有系統、一系列的介紹人類致病基因定位的策略與方法
協調老師:孫孝芳 (Office: 9B-112 ; Phone: 3648)
參考書:Current protocols in human genetics Analysis of Human Genetic Linkage (Jurg Ott, Third Edition)
Date
Lecture
Speaker
Topic
2007-03-07
1
孫孝芳(成大分醫所)
Basic concepts of linkage analysis
2007-03-14
2
林秀娟(成醫小兒科)
Collection of clinical data for genetic studies
2007-03-21
3
孫孝芳(成大分醫所)
Determining the genetic component of a disease
2007-03-28
4
孫孝芳(成大分醫所)
Positional cloning
2007-04-11
5
孫孝芳(成大分醫所)
Alternative study designs (Sib-pair analysis and homozygosity mapping)
2007-04-18
6
呂政展(成大病理部)
Allelic association and Transmission Disequilibrium Test
2007-04-25
7
張志欽(成大環醫所)
Genetic epidemiology
2007-05-02
8
孫孝芳(成大分醫所)
Midterm examine
2007-05-09
9
王憶卿(成大藥理所)
Gene mapping by genetic and epigenetic approaches in cancer
2007-05-16
10
張堯(NHRI臨床研究組)
Transforming genes of EBV in related human malignancies
2007-05-23
11
孫孝芳(成大分醫所)
Methods in identification of sequence variants
2007-05-30
12
郭保麟(成大婦產科)
Identification of genes involved in male infertility
2007-06-06
13
孫孝芳(成大分醫所)
Paper discussion Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase.A genome-wide association study identifies novel risk loci for type 2 diabetes.
2007-06-13
14
孫孝芳(成大分醫所)
Paper discussion Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.
2007-06-20
15
孫孝芳(成大分醫所)
Paper discussion Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.
2007-06-27
16
孫孝芳(成大分醫所)
Paper discussion A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14.Functional variants in the promoter region of Chitinase 3-like 1 (CHI3L1) and susceptibility to schizophrenia.
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