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分子與基因醫學研究所
蔡世峯
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Trans-ethnic comprehensive genomic ...
GATA3 mutation of luminal-type brea...
Immune tolerance and intolerance in...
Detection of common mutations in sp...
Identification of MCP-1 as a key ef...
Identification of MCP-1 as a key ef...
Human versus chimpanzee chromosome-...
Spatial and temporal control of the...
Mutation in the tyrosine kinase dom...
Mutations in either the OSMR or IL3...
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2023-02
Trans-ethnic comprehensive genomic cluster stratification of upper tract urothelial carcinoma
European Urology. 2023 Feb;83(Suppl. 1):S1695.
2018-07
GATA3 mutation of luminal-type breast cancer patients in Taiwan
Cancer Research. 2018 Jul;78(13, Suppl.):Meeting Abstract 3439.
2015-12
Immune tolerance and intolerance in IgG repertoires of hepatitis B carrier children
Journal of Gastroenterology and Hepatology. 2015 Dec;30(Suppl. S4):23.
2014-09
Detection of common mutations in sporadic primary localized cutaneous amyloidosis by DNA mass spectrometry
Journal of Investigative Dermatology. 2014 Sep;134(S2):S56.
2013-02
Identification of MCP-1 as a key effector of IL-31 signaling in Familial Primary Cutaneous Amyloidosis
Journal of Dermatological Science. 2013 Feb;69(2):e54.
2012-09
Identification of MCP-1 as a key effector of IL-31 signaling in Primary Cutaneous Amyloidosis
Journal of Investigative Dermatology. 2012 Sep;132(Suppl. 2):S91.
2009-09
Mutations in either the OSMR or IL31RA genes underlie familial primary cutaneous amyloidosis
Journal of Investigative Dermatology. 2009 Sep;129(S2):S46.
2005-06
Mutation in the tyrosine kinase domain of epidermal growth factor receptor is a predictive and prognostic factor for gefitinib treatment in patients with non-small cell lung cancer
Journal of Clinical Oncology. 2005 Jun;23(16):Abstract number 641S.
2003
Human versus chimpanzee chromosome-wide sequence comparison and its evolutionary implication
Cold Spring Harbor Symposia on Quantitative Biology. 2003;68:455-460.
2001-10
Spatial and temporal control of the human ADH gene complexes in BAC transgenic mice
American Journal of Human Genetics. 2001 Oct;69(4 Suppl. 1):357.
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