Browsing by Author rp00418

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TitleAuthor(s)Issue Date
 
A founder mutation of hMSH2 in Chinese with early-onset colorectal cancer
Proceeding/Conference:Proceedings of the American Association for Cancer Research
Chan, TLLeung, SYHo, JWCChan, ASYLam, PWYTse, CWLee, KCGwi, EYuen, ST
2002
 
Frequent Inactivation of Axon Guidance Molecule RGMA in Human Colon Cancer Through Genetic and Epigenetic Mechanisms
Journal:Gastroenterology
Li, VSWYuen, STChan, TLYan, HHNLaw, WLYeung, BHYChan, ASYTsui, WYSo, SChen, XLeung, SY
2009
 
Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer
Journal:Journal of the National Cancer Institute
Chan, TLYuen, STChung, LPHo, JWCKwan, KYMChan, ASYHo, JCYLeung, SYWyllie, AH
1999
 
Gene expression patterns of human colon tops and basal crypts and BMP antagonists as intestinal stem cell niche factors
Journal:Proceedings of the National Academy of Sciences of the United States of America
Kosinski, CLi, VSWChan, ASYZhang, JHo, CWai, YTTsun, LCMifflin, RCPowell, DWSiu, TYSuet, YLChen, X
2007
 
Gene expression profiling of human colon top versus basal crypts and identification of BMP antagonists as candidates for intestinal stem cell niche
Proceeding/Conference:Keystone Symposium on Frontiers in Gastrointestinal Cancer: Molecular Genetics, Inflammation, Early Detection & Therapy
Li, VSWKosinski, CChan, ASYZhang, JHo, CTsui, WYChan, TLMifflin, RCPowell, DWYuen, STLeung, SYChen, X
2007
 
Genetic diagnosis for herediary colorectal cancer syndromes
Proceeding/Conference:1st Hong Kong Medical Genetics Conference
Yuen, STChung, LPHo, JWCChan, TLSo, KCLeung, SY
1997
 
Genetic screening for familial adenomatous polyposis
Proceeding/Conference:HKICC 1996 & 7th International EBV Symposium
Yuen, STChung, LPHo, JWCSo, KCChan, CTLLeung, SY
1996
 
Germline epimutation of MLH1 in early-onset colorectal cancer
Proceeding/Conference:Cancer Research
Chan, TLTsui, WYChan, YWChan, ASYLee, TYHYuen, STLeung, SY
2008
 
Germline hMSH2 and differential somatic mutations in patients with Turcot's syndrome
Journal:Genes Chromosomes and Cancer
Chan, TLYuen, STChung, LPHo, JWCKwan, KFan, YWChan, ASYLeung, SY
1999
 
Germline methylation of the MSH2 promoter as a cause of Hereditary Non-Polyposis Colorectal Cancer
Proceeding/Conference:Cancer Research
Chan, TLYuen, STHo, JWCChan, YWChan, ASYChan, EMSLeung, SY
2005
 
Germline PALB2 mutation in high-risk Chinese breast and/or ovarian cancer patients
Journal:Cancers
Kwong, AShin, VYHo, CYSKhalid, AAu, CHChan, KKLNgan, HYSChan, TLMa, ESK
2021
 
Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers
Journal:Oncogene
Yuen, STChan, TLHo, JWCChan, ASYChung, LPLam, PWYTse, CWWyllie, AHLeung, SY
2002
 
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer
Journal:Nature Genetics
Chan, TLYuen, STKong, CKChan, YWChan, ASYNg, WFTsui, WYLo, MWSTam, WYLi, VSWLeung, SY
2006
 
Heritable germline epimutation of MSH2 in a hereditary nonpolyposis colorectal cancer family
Proceeding/Conference:Biennial Scientific Meeting of the International Society for Gastrointestinal Hereditary Tumours, InSiGHT 2007
Chan, TLYuen, STKong, CKChan, YWChan, ASYLeung, SY
2007
 
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
Journal:Nature Genetics
Ligtenberg, MJLKuiper, RPChan, TLGoossens, MHebeda, KMVoorendt, MLee, TYHBodmer, DHoenselaar, EHendriksCornelissen, SJBTsui, WYKong, CKBrunner, HGVan Kessel, AGYuen, STVan Krieken, JHJMLeung, SYHoogerbrugge, N
2009
 
High throughput germline mutation screening for hereditary breast cancer in Southern Chinese patients by massively parallel DNA sequencing
Proceeding/Conference:The Journal of Molecular Diagnostics
Au, CHLaw, FBFHo, DNIp, BKWong, ATCChan, TLKwong, AMa, ESK
2013
 
How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?
Journal:BMC Medical Genomics
Kwong, AHo, CYSShin, VYAu, CHChan, TLMa, ESK
2022
 
Identification of BRCA1/2 germline mutations by integrated approach
Proceeding/Conference:The Breast
Kwong, AChen, JShin, VLaw, FChan, TLFord, J
2015
 
Immunohistochemical staining on tissue microarray of colorectal cancers constitutes a convenient means to rapidly screen for MMR deficiency
Proceeding/Conference:Biennial Scientific Meeting of the International Society for Gastrointestinal Hereditary Tumours, InSiGHT 2007
Chan, TLGuo, DYuen, STChan, YWChan, ASYLeung, SY
2007
 
Insight from a breast and ovarian cancer patient with double BRCA1 mutation
Proceeding/Conference:International Breast Cancer Symposium, IBCS 2014
Ip, BKHo, DNUAu, CHLaw, FBFChoy, GKCChu, TWAShin, VYWong, ATCChan, TLMa, ESKKwong, A
2014
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