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Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer

Nature genetics, 2011-12, Vol.43 (12), p.1219-1223

2011

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Gene expression patterns of human colon tops and basal crypts and BMP antagonists as intestinal stem cell niche factors

Proceedings of the National Academy of Sciences - PNAS, 2007-09, Vol.104 (39), p.15418-15423

2007

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Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

Nature genetics, 2006-10, Vol.38 (10), p.1178-1183

2006

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Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles

Gut, 2020-12, Vol.69 (12), p.2165

2020

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A Comprehensive Human Gastric Cancer Organoid Biobank Captures Tumor Subtype Heterogeneity and Enables Therapeutic Screening

Cell stem cell, 2018-12, Vol.23 (6), p.882-897.e11

2018

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Whole-genome sequencing and comprehensive molecular profiling identify new driver mutations in gastric cancer

Nature genetics, 2014-06, Vol.46 (6), p.573-582

2014

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RNF43 germline and somatic mutation in serrated neoplasia pathway and its association with BRAF mutation

Gut, 2017-09, Vol.66 (9), p.1645

2017

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Reduced expression of EphB2 that parallels invasion and metastasis in colorectal tumours

Carcinogenesis (New York), 2006-03, Vol.27 (3), p.454-464

2006

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Phospholipase A2 Group IIA Expression in Gastric Adenocarcinoma Is Associated with Prolonged Survival and Less Frequent Metastasis

Proceedings of the National Academy of Sciences - PNAS, 2002-12, Vol.99 (25), p.16203-16208

2002

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Escape from cell-cell and cell-matrix adhesion dependence underscores disease progression in gastric cancer organoid models

Gut, 2023-02, Vol.72 (2), p.242

2023

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Mutational landscape of normal epithelial cells in Lynch Syndrome patients

Nature communications, 2022-05, Vol.13 (1), p.2710-2710, Article 2710

2022

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Comprehensive analysis of the gene expression profiles in human gastric cancer cell lines

Oncogene, 2002-09, Vol.21 (42), p.6549-6556

2002

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MSH2 c.1452–1455delAATG Is a Founder Mutation and an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Southern Chinese Population

American journal of human genetics, 2004-05, Vol.74 (5), p.1035-1042

2004

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Epigenetic-Genetic Interactions in the APC/WNT, RAS/RAF, and P53 Pathways in Colorectal Carcinoma

Clinical cancer research, 2008-05, Vol.14 (9), p.2560-2569

2008

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Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia

Cancer research (Chicago, Ill.), 2002-11, Vol.62 (22), p.6451-6455

2002

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Microsatellite Instability and Mutation of DNA Mismatch Repair Genes in Gliomas

The American journal of pathology, 1998-10, Vol.153 (4), p.1181-1188

1998

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Lack of mismatch repair enhances resistance to methylating agents for cells deficient in oxidative demethylation

The Journal of biological chemistry, 2024-08, Vol.300 (8), p.107492, Article 107492

2024

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Frequent Inactivation of Axon Guidance Molecule RGMA in Human Colon Cancer Through Genetic and Epigenetic Mechanisms

Gastroenterology (New York, N.Y. 1943), 2009-07, Vol.137 (1), p.176-187

2009

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A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing : a founder mutation in the Chinese population

Oncogene, 2001-05, Vol.20 (23), p.2976-2981

2001

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Variation in gene expression patterns in human gastric cancers

Molecular biology of the cell, 2003-08, Vol.14 (8), p.3208-3215

2003

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Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers

Oncogene, 2002-10, Vol.21 (49), p.7585-7592

2002

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Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes

Oncogene, 2001-08, Vol.20 (35), p.4871-4876

2001

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Mutations of BRAF and KRAS in gastric cancer and their association with microsatellite instability

International journal of cancer, 2004-01, Vol.108 (1), p.167-169

2004

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Evaluating the Chinese University Summer Gifted Program for Junior Secondary Students in Hong Kong

The Journal of secondary gifted education, 2000-02, Vol.11 (3), p.136-143

2000

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Abstract 1448: Unraveling the oncogenic pathway of serrated polyposis syndrome driven by RNF43 germline mutation

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.1448-1448

2017

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Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer

Gene expression patterns of human colon tops and basal crypts and BMP antagonists as intestinal stem cell niche factors

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles

A Comprehensive Human Gastric Cancer Organoid Biobank Captures Tumor Subtype Heterogeneity and Enables Therapeutic Screening

Whole-genome sequencing and comprehensive molecular profiling identify new driver mutations in gastric cancer

RNF43 germline and somatic mutation in serrated neoplasia pathway and its association with BRAF mutation

Reduced expression of EphB2 that parallels invasion and metastasis in colorectal tumours

Phospholipase A2 Group IIA Expression in Gastric Adenocarcinoma Is Associated with Prolonged Survival and Less Frequent Metastasis

Escape from cell-cell and cell-matrix adhesion dependence underscores disease progression in gastric cancer organoid models

Mutational landscape of normal epithelial cells in Lynch Syndrome patients

Comprehensive analysis of the gene expression profiles in human gastric cancer cell lines

MSH2 c.1452–1455delAATG Is a Founder Mutation and an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Southern Chinese Population

Epigenetic-Genetic Interactions in the APC/WNT, RAS/RAF, and P53 Pathways in Colorectal Carcinoma

Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia

Microsatellite Instability and Mutation of DNA Mismatch Repair Genes in Gliomas

Lack of mismatch repair enhances resistance to methylating agents for cells deficient in oxidative demethylation

Frequent Inactivation of Axon Guidance Molecule RGMA in Human Colon Cancer Through Genetic and Epigenetic Mechanisms

A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing : a founder mutation in the Chinese population

Variation in gene expression patterns in human gastric cancers

Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers

Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes

Mutations of BRAF and KRAS in gastric cancer and their association with microsatellite instability

Evaluating the Chinese University Summer Gifted Program for Junior Secondary Students in Hong Kong

Abstract 1448: Unraveling the oncogenic pathway of serrated polyposis syndrome driven by RNF43 germline mutation

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