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Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines

Journal of clinical oncology, 2015-01, Vol.33 (2), p.209-217

2015

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β-Catenin destruction complex-independent regulation of Hippo-YAP signaling by APC in intestinal tumorigenesis

Genes & development, 2015-07, Vol.29 (14), p.1493-1506

2015

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Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

American journal of human genetics, 2016-05, Vol.98 (5), p.830-842

2016

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Mouse models of intestinal cancer

The Journal of pathology, 2016-01, Vol.238 (2), p.141-151

2016

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Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations

Archives of pathology & laboratory medicine (1976), 2019-11, Vol.143 (11), p.1382-1398

2019

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The microbiome, genetics, and gastrointestinal neoplasms: the evolving field of molecular pathological epidemiology to analyze the tumor–immune–microbiome interaction

Human genetics, 2021-05, Vol.140 (5), p.725-746

2021

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PLK1 has tumor-suppressive potential in APC-truncated colon cancer cells

Nature communications, 2018-03, Vol.9 (1), p.1106-17, Article 1106

2018

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Epithelial cell extrusion: Pathways and pathologies

Seminars in cell & developmental biology, 2017-07, Vol.67, p.132-140

2017

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The adenomatous polyposis coli protein 30 years on

Seminars in cell & developmental biology, 2023-12, Vol.150-151, p.28-34

2023

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Microenvironmental changes in familial adenomatous polyposis during colorectal cancer carcinogenesis

Cancer letters, 2024-05, Vol.589, p.216822-216822, Article 216822

2024

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Integrated genotype–phenotype analysis of familial adenomatous polyposis-associated hepatocellular adenomas

Virchows Archiv : an international journal of pathology, 2024-04, Vol.484 (4), p.587-595

2024

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High cumulative risk of colorectal cancers and desmoid tumours and fibromatosis in South Asian APC mutation carriers

Journal of medical genetics, 2022-05, Vol.59 (5), p.492-495

2022

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Resorting the function of the colorectal cancer gatekeeper adenomatous polyposis coli

International journal of cancer, 2020-02, Vol.146 (4), p.1064-1074

2020

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A pan-cancer analysis on the carcinogenic effect of human adenomatous polyposis coli

PloS one, 2022-03, Vol.17 (3), p.e0265655

2022

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Low adenoma burden in unselected patients with a pathogenic APC variant

Genetics in medicine, 2023-12, Vol.25 (12), p.100949, Article 100949

2023

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Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancer

Journal of medical genetics, 2022-10, Vol.59 (10), p.976-983

2022

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Molecular Pathways of Carcinogenesis in Familial Adenomatous Polyposis

International journal of molecular sciences, 2023-03, Vol.24 (6), p.5687

2023

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Myc deletion rescues Apc deficiency in the small intestine

Nature, 2007-04, Vol.446 (7136), p.676-679

2007

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A novel APC mutation associated with Gardner syndrome in a Chinese family

Gene, 2024-02, Vol.896, p.148051-148051, Article 148051

2024

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A one‐stop approach to diagnosing hereditary colorectal cancer in the Chinese population

Journal of gastroenterology and hepatology, 2023-11, Vol.38 (11), p.1980-1987

2023

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Genome sequencing-based discovery of a novel deep intronic APC pathogenic variant causing exonization

European journal of human genetics : EJHG, 2023-07, Vol.31 (7), p.841-845

2023

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Modeling APC mutagenesis and familial adenomatous polyposis using human iPS cells

PloS one, 2018-07, Vol.13 (7), p.e0200657

2018

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Wnt-Independent and Wnt-Dependent Effects of APC Loss on the Chemotherapeutic Response

International journal of molecular sciences, 2020-10, Vol.21 (21), p.7844

2020

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The 15-Amino Acid Repeat Region of Adenomatous Polyposis Coli Is Intrinsically Disordered and Retains Conformational Flexibility upon Binding β-Catenin

Biochemistry (Easton), 2020-10, Vol.59 (41), p.4039-4050

2020

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Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas

JAMA : the journal of the American Medical Association, 2012-08, Vol.308 (5), p.485

2012

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Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines

β-Catenin destruction complex-independent regulation of Hippo-YAP signaling by APC in intestinal tumorigenesis

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

Mouse models of intestinal cancer

Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations

The microbiome, genetics, and gastrointestinal neoplasms: the evolving field of molecular pathological epidemiology to analyze the tumor–immune–microbiome interaction

PLK1 has tumor-suppressive potential in APC-truncated colon cancer cells

Epithelial cell extrusion: Pathways and pathologies

The adenomatous polyposis coli protein 30 years on

Microenvironmental changes in familial adenomatous polyposis during colorectal cancer carcinogenesis

Integrated genotype–phenotype analysis of familial adenomatous polyposis-associated hepatocellular adenomas

High cumulative risk of colorectal cancers and desmoid tumours and fibromatosis in South Asian APC mutation carriers

Resorting the function of the colorectal cancer gatekeeper adenomatous polyposis coli

A pan-cancer analysis on the carcinogenic effect of human adenomatous polyposis coli

Low adenoma burden in unselected patients with a pathogenic APC variant

Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancer

Molecular Pathways of Carcinogenesis in Familial Adenomatous Polyposis

Myc deletion rescues Apc deficiency in the small intestine

A novel APC mutation associated with Gardner syndrome in a Chinese family

A one‐stop approach to diagnosing hereditary colorectal cancer in the Chinese population

Genome sequencing-based discovery of a novel deep intronic APC pathogenic variant causing exonization

Modeling APC mutagenesis and familial adenomatous polyposis using human iPS cells

Wnt-Independent and Wnt-Dependent Effects of APC Loss on the Chemotherapeutic Response

The 15-Amino Acid Repeat Region of Adenomatous Polyposis Coli Is Intrinsically Disordered and Retains Conformational Flexibility upon Binding β-Catenin

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas

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