Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

Mev Dominguez; Christina Therkildsen; Srinivas Veerla; Mats Jönsson; Inge Bernstein; Åke Borg; Mef Nilbert

doi:10.1371/journal.pone.0071755

Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

Mev Dominguez, Christina Therkildsen, Srinivas Veerla, Mats Jönsson, Inge Bernstein, Åke Borg, Mef Nilbert

Research output: Contribution to journal › Article › peer-review

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Abstract

Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects.

Original language	English
Article number	e71755
Journal	PLoS ONE
Volume	8
Issue number	8
DOIs	https://doi.org/10.1371/journal.pone.0071755
Publication status	Published - 2013

Subject classification (UKÄ)

Cancer and Oncology

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1371/journal.pone.0071755

Dominguez-Valentin_et_al

http://www.ncbi.nlm.nih.gov/pubmed/23951239?dopt=Abstract

Precision Medicine in Hereditary Cancer and Sarcoma; targeted surveillance, immunotherapy and individualized follow-up
Nilbert, M. (PI), Rambech, E. (Researcher), Jönsson, M. (Researcher), Styring, E. (Assistant supervisor), Nyström, H. (Research student) & Rosell, L. (Research student)
Project: Research

Cite this

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title = "Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.",

abstract = "Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects.",

author = "Mev Dominguez and Christina Therkildsen and Srinivas Veerla and Mats J{\"o}nsson and Inge Bernstein and {\AA}ke Borg and Mef Nilbert",

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AU - Therkildsen, Christina

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AU - Bernstein, Inge

AU - Borg, Åke

AU - Nilbert, Mef

PY - 2013

Y1 - 2013

N2 - Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects.

AB - Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects.

U2 - 10.1371/journal.pone.0071755

DO - 10.1371/journal.pone.0071755

M3 - Article

C2 - 23951239

SN - 1932-6203

VL - 8

JO - PLoS ONE

JF - PLoS ONE

IS - 8

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Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

Abstract

Subject classification (UKÄ)

UN SDGs

Access to Document

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Projects

Precision Medicine in Hereditary Cancer and Sarcoma; targeted surveillance, immunotherapy and individualized follow-up

Cite this