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

Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

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Sammanfattning

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.

Originalspråk	engelska
Artikelnummer	e71755
Tidskrift	PLoS ONE
Volym	8
Nummer	8
DOI	https://doi.org/10.1371/journal.pone.0071755
Status	Published - 2013

Ämnesklassifikation (UKÄ)

Cancer och onkologi

Tillgång till dokument

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., Rambech, E., Jönsson, M., Styring, E., Nyström, H. & Rosell, L.
Projekt: Forskning

Citera det här

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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",

year = "2013",

doi = "10.1371/journal.pone.0071755",

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AU - Dominguez, Mev

AU - Therkildsen, Christina

AU - Veerla, Srinivas

AU - Jönsson, Mats

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

VL - 8

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 8

M1 - e71755

ER -

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

Sammanfattning

Ämnesklassifikation (UKÄ)

Tillgång till dokument

Fingeravtryck

Projekt

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

Citera det här