DNA methylation subgroups in melanoma are associated with proliferative and immunological processes.

Martin Lauss; Markus Ringnér; Anna F Karlsson; Katja Harbst; Christian Busch; Jürgen Geisler; Per Eystein Lønning; Johan Staaf; Göran B Jönsson

doi:10.1186/s12920-015-0147-4

DNA methylation subgroups in melanoma are associated with proliferative and immunological processes.

Martin Lauss, Markus Ringnér, Anna F Karlsson, Katja Harbst, Christian Busch, Jürgen Geisler, Per Eystein Lønning, Johan Staaf, Göran B Jönsson

Bröstcancer-genetik

University of Bergen

Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Sammanfattning

DNA methylation at CpG dinucleotides is modified in tumorigenesis with potential impact on transcriptional activity.

Originalspråk	engelska
Artikelnummer	73
Tidskrift	BMC Medical Genomics
Volym	8
Nummer	1
DOI	https://doi.org/10.1186/s12920-015-0147-4
Status	Published - 2015

Ämnesklassifikation (UKÄ)

Cancer och onkologi

FN:s Globala mål

Denna forskningsoutput relaterar till följande Globala mål

Tillgång till dokument

10.1186/s12920-015-0147-4Licens: CC BY

http://www.ncbi.nlm.nih.gov/pubmed/26545983?dopt=Abstract

Citera det här

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title = "DNA methylation subgroups in melanoma are associated with proliferative and immunological processes.",

abstract = "DNA methylation at CpG dinucleotides is modified in tumorigenesis with potential impact on transcriptional activity.",

author = "Martin Lauss and Markus Ringn{\'e}r and Karlsson, {Anna F} and Katja Harbst and Christian Busch and J{\"u}rgen Geisler and L{\o}nning, {Per Eystein} and Johan Staaf and J{\"o}nsson, {G{\"o}ran B}",

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AU - Lauss, Martin

AU - Ringnér, Markus

AU - Karlsson, Anna F

AU - Harbst, Katja

AU - Busch, Christian

AU - Geisler, Jürgen

AU - Lønning, Per Eystein

AU - Staaf, Johan

AU - Jönsson, Göran B

PY - 2015

Y1 - 2015

N2 - DNA methylation at CpG dinucleotides is modified in tumorigenesis with potential impact on transcriptional activity.

AB - DNA methylation at CpG dinucleotides is modified in tumorigenesis with potential impact on transcriptional activity.

U2 - 10.1186/s12920-015-0147-4

DO - 10.1186/s12920-015-0147-4

M3 - Article

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SN - 1755-8794

VL - 8

JO - BMC Medical Genomics

JF - BMC Medical Genomics

IS - 1

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