The Gln/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys/Gln as an important predictor for melanoma progression : A case control study in the Swedish population
- Author
- KERTAT, Khadija1 ; ROSDAHL, Inger1 ; SUN, Xiao-Feng2 ; SYNNERSTAD, Ingrid1 ; HONG ZHANG1 3
[1] Division of Dermatology, Department of Experimental and Clinical Medicine, Linköping University, 581 85 Linköping, Sweden
[2] Division of Oncology, Department of Experimental and Clinical Medicine, Linköping University, 581 85 Linköping, Sweden
[3] School of Life Sciences, University of Skövde, 541 28 Skövde, Sweden - Source
Oncology reports. 2008, Vol 20, Num 1, pp 179-183, 5 p ; ref : 22 ref
- ISSN
- 1021-335X
- Scientific domain
- Medical oncology
- Publisher
- [S.n.], Athens
- Publication country
- Greece
- Document type
- Article
- Language
- English
- Author keyword
- melanoma polymorphism progression risk xeroderma pigmentosum complementation group D
- Keyword (fr)
- Cancérologie Codon Complémentation Etude cas témoin Facteur prédictif Facteur risque Gène réparation Génotype Homme Marqueur génétique Mélanome malin Polymorphisme Progression carcinogenèse Variabilité génétique Xeroderma pigmentosum Gène ERCC2 Réparation par excision de nucléotide Suède Cancer Maladie héréditaire Pathologie de la peau Photodermatose Photosensibilité Trouble de la pigmentation Tumeur maligne Europe
- Keyword (en)
- Cancerology Codon Complementation Case control study Predictive factor Risk factor Repair gene Genotype Human Genetic marker Malignant melanoma Polymorphism Tumor progression Genetic variability Xeroderma pigmentosum Nucleotide excision repair Sweden Cancer Genetic disease Skin disease Photodermatosis Photosensitivity Pigmentation disorder Malignant tumor Europe
- Keyword (es)
- Cancerología Codón Complementación Estudio caso control Factor predictivo Factor riesgo Gen reparación Genotipo Hombre Marcador genético Melanoma maligno Polimorfismo Progresión carcinogénesis Variabilidad genética Xeroderma pigmentoso Reparación por excisión de nucleótido Suecia Cáncer Enfermedad hereditaria Piel patología Fotodermatosis Fotosensibilidad Trastorno pigmentación Tumor maligno Europa
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B08 Dermatology / 002B08A Tumors of the skin and soft tissue. Premalignant lesions
- Discipline
- Dermatology Tumours
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20474410
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
Install on your browser
"O:13:\"PanistOpenUrl\":36:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000idc\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:0:\"\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:9:\"\u0000*\u0000jtitle\";s:16:\"Oncology reports\";s:9:\"\u0000*\u0000stitle\";s:10:\"Oncol. rep\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"20\";s:8:\"\u0000*\u0000issue\";s:1:\"1\";s:8:\"\u0000*\u0000spage\";s:3:\"179\";s:8:\"\u0000*\u0000epage\";s:3:\"183\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1021-335X\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"KERTAT\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Khadija\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"ROSDAHL, Inger\";i:1;s:14:\"SUN, Xiao-Feng\";i:2;s:18:\"SYNNERSTAD, Ingrid\";i:3;s:10:\"HONG ZHANG\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:8:\"\u0000*\u0000place\";s:6:\"Athens\";s:6:\"\u0000*\u0000pub\";s:6:\"[S.n.]\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"5\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Panist access
"O:12:\"IstexOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:0:\"\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:9:\"\u0000*\u0000jtitle\";s:16:\"Oncology reports\";s:9:\"\u0000*\u0000stitle\";s:10:\"Oncol. rep\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"20\";s:8:\"\u0000*\u0000issue\";s:1:\"1\";s:8:\"\u0000*\u0000spage\";s:3:\"179\";s:8:\"\u0000*\u0000epage\";s:3:\"183\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1021-335X\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"KERTAT\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Khadija\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"ROSDAHL, Inger\";i:1;s:14:\"SUN, Xiao-Feng\";i:2;s:18:\"SYNNERSTAD, Ingrid\";i:3;s:10:\"HONG ZHANG\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:8:\"\u0000*\u0000place\";s:6:\"Athens\";s:6:\"\u0000*\u0000pub\";s:6:\"[S.n.]\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"5\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Istex access
"O:16:\"EuropePMCOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:0:\"\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:9:\"\u0000*\u0000jtitle\";s:16:\"Oncology reports\";s:9:\"\u0000*\u0000stitle\";s:10:\"Oncol. rep\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"20\";s:8:\"\u0000*\u0000issue\";s:1:\"1\";s:8:\"\u0000*\u0000spage\";s:3:\"179\";s:8:\"\u0000*\u0000epage\";s:3:\"183\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1021-335X\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"KERTAT\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Khadija\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"ROSDAHL, Inger\";i:1;s:14:\"SUN, Xiao-Feng\";i:2;s:18:\"SYNNERSTAD, Ingrid\";i:3;s:10:\"HONG ZHANG\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:8:\"\u0000*\u0000place\";s:6:\"Athens\";s:6:\"\u0000*\u0000pub\";s:6:\"[S.n.]\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"5\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Europe PubMed Central access
"O:11:\"BaseOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:0:\"\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:9:\"\u0000*\u0000jtitle\";s:16:\"Oncology reports\";s:9:\"\u0000*\u0000stitle\";s:10:\"Oncol. rep\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"20\";s:8:\"\u0000*\u0000issue\";s:1:\"1\";s:8:\"\u0000*\u0000spage\";s:3:\"179\";s:8:\"\u0000*\u0000epage\";s:3:\"183\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1021-335X\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"KERTAT\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Khadija\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"ROSDAHL, Inger\";i:1;s:14:\"SUN, Xiao-Feng\";i:2;s:18:\"SYNNERSTAD, Ingrid\";i:3;s:10:\"HONG ZHANG\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:8:\"\u0000*\u0000place\";s:6:\"Athens\";s:6:\"\u0000*\u0000pub\";s:6:\"[S.n.]\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"5\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Base Search access
"O:12:\"ArXivOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:0:\"\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:9:\"\u0000*\u0000jtitle\";s:16:\"Oncology reports\";s:9:\"\u0000*\u0000stitle\";s:10:\"Oncol. rep\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"20\";s:8:\"\u0000*\u0000issue\";s:1:\"1\";s:8:\"\u0000*\u0000spage\";s:3:\"179\";s:8:\"\u0000*\u0000epage\";s:3:\"183\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1021-335X\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"KERTAT\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Khadija\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:4:{i:0;s:14:\"ROSDAHL, Inger\";i:1;s:14:\"SUN, Xiao-Feng\";i:2;s:18:\"SYNNERSTAD, Ingrid\";i:3;s:10:\"HONG ZHANG\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:187:\"The Gln\/Gln genotype of XPD codon 751 as a genetic marker for melanoma risk and Lys\/Gln as an important predictor for melanoma progression : A case control study in the Swedish population\";s:8:\"\u0000*\u0000place\";s:6:\"Athens\";s:6:\"\u0000*\u0000pub\";s:6:\"[S.n.]\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"5\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
arXiv access
