Deletion of theMGMTgene in familial melanoma

Author:

Appelqvist Frida1,Yhr Maria2,Erlandson Anna2,Martinsson Tommy2,Enerbäck Charlotta3

Affiliation:

1. Department of Dermatology, Institute of Clinical Sciences; Sahlgrenska University Hospital; SE-413 45 Göteborg Sweden

2. Department of Clinical Genetics, Institute of Biomedicine; Sahlgrenska University Hospital; SE-413 45 Göteborg Sweden

3. Department of Clinical and Experimental Medicine, Division of Cell Biology and Dermatology; Linköping University; SE-581 85 Linköping Sweden

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference51 articles.

1. Expression of the endogenous O6-methylguanine-DNA-methyltransferase protects Chinese hamster ovary cells from spontaneous G:C to A:T transitions;Aquilina;Cancer Res,1992

2. Prevalence of common and dysplastic naevi in a Swedish population;Augustsson;Br J Dermatol,1991

3. The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation;Bergman;Eur J Hum Genet,2001

4. Identification of CDK4 sequences involved in cyclin D1 and p16 binding;Coleman;J Biol Chem,1997

5. The polymorphisms in the MGMT gene and the risk of cancer: A meta-analysis;Du;Tumor Biol,2013

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