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GNAQ and GNA11 mutations and downstream YAP activation in choroidal nevi
Genomic analysis and clinical management of adolescent cutaneous melanoma
Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families
Germline TERT promoter mutations are rare in familial melanoma
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Prognostic Significance of Promoter Hypermethylation and Diminished Gene Expression of SYNPO2 in Melanoma
MC1R gene variants and non-melanoma skin cancer: a pooled-analysis from the M-SKIP project
Development and Validation of a Melanoma Risk Score Based on Pooled Data from 16 Case-Control Studies
Histologic features of melanoma associated with CDKN2A genotype
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma
MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project
Promoter CpG Island Hypermethylation in Dysplastic Nevus and Melanoma: CLDN11 as an Epigenetic Biomarker for Malignancy
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
Cutaneous melanoma: Medical specialists' opinions on follow-up and sentinel lymph node biopsy
In-vitro melanoma models: invasive growth is determined by dermal matrix and basement membrane
POT1 loss-of-function variants predispose to familial melanoma
An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study

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