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Increased C-MYC copy numbers on the background of CDKN2A loss is associated with improved survival in nodular melanoma.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2007, v. 133, n. 2, p. 117, doi. 10.1007/s00432-006-0150-4
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- Publication type:
- Article
Acquired Melanocytic Nevi in Childhood and Familial Melanoma.
- Published in:
- JAMA Dermatology, 2014, v. 150, n. 1, p. 35, doi. 10.1001/jamadermatol.2013.5588
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- Publication type:
- Article
INK4a‐deficient human diploid fibroblasts are resistant to RAS‐induced senescence.
- Published in:
- EMBO Journal, 2002, v. 21, n. 12, p. 2936, doi. 10.1093/emboj/cdf289
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- Publication type:
- Article
INK4a-deficient human diploid fibroblasts are resistant to RAS-induced senescence.
- Published in:
- EMBO Journal, 2002, v. 21, n. 12, p. 2936, doi. 10.1093/emboj/cdf289
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- Publication type:
- Article
A road map for efficient and reliable human genome epidemiology.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 3, doi. 10.1038/ng0106-3
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- Publication type:
- Article
Genome‐wide characterization of 5‐hydoxymethylcytosine in melanoma reveals major differences with nevus.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 6, p. 366, doi. 10.1002/gcc.22837
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- Publication type:
- Article
Genome-Wide Analysis of Gene and Protein Expression of Dysplastic Naevus Cells.
- Published in:
- Journal of Skin Cancer, 2012, p. 1, doi. 10.1155/2012/981308
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- Publication type:
- Article
Genetic testing in familial melanoma: uptake and implications.
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- Psycho-Oncology, 2008, v. 17, n. 8, p. 790, doi. 10.1002/pon.1377
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- Publication type:
- Article
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
- Published in:
- 2002
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- Publication type:
- journal article
A mutation hotspot at the p14ARF splice site.
- Published in:
- Oncogene, 2005, v. 24, n. 28, p. 4604, doi. 10.1038/sj.onc.1208678
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- Publication type:
- Article
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
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- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1135, doi. 10.1038/ejhg.2008.72
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- Publication type:
- Article
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
- Published in:
- 2008
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- Publication type:
- Correction Notice
The importance of motivation in selecting undergraduate medical students for extracurricular research programmes.
- Published in:
- PLoS ONE, 2021, v. 16, n. 11, p. 1, doi. 10.1371/journal.pone.0260193
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- Publication type:
- Article
Interplay between TERT promoter mutations and methylation culminates in chromatin accessibility and TERT expression.
- Published in:
- PLoS ONE, 2020, v. 15, n. 4, p. 1, doi. 10.1371/journal.pone.0231418
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- Publication type:
- Article
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families.
- Published in:
- 2021
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- Publication type:
- journal article
A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes.
- Published in:
- International Journal of Cancer, 2009, v. 124, n. 2, p. 420, doi. 10.1002/ijc.23869
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- Publication type:
- Article
Expression profiling reveals that methylation of TIMP3 is involved in uveal melanoma development.
- Published in:
- International Journal of Cancer, 2003, v. 106, n. 4, p. 472, doi. 10.1002/ijc.11262
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- Publication type:
- Article
Prognostic Significance of Promoter Hypermethylation and Diminished Gene Expression of SYNPO2 in Melanoma.
- Published in:
- Journal of Investigative Dermatology, 2015, v. 135, n. 9, p. 2328, doi. 10.1038/jid.2015.163
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- Publication type:
- Article
Promoter CpG Island Hypermethylation in Dysplastic Nevus and Melanoma: CLDN11 as an Epigenetic Biomarker for Malignancy.
- Published in:
- Journal of Investigative Dermatology, 2014, v. 134, n. 12, p. 2957, doi. 10.1038/jid.2014.270
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- Publication type:
- Article
Primary Melanoma Tumors from CDKN2A Mutation Carriers Do Not Belong to a Distinct Molecular Subclass.
- Published in:
- Journal of Investigative Dermatology, 2014, v. 134, n. 12, p. 3000, doi. 10.1038/jid.2014.272
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- Publication type:
- Article
Somatic BRAF and NRAS Mutations in Familial Melanomas with Known Germline CDKN2A Status: A GenoMEL Study.
- Published in:
- Journal of Investigative Dermatology, 2014, v. 134, n. 1, p. 287, doi. 10.1038/jid.2013.270
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- Publication type:
- Article
Melanocortin 1 Receptor Function: Shifting Gears from Determining Skin and Nevus Phenotype to Fetal Growth.
- Published in:
- Journal of Investigative Dermatology, 2012, v. 132, n. 8, p. 1953, doi. 10.1038/jid.2012.216
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- Publication type:
- Article
A Flexible Multiplex Bead-Based Assay for Detecting Germline CDKN2A and CDK4 Variants in Melanoma-Prone Kindreds.
- Published in:
- Journal of Investigative Dermatology, 2011, v. 131, n. 2, p. 480, doi. 10.1038/jid.2010.331
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- Publication type:
- Article
Absence of Germline Epimutation of the CDKN2A Gene in Familial Melanoma.
- Published in:
- 2009
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- Publication type:
- Letter
MICA Gene Polymorphism is Not Associated With an Increased Risk for Skin Cancer.
- Published in:
- Journal of Investigative Dermatology, 2002, v. 118, n. 4, p. 686, doi. 10.1046/j.1523-1747.2002.01712.x
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- Publication type:
- Article
Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color.
- Published in:
- Journal of Investigative Dermatology, 2001, v. 117, n. 2, p. 294, doi. 10.1046/j.0022-202x.2001.01421.x
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- Publication type:
- Article
Excess Cancer Mortality in six Dutch Pedigrees with the Familial Atypical Multiple Mole...
- Published in:
- Journal of Investigative Dermatology, 1998, v. 110, n. 5, p. 788, doi. 10.1046/j.1523-1747.1998.00185.x
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- Publication type:
- Article
Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies.
- Published in:
- BMC Medical Research Methodology, 2012, v. 12, n. 1, p. 116, doi. 10.1186/1471-2288-12-116
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- Publication type:
- Article
Cutaneous squamous cell carcinoma and p53 codon 72 polymorphism: A need for screening?
- Published in:
- Molecular Carcinogenesis, 2001, v. 30, n. 1, p. 56, doi. 10.1002/1098-2744(200101)30:1<56::AID-MC1013>3.0.CO;2-2
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- Publication type:
- Article
Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non‐CDKN2A/CDK4 melanoma families.
- Published in:
- International Journal of Cancer, 2019, v. 144, n. 10, p. 2453, doi. 10.1002/ijc.31984
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- Publication type:
- Article
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 6, p. 1351, doi. 10.1002/ijc.29099
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- Publication type:
- Article
MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 3, p. 618, doi. 10.1002/ijc.29018
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- Publication type:
- Article
Genome-wide analysis of constitutional DNA methylation in familial melanoma.
- Published in:
- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00831-7
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- Publication type:
- Article
Genetics of Seven Dutch Familial Atypcial Multiple Mole-Menaloma Syndrome Families: A Review of Linkage Results Including Chromosomes 1 and 9.
- Published in:
- Journal of Investigative Dermatology, 1994, v. 103, p. 122S, doi. 10.1038/jid.1994.22
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- Publication type:
- Article
Genetic Linkage Between the Collagen VII (COL7A1) Gene and the Autosomal Dominant Form of Dystrophic Epidermolysis Bullosa in Two Dutch Kindreds.
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- Journal of Investigative Dermatology, 1992, v. 99, n. 5, p. 528, doi. 10.1111/1523-1747.ep12658066
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- Publication type:
- Article
Progress report on the major clinical advances in patient-oriented research into familial melanoma (2013–2018).
- Published in:
- Familial Cancer, 2019, v. 18, n. 2, p. 267, doi. 10.1007/s10689-018-00115-3
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- Publication type:
- Article
Germline TERT promoter mutations are rare in familial melanoma.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 139, doi. 10.1007/s10689-015-9841-9
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- Publication type:
- Article
Familial melanoma: a complex disorder leading to controversy on DNA testing.
- Published in:
- Familial Cancer, 2003, v. 2, n. 2, p. 109, doi. 10.1023/A:1025758527675
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- Publication type:
- Article
Affected members of melanoma-prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19<sup>ARF</sup>.
- Published in:
- Genes, Chromosomes & Cancer, 1997, v. 19, n. 1, p. 52, doi. 10.1002/(SICI)1098-2264(199705)19:1<52::AID-GCC8>3.0.CO;2-#
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- Publication type:
- Article
Author Correction: Telomere length and survival in primary cutaneous melanoma patients.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls.
- Published in:
- International Journal of Epidemiology, 2009, v. 38, n. 3, p. 814, doi. 10.1093/ije/dyp166
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- Publication type:
- Article
The melanocortin-1-receptor gene is the major freckle gene.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 16, p. 1701, doi. 10.1093/hmg/10.16.1701
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- Publication type:
- Article
Genomic analysis and clinical management of adolescent cutaneous melanoma.
- Published in:
- Pigment Cell & Melanoma Research, 2017, v. 30, n. 3, p. 307, doi. 10.1111/pcmr.12574
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- Publication type:
- Article
An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a Bio Geno MEL study.
- Published in:
- Pigment Cell & Melanoma Research, 2014, v. 27, n. 2, p. 234, doi. 10.1111/pcmr.12193
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- Publication type:
- Article
Genome-wide promoter methylation analysis identifies epigenetic silencing of MAPK 13 in primary cutaneous melanoma.
- Published in:
- Pigment Cell & Melanoma Research, 2013, v. 26, n. 4, p. 542, doi. 10.1111/pcmr.12096
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- Publication type:
- Article
Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study.
- Published in:
- Pigment Cell & Melanoma Research, 2012, v. 25, n. 3, p. 384, doi. 10.1111/j.1755-148X.2012.00982.x
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- Publication type:
- Article
Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations.
- Published in:
- Human Mutation, 1998, v. 11, n. 6, p. 424, doi. 10.1002/(SICI)1098-1004(1998)11:6<424::AID-HUMU2>3.0.CO;2-2
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- Publication type:
- Article
Germline Mutations of the CDKN2 Gene in UK Melanoma Families.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2061, doi. 10.1093/hmg/6.12.2061
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- Publication type:
- Article