A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma (original) (raw)
2011, Nature
visibility
…
description
8 pages
link
1 file
Related papers
2020
Loss of Heterozygosity in the MXI1 Gene Is a Frequent Occurrence in Melanoma
Modern Pathology, 2003
Identification of new genes associated with melanoma
Experimental Dermatology, 2011
Altered molecular pathways in melanocytic lesions
International Journal of Cancer, 2009
Clinical characteristics associated with BRAF, NRAS and KIT mutations in Japanese melanoma patients
Journal of Dermatological Science, 2015
BMC Cancer
Paola Queirolo, Lorenza Pastorino
Pigment Cell & Melanoma Research, 2013
Subscribe to PCMR and stay up-to-date with the only journal committed to publishing basic research in melanoma and pigment cell biology As a member of the IFPCS or the SMR you automatically get online access to PCMR. Sign up as a member today at www.ifpcs.org or at www.societymelanomaresarch.org
High- and low-penetrance cutaneous melanoma susceptibility genes
Expert Review of Anticancer Therapy, 2006
Oncogene, 2006
The Genomic Landscape of Childhood and Adolescent Melanoma
Journal of Investigative Dermatology, 2015
Loading Preview
Sorry, preview is currently unavailable. You can download the paper by clicking the button above.
Related papers
BRAF V600 mutations and pathological features in Japanese melanoma patients
Melanoma Research, 2015
Genes and signaling pathways affecting the pathogenesis of melanoma
Postdoc Journal, 2013
MC1R Genotype Modifies Risk of Melanoma in Families Segregating CDKN2A Mutations
The American Journal of Human Genetics, 2001
Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients
Journal of Translational Medicine
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma
Nature Genetics, 2011
Genomewide association study identifies a new melanoma susceptibility locus at 1q21.3.Nat.Genet
2011
Variants of the MATP / SLC45A2 gene are protective for melanoma in the French population
Human Mutation, 2008
British Journal of Cancer, 2000
Pigment Cell & Melanoma Research, 2014
Editorial: Advancements in Molecular Diagnosis and Treatment of Melanoma
Frontiers in Oncology
JAMA dermatology, 2015
Journal of Medical Genetics, 2006
European Journal of Human Genetics, 2005
Oncology Reports, 2017
Common sequence variants on 20q11.22 confer melanoma susceptibility
Nature Genetics, 2008
Nodular melanoma in an MITF p.E318K carrier patient: The Wolf in Little Red Riding Hood
Australasian Journal of Dermatology, 2020
Journal of the American Academy of Dermatology, 2016
International Journal of Oncology, 1993
Clinical genetic testing for familial melanoma in Italy: A cooperative study
Journal of the American Academy of Dermatology, 2009
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
Nicolas Janin, Valérie Bonadona
Nature, 2011
Related topics
BiologyMedicineMultidisciplinaryNatureMutationMelanomaYoung AdultAgedSumoylation