A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Authors
Keywords
-
Journal
NATURE
Volume 480, Issue 7375, Pages 99-103
Publisher
Springer Nature
Online
2011-11-11
DOI
10.1038/nature10630
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Essential role of microphthalmia transcription factor for DNA replication, mitosis and genomic stability in melanoma
- (2011) T Strub et al. ONCOGENE
- Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factor
- (2011) Glen M. Boyle et al. Pigment Cell & Melanoma Research
- IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma
- (2010) David L. Duffy et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Melanocytic Nevi, Nevus Genes, and Melanoma Risk in a Large Case-Control Study in the United Kingdom
- (2010) J. A. Newton-Bishop et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- No Association between TERT-CLPTM1L Single Nucleotide Polymorphism rs401681 and Mean Telomere Length or Cancer Risk
- (2010) K. A. Pooley et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- Melanocortin 1 receptor and risk of cutaneous melanoma: A meta-analysis and estimates of population burden
- (2010) Patricia F. Williams et al. INTERNATIONAL JOURNAL OF CANCER
- Population-based, Case-Control-Family Design to Investigate Genetic and Environmental Influences on Melanoma Risk: Australian Melanoma Family Study
- (2009) A. E. Cust et al. AMERICAN JOURNAL OF EPIDEMIOLOGY
- Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry
- (2009) Hongmei Nan et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
- (2009) Mario Falchi et al. NATURE GENETICS
- Genome-wide association study identifies three loci associated with melanoma risk
- (2009) D Timothy Bishop et al. NATURE GENETICS
- Frequent mutations in the MITF pathway in melanoma
- (2009) Julia C. Cronin et al. Pigment Cell & Melanoma Research
- Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays
- (2009) R. Drmanac et al. SCIENCE
- TRPM1 Forms Ion Channels Associated with Melanin Content in Melanocytes
- (2009) E. Oancea et al. Science Signaling
- Common Single-Nucleotide Polymorphisms in DNA Double-Strand Break Repair Genes and Breast Cancer Risk
- (2008) K. A. Pooley et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes
- (2008) Yu-mei Chang et al. INTERNATIONAL JOURNAL OF CANCER
- Common sequence variants on 20q11.22 confer melanoma susceptibility
- (2008) Kevin M Brown et al. NATURE GENETICS
- ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
- (2008) Daniel F Gudbjartsson et al. NATURE GENETICS
- Increased Melanogenesis is a Risk Factor for Oxidative DNA Damage— Study on Cultured Melanocytes and Atypical Nevus Cells
- (2008) Nico P. M. Smit et al. PHOTOCHEMISTRY AND PHOTOBIOLOGY
- Novel MITF targets identified using a two-step DNA microarray strategy
- (2008) Keith S. Hoek et al. Pigment Cell & Melanoma Research
- The Queensland Study of Melanoma: Environmental and Genetic Associations (Q-MEGA); Study Design, Baseline Characteristics, and Repeatability of Phenotype and Sun Exposure Measures
- (2008) Amanda J. Baxter et al. Twin Research and Human Genetics
- A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation
- (2008) Jiali Han et al. PLoS Genetics
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started