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ESMO Open|September 21, 2018
Somatic cancer genetics in the UK: real-world data from phase I of the Cancer Research UK Stratified Medicine ProgrammeColin R Lindsay, Emily C Shaw, Fiona Blackhall, et al.Biorxiv : the Preprint Server for Biology|May 8, 2026
Functional characterization of the 9q34.13 locus identifies RAPGEF1 as modulating risk for melanoma and nevi via RAS activationRohit Thakur, Mai Xu, Alexandra M Thornock, et al.Pigment Cell & Melanoma Research|November 14, 2013
An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL studyJohn R Davies, Sinead Field, Juliette Randerson-Moor, et al.BMC Medical Research Methodology|August 7, 2012
Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studiesSara Raimondi, Sara Gandini, Maria Concetta Fargnoli, et al.European Geriatric Medicine|June 12, 2025
Falls prevention in community-dwelling older adults and implementation of world falls guidelines: a call for action across Europe by the European Geriatric Medicine Society Special Interest Group on Falls and FracturesNathalie van der Velde, Lotta J Seppala, Alvaro Casas Herrero, et al.Plos One|December 24, 2015
A Transcriptional Signature of Fatigue Derived from Patients with Primary Sjögren's SyndromeKatherine James, Shereen Al-Ali, Jessica Tarn, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 26, 2015
Development and validation of a melanoma risk score based on pooled data from 16 case-control studiesJohn R Davies, Yu-mei Chang, D Timothy Bishop, et al.Journal of the American Academy of Dermatology|September 16, 2009
Selection criteria for genetic assessment of patients with familial melanomaSancy A Leachman, John Carucci, Wendy Kohlmann, et al.International Journal of Cancer|February 19, 2014
Inherited variation in the PARP1 gene and survival from melanomaJohn R Davies, Rosalyn Jewell, Paul Affleck, et al.Journal of Medical Genetics|June 9, 2017
Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcomaFanélie Jouenne, Isaure Chauvot de Beauchene, Emeline Bollaert, et al.Pageof 20