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Genetics of melanoma predispositionHAYWARD, Nicholas K.Oncogene (Basingstoke). 2003, Vol 22, Num 20, pp 3053-3062, issn 0950-9232, 10 p.Article

Molecular Pathways: Mitogen-Activated Protein Kinase Pathway Mutations and Drug ResistancePRITCHARD, Antonia L; HAYWARD, Nicholas K.Clinical cancer research (Print). 2013, Vol 19, Num 9, pp 2301-2309, issn 1078-0432, 9 p.Article

Pathways to melanoma development: Lessons from the mouseWALKER, Graeme J; HAYWARD, Nicholas K.Journal of investigative dermatology. 2002, Vol 119, Num 4, pp 783-792, issn 0022-202X, 10 p.Article

Meta-Analysis Combining New and Existing Data Sets Confirms that the TERT-CLPTM1L Locus Influences Melanoma RiskLAW, Matthew H; MONTGOMERY, Grant W; BROWN, Kevin M et al.Journal of investigative dermatology. 2012, Vol 132, Num 2, pp 485-487, issn 0022-202X, 3 p.Article

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47ANDERSON, Carl A; BOUCHER, Gabrielle; LAGACE, Caroline et al.Nature genetics. 2011, Vol 43, Num 3, pp 246-252, issn 1061-4036, 7 p.Article

A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaYOKOYAMA, Satoru; WOODS, Susan L; TAYLOR, John C et al.Nature (London). 2011, Vol 480, Num 7375, pp 99-103, issn 0028-0836, 5 p.Article

Predictors of Sun Protection Behaviors and Severe Sunburn in an International Online StudyBRÄNSTRÖM, Richard; KASPARIAN, Nadine A; BRUNO, William et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 9, pp 2199-2210, issn 1055-9965, 12 p.Article

A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to LiabilitySHEKAR, Sri N; DUFFY, David L; MARTIN, Nicholas G et al.Journal of investigative dermatology. 2009, Vol 129, Num 9, pp 2211-2219, issn 0022-202X, 9 p.Article

Genome-wide association study identifies three loci associated with melanoma riskBISHOP, D. Timothy; DEMENAIS, Florence; BAKKER, Bert et al.Nature genetics. 2009, Vol 41, Num 8, pp 920-925, issn 1061-4036, 6 p.Article

MC1R Variants Increase Risk of Melanomas Harboring BRAF Mutations. CommentaryHACKER, Elke; HAYWARD, Nicholas K; SEIDENARI, Stefania et al.Journal of investigative dermatology. 2008, Vol 128, Num 10, issn 0022-202X, 2354-2356, 2485-2490 [9 p.]Article

Features associated with germline CDKN2A mutations : a GenoMEL study of melanoma-prone families from three continentsGOLDSTEIN, Alisa M; CHAN, May; CALISTA, Donato et al.Journal of medical genetics. 2007, Vol 44, Num 2, pp 99-106, issn 0022-2593, 8 p.Article

Invasion and metastasis markers in cancersCHIN, David; BOYLE, Glen M; KANE, Anthony J et al.British journal of plastic surgery. 2005, Vol 58, Num 4, pp 466-474, issn 0007-1226, 9 p.Article

Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific regionHANDOKO, Herlina Y; NANCARROW, Derek J; SRINIVASAN, T. N et al.American journal of medical genetics. 2003, Vol 121A, Num 2, pp 1-6, issn 0148-7299, 6 p.Article

BRAF mutation status is an independent prognostic factor for resected stage IIIB and IIIC melanoma: Implications for melanoma staging and adjuvant therapyBARBOUR, Andrew P; YUE HANG TANG; HAYWARD, Nicholas K et al.European journal of cancer (1990). 2014, Vol 50, Num 15, pp 2668-2676, issn 0959-8049, 9 p.Article

SOX10 Ablation Arrests Cell Cycle, Induces Senescence, and Suppresses MelanomagenesisCRONIN, Julia C; WATKINS-CHOW, Dawn E; PAVAN, William J et al.Cancer research (Chicago, Ill.). 2013, Vol 73, Num 18, pp 5709-5718, issn 0008-5472, 10 p.Article

Exome sequencing identifies recurrent somatic RAC1 mutations in melanomaKRAUTHAMMER, Michael; YONGKONG; ARIYAN, Stephan et al.Nature genetics. 2012, Vol 44, Num 9, pp 1006-1014, issn 1061-4036, 9 p.Article

Nevi, Family History, and Fair Skin Increase the Risk of Second Primary MelanomaSISKIND, Victor; HUGHES, Maria Celia B; PALMER, Jane M et al.Journal of investigative dermatology. 2011, Vol 131, Num 2, pp 461-467, issn 0022-202X, 7 p.Article

Gene expression analysis in absence epilepsy using a monozygotic twin designHELBIG, Ingo; MATIGIAN, Nicholas A; DIBBENS, Leanne M et al.Epilepsia (Copenhagen). 2008, Vol 49, Num 9, pp 1546-1554, issn 0013-9580, 9 p.Article

ATG16L1 T300A Shows Strong Associations With Disease Subgroups in a Large Australian IBD Population : Further Support for Significant Disease HeterogeneityFOWLER, Elizabeth V; DOECKE, James; RADFORD-SMITH, Graham L et al.The American journal of gastroenterology. 2008, Vol 103, Num 10, pp 2519-2526, issn 0002-9270, 8 p.Article

A genome-wide scan for naevus count : linkage to CDKN2A and to other chromosome regionsGU ZHU; MONTGOMERY, Grant W; JAMES, Michael R et al.European journal of human genetics. 2007, Vol 15, Num 1, pp 94-102, issn 1018-4813, 9 p.Article

Novel variants in growth differentiation factor 9 in mothers of dizygotic twinsPALMER, James S; ZHEN ZHEN ZHAO; HOEKSTRA, Chantal et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 11, pp 4713-4716, issn 0021-972X, 4 p.Article

Cell cycle alterations in biopsied olfactory neuroepithelium in schizophrenia and bipolar I disorder using cell culture and gene expression analysesMCCURDY, Richard D; FERON, Francois; PERRY, Chris et al.Schizophrenia research. 2006, Vol 82, Num 2-3, pp 163-173, issn 0920-9964, 11 p.Article

Microarray expression profiling in melanoma reveals a BRAF mutation signaturePAVEY, Sandra; JOHANSSON, Peter; HANSEN, Katherine et al.Oncogene (Basingstoke). 2004, Vol 23, Num 23, pp 4060-4067, issn 0950-9232, 8 p.Article

Chromosomal gains and losses in ocular melanoma detected by comparative genomic hybridization in an Australian population-based studyVAJDIC, Claire M; HUTCHINS, Anne-Marie; KRICKER, Anne et al.Cancer genetics and cytogenetics. 2003, Vol 144, Num 1, pp 12-17, issn 0165-4608, 6 p.Article

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutationsBOX, Neil F; DUFFY, David L; WEI CHEN et al.American journal of human genetics. 2001, Vol 69, Num 4, pp 765-773, issn 0002-9297Article

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