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Prognostic and Clinicopathologic Associations of Oncogenic BRAF in Metastatic MelanomaLONG, Georgina V; MENZIES, Alexander M; NAGRIAL, Adnan M et al.Journal of clinical oncology. 2011, Vol 29, Num 10, pp 1239-1246, issn 0732-183X, 8 p.Article

Selection criteria for genetic assessment of patients with familial melanomaLEACHMAN, Sancy A; CARUCCI, John; CURIEL-LEWANDROWSKI, Clara et al.Journal of the American Academy of Dermatology. 2009, Vol 61, Num 4, pp 677-684, issn 0190-9622, 8 p.Article

Frequent loss of heterozygosity targeting the inactive X chromosome in melanomaINDSTO, James O; NASSIF, Najah T; KEFFORD, Richard F et al.Clinical cancer research. 2003, Vol 9, Num 17, pp 6476-6482, issn 1078-0432, 7 p.Article

Online Prostate Cancer Screening Decision Aid for At-Risk Men: A Randomized TrialWATTS, Kaaren J; MEISER, Bettina; BARRATT, Alexandra L et al.Health psychology (Hillsdale, N.J.). 2014, Vol 33, Num 9, pp 986-997, issn 0278-6133, 12 p.Article

The melanoma-associated 24 base pair duplication in p16INK4a is functionally impairedBECKER, Therese M; AYUB, Ana L; KEFFORD, Richard F et al.International journal of cancer. 2005, Vol 117, Num 4, pp 569-573, issn 0020-7136, 5 p.Article

EDD, the human orthologue of the hyperplastic discs tumour suppressor gene, is amplified and overexpressed in cancerCLANCY, Jennifer L; HENDERSON, Michelle J; BRADY, Ged et al.Oncogene (Basingstoke). 2003, Vol 22, Num 32, pp 5070-5081, issn 0950-9232, 12 p.Article

Dominant negative ATM mutations in breast cancer familiesCHENEVIX-TRENCH, Georgia; SPURDLE, Amanda B; SCOTT, Clare et al.Journal of the National Cancer Institute. 2002, Vol 94, Num 3, pp 205-215, issn 0027-8874Article

The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthILES, Mark M; BISHOP, D. Timothy; ANDRESEN, Per A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 10, issn 0027-8874, 267.1-267.5Article

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3MACGREGOR, Stuart; MONTGOMERY, Grant W; PAINTER, Jodie N et al.Nature genetics. 2011, Vol 43, Num 11, pp 1114-1118, issn 1061-4036, 5 p.Article

A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL)HARLAND, Mark; GOLDSTEIN, Alisa M; HAYWARD, Nicholas K et al.European journal of cancer (1990). 2008, Vol 44, Num 9, pp 1269-1274, issn 0959-8049, 6 p.Article

Low prevalence of RAS-RAF-activating mutations in Spitz melanocytic nevi compared with other melanocytic lesionsINDSTO, James O; KUMAR, Swapna; LIXIANG WANG et al.Journal of cutaneous pathology. 2007, Vol 34, Num 6, pp 448-455, issn 0303-6987, 8 p.Article

High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMELGOLDSTEIN, Alisa M; CHAN, May; BRUNO, William et al.Cancer research (Baltimore). 2006, Vol 66, Num 20, pp 9818-9828, issn 0008-5472, 11 p.Article

X inactivation, DNA deletion, and microsatellite instability in common acquired melanocytic neviINDSTO, James O; CACHIA, Adrian R; KEFFORD, Richard F et al.Clinical cancer research. 2001, Vol 7, Num 12, pp 4054-4059, issn 1078-0432Article

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

Review and Cross-Validation of Gene Expression Signatures and Melanoma PrognosisSCHRAMM, Sarah-Jane; CAMPAIN, Anna E; SCOLYER, Richard A et al.Journal of investigative dermatology. 2012, Vol 132, Num 2, pp 274-283, issn 0022-202X, 10 p.Article

Sunbed use during adolescence and early adulthood is associated with increased risk of early-onset melanomaCUST, Anne E; ARMSTRONG, Bruce K; GOUMAS, Chris et al.International journal of cancer (Print). 2011, Vol 128, Num 10, pp 2425-2435, issn 0020-7136, 11 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

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

Population-based, Case-Control-Family Design to Investigate Genetic and Environmental Influences on Melanoma Risk: Australian Melanoma Family StudyCUST, Anne E; SCHMID, Helen; GILES, Graham G et al.American journal of epidemiology. 2009, Vol 170, Num 12, pp 1541-1554, issn 0002-9262, 14 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

Predictors of vinorelbine pharmacokinetics and pharmacodvnamics in patients with cancerWONG, Mark; BALLEINE, Rosemary L; HOSKINS, Janelle M et al.Journal of clinical oncology. 2006, Vol 24, Num 16, pp 2448-2455, issn 0732-183X, 8 p.Article

Hepatic technetium Tc 99m-labeled sestamibi elimination rate and ABCB1 (MDR1) genotype as indicators of ABCB1 (P-glycoprotein) activity in patients with cancerWONG, Mark; EVANS, Scott; RIVORY, Laurent P et al.Clinical pharmacology and therapeutics. 2005, Vol 77, Num 1, pp 33-42, issn 0009-9236, 10 p.Article

Geographical variation in the penetrance of CDKN2A mutations for melanomaBISHOP, D. Timothy; DEMENAIS, Florence; HARLAND, Mark et al.Journal of the National Cancer Institute. 2002, Vol 94, Num 12, pp 894-903, issn 0027-8874, 10 p.Article

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