Inhibition of DNA, RNA and protein synthesis and chromatin alteration by N-hydroxyphenacetinHAYWARD, N. K; LAVIN, M. F.Xenobiotica (London. Print). 1987, Vol 17, Num 1, pp 115-124, issn 0049-8254Article

p-Aminophenol induced DNA damage and cytotoxycity enhenced by autoxidationHAYWARD, N. K; LAVIN, M. F.Life sciences (1973). 1985, Vol 36, Num 21, pp 2039-2046, issn 0024-3205Article

p-Aminophenol induced DNA damage and cytotoxycity enhenced by autoxidationHAYWARD, N. K; LAVIN, M. F.Life sciences (1973). 1985, Vol 36, Num 21, pp 2039-2046, issn 0024-3205Article

Prophylactic but not therapeutic activity of a monoclonal antibody that neutralizes the binding of VEGF-B to VEGFR-1 in a murine collagen-induced arthritis modelMOULD, A. W; SCOTNEY, P; GRECO, S. A et al.Rheumatology (Oxford. Print). 2008, Vol 47, Num 3, pp 263-266, issn 1462-0324, 4 p.Article

Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C β3 gene (PLCB3)LAGERCRANTZ, J; CARSON, E; PHELAN, C et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 467-472, issn 0888-7543Article

The phospholipase C β3 gene located in the MEN1 region shows loss of expression in endocrine tumoursWEBER, G; FRIEDMAN, E; CARSON, E et al.Human molecular genetics (Print). 1994, Vol 3, Num 10, pp 1775-1781, issn 0964-6906Article

Single base mutation in the hormone binding domain of the thyroid hormone receptor β gene in generalised thyroid hormone resistance demonstrated by single stranded conformation polymorphism analysisBOOTHROYD, C. V; TEH, B. T; HAYWARD, N. K et al.Biochemical and biophysical research communications (Print). 1991, Vol 178, Num 2, pp 606-612, issn 0006-291XArticle

A Taq I polymorphism for the human transforming growth factor alpha gene (TGFA)HAYWARD, N. K; NANCARROW, D. J; BELL, G. I et al.Nucleic acids research. 1987, Vol 15, Num 13, issn 0305-1048, 5503Article

Evidence for microsatellite instability in bilateral breast carcinomasIMYANITOV, E. N; TOGO, A. V; LAVIN, M. F et al.Cancer letters. 2000, Vol 154, Num 1, pp 9-17, issn 0304-3835Article

Involvement of p16^CDKN2A in cell cycle delays after low dose UV irradiationMILLIGAN, A; GABRIELLI, B. G; CLARK, J. M et al.Mutation research. 1998, Vol 422, Num 1, pp 43-53, issn 0027-5107Conference Paper

Low frequency of p16/CDKN2A methylation in sporadic melanoma: Comparative approaches for methylation analysis of primary tumorsGONZALGO, M. L; BENDER, C. M; YOU, E. H et al.Cancer research (Baltimore). 1997, Vol 57, Num 23, pp 5336-5347, issn 0008-5472Article

A linkage study of schizophrenia to markers within Xp11 near the MAOB geneDANN, J; DELISI, L. E; COMAZZI, M et al.Psychiatry research. 1997, Vol 70, Num 3, pp 131-143, issn 0165-1781Article

Simple tandem repeat allelic deletions confirm the preferential loss of distal chromosome 6q in melanomaWALKER, G. J; PALMER, J. M; WALTERS, M. K et al.International journal of cancer. 1994, Vol 58, Num 2, pp 203-206, issn 0020-7136Article

Confirmation of chromosome 9p linkage familial melanomaNANCARROW, D. J; MANN, G. J; FOUNTAIN, J. W et al.American journal of human genetics. 1993, Vol 53, Num 4, pp 936-942, issn 0002-9297Article

c-Ha-ras-1 alleles in bladder cancer, Wilms' tumour and malignant melanomaHAYWARD, N. K; KEEGAN, R; NANCARROW, D. J et al.Human genetics. 1988, Vol 78, Num 2, pp 115-120, issn 0340-6717Article

Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindredsFLORES, J. F; POLLOCK, P. M; WALKER, G. J et al.Oncogene (Basingstoke). 1997, Vol 15, Num 24, pp 2999-3005, issn 0950-9232Article

Confirmation of a susceptibility locus on chromosome 13 in Australian breast cancer familiesGRIMMOND, S. M; PALMER, J. M; WETZIG, N et al.Human genetics. 1996, Vol 98, Num 1, pp 80-85, issn 0340-6717Article

Loss of the p16^INK4a and p15^INK4b genes, as well as neighboring 9p21 markers, in sporadic melanomaFLORES, J. F; WALKER, G. J; BARNHILL, R. L et al.Cancer research (Baltimore). 1996, Vol 56, Num 21, pp 5023-5032, issn 0008-5472Article

Predictive diagnosis of multiple endocrine neoplasia (MEN 1) in four Australian kindredsGRIMMOND, S. M; TEH, B. T; BOYAGES, S et al.Australian and New Zealand journal of medicine. 1996, Vol 26, Num 1, pp 27-32, issn 0004-8291Conference Paper

Candidate genes for multiple endocrine neoplasia type 1 : Multiple endocrine neoplasia 1LAGERCRANTZ, J; LARSSON, C; HAYWARD, N. K et al.Journal of internal medicine. 1995, Vol 238, Num 3, pp 245-248, issn 0954-6820Article

The MLLT3 gene maps between D9S156 and D9S171 and contains an unstable polymorphic trinucleotide repeatWALKER, G. J; WALTERS, M. K; PALMER, J. M et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 3, pp 490-491, issn 0888-7543Article

Analysis of gene amplification in head-and-neck squamous-cell carcinomasLEONARD, J. H; KEARSLEY, J. H; CHENEVIX-TRENCH, G et al.International journal of cancer. 1991, Vol 48, Num 4, pp 511-515, issn 0020-7136Article

Clonal loss of INT-2 alleles in sporadic and familial pancreatic endocrine tumoursTEH, B. T; HAYWARD, N. K; WILKINSON, S et al.British journal of cancer. 1990, Vol 62, Num 2, pp 253-254, issn 0007-0920, 2 p.Article

Rare c-Ha-ras-1 alleles in human leukaemiaBAXTER, G. D; HAYWARD, N. K; COLLINS, R. J et al.Nucleic acids research. 1989, Vol 17, Num 12, issn 0305-1048, 4903 [1 p.]Article

Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL StudyDEMENAIS, F; MOHAMDI, H; AVRIL, M. F et al.Journal of the National Cancer Institute. 2010, Vol 102, Num 20, pp 1568-1583, issn 0027-8874, 16 p.Article