Items for Mayne, Lynne

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Number of items: 9.

Article

Rulten, S L, Hodder, E, Ripley, Tamzin, Stephens, D N and Mayne, L V (2008) Alcohol induces DNA damage and the Fanconi anemia D2 protein implicating FANCD2 in the DNA damage response pathways in brain. Alcoholism: Clinical and Experimental Research, 32 (7). pp. 1186-1196. ISSN 0145-6008

Rulten, Stuart L, Ripley, Tamzin, Manerakis, Ektor, Stephens, David N and Mayne, Lynne V (2006) Ethanol modifies the effect of handling stress on gene expression: problems in the analysis of two-way gene expression studies in mouse brain. Brain Research, 1102 (-). ISSN 0006-8993

Mead, A N, Morris, H V, Dixon, C I, Rulten, S L, Mayne, L V, Zamanillo, D and Stephens, D N (2006) AMPA receptor GluR2, but not GluR1 subunit deletion impairs emotional response conditioning in mice. Behavioral Neuroscience, 120 (2). pp. 241-8. ISSN 0735-7044

Rulten, S L, Ripley, Tamzin, Hunt, C L, Stephens, D N and Mayne, L V (2006) Sp1 and NFkappaB pathways are regulated in brain in response to acute and chronic ethanol. Genes, Brain and Behavior, 5 (3). pp. 257-273. ISSN 1601-1848

Rulten, Stuart, Ripley, Tamzin and Mayne, Lynne (2002) Uniform Microarray Hybridisation: A Comparative Study. International Biotechnology Laboratory.

Brown, A J H, Hutchings, C, Burke, J F and Mayne, L V (1999) Application of a Rapid Method (Targeted Display) for the Identification of Differentially Expressed mRNAs following NGF-induced Neuronal Differentiation in PC12 cells. Molecular and Cellular Neuroscience, 13. pp. 119-130. ISSN 1044-7431

Biggart, S, Chin, D, Fauchon, M, Cardew, G, du Fou, L, Harker, N, Quinn, E, Keller, C, Vincent, R and Mayne, L (1998) Association of genetic polymorphisms in the ACE ApoE and TGFb genes with premature ischaemic heart disease. Clinical Cardiology, 21. pp. 831-836.

Moorwood, Kim, Price, Toby N C and Mayne, Lynne V (1996) Mutation of p53 is not a prerequisite for immortaliation of human fibroblasts by SV40 T antigen. Experimental Cell Research, 223 (2). pp. 308-313.

Chu, Gilbert and Mayne, Lynne (1996) Xeroderma pigmentosum Cockayne syndrome and trichothiodystrophy: Do the genes explain the Diseases? Trends in Genetics, 12. pp. 187-192.

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