Messenger RNA processing and its role in diabetesHARRIES, L. W.Diabetic medicine. 2011, Vol 28, Num 9, pp 1010-1017, issn 0742-3071, 8 p.Article

Reduced peripheral blood mitochondrial DNA content is not a risk factor for Type 2 diabetesSINGH, R; HATTERSLEY, A. T; HARRIES, L. W et al.Diabetic medicine. 2007, Vol 24, Num 7, pp 784-787, issn 0742-3071, 4 p.Article

The glutathione S-transferase GSTP1 polymorphism : effects on susceptibility to oral/pharyngeal and laryngeal carcinomasMATTHIAS, C; BOCKMÜHL, U; STRANGE, R. C et al.Pharmacogenetics (London). 1998, Vol 8, Num 1, pp 1-6, issn 0960-314XArticle

Variants in the isoform-specific coding regions of the HNF1A, HNF4A and HNF1B genes are not a common cause of familial, young-onset diabetes or renal cysts and diabetes (RCAD)LOCKE, J. M; ELLARD, S; NORWOOD, V. F et al.Diabetic medicine. 2009, Vol 26, Num 5, pp 569-570, issn 0742-3071, 2 p.Article

Molecular genetics of the human cytochrome P450 monooxygenase superfamilySMITH, G; STUBBINS, M. J; HARRIES, L. W et al.Xenobiotica (London. Print). 1998, Vol 28, Num 12, pp 1129-1165, issn 0049-8254Article

Genotypes of glutathione transferase M1 and P1 and their significance for lung DNA adduct levels and cancer riskRYBERG, D; SKAUG, V; HEWER, A et al.Carcinogenesis (New York. Print). 1997, Vol 18, Num 7, pp 1285-1289, issn 0143-3334Article

An alternative polyadenylation signal in TCF7L2 generates isoforms that inhibit T cell factor/lymphoid-enhancer factor (TCF/LEF)-dependent target genesLOCKE, J. M; DA SILVA XAVIER, G; RUTTER, G. A et al.Diabetologia (Berlin). 2011, Vol 54, Num 12, pp 3078-3082, issn 0012-186X, 5 p.Article

Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitroWIRSING, A; JOHNSTONE, K. A; HARRIES, L. W et al.Diabetic medicine. 2010, Vol 27, Num 6, pp 631-635, issn 0742-3071, 5 p.Article

Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndromeHARRIES, L. W; ELLARD, S; JONES, R. W. A et al.Diabetologia (Berlin). 2004, Vol 47, Num 5, pp 937-942, issn 0012-186X, 6 p.Article

Increased expression of miR-187 in human islets from individuals with type 2 diabetes is associated with reduced glucose-stimulated insulin secretionLOCKE, J. M; DA SILVA XAVIER, G; DAWE, H. R et al.Diabetologia (Berlin). 2014, Vol 57, Num 1, pp 122-128, issn 0012-186X, 7 p.Article

Severe Intrauterine Growth Retardation and Atypical Diabetes Associated with a Translocation Breakpoint Disrupting Regulation of the Insulin-Like Growth Factor 2 GeneMURPHY, R; BAPTISTA, J; HOLLY, J et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 11, pp 4373-4380, issn 0021-972X, 8 p.Article

Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the youngELLARD, S; THOMAS, K; EIBERG, H et al.Diabetologia (Berlin). 2007, Vol 50, Num 11, pp 2313-2317, issn 0012-186X, 5 p.Article

Identification of genetic polymorphisms at the glutathione S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancerHARRIES, L. W; STUBBINS, M. J; FORMAN, D et al.Carcinogenesis (New York. Print). 1997, Vol 18, Num 4, pp 641-644, issn 0143-3334Article

Analysis of haematopoietic chimaerism by quantitative real-time polymerase chain reactionHARRIES, L. W; WICKHAM, C. L; EVANS, J. C et al.Bone marrow transplantation (Basingstoke). 2005, Vol 35, Num 3, pp 283-290, issn 0268-3369, 8 p.Article

The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decayHARRIES, L. W; BINGHAM, Coralie; BELLANNE-CHANTELOT, Christine et al.Human genetics. 2005, Vol 118, Num 2, pp 214-224, issn 0340-6717, 11 p.Article

Abnormal splicing of hepatocyte nuclear factor 1 alpha in maturity-onset diabetes of the youngBULMAN, M. P; HARRIES, L. W; HANSEN, T et al.Diabetologia (Berlin). 2002, Vol 45, Num 10, pp 1463-1467, issn 0012-186X, 5 p.Article

Genetic analysis of the human cytochrome P450 CYP2C9 locusSTUBBINS, M. J; HARRIES, L. W; SMITH, G et al.Pharmacogenetics (London). 1996, Vol 6, Num 5, pp 429-439, issn 0960-314XArticle