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Advances in Experimental Medicine and Biology|June 23, 2004
Levels of purine, kynurenine and lipid peroxidation products in patients with inflammatory bowel diseaseCaroline M Forrest, Stuart R Gould, L Gail Darlington, et al.Development (Cambridge, England)|November 5, 2004
Temporal complexity within a translational control element in the nanos mRNAKevin M Forrest, Ira E Clark, Roshan A Jain, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 21, 2000
Population-specific polymorphisms of the human FMO3 gene: significance for detoxicationJ R Cashman, B R Akerman, S M Forrest, et al.Clinical Nutrition (Edinburgh, Scotland)|September 15, 2009
The relationship between the insulin-like growth factor-1 axis, weight loss, an inflammation-based score and survival in patients with inoperable non-small cell lung cancerClaire L Meek, A Michael Wallace, Lynn M Forrest, et al.Journal of Medical Genetics|August 1, 1994
Maternal uniparental disomy of chromosome 13 in a phenotypically normal childH Slater, J H Shaw, G Dawson, et al.Journal of Neural Engineering|May 24, 2024
Neuronal functional connectivity is impaired in a layer dependent manner near chronically implanted intracortical microelectrodes in C57BL6 wildtype miceKeying Chen, Adam M Forrest, Guillermo Gonzalez Burgos, et al.American Journal of Human Genetics|August 1, 1990
Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiencyD W Howells, S M Forrest, H H Dahl, et al.Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 20Elsdon Storey, Melanie A Knight, Susan M Forrest, et al.Marine Pollution Bulletin|February 8, 2014
Spatial and temporal dynamics in macrobenthos during recovery from salmon farm induced organic enrichment: when is recovery complete?Nigel B Keeley, Catriona K Macleod, Grant A Hopkins, et al.Human Genetics|September 1, 1992
CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase geneS J Ramus, S M Forrest, J A Saleeba, et al.Pageof 185