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Oecologia|April 2, 2011
Fitness consequences of individual specialisation in resource use and trophic morphology in European eelsJulien Cucherousset, Anthony Acou, Simon Blanchet, et al.
Experimental Cell Research|January 1, 1983
Maintenance and reversibility of active albumin secretion by adult rat hepatocytes co-cultured with another liver epithelial cell typeC Guguen-Guillouzo, B Clément, G Baffet, et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|June 5, 2025
Characteristics of Combined Movement Behavior Interventions in Children and Adolescents: A Scoping ReviewCiaran M C Maloney, Andrew J Atkin, Lee C Beaumont, et al.
American Journal of Human Genetics|February 1, 1996
Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase alleleL Gouya, J C Deybach, J Lamoril, et al.
Annals of Human Genetics|May 1, 1984
Assignment of the human gene for delta aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassayC Beaumont, C Foubert, B Grandchamp, et al.
Plos One|April 9, 2026
Adolescents' time-use and academic attainment: A longitudinal, compositional analysis in the Millennium Cohort StudyCiaran M C Maloney, Andrew J Atkin, Lee C Beaumont, et al.
Blood|November 24, 1999
H-ferritin subunit overexpression in erythroid cells reduces the oxidative stress response and induces multidrug resistance propertiesS Epsztejn, H Glickstein, V Picard, et al.
Nucleic Acids Research|August 25, 1989
A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyriaB Grandchamp, C Picat, F de Rooij, et al.
Journal of Fish Biology|February 1, 2018
Atlantic salmon Salmo salar in the chalk streams of England are genetically uniqueC Ikediashi, J R Paris, R A King, et al.
Genomics|July 1, 1991
Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19A K Yachou, F Renaudie, J L Guenet, et al.
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