The Canadian Rutherford lecture. An evolutionary view of disease in man

A Commentary on Multiple Screening for Aminoacidopathies in the Newborn Infant.

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What we know that could influence future treatment of phenylketonuria.

Journal of inherited metabolic disease·2008

The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East England.

Annals of human genetics·2008

Recommendations for locus-specific databases and their curation.

Human mutation·2007

CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene.

Human mutation·2006

After the genome--the phenome?

Journal of inherited metabolic disease·2004

Studies on the mechanism of action of picrotoxinin and other convulsants at the crustacean muscle GABA receptor.

Proceedings of the Royal Society of London. Series B, Biological sciences·2015

Selectivity in phagocytosis and persistence of symbiotic algae in the scyphistoma stage of the jellyfish Cassiopeia xamachana.

Proceedings of the Royal Society of London. Series B, Biological sciences·2012

AMPK activation by Aldometanib from Bigujing improves metabolic and cognitive dysfunction in aging mice.

Metabolic brain disease·2026

Open resection and primary anastomosis repair of giant, symptomatic extracranial internal carotid artery aneurysm.

Journal of vascular surgery cases and innovative techniques·2026

Metabolism and oxygen tension in Alzheimer's disease mouse model using two-photon FLIM-PLIM microscopy.

Neurophotonics·2026

Separating Faces in ARMS Metabarcoding Improves Marine Biodiversity Monitoring: A Comparison Across Protocols, Experimental Designs and Photographic Surveys.

Molecular ecology resources·2026

Landscape of retron diversity across the SPIRE microbial metagenome resource reveals candidate novel type XI-like lineages.

mSystems·2026

Is There a Fly in My Soup? To What Extent Do Metabarcoding and Individual Barcoding Tell the Same Story?

Molecular ecology resources·2026

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A Commentary on Multiple Screening for Aminoacidopathies in the Newborn Infant.

What we know that could influence future treatment of phenylketonuria.

The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East England.

Recommendations for locus-specific databases and their curation.

CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene.

After the genome--the phenome?

Studies on the mechanism of action of picrotoxinin and other convulsants at the crustacean muscle GABA receptor.

Selectivity in phagocytosis and persistence of symbiotic algae in the scyphistoma stage of the jellyfish Cassiopeia xamachana.

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