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Publications by David R. Thorburn

A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome

Molecular Medicine

Molecular Biology

English

Delayed Diagnosis of Congenital Myasthenia Due to Associated Mitochondrial Enzyme Defect

Neuromuscular Disorders

English

New DGK Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome

Archives of Neurology

English

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Multidimensional Proteomics for Cell Biology

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DNA Methylation Pathways and Their Crosstalk With Histone Methylation

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Transcriptional Integration of Metabolism by the Nuclear Sterol-Activated Receptors LXR and FXR

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Tail-Anchored Membrane Protein Insertion Into the Endoplasmic Reticulum

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Dynamin, a Membrane-Remodelling GTPase

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Regulating the Regulator: Post-Translational Modification of RAS

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Trithorax Group Proteins: Switching Genes on and Keeping Them Active

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