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Publications by T C Wood

Human Thiopurine Methyltransferase Pharmacogenetics. Kindred With a Terminal Exon Splice Junction Mutation That Results in Loss of Activity.

Journal of Clinical Investigation

English

Related publications

A Single Point Mutation Leading to Loss of Catalytic Activity in Human Thiopurine S-Methyltransferase.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Thiopurine S-Methyltransferase Pharmacogenetics: Autophagy as a Mechanism for Variant Allozyme Degradation

Pharmacogenetics and Genomics

Molecular Medicine

Molecular Biology

English

Thiopurine Metabolites and the Role of Thiopurine Methyltransferase Activity in Inflammatory Bowel Disease

Gastroenterology

English

Mutation in an Intervening Sequence Splice Junction in Man.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Exon Junction Complexes Suppress Spurious Splice Sites to Safeguard Transcriptome Integrity

Molecular Biology

English

A Novel Splice Site Mutation inSMARCAL1results in Aberrant Exon Definition in a Child With Schimke Immunoosseous Dysplasia

American Journal of Medical Genetics, Part A

English

Azathioprine Therapy in Multiple Sclerosis: Phosphoribosylated Metabolites and Thiopurine Methyltransferase Activity

The Open Neuroscience Journal

English

Clinical Pharmacogenomics of Thiopurine S-Methyltransferase

Current Clinical Pharmacology

English

The Effect of Thiopurine Methyltransferase Expression on Sensitivity to Thiopurine Drugs

Molecular Pharmacology

Molecular Medicine

English