M Town

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

Tom Vulliamy, Michele D’Urso, G. Battistuzzi et al. · Proceedings of the National Academy of Sciences · 1988 · 252 citations · Full text

Genetics, Human Polymorphism, Molecular Biology +16

Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin

Marlene Attard, G Jean, Lionel Forestier et al. · Human Molecular Genetics · 1999 · 148 citations · Full text

Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific).

Mary Ganczakowski, M Town, D. K. Bowden et al. · Europe PMC (PubMed Central) · 1995 · 96 citations

Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA

Valeria Poggi, M Town, Nicholas S. Foulkes et al. · Biochemical Journal · 1990 · 83 citations · Full text

Genetics, Molecular Biology, Molecular Genetics +17

Behavior of Adult Human Mesenchymal Stem Cells Entrapped in Alginate-GRGDY Beads

Julia F. Markusen, Christopher Mason, Dearbhla A. Hull et al. · Tissue Engineering · 2006 · 82 citations

Tissue Engineering, Engineering, Adult Stem Cell +20