Derek J. Blake

The utrophin and dystrophin genes share similarities in genomic structure.

A. Monaco, K. Davies, D. Blake, 1993, Human molecular genetics.

Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cells.

C. Esapa, D. Blake, R. McIlhinney, 2005, Human molecular genetics.

Increasing complexity of the dystrophin-associated protein complex.

K. Davies, D. Blake, D J Blake, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Coiled-coil regions in the carboxy-terminal domains of dystrophin and related proteins: potentials for protein-protein interactions.

K. Davies, S. Winder, A. Knight, 1995, Trends in biochemical sciences.

Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site.

K. Davies, D. Blake, J. Tinsley, 1993, Human molecular genetics.

The genetic basis of neuromuscular disorders.

K. Davies, D. Blake, R. Nawrotzki, 1996, Trends in genetics : TIG.

The effect of glucocorticoids on the accumulation of utrophin by cultured normal and dystrophic human skeletal muscle satellite cells

K. Davies, G. Karpati, P. Holland, 1995, Neuromuscular Disorders.

G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain.

K. Davies, E. Barnard, D. Górecki, 1995, Proceedings of the National Academy of Sciences of the United States of America.