P. Dopping-Hepenstal

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

DebbieM Hunt, Lisa Rickman, NeilV Whittock et al. · European Journal of Human Genetics · 2001 · 104 citations

Medicine, Dermatology, Genetics +13

The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen

Peter C. van den Akker, Jemima E. Mellerio, Anna E. Martinez et al. · Journal of Medical Genetics · 2010 · 70 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Limitation of substratum size alters cytoskeletal organization and behaviour of Swiss 3T3 fibroblasts

Grenham W. Ireland, P. Dopping-Hepenstal, Paul Jordan et al. · Cell Biology International Reports · 1989 · 14 citations

Life Sciences, Biophysics, Cell Biology +12