R. Williamson

发表

Gene delivery and expression mediated by an integrin-binding peptide.

A. Miller, S. Hart, R. Harbottle, 1995, Gene therapy.

Cell binding and internalization by filamentous phage displaying a cyclic Arg-Gly-Asp-containing peptide.

S. Hart, R. Harbottle, C. Coutelle, 1994, The Journal of biological chemistry.

New treatments for cystic fibrosis.

D. Geddes, E. Alton, N. Caplen, 1992, British medical bulletin.

In vitro liposome-mediated DNA transfection of epithelial cell lines using the cationic liposome DC-Chol/DOPE.

N. Caplen, D. Geddes, E. Kinrade, 1995, Gene therapy.

Non–invasive liposome–mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

A. Miller, S. Hart, E. Alton, 1993 .

Atomic force microscopy imaging of DNA–cationic liposome complexes optimised for gene transfection into neuronal cells

J. Carlin, T. Senden, D. Jans, 2001, The journal of gene medicine.

The introduction of two silent mutations into a CFTR cDNA construct allows improved detection of exogenous mRNA in gene transfer experiments.

S. Hart, E. Alton, C. Coutelle, 1995, Human Molecular Genetics.

Gene therapy for cystic fibrosis.

C. Coutelle, C. Huxley, S. Hart, 1993, Archives of disease in childhood.

Genetic analysis of DNA from single human oocytes: A model for preimplantation diagnosis of cystic fibrosis

R. Williamson, A. Handyside, C. Coutelle, 1990, BMJ.

Corrigendum: Non–invasive liposome–mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

S. Hart, E. Alton, P. Jeffery, 1993, Nature Genetics.