C. Higgins

Towards gene therapy for cystic fibrosis: a clinical progress report

D. Gill, E. Alton, J. Innes, 1998, Gene Therapy.

Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis

D. Gill, L. Huang, F. Sorgi, 2000, Gene Therapy.

Chloride secretion in the trachea of null cystic fibrosis mice: the effects of transfection with pTrial10‐CFTR2.

M. Evans, S. Hyde, D. Gill, 1997, The Journal of physiology.

The multidrug resistance and cystic fibrosis genes have complementary patterns of epithelial expression.

C. Higgins, A. E. Trezíse, S. Hyde, 1992, The EMBO journal.

Measure and interpretation of CF gene therapy trial results.

D. Porteous, D. Gill, J. Innes, 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

ABCB4 gene sequence variation in women with intrahepatic cholestasis of pregnancy

M. McCarthy, S. Wiltshire, K. Linton, 2003 .

A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis

D. Gill, F. Sorgi, D. Bilton, 1997, Gene Therapy.

Tamoxifen blocks chloride channels. A possible mechanism for cataract formation.

C. Higgins, A. E. Trezíse, M. Valverde, 1994, The Journal of clinical investigation.

A second dose of a CFTR cDNA–liposome complex is as effective as the first dose in restoring cAMP-dependent chloride secretion to null CF mice trachea

D. Gill, W. Colledge, C. Goddard, 1997, Gene Therapy.