W. H. Colledge

Details der Publikationsliste

Zeitraum

1995 - 2005

Anzahl

34

Co-Autoren

In vivo gene expression: DNA electrotransfer (2003)

Trezise, A. E., Palazon, L., Davies, W. L., Colledge, W. H.

The use of electric pulses to deliver therapeutic molecules to tissues and organs in vivo is a rapidly growing field of research. Electrotransfer can be used to deliver a wide range of potentially...

In vivo gene expression: DNA electrotransfer (2003)

Trezise, A. E., Palazon, L., Davies, W. L., Colledge, W. H.

The use of electric pulses to deliver therapeutic molecules to tissues and organs in vivo is a rapidly growing field of research. Electrotransfer can be used to deliver a wide range of potentially...

Mucus altering agents as adjuncts for nonviral gene transfer to airway epithelium (2001)

Ferrari, S., Kitson, C., Farley, R., Steel, R., Marriott, C., Parkins, D. A., ...

Nonviral vectors have been shown to be a safe and valid alternative to recombinant viruses for gene therapy of cystic fibrosis (CF). Nevertheless, gene transfer efficiency needs to be increased...

Mucus altering agents as adjuncts for nonviral gene transfer to airway epithelium (2001)

Ferrari, S., Kitson, C., Farley, R., Steel, R., Marriott, C., Parkins, D. A., ...

Nonviral vectors have been shown to be a safe and valid alternative to recombinant viruses for gene therapy of cystic fibrosis (CF). Nevertheless, gene transfer efficiency needs to be increased...

Cystic fibrosis gene therapy (1995)

Colledge, W H, Evans, M J

Cystic fibrosis is a common severe autosomal recessive genetic disease which is caused by dysfunction of an epithelial cell surface cAMP activated CI– channel. The effects of this dysfunction are...

Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis mice.

Valverde, M A, O'Brien, J A, Sepúlveda, F V, Ratcliff, R A, Evans, M J, Colledge, W H

Cystic fibrosis is a disease characterized by abnormalities in the epithelia of the lungs, intestine, salivary and sweat glands, liver, and reproductive systems, often as a result of inadequate...

Site-directed mutagenesis of polyomavirus middle-T antigen sequences encoding tyrosine 315 and tyrosine 250.

Markland, W, Oostra, B A, Harvey, R, Markham, A F, Colledge, W H, Smith, A E

Tyrosine residues of middle-T and tyrosine phosphorylation are thought to be important in the transformation of cultured rodent cells by polyomavirus. Of the potential tyrosine sites in the...

Null Mutation of the Lmo4 Gene or a Combined Null Mutation of the Lmo1/Lmo3 Genes Causes Perinatal Lethality, and Lmo4 Controls Neural Tube Development in Mice

Tse, E., Smith, A. J. H., Hunt, S., Lavenir, I., Forster, A., Warren, A. J., ...

The LIM-only family of proteins comprises four members; two of these (LMO1 and LMO2) are involved in human T-cell leukemia via chromosomal translocations, and LMO2 is a master regulator of...

Extensive mutagenesis of the nuclear location signal of simian virus 40 large-T antigen.

Colledge, W H, Richardson, W D, Edge, M D, Smith, A E

Site-directed mutagenesis was used to change Lys-128 of the simian virus 40 large-T nuclear location signal to Met, Ile, Arg, Gln, Asn, Leu, or His. Except for the large-T antigen of the Arg...

Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY3-36

Challis, B. G., Coll, A. P., Yeo, G. S. H., Pinnock, S. B., Dickson, S. L., Thresher, R. R., ...

Inactivating mutations of the pro-opiomelanocortin (POMC) gene in both mice and humans leads to hyperphagia and obesity. To further examine the mechanisms whereby POMC-deficiency leads to disordered...

Complementation of null CF mice with a human CFTR YAC transgene.

Manson, A L, Trezise, A E, MacVinish, L J, Kasschau, K D, Birchall, N, Episkopou, V, ...

We have made transgenic mice carrying a 320 kb YAC with the intact human cystic fibrosis transmembrane regulator (CFTR) gene. Mice that only express the human transgene were obtained by breeding with...

Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lens.

Gilmour, D T, Lyon, G J, Carlton, M B, Sanes, J R, Cunningham, J M, Anderson, J R, ...

SPARC (secreted protein acidic and rich in cysteine, also known as osteonectin/BM40) is a secreted Ca2+-binding glycoprotein that interacts with a range of extracellular matrix molecules, including...

The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study.

Cuthbert, A W, Halstead, J, Ratcliff, R, Colledge, W H, Evans, M J

1. The delta F508 mutation of the cystic fibrosis (CF) gene is of high frequency in man (1 in 25) and in homozygotes causes cystic fibrosis. It is suggested that cystic fibrosis heterozygotes...

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

MacVinish, L J, Gill, D R, Hyde, S C, Mofford, K A, Evans, M J, Higgins, C F, ...

1. An improved novel plasmid backbone, pTrial10, has been developed. We have used this vector to deliver the cDNA for the cystic fibrosis transmembrane conductance regulator (CFTR) to cells, both in...

A functional CFTR protein is required for mouse intestinal cAMP-, cGMP- and Ca(2+)-dependent HCO3- secretion.

Seidler, U, Blumenstein, I, Kretz, A, Viellard-Baron, D, Rossmann, H, Colledge, W H, ...

1. Most segments of the gastrointestinal tract secrete HCO3-, but the molecular nature of the secretory mechanisms has not been identified. We had previously speculated that the regulator for...

Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis mice.

Valverde, M A, O'Brien, J A, Sepúlveda, F V, Ratcliff, R A, Evans, M J, Colledge, W H

Cystic fibrosis is a disease characterized by abnormalities in the epithelia of the lungs, intestine, salivary and sweat glands, liver, and reproductive systems, often as a result of inadequate...

Site-directed mutagenesis of polyomavirus middle-T antigen sequences encoding tyrosine 315 and tyrosine 250.

Markland, W, Oostra, B A, Harvey, R, Markham, A F, Colledge, W H, Smith, A E

Tyrosine residues of middle-T and tyrosine phosphorylation are thought to be important in the transformation of cultured rodent cells by polyomavirus. Of the potential tyrosine sites in the...

Null Mutation of the Lmo4 Gene or a Combined Null Mutation of the Lmo1/Lmo3 Genes Causes Perinatal Lethality, and Lmo4 Controls Neural Tube Development in Mice

Tse, E., Smith, A. J. H., Hunt, S., Lavenir, I., Forster, A., Warren, A. J., ...

The LIM-only family of proteins comprises four members; two of these (LMO1 and LMO2) are involved in human T-cell leukemia via chromosomal translocations, and LMO2 is a master regulator of...

Extensive mutagenesis of the nuclear location signal of simian virus 40 large-T antigen.

Colledge, W H, Richardson, W D, Edge, M D, Smith, A E

Site-directed mutagenesis was used to change Lys-128 of the simian virus 40 large-T nuclear location signal to Met, Ile, Arg, Gln, Asn, Leu, or His. Except for the large-T antigen of the Arg...

Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY3-36

Challis, B. G., Coll, A. P., Yeo, G. S. H., Pinnock, S. B., Dickson, S. L., Thresher, R. R., ...

Inactivating mutations of the pro-opiomelanocortin (POMC) gene in both mice and humans leads to hyperphagia and obesity. To further examine the mechanisms whereby POMC-deficiency leads to disordered...

The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study.

Cuthbert, A W, Halstead, J, Ratcliff, R, Colledge, W H, Evans, M J

1. The delta F508 mutation of the cystic fibrosis (CF) gene is of high frequency in man (1 in 25) and in homozygotes causes cystic fibrosis. It is suggested that cystic fibrosis heterozygotes...

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

MacVinish, L J, Gill, D R, Hyde, S C, Mofford, K A, Evans, M J, Higgins, C F, ...

1. An improved novel plasmid backbone, pTrial10, has been developed. We have used this vector to deliver the cDNA for the cystic fibrosis transmembrane conductance regulator (CFTR) to cells, both in...

A functional CFTR protein is required for mouse intestinal cAMP-, cGMP- and Ca(2+)-dependent HCO3- secretion.

Seidler, U, Blumenstein, I, Kretz, A, Viellard-Baron, D, Rossmann, H, Colledge, W H, ...

1. Most segments of the gastrointestinal tract secrete HCO3-, but the molecular nature of the secretory mechanisms has not been identified. We had previously speculated that the regulator for...

Complementation of null CF mice with a human CFTR YAC transgene.

Manson, A L, Trezise, A E, MacVinish, L J, Kasschau, K D, Birchall, N, Episkopou, V, ...

We have made transgenic mice carrying a 320 kb YAC with the intact human cystic fibrosis transmembrane regulator (CFTR) gene. Mice that only express the human transgene were obtained by breeding with...

Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lens.

Gilmour, D T, Lyon, G J, Carlton, M B, Sanes, J R, Cunningham, J M, Anderson, J R, ...

SPARC (secreted protein acidic and rich in cysteine, also known as osteonectin/BM40) is a secreted Ca2+-binding glycoprotein that interacts with a range of extracellular matrix molecules, including...

Markedly reduced effects of (−)-isoprenaline but not of (−)-CGP12177 and unchanged affinity of β-blockers at Gly389-β1-adrenoceptors compared to Arg389-β1-adrenoceptors

Joseph, S S, Lynham, J A, Grace, A A, Colledge, W H, Kaumann, A J

Substitution of arginine by glycine at position 389, a frequent β1-adrenoceptor polymorphism, reduces adenylyl cyclase stimulation by (−)-isoprenaline. β1-Adrenoceptors mediate the effects of...

Chloride secretion in response to guanylin in colonic epithelial from normal and transgenic cystic fibrosis mice.

Cuthbert, A. W., Hickman, M. E., MacVinish, L. J., Evans, M. J., Colledge, W. H., Ratcliff, R., ...

1. Guanylin, a 15 amino acid endogenous gut peptide, increased the short circuit current (SCC) in the epithelium of the mouse colon, but only when applied to the apical and not the basolateral...

Evidence for cystic fibrosis transmembrane conductance regulator-dependent sodium reabsorption in kidney, using Cftrtm2cammice

Kibble, J D, Neal, A M, Colledge, W H, Green, R, Taylor, C J

The aims of this study were to investigate (a) if renal Na+ handling was normal in Cftrtm2camΔF508 cystic fibrosis mice, (b) whether adaptation to dietary salt depletion was preserved and (c)...

Expression and regulation of the Na+-K+-2Cl− cotransporter NKCC1 in the Normal and CFTR-deficient murine colon

Bachmann, O, Wüchner, K, Rossmann, H, Leipziger, J, Osikowska, B, Colledge, W H, ...

Defective regulation and/or reduced expression of the Na+-K+-2Cl− cotransporter NKCC1 may contribute to the severe secretory defect that is observed in cystic fibrosis, but data concerning the...

Mutation analysis of the c-mos proto-oncogene in human ovarian teratomas.

De Foy, K. A., Gayther, S. A., Colledge, W. H., Crockett, S., Scott, I. V., Evans, M. J., ...

Female transgenic mice lacking a functional c-mos proto-oncogene develop ovarian teratomas, indicating that c-mos may behave as a tumour-suppressor gene for this type of tumour. We have analysed the...