Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Helen Garside"'
Autor:
Mark Graham, Emma Thompson, Martin R. Brown, Saseela Atwal, Chloe Bean, Michael Sullivan, Helen Garside, Tony Goodall
Publikováno v:
Toxicological Sciences. 160:408-419
Significant prolonged aryl hydrocarbon receptor (AHR) activation, classically exhibited following exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin, can cause a variety of undesirable toxicological effects. Novel pharmaceutical chemistries also have th
Autor:
Karen Oldman, Mark Pilling, Martin R. Brown, Chris Pollard, Najah Abi-Gerges, Clare E. Sefton, Amy Pointon, Helen Garside
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 83:1-15
Cardiovascular toxicity is a prominent reason for failures in drug development, resulting in the demand for assays that can predict this liability in early drug discovery. We investigated whether iCell® cardiomyocytes have utility as an early QT/TdP
Autor:
Chris Pollard, Najah Abi-Gerges, Joanne Bowes, Ian L. Dale, Amy Pointon, Helen Garside, Alexander R. Harmer
Publikováno v:
Toxicological Sciences. 144:227-237
Functional changes to cardiomyocytes are a common cause of attrition in preclinical and clinical drug development. Current approaches to assess cardiomyocyte contractility in vitro are limited to low-throughput methods not amenable to early drug disc
Autor:
Najah, Abi-Gerges, Amy, Pointon, Karen L, Oldman, Martin R, Brown, Mark A, Pilling, Clare E, Sefton, Helen, Garside, Christopher E, Pollard
Publikováno v:
Journal of pharmacological and toxicological methods. 83
Cardiovascular toxicity is a prominent reason for failures in drug development, resulting in the demand for assays that can predict this liability in early drug discovery. We investigated whether iCell® cardiomyocytes have utility as an early QT/TdP
Publikováno v:
Molecular and Cellular Biochemistry. 341:73-78
Within the liver, hormonal control of glycogen metabolism allows for rapid release and uptake of glucose from the circulation, providing a reserve of glucose that can be utilised by other organs. Traditionally, cellular glycogen storage has been dete
Autor:
Fiona H Blackhall, Ian J. Stratford, Leo A. H. Zeef, Helen Garside, Anne White, Dave Singh, Lisa Rice, Charlotte E Waters, Adam Stevens, Paul Kay, David W. Ray, Robert Clarke, Jennifer Eccles, Brian A. Telfer, Paula Sommer
Publikováno v:
The Journal of Endocrinology
Glucocorticoid (GC) receptors (GRs) have profound anti-survival effects on human small cell lung cancer (SCLC). To explore the basis of these effects, protein partners for GRs were sought using a yeast two-hybrid screen. We discovered a novel gene, F
Publikováno v:
Xenobiotica. 38:1-20
Early identification of toxicity associated with new chemical entities is important for reducing compound attrition in late stage drug discovery. Activation of the aryl hydrocarbon receptor (AhR) by xenobiotics is a recognised mechanism of toxicity:
Autor:
Andrew Jermy, Stephanie Carter, Martin Willer, Helen Garside, Gregor J. Steel, Colin J. Stirling
Publikováno v:
Biochemistry. 42:7171-7177
The signal recognition particle (SRP) is required for co-translational targeting of polypeptides to the endoplasmic reticulum (ER). Once at the membrane, the precursor interacts with a complex proteinaceous machinery that mediates its translocation a
Publikováno v:
Molecular Endocrinology. 17:845-859
Within the human glucocorticoid receptor (GR) steroid binding pocket, tyrosine 735 makes hydrophobic contact with the steroid D ring. Substitution of tyrosine735 selectively impairs glucocorticoid transactivation but not transrepression. We now show,
Autor:
Andrew Berry, David W. Ray, Laura Matthews, Jacqueline Ohanian, Helen Garside, Vasken Ohanian
Publikováno v:
Matthews, L, Berry, A, Ohanian, V, Ohanian, J, Garside, H & Ray, D 2008, ' Caveolin mediates rapid glucocorticoid effects and couples glucocorticoid action to the antiproliferative program ', Molecular Endocrinology, vol. 22, no. 6, pp. 1320-1330 . https://doi.org/10.1210/me.2007-0154
Many glucocorticoid (Gc) actions are of rapid onset and therefore require acute regulation of intracellular signaling cascades. Integration of diverse extracellular signals requires cross-talk between intracellular pathways, suggesting the existence