Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Laura E, Randle"'
Autor:
Ross A Kelly, Joseph Leedale, Andy Harrell, Daniel A Beard, Laura E Randle, Amy E Chadwick, Steven D Webb
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0207803 (2018)
Cancer cells depend on glucose metabolism via glycolysis as a primary energy source, despite the presence of oxygen and fully functioning mitochondria, in order to promote growth, proliferation and longevity. Glycolysis relies upon NAD+ to accept ele
Externí odkaz:
https://doaj.org/article/6175f3db99624567aabd4c19c5b8a565
Autor:
Said Alizadeh-Shekalgourabi, Sam P. de Visser, James F. Dunn, Alistair J. Fielding, Michael G. B. Drew, Fyaz M.D. Ismail, Fabián G. Cantú Reinhard, Alessio del Casino, Nicola M. Dempster, Philip G. Evans, Verity Male, Dascombe Mj, Valentina Lukinović, Roger H. Bisby, Lutfun Nahar, Satyajit D. Sarker, Laura E. Randle
Publikováno v:
Fielding, A, Lukinović, V, Evans, P G, Alizadeh-Shekalgourabi, S, Bisby, R H, Drew, M G B, ADel Casino, A, Dunn, J F, Randle, L E, Dempster, N M, Nahar, L, Sarker, S D, Cantu Reinhard, F, De Visser, S, Dascombe, M & Ismail, F M D 2017, ' Modulation of Antimalarial Activity at a Putative Bisquinoline Receptor in vivo Using Fluorinated Bisquinolines ', Chemistry: A European Journal, vol. 23, no. 28, pp. 6811-6828 . https://doi.org/10.1002/chem.201605099
Antimalarials can interact with heme covalently, by π⋅⋅⋅π interactions or by hydrogen bonding. Consequently, the prototropy of 4-aminoquinolines and quinoline methanols was investigated by using quantum mechanics. Calculations showed mefloqui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d03c9f8537ab54ae4ac5893b4cee3db
https://www.ccdc.cam.ac.uk/structures/search?id=doi:10.5517/ccdc.csd.cc7h472&sid=DataCite
https://www.ccdc.cam.ac.uk/structures/search?id=doi:10.5517/ccdc.csd.cc7h472&sid=DataCite
Autor:
John Farrell, Sophie L. Regan, Dominic P. Williams, Neil R. Kitteringham, Alvin J. L. Chia, Laura E. Randle, Abhishek Srivastava, Christopher E. Goldring, Andrew V. Stachulski, Dean J. Naisbitt, Daniel J. Antoine, Thomas A. Baillie, Martin S. Lennard, J. Luis Castrejon, Hayley Callan, B. Kevin Park, Deepak Dalvie, R. Scott Obach
Publikováno v:
Medicinal Research Reviews. 33:985-1080
The decline in approval of new drugs during the past decade has led to a close analysis of the drug discovery process. One of the main reasons for attrition is preclinical toxicity, frequently attributed to the generation of protein-reactive drug met
Autor:
Neil R. Kitteringham, Samantha J. Williams, Laura E. Randle, B. Kevin Park, Christopher M. Sanderson, Azman Abdullah, Christopher E. Goldring, Rowena L. Sison, Joanne Walsh, Rosalind E. Jenkins, John D. Hayes, Larry G. Higgins, Helen Powell, Masayuki Yamamoto
Publikováno v:
Journal of Proteomics
The transcription factor Nrf2 regulates expression of multiple cellular defence proteins through the antioxidant response element (ARE). Nrf2-deficient mice (Nrf2−/−) are highly susceptible to xenobiotic-mediated toxicity, but the precise molecul
Autor:
Dominic P. Williams, Neil R. Kitteringham, Laura E. Randle, Jean G. Sathish, B.K. Park, I Macdonald
Publikováno v:
British Journal of Pharmacology. 153:820-830
Background and purpose: Paracetamol, a major cause of acute liver failure (ALF) represents a significant clinical problem. Adrenoceptor stimulation or antagonism can modulate chemical-induced hepatotoxicity. We investigated the role of endogenous cat
Autor:
Andrew V, Stachulski, Thomas A, Baillie, B Kevin, Park, R Scott, Obach, Deepak K, Dalvie, Dominic P, Williams, Abhishek, Srivastava, Sophie L, Regan, Daniel J, Antoine, Christopher E P, Goldring, Alvin J L, Chia, Neil R, Kitteringham, Laura E, Randle, Hayley, Callan, J Luis, Castrejon, John, Farrell, Dean J, Naisbitt, Martin S, Lennard
Publikováno v:
Medicinal research reviews. 33(5)
The decline in approval of new drugs during the past decade has led to a close analysis of the drug discovery process. One of the main reasons for attrition is preclinical toxicity, frequently attributed to the generation of protein-reactive drug met
Autor:
Alvin J. L. Chia, John D. Hayes, B. Kevin Park, Christopher E. Goldring, Neil R. Kitteringham, Rosalind E. Jenkins, Laura E. Randle, Ian M. Copple
Publikováno v:
Hepatology (Baltimore, Md.). 48(4)
The transcription factor Nrf2 regulates the expression of numerous cytoprotective genes in mammalian cells. We have demonstrated previously that acetaminophen activates Nrf2 in mouse liver following administration of non-hepatotoxic and hepatotoxic d
Autor:
Dominic P. Williams, Christopher E. Goldring, Peter Metcalfe, Craig Benson, B. Kevin Park, Neil R. Kitteringham, Laura E. Randle
Publikováno v:
Toxicology. 243(3)
The Keap1-Nrf2-ARE signalling pathway has emerged as an important regulator of the mammalian defence system to enable detoxification and clearance of foreign chemicals. Recent studies by our group using paracetamol (APAP), diethylmaleate and buthioni
Autor:
Julian Blagg, Dominic P. Williams, Daniel J. Antoine, Laura E. Randle, Martin Howard, Russell Jones, B. Kevin Park, Iain Gardner, Philip J. Butler, Anthony Payne
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 322(3)
Furosemide, a loop diuretic, causes hepatic necrosis in mice. Previous evidence suggested hepatotoxicity arises from metabolic bioactivation to a chemically reactive metabolite that binds to hepatic proteins. To define the nature of the toxic metabol
Autor:
Cerys A. Lovatt, Dominic P. Williams, Andrew Owen, Wolfgang Hillen, Philip J. Butler, Xiao-Ping Liu, Christian Berens, Azman Abdullah, Peter Metcalfe, Rosalind E. Jenkins, B. Kevin Park, Alec W.M. Simpson, Neil R. Kitteringham, Laura E. Randle, Lesley I. McLellan, Christopher E. Goldring, Brian Foster
Publikováno v:
American journal of physiology. Cell physiology. 290(1)
Precise control of the level of protein expression in cells can yield quantitative and temporal information on the role of a given gene in normal cellular physiology and on exposure to chemicals and drugs. This is particularly relevant to liver cells