Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Christopher J, Caunt"'
Autor:
Andrew M. Kidger, Mark K. Saville, Linda K. Rushworth, Jane Davidson, Julia Stellzig, Motoharu Ono, Ludwig A. Kuebelsbeck, Klaus-Peter Janssen, Bernhard Holzmann, Jennifer P. Morton, Owen J. Sansom, Christopher J. Caunt, Stephen M. Keyse
Publikováno v:
Oncogene. 41:2811-2823
The cytoplasmic phosphatase DUSP6 and its nuclear counterpart DUSP5 are negative regulators of RAS/ERK signalling. Here we use deletion of either Dusp5 or Dusp6 to explore the roles of these phosphatases in a murine model of KRASG12D-driven pancreati
Autor:
Fiona Hey, Catherine Andreadi, Catherine Noble, Bipin Patel, Hong Jin, Tamihiro Kamata, Kees Straatman, Jinli Luo, Kathryn Balmanno, David T.W. Jones, V. Peter Collins, Simon J. Cook, Christopher J. Caunt, Catrin Pritchard
Publikováno v:
Heliyon, Vol 4, Iss 12, Pp e01065- (2018)
BRAF is a cytoplasmic protein kinase, which activates the MEK-ERK signalling pathway. Deregulation of the pathway is associated with the presence of BRAF mutations in human cancer, the most common being V600EBRAF, although structural rearrangements,
Externí odkaz:
https://doaj.org/article/fd31fb97d68f4aaf961cf388c3e1c07c
Autor:
Andrew M, Kidger, Mark K, Saville, Linda K, Rushworth, Jane, Davidson, Julia, Stellzig, Motoharu, Ono, Ludwig A, Kuebelsbeck, Klaus-Peter, Janssen, Bernhard, Holzmann, Jennifer P, Morton, Owen J, Sansom, Christopher J, Caunt, Stephen M, Keyse
Publikováno v:
Oncogene. 41(20)
The cytoplasmic phosphatase DUSP6 and its nuclear counterpart DUSP5 are negative regulators of RAS/ERK signalling. Here we use deletion of either Dusp5 or Dusp6 to explore the roles of these phosphatases in a murine model of KRAS
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e40077 (2012)
Gonadotropin-releasing hormone receptors (GnRHR) mediate activation and nuclear translocation of the extracellular signal regulated kinases 1 and 2 (ERK) by phosphorylation on the TEY motif. This is necessary for GnRH to initiate transcriptional prog
Externí odkaz:
https://doaj.org/article/e18885e77410470cade7adf1bb83764a
Autor:
Sylvain Meloche, Simon J. Cook, Christopher J. Caunt, Honorine Lebraud, Marc K. Saba-El-Leil, Hanneke Okkenhaug, Rebecca Gilley, Andrew M. Kidger, Tom D. Heightman, James Sipthorp
Publikováno v:
Bioconjugate Chemistry. 28:1677-1683
The RAS-RAF-MEK-ERK pathway has been intensively studied in oncology, with RAS known to be mutated in ∼30% of all human cancers. The recent emergence of ERK1/2 inhibitors and their ongoing clinical investigation demands a better understanding of ER
Autor:
Clive G. Bowsher, Craig A. McArdle, Thanh Pham, Kathryn Garner, George R. Pope, Christopher J. Caunt, Rebecca M. Perrett, Margaritis Voliotis, Krasimira Tsaneva-Atanasova
Publikováno v:
Journal of Biological Chemistry. 291:2246-2259
Cell signaling pathways are noisy communication channels, and statistical measures derived from information theory can be used to quantify the information they transfer. Here we use single cell signaling measures to calculate mutual information as a
Autor:
Julia Stellzig, Linda K. Rushworth, Cassidy Bayley, Stephen M. Keyse, Jane Davidson, Andrew M. Kidger, Edward Caddye, Tim Rogers, Christopher J. Caunt, Christopher J. Bryant
Publikováno v:
Proceedings of the National Academy of Sciences. 114
Deregulated extracellular signal-regulated kinase (ERK) signaling drives cancer growth. Normally, ERK activity is self-limiting by the rapid inactivation of upstream kinases and delayed induction of dual-specificity MAP kinase phosphatases (MKPs/DUSP
Autor:
Craig A. McArdle, Robert C. Fowkes, Christopher J. Caunt, Rebecca M. Perrett, Clive G. Bowsher, Krasimira Tsaneva-Atanasova
Publikováno v:
Journal of Biological Chemistry. 288:21001-21014
Many extracellular signals act via the Raf/MEK/ERK cascade in which kinetics, cell-cell variability, and sensitivity of the ERK response can all influence cell fate. Here we used automated microscopy to explore the effects of ERK-mediated negative fe
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1447
The spatiotemporal regulation of the Ras/ERK pathway is critical in determining the physiological and pathophysiological outcome of signaling. Dual-specificity mitogen-activated protein kinase (MAPK) phosphatases (DUSPs or MKPs) are key regulators of
Publikováno v:
Caunt, C J, Kidger, A M & Keyse, S M 2016, Visualizing and quantitating the spatiotemporal regulation of Ras/ERK signaling by dual-specificity mitogen-activated protein phosphatases (MKPs) . in R Pulido (ed.), Protein Tyrosine Phosphatases : Methods and Protocols . Methods in Molecular Biology, vol. 1447, Springer, pp. 197-215 . https://doi.org/10.1007/978-1-4939-3746-2_12
Methods in Molecular Biology ISBN: 9781493937448
Methods in Molecular Biology ISBN: 9781493937448
The spatiotemporal regulation of the Ras/ERK pathway is critical in determining the physiological and pathophysiological outcome of signaling. Dual-specificity mitogen-activated protein kinase (MAPK) phosphatases (DUSPs or MKPs) are key regulators of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c46614781c9e0b404f3334e91a6c1938
https://purehost.bath.ac.uk/ws/files/146949043/Methods_chapter_PDF.pdf
https://purehost.bath.ac.uk/ws/files/146949043/Methods_chapter_PDF.pdf