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Becky Saunders
Becky Saunders
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Cited by
Year
Acetyl-CoA synthetase 2 promotes acetate utilization and maintains cancer cell growth under metabolic stress
ZT Schug, B Peck, DT Jones, Q Zhang, S Grosskurth, IS Alam, ...
Cancer cell 27 (1), 57-71, 2015
7022015
The glutathione redox system is essential to prevent ferroptosis caused by impaired lipid metabolism in clear cell renal cell carcinoma
H Miess, B Dankworth, AM Gouw, M Rosenfeldt, W Schmitz, M Jiang, ...
Oncogene 37 (40), 5435-5450, 2018
2752018
Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)
C Licht, S Heinen, M Jozsi, I Löschmann, RE Saunders, SJ Perkins, ...
Kidney international 70 (1), 42-50, 2006
2472006
Inhibition of fatty acid desaturation is detrimental to cancer cell survival in metabolically compromised environments
B Peck, ZT Schug, Q Zhang, B Dankworth, DT Jones, E Smethurst, ...
Cancer & metabolism 4, 1-18, 2016
2172016
Reduced NF1 Expression Confers Resistance to EGFR Inhibition in Lung Cancer
EC de Bruin, C Cowell, PH Warne, M Jiang, RE Saunders, MA Melnick, ...
Cancer discovery 4 (5), 606-619, 2014
2112014
Determination of synthetic lethal interactions in KRAS oncogene-dependent cancer cells reveals novel therapeutic targeting strategies
M Steckel, M Molina-Arcas, B Weigelt, M Marani, PH Warne, H Kuznetsov, ...
Cell research 22 (8), 1227-1245, 2012
1982012
The interactive Factor H–atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with …
RE Saunders, C Abarrategui‐Garrido, V Frémeaux‐Bacchi, ...
Human mutation 28 (3), 222-234, 2007
1952007
Multiomic analysis of the UV-induced DNA damage response
S Boeing, L Williamson, V Encheva, I Gori, RE Saunders, R Instrell, ...
Cell reports 15 (7), 1597-1610, 2016
1802016
Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions
M Józsi, S Heinen, A Hartmann, CW Ostrowicz, S Hälbich, H Richter, ...
Journal of the American Society of Nephrology 17 (1), 170-177, 2006
1592006
Genome‐wide RNA interference analysis of renal carcinoma survival regulators identifies MCT4 as a Warburg effect metabolic target
M Gerlinger, CR Santos, B Spencer‐Dene, P Martinez, D Endesfelder, ...
The Journal of pathology 227 (2), 146-156, 2012
1382012
Genome‐wide siRNA screen reveals amino acid starvation‐induced autophagy requires SCOC and WAC
NC McKnight, HBJ Jefferies, EA Alemu, RE Saunders, M Howell, ...
The EMBO journal 31 (8), 1931-1946, 2012
1242012
Salt-inducible kinases regulate growth through the Hippo signalling pathway in Drosophila
MC Wehr, MV Holder, I Gailite, RE Saunders, TM Maile, E Ciirdaeva, ...
Nature cell biology 15 (1), 61-71, 2013
1122013
An interactive web database of factor H‐associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease‐associated mutations
RE Saunders, THJ Goodship, PF Zipfel, SJ Perkins
Human mutation 27 (1), 21-30, 2006
112*2006
Functional screening identifies MCT4 as a key regulator of breast cancer cell metabolism and survival
F Baenke, S Dubuis, C Brault, B Weigelt, B Dankworth, B Griffiths, M Jiang, ...
The Journal of pathology 237 (2), 152-165, 2015
962015
Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis tools
RE Saunders, NM O'Connell, CA Lee, DJ Perry, SJ Perkins
Human mutation 26 (3), 192-198, 2005
832005
A CRISPR platform for targeted in vivo screens identifies Toxoplasma gondii virulence factors in mice
J Young, C Dominicus, J Wagener, S Butterworth, X Ye, G Kelly, M Ordan, ...
Nature Communications 10 (1), 3963, 2019
632019
Charge environments around phosphorylation sites in proteins
J Kitchen, RE Saunders, J Warwicker
BMC structural biology 8, 1-11, 2008
422008
Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illness
MM Edey, PA Mead, RE Saunders, L Strain, SJ Perkins, THJ Goodship, ...
American journal of kidney diseases 51 (3), 487-490, 2008
392008
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency
RE Saunders, N Shiltagh, K Gomez, G Mellars, C Cooper, DJ Perry, ...
Thrombosis and haemostasis 102 (08), 287-301, 2009
382009
Control of skeletal morphogenesis by the Hippo-YAP/TAZ pathway
HK Vanyai, F Prin, O Guillermin, B Marzook, S Boeing, A Howson, ...
Development 147 (21), dev187187, 2020
362020
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