Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Nicola E. Potter"'
Autor:
Sara G.M. Piccirillo, Sue Colman, Nicola E. Potter, Frederik W. van Delft, Suzanne Lillis, Maria-Jose Carnicer, Lyndal Kearney, Colin Watts, Mel Greaves
Publikováno v:
Stem Cell Reports, Vol 4, Iss 1, Pp 7-15 (2015)
Summary: Glioblastoma (GBM) is a lethal malignancy whose clinical intransigence has been linked to extensive intraclonal genetic and phenotypic diversity and the common emergence of therapeutic resistance. This interpretation embodies the implicit as
Externí odkaz:
https://doaj.org/article/cc79c6f4f2a04f6ab01f6a39a4454a9b
Autor:
Nigel H. Russell, David Grimwade, Michael Dennis, Richard Dillon, Nicola Foot, Sandrine Jayne, Nicola E. Potter, Kavita Raj, Mikel Valganon, Matthew J. Ahearne, Lynn Quek, Sudhir Tauro, Jelena V. Jovanovic, Ellen Solomon, Martin J. S. Dyer
Publikováno v:
Leukemia
Publikováno v:
British Journal of Haematology. 193:231-244
In recent years there have been major advances in the use of molecular diagnostic and monitoring techniques for patients with acute myeloid leukaemia (AML). Coupled with the simultaneous explosion of new therapeutic agents, this has sown the seeds fo
Autor:
Nicola E. Potter, Manohursingh Runglall, Adam Ivey, Anthony P. Schwarer, Kavita Raj, Phillip C. Nguyen, Nigel H. Russell, Chun Yew Fong, Annie‐Louise Latif, Andrew H. Wei, Tse-Chieh Teh, Andrew Grigg, Nicholas James Cummings, Ing Soo Tiong, Richard Dillon, David Taussig
Publikováno v:
British Journal of Haematology
Summary Based on promising results in older adults with acute myeloid leukaemia (AML), we treated patients with NPM1 mut measurable residual disease (MRD) using off‐label venetoclax in combination with low‐dose cytarabine or azacitidine. Twelve c
Autor:
Claire Hemmaway, Andrew H. Wei, Chung H. Kok, Nicola E. Potter, Richard Dillon, Ashish Bajel, Nigel H. Russell, Amanda F. Gilkes, James Anton Kuzich, Devendra K Hiwase, Adam Ivey, Jake Shortt, Abin Thomas, Emad Uddin Abro, Nisha Thiagarajah, James P Rowland, Matthew L. Smith, Kirsty Sharplin, Aditya Tedjaseputra, Carolyn S. Grove, Ing Soo Tiong
Monitoring of NPM1 mutant (NPM1mut) measurable residual disease (MRD) in acute myeloid leukemia (AML) has an established role in patients who are treated with intensive chemotherapy. The European LeukemiaNet has defined molecular persistence at low c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::286cfe6c9b290acbd9859864007fb26f
https://orca.cardiff.ac.uk/id/eprint/146658/1/advancesadv2021005455.pdf
https://orca.cardiff.ac.uk/id/eprint/146658/1/advancesadv2021005455.pdf
Autor:
Nisha Thiagarajah, Richard Dillon, Nigel H. Russell, Amanda F. Gilkes, Ashish Bajel, Ing Soo Tiong, Andrew H. Wei, Claire Hemmaway, Abin Thomas, Nicola E. Potter, Matthew Smith, James Anton Kuzich, Chung H. Kok, Adam Ivey
Publikováno v:
Blood. 136:25-27
Introduction Molecular MRD assays targeting NPM1 mutant (mut) transcripts have an established role for monitoring treatment efficacy in patients with NPM1mut AML. Approximately 25% of NPM1mut patients show persistent MRD level in the bone marrow (BM)
Autor:
Chuling Ding, Mark Lynch, Phil Ancliff, José Afonso Guerra-Assunção, Sten Eirik W. Jacobsen, Nicola E. Potter, Maxime Tarabichi, Amy P. Webster, Peter Van Loo, Agne Daneviciute, Mel Greaves, Rajeev Gupta, Chela James, Stephan Beck, Javier Herrero, Virginia Turati, Giovanni Cazzaniga, Lucia Conde, John Brown, Lisa J. Russell, Iain C. Macaulay, Georgina W. Hall, Andrea Biondi, Mike Hubank, Sarah Inglott, Tariq Enver, Gillian May, Simone Ecker
Publikováno v:
Nature cancer
Comparison of intratumor genetic heterogeneity in cancer at diagnosis and relapse suggests that chemotherapy induces bottleneck selection of subclonal genotypes. However, evolutionary events subsequent to chemotherapy could also explain changes in cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dc28217667eec84f4b36c5273edf387
http://hdl.handle.net/10281/336812
http://hdl.handle.net/10281/336812
Autor:
Jelena V. Jovanovic, Michael Dennis, Manohursingh Runglall, Nicola E. Potter, Anju Kanda, Pramila Krishnamurthy, Igor Novitzky-Basso, Anjum Bashir Khan, Emmanouil Nikolousis, Alan Kenneth Burnett, Robert Kerrin Hills, Samah Alimam, David Grimwade, Ulrik Malthe Overgaard, Charles Craddock, Rosemary E. Gale, Asim Khwaja, Kate Hill, Richard Dillon, Nicola Foot, Adam Ivey, Rahuman Salim, Priyanka Mehta, Damian Finnegan, Erin Hurst, Amanda F. Gilkes, Sylvie D. Freeman, Matthew Lee Smith, David Taussig, Steven Knapper, Nigel H. Russell, Jamie Cavenagh, Mikel Valganon, Ruth Spearing, Hans Beier Ommen, Robert Danby, Kavita Raj, Harpreet Kaur, Peter R. E. Johnson
Publikováno v:
Dillon, R, Hills, R K, Freeman, S D, Potter, N, Jovanovic, J, Ivey, A, Kanda, A, Runglall, M, Foot, N, Valganon, M, Khwaja, A, Cavenagh, J, Smith, M L, Ommen, H B, Overgaard, U, Dennis, M, Knapper, S, Kaur, H, Taussig, D C, Mehta, P, Raj, K, Novitzky-Basso, I, Nikolousis, E, Danby, R D, Krishnamurthy, P, Hill, K, Finnegan, D, Alimam, S, Hurst, E, Johnson, P, Khan, A B, Salim, R, Craddock, C F, Spearing, R L, Gilkes, A F, Gale, R E, Burnett, A K, Russell, N H & Grimwade, D 2020, ' Molecular MRD status and outcome after transplantation in NPM1 mutated AML ', Blood, vol. 135, no. 9, pp. 680-688 . https://doi.org/10.1182/blood.2019002959
Dillon, R, Hills, R, Freeman, S, Potter, N, Jovanovic, J, Ivey, A, Kanda, A S, Runglall, M, Foot, N, Valganon, M, Khwaja, A, Cavenagh, J, Smith, M, Ommen, H B, Overgaard, U M, Dennis, M, Knapper, S, Kaur, H, Taussig, D, Mehta, P, Raj, K, Novitzky-Basso, I, Nikolousis, E, Danby, R, Krishnamurthy, P, Hill, K, Finnegan, D, Alimam, S, Hurst, E, Johnson, P, Khan, A, Salim, R, Craddock, C, Spearing, R, Gilkes, A, Gale, R, Burnett, A, Russell, N H & Grimwade, D 2020, ' Molecular MRD status and outcome after transplantation in NPM1-mutated AML ', Blood, vol. 135, no. 9, pp. 680-688 . https://doi.org/10.1182/blood.2019002959
Dillon, R, Hills, R, Freeman, S, Potter, N, Jovanovic, J, Ivey, A, Kanda, A S, Runglall, M, Foot, N, Valganon, M, Khwaja, A, Cavenagh, J, Smith, M, Ommen, H B, Overgaard, U M, Dennis, M, Knapper, S, Kaur, H, Taussig, D, Mehta, P, Raj, K, Novitzky-Basso, I, Nikolousis, E, Danby, R, Krishnamurthy, P, Hill, K, Finnegan, D, Alimam, S, Hurst, E, Johnson, P, Khan, A, Salim, R, Craddock, C, Spearing, R, Gilkes, A, Gale, R, Burnett, A, Russell, N H & Grimwade, D 2020, ' Molecular MRD status and outcome after transplantation in NPM1-mutated AML ', Blood, vol. 135, no. 9, pp. 680-688 . https://doi.org/10.1182/blood.2019002959
Relapse remains the most common cause of treatment failure for patients with acute myeloid leukemia (AML) who undergo allogeneic stem cell transplantation (alloSCT), and carries a grave prognosis. Multiple studies have identified the presence of meas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b21c643cbf633633d68fcbce8813cce
https://kclpure.kcl.ac.uk/en/publications/16321efb-66e2-4258-8991-eac3a8316f55
https://kclpure.kcl.ac.uk/en/publications/16321efb-66e2-4258-8991-eac3a8316f55
Autor:
Lyndal Kearney, Nicola E. Potter, Sabine Strehl, Christine J. Harrison, Helen J. Blair, Lisa Jones, Lisa J. Russell, Mel Greaves
Publikováno v:
Leukemia
Deregulated expression of the type I cytokine receptor, CRLF2, is observed in 5-15% of precursor B-cell acute lymphoblastic leukaemia (B-ALL). We have previously reported the genomic landscape of patients with CRLF2 rearrangements (CRLF2-r) using bot
Autor:
Marcela B. Mansur, Luca Ermini, Donát Alpár, Lyndal Kearney, Tomasz Szczepański, Ian Titley, D. Wren, Anthony M. Ford, F W van Delft, Mel Greaves, David Gonzalez, Nicola E. Potter, Caroline M. Bateman
Publikováno v:
Leukemia. 29:839-846
Studies on twins with concordant acute lymphoblastic leukemia (ALL) have revealed that ETV6-RUNX1 gene fusion is a common, prenatal genetic event with other driver aberrations occurring subclonally and probably postnatally. The fetal cell type that i