Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anthony, Cutts"'
Autor:
Angela Hamblin, Sarah Wordsworth, Jilles M Fermont, Suzanne Page, Kulvinder Kaur, Carme Camps, Pamela Kaisaki, Avinash Gupta, Denis Talbot, Mark Middleton, Shirley Henderson, Anthony Cutts, Dimitrios V Vavoulis, Nick Housby, Ian Tomlinson, Jenny C Taylor, Anna Schuh
Publikováno v:
PLoS Medicine, Vol 14, Iss 2, p e1002230 (2017)
BackgroundSingle gene tests to predict whether cancers respond to specific targeted therapies are performed increasingly often. Advances in sequencing technology, collectively referred to as next generation sequencing (NGS), mean the entire cancer ge
Externí odkaz:
https://doaj.org/article/30d53926b96445d9a9f524a7a39674d7
Autor:
Pamela J Kaisaki, Anthony Cutts, Niko Popitsch, Carme Camps, Melissa M Pentony, Gareth Wilson, Suzanne Page, Kulvinder Kaur, Dimitris Vavoulis, Shirley Henderson, Avinash Gupta, Mark R Middleton, Ioannis Karydis, Denis C Talbot, Anna Schuh, Jenny C Taylor
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162809 (2016)
Use of circulating tumour DNA (ctDNA) as a liquid biopsy has been proposed for potential identification and monitoring of solid tumours. We investigate a next-generation sequencing approach for mutation detection in ctDNA in two related studies using
Externí odkaz:
https://doaj.org/article/c84931d42bd34e6883e57ececea2c9cd
Autor:
Mary Petrou, Anthony Cutts, Barnaby Clark, Dimitrios V Vavoulis, Anna Schuh, Frances Smith, Shirley Henderson
Publikováno v:
Blood. 134:1190-1193
TO THE EDITOR: Since the discovery of circulating cell-free DNA (cfDNA) in the plasma of pregnant women in the late 1990s,[1][1],[2][2] its potential for prenatal diagnosis has been the focus of intensive technological innovation. Screening for chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3adc14981418ca25d2387cdb2a52c024
https://doi.org/10.1182/blood.2019002099
https://doi.org/10.1182/blood.2019002099
Publikováno v:
Bioinformatics
Tumours are composed of genotypically and phenotypically distinct cancer cell populations (clones), which are subject to a process of Darwinian evolution in response to changes in their local micro-environment, such as drug treatment. In a cancer pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74be03d80e6aa10f20d96ff33cd16947
Autor:
Helene Marie-Pierre Dreau, Josh Caddy, Anna Schuh, Laura Lopez Pascua, Andrew Davies, Edward Wilson, Pek Sang Tang, Katy Mercer, Peter Johnson, Louise Stanton, Anthony Cutts
Publikováno v:
Blood. 136:24-25
Introduction Plasma cell-free DNA (cfDNA) and circulating tumor DNA (ctDNA) genotyping in Diffuse Large B-cell Lymphoma (DLBCL) holds great promise for early detection and response prediction. DLBCL is a highly heterogenous disease with diverse tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7cba7574d96c8abf04d9814cd67405e
https://doi.org/10.1182/blood-2020-137439
https://doi.org/10.1182/blood-2020-137439
Autor:
Frances Smith, Dimitrios V Vavoulis, Barnaby Clark, Shirley Henderson, Mary Petrou, Anna Schuh, Anthony Cutts
Non-invasive prenatal testing (NIPT) to date is used in the clinic primarily to detect foetal aneuploidy. Few studies so far have focused on the detection of monogenic autosomal recessive disorders where mother and foetus carry the same mutation. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bd8d925ec3d9510b84a7f1ccd9672bc
https://doi.org/10.1101/635342
https://doi.org/10.1101/635342
Autor:
Anthony Cutts, Oliver Venn, Alexander Dilthey, Avinash Gupta, Dimitris Vavoulis, Helene Dreau, Mark Middleton, Gil McVean, Jenny C. Taylor, Anna Schuh
Publikováno v:
NPJ Genomic Medicine
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-8 (2017)
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-8 (2017)
Cancer is characterised by complex somatically acquired genetic aberrations that manifest as intra-tumour and inter-tumour genetic heterogeneity and can lead to treatment resistance. In this case study, we characterise the genome-wide somatic mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::68b52849c0757cbc9a05ee19f18f9495
https://doi.org/10.1038/s41525-017-0030-7
https://doi.org/10.1038/s41525-017-0030-7
Autor:
Angela, Hamblin, Sarah, Wordsworth, Jilles M, Fermont, Suzanne, Page, Kulvinder, Kaur, Carme, Camps, Pamela, Kaisaki, Avinash, Gupta, Denis, Talbot, Mark, Middleton, Shirley, Henderson, Anthony, Cutts, Dimitrios V, Vavoulis, Nick, Housby, Ian, Tomlinson, Jenny C, Taylor, Anna, Schuh
Publikováno v:
PLoS Medicine, Vol 14, Iss 2, p e1002230 (2017)
PLoS Medicine
PLoS Medicine
Background Single gene tests to predict whether cancers respond to specific targeted therapies are performed increasingly often. Advances in sequencing technology, collectively referred to as next generation sequencing (NGS), mean the entire cancer g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6032383a8d73172aa0f15760e1e5db6a
https://ora.ox.ac.uk/objects/uuid:885a2715-5860-4ad3-bf89-31a4143ec52f
https://ora.ox.ac.uk/objects/uuid:885a2715-5860-4ad3-bf89-31a4143ec52f
Autor:
Anna Schuh, Ming-Qing Du, O. Salminen, N. Vaughan-Spickers, S. Barrans, R.T. Mizani, P. Johnson, Helene Marie-Pierre Dreau, Anthony Cutts, D. Joke, Francesco Cucco, C. Burton, Sophia Ahmed, Alexandra Clipson, Laura Lopez Pascua, M. Van Hoppe
Publikováno v:
Hematological Oncology. 35:281-281
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c09d33c8286a70c2d55351305c773ef1
https://doi.org/10.1002/hon.2439_6
https://doi.org/10.1002/hon.2439_6