Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Anthony E. Reeve"'
Autor:
Tyler McInnes, Donghui Zou, Dasari S. Rao, Francesca M. Munro, Vicky L. Phillips, John L. McCall, Michael A. Black, Anthony E. Reeve, Parry J. Guilford
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background Aberrant DNA methylation profiles are a characteristic of all known cancer types, epitomized by the CpG island methylator phenotype (CIMP) in colorectal cancer (CRC). Hypermethylation has been observed at CpG islands throughout th
Externí odkaz:
https://doaj.org/article/b983699b554c4626aa4eff65786a812f
Autor:
Anthony E. Reeve, Bernhard Holzmann, Jörg Rüdiger Siewert, John L. McCall, Han-Seung Yoon, Andre van Rij, Arend E. Merrie, Tumi Toro, Nikola Kasabov, Mark Thompson-Fawcett, Vicky Phillips, Parry J. Guilford, Robert Rosenberg, Jörg Mages, Michael A. Black, Jan Friederichs, Yu-Hsin Lin
Supplementary Tables 1-2 from Multiple Gene Expression Classifiers from Different Array Platforms Predict Poor Prognosis of Colorectal Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b34a66a1e0930f9da25d4940aedad96
https://doi.org/10.1158/1078-0432.22440696
https://doi.org/10.1158/1078-0432.22440696
Autor:
Anthony E. Reeve, Bernhard Holzmann, Jörg Rüdiger Siewert, John L. McCall, Han-Seung Yoon, Andre van Rij, Arend E. Merrie, Tumi Toro, Nikola Kasabov, Mark Thompson-Fawcett, Vicky Phillips, Parry J. Guilford, Robert Rosenberg, Jörg Mages, Michael A. Black, Jan Friederichs, Yu-Hsin Lin
Purpose: This study aimed to develop gene classifiers to predict colorectal cancer recurrence. We investigated whether gene classifiers derived from two tumor series using different array platforms could be independently validated by application to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe5cf06768ab427321bfbbed4e7f828
https://doi.org/10.1158/1078-0432.c.6517992.v1
https://doi.org/10.1158/1078-0432.c.6517992.v1
Autor:
Bryan R.G. Williams, Jane Skeen, Rosemary Heathcott, Anthony E. Reeve, Jennifer Alami, Herman Yeger, Patricia Kessler, Wenliang Li
Supplementary Table 1 from A Gene Expression Signature for Relapse of Primary Wilms Tumors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24b5046963294e3d16f3d90c53ebfe37
https://doi.org/10.1158/0008-5472.22364190.v1
https://doi.org/10.1158/0008-5472.22364190.v1
Autor:
Benjamin J Halliday, Ryuji Fukuzawa, David M Markie, Richard G Grundy, Jackie L Ludgate, Michael A Black, Jane E Skeen, Robert J Weeks, Daniel R Catchpoole, Aedan G K Roberts, Anthony E Reeve, Ian M Morison
Publikováno v:
PLoS Genetics, Vol 14, Iss 6, p e1007399 (2018)
Wilms tumour is a childhood tumour that arises as a consequence of somatic and rare germline mutations, the characterisation of which has refined our understanding of nephrogenesis and carcinogenesis. Here we report that germline loss of function mut
Externí odkaz:
https://doaj.org/article/40aef522afc74369a20470895065cac4
Autor:
Pardeep Kaurah, Magali Svrcek, Toshikazu Ushijima, James Whitworth, Yasmin Nouri, Kirsty L. Harris, Emily Schulpen, Jeremy L. Davis, Lynn DeGregorio, Hidetaka Yamada, Richard H. Hardwick, Tanis D Godwin, Julie Arnold, Carla Oliveira, Jolanda M. van Dieren, Helen L. Fisher, Bostjan Humar, Katharine Nichole Holm, Han Kwang Yang, Parry Guilford, Joana Figueiredo, Fátima Carneiro, Sonia S. Kupfer, Daniel G. Coit, Paul F. Mansfield, Andrew Latchford, Ana Sofia Ribeiro, Rebecca C. Fitzgerald, Anthony E. Reeve, Nicola Bougen-Zhukov, Patrick R. Benusiglio, Enrique Norero, Kimberley Gamet, Erin Gardner, Andrew A. Sporle, Patrícia Carneiro, Joao Sanches, Johanna L. D'Addario, Marc Tischkowitz, Maybelle McLeod, Tom Brew, Elizabeth C. Monroe, Alex Boussioutas, Rachel S. van der Post, Nicoline Hoogerbrugge, Mark D. Muller, Simone Busija, Haruhiko Sugimura, Irene Gullo, Tanya M. Bisseling, Karyn Paringatai, Liying Zhang, Joana Paredes, Raquel Seruca, David G. Huntsman, Karen E Chelcun Schreiber, James M. Ford, Jeremy Rossaak, Vanessa Blair, Amanda Charlton, Susan Parry, Takeshi Nakajima, Massimiliano di Pietro, C. J. Lintott, Adrian Claydon, Annemieke Cats
Publikováno v:
Lancet Oncology, 21, 8, pp. e386-e397
Lancet Oncol
Lancet Oncology, 21, e386-e397
Lancet Oncol
Lancet Oncology, 21, e386-e397
Contains fulltext : 225261.pdf (Publisher’s version ) (Closed access) Hereditary diffuse gastric cancer (HDGC) is an autosomal dominant cancer syndrome that is characterised by a high prevalence of diffuse gastric cancer and lobular breast cancer.
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 10, p e0186333 (2017)
PLoS ONE, Vol 12, Iss 10, p e0186333 (2017)
Wilms tumour (WT) is an embryonal tumour that recapitulates kidney development. The normal kidney is formed from two distinct embryological origins: the metanephric mesenchyme (MM) and the ureteric bud (UB). It is generally accepted that WT arises fr
Autor:
Anthony E. Reeve, Tyler McInnes, John L. McCall, Parry Guilford, Michael A. Black, Vicky L. Phillips, Donghui Zou, Dasari S. Rao, Francesca M. Munro
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
BMC Cancer
BMC Cancer
Background Aberrant DNA methylation profiles are a characteristic of all known cancer types, epitomized by the CpG island methylator phenotype (CIMP) in colorectal cancer (CRC). Hypermethylation has been observed at CpG islands throughout the genome,
Autor:
Catherine S. Choong, Nelly Sabbaghian, Donghui Zou, Mona Wu, T.Y. Tan, Paul Goodyer, S. Addidou-Kalucki, Bin Xu, Caroline Cole, Diana M. Iglesias, Adrian Charles, Anthony E. Reeve, William D. Foulkes, Michael R. Eccles, Chantal Bernard
Publikováno v:
The Journal of Pathology. 230:154-164
DICER1 is an endoribonuclease central to the generation of microRNAs (miRNAs) and short interfering RNAs (siRNAs). Germline mutations in DICER1 have been associated with a pleiotropic tumour predisposition syndrome and Wilms tumour (WT) is a rare man
Autor:
Ian M. Morison, Robert J. Weeks, Euan J. Rodger, Anthony E. Reeve, Jackie L. Ludgate, Ryuji Fukuzawa, Gwenn Le Mée
Publikováno v:
Genes, Chromosomes and Cancer. 52:174-184
Epigenetic abnormalities at the IGF2/H19 locus play a key role in the onset of Wilms tumor. These tumors can be classified into three molecular subtypes depending on the events occurring at this locus: loss of imprinting (LOI), loss of heterozygosity