Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Keith W. Brown"'
Autor:
Danny Legge, Ling Li, Whei Moriarty, David Lee, Marianna Szemes, Asef Zahed, Leonidas Panousopoulos, Wan Yun Chung, Yara Aghabi, Jasmin Barratt, Richard Williams, Kathy Pritchard‐Jones, Karim T.A. Malik, Sebastian Oltean, Keith W. Brown
Publikováno v:
Molecular Oncology, Vol 16, Iss 3, Pp 630-647 (2022)
Wilms tumour (WT), an embryonal kidney cancer, has been extensively characterised for genetic and epigenetic alterations, but a proportion of WTs still lack identifiable abnormalities. To uncover DNA methylation changes critical for WT pathogenesis,
Externí odkaz:
https://doaj.org/article/4fdb93ca44e444e2810400925199bb7a
Autor:
Laxmi Chilukamarri, Anne L. Hancock, Sally Malik, Joanna Zabkiewicz, Jenny A. Baker, Alexander Greenhough, Anthony R. Dallosso, Tim Hui-Ming Huang, Brigitte Royer-Pokora, Keith W. Brown, Karim Malik
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 9, Iss 11, Pp 970-978 (2007)
Wilms tumors (WTs) have a complex etiology, displaying genetic and epigenetic changes, including loss of imprinting (LOI) and tumor suppressor gene silencing. To identify new regions of epigenetic perturbation in WTs, we screened kidney and tumor DNA
Externí odkaz:
https://doaj.org/article/21d16ee5da0347cb9bba27ed239044f5
Autor:
Anthony R. Dallosso, Anne L. Hancock, Marianna Szemes, Kim Moorwood, Laxmi Chilukamarri, Hsin-Hao Tsai, Abby Sarkar, Jonathan Barasch, Raisa Vuononvirta, Chris Jones, Kathy Pritchard-Jones, Brigitte Royer-Pokora, Sean Bong Lee, Ceris Owen, Sally Malik, Yi Feng, Marcus Frank, Andrew Ward, Keith W. Brown, Karim Malik
Publikováno v:
PLoS Genetics, Vol 5, Iss 12 (2009)
Externí odkaz:
https://doaj.org/article/12cff33d5872435d98ea3c6115388187
Supplementary Data from Frequency and Timing of Loss of Imprinting at 11p13 and 11p15 in Wilms' Tumor Development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d66c807339e545de32c42d08562aa5
https://doi.org/10.1158/1541-7786.22518706
https://doi.org/10.1158/1541-7786.22518706
Epigenetic changes occur frequently in Wilms' tumor (WT), especially loss of imprinting (LOI) of IGF2/H19 at 11p15. Our previous results have identified imprinted transcripts (WT1-AS and AWT1) from the WT1 locus at 11p13 and showed LOI of these in so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5124f64b0d1108090e527dcf3804e65
https://doi.org/10.1158/1541-7786.c.6542083
https://doi.org/10.1158/1541-7786.c.6542083
Autor:
Marianna Szemes, Danny Legge, Karim Malik, Wan Yun Chung, David A. Lee, Richard D. Williams, Whei Moriarty, Sebastian Oltean, Asef Zahed, Kathy Pritchard-Jones, Leonidas Panousopoulos, Keith W. Brown, Jasmin Barratt, Ling Li, Yara Aghabi
Publikováno v:
Molecular Oncology, Vol 16, Iss 3, Pp 630-647 (2022)
Legge, D N, Moriarty, W F, Lee, D A, Szemes, M, Zahed, A, Panousopoulos, L, Chung, W Y, Aghabi, Y, Barratt, J, Williams, R, Pritchard-Jones, K, Malik, K T A, Oltean, S & Brown, K W 2021, ' The epithelial splicing regulator ESRP2 is epigenetically repressed by DNA hypermethylation in Wilms tumour and acts as a tumour suppressor ', Molecular Oncology . https://doi.org/10.1002/1878-0261.13101
Molecular Oncology
Legge, D N, Moriarty, W F, Lee, D A, Szemes, M, Zahed, A, Panousopoulos, L, Chung, W Y, Aghabi, Y, Barratt, J, Williams, R, Pritchard-Jones, K, Malik, K T A, Oltean, S & Brown, K W 2021, ' The epithelial splicing regulator ESRP2 is epigenetically repressed by DNA hypermethylation in Wilms tumour and acts as a tumour suppressor ', Molecular Oncology . https://doi.org/10.1002/1878-0261.13101
Molecular Oncology
Wilms tumour (WT), an embryonal kidney cancer, has been extensively characterised for genetic and epigenetic alterations, but a proportion of WTs still lack identifiable abnormalities. To uncover DNA methylation changes critical for WT pathogenesis,
Autor:
Asef Zahed, Keith W. Brown, Danny Legge, David A. Lee, Whei Moriarty, Ling Li, Wan Yun Chung, Karim Malik, Richard D. Williams, Jasmin Barratt, Sebastian Oltean, Kathy Pritchard-Jones, Leonidas Panousopoulos, Marianna Szemes, Yara Aghabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf8b5bf5d11692f1307cfb2fe01d61dd
https://doi.org/10.1002/1878-0261.13101/v2/response1
https://doi.org/10.1002/1878-0261.13101/v2/response1
Autor:
Richard D. Williams, Danny Legge, Yara Aghabi, Ling Li, David A. Lee, Karim Malik, Sebastian Oltean, Whei Moriarty, Jasmin Barratt, Kathy Pritchard-Jones, Keith W. Brown, Leonidas Panousopoulus, Marianna Szemes, Asef Zahed, Wan Yun Chung
Wilms tumour (WT), a childhood kidney cancer with embryonal origins, has been extensively characterised for genetic and epigenetic alterations, but a proportion of WTs still lack identifiable abnormalities. To uncover DNA methylation changes critical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c11b34878d4c356105febccee6f624be
https://doi.org/10.1101/2020.11.02.364570
https://doi.org/10.1101/2020.11.02.364570
Autor:
Jessica Charlet, Keith W. Brown, Karim Malik, Bader Almutairi, Heather C. Etchevers, Anthony R. Dallosso, Marianna Szemes
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, pp.18934. ⟨10.1038/s41598-019-55382-6⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Almutairi, B, Charlet, J, Dallosso, A R, Szemes, M, Etchevers, H C, Malik, K T A & Brown, K W 2019, ' Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes ', Scientific Reports, vol. 9, 18934 (2019) . https://doi.org/10.1038/s41598-019-55382-6
Scientific Reports, Nature Publishing Group, 2019, pp.18934. ⟨10.1038/s41598-019-55382-6⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Almutairi, B, Charlet, J, Dallosso, A R, Szemes, M, Etchevers, H C, Malik, K T A & Brown, K W 2019, ' Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes ', Scientific Reports, vol. 9, 18934 (2019) . https://doi.org/10.1038/s41598-019-55382-6
International audience; To discover epigenetic changes that may underly neuroblastoma pathogenesis, we identified differentially methylated genes in neuroblastoma cells compared to neural crest cells, the presumptive precursors cells for neuroblastom
Autor:
Caroline Jarrett, Jeffrey M P Holly, Keith W. Brown, Kathleen M Gillespie, Li Zeng, Claire M Perks
Publikováno v:
Experimental Cell Research. 319:2282-2295
Breast cancer progression is associated with loss of estrogen receptor (ER-α), often due to epigenetic silencing. IGFBP genes have consistently been identified among the most common to be aberrantly methylated in tumours. To understand the impact of