Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Laxmi Chilukamarri"'
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
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 11, p e1000745 (2009)
Wilms' tumour (WT) is a pediatric tumor of the kidney that arises via failure of the fetal developmental program. The absence of identifiable mutations in the majority of WTs suggests the frequent involvement of epigenetic aberrations in WT. We there
Externí odkaz:
https://doaj.org/article/7af8fa26a11e4c70987e9295678bdc7f
Publikováno v:
Scientia Horticulturae. 280:109899
In-vitro grafting involves grafting a micro-scion onto a micro-rootstock under aseptic conditions. Due to juvenility and health status of the source plants for microscion / microrootstock, in-vitro grafting possesses many advantages over traditional
Autor:
Keith W. Brown, Karim Malik, Yi Feng, Marianna Szemes, Hsin-Hao Tsai, Jonathan Barasch, Anthony R. Dallosso, Andrew Ward, Laxmi Chilukamarri, Ceris Owen, Kathy Pritchard-Jones, Anne L. Hancock, Brigitte Royer-Pokora, Raisa Vuononvirta, Kim Moorwood, Sean Bong Lee, Abby Sarkar, Chris Jones, Marcus Frank, Sally Malik
Publikováno v:
Dallosso, A R, Hancock, A L, Szemes, M, Moorwood, K, Chilukamarri, L, Tsai, H-H, Sarkar, A, Barasch, J, Vuononvirta, R, Jones, C, Pritchard-Jones, K, Royer-Pokora, B, Lee, S B, Owen, C, Malik, S, Feng, Y, Frank, M, Ward, A, Brown, K W & Malik, K 2009, ' Frequent long-range epigenetic silencing of protocadherin gene clusters on chromosome 5q31 in Wilms' tumor ', PLoS Genetics, vol. 5, no. 11, e1000745 . https://doi.org/10.1371/journal.pgen.1000745
PLOS GENET, 5 (11), Article e1000745. (2009)
PLoS Genetics
Dallosso, A R, Hancock, A L, Szemes, M, Moorwood, K, Chilukamarri, L, Tsai, H H, Sarkar, A, Barasch, J, Vuononvirta, R, Jones, C, Pritchard-Jones, K, Royer-Pokora, B, Lee, S B, Owen, C, Malik, S, Feng, Y, Frank, M, Ward, A, Brown, K W & Malik, K 2009, ' Frequent long-range epigenetic silencing of Protocadherin gene clusters on chromosome 5q31 in Wilms' Tumor ', Plos Genetics, vol. 5, no. 11, e1000745 . https://doi.org/10.1371/journal.pgen.1000745
PLoS Genetics, Vol 5, Iss 11, p e1000745 (2009)
PLOS GENET, 5 (11), Article e1000745. (2009)
PLoS Genetics
Dallosso, A R, Hancock, A L, Szemes, M, Moorwood, K, Chilukamarri, L, Tsai, H H, Sarkar, A, Barasch, J, Vuononvirta, R, Jones, C, Pritchard-Jones, K, Royer-Pokora, B, Lee, S B, Owen, C, Malik, S, Feng, Y, Frank, M, Ward, A, Brown, K W & Malik, K 2009, ' Frequent long-range epigenetic silencing of Protocadherin gene clusters on chromosome 5q31 in Wilms' Tumor ', Plos Genetics, vol. 5, no. 11, e1000745 . https://doi.org/10.1371/journal.pgen.1000745
PLoS Genetics, Vol 5, Iss 11, p e1000745 (2009)
Wilms' tumour (WT) is a pediatric tumor of the kidney that arises via failure of the fetal developmental program. The absence of identifiable mutations in the majority of WTs suggests the frequent involvement of epigenetic aberrations in WT. We there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012c60532b00d73f79f85e1a94f89b74
https://www.pure.ed.ac.uk/ws/files/8144707/Frequent_long_range_epigenetic_silencing_of_protocadherin_gene_clusters_on_chromosome_5q31_in_Wilms_tumor.pdf
https://www.pure.ed.ac.uk/ws/files/8144707/Frequent_long_range_epigenetic_silencing_of_protocadherin_gene_clusters_on_chromosome_5q31_in_Wilms_tumor.pdf
Autor:
Alexander Greenhough, Tim H M Huang, Jenny A. Baker, Joanna Zabkiewicz, Karim Malik, Sally Malik, Keith W. Brown, Brigitte Royer-Pokora, Anne L. Hancock, Laxmi Chilukamarri, Anthony R. Dallosso
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