Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anthony McGuigan"'
Autor:
Anja L Frei, Anthony McGuigan, Ritik RAK Sinha, Mark A Glaire, Faiz Jabbar, Luciana Gneo, Tijana Tomasevic, Andrea Harkin, Tim J Iveson, Mark Saunders, Karin Oein, Noori Maka, Francesco Pezella, Leticia Campo, Jennifer Hay, Joanne Edwards, Owen J Sansom, Caroline Kelly, Ian Tomlinson, Wanja Kildal, Rachel S Kerr, David J Kerr, Håvard E Danielsen, Enric Domingo, TransSCOT Consortium, David N Church, Viktor H Koelzer
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 9, Iss 6, Pp 449-463 (2023)
Abstract Multiplex immunofluorescence (mIF) imaging can provide comprehensive quantitative and spatial information for multiple immune markers for tumour immunoprofiling. However, application at scale to clinical trial samples sourced from multiple i
Externí odkaz:
https://doaj.org/article/d2fd350d290249e6b38f3b09f966ff54
Autor:
Anja Laura Frei, Anthony McGuigan, Ritik RAK Sinha, Mark A Glaire, Faiz Jabbar, Luciana Gneo, Tijana Tomasevic, Andrea Harkin, Tim Iveson, Mark Saunders, Karin Oien, Noori Maka, Francesco Pezzella, Leticia Campo, Jennifer Hay, Joanne Edwards, Owen Sansom, Caroline Kelly, Ian Tomlinson, Wanja Kildal, Rachel Kerr, David Kerr, Havard Emil Danielsen, Enric Domingo, David N Church, Viktor Hendrik Koelzer
Background: Tumour immunoprofiling captures tumour-microenvironment interactions and enables precision medicine. Multiplex immunofluorescence (mIF) imaging can provide comprehensive quantitative and spatial information for multiple immune markers. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f8335b8a6f4dafad80bfbed52bc50e1
https://doi.org/10.1101/2023.05.19.23290216
https://doi.org/10.1101/2023.05.19.23290216
Autor:
Prabhu Arumugam, Anthony McGuigan, James Whitworth, Marta Bleda, Arianna Tucci, Tom Fowler, Avgi Andreou
Publikováno v:
European Journal of Human Genetics. 30:265-270
Multi-locus Inherited Neoplasia Allele Syndrome (MINAS) refers to individuals with germline pathogenic variants in two or more cancer susceptibility genes(CSGs). With increased use of exome/genome sequencing it would be predicted that detection of MI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bef0d79a77019eadbe06a8f6981f2065
https://doi.org/10.1038/s41431-021-01013-6
https://doi.org/10.1038/s41431-021-01013-6