Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pamela Kaisaki"'
Autor:
Adrian M. Shields, Alistair T. Pagnamenta, Andrew J. Pollard, OxClinWGS, Jenny C. Taylor, Holger Allroggen, Smita Y. Patel, Samantha J. L. Knight, Niko Popitsch, Carme Camps, Melissa M. Pentony, Erika M. Kvikstad, Lukas Lange, Mona Hashim, Steve Harris, Mark Tilley, Dimitris Vavoulis, Pamela Kaisaki, Vassilis Ragoussis, Matteo Feral
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Deficiency of complement factor I is a rare immunodeficiency that typically presents with increased susceptibility to encapsulated bacterial infections. However, non-infectious presentations including rheumatological, dermatological and neurological
Externí odkaz:
https://doaj.org/article/b00ed76bf8364c97a638ff44d5f2c49e
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:
Jenny F. Seligmann, Enric Domingo, David Fisher, Faye Elliott, Louise C. Brown, Matthew T. Seymour, Susan Richman, Philip Quirke, Rachel Butler, Helen Roberts, Carme Camps, Pamela Kaisaki, David N. Church, David James Kerr, Rachel Kerr, Richard H. Wilson, Oliver Sieber, Jenny Taylor, Ian Tomlinson, Tim Maughan
Publikováno v:
Journal of Clinical Oncology. 40:3540-3540
3540 Background: The relevance of individual RAS (KRAS and NRAS) and TP53 mutations in CRC is well described, but the impact of the combination of both mutations together is less understood. RAS/TP53-mutant (mut) patients (pts) were selected in FOCUS
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:
Richard, Mott, Wei, Yuan, Pamela, Kaisaki, Xiangchao, Gan, James, Cleak, Andrew, Edwards, Amelie, Baud, Jonathan, Flint
Publikováno v:
Cell. 156(1-2)
The number of imprinted genes in the mammalian genome is predicted to be small, yet we show here, in a survey of 97 traits measured in outbred mice, that most phenotypes display parent-of-origin effects that are partially confounded with family struc