Zobrazeno 1 - 4
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pro vyhledávání: '"Sarah L. Pashley"'
Publikováno v:
Cells, Vol 13, Iss 23, p 1954 (2024)
The EML4–ALK oncogene drives tumour progression in approximately 5% of cases of non-small-cell lung cancers. At least 15 EML4–ALK variants have been identified, which elicit differential responses to conventional ALK inhibitors. Unfortunately, mo
Externí odkaz:
https://doaj.org/article/d692f3eb5ada4108bcb59f1356a8c204
Autor:
Kellie Lucken, Laura O'Regan, Jene Choi, Josephina Sampson, Sarah L. Pashley, Richard Bayliss, Sam Khan, Andrew M. Fry
Publikováno v:
Mol Cancer Res
EML4-ALK is an oncogenic fusion protein present in approximately 5% of non–small cell lung cancers (NSCLC). Alternative breakpoints in the gene encoding EML4 result in distinct variants that are linked to markedly different patient outcomes. Patien
Autor:
Andrew M. Fry, Sam Khan, Richard Bayliss, Sarah L. Pashley, Josephina Sampson, Jene Choi, Laura O'Regan, Kellie Lucken
Supplementary Figure from EML4-ALK Variant 3 Promotes Mitotic Errors and Spindle Assembly Checkpoint Deficiency Leading to Increased Microtubule Poison Sensitivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bcd3bad71aec51f613a94963a943449
https://doi.org/10.1158/1541-7786.22527450.v1
https://doi.org/10.1158/1541-7786.22527450.v1
Autor:
Savvas Papageorgiou, Sarah L. Pashley, Laura O’Regan, Sam Khan, Richard Bayliss, Andrew M. Fry
Publikováno v:
Cancers. 14:3452
EML4-ALK is an oncogenic fusion protein that accounts for approximately 5% of NSCLC cases. Targeted inhibitors of ALK are the standard of care treatment, often leading to a good initial response. Sadly, some patients do not respond well, and most wil