👤 Paulette Bioulac Sage

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3
Articles
3
Name variants
Also published as: Helen Sage, Julien Sage,
articles
Sandra Cristea, Garry L Coles, Daniel Hornburg +13 more · 2020 · Cancer research · added 2026-04-24
Small-cell lung cancer (SCLC) is an aggressive form of lung cancer with dismal survival rates. While kinases often play key roles driving tumorigenesis, there are strikingly few kinases known to promo Show more
Small-cell lung cancer (SCLC) is an aggressive form of lung cancer with dismal survival rates. While kinases often play key roles driving tumorigenesis, there are strikingly few kinases known to promote the development of SCLC. Here, we investigated the contribution of the MAPK module MEK5-ERK5 to SCLC growth. MEK5 and ERK5 were required for optimal survival and expansion of SCLC cell lines Show less
📄 PDF DOI: 10.1158/0008-5472.CAN-19-1027
MAP2K5
Andrew R Harper, Michael Bowman, Jesse B G Hayesmoore +17 more · 2020 · Circulation. Genomic and precision medicine · added 2026-04-24
The common intronic deletion, Sequence data from 2 HCM cohorts (n=5393) was analyzed to determine Our data suggest that the risk of HCM, previously attributed to The
no PDF DOI: 10.1161/CIRCGEN.119.002783
MYBPC3
Quentin Bayard, Stefano Caruso, Gabrielle Couchy +14 more · 2020 · Gut · added 2026-04-24
Inflammatory hepatocellular adenomas (IHCAs) are benign liver tumours characterised by an activation of the janus kinase (JAK)/signal transducers and activators of transcription (STAT) pathway caused Show more
Inflammatory hepatocellular adenomas (IHCAs) are benign liver tumours characterised by an activation of the janus kinase (JAK)/signal transducers and activators of transcription (STAT) pathway caused by oncogenic activating mutations. However, a subset of IHCA lacks of identified mutation explaining the inflammatory phenotype. 657 hepatocellular adenomas developed in 504 patients were analysed for gene expression of 17 genes and for mutations in seven genes by sequencing. 22 non-mutated IHCAs were analysed by whole-exome and/or RNA sequencing. We identified 296 IHCA (45%), 81% of them were mutated in either Recurrent chromosomal alterations involving Show less
no PDF DOI: 10.1136/gutjnl-2019-319790
SEC16B