Author Correction: Oncogene ablation-resistant pancreatic cancer cells depend on mitochondrial function
Andrea Viale, Piergiorgio Pettazzoni, Costas A. Lyssiotis, Haoqiang Ying et autres
us, it (code pays fourni par la source)
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
Andrea Viale, Piergiorgio Pettazzoni, Costas A. Lyssiotis, Haoqiang Ying et autres
us, it (code pays fourni par la source)
Gargi D. Basu, Nick Johnson, Angela K. Deem, Judith Frederick et autres
Abstract Tumor molecular profiling may reveal distinct biological behaviors by identifying actionable alterations (AAs), informing precision oncology. However, the effect of molecular characteristics on ctDNA detection and monitoring is not well studied. Here, we evaluated patients with breast cancer (BC; all subtypes) …
us (code pays fourni par la source)
Gargi D. Basu, Paige Innis, Angela K. Deem, Arthur Starodynov et autres
BACKGROUND: ESR1 alterations present a common mechanism of resistance to endocrine therapy (ET) in hormonally driven tumors. The clinical significance of these alterations continues to evolve with newly approved targeted therapies and a range of ongoing investigational trials. METHODS: A retrospective study …
us (code pays fourni par la source)
Gargi D. Basu, Paige Innis, Angela K. Deem, Arthur Starodynov et autres
Abstract Background ESR1 alterations present a common mechanism of resistance to endocrine therapy (ET) in hormonally driven tumors. The clinical significance of these alterations continues to evolve with newly approved targeted therapies and a range of ongoing investigational trials. Methods A retrospective …
us (code pays fourni par la source)
Gargi D. Basu, Paige Innis, Angela K. Deem, Arthur Starodynov et autres
Supplementary material 1
us (code pays fourni par la source)
Gargi D. Basu, Paige Innis, Angela K. Deem, Arthur Starodynov et autres
Abstract Background ESR1 alterations present a common mechanism of resistance to endocrine therapy (ET) in hormonally driven tumors. The clinical significance of these alterations continues to evolve with newly approved targeted therapies and a range of ongoing investigational trials. Methods A retrospective …
us (code pays fourni par la source)
Gargi D. Basu, Paige Innis, Angela K. Deem, Arthur Starodynov et autres
Supplementary material 1
us (code pays fourni par la source)
Jean-Paul De La O, Jess Hoag, Angela K. Deem, Min Wang et autres
// Jean-Paul De La O 1 , Jess R. Hoag 1 , Angela K. Deem 1 , Min Wang 1 , Arthur Starodynov 1 , Sameer S. Udhane 1 , Janine R. LoBello 1 , Nishitha Therala 1 , David W. Hall …
us (code pays fourni par la source)
Madelaine Skolastika Theardy, Mitsunobu Takeda, Alexey V. Sorokin, Shuaitong Chen et autres
The therapeutic benefit of recently developed mutant KRAS (KRAS∗) inhibitors remains limited by the rapid onset of resistance. Here, we aim to delineate mechanisms underlying acquired resistance and identify actionable targets for overcoming this clinical challenge. Previously, we identified syndecan-1 (SDC1) as …
us, jp (code pays fourni par la source)
Sameer S. Udhane, Pawan Noel, Fadel Alyaqoub, Ariane Kemkes et autres
Abstract Background: Breast cancer (BC) in younger women is often more aggressive and diagnosed at a later stage. The choice of endocrine therapy (ET) for women with hormone-receptor positive (HR+) BC varies based on whether she is premenopausal (preM) or postmenopausal (postM): …
Jean–Paul De La O, Jess Hoag, Gargi D. Basu, Arthur Starodynov et autres
781 Background: Genomic profiling has brought to the forefront the clinical relevance of intratumoral heterogeneity. Oncogenic KRAS mutation is the most common driver event in pancreatic ductal adenocarcinoma (PDAC), but little is known about how KRAS alteration may cooperate with other genetic …
us (code pays fourni par la source)
Francesca Citron, I-Lin Ho, Chiara Balestrieri, Zhaoliang Liu et autres
It is unclear how cells counteract the potentially harmful effects of uncoordinated DNA replication in the context of oncogenic stress. Here, we identify the WRAD (WDR5/RBBP5/ASH2L/DPY30) core as a modulator of DNA replication in pancreatic ductal adenocarcinoma (PDAC) models. Molecular analyses demonstrated …
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