Results 171 to 180 of about 9,897,717 (308)
This study identifies somatostatin receptor 4 (Sstr4) as a critical tumor suppressor against skin and head/neck cancers (HNSCC, cSCC, and BCC). The loss of Sstr4 removes a check on cell growth, causing hyperactivation of the MAPK‐ERK signaling pathway (↑).
Ali Taqvi +6 more
wiley +1 more source
Stratégie de recherche du ministère de la Culture 2017-2020 (La) [PDF]
Ce rapport, présentant la stratégie de recherche 2017-2020 du ministère de la Culture, repose sur le travail accompli entre 2014 et 2016 par un comité de pilotage de la recherche Culture.
Ministère de la Culture
core
A macrophage-intestinal organoid co-culture model captures balanced epithelial homeostasis and inflammation. [PDF]
Tonini L +5 more
europepmc +1 more source
We show that emergence of castration‐resistant prostate (CRPC) is associated with significant upregulation of cyclins that positively regulate cyclin‐dependent kinase 2 (CDK2) and concomitant downregulation of CDK4 cyclins. This renders CRPC cells dependent on the high activity of CDK2, and CDK2 inhibitors synergistically sensitize CRPC cells to both ...
Joyeeta Chatterjee +3 more
wiley +1 more source
Different co-culture approaches to increase metabolites in foods. [PDF]
Uysal GS, Yıldırım HK.
europepmc +1 more source
Partial inhibition of focal adhesion kinase (FAK) can paradoxically promote tumor growth, rather than simply producing a weaker antitumor effect than that observed with strong FAK suppression. In breast cancer and melanoma models, targeting p110δ PI3K, particularly in macrophages, counteracted these tumor‐promoting effects, highlighting the importance ...
Lydia Xenou +4 more
wiley +1 more source
The 1841 Pigot & Co.'s directory of York, Leicester & Rutland, Lincoln, Northampton and Nottingham, and includes ...
Pigot & Co. historical directories;
core
Uptake and Transport of Monotropein and Monotropein Esters in a Caco-2/HT29-MTX-E12 Co-Culture Model. [PDF]
Zielinski C +7 more
europepmc +1 more source
Mechanisms and therapeutic opportunities of the ribotoxic stress response in cancer
Cancer cells' high translational demand creates opportunities to therapeutically target ribosome function. Ribosome stalling and collisions activate ZAKα and the ribotoxic stress response (RSR), which can trigger rapid, p53‐independent apoptosis in cancer.
Anastassiya Kim +7 more
wiley +1 more source

