Results 181 to 190 of about 11,636,692 (262)
Meta-analysis reveals asymmetric root and microbial phenology shifts under global change. [PDF]
Zhao C +5 more
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
Biological traits predict species' time-varying responses to multiple global change drivers. [PDF]
Sasaki T +15 more
europepmc +1 more source
Articulating the JACC Journals' Direction in Times of Global Change. [PDF]
Krumholz HM +9 more
europepmc +5 more sources
Unraveling the epigenetic code in cancer cell–tumor microenvironment crosstalk
Epigenetic regulation is a key driver of cancer development and progression. Diverse epigenetic alterations in cancer cells and components of the tumor microenvironment (TME) orchestrate their communication through multiple mechanisms. We discuss how the epigenetic code coordinates bidirectional cancer cell–TME crosstalk to promote cancer progression ...
Ji Hoon Park, Mi‐Young Kim
wiley +1 more source
Congo Basin Carbon Cycle Responses to Global Change. [PDF]
Worden S +17 more
europepmc +1 more source
Arginine methylation can be viewed as a persistence‐prone post‐translational modification regulated by a network of PRMTs. Competitive and compensatory interactions among PRMTs can redistribute methylation across substrate pools shaped by sequence, structural, spatial, and environmental layers, reinforcing RNA‐processing, chromatin, and signaling ...
So Hyun Kwon, Ji Min Lee
wiley +1 more source
Contrasting vulnerability profiles for insular assemblages of birds and mammals facing global change. [PDF]
Marino C +13 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
Advancing the science of systemic environmental risk in an era of global change. [PDF]
Wang G, Cao S, Wu J.
europepmc +1 more source

