In over 50% of non‐metastatic breast cancer patients, circulating tumor cells (CTCs) along the whole epithelial‐mesenchymal transition spectrum are detected. Total CTC number and individual phenotypes relate to aggressive disease characteristics, including lymph node involvement and higher tumor proliferation. At the single‐cell level, mesenchymal CTCs
Justyna Topa +14 more
wiley +1 more source
Identification and application of bioparts for plant synthetic biology. [PDF]
Koo H, Jung M, Lee S, Go S, Kim YM.
europepmc +1 more source
Standard virtual biological parts: a repository of modular modeling components for synthetic biology [PDF]
Michael T. Cooling +6 more
openalex +1 more source
Aggressive prostate cancer is associated with pericyte dysfunction
Tumor‐produced TGF‐β drives pericyte dysfunction in prostate cancer. This dysfunction is characterized by downregulation of some canonical pericyte markers (i.e., DES, CSPG4, and ACTA2) while maintaining the expression of others (i.e., PDGFRB, NOTCH3, and RGS5).
Anabel Martinez‐Romero +11 more
wiley +1 more source
Unveiling the Frontiers of Synthetic Biology in Brazil: Pioneering the National Synthetic Biology Network. [PDF]
Santos LV +12 more
europepmc +1 more source
Design and characterization of molecular tools for a Synthetic Biology approach towards developing cyanobacterial biotechnology [PDF]
Hsin-Ho Huang +3 more
openalex +1 more source
ERRFI1, a neural crest (NC)‐associated gene, was upregulated in melanoma and negatively correlated with the expression of melanocytic differentiation markers and the susceptibility of melanoma cells toward BRAF inhibitors (BRAFi). Knocking down ERRFI1 significantly increased the sensitivity of melanoma cells to BRAFi.
Nina Wang +8 more
wiley +1 more source
Synthetic biology for space exploration. [PDF]
Onofri S +20 more
europepmc +1 more source
Engineering of a genome-reduced host: practical application of synthetic biology in the overproduction of desired secondary metabolites [PDF]
Hong Gao +3 more
openalex +1 more source
Survivin and Aurora Kinase A control cell fate decisions during mitosis
Aurora A interacts with survivin during mitosis and regulates its centromeric role. Loss of Aurora A activity mislocalises survivin, the CPC and BubR1, leading to disruption of the spindle checkpoint and triggering premature mitotic exit, which we refer to as ‘mitotic slippage’.
Hana Abdelkabir +2 more
wiley +1 more source

