Two “NEUcrest” ITN Early Stage Researcher PhD positions for 3 years (# of pos: 2)

Updated: about 1 month ago
Deadline: 31 Oct 2019

Two “NEUcrest” ITN Early Stage Researcher PhD positions for 3 years available in the lab of Prof. M. Angela Nieto, “Cell movements in development and disease” at Institute for Neuroscience (CSIC-UMH) in Alicante, Spain ( ). These full-time positions are funded by the European Commission H2020 / Marie Skłodowska-Curie Actions, and the remuneration will be in line with the rules for MSCA grant holders (ESR, Initial Training Network).

In the lab, we study cell plasticity in health and disease, and in particular the epithelial to mesenchymal transition (EMT). The EMT is crucial for the formation of multiple tissues and organs including the neural crest and it is reactivated in the adult during wound healing, tumor progression and organ degeneration. We use zebrafish, mouse and chick embryos as model systems together with cultured cells and samples from patients, and we have a high interest in Cell Biology, Evo-Devo, Biomedicine, state-of-the-art imaging, transgenesis and gene expression profiling. These two PhD projects are devoted to the following themes:

From transcriptomics to cell behaviour in vertebrate neural crest

EMT and cell behaviour in normal and pathological vertebrate neural crest

Selected references:

  • Ocaña, O.H., et al. (2012) Metastatic colonization requires the repression of the epithelial-mesenchymal transition inducer Prrx1. Cancer Cell 22, 709-724.
  • Grande et al. (2015). Snail1-induced partial epithelial-to-mesenchymal transition drives renal fibrosis in mice and can be targeted to reverse established disease. Nat. Med. 21, 989-997.
  • Nieto et al. (2016). EMT: 2016. Cell 166, 21-45.
  • Ocaña et al. (2017) A right-handed signalling pathway drives heart looping in vertebrates. Nature 549, 86-90
  • Fazilaty et al. (2019). A Gene Regulatory Network to Control EMT Programs in Development and Disease Nat. Comm. in press.

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