RESEARCH FIELDBiological sciencesNeurosciences
RESEARCHER PROFILEFirst Stage Researcher (R1)
APPLICATION DEADLINE03/07/2020 23:00 - Europe/Brussels
LOCATIONNetherlands › Nijmegen
France › Paris
TYPE OF CONTRACTTemporary
HOURS PER WEEK35-40
OFFER STARTING DATE01/09/2020
EU RESEARCH FRAMEWORK PROGRAMMEH2020 / Marie Skłodowska-Curie Actions
REFERENCE NUMBERSCilS - 861329
MARIE CURIE GRANT AGREEMENT NUMBER861329
Primary cilia are microtubule-based projections from the cell surface of nearly every cell in our body. In the last two decades it has become clear that primary cilia have evolved to be key signalling hubs of the cells, as they concentrate or segregate components of major cellular signalling pathways.
Dysfunctional cilia can lead to over 35 severe human genetic traits (ciliopathies) with highly heterogeneous, overlapping phenotypes, affecting as many as 1 in 400 people. We now know that humans critically depend on cilia to see, hear, smell, breathe, excrete and reproduce. Such activities require a high degree of regulation and critical feedback to ensure robustness in development and cellular homeostasis of different tissues and organs.
Nijmegen, NL: ESR8 will use three selected Joubert syndrome patient-derived hiPSCs from ciliary protein modules that are differentially localized across the ciliary axoneme, as well as isogenic CRIPSR/Cas9-edited lines for neuronal network measurements using microelectrode arrays (MEAs) and generate a developmental network MEA fingerprint that functionally describes the properties of the neural signalling circuits.
Paris, FR: ESR10 will use cellular and omics analyses (transcriptomic and proteomic) in CRISPR invalidated epithelial cells or urinary epithelial renal cells collected from patients to characterize the pathophysiological processes and determine common and specific signaling pathways altered in patients with NPH. ESR10 will use inhibitors/activators and biosensors (FRET) of the altered pathways to examine their role in NPH-associated phenotype in iPSC-derived kidney organoids and animal models (zebrafish, mouse)
- The positions are funded for three years by the EU Marie Curie ITN SCilS, with the intention for 12 months additional funding from other sources to complete the PhD training (if applicable).
Applicants should not have resided or performed their main activity in the country of the host institution for more than 12 months in the 3 year period immediately prior to the start date of the fellowship.
Early Stage Researcher:
Applicants should be in the first 4 years (full-time equivalent) of their research careers, including the period of research training, starting at the date of obtaining the degree which would formally entitle them to embark on a doctorate.
Applicants should submit:
• a personal statement explaining their motivation and project interests and the contact details of 2 academic referees
• a CV in EU format, other formats are NOT accepted
Please send these documents via email to email@example.com
Intended starting date is September 2020. The positions are open until filled.
PLEASE NOTE that applications that do not meet the requirements WILL NOT BE CONSIDERED.
Web site for additional job details
REQUIRED EDUCATION LEVELBiological sciences: Master Degree or equivalentNeurosciences: Master Degree or equivalent
REQUIRED LANGUAGESENGLISH: Excellent
- Academic degree (MSc) in molecular life sciences, biomedical sciences or a related discipline.
- A strong background in molecular and cellular neuroscience, cellular biology
- Experience with cell culture, culture of primary neurons and induced pluripotent stem cells.
- Highly motivated to work in an interdisciplinary environment at the cutting edge of science
- Excellent interpersonal and communication skills are essential, as is a willingness to work flexibly
EURAXESS offer ID: 529274
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