Published | Deadline | Location |
---|---|---|
today | 17 Oct | Rotterdam |
Job description
This project will study how genetic variants in the DJ-1 and MPAN genes lead to neurodegenerative disease. To address the research questions, the candidate will use a multi-omics approach to study the pathogenic pathways activated by these genetic variants in patient iPS derived midbrain organoids. Midbrain organoids closely recapitulate the physiology and complexity of the human midbrain, and this technology has recently been introduced in our lab. Using these models, the lab anticipates to increase knowledge about important molecular changes associated with these neurodegenerative diseases that may contribute to the development of biomarkers as well as novel therapeutic opportunities.
To this end, the candidate will employ a multidisciplinary approach, including but not limited to iPS cell differentiation and organoid culture protocols, use various molecular biology assays, (sc)RNA sequencing, and (super resolution) microscopy.
Specifications
Erasmus MC (University Medical Center Rotterdam)
Requirements
Conditions of employment
Employer
Erasmus MC
The research section at the Clinical Genetics department conducts basic research to understand the molecular mechanisms of hereditary diseases. The results are converted into practical applications for patient care. The section’s mission is to improve the identification, treatment and prevention of hereditary diseases. They do this by the use of multiple state-of-the-art omics technologies.
In the research group of Molecular mechanisms of movement disorders , we are searching for genes involved in Parkinson’s disease (PD) and other movement disorders. The search may provide clues for understanding of disease mechanisms and identifying novel targets for therapies to stop and prevent these diseases. PD is a common degenerative disease of the brain with progressive loss of dopaminergic neurons and the formation of neuronal inclusions (Lewy bodies) in the surviving neurons. Much of the pathogenesis of PD is unknown. Yet, a growing list of gene defects identified in some inherited forms offers unprecedented, exciting opportunities to disentangle the complex molecular pathways leading to PD. The lab uses a number of unbiased strategies to identify novel genes causing or predisposing to PD and other movement disorders, such as dystonias, paroxysmal dyskinesias, and restless legs syndrome. Our experimental approaches include family-based linkage mapping, homozygosity mapping, positional cloning, next-generation sequencing technologies (exome sequencing and whole genome sequencing), and tools for in-silico analysis of DNA and protein sequence data. Each of the Mendelian forms of disease might provide important clues for understanding of the pathogenesis; also in the more common, complex forms of the disease.
To investigate the function of genetic variants that cause movement disorders, we use iPS-derived
If you are excited by the thought of this position and would like to apply, please do so by using the application form on our website.
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Application procedure
For more information about this position, please contact Wim Mandemakers, PhD, staff scientist, phone number: +31 10 703 87 87 or e-mail: w.mandemakers@erasmusmc.nl.
In case of other requirements to apply:
Your application must include the following documents:
If you are excited by the thought of this position and would like to apply, please do so by using the application form on our website.
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