- The candidate should have a strong academic record and hold a Master's degree in any area of Biology or Biomedical Sciences (Medicine, Biomedical Sciences, Biology, BioEngineering (Cell- and Genebiotechnology), Neuroscience,..).
- Previous research experience, especially regarding cell culture is a plus, but not essential.
- English is the main language and proficiency in written and spoken English is crucial.
- You are a good writer, and you are not afraid of public speaking (e.g., delivering a conference presentation, ...)
- The selected candidate is expected to write a doctoral thesis after 4 years.
- We offer employment as a full-time doctoral researcher in a stimulating expert environment, but the student will be asked to apply for FWO funding at least once.
- The possibility to participate in international conferences and collaborations.
- Doctoral training at the Leuven International Doctoral School of Biomedical Sciences
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PhD: studying neurodegeneration using iPSC and xenotransplantation models
Gevonden in: Talent BE 2A C2 - 1 dag geleden
KU Leuven Leuven, BelgiëDe kandidaat heeft een master in geneeskunde, biomedische wetenschappen, farmaceutische wetenschappen, biologie, bioscience engineering, biochemische wetenschappen of een verwante discipline. · Ervaring met humane geïnduceerde pluripotente stamcellen (iPSC's) is een plus · Ervari ...
PhD: Linking neurodevelopment and mitochondria in human neurons using iPSC and xenotransplantation - Leuven, België - VIB
Beschrijving
PhD position: Linking neurodevelopmental disorders and mitochondria in human neurons, using iPSC and xenotransplantation
We are looking for an ambitious PhD student with a broad interest in interdisciplinary research working in the exciting field of Neuroscience.
Project
While most genes associated with neurodevelopmental disorders (NDD) encode proteins involved in transcriptional/epigenetic regulation or synaptic function, increasing evidence suggests that mitochondria dynamics or function may be affected in at least some of these conditions.
Among NDD potentially linked to mitochondria are Rett syndrome (RTT) and MECP2 duplication syndrome, both caused by abnormal dosage of MECP2 protein. We have developed a xenotransplantation model for both disorders, as well as novel ways to investigate the mitochondrial phenotypes in human diseased neurons (Nageshappa et al. Mol Psychiatry ;21(2):178-88; Linaro et al. Neuron :972-986; Iwata et al. Science : 1-9 science.abn4705). Here we will explore whether and how mitochondrial abnormalities contribute to the neurological pathology in human neurons in vitro and in vivo. This project will lead to novel insights into NDD mechanisms and potentially to innovative therapeutic venues.
Profile
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