DC 6

Primary airway cell culture, gene editing, and functional analysis for rare disease drug discovery and validation

About this project

The aim of this PhD project is to use state-of-the-art CRISPR-Cas9 genetic perturbations of primary airway 2D- and 3D-cell models for assay development and structure-function analyses in the context of the genetic disease Cystic Fibrosis (CF).

The PhD candidate will use conventional CRISPR-Cas9 and base-editing technologies for (large-scale) targeted manipulation of CFTR, followed by molecular and functional typing of cells using label-free, high-throughput robotic screening platforms and high-resolution imaging technologies.

Lead Supervisor: Jeff Beekman

Host Institution

Aditi Shekhar

Aditi Shekhar

DC6

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