Novel therapy approach for treatment of lung fibrosis

WarpDemuX - Method for Demultiplexing of RNA-sequencing DATA

CrispRGold - Design of efficient CrispR/Cas sgRNA sequences and off-target prediction

Human TCR constructs for adoptive cell therapy of cancer

Liver stem cell generation for therapeutic applications

AAV Vector Variants for Ocular Gene Delivery

Next generation allogeneic CAR-NK cell platform for treatment of malignant diseases

Reprogramming immune cells for CAR cell-based therapies

Immunosuppressant resistance in anti-viral T cell products 

High-level recombinant adeno-associated virus production

The CXCR3alt-CXCL11 chemokine system for therapeutic use in solid cancer

Base editing enzymes for multiplex editing with simultaneous gene knock-in and knock-out

Gene editing of the proteinase 3 autoantigen as a novel treatment for ANCA-associated vasculitis

An engineered serine integrase for targeted gene transfer in human cells

BreakTag - Novel method for detection of ds-breaks and analysis of CRISPR-induced on- and off-target effects