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- 2023
-
Mark
Prime editing to correct disease causative mutations in patient-derived Gaucher iPSC lines
(
- Master (Two yrs)
- 2022
-
Mark
Generation of α-synuclein reporter iPSC lines using CRISPR/Cas9 for studies on Lysosomal Storage Disorders
(
- Master (Two yrs)
- 2021
-
Mark
Brain and cellular alterations caused by CYP27A1 deficiency in mouse and human models
(
- Master (Two yrs)
- 2020
-
Mark
Modeling neuronopathic Gaucher's Disease using pluripotent stem cells and genome engineering
(
- Master (Two yrs)
- 2016
-
Mark
Efficient induction of astrocyte-like cells from human embryonic fibroblasts by defined factors
(
- Master (Two yrs)