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Ribosome profiling of G2019S LRRK2 human dopamine neurons
Modelling G2019S-LRRK2 sporadic Parkinson’s disease in 3D midbrain organoids
RNA-Seq of LRRK2 G2019S Parkinson’s iPSC-derived astrocytes
Transcriptome analysis of isogenic Neural stem cell for LRRK2 G2019S mutation.
The Parkinson's disease associated mutation LRRK2-G2019S affects astrocyte specification
Differential serum microRNAs in premotor LRRK2 G2019S carriers from Parkinson’s disease
Parkinson’s disease (PD) has a neuro-developmental component with multiple genetic predispositions. The most prevalent mutation, LRRK2-G2019S is linked to familial and sporadic PD. Based on the multiple origins of PD and the incomplete penetrance of LRRK2-G2019S, we hypothesize that modifiers in the...
ORGANISM(S): Homo sapiens 
2018-03-07 | GSE101534 | GEO
G2019S mutaion of LRRK2 is known to increase mRNA translation. We perform ribosome profiling to study defective translation using human dopamine neuron models. Patient-derived human dopamine neurons with G2019S LRRK2 mutation were generated and used. Also a mutation-corrected isogenic pair line was ...
ORGANISM(S): Homo sapiens 
2018-07-01 | GSE90469 | GEO
Genetic mutations on leucine-rich repeat kinase 2 (LRRK2) have been associated with an increased risk of Parkinson's disease. The Gly2019Ser (G2019S) mutation on LRRK2 gene is a relatively common cause of familial Parkinson's disease in Caucasian population. In this study, we generated human induced...
ORGANISM(S): Homo sapiens 
Recent advances in generating 3 dimensional (3D) organoid systems from stem cells offer new possibilities for disease modeling. In this study, we generate isogenic 3D midbrain organoids with or without a Parkinson’s disease-associated LRRK2 G2019S mutation. LRRK2-G2019S midbrain organoids derived fr...
ORGANISM(S): Homo sapiens 
2019-02-02 | GSE125234 | GEO
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