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A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson's disease.
- Published in:
- Science Translational Medicine, 2020, v. 12, n. 560, p. 1, doi. 10.1126/scitranslmed.aau3960
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- Article
Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient‐Derived Neurons.
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- Movement Disorders, 2021, v. 36, n. 3, p. 704, doi. 10.1002/mds.28365
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- Article
Using High-Content Screening to Generate Single-Cell Gene-Corrected Patient-Derived iPS Clones Reveals Excess Alpha-Synuclein with Familial Parkinson's Disease Point Mutation A30P.
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- Cells (2073-4409), 2020, v. 9, n. 9, p. 2065, doi. 10.3390/cells9092065
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- Article
Gene-corrected p.A30P SNCA patient-derived isogenic neurons rescue neuronal branching and function.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-01505-x
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- Article
Haploinsufficiency due to a novel ACO2 deletion causes mitochondrial dysfunction in fibroblasts from a patient with dominant optic nerve atrophy.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-73557-4
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- Article
Impaired mitochondrial–endoplasmic reticulum interaction and mitophagy in Miro1-mutant neurons in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 8, p. 1353, doi. 10.1093/hmg/ddaa066
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- Article