Genetic predispositions of Parkinson's disease revealed in patient-derived brain cells
J Tran, H Anastacio, C Bardy - NPJ Parkinson's disease, 2020 - nature.com
Parkinson's disease (PD) is the second most prevalent neurological disorder and has been
the focus of intense investigations to understand its etiology and progression, but it still lacks …
the focus of intense investigations to understand its etiology and progression, but it still lacks …
[HTML][HTML] Studying human neurological disorders using induced pluripotent stem cells: from 2D monolayer to 3D organoid and blood brain barrier models
S Logan, T Arzua, SG Canfield… - Comprehensive …, 2019 - ncbi.nlm.nih.gov
Neurological disorders have emerged as a predominant healthcare concern in recent years
due to their severe consequences on quality of life and prevalence throughout the world …
due to their severe consequences on quality of life and prevalence throughout the world …
Metabolic alterations in Parkinson's disease astrocytes
TM Sonninen, RH Hämäläinen, M Koskuvi… - Scientific reports, 2020 - nature.com
In Parkinsons disease (PD), the loss of dopaminergic (DA) neurons in the substantia nigra
pars compacta is associated with Lewy bodies arising from the accumulation of alpha …
pars compacta is associated with Lewy bodies arising from the accumulation of alpha …
Th17 lymphocytes induce neuronal cell death in a human iPSC-based model of Parkinson's disease
A Sommer, F Marxreiter, F Krach, T Fadler, J Grosch… - Cell stem cell, 2018 - cell.com
Parkinson's disease (PD) is a neurodegenerative disorder characterized by the progressive
degeneration of midbrain neurons (MBNs). Recent evidence suggests contribution of the …
degeneration of midbrain neurons (MBNs). Recent evidence suggests contribution of the …
Post-translational proteomics platform identifies neurite outgrowth impairments in Parkinson's disease GBA-N370S dopamine neurons
H Bogetofte, BJ Ryan, P Jensen, SI Schmidt… - Cell Reports, 2023 - cell.com
Variants at the GBA locus, encoding glucocerebrosidase, are the strongest common genetic
risk factor for Parkinson's disease (PD). To understand GBA-related disease mechanisms …
risk factor for Parkinson's disease (PD). To understand GBA-related disease mechanisms …
Stress-induced unfolded protein response contributes to Zika virus–associated microcephaly
I Gladwyn-Ng, L Cordón-Barris, C Alfano… - Nature …, 2018 - nature.com
Accumulating evidence support a causal link between Zika virus (ZIKV) infection during
gestation and congenital microcephaly. However, the mechanism of ZIKV-associated …
gestation and congenital microcephaly. However, the mechanism of ZIKV-associated …
Early degeneration of both dopaminergic and serotonergic axons–a common mechanism in Parkinson's disease
Motor symptoms in Parkinson's disease (PD) are tightly linked to the degeneration of
substantia nigra dopaminergic neurons and their projections into the striatum. Moreover, a …
substantia nigra dopaminergic neurons and their projections into the striatum. Moreover, a …
In vitro genome editing rescues parkinsonism phenotypes in induced pluripotent stem cells-derived dopaminergic neurons carrying LRRK2 p.G2019S mutation
KH Chang, CY Huang, CH Ou-Yang, CH Ho… - Stem cell research & …, 2021 - Springer
Abstract Background The c. G6055A (p. G2019S) mutation in leucine-rich repeat kinase 2
(LRRK2) is the most prevalent genetic cause of Parkinson's disease (PD). CRISPR/Cas9 …
(LRRK2) is the most prevalent genetic cause of Parkinson's disease (PD). CRISPR/Cas9 …
[HTML][HTML] An integrated transcriptomics and proteomics analysis reveals functional endocytic dysregulation caused by mutations in LRRK2
N Connor-Robson, H Booth, JG Martin, B Gao… - Neurobiology of …, 2019 - Elsevier
Background Mutations in LRRK2 are the most common cause of autosomal dominant
Parkinson's disease, and the relevance of LRRK2 to the sporadic form of the disease is …
Parkinson's disease, and the relevance of LRRK2 to the sporadic form of the disease is …
Parkinson-causing mutations in LRRK2 impair the physiological tetramerization of endogenous α-synuclein in human neurons
L Fonseca-Ornelas, JMS Stricker… - npj Parkinson's …, 2022 - nature.com
Abstract α-Synuclein (αSyn) aggregation in Lewy bodies and neurites defines both familial
and 'sporadic'Parkinson's disease. We previously identified α-helically folded αSyn …
and 'sporadic'Parkinson's disease. We previously identified α-helically folded αSyn …