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Crosstalk of organelles in Parkinson’s disease – MiT family transcription factors as central players in signaling pathways connecting mitochondria and lysosomes

Molecular neurodegeneration, 2022-07, Vol.17 (1), p.1-50, Article 50

2022

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Dopamine‑iron homeostasis interaction rescues mitochondrial fitness in Parkinson's disease

Neurobiology of disease, 2024-06, Vol.196, p.106506-106506, Article 106506

2024

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Interaction of Alpha-Synuclein With Lipids: Mitochondrial Cardiolipin as a Critical Player in the Pathogenesis of Parkinson’s Disease

Frontiers in neuroscience, 2020-10, Vol.14, p.578993-578993

2020

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Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2

Journal of translational medicine, 2024-01, Vol.22 (1), p.59-18, Article 59

2024

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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

PLoS medicine, 2013-06, Vol.10 (6), p.e1001462-e1001462

2013

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Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy

Biochimica et biophysica acta. Molecular basis of disease, 2018-12, Vol.1864 (12), p.3588-3597

2018

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Frequency of Heterozygous Parkin ( PRKN ) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort

Frontiers in neurology, 2021-08, Vol.12, p.706145-706145

2021

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Exome-wide association study of levodopa-induced dyskinesia in Parkinson’s disease

Scientific reports, 2021-10, Vol.11 (1), p.19582-19582, Article 19582

2021

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Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance

Parkinson's disease, 2018-01, Vol.2018 (2018), p.1-8

2018

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Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family

Stem cell research, 2022-04, Vol.60, p.102692-102692, Article 102692

2022

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Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson’s disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method

Stem cell research, 2022-04, Vol.60, p.102713-102713, Article 102713

2022

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Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells

International journal of molecular sciences, 2019-02, Vol.20 (3), p.748

2019

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Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers

NPJ Parkinson's Disease, 2023-04, Vol.9 (1), p.65-65, Article 65

2023

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Profiling of Parkin-binding partners using tandem affinity purification

PloS one, 2013-11, Vol.8 (11), p.e78648-e78648

2013

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Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene

Stem cell research, 2019-12, Vol.41, p.101624-101624, Article 101624

2019

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The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1

Frontiers in molecular neuroscience, 2018-02, Vol.11, p.64-64

2018

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Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture

Frontiers in cell and developmental biology, 2021-08, Vol.9, p.708389-708389

2021

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SLP-2: a potential new target for improving mitochondrial function in Parkinson's disease

Neural regeneration research, 2017-09, Vol.12 (9), p.1435-1436

2017

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Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

PLoS medicine, 2013-06, Vol.10 (6)

2013

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A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson’s disease by highlighting the use of cybrid models

Cellular and molecular life sciences : CMLS, 2022-05, Vol.79 (5), p.283-283, Article 283

2022

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Parkin R274W mutation affects muscle and mitochondrial physiology

Biochimica et biophysica acta. Molecular basis of disease, 2024-10, Vol.1870 (7), p.167302, Article 167302

2024

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The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives

BMC medical genetics, 2007-06, Vol.8 (1), p.29-29, Article 29

2007

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Co-occurrence of restless legs syndrome and Parkin mutations in two families

Movement disorders, 2006-02, Vol.21 (2), p.258-263

2006

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Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PD

Neurology, 2015-02, Vol.84 (7), p.645-653

2015

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Crosstalk of organelles in Parkinson’s disease – MiT family transcription factors as central players in signaling pathways connecting mitochondria and lysosomes

Dopamine‑iron homeostasis interaction rescues mitochondrial fitness in Parkinson's disease

Interaction of Alpha-Synuclein With Lipids: Mitochondrial Cardiolipin as a Critical Player in the Pathogenesis of Parkinson’s Disease

Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy

Frequency of Heterozygous Parkin ( PRKN ) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort

Exome-wide association study of levodopa-induced dyskinesia in Parkinson’s disease

Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance

Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family

Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson’s disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method

Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells

Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers

Profiling of Parkin-binding partners using tandem affinity purification

Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene

The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1

Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels

Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture

SLP-2: a potential new target for improving mitochondrial function in Parkinson's disease

Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson’s disease by highlighting the use of cybrid models

Parkin R274W mutation affects muscle and mitochondrial physiology

The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives

Co-occurrence of restless legs syndrome and Parkin mutations in two families

Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PD

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