UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 185

Sortiert nach

Dysregulation of mitochondria-lysosome contacts by GBA1 dysfunction in dopaminergic neuronal models of Parkinson's disease

Nature communications, 2021-03, Vol.12 (1), p.1807-1807, Article 1807

2021

Link zum Volltext

Verfügbarkeit prüfen

Mitochondria-lysosome contacts regulate mitochondrial fission via RAB7 GTP hydrolysis

Nature (London), 2018-02, Vol.554 (7692), p.382-386

2018

Link zum Volltext

Verfügbarkeit prüfen

Mitochondria-lysosome contacts regulate mitochondrial Ca2+ dynamics via lysosomal TRPML1

Proceedings of the National Academy of Sciences - PNAS, 2020-08, Vol.117 (32), p.19266-19275

2020

Link zum Volltext

Verfügbarkeit prüfen

Zn2+ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation

Human molecular genetics, 2014-06, Vol.23 (11), p.2791-2801

2014

Link zum Volltext

Verfügbarkeit prüfen

Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson’s Disease

Trends in neurosciences (Regular ed.), 2019-02, Vol.42 (2), p.140-149

2019

Link zum Volltext

Verfügbarkeit prüfen

Regulation and Function of Mitochondria–Lysosome Membrane Contact Sites in Cellular Homeostasis

Trends in cell biology, 2019-06, Vol.29 (6), p.500-513

2019

Link zum Volltext

Verfügbarkeit prüfen

Parkin Modulates Endosomal Organization and Function of the Endo-Lysosomal Pathway

The Journal of neuroscience, 2016-02, Vol.36 (8), p.2425-2437

2016

Link zum Volltext

Verfügbarkeit prüfen

α-Synuclein–induced lysosomal dysfunction occurs through disruptions in protein trafficking in human midbrain synucleinopathy models

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (7), p.1931-1936

2016

Link zum Volltext

Verfügbarkeit prüfen

Lysosomal Regulation of Inter-mitochondrial Contact Fate and Motility in Charcot-Marie-Tooth Type 2

Developmental cell, 2019-08, Vol.50 (3), p.339-354.e4

2019

Link zum Volltext

Verfügbarkeit prüfen

Mutant Huntingtin Is Secreted via a Late Endosomal/Lysosomal Unconventional Secretory Pathway

The Journal of neuroscience, 2017-09, Vol.37 (37), p.9000-9012

2017

Link zum Volltext

Verfügbarkeit prüfen

LRRK2 kinase activity regulates lysosomal glucocerebrosidase in neurons derived from Parkinson's disease patients

Nature communications, 2019-12, Vol.10 (1), p.5570-9, Article 5570

2019

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial Parkin recruitment is impaired in neurons derived from mutant PINK1 induced pluripotent stem cells

The Journal of neuroscience, 2011-04, Vol.31 (16), p.5970-5976

2011

Link zum Volltext

Verfügbarkeit prüfen

Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease

Science (American Association for the Advancement of Science), 2017-09, Vol.357 (6357), p.1255-1261

2017

Link zum Volltext

Verfügbarkeit prüfen

Progranulin mutations result in impaired processing of prosaposin and reduced glucocerebrosidase activity

Human molecular genetics, 2020-03, Vol.29 (5), p.716-726

2020

Link zum Volltext

Verfügbarkeit prüfen

Functional Impairment in Miro Degradation and Mitophagy Is a Shared Feature in Familial and Sporadic Parkinson’s Disease

Cell stem cell, 2016-12, Vol.19 (6), p.709-724

2016

Link zum Volltext

Verfügbarkeit prüfen

Emerging links between pediatric lysosomal storage diseases and adult parkinsonism

Movement disorders, 2019-05, Vol.34 (5), p.614-624

2019

Link zum Volltext

Verfügbarkeit prüfen

Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients

Human molecular genetics, 2017-12, Vol.26 (24), p.4861-4872

2017

Link zum Volltext

Verfügbarkeit prüfen

The role of dopamine in the pathogenesis of GBA1-linked Parkinson's disease

Neurobiology of disease, 2019-12, Vol.132, p.104545-104545, Article 104545

2019

Link zum Volltext

Verfügbarkeit prüfen

Dopamine metabolism by a monoamine oxidase mitochondrial shuttle activates the electron transport chain

Nature neuroscience, 2020-01, Vol.23 (1), p.15

2020

Link zum Volltext

Verfügbarkeit prüfen

Identification of ASCL1 as a determinant for human iPSC-derived dopaminergic neurons

Scientific reports, 2021-11, Vol.11 (1), p.22257-22257, Article 22257

2021

Link zum Volltext

Verfügbarkeit prüfen

Protocol to investigate Parkinson’s patient-derived dopaminergic neurons by live-cell microscopy and oxidized dopamine assays

STAR protocols, 2024-03, Vol.5 (1), p.102889-102889, Article 102889

2024

Link zum Volltext

Verfügbarkeit prüfen

Human iPSC-Based Modeling of Late-Onset Disease via Progerin-Induced Aging

Cell stem cell, 2013-12, Vol.13 (6), p.691-705

2013

Link zum Volltext

Verfügbarkeit prüfen

Rapamycin reverses cellular phenotypes and enhances mutant protein clearance in Hutchinson-Gilford progeria syndrome cells

Science translational medicine, 2011-06, Vol.3 (89), p.89ra58

2011

Link zum Volltext

Verfügbarkeit prüfen

Sirt1 mediates neuroprotection from mutant huntingtin by activation of the TORC1 and CREB transcriptional pathway

Nature medicine, 2012-01, Vol.18 (1), p.159-165

2012

Link zum Volltext

Verfügbarkeit prüfen

Lysosomal dysfunction in neurodegeneration: The role of ATP13A2/PARK9

Autophagy, 2012-06, Vol.8 (6), p.987-988

2012

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 185

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(178)
Mit Volltextzugriff
(159)

Publikationsform

Sprache

Englisch
(185)
Japanisch
(44)

Erscheinungsjahr

n.n

Thema

Science & Technology
(143)
Humans
(119)
Life Sciences & Biomedicine
(115)
Animals
(56)
Neurosciences & Neurology
(56)
Mutation
(40)
Neurosciences
(40)
Mice
(39)
Cell Biology
(32)
Parkinson Disease - Genetics
(32)
Parkinson's Disease
(32)
Alpha-Synuclein - Metabolism
(30)
Lysosomes - Metabolism
(30)
Neurons
(29)
Clinical Neurology
(28)
Parkinson Disease - Metabolism
(27)
Biochemistry & Molecular Biology
(26)
Male
(26)
Proteins
(25)
Science & Technology - Other Topics
(25)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Dysregulation of mitochondria-lysosome contacts by GBA1 dysfunction in dopaminergic neuronal models of Parkinson's disease

Mitochondria-lysosome contacts regulate mitochondrial fission via RAB7 GTP hydrolysis

Mitochondria-lysosome contacts regulate mitochondrial Ca2+ dynamics via lysosomal TRPML1

Zn2+ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation

Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson’s Disease

Regulation and Function of Mitochondria–Lysosome Membrane Contact Sites in Cellular Homeostasis

Parkin Modulates Endosomal Organization and Function of the Endo-Lysosomal Pathway

α-Synuclein–induced lysosomal dysfunction occurs through disruptions in protein trafficking in human midbrain synucleinopathy models

Lysosomal Regulation of Inter-mitochondrial Contact Fate and Motility in Charcot-Marie-Tooth Type 2

Mutant Huntingtin Is Secreted via a Late Endosomal/Lysosomal Unconventional Secretory Pathway

LRRK2 kinase activity regulates lysosomal glucocerebrosidase in neurons derived from Parkinson's disease patients

Mitochondrial Parkin recruitment is impaired in neurons derived from mutant PINK1 induced pluripotent stem cells

Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease

Progranulin mutations result in impaired processing of prosaposin and reduced glucocerebrosidase activity

Functional Impairment in Miro Degradation and Mitophagy Is a Shared Feature in Familial and Sporadic Parkinson’s Disease

Emerging links between pediatric lysosomal storage diseases and adult parkinsonism

Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients

The role of dopamine in the pathogenesis of GBA1-linked Parkinson's disease

Dopamine metabolism by a monoamine oxidase mitochondrial shuttle activates the electron transport chain

Identification of ASCL1 as a determinant for human iPSC-derived dopaminergic neurons

Protocol to investigate Parkinson’s patient-derived dopaminergic neurons by live-cell microscopy and oxidized dopamine assays

Human iPSC-Based Modeling of Late-Onset Disease via Progerin-Induced Aging

Rapamycin reverses cellular phenotypes and enhances mutant protein clearance in Hutchinson-Gilford progeria syndrome cells

Sirt1 mediates neuroprotection from mutant huntingtin by activation of the TORC1 and CREB transcriptional pathway

Lysosomal dysfunction in neurodegeneration: The role of ATP13A2/PARK9

Suchergebnisse filtern