UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration

PLoS genetics, 2016-03, Vol.12 (3), p.e1005944-e1005944

2016

Volltextzugriff (PDF)

Glucocerebrosidase deficiency promotes protein aggregation through dysregulation of extracellular vesicles

PLoS genetics, 2018-09, Vol.14 (9), p.e1007694-e1007694

2018

Volltextzugriff (PDF)

Glucocerebrosidase reduces the spread of protein aggregation in a Drosophila melanogaster model of neurodegeneration by regulating proteins trafficked by extracellular vesicles

PLoS genetics, 2021-02, Vol.17 (2), p.e1008859-e1008859

2021

Volltextzugriff (PDF)

Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration

PLoS genetics, 2016-03, Vol.12 (3), p.e1005944

2016

Volltextzugriff (PDF)

Predictive Modeling of Alzheimer's and Parkinson's Disease Using Metabolomic and Lipidomic Profiles from Cerebrospinal Fluid

Metabolites, 2022-03, Vol.12 (4), p.277

2022

Volltextzugriff (PDF)

Diagnostic Validation for Participants in the Washington State Parkinson Disease Registry

Parkinson's disease, 2018-01, Vol.2018 (2018), p.1-6

2018

Volltextzugriff (PDF)

Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients

Acta neuropathologica, 2024-06, Vol.147 (1), p.28, Article 28

2024

Volltextzugriff (PDF)

Parkinsonism syndrome in heterozygotes for Niemann–Pick C1

Journal of the neurological sciences, 2013-12, Vol.335 (1), p.219-220

2013

Volltextzugriff (PDF)

Vreteno, a gonad-specific protein, is essential for germline development and primary piRNA biogenesis in Drosophila

Development (Cambridge), 2011-09, Vol.138 (18), p.4039-4050

2011

Volltextzugriff (PDF)

Movement Disorders in Multiple Sclerosis

Physical medicine and rehabilitation clinics of North America, 2013-11, Vol.24 (4), p.639-651

2013

Volltextzugriff (PDF)

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Brain (London, England : 1878), 2023-05, Vol.146 (5), p.2003-2015

2023

Volltextzugriff (PDF)

Unusually long duration and delayed penetrance in a family with FTD and mutation in MAPT (V337M)

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-01, Vol.174 (1), p.70-74

2017

Volltextzugriff (PDF)

The co-occurrence of Alzheimer's disease and Huntington's disease: a neuropathological study of 15 elderly Huntington's disease subjects

Journal of Huntington's disease, 2014, Vol.3 (2), p.209-217

2014

Volltextzugriff (PDF)

The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2016-10, Vol.171B (7), p.925-930

2016

Volltextzugriff (PDF)

PNPLA6‐Related Disorder with Levodopa‐Responsive Parkinsonism

Movement disorders clinical practice (Hoboken, N.J.), 2023-02, Vol.10 (2), p.338-340

2023

Volltextzugriff (PDF)

Novel mutations in ataxia telangiectasia and AOA2 associated with prolonged survival

Journal of the neurological sciences, 2013-12, Vol.335 (1), p.134-138

2013

Volltextzugriff (PDF)

The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-01, Vol.174 (1), p.113-113

2017

Volltextzugriff (PDF)

Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias

Movement disorders clinical practice (Hoboken, N.J.), 2024-05, Vol.11 (5), p.496-503

2024

Volltextzugriff (PDF)

Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5‐Dyskinesia

Movement disorders clinical practice (Hoboken, N.J.), 2020-01, Vol.7 (1), p.70-77

2020

Volltextzugriff (PDF)

Investigating a Neuroprotective Role for GBA in Astrocytes (P8-11.008)

Neurology, 2022-05, Vol.98 (18_supplement)

2022

Volltextzugriff (PDF)

Glucocerebrosidase Deficiency Mediates Propagation of Protein Aggregation in a Drosophila Model of Neurodegeneration via Modification of Extracellular Vesicles (S53.004)

Neurology, 2019-04, Vol.92 (15_supplement)

2019

Volltextzugriff (PDF)

Cover Image, Volume 174B, Number 1, January 2017

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-01, Vol.174 (1)

2017

Volltextzugriff (PDF)

Modifications in Synthesis Strategy Improve the Yield and Efficacy of Geldanamycin−Herceptin Immunoconjugates

Bioconjugate chemistry, 2002-07, Vol.13 (4), p.786-791

2002

Volltextzugriff (PDF)

1 – 25 von 149

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(139)
Mit Volltextzugriff
(116)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration

Glucocerebrosidase deficiency promotes protein aggregation through dysregulation of extracellular vesicles

Glucocerebrosidase reduces the spread of protein aggregation in a Drosophila melanogaster model of neurodegeneration by regulating proteins trafficked by extracellular vesicles

Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration

Predictive Modeling of Alzheimer's and Parkinson's Disease Using Metabolomic and Lipidomic Profiles from Cerebrospinal Fluid

Diagnostic Validation for Participants in the Washington State Parkinson Disease Registry

Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease

Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations

Parkinsonism syndrome in heterozygotes for Niemann–Pick C1

Vreteno, a gonad-specific protein, is essential for germline development and primary piRNA biogenesis in Drosophila

Movement Disorders in Multiple Sclerosis

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Unusually long duration and delayed penetrance in a family with FTD and mutation in MAPT (V337M)

The co-occurrence of Alzheimer's disease and Huntington's disease: a neuropathological study of 15 elderly Huntington's disease subjects

The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

PNPLA6‐Related Disorder with Levodopa‐Responsive Parkinsonism

Novel mutations in ataxia telangiectasia and AOA2 associated with prolonged survival

The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias

Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5‐Dyskinesia

Investigating a Neuroprotective Role for GBA in Astrocytes (P8-11.008)

Glucocerebrosidase Deficiency Mediates Propagation of Protein Aggregation in a Drosophila Model of Neurodegeneration via Modification of Extracellular Vesicles (S53.004)

Cover Image, Volume 174B, Number 1, January 2017

Modifications in Synthesis Strategy Improve the Yield and Efficacy of Geldanamycin−Herceptin Immunoconjugates

Suchergebnisse filtern