UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 339

Sortiert nach

GREGOR: Optics redesign and updates from 2018–2020

Astronomy and astrophysics (Berlin), 2020-09, Vol.641, p.A27

2020

Link zum Volltext

Verfügbarkeit prüfen

Intracranial AAV‐IFN‐β gene therapy eliminates invasive xenograft glioblastoma and improves survival in orthotopic syngeneic murine model

Molecular oncology, 2017-02, Vol.11 (2), p.180-193

2017

Link zum Volltext

Verfügbarkeit prüfen

Design of new modular metal pallets: Experimental validation and life cycle analysis

Materials & design, 2022-02, Vol.214, p.110425, Article 110425

2022

Link zum Volltext

Verfügbarkeit prüfen

Corrigendum to “Modelling of layers interactions on the structural behaviour of insulating glasses. Vertical deflection analyses” [Case Stud. Constr. Mater. 18 (2023) 2129]

Case Studies in Construction Materials, 2023-12, Vol.19, p.e02473, Article e02473

2023

Link zum Volltext

Verfügbarkeit prüfen

Modelling of layers interactions on the structural behaviour of insulating glasses. Vertical deflection analyses

Case Studies in Construction Materials, 2023-07, Vol.18, p.e02129, Article e02129

2023

Link zum Volltext

Verfügbarkeit prüfen

Cerebral organoids derived from Sandhoff disease-induced pluripotent stem cells exhibit impaired neurodifferentiation[S]

Journal of lipid research, 2018-03, Vol.59 (3), p.550-563

2018

Link zum Volltext

Verfügbarkeit prüfen

Several rAAV Vectors Efficiently Cross the Blood–brain Barrier and Transduce Neurons and Astrocytes in the Neonatal Mouse Central Nervous System

Molecular therapy, 2011-08, Vol.19 (8), p.1440-1448

2011

Link zum Volltext

Verfügbarkeit prüfen

Analytical modelling and experimental assessment of metal pallets. Mechanical behaviour and durability performance under microbiological, chemical and environmental attacks

Case Studies in Construction Materials, 2024-07, Vol.20, p.e02735, Article e02735

2024

Link zum Volltext

Verfügbarkeit prüfen

Microvesicle-associated AAV Vector as a Novel Gene Delivery System

Molecular therapy, 2012-05, Vol.20 (5), p.960-971

2012

Link zum Volltext

Verfügbarkeit prüfen

Adeno Associated Viral Vector Delivered RNAi for Gene Therapy of SOD1 Amyotrophic Lateral Sclerosis

Frontiers in molecular neuroscience, 2016-08, Vol.9, p.56-56

2016

Link zum Volltext

Verfügbarkeit prüfen

Bis(monoacylglycero)phosphate: a secondary storage lipid in the gangliosidoses

Journal of lipid research, 2015-05, Vol.56 (5), p.1005-1006

2015

Link zum Volltext

Verfügbarkeit prüfen

A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis

EBioMedicine, 2023-06, Vol.92, p.104627-104627, Article 104627

2023

Link zum Volltext

Verfügbarkeit prüfen

Brain-Derived Neurotrophic Factor Regulates Hedonic Feeding by Acting on the Mesolimbic Dopamine System

The Journal of neuroscience, 2010-02, Vol.30 (7), p.2533-2541

2010

Link zum Volltext

Verfügbarkeit prüfen

Selection of an Efficient AAV Vector for Robust CNS Transgene Expression

Molecular therapy. Methods & clinical development, 2019-12, Vol.15, p.320-332

2019

Link zum Volltext

Verfügbarkeit prüfen

Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia

Nature communications, 2024-03, Vol.15 (1), p.2497-2497, Article 2497

2024

Link zum Volltext

Verfügbarkeit prüfen

Mutant Huntingtin Impairs Vesicle Formation from Recycling Endosomes by Interfering with Rab11 Activity

Molecular and Cellular Biology, 2009-11, Vol.29 (22), p.6106-6116

2009

Link zum Volltext

Verfügbarkeit prüfen

EZH2 inhibition reactivates epigenetically silenced FMR1 and normalizes molecular and electrophysiological abnormalities in fragile X syndrome neurons

Frontiers in neuroscience, 2024-02, Vol.18, p.1348478-1348478

2024

Link zum Volltext

Verfügbarkeit prüfen

Disruption of Rab11 activity in a knock-in mouse model of Huntington's disease

Neurobiology of disease, 2009-11, Vol.36 (2), p.374-383

2009

Link zum Volltext

Verfügbarkeit prüfen

Human GLB1 knockout cerebral organoids: A model system for testing AAV9-mediated GLB1 gene therapy for reducing GM1 ganglioside storage in GM1 gangliosidosis

Molecular genetics and metabolism reports, 2019-12, Vol.21, p.100513-100513, Article 100513

2019

Link zum Volltext

Verfügbarkeit prüfen

Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons

International journal of molecular sciences, 2022-12, Vol.23 (24), p.16013

2022

Link zum Volltext

Verfügbarkeit prüfen

Social media use by cardiovascular healthcare professionals in Portugal

Revista portuguesa de cardiologia, 2023-04, Vol.42 (4), p.349-357

2023

Link zum Volltext

Verfügbarkeit prüfen

Focused Ultrasound-Mediated Disruption of the Blood–Brain Barrier for AAV9 Delivery in a Mouse Model of Huntington’s Disease

Pharmaceutics, 2024-05, Vol.16 (6), p.710

2024

Link zum Volltext

Verfügbarkeit prüfen

Induced Pluripotent Stem Cell Models of Progranulin-Deficient Frontotemporal Dementia Uncover Specific Reversible Neuronal Defects

Cell reports (Cambridge), 2012-10, Vol.2 (4), p.789-798

2012

Link zum Volltext

Verfügbarkeit prüfen

Upregulating β-hexosaminidase activity in rodents prevents α-synuclein lipid associations and protects dopaminergic neurons from α-synuclein-mediated neurotoxicity

Acta neuropathologica communications, 2020-08, Vol.8 (1), p.127-14, Article 127

2020

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 339

Suche als RSS-Feed

Aktive Filter

KollektionEZB Electronic Journals Library

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(299)
Mit Volltextzugriff
(334)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Molecular Therapy
(33)
Plos One
(16)
Blood
(14)
Análise Social
(8)
Arquivos Brasileiros De Cardiologia
(7)
Molecular Therapy. Methods & Clinical Development
(7)
Grasas Y Aceites
(6)
História
(4)
Human Brain Mapping
(4)
Jornal De Pediatria
(4)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(6)
... seit 90 Tagen
(11)

Menü

Weitere Dienste

Einstellungen

Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis

GREGOR: Optics redesign and updates from 2018–2020

Intracranial AAV‐IFN‐β gene therapy eliminates invasive xenograft glioblastoma and improves survival in orthotopic syngeneic murine model

Design of new modular metal pallets: Experimental validation and life cycle analysis

Corrigendum to “Modelling of layers interactions on the structural behaviour of insulating glasses. Vertical deflection analyses” [Case Stud. Constr. Mater. 18 (2023) 2129]

Modelling of layers interactions on the structural behaviour of insulating glasses. Vertical deflection analyses

Cerebral organoids derived from Sandhoff disease-induced pluripotent stem cells exhibit impaired neurodifferentiation[S]

Several rAAV Vectors Efficiently Cross the Blood–brain Barrier and Transduce Neurons and Astrocytes in the Neonatal Mouse Central Nervous System

Analytical modelling and experimental assessment of metal pallets. Mechanical behaviour and durability performance under microbiological, chemical and environmental attacks

Microvesicle-associated AAV Vector as a Novel Gene Delivery System

Adeno Associated Viral Vector Delivered RNAi for Gene Therapy of SOD1 Amyotrophic Lateral Sclerosis

Bis(monoacylglycero)phosphate: a secondary storage lipid in the gangliosidoses

A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis

Brain-Derived Neurotrophic Factor Regulates Hedonic Feeding by Acting on the Mesolimbic Dopamine System

Selection of an Efficient AAV Vector for Robust CNS Transgene Expression

Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia

Mutant Huntingtin Impairs Vesicle Formation from Recycling Endosomes by Interfering with Rab11 Activity

EZH2 inhibition reactivates epigenetically silenced FMR1 and normalizes molecular and electrophysiological abnormalities in fragile X syndrome neurons

Disruption of Rab11 activity in a knock-in mouse model of Huntington's disease

Human GLB1 knockout cerebral organoids: A model system for testing AAV9-mediated GLB1 gene therapy for reducing GM1 ganglioside storage in GM1 gangliosidosis

Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons

Social media use by cardiovascular healthcare professionals in Portugal

Focused Ultrasound-Mediated Disruption of the Blood–Brain Barrier for AAV9 Delivery in a Mouse Model of Huntington’s Disease

Induced Pluripotent Stem Cell Models of Progranulin-Deficient Frontotemporal Dementia Uncover Specific Reversible Neuronal Defects

Upregulating β-hexosaminidase activity in rodents prevents α-synuclein lipid associations and protects dopaminergic neurons from α-synuclein-mediated neurotoxicity

Aktive Filter

Suchergebnisse filtern