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...

Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease

Cell metabolism, 2013-06, Vol.17 (6), p.941-953

2013

Volltextzugriff (PDF)

Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis

Lancet neurology, 2019-01, Vol.18 (1), p.107-116

2019

Volltextzugriff (PDF)

Clinical and Molecular Features of Early Infantile Niemann Pick Type C Disease

International journal of molecular sciences, 2020-07, Vol.21 (14), p.5059

2020

Volltextzugriff (PDF)

Fetal gene therapy for neurodegenerative disease of infants

Nature medicine, 2018-09, Vol.24 (9), p.1317-1323

2018

Volltextzugriff (PDF)

Diabetes drugs activate neuroprotective pathways in models of neonatal hypoxic-ischemic encephalopathy

EMBO molecular medicine, 2024-06, Vol.16 (6), p.1284-1309

2024

Volltextzugriff (PDF)

Dysregulated Wnt and NFAT signaling in a Parkinson’s disease LRRK2 G2019S knock-in model

Scientific reports, 2024-05, Vol.14 (1), p.12393-22, Article 12393

2024

Volltextzugriff (PDF)

Delineating pathological pathways in a chemically induced mouse model of Gaucher disease

The Journal of pathology, 2016-08, Vol.239 (4), p.496-509

2016

Volltextzugriff (PDF)

Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer

Nature communications, 2018-08, Vol.9 (1), p.3505-14, Article 3505

2018

Volltextzugriff (PDF)

Using Stem Cells to Grow Artificial Tissue for Peripheral Nerve Repair

Stem cells international, 2016-01, Vol.2016 (2016), p.1-18

2016

Volltextzugriff (PDF)

Gene Therapy for Lysosomal Storage Disorders: Ongoing Studies and Clinical Development

Biomolecules (Basel, Switzerland), 2021-04, Vol.11 (4), p.611

2021

Volltextzugriff (PDF)

Neuroprotective Effects of Diabetes Drugs for the Treatment of Neonatal Hypoxia-Ischemia Encephalopathy

Frontiers in cellular neuroscience, 2020-05, Vol.14, p.112

2020

Volltextzugriff (PDF)

Inhibition of Mitochondrial Complex I Impairs Release of α-Galactosidase by Jurkat Cells

International journal of molecular sciences, 2019-09, Vol.20 (18), p.4349

2019

Volltextzugriff (PDF)

Intravenous administration of AAV2/9 to the fetal and neonatal mouse leads to differential targeting of CNS cell types and extensive transduction of the nervous system

The FASEB journal, 2011-10, Vol.25 (10), p.3505-3518

2011

Volltextzugriff (PDF)

An autonucleolytic suspension HEK293F host cell line for high-titer serum-free AAV5 and AAV9 production with reduced levels of DNA impurity

Molecular therapy. Methods & clinical development, 2024-09, Vol.32 (3), p.101317, Article 101317

2024

Volltextzugriff (PDF)

Gene therapy for global brain diseases: one small step for mice, one giant leap for humans

Brain (London, England : 1878), 2020-07, Vol.143 (7), p.1964-1966

2020

Volltextzugriff (PDF)

Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes

Journal of inherited metabolic disease, 2013-09, Vol.36 (5), p.869-872

2013

Volltextzugriff (PDF)

Current therapies for the soluble lysosomal forms of neuronal ceroid lipofuscinosis

Biochemical Society transactions, 2010-12, Vol.38 (6), p.1484-1488

2010

Volltextzugriff (PDF)

Perinatal gene transfer to the liver

Current pharmaceutical design, 2011-08, Vol.17 (24), p.2528-2541

2011

Volltextzugriff (PDF)

Epilepsy Gene Therapy Using an Engineered Potassium Channel

The Journal of neuroscience, 2019-04, Vol.39 (16), p.3159-3169

2019

Volltextzugriff (PDF)

Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice

Molecular therapy. Nucleic acids, 2018-09, Vol.12, p.626-634

2018

Volltextzugriff (PDF)

Neuroprotective exendin-4 enhances hypothermia therapy in a model of hypoxic-ischaemic encephalopathy

Brain (London, England : 1878), 2018-10, Vol.141 (10), p.2925-2942

2018

Volltextzugriff (PDF)

Special edition: The NCLs/Batten disease

Biochimica et biophysica acta. Molecular basis of disease, 2020-09, Vol.1866 (9), p.165824-165824, Article 165824

2020

Volltextzugriff (PDF)

Comparison of different promoters to improve AAV vector-mediated gene therapy for neuronopathic Gaucher disease

Human molecular genetics, 2024-05, Vol.33 (17), p.1467-1480

2024

Volltextzugriff (PDF)

A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency

Brain (London, England : 1878), 2018-07, Vol.141 (7), p.2014-2031

2018

Volltextzugriff (PDF)

Microfluidic production of nanogels as alternative triple transfection reagents for the manufacture of adeno-associated virus vectors

Nanoscale, 2023-03, Vol.15 (12), p.5865-5876

2023

Volltextzugriff (PDF)

1 – 25 von 99

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(88)
Mit Volltextzugriff
(76)

Publikationsform

Sprache

Englisch
(98)
Persisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(71)
Life Sciences & Biomedicine
(60)
Animals
(44)
Humans
(38)
Mice
(28)
Gene Therapy
(27)
Biochemistry & Molecular Biology
(21)
Cell Biology
(14)
Genetic Vectors
(14)
Medicine, Research & Experimental
(14)
Mutation
(14)
Research & Experimental Medicine
(14)
Gene Expression
(13)
Disease Models, Animal
(12)
Genetic Therapy
(12)
Genetics & Heredity
(12)
Science & Technology - Other Topics
(11)
Female
(10)
Neonates
(10)
Physical Sciences
(10)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

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

Menü

Weitere Dienste

Einstellungen

Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease

Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis

Clinical and Molecular Features of Early Infantile Niemann Pick Type C Disease

Fetal gene therapy for neurodegenerative disease of infants

Diabetes drugs activate neuroprotective pathways in models of neonatal hypoxic-ischemic encephalopathy

Dysregulated Wnt and NFAT signaling in a Parkinson’s disease LRRK2 G2019S knock-in model

Delineating pathological pathways in a chemically induced mouse model of Gaucher disease

Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer

Using Stem Cells to Grow Artificial Tissue for Peripheral Nerve Repair

Gene Therapy for Lysosomal Storage Disorders: Ongoing Studies and Clinical Development

Neuroprotective Effects of Diabetes Drugs for the Treatment of Neonatal Hypoxia-Ischemia Encephalopathy

Inhibition of Mitochondrial Complex I Impairs Release of α-Galactosidase by Jurkat Cells

Intravenous administration of AAV2/9 to the fetal and neonatal mouse leads to differential targeting of CNS cell types and extensive transduction of the nervous system

An autonucleolytic suspension HEK293F host cell line for high-titer serum-free AAV5 and AAV9 production with reduced levels of DNA impurity

Gene therapy for global brain diseases: one small step for mice, one giant leap for humans

Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes

Current therapies for the soluble lysosomal forms of neuronal ceroid lipofuscinosis

Perinatal gene transfer to the liver

Epilepsy Gene Therapy Using an Engineered Potassium Channel

Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice

Neuroprotective exendin-4 enhances hypothermia therapy in a model of hypoxic-ischaemic encephalopathy

Special edition: The NCLs/Batten disease

Comparison of different promoters to improve AAV vector-mediated gene therapy for neuronopathic Gaucher disease

A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency

Microfluidic production of nanogels as alternative triple transfection reagents for the manufacture of adeno-associated virus vectors

Suchergebnisse filtern