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...

Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice

BioMed research international, 2016-01, Vol.2016 (2016), p.1-9

2016

Volltextzugriff (PDF)

Automated Five-Color Multiplex Co-detection of MicroRNA and Protein Expression in Fixed Tissue Specimens

Methods in molecular biology (Clifton, N.J.), 2020, Vol.2148, p.257

2020

Volltextzugriff (PDF)

Multiplexed Quantitative In Situ Hybridization with Subcellular or Single-Molecule Resolution Within Whole-Mount Vertebrate Embryos: qHCR and dHCR Imaging (v3.0)

Methods in molecular biology (Clifton, N.J.), 2020, Vol.2148, p.159

2020

Volltextzugriff (PDF)

Simultaneous Visualization of RNA and Protein Expression in Tissue Using a Combined RNAscope™ In Situ Hybridization and Immunofluorescence Protocol

Methods in molecular biology (Clifton, N.J.), 2020, Vol.2148, p.301

2020

Volltextzugriff (PDF)

Dual-color ultrasensitive bright-field RNA in situ hybridization with RNAscope

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1211, p.139

2014

Volltextzugriff (PDF)

Fluorescence in situ hybridization for detection of small RNAs on frozen tissue sections

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1211, p.95

Silahtaroglu, Asli

2014

Volltextzugriff (PDF)

Identification of low-expressing transcripts of the NPY receptors' family in the murine lingual epithelia

Methods in molecular biology (Clifton, N.J.), 2014, Vol.1211, p.213

Zolotukhin, Sergei

2014

Volltextzugriff (PDF)

Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors

PloS one, 2013-04, Vol.8 (4), p.e62097-e62097

2013

Volltextzugriff (PDF)

Improving retinal vascular endothelial cell tropism through rational rAAV capsid design

PloS one, 2023-05, Vol.18 (5), p.e0285370-e0285370

2023

Volltextzugriff (PDF)

rAAV2 5 gene-targeting to rods:dose-dependent efficiency and complications associated with different promoters

Gene therapy, 2010-09, Vol.17 (9), p.1162-1174

2010

Volltextzugriff (PDF)

Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus

Gene therapy, 2013-08, Vol.20 (8), p.824-833

2013

Volltextzugriff (PDF)

Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber’s hereditary optic neuropathy in a mouse model

Proceedings of the National Academy of Sciences - PNAS, 2012-05, Vol.109 (20), p.E1238-E1247

2012

Volltextzugriff (PDF)

SARM1 depletion rescues NMNAT1-dependent photoreceptor cell death and retinal degeneration

eLife, 2020-10, Vol.9

2020

Volltextzugriff (PDF)

Capsid Mutated Adeno-Associated Virus Delivered to the Anterior Chamber Results in Efficient Transduction of Trabecular Meshwork in Mouse and Rat

PloS one, 2015-06, Vol.10 (6), p.e0128759

2015

Volltextzugriff (PDF)

Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency

Gene therapy, 2010-07, Vol.17 (7), p.815-826

2010

Volltextzugriff (PDF)

Functional and behavioral restoration of vision by gene therapy in the guanylate cyclase-1 (GC1) knockout mouse

PloS one, 2010-06, Vol.5 (6), p.e11306-e11306

2010

Volltextzugriff (PDF)

Promotion of endoplasmic reticulum retrotranslocation by overexpression of E3 ubiquitin‐protein ligase synoviolin 1 reduces endoplasmic reticulum stress and preserves cone photoreceptors in cyclic nucleotide‐gated channel deficiency

The FASEB journal, 2024-09, Vol.38 (17), p.e70021-n/a

2024

Volltextzugriff (PDF)

Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

Human molecular genetics, 2015-11, Vol.24 (21), p.6229-6239

2015

Volltextzugriff (PDF)

Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque

Human gene therapy, 2019-05, Vol.30 (5), p.571-589

2019

Volltextzugriff (PDF)

Optimization of Capillary-Based Western Blotting for MYO7A

Advances in experimental medicine and biology, 2023, Vol.1415, p.125-130

2023

Volltextzugriff (PDF)

Long-term Retinal Function and Structure Rescue Using Capsid Mutant AAV8 Vector in the rd10 Mouse, a Model of Recessive Retinitis Pigmentosa

Molecular therapy, 2011-02, Vol.19 (2), p.234-242

2011

Volltextzugriff (PDF)

The human rhodopsin kinase promoter in an AAV5 vector confers rod- and cone-specific expression in the primate retina

Human gene therapy, 2012-10, Vol.23 (10), p.1101-1115

2012

Volltextzugriff (PDF)

Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy

PloS one, 2014-03, Vol.9 (3), p.e92928-e92928

2014

Volltextzugriff (PDF)

Virally delivered Channelrhodopsin-2 Safely and Effectively Restores Visual Function in Multiple Mouse Models of Blindness

Molecular therapy, 2011-07, Vol.19 (7), p.1220-1229

2011

Volltextzugriff (PDF)

Novel AAV44.9-Based Vectors Display Exceptional Characteristics for Retinal Gene Therapy

Molecular therapy, 2020-06, Vol.28 (6), p.1464-1478

2020

Volltextzugriff (PDF)

1 – 25 von 246

Suche als RSS-Feed

Aktive Filter

ThemaMice

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(233)
Mit Volltextzugriff
(208)

Publikationsform

Artikel
(245)
Buchkapitel
(1)

Sprache

Englisch
(244)
Französisch
(2)

Erscheinungsjahr

n.n

Thema

Animals
(243)
Science & Technology
(204)
Life Sciences & Biomedicine
(174)
Humans
(104)
Female
(61)
Male
(54)
Mice, Inbred C57bl
(50)
Mice, Knockout
(50)
Biological And Medical Sciences
(45)
Disease Models, Animal
(42)
Retina
(39)
Gene Therapy
(38)
Dependovirus - Genetics
(37)
Rodents
(36)
Biochemistry & Molecular Biology
(33)
Medicine, Research & Experimental
(33)
Research & Experimental Medicine
(33)
Science & Technology - Other Topics
(32)
Genetics & Heredity
(31)

14 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice

Automated Five-Color Multiplex Co-detection of MicroRNA and Protein Expression in Fixed Tissue Specimens

Multiplexed Quantitative In Situ Hybridization with Subcellular or Single-Molecule Resolution Within Whole-Mount Vertebrate Embryos: qHCR and dHCR Imaging (v3.0)

Simultaneous Visualization of RNA and Protein Expression in Tissue Using a Combined RNAscope™ In Situ Hybridization and Immunofluorescence Protocol

Dual-color ultrasensitive bright-field RNA in situ hybridization with RNAscope

Fluorescence in situ hybridization for detection of small RNAs on frozen tissue sections

Identification of low-expressing transcripts of the NPY receptors' family in the murine lingual epithelia

Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors

Improving retinal vascular endothelial cell tropism through rational rAAV capsid design

rAAV2 5 gene-targeting to rods:dose-dependent efficiency and complications associated with different promoters

Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus

Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber’s hereditary optic neuropathy in a mouse model

SARM1 depletion rescues NMNAT1-dependent photoreceptor cell death and retinal degeneration

Capsid Mutated Adeno-Associated Virus Delivered to the Anterior Chamber Results in Efficient Transduction of Trabecular Meshwork in Mouse and Rat

Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency

Functional and behavioral restoration of vision by gene therapy in the guanylate cyclase-1 (GC1) knockout mouse

Promotion of endoplasmic reticulum retrotranslocation by overexpression of E3 ubiquitin‐protein ligase synoviolin 1 reduces endoplasmic reticulum stress and preserves cone photoreceptors in cyclic nucleotide‐gated channel deficiency

Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque

Optimization of Capillary-Based Western Blotting for MYO7A

Long-term Retinal Function and Structure Rescue Using Capsid Mutant AAV8 Vector in the rd10 Mouse, a Model of Recessive Retinitis Pigmentosa

The human rhodopsin kinase promoter in an AAV5 vector confers rod- and cone-specific expression in the primate retina

Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy

Virally delivered Channelrhodopsin-2 Safely and Effectively Restores Visual Function in Multiple Mouse Models of Blindness

Novel AAV44.9-Based Vectors Display Exceptional Characteristics for Retinal Gene Therapy

Aktive Filter

Suchergebnisse filtern