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...

Drusen in patient-derived hiPSC-RPE models of macular dystrophies

Proceedings of the National Academy of Sciences - PNAS, 2017-09, Vol.114 (39), p.E8214-E8223

2017

Volltextzugriff (PDF)

Development of a CRISPRi Human Retinal Pigmented Epithelium Model for Functional Study of Age-Related Macular Degeneration Genes

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3417

2023

Volltextzugriff (PDF)

AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell models

Scientific reports, 2022-06, Vol.12 (1), p.9525-9525, Article 9525

2022

Volltextzugriff (PDF)

Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells

Stem Cells International, 2016-01, Vol.2016 (2016), p.578-589-046

2016

Volltextzugriff (PDF)

Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis

BMC medical genomics, 2018-07, Vol.11 (1), p.61-61, Article 61

2018

Volltextzugriff (PDF)

AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo

Investigative ophthalmology & visual science, 2016-06, Vol.57 (7), p.3470-3476

2016

Volltextzugriff (PDF)

Combinatorial Approach of Binary Colloidal Crystals and CRISPR Activation to Improve Induced Pluripotent Stem Cell Differentiation into Neurons

ACS applied materials & interfaces, 2022-02, Vol.14 (7), p.8669-8679

2022

Volltextzugriff (PDF)

Enriched retinal ganglion cells derived from human embryonic stem cells

Scientific reports, 2016-08, Vol.6 (1), p.30552-30552, Article 30552

2016

Volltextzugriff (PDF)

Utility of Self-Destructing CRISPR/Cas Constructs for Targeted Gene Editing in the Retina

Human gene therapy, 2019-11, Vol.30 (11), p.1349-1360

2019

Volltextzugriff (PDF)

Comparison of CRISPR/Cas Endonucleases for in vivo Retinal Gene Editing

Frontiers in cellular neuroscience, 2020-09, Vol.14, p.570917-570917

2020

Volltextzugriff (PDF)

Potentials of Cellular Reprogramming as a Novel Strategy for Neuroregeneration

Frontiers in cellular neuroscience, 2018-11, Vol.12, p.460-460

2018

Volltextzugriff (PDF)

A Simple Cloning-free Method to Efficiently Induce Gene Expression Using CRISPR/Cas9

Molecular therapy. Nucleic acids, 2019-03, Vol.14, p.184-191

2019

Volltextzugriff (PDF)

Corrigendum: Potentials of Cellular Reprogramming as a Novel Strategy for Neuroregeneration

Frontiers in cellular neuroscience, 2019-05, Vol.13, p.147-147

2019

Volltextzugriff (PDF)

Repression of global protein synthesis by Eif1a-like genes that are expressed specifically in the two-cell embryos and the transient Zscan4-positive state of embryonic stem cells

DNA research, 2013-08, Vol.20 (4), p.391-402

2013

Volltextzugriff (PDF)

A single‐cell transcriptome atlas of the adult human retina

The EMBO journal, 2019-09, Vol.38 (18), p.e100811-n/a

2019

Volltextzugriff (PDF)

A phospho-proteomic screen identifies novel S6K1 and mTORC1 substrates revealing additional complexity in the signaling network regulating cell growth

Cellular signalling, 2011-08, Vol.23 (8), p.1338-1347

2011

Volltextzugriff (PDF)

Drug discovery using induced pluripotent stem cell models of neurodegenerative and ocular diseases

Pharmacology & therapeutics (Oxford), 2017-09, Vol.177, p.32-43

2017

Volltextzugriff (PDF)

Genome engineering in ophthalmology: Application of CRISPR/Cas to the treatment of eye disease

Progress in retinal and eye research, 2016-07, Vol.53, p.1-20

2016

Volltextzugriff (PDF)

Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy

Aging (Albany, NY.), 2017-04, Vol.9 (4), p.1341-1350

2017

Volltextzugriff (PDF)

Knockout of AMD-associated gene POLDIP2 reduces mitochondrial superoxide in human retinal pigment epithelial cells

Aging (Albany, NY.), 2023-02, Vol.15 (6), p.1713-1733

2023

Volltextzugriff (PDF)

Study of mitochondrial respiratory defects on reprogramming to human induced pluripotent stem cells

Aging (Albany, NY.), 2016-05, Vol.8 (5), p.945-957

2016

Volltextzugriff (PDF)

Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencing

NAR genomics and bioinformatics, 2020-06, Vol.2 (2)

2020

Volltextzugriff (PDF)

Generation of Integration-free Human Induced Pluripotent Stem Cells Using Hair-derived Keratinocytes

Journal of visualized experiments, 2015-08 (102), p.e53174-e53174

2015

Volltextzugriff (PDF)

NF-κB-independent induction of endothelial cell apoptosis by the vascular disrupting agent DMXAA

Anticancer research, 2007, Vol.27 (1A), p.327-334

2007

Volltextzugriff (PDF)

NF-kappaB-independent induction of endothelial cell apoptosis by the vascular disrupting agent DMXAA

Anticancer research, 2007-01, Vol.27 (1A), p.327-334

2007

Volltextzugriff (PDF)

1 – 25 von 55

Suche als RSS-Feed

Aktive Filter

SpracheJapanisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(49)
Mit Volltextzugriff
(50)

Publikationsform

Sprache

Englisch
(55)
Chinesisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Drusen in patient-derived hiPSC-RPE models of macular dystrophies

Development of a CRISPRi Human Retinal Pigmented Epithelium Model for Functional Study of Age-Related Macular Degeneration Genes

AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell models

Electrical Stimulation Promotes Cardiac Differentiation of Human Induced Pluripotent Stem Cells

Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis

AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo

Combinatorial Approach of Binary Colloidal Crystals and CRISPR Activation to Improve Induced Pluripotent Stem Cell Differentiation into Neurons

Enriched retinal ganglion cells derived from human embryonic stem cells

Utility of Self-Destructing CRISPR/Cas Constructs for Targeted Gene Editing in the Retina

Comparison of CRISPR/Cas Endonucleases for in vivo Retinal Gene Editing

Potentials of Cellular Reprogramming as a Novel Strategy for Neuroregeneration

A Simple Cloning-free Method to Efficiently Induce Gene Expression Using CRISPR/Cas9

Corrigendum: Potentials of Cellular Reprogramming as a Novel Strategy for Neuroregeneration

Repression of global protein synthesis by Eif1a-like genes that are expressed specifically in the two-cell embryos and the transient Zscan4-positive state of embryonic stem cells

A single‐cell transcriptome atlas of the adult human retina

A phospho-proteomic screen identifies novel S6K1 and mTORC1 substrates revealing additional complexity in the signaling network regulating cell growth

Drug discovery using induced pluripotent stem cell models of neurodegenerative and ocular diseases

Genome engineering in ophthalmology: Application of CRISPR/Cas to the treatment of eye disease

Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy

Knockout of AMD-associated gene POLDIP2 reduces mitochondrial superoxide in human retinal pigment epithelial cells

Study of mitochondrial respiratory defects on reprogramming to human induced pluripotent stem cells

Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencing

Generation of Integration-free Human Induced Pluripotent Stem Cells Using Hair-derived Keratinocytes

NF-κB-independent induction of endothelial cell apoptosis by the vascular disrupting agent DMXAA

NF-kappaB-independent induction of endothelial cell apoptosis by the vascular disrupting agent DMXAA

Aktive Filter

Suchergebnisse filtern