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...

Transcriptomic Analysis of Cultured Corneal Endothelial Cells as a Validation for Their Use in Cell Replacement Therapy

Cell transplantation, 2016-06, Vol.25 (6), p.1159-1176

2016

Volltextzugriff (PDF)

Phenotypic and functional characterization of corneal endothelial cells during in vitro expansion

Scientific reports, 2020-05, Vol.10 (1), p.7402-7402, Article 7402

2020

Volltextzugriff (PDF)

Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1

PloS one, 2017-01, Vol.12 (1), p.e0169215-e0169215

2017

Volltextzugriff (PDF)

Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants

American Journal of Physiology: Cell Physiology, 2016-11, Vol.311 (5), p.C820-C830

2016

Volltextzugriff (PDF)

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing

PloS one, 2019-06, Vol.14 (6), p.e0218279-e0218279

2019

Volltextzugriff (PDF)

Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy

Investigative ophthalmology & visual science, 2017-06, Vol.58 (7), p.3202-3214

2017

Volltextzugriff (PDF)

Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12

PloS one, 2014-04, Vol.9 (4), p.e95037

2014

Volltextzugriff (PDF)

Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus

PloS one, 2016-06, Vol.11 (6), p.e0158467-e0158467

2016

Volltextzugriff (PDF)

Site-Specific Production of IL-6 in the Central Nervous System Retargets and Enhances the Inflammatory Response in Experimental Autoimmune Encephalomyelitis

The Journal of immunology (1950), 2009-08, Vol.183 (3), p.2079-2088

2009

Volltextzugriff (PDF)

Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24

PloS one, 2016-06, Vol.11 (6), p.e0157418-e0157418

2016

Volltextzugriff (PDF)

A novel method to establish microglia-free astrocyte cultures: Comparison of matrix metalloproteinase expression profiles in pure cultures of astrocytes and microglia

Glia, 2008-08, Vol.56 (11), p.1187-1198

2008

Volltextzugriff (PDF)

Elevated ATG5 expression in autoimmune demyelination and multiple sclerosis

Autophagy, 2009-02, Vol.5 (2), p.152-158

2009

Volltextzugriff (PDF)

Persistent Macrophage/Microglial Activation and Myelin Disruption after Experimental Autoimmune Encephalomyelitis in Tissue Inhibitor of Metalloproteinase-1-Deficient Mice

The American journal of pathology, 2006-12, Vol.169 (6), p.2104-2116

2006

Volltextzugriff (PDF)

Coxsackievirus Preferentially Replicates and Induces Cytopathic Effects in Undifferentiated Neural Progenitor Cells

Journal of Virology, 2011-06, Vol.85 (12), p.5718-5732

2011

Volltextzugriff (PDF)

Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy

Journal of Ophthalmology, 2016-01, Vol.2016 (2016), p.271-279-037

2016

Volltextzugriff (PDF)

Nanocrystalline Silver Layer of Knitted Polyester Outperforms Other Silver-Containing Wound Dressings in an In Vitro Wound Model

Curēus (Palo Alto, CA), 2023-07

2023

Volltextzugriff (PDF)

Multimodal Imaging of Pre-Descemet Corneal Dystrophy Associated With X-Linked Ichthyosis and Deletion of the STS Gene

Cornea, 2020-11, Vol.39 (11), p.1442-1445

2020

Volltextzugriff (PDF)

Transcriptome analysis of the human corneal endothelium

Investigative ophthalmology & visual science, 2014-11, Vol.55 (12), p.7821-7830

2014

Volltextzugriff (PDF)

Astrocytic tissue inhibitor of metalloproteinase-1 (TIMP-1) promotes oligodendrocyte differentiation and enhances CNS myelination

The Journal of neuroscience, 2011-04, Vol.31 (16), p.6247-6254

2011

Volltextzugriff (PDF)

Functional impact of ZEB1 mutations associated with posterior polymorphous and Fuchs' endothelial corneal dystrophies

Investigative ophthalmology & visual science, 2014-10, Vol.55 (10), p.6159-6166

2014

Volltextzugriff (PDF)

Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening

JAMA ophthalmology, 2013-12, Vol.131 (12), p.1583

2013

Volltextzugriff (PDF)

Variant lattice corneal dystrophy associated with compound heterozygous mutations in the TGFBI gene

British journal of ophthalmology, 2017-04, Vol.101 (4), p.509-513

2017

Volltextzugriff (PDF)

Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum

Vision research (Oxford), 2014-07, Vol.100, p.88-92

2014

Volltextzugriff (PDF)

Corneal ectasia associated with posterior lamellar opacification

Ophthalmic genetics, 2021-08, Vol.42 (4), p.486-492

2021

Volltextzugriff (PDF)

Investigating the Molecular Basis of PPCD3: Characterization of ZEB1 Regulation of COL4A3 Expression

Investigative ophthalmology & visual science, 2016-08, Vol.57 (10), p.4136-4143

2016

Volltextzugriff (PDF)

1 – 25 von 59

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(42)

Publikationsform

Artikel
(54)
Berichte
(5)

Sprache

Englisch
(58)
Portugiesisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(37)
Life Sciences & Biomedicine
(30)
Humans
(26)
Corneal Dystrophies, Hereditary - Genetics
(20)
Ophthalmology
(20)
Male
(19)
Female
(18)
Cornea
(12)
Mutation
(11)
Pedigree
(11)
Animals
(10)
Mice
(10)
Adult
(9)
Adolescent
(8)
Corneal Dystrophy
(8)
Middle Aged
(8)
Child
(7)
Corneal Dystrophies, Hereditary - Diagnosis
(7)
Corneal Dystrophies, Hereditary - Metabolism
(7)
Gene Expression
(7)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Transcriptomic Analysis of Cultured Corneal Endothelial Cells as a Validation for Their Use in Cell Replacement Therapy

Phenotypic and functional characterization of corneal endothelial cells during in vitro expansion

Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1

Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing

Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy

Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12

Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus

Site-Specific Production of IL-6 in the Central Nervous System Retargets and Enhances the Inflammatory Response in Experimental Autoimmune Encephalomyelitis

Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24

A novel method to establish microglia-free astrocyte cultures: Comparison of matrix metalloproteinase expression profiles in pure cultures of astrocytes and microglia

Elevated ATG5 expression in autoimmune demyelination and multiple sclerosis

Persistent Macrophage/Microglial Activation and Myelin Disruption after Experimental Autoimmune Encephalomyelitis in Tissue Inhibitor of Metalloproteinase-1-Deficient Mice

Coxsackievirus Preferentially Replicates and Induces Cytopathic Effects in Undifferentiated Neural Progenitor Cells

Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy

Nanocrystalline Silver Layer of Knitted Polyester Outperforms Other Silver-Containing Wound Dressings in an In Vitro Wound Model

Multimodal Imaging of Pre-Descemet Corneal Dystrophy Associated With X-Linked Ichthyosis and Deletion of the STS Gene

Transcriptome analysis of the human corneal endothelium

Astrocytic tissue inhibitor of metalloproteinase-1 (TIMP-1) promotes oligodendrocyte differentiation and enhances CNS myelination

Functional impact of ZEB1 mutations associated with posterior polymorphous and Fuchs' endothelial corneal dystrophies

Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening

Variant lattice corneal dystrophy associated with compound heterozygous mutations in the TGFBI gene

Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum

Corneal ectasia associated with posterior lamellar opacification

Investigating the Molecular Basis of PPCD3: Characterization of ZEB1 Regulation of COL4A3 Expression

Suchergebnisse filtern