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...

Deficiency in Lyst function leads to accumulation of secreted proteases and reduced retinal adhesion

PloS one, 2022-03, Vol.17 (3), p.e0254469

2022

Volltextzugriff (PDF)

Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10419

2022

Volltextzugriff (PDF)

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model

PLoS genetics, 2022-06, Vol.18 (6), p.e1009798

2022

Volltextzugriff (PDF)

Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1615

2022

Volltextzugriff (PDF)

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Human molecular genetics, 2011-02, Vol.20 (3), p.482-496

2011

Volltextzugriff (PDF)

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Journal of neurophysiology, 2012-11, Vol.108 (9), p.2442-2451

2012

Volltextzugriff (PDF)

Degradation of IRS1 leads to impaired glucose uptake in adipose tissue of the type 2 diabetes mouse model TALLYHO/Jng

Journal of endocrinology, 2009-10, Vol.203 (1), p.65-74

2009

Volltextzugriff (PDF)

Epithelial mechanics are maintained by inhibiting cell fusion with age in Drosophila

Journal of cell science, 2023-10, Vol.136 (20)

2023

Volltextzugriff (PDF)

Mouse Model Resources for Vision Research

Journal of ophthalmology, 2011-01, Vol.2011 (2011), p.1-12

2011

Volltextzugriff (PDF)

Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

Molecular and cellular neuroscience, 2007-05, Vol.35 (1), p.161-170

2007

Volltextzugriff (PDF)

Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments

Visual neuroscience, 2008-07, Vol.25 (4), p.563-574

2008

Volltextzugriff (PDF)

Genetic Analysis of a New Mouse Model for Non-Insulin-Dependent Diabetes

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.273-286

2001

Volltextzugriff (PDF)

A new mouse model of metabolic syndrome and associated complications

Journal of endocrinology, 2009-07, Vol.202 (1), p.17-28

2009

Volltextzugriff (PDF)

Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ

Investigative ophthalmology & visual science, 2016-03, Vol.57 (3), p.877-888

2016

Volltextzugriff (PDF)

Microtubule-associated protein 1A is a modifier of tubby hearing ( moth1 )

Nature genetics, 2002-04, Vol.30 (4), p.401-405

2002

Volltextzugriff (PDF)

An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency

Human molecular genetics, 2018-10, Vol.27 (19), p.3340-3352

2018

Volltextzugriff (PDF)

Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele

Investigative ophthalmology & visual science, 2018-10, Vol.59 (12), p.5127-5139

2018

Volltextzugriff (PDF)

Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa

Human molecular genetics, 2013-02, Vol.22 (3), p.558-567

2013

Volltextzugriff (PDF)

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1 rd8 mouse model

PLoS genetics, 2022-06, Vol.18 (6), p.e1009798

2022

Volltextzugriff (PDF)

Bright-Field Imaging and Optical Coherence Tomography of the Mouse Posterior Eye

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1438, p.395

2016

Volltextzugriff (PDF)

Defective carbohydrate metabolism in mice homozygous for the tubby mutation

Physiological genomics, 2006-10, Vol.27 (2), p.131-140

2006

Volltextzugriff (PDF)

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina

Human molecular genetics, 2003-09, Vol.12 (17), p.2179-2189

2003

Volltextzugriff (PDF)

Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction

Experimental eye research, 2009-09, Vol.89 (3), p.365-372

2009

Volltextzugriff (PDF)

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

Investigative ophthalmology & visual science, 2015-06, Vol.56 (6), p.3776-3787

2015

Volltextzugriff (PDF)

Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis

Investigative ophthalmology & visual science, 2012-02, Vol.53 (2), p.967-974

2012

Volltextzugriff (PDF)

1 – 25 von 93

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(89)
Mit Volltextzugriff
(89)

Publikationsform

Artikel
(92)
Buchkapitel
(1)

Sprache

Englisch
(92)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Animals
(61)
Science & Technology
(57)
Mice
(55)
Life Sciences & Biomedicine
(54)
Mice, Inbred C57bl
(29)
Biological And Medical Sciences
(23)
Male
(23)
Ophthalmology
(21)
Mutation
(20)
Disease Models, Animal
(19)
Biochemistry & Molecular Biology
(16)
Female
(16)
Fundamental And Applied Biological Sciences. Psychology
(16)
Retinal Degeneration - Genetics
(15)
Chromosome Mapping
(14)
Genetics & Heredity
(14)
Phenotype
(14)
Electroretinography
(11)
Alleles
(10)
Mice, Mutant Strains
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Deficiency in Lyst function leads to accumulation of secreted proteases and reduced retinal adhesion

Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model

Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Degradation of IRS1 leads to impaired glucose uptake in adipose tissue of the type 2 diabetes mouse model TALLYHO/Jng

Epithelial mechanics are maintained by inhibiting cell fusion with age in Drosophila

Mouse Model Resources for Vision Research

Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments

Genetic Analysis of a New Mouse Model for Non-Insulin-Dependent Diabetes

A new mouse model of metabolic syndrome and associated complications

Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ

Microtubule-associated protein 1A is a modifier of tubby hearing ( moth1 )

An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency

Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele

Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1 rd8 mouse model

Bright-Field Imaging and Optical Coherence Tomography of the Mouse Posterior Eye

Defective carbohydrate metabolism in mice homozygous for the tubby mutation

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina

Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis

Aktive Filter

Suchergebnisse filtern