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)

Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations

Annual review of neuroscience, 2003-01, Vol.26, p.657-700

2003

Volltextzugriff (PDF)

Mouse Model Resources for Vision Research

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

2011

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)

The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina

Advances in experimental medicine and biology, 2018, Vol.1074, p.545-551

2018

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)

Lysosomal Trafficking Regulator (LYST)

Advances in experimental medicine and biology, 2016-01, Vol.854, p.745-750

2016

Volltextzugriff (PDF)

New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

Human molecular genetics, 2009-01, Vol.18 (1), p.178-192

2009

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)

A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density

Molecular vision, 2017-03, Vol.23, p.140-148

2017

Volltextzugriff (PDF)

A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects

Advances in experimental medicine and biology, 2016-01, Vol.854, p.177-183

2016

Volltextzugriff (PDF)

Myosin 6 is required for iris development and normal function of the outer retina

Investigative ophthalmology & visual science, 2013-11, Vol.54 (12), p.7223-7233

2013

Volltextzugriff (PDF)

An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice

Investigative ophthalmology & visual science, 2012-03, Vol.53 (3), p.1663-1669

2012

Volltextzugriff (PDF)

An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration

Investigative ophthalmology & visual science, 2011-06, Vol.52 (7), p.4703-4709

2011

Volltextzugriff (PDF)

Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis

Experimental eye research, 2014-01, Vol.118, p.30-35

2014

Volltextzugriff (PDF)

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6

Human molecular genetics, 2002-08, Vol.11 (16), p.1879-1886

2002

Volltextzugriff (PDF)

Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2

Investigative ophthalmology & visual science, 2010-06, Vol.51 (6), p.3264-3272

2010

Volltextzugriff (PDF)

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosa

Nature genetics, 1998-02, Vol.18 (2), p.174-176

1998

Volltextzugriff (PDF)

The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation

Visual neuroscience, 2006-11, Vol.23 (6), p.917-929

2006

Volltextzugriff (PDF)

Translational vision research models program

Advances in experimental medicine and biology, 2012, Vol.723, p.391

2012

Volltextzugriff (PDF)

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene

Human molecular genetics, 2000-01, Vol.9 (2), p.155-163

2000

Volltextzugriff (PDF)

Cell-Specific Expression of Tubby Gene Family Members (tub, Tulp1, 2, and 3) in the Retina

Investigative ophthalmology & visual science, 1999-10, Vol.40 (11), p.2706-2712

1999

Volltextzugriff (PDF)

Severe Ocular Abnormalities in C57BL/6 but Not in 129/Sv p53-Deficient Mice

Investigative ophthalmology & visual science, 1999-07, Vol.40 (8), p.1874-1878

1999

Volltextzugriff (PDF)

1 – 25 von 36

Suche als RSS-Feed

Aktive Filter

ThemaOphthalmology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(35)
Mit Volltextzugriff
(32)

Publikationsform

Artikel
(35)
Buchkapitel
(1)

Sprache

Englisch
(36)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations

Mouse Model Resources for Vision Research

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

The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina

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

Lysosomal Trafficking Regulator (LYST)

New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

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

A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density

A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects

Myosin 6 is required for iris development and normal function of the outer retina

An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice

An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration

Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6

Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosa

The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation

Translational vision research models program

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene

Cell-Specific Expression of Tubby Gene Family Members (tub, Tulp1, 2, and 3) in the Retina

Severe Ocular Abnormalities in C57BL/6 but Not in 129/Sv p53-Deficient Mice

Aktive Filter

Suchergebnisse filtern