UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 53

Sortiert nach

In Vivo Assessment of Potential Therapeutic Approaches for USH2A-Associated Diseases

Advances in experimental medicine and biology, 2019, Vol.1185, p.91-96

2019

Volltextzugriff (PDF)

Intrinsic Circadian Clock of the Mammalian Retina: Importance for Retinal Processing of Visual Information

Cell, 2007-08, Vol.130 (4), p.730-741

2007

Volltextzugriff (PDF)

Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis

Cancer cell, 2006, Vol.9 (1), p.13-22

2006

Volltextzugriff (PDF)

LKB1 and AMPK regulate synaptic remodeling in old age

Nature neuroscience, 2014-09, Vol.17 (9), p.1190-1197

2014

Volltextzugriff (PDF)

Elastic fiber homeostasis requires lysyl oxidase-like 1 protein

Nature genetics, 2004-02, Vol.36 (2), p.178-182

2004

Volltextzugriff (PDF)

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (11), p.4413-4418

2007

Volltextzugriff (PDF)

Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss

PLoS genetics, 2010-05, Vol.6 (5), p.e1000955-e1000955

2010

Volltextzugriff (PDF)

MEF2D Drives Photoreceptor Development through a Genome-wide Competition for Tissue-Specific Enhancers

Neuron (Cambridge, Mass.), 2015-04, Vol.86 (1), p.247-263

2015

Volltextzugriff (PDF)

Gene Therapy Preserves Retinal Structure and Function in a Mouse Model of NMNAT1-Associated Retinal Degeneration

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.582-594

2020

Volltextzugriff (PDF)

Failure of Elastic Fiber Homeostasis Leads to Pelvic Floor Disorders

The American journal of pathology, 2006-02, Vol.168 (2), p.519-528

2006

Volltextzugriff (PDF)

Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors

Human molecular genetics, 2009-06, Vol.18 (12), p.2099-2114

2009

Volltextzugriff (PDF)

Gene Replacement Therapy Rescues Photoreceptor Degeneration in a Murine Model of Leber Congenital Amaurosis Lacking RPGRIP

Investigative ophthalmology & visual science, 2005-09, Vol.46 (9), p.3039-3045

2005

Volltextzugriff (PDF)

Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis

Human gene therapy, 2010-08, Vol.21 (8), p.993

2010

Volltextzugriff (PDF)

A Retinitis Pigmentosa GTPase Regulator (RPGR)-Deficient Mouse Model for X-Linked Retinitis Pigmentosa (RP3)

Proceedings of the National Academy of Sciences - PNAS, 2000-03, Vol.97 (7), p.3649-3654

2000

Volltextzugriff (PDF)

AAV-Mediated Expression Targeting of Rod and Cone Photoreceptors with a Human Rhodopsin Kinase Promoter

Investigative ophthalmology & visual science, 2007-09, Vol.48 (9), p.3954-3961

2007

Volltextzugriff (PDF)

The Retinitis Pigmentosa GTPase Regulator (RPGR)-Interacting Protein: Subserving RPGR Function and Participating in Disk Morphogenesis

Proceedings of the National Academy of Sciences - PNAS, 2003-04, Vol.100 (7), p.3965-3970

2003

Volltextzugriff (PDF)

The Ciliary Rootlet Maintains Long-Term Stability of Sensory Cilia

Molecular and Cellular Biology, 2005-05, Vol.25 (10), p.4129-4137

2005

Volltextzugriff (PDF)

RPGR Isoforms in Photoreceptor Connecting Cilia and the Transitional Zone of Motile Cilia

Investigative ophthalmology & visual science, 2003-06, Vol.44 (6), p.2413-2421

2003

Volltextzugriff (PDF)

Increased light exposure alleviates one form of photoreceptor degeneration marked by elevated calcium in the dark

PloS one, 2009-12, Vol.4 (12), p.e8438

2009

Volltextzugriff (PDF)

An Experimental Animal Model of Photodynamic Optic Nerve Head Injury (PONHI)

Current eye research, 2016-11, Vol.41 (11), p.1498-1506

2016

Volltextzugriff (PDF)

Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial function

The EMBO journal, 2004-01, Vol.23 (1), p.89-99

2004

Volltextzugriff (PDF)

AIPL1, the Protein That Is Defective in Leber Congenital Amaurosis, Is Essential for the Biosynthesis of Retinal Rod cGMP Phosphodiesterase

Proceedings of the National Academy of Sciences - PNAS, 2004-09, Vol.101 (38), p.13903-13908

2004

Volltextzugriff (PDF)

Rod and Cone Opsin Mislocalization in an Autopsy Eye From a Carrier of X-linked Retinitis Pigmentosa With a Gly436Asp Mutation in the RPGR Gene

American journal of ophthalmology, 2006-09, Vol.142 (3), p.515-518

2006

Volltextzugriff (PDF)

A Single, Abbreviated RPGR-ORF15 Variant Reconstitutes RPGR Function In Vivo

Investigative ophthalmology & visual science, 2005-02, Vol.46 (2), p.435-441

2005

Volltextzugriff (PDF)

Genetic Replacement of Cyclin D1 Function in Mouse Development by Cyclin D2

Molecular and Cellular Biology, 2005-02, Vol.25 (3), p.1081-1088

2005

Volltextzugriff (PDF)

1 – 25 von 53

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(52)
Mit Volltextzugriff
(50)

Publikationsform

Artikel
(53)

Sprache

Englisch
(53)
Japanisch
(20)

Erscheinungsjahr

n.n

Thema

Science & Technology
(47)
Animals
(41)
Life Sciences & Biomedicine
(41)
Mice
(34)
Biological And Medical Sciences
(26)
Ophthalmology
(23)
Electroretinography
(19)
Retina
(16)
Fundamental And Applied Biological Sciences. Psychology
(15)
Medical Sciences
(15)
Humans
(14)
Mice, Inbred C57bl
(13)
Mice, Knockout
(13)
Disease Models, Animal
(11)
Mice, Transgenic
(11)
Photoreceptors
(11)
Biochemistry & Molecular Biology
(10)
Eye And Associated Structures. Visual Pathways And Centers. Vision
(10)
Female
(10)
Mutation
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

In Vivo Assessment of Potential Therapeutic Approaches for USH2A-Associated Diseases

Intrinsic Circadian Clock of the Mammalian Retina: Importance for Retinal Processing of Visual Information

Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis

LKB1 and AMPK regulate synaptic remodeling in old age

Elastic fiber homeostasis requires lysyl oxidase-like 1 protein

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss

MEF2D Drives Photoreceptor Development through a Genome-wide Competition for Tissue-Specific Enhancers

Gene Therapy Preserves Retinal Structure and Function in a Mouse Model of NMNAT1-Associated Retinal Degeneration

Failure of Elastic Fiber Homeostasis Leads to Pelvic Floor Disorders

Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors

Gene Replacement Therapy Rescues Photoreceptor Degeneration in a Murine Model of Leber Congenital Amaurosis Lacking RPGRIP

Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis

A Retinitis Pigmentosa GTPase Regulator (RPGR)-Deficient Mouse Model for X-Linked Retinitis Pigmentosa (RP3)

AAV-Mediated Expression Targeting of Rod and Cone Photoreceptors with a Human Rhodopsin Kinase Promoter

The Retinitis Pigmentosa GTPase Regulator (RPGR)-Interacting Protein: Subserving RPGR Function and Participating in Disk Morphogenesis

The Ciliary Rootlet Maintains Long-Term Stability of Sensory Cilia

RPGR Isoforms in Photoreceptor Connecting Cilia and the Transitional Zone of Motile Cilia

Increased light exposure alleviates one form of photoreceptor degeneration marked by elevated calcium in the dark

An Experimental Animal Model of Photodynamic Optic Nerve Head Injury (PONHI)

Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial function

AIPL1, the Protein That Is Defective in Leber Congenital Amaurosis, Is Essential for the Biosynthesis of Retinal Rod cGMP Phosphodiesterase

Rod and Cone Opsin Mislocalization in an Autopsy Eye From a Carrier of X-linked Retinitis Pigmentosa With a Gly436Asp Mutation in the RPGR Gene

A Single, Abbreviated RPGR-ORF15 Variant Reconstitutes RPGR Function In Vivo

Genetic Replacement of Cyclin D1 Function in Mouse Development by Cyclin D2

Suchergebnisse filtern