相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Nanomedicine for the treatment of retinal and optic nerve diseases
Marco Attilio Zarbin et al.
CURRENT OPINION IN PHARMACOLOGY (2013)
From channelrhodopsins to optogenetics
Peter Hegemann et al.
EMBO MOLECULAR MEDICINE (2013)
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement
Artur V. Cideciyan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
A review and update on the current status of stem cell therapy and the retina
J. M. Ong et al.
BRITISH MEDICAL BULLETIN (2012)
CRB1 Mutations in Inherited Retinal Dystrophies
Kinga Bujakowska et al.
HUMAN MUTATION (2012)
Interim Results from the International Trial of Second Sight's Visual Prosthesis
Mark S. Humayun et al.
OPHTHALMOLOGY (2012)
Phosphene Thresholds Elicited by Transcorneal Electrical Stimulation in Healthy Subjects and Patients with Retinal Diseases
Lubka Naycheva et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2012)
A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews
Lina Zelinger et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa
Stephan Zuechner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Optogenetic approaches to restoring visual function in retinitis pigmentosa
Volker Busskamp et al.
CURRENT OPINION IN NEUROBIOLOGY (2011)
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy
Artur V. Cideciyan et al.
HUMAN MOLECULAR GENETICS (2011)
Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations
Sanae Sakami et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
ANATOMICAL CORRELATES TO THE BANDS SEEN IN THE OUTER RETINA BY OPTICAL COHERENCE TOMOGRAPHY Literature Review and Model
Richard F. Spaide et al.
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES (2011)
Intravitreal Injection of AAV2 Transduces Macaque Inner Retina
Lu Yin et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
Human CRB1-Associated Retinal Degeneration: Comparison with the rd8 Crb1-Mutant Mouse Model
Tomas S. Aleman et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
The Genomic, Biochemical, and Cellular Responses of the Retina in Inherited Photoreceptor Degenerations and Prospects for the Treatment of These Disorders
Alexa N. Bramall et al.
ANNUAL REVIEW OF NEUROSCIENCE, VOL 33 (2010)
Microbial rhodopsins in the spotlight
Christian Bamann et al.
CURRENT OPINION IN NEUROBIOLOGY (2010)
Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait
Alan F. Wright et al.
NATURE REVIEWS GENETICS (2010)
Treatment Possibilities for Retinitis Pigmentosa.
Samuel G. Jacobson et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy
Artur V. Cideciyan
PROGRESS IN RETINAL AND EYE RESEARCH (2010)
Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa
Volker Busskamp et al.
SCIENCE (2010)
Differential Macular Morphology in Patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-Related Leber Congenital Amaurosis
Sirichai Pasadhika et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate
Tadao Maeda et al.
HUMAN MOLECULAR GENETICS (2009)
CERKL Mutations Cause an Autosomal Recessive Cone-Rod Dystrophy with Inner Retinopathy
Tomas S. Aleman et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Disease Boundaries in the Retina of Patients with Usher Syndrome Caused by MYO7A Gene Mutations
Samuel G. Jacobson et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Leber congenital amaurosis: Genes, proteins and disease mechanisms
Anneke I. den Hollander et al.
PROGRESS IN RETINAL AND EYE RESEARCH (2008)
Retinal Laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations
Tomas S. Aleman et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2008)
Centrosomal,Ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of Photoreceptors and visual brain: Implications for therapy of Leber congenital amaurosis
Artur V. Cideciyan et al.
HUMAN MUTATION (2007)
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations
Tomas S. Aleman et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2007)
Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutation
Geoffrey K. Aguirre et al.
PLOS MEDICINE (2007)
RDH12 and RPE65, visual cycle genes causing Leber congenital amaurosis, differ in disease expression
Samuel G. Jacobson et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2007)
Evaluation of residual retinal function by pupillary constrictions and phosphenes using transcorneal electrical stimulation in patients with retinal degeneration
Takeshi Morimoto et al.
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2006)
Remodeling of the human retina in choroideremia:: Rab escort protein 1 (REP-1) mutations
Samuel G. Jacobson et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
SG Jacobson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination
SG Jacobson et al.
HUMAN MOLECULAR GENETICS (2003)
Mutations in the CRB1 gene cause Leber congenital amaurosis
AJ Lotery et al.
ARCHIVES OF OPHTHALMOLOGY (2001)
分享论文
