Literature DB >> 27928030

Emerging therapies for inherited retinal degeneration.

Hendrik P N Scholl1,2, Rupert W Strauss2,3,4,5,6, Mandeep S Singh2, Deniz Dalkara7,8,9, Botond Roska10,11, Serge Picaud7,8,9, José-Alain Sahel7,8,9,12,13,14.   

Abstract

Inherited retinal degenerative diseases, a genetically and phenotypically heterogeneous group of disorders, affect the function of photoreceptor cells and are among the leading causes of blindness. Recent advances in molecular genetics and cell biology are elucidating the pathophysiological mechanisms underlying these disorders and are helping to identify new therapeutic approaches, such as gene therapy, stem cell therapy, and optogenetics. Several of these approaches have entered the clinical phase of development. Artificial replacement of dying photoreceptor cells using retinal prostheses has received regulatory approval. Precise retinal imaging and testing of visual function are facilitating more efficient clinical trial design. In individual patients, disease stage will determine whether the therapeutic strategy should comprise photoreceptor cell rescue to delay or arrest vision loss or retinal replacement for vision restoration.
Copyright © 2016, American Association for the Advancement of Science.

Entities:  

Mesh:

Year:  2016        PMID: 27928030     DOI: 10.1126/scitranslmed.aaf2838

Source DB:  PubMed          Journal:  Sci Transl Med        ISSN: 1946-6234            Impact factor:   17.956


  68 in total

Review 1.  Applications of CRISPR/Cas9 in retinal degenerative diseases.

Authors:  Ying-Qian Peng; Luo-Sheng Tang; Shigeo Yoshida; Ye-Di Zhou
Journal:  Int J Ophthalmol       Date:  2017-04-18       Impact factor: 1.779

Review 2.  Relevance of tissue specific subunit expression in channelopathies.

Authors:  Hartwig Seitter; Alexandra Koschak
Journal:  Neuropharmacology       Date:  2017-06-29       Impact factor: 5.250

Review 3.  [Imaging and molecular genetic diagnostics for the characterization of retinal dystrophies].

Authors:  J Birtel; M Gliem; F G Holz; P Herrmann
Journal:  Ophthalmologe       Date:  2018-12       Impact factor: 1.059

Review 4.  [Genetic diagnostics of retinal dystrophies : Breakthrough with new methods of DNA sequencing].

Authors:  H J Bolz
Journal:  Ophthalmologe       Date:  2018-12       Impact factor: 1.059

5.  Effect of MMP-9 gene knockout on retinal vascular form and function.

Authors:  Akash K George; Rubens P Homme; Avisek Majumder; Suresh C Tyagi; Mahavir Singh
Journal:  Physiol Genomics       Date:  2019-11-11       Impact factor: 3.107

6.  Stable Retinoid Analogue Targeted Dual pH-Sensitive Smart Lipid ECO/pDNA Nanoparticles for Specific Gene Delivery in the Retinal Pigment Epithelium.

Authors:  Da Sun; Rebecca M Schur; Avery E Sears; Song-Qi Gao; Wenyu Sun; Amirreza Naderi; Timothy Kern; Krzysztof Palczewski; Zheng-Rong Lu
Journal:  ACS Appl Bio Mater       Date:  2020-04-03

7.  In vivo-directed evolution of adeno-associated virus in the primate retina.

Authors:  Leah C Byrne; Timothy P Day; Meike Visel; Jennifer A Strazzeri; Cécile Fortuny; Deniz Dalkara; William H Merigan; David V Schaffer; John G Flannery
Journal:  JCI Insight       Date:  2020-05-21

8.  Longitudinal Microperimetric Changes of Macular Sensitivity in Stargardt Disease After 12 Months: ProgStar Report No. 13.

Authors:  Etienne M Schönbach; Rupert W Strauss; Beatriz Muñoz; Yulia Wolfson; Mohamed A Ibrahim; David G Birch; Eberhart Zrenner; Janet S Sunness; Michael S Ip; SriniVas R Sadda; Sheila K West; Hendrik P N Scholl
Journal:  JAMA Ophthalmol       Date:  2020-07-01       Impact factor: 7.389

9.  Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10.

Authors:  Xiangrong Kong; Kaoru Fujinami; Rupert W Strauss; Beatriz Munoz; Sheila K West; Artur V Cideciyan; Michel Michaelides; Mohamed Ahmed; Ann-Margret Ervin; Etienne Schönbach; Janet K Cheetham; Hendrik P N Scholl
Journal:  JAMA Ophthalmol       Date:  2018-08-01       Impact factor: 7.389

10.  A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families.

Authors:  Revital Bronstein; Elizabeth E Capowski; Sudeep Mehrotra; Alex D Jansen; Daniel Navarro-Gomez; Mathew Maher; Emily Place; Riccardo Sangermano; Kinga M Bujakowska; David M Gamm; Eric A Pierce
Journal:  Hum Mol Genet       Date:  2020-04-15       Impact factor: 6.150

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