microRNAs and inherited retinal dystrophies.
作者信息
Xu Shunbin
机构信息
Department of Ophthalmology/Kresge Eye Institute and Department of Anatomy & Cell Biology, School of Medicine, Wayne State University, Detroit, MI 48201
出版信息
Proc Natl Acad Sci U S A. 2015 Jul 21;112(29):8805-6. doi: 10.1073/pnas.1511019112. Epub 2015 Jul 9.
Abstract
摘要
相似文献
1
microRNAs and inherited retinal dystrophies.
Proc Natl Acad Sci U S A. 2015 Jul 21;112(29):8805-6. doi: 10.1073/pnas.1511019112. Epub 2015 Jul 9.
2
MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma.
Proc Natl Acad Sci U S A. 2015 Jun 23;112(25):E3236-45. doi: 10.1073/pnas.1401464112. Epub 2015 Jun 8.
3
[Human genetic diagnostics in hereditary eye diseases : What does the ophthalmologist need to know].
Ophthalmologie. 2023 Jun;120(6):679-688. doi: 10.1007/s00347-023-01878-6. Epub 2023 Jun 2.
4
Gene discovery and prevalence in inherited retinal dystrophies.
C R Biol. 2014 Mar;337(3):160-6. doi: 10.1016/j.crvi.2013.12.001. Epub 2014 Mar 4.
5
[Gene Replacement Therapy for Inherited Retinal Dystrophies].
Klin Monbl Augenheilkd. 2017 Mar;234(3):320-328. doi: 10.1055/s-0043-101817. Epub 2017 Mar 29.
6
Development of Refractive Errors-What Can We Learn From Inherited Retinal Dystrophies?
Am J Ophthalmol. 2017 Oct;182:81-89. doi: 10.1016/j.ajo.2017.07.008. Epub 2017 Jul 25.
7
Design and In Vitro Use of Antisense Oligonucleotides to Correct Pre-mRNA Splicing Defects in Inherited Retinal Dystrophies.
Methods Mol Biol. 2018;1715:61-78. doi: 10.1007/978-1-4939-7522-8_5.
8
Therapies for Inherited Retinal Dystrophies: What is Enough?
Drug Discov Today. 2024 Sep;29(9):104095. doi: 10.1016/j.drudis.2024.104095. Epub 2024 Jul 9.
9
The current status of molecular diagnosis of inherited retinal dystrophies.
Curr Opin Ophthalmol. 2015 Jul;26(5):346-51. doi: 10.1097/ICU.0000000000000185.
10
[Genetic diagnostic testing in inherited retinal dystrophies].
Klin Monbl Augenheilkd. 2013 Mar;230(3):243-6. doi: 10.1055/s-0032-1327929. Epub 2012 Dec 3.
引用本文的文献
1
New insight into the neuroimmune interplay in Pseudomonas aeruginosa keratitis.
Ocul Surf. 2025 Jul 24;38:170-183. doi: 10.1016/j.jtos.2025.07.008.
2
New Insight Into the Neuroimmune Interplay In Keratitis.
bioRxiv. 2025 Mar 11:2025.03.06.641908. doi: 10.1101/2025.03.06.641908.
3
Exploring Histone Modifications in Inherited Retinal Disorders.
Adv Exp Med Biol. 2025;1468:189-193. doi: 10.1007/978-3-031-76550-6_31.
4
The miR-183/96/182 cluster regulates sensory innervation, resident myeloid cells and functions of the cornea through cell type-specific target genes.
Sci Rep. 2024 Apr 1;14(1):7676. doi: 10.1038/s41598-024-58403-1.
5
Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy.
Front Cell Dev Biol. 2020 Dec 23;8:619641. doi: 10.3389/fcell.2020.619641. eCollection 2020.
6
MicroRNAs in Ocular Infection.
Microorganisms. 2019 Sep 17;7(9):359. doi: 10.3390/microorganisms7090359.
7
Multimodal Regulation Orchestrates Normal and Complex Disease States in the Retina.
Sci Rep. 2017 Apr 6;7(1):690. doi: 10.1038/s41598-017-00788-3.
8
Genome-Wide Scleral Micro- and Messenger-RNA Regulation During Myopia Development in the Mouse.
Invest Ophthalmol Vis Sci. 2016 Nov 1;57(14):6089-6097. doi: 10.1167/iovs.16-19563.
本文引用的文献
1
MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma.
Proc Natl Acad Sci U S A. 2015 Jun 23;112(25):E3236-45. doi: 10.1073/pnas.1401464112. Epub 2015 Jun 8.
2
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance.
Nucleic Acids Res. 2014 Jul;42(12):7793-806. doi: 10.1093/nar/gku498. Epub 2014 Jun 3.
3
Genes and mutations causing retinitis pigmentosa.
Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
4
Pax6 regulates gene expression in the vertebrate lens through miR-204.
PLoS Genet. 2013;9(3):e1003357. doi: 10.1371/journal.pgen.1003357. Epub 2013 Mar 14.
5
Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degeneration.
Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):E507-16. doi: 10.1073/pnas.1212655110. Epub 2013 Jan 22.
6
A single-base substitution in the seed region of miR-184 causes EDICT syndrome.
Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):348-53. doi: 10.1167/iovs.11-8783.
7
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.
Hum Mol Genet. 2012 Feb 1;21(3):577-85. doi: 10.1093/hmg/ddr493. Epub 2011 Oct 28.
8
Mutation altering the miR-184 seed region causes familial keratoconus with cataract.
Am J Hum Genet. 2011 Nov 11;89(5):628-33. doi: 10.1016/j.ajhg.2011.09.014. Epub 2011 Oct 11.
9
miR-204 is required for lens and retinal development via Meis2 targeting.
Proc Natl Acad Sci U S A. 2010 Aug 31;107(35):15491-6. doi: 10.1073/pnas.0914785107. Epub 2010 Aug 16.
10
A mutation in the 3'-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia.
Hum Mol Genet. 2010 May 15;19(10):2015-27. doi: 10.1093/hmg/ddq083. Epub 2010 Feb 24.
Zotero 插件