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The Pervasive Role of the miR-181 Family in Development, Neurodegeneration, and Cancer

International journal of molecular sciences, 2020-03, Vol.21 (6), p.2092

2020

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lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA

PloS one, 2014-06, Vol.9 (6), p.e98965-e98965

2014

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Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease

PloS one, 2011-10, Vol.6 (10), p.e25443-e25443

2011

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A Gene Network Regulating Lysosomal Biogenesis and Function

Science (American Association for the Advancement of Science), 2009-07, Vol.325 (5939), p.473-477

2009

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miRNeye: a microRNA expression atlas of the mouse eye

BMC genomics, 2010-12, Vol.11 (1), p.715-715, Article 715

2010

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High-resolution analysis of the human retina miRNome reveals isomiR variations and novel microRNAs

Nucleic acids research, 2016-02, Vol.44 (4), p.1525-1540

2016

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Identification and Characterization of MicroRNAs Expressed in the Mouse Eye

Investigative ophthalmology & visual science, 2007-02, Vol.48 (2), p.509-515

2007

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Identification of microRNA-regulated gene networks by expression analysis of target genes

Genome research, 2012-06, Vol.22 (6), p.1163-1172

2012

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UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs

Nucleic acids research, 2010-01, Vol.38 (Database issue), p.D75-D80

2010

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The long noncoding RNA Vax2os1 controls the cell cycle progression of photoreceptor progenitors in the mouse retina

RNA (Cambridge), 2012-01, Vol.18 (1), p.111-123

2012

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miR-204 is required for lens and retinal development via Meis2 targeting

Proceedings of the National Academy of Sciences - PNAS, 2010-08, Vol.107 (35), p.15491-15496

2010

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Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy

Scientific reports, 2022-12, Vol.12 (1), p.20815-20815, Article 20815

2022

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Light‐responsive microRNA miR‐211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance

The EMBO journal, 2020-04, Vol.39 (8), p.e102468-n/a

2020

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Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy

Scientific reports, 2022-10, Vol.12 (1), p.17637-17637, Article 17637

2022

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Gene therapy of inherited retinal degenerations: prospects and challenges

Human gene therapy, 2015-04, Vol.26 (4), p.193-200

2015

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MicroRNA target prediction by expression analysis of host genes

Genome Research, 2009-03, Vol.19 (3), p.481-490

2009

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Novel and Recurrent Copy Number Variants in ABCA4 -Associated Retinopathy

International journal of molecular sciences, 2024-05, Vol.25 (11), p.5940

2024

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TGF-β Controls miR-181/ERK Regulatory Network during Retinal Axon Specification and Growth

PloS one, 2015-12, Vol.10 (12), p.e0144129-e0144129

2015

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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome

Genetics in medicine, 2020-11, Vol.22 (11), p.1838-1850

2020

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Sophisticated Gene Regulation for a Complex Physiological System: The Role of Non-coding RNAs in Photoreceptor Cells

Frontiers in cell and developmental biology, 2021-01, Vol.8, p.629158-629158

2021

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An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs

Human molecular genetics, 2020-08, Vol.29 (13), p.2250-2260

2020

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Non-coding RNAs in retinal development and function

Human genetics, 2019-09, Vol.138 (8-9), p.957-971

2019

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Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder

European journal of human genetics : EJHG, 2019-09, Vol.27 (9), p.1475-1480

2019

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MiR-211 is essential for adult cone photoreceptor maintenance and visual function

Scientific reports, 2017-12, Vol.7 (1), p.17004-13, Article 17004

2017

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Hmgb3 is regulated by microRNA-206 during muscle regeneration

PloS one, 2012-08, Vol.7 (8), p.e43464-e43464

2012

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The Pervasive Role of the miR-181 Family in Development, Neurodegeneration, and Cancer

lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA

Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease

A Gene Network Regulating Lysosomal Biogenesis and Function

miRNeye: a microRNA expression atlas of the mouse eye

High-resolution analysis of the human retina miRNome reveals isomiR variations and novel microRNAs

Identification and Characterization of MicroRNAs Expressed in the Mouse Eye

Identification of microRNA-regulated gene networks by expression analysis of target genes

UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs

The long noncoding RNA Vax2os1 controls the cell cycle progression of photoreceptor progenitors in the mouse retina

miR-204 is required for lens and retinal development via Meis2 targeting

Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy

Light‐responsive microRNA miR‐211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance

Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy

Gene therapy of inherited retinal degenerations: prospects and challenges

MicroRNA target prediction by expression analysis of host genes

Novel and Recurrent Copy Number Variants in ABCA4 -Associated Retinopathy

TGF-β Controls miR-181/ERK Regulatory Network during Retinal Axon Specification and Growth

De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome

Sophisticated Gene Regulation for a Complex Physiological System: The Role of Non-coding RNAs in Photoreceptor Cells

An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs

Non-coding RNAs in retinal development and function

Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder

MiR-211 is essential for adult cone photoreceptor maintenance and visual function

Hmgb3 is regulated by microRNA-206 during muscle regeneration

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