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Transcription elongation factor AFF2/FMR2 regulates expression of expanded GGGGCC repeat-containing C9ORF72 allele in ALS/FTD

Nature communications, 2019-11, Vol.10 (1), p.5466-14, Article 5466

2019

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MicroRNA-9: Functional evolution of a conserved small regulatory RNA

RNA biology, 2011-07, Vol.8 (4), p.557-564

2011

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Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Scientific reports, 2024-01, Vol.14 (1), p.2153-2153, Article 2153

2024

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Author Correction: Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Scientific reports, 2024-04, Vol.14 (1), p.9346-9346, Article 9346

2024

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Downregulation of the Host Gene jigr1 by miR-92 Is Essential for Neuroblast Self-Renewal in Drosophila

PLoS genetics, 2015-05, Vol.11 (5), p.e1005264-e1005264

2015

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Different modes of APC/C activation control growth and neuron-glia interaction in the developing Drosophila eye

Development (Cambridge), 2017-12, Vol.144 (24), p.4673-4683

2017

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Antagonistic feedback loops involving Rau and Sprouty in the Drosophila eye control neuronal and glial differentiation

Science signaling, 2013-11, Vol.6 (300), p.ra96

2013

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Long‐range signaling systems controlling glial migration in the Drosophila eye

Developmental neurobiology (Hoboken, N.J.), 2011-12, Vol.71 (12), p.1310-1316

2011

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The eye imaginal disc as a model to study the coordination of neuronal and glial development

Fly (Austin, Tex.), 2010-01, Vol.4 (1), p.71-79

2010

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Progranulin upregulation by antisense oligonucleotides targeting regRNAs for treatment of FTD‐GRN

Alzheimer's & dementia, 2022-12, Vol.18 (S10), p.n/a

2022

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Glial Cell Migration in the Eye Disc

The Journal of neuroscience, 2007-11, Vol.27 (48), p.13130-13139

2007

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Insights into C9ORF72-Related ALS/FTD from Drosophila and iPSC Models

Trends in neurosciences (Regular ed.), 2018-07, Vol.41 (7), p.457-469

2018

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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 21 as a milder allelic variant of congenital muscular dystrophy MDC1C

Human molecular genetics, 2001-12, Vol.10 (25), p.2851-2859

2001

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Abnormalities in α-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies

The American journal of pathology, 2004-02, Vol.164 (2), p.727-737

2004

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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2i as a milder allelic variant of congenital muscular dystrophy MDC1C

Human molecular genetics, 2001-12, Vol.10 (25), p.2851-2859

2001

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Phenotypic spectrum associated with mutations in the fukutin-related protein gene

Annals of neurology, 2003-04, Vol.53 (4), p.537-542

2003

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Downregulation of Hsp90 and the antimicrobial peptide Mtk suppresses poly(GR)-induced neurotoxicity in C9ORF72-ALS/FTD

Neuron (Cambridge, Mass.), 2023-05, Vol.111 (9), p.1381-1390.e6

2023

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Switch in FGF signalling initiates glial differentiation in the Drosophila eye

Nature (London), 2009-08, Vol.460 (7256), p.758-761

2009

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Spinster controls Dpp signaling during glial migration in the Drosophila eye

The Journal of neuroscience, 2011-05, Vol.31 (19), p.7005-7015

2011

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Downregulation of the Host Gene jigr1 by miR-92 Is Essential for Neuroblast Self-Renewal in Drosophila: e1005264

PLoS genetics, 2015-05, Vol.11 (5)

2015

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A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan

Neuromuscular disorders : NMD, 2003-12, Vol.13 (10), p.771-778

2003

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Prenatal diagnosis of Ullrich congenital muscular dystrophy using haplotype analysis and collagen VI immunocytochemistry

Prenatal diagnosis, 2004-06, Vol.24 (6), p.440-444

2004

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Evaluation of C/Ebp(Formula) as a Candidate Tumor Suppressor Gene in Hepatocellular Carcinoma

Yuva, Yeliz

2004

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Abnormalities in {alpha}-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies

The American journal of pathology, 2004-02, Vol.164 (2), p.727

2004

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Transcription elongation factor AFF2/FMR2 regulates expression of expanded GGGGCC repeat-containing C9ORF72 allele in ALS/FTD

MicroRNA-9: Functional evolution of a conserved small regulatory RNA

Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Author Correction: Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Downregulation of the Host Gene jigr1 by miR-92 Is Essential for Neuroblast Self-Renewal in Drosophila

Different modes of APC/C activation control growth and neuron-glia interaction in the developing Drosophila eye

Antagonistic feedback loops involving Rau and Sprouty in the Drosophila eye control neuronal and glial differentiation

Long‐range signaling systems controlling glial migration in the Drosophila eye

The eye imaginal disc as a model to study the coordination of neuronal and glial development

Progranulin upregulation by antisense oligonucleotides targeting regRNAs for treatment of FTD‐GRN

Glial Cell Migration in the Eye Disc

Insights into C9ORF72-Related ALS/FTD from Drosophila and iPSC Models

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 21 as a milder allelic variant of congenital muscular dystrophy MDC1C

Abnormalities in α-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2i as a milder allelic variant of congenital muscular dystrophy MDC1C

Phenotypic spectrum associated with mutations in the fukutin-related protein gene

Downregulation of Hsp90 and the antimicrobial peptide Mtk suppresses poly(GR)-induced neurotoxicity in C9ORF72-ALS/FTD

Switch in FGF signalling initiates glial differentiation in the Drosophila eye

Spinster controls Dpp signaling during glial migration in the Drosophila eye

Downregulation of the Host Gene jigr1 by miR-92 Is Essential for Neuroblast Self-Renewal in Drosophila: e1005264

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan

Prenatal diagnosis of Ullrich congenital muscular dystrophy using haplotype analysis and collagen VI immunocytochemistry

Evaluation of C/Ebp(Formula) as a Candidate Tumor Suppressor Gene in Hepatocellular Carcinoma

Abnormalities in {alpha}-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies

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