Mef2d is essential for the maturation and integrity of retinal photoreceptor and bipolar cells. (Q50596815)

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2 March 2020

title

Mef2d is essential for the maturation and integrity of retinal photoreceptor and bipolar cells (English)

1 reference

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2 March 2020

main subject

photoreceptor protein

0 references

1 reference

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2 March 2020

Yoshihiro Omori

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2 March 2020

Tamiki Kitamura

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2 March 2020

Satoyo Yoshida

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2 March 2020

Taro Chaya

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2 March 2020

Shoichi Irie

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2 March 2020

Takahisa Furukawa

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2 March 2020

publication date

11 March 2015

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2 March 2020

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2 March 2020

volume

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2 March 2020

issue

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2 March 2020

page(s)

408-426

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The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10

2 March 2020

cites work

1 reference

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

21 January 2018

1 reference

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

21 January 2018

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MEF2C transcription factor controls chondrocyte hypertrophy and bone development

21 January 2018

1 reference

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness

21 January 2018

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Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins

21 January 2018

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Synaptogenesis in the photoreceptor terminal of the mouse retina

21 January 2018

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Cell fate determination in the vertebrate retina

21 January 2018

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A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome.

21 January 2018

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A typology of photoreceptor gene expression patterns in the mouse

21 January 2018

1 reference

p300/cAMP-response-element-binding-protein ('CREB')-binding protein (CBP) modulates co-operation between myocyte enhancer factor 2A (MEF2A) and thyroid hormone receptor-retinoid X receptor

21 January 2018

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Fibroblast growth factor receptor 3 is a negative regulator of bone growth

21 January 2018

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Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1.

21 January 2018

1 reference

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

21 January 2018

1 reference

Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

21 January 2018

1 reference

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

21 January 2018

1 reference

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness

21 January 2018

1 reference

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

21 January 2018

1 reference

Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysis

21 January 2018

1 reference

The transcription factor neural retina leucine zipper (NRL) controls photoreceptor-specific expression of myocyte enhancer factor Mef2c from an alternative promoter

21 January 2018

1 reference

21 January 2018

1 reference

The cis-regulatory logic of the mammalian photoreceptor transcriptional network

21 January 2018

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21 January 2018

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A calcium channel mutation causing hypokalemic periodic paralysis

21 January 2018

1 reference

Blimp1 suppresses Chx10 expression in differentiating retinal photoreceptor precursors to ensure proper photoreceptor development

21 January 2018

1 reference

Activation of the myogenic lineage by MEF2A, a factor that induces and cooperates with MyoD.

21 January 2018

1 reference

The MEF2D transcription factor mediates stress-dependent cardiac remodeling in mice

21 January 2018

1 reference

A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia

21 January 2018

1 reference

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade

21 January 2018

1 reference

Kinetics of rod outer segment renewal in the developing mouse retina

21 January 2018

1 reference

Myocyte-specific enhancer factor 2 and thyroid hormone receptor associate and synergistically activate the alpha-cardiac myosin heavy-chain gene

21 January 2018

1 reference

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans

21 January 2018

1 reference

Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C

21 January 2018

1 reference

A Mef2 gene that generates a muscle-specific isoform via alternative mRNA splicing

21 January 2018

1 reference

Nrl is required for rod photoreceptor development

21 January 2018

1 reference

The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation

21 January 2018

1 reference

Cooperative activation of muscle gene expression by MEF2 and myogenic bHLH proteins

21 January 2018

1 reference

GATA-dependent recruitment of MEF2 proteins to target promoters

21 January 2018

1 reference

Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice

21 January 2018

1 reference

Gene expression analysis of embryonic photoreceptor precursor cells using BAC-Crx-EGFP transgenic mouse

21 January 2018

1 reference

An essential role for RAX homeoprotein and NOTCH-HES signaling in Otx2 expression in embryonic retinal photoreceptor cell fate determination

21 January 2018

1 reference

Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factor

21 January 2018

1 reference

A thyroid hormone receptor that is required for the development of green cone photoreceptors

21 January 2018

1 reference

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development

21 January 2018

1 reference

Analysis of Transcriptional Regulatory Pathways of Photoreceptor Genes by Expression Profiling of the Otx2-Deficient Retina

21 January 2018

1 reference

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1

21 January 2018

1 reference

The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes

21 January 2018

1 reference

Deciphering the contribution of known cis-elements in the mouse cone arrestin gene to its cone-specific expression

21 January 2018

1 reference

MEF2: a central regulator of diverse developmental programs

21 January 2018

1 reference

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

21 January 2018

1 reference

High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP

21 January 2018

1 reference

A Transgenic Mouse Line That Retains Cre Recombinase Activity in Mature Oocytes Irrespective of thecreTransgene Transmission

21 January 2018

1 reference

miR-124a is required for hippocampal axogenesis and retinal cone survival through Lhx2 suppression

21 January 2018

1 reference

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation

21 January 2018

1 reference

Tissue-specific splicing of a ubiquitously expressed transcription factor is essential for muscle differentiation

21 January 2018

1 reference

The MADS-box family of transcription factors

21 January 2018

1 reference

Rbfox2-coordinated alternative splicing of Mef2d and Rock2 controls myoblast fusion during myogenesis

21 January 2018

1 reference

GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy

21 January 2018

1 reference

Structure and function of ribbon synapses

21 January 2018

1 reference

The cell biology of vision

21 January 2018

1 reference

Localization of Cacna1s to ON bipolar dendritic tips requires mGluR6-related cascade elements

21 January 2018

1 reference

Basolateral Mg2+ extrusion via CNNM4 mediates transcellular Mg2+ transport across epithelia: a mouse model

21 January 2018

1 reference

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

21 January 2018

1 reference

Mouse cone arrestin gene characterization: promoter targets expression to cone photoreceptors

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/GTC.12233

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25757744%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference

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