Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy (Q36007472)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17823282%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

title

Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy (English)

1 reference

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6 January 2020

0 references

1 reference

Marta Barrachina

1

1 reference

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6 January 2020

Jesús Moreno

series ordinal

2

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6 January 2020

Salvador Juvés

series ordinal

3

1 reference

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6 January 2020

Dolores Moreno

series ordinal

4

1 reference

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6 January 2020

language of work or name

English

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publication date

6 September 2007

1 reference

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The American Journal of Pathology

6 January 2020

published in

1 reference

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6 January 2020

volume

171

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6 January 2020

issue

4

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6 January 2020

page(s)

1312-1323

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Comparative genomics modeling of the NRSF/REST repressor network: from single conserved sites to genome-wide repertoire

6 January 2020

cites work

1 reference

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Different early pathogenesis in myotilinopathy compared to primary desminopathy.

2 October 2017

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Reciprocal actions of REST and a microRNA promote neuronal identity

2 October 2017

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A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

2 October 2017

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MatInspector and beyond: promoter analysis based on transcription factor binding sites

2 October 2017

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Mutations in ZASP define a novel form of muscular dystrophy in humans

2 October 2017

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Genome-wide analysis of repressor element 1 silencing transcription factor/neuron-restrictive silencing factor (REST/NRSF) target genes

2 October 2017

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2 October 2017

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Mutations in myotilin cause myofibrillar myopathy

2 October 2017

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2 October 2017

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Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

2 October 2017

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Ubiquitin carboxy-terminal hydrolase L1 binds to and stabilizes monoubiquitin in neuron

2 October 2017

1 reference

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RE-1 silencing transcription factor (REST) regulates human synaptophysin gene transcription through an intronic sequence-specific DNA-binding site

2 October 2017

1 reference

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The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility

2 October 2017

1 reference

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Corepressor-dependent silencing of chromosomal regions encoding neuronal genes

2 October 2017

1 reference

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Regulation of neuronal traits by a novel transcriptional complex

2 October 2017

1 reference

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Methylation status in the promoter region of the human PGP9.5 gene in cancer and normal tissues

2 October 2017

1 reference

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Constitutive expression of the neuron-restrictive silencer factor (NRSF)/REST in differentiating neurons disrupts neuronal gene expression and causes axon pathfinding errors in vivo

2 October 2017

1 reference

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Expression and functional analysis of Uch-L3 during mouse development

2 October 2017

1 reference

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Transcriptional repression by REST: recruitment of Sin3A and histone deacetylase to neuronal genes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Biological activity and modular structure of RE-1-silencing transcription factor (REST), a repressor of neuronal genes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

A dysfunctional desmin mutation in a patient with severe generalized myopathy

2 October 2017

1 reference

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A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

2 October 2017

1 reference

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Neuronal expression of zinc finger transcription factor REST/NRSF/XBR gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

A single zinc finger motif in the silencing factor REST represses the neural-specific type II sodium channel promoter.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Identification of potential target genes for the neuron-restrictive silencer factor

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Cloning and sequence analysis of the human SNAP25 cDNA

2 October 2017

1 reference

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The neuron-restrictive silencer factor (NRSF): a coordinate repressor of multiple neuron-specific genes

2 October 2017

1 reference

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REST: a mammalian silencer protein that restricts sodium channel gene expression to neurons

2 October 2017

1 reference

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The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase

2 October 2017

1 reference

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The structure of the human gene encoding protein gene product 9.5 (PGP9.5), a neuron-specific ubiquitin C-terminal hydrolase

2 October 2017

1 reference

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The 5'-flanking region of the synapsin I gene. A G+C-rich, TATA- and CAAT-less, phylogenetically conserved sequence with cell type-specific promoter function

2 October 2017

1 reference

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Complete structure of the human gene encoding neuron-specific enolase

2 October 2017

1 reference

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The gene for human neurone specific ubiquitin C-terminal hydrolase(UCHLl, PGP9.5) maps to chromosome 4p14

2 October 2017

1 reference

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Comparative sequence analysis reveals an intricate network among REST, CREB and miRNA in mediating neuronal gene expression

2 October 2017

1 reference

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NRSF/REST is required in vivo for repression of multiple neuronal target genes during embryogenesis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

TaqMan PCR assay in the control of RNA normalization in human post-mortem brain tissue.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Myotilinopathy: refining the clinical and myopathological phenotype

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Involvement of clusterin and the aggresome in abnormal protein deposits in myofibrillar myopathies and inclusion body myositis.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutations.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Myofibrillar myopathy with abnormal foci of desmin positivity. II. Immunocytochemical analysis reveals accumulation of multiple other proteins

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Identification of evolutionary conserved regulatory sequences in the 5' untranscribed region of the neural-specific ubiquitin C-terminal hydrolase (PGP9.5) gene.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1988880

Expression of the gene for the neuronal intermediate filament protein alpha-internexin coincides with the onset of neuronal differentiation in the developing rat nervous system

23 September 2018

1 reference

12 December 2020

Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases

1 reference

12 December 2020

Myofibrillar myopathy. III. Abnormal expression of cyclin-dependent kinases and nuclear proteins

1 reference

12 December 2020

A bi-functional activator/repressor element required for transcriptional activity of the human UCH-L1 gene assembles a neuron-specific protein: single-strand DNA complex

1 reference

12 December 2020

1 reference

12 December 2020

Stimulation of the murine Uchl1 gene promoter by the B-Myb transcription factor

1 reference

12 December 2020

Expression of mutant ubiquitin (UBB+1) and p62 in myotilinopathies and desminopathies

1 reference

12 December 2020

10.2353/AJPATH.2007.070520

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17823282%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17823282%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

PubMed publication ID

17823282

1 reference