hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome (Q37089623)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806275%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806275%20AND%20SRC:MED&resulttype=core&format=json

congenital myasthenic syndrome

14 January 2020

main subject

congenital disorder

0 references

1 reference

6

1 reference

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14 January 2020

author name string

Akio Masuda

1

1 reference

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14 January 2020

Xin-Ming Shen

2

1 reference

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14 January 2020

Mikako Ito

3

1 reference

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14 January 2020

Tohru Matsuura

4

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14 January 2020

Andrew G Engel

5

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14 January 2020

publication date

20 September 2008

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14 January 2020

published in

Human Molecular Genetics

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14 January 2020

volume

17

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14 January 2020

issue

24

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14 January 2020

page(s)

4022-4035

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Human branch point consensus sequence is yUnAy

14 January 2020

cites work

1 reference

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In vitro and in silico analysis reveals an efficient algorithm to predict the splicing consequences of mutations at the 5' splice sites

29 September 2017

1 reference

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Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs)

29 September 2017

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Seemingly neutral polymorphic variants may confer immunity to splicing-inactivating mutations: a synonymous SNP in exon 5 of MCAD protects from deleterious mutations in a flanking exonic splicing enhancer

29 September 2017

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SRp54 (SFRS11), a regulator for tau exon 10 alternative splicing identified by an expression cloning strategy

29 September 2017

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29 September 2017

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SC35 and heterogeneous nuclear ribonucleoprotein A/B proteins bind to a juxtaposed exonic splicing enhancer/exonic splicing silencer element to regulate HIV-1 tat exon 2 splicing

29 September 2017

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Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays

29 September 2017

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Sleuthing molecular targets for neurological diseases at the neuromuscular junction

29 September 2017

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Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating.

29 September 2017

1 reference

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Congenital myasthenic syndrome caused by low-expressor fast-channel AChR delta subunit mutation

29 September 2017

1 reference

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BRCA2 T2722R is a deleterious allele that causes exon skipping

29 September 2017

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Alternative splicing: multiple control mechanisms and involvement in human disease

29 September 2017

1 reference

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Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1.

29 September 2017

1 reference

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Both ran and importins have the ability to function as nuclear mRNA export factors

29 September 2017

1 reference

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A new type of mutation causes a splicing defect in ATM.

29 September 2017

1 reference

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SR proteins and hnRNP H regulate the splicing of the HIV-1 tev-specific exon 6D.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Modulation of survival motor neuron pre-mRNA splicing by inhibition of alternative 3' splice site pairing

29 September 2017

1 reference

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Determination of the RNA binding specificity of the heterogeneous nuclear ribonucleoprotein (hnRNP) H/H'/F/2H9 family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

A second exon splicing silencer within human immunodeficiency virus type 1 tat exon 2 represses splicing of Tat mRNA and binds protein hnRNP H.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations

29 September 2017

1 reference

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Alternative pre-mRNA splicing: the logic of combinatorial control

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Conversion of diploidy to haploidy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Characterization of the 415G>A (E139K) PMM2 mutation in carbohydrate-deficient glycoprotein syndrome type Ia disrupting a splicing enhancer resulting in exon 5 skipping

29 September 2017

1 reference

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Mutation causing congenital myasthenia reveals acetylcholine receptor beta/delta subunit interaction essential for assembly

29 September 2017

1 reference

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Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism

29 September 2017

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Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

29 September 2017

1 reference

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Binding of hnRNP H to an exonic splicing silencer is involved in the regulation of alternative splicing of the rat beta-tropomyosin gene

29 September 2017

1 reference

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hnRNP H is a component of a splicing enhancer complex that activates a c-src alternative exon in neuronal cells

29 September 2017

1 reference

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Identification of a neuregulin and protein-tyrosine phosphatase response element in the nicotinic acetylcholine receptor epsilon subunit gene: regulatory role of an Rts transcription factor

29 September 2017

1 reference

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Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Precise branch point mapping and quantification of splicing intermediates

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Acetylcholine receptor alpha-subunit isoforms are differentially expressed in thymuses from myasthenic patients.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

End-plate acetylcholine receptor deficiency due to nonsense mutations in the epsilon subunit

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Functional and non-functional isoforms of the human muscle acetylcholine receptor.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Human nicotinic acetylcholine receptor alpha-subunit isoforms: origins and expression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Congenital myasthenic syndromes: II. Syndrome attributed to abnormal interaction of acetylcholine with its receptor

29 September 2017

1 reference

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In vivo and in vitro analysis of electrical activity-dependent expression of muscle acetylcholine receptor genes using adenovirus

29 September 2017

1 reference

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Regulation of acetylcholine receptor alpha subunit variants in human myasthenia gravis. Quantification of steady-state levels of messenger RNA in muscle biopsy using the polymerase chain reaction.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Identification of a DNA element determining synaptic expression of the mouse acetylcholine receptor delta-subunit gene

29 September 2017

1 reference

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The human medulloblastoma cell line TE671 expresses a muscle-like acetylcholine receptor. Cloning of the alpha-subunit cDNA

29 September 2017

1 reference

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

29 September 2017

1 reference

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A muscle acetylcholine receptor is expressed in the human cerebellar medulloblastoma cell line TE671.

29 September 2017

1 reference

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The human muscle nicotinic acetylcholine receptor alpha-subunit exist as two isoforms: a novel exon

29 September 2017

1 reference

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PLP/DM20 ratio is regulated by hnRNPH and F and a novel G-rich enhancer in oligodendrocytes

29 September 2017

1 reference

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C-terminal and heparin-binding domains of collagenic tail subunit are both essential for anchoring acetylcholinesterase at the synapse

27 June 2018

1 reference

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Congenital endplate acetylcholinesterase deficiency

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Scanning from an independently specified branch point defines the 3' splice site of mammalian introns

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Functional differences among nonerythroid anion exchangers expressed in a transfected human cell line

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

A frameshifting mutation in CHRNE unmasks skipping of the preceding exon

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Identification of an element crucial for the sub-synaptic expression of the acetylcholine receptor epsilon-subunit gene.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptor.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638575

A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy

3 September 2018

1 reference

12 December 2020

Ultrastructural localization of the acetylcholine receptor in myasthenia gravis and in its experimental autoimmune model

1 reference

12 December 2020

Separate pathways for synapse-specific and electrical activity-dependent gene expression in skeletal muscle

1 reference

12 December 2020

Adenosine deaminase deficiency in adults

1 reference

12 December 2020

Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunit

1 reference

12 December 2020

Association of acetylcholine receptor alpha-subunit gene expression in mixed thymoma with myasthenia gravis

1 reference

12 December 2020

Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency

1 reference

12 December 2020

An exon splice enhancer mutation causes autosomal dominant GH deficiency

1 reference

12 December 2020

Congenital myasthenic syndrome caused by a mutation in the Ets-binding site of the promoter region of the acetylcholine receptor epsilon subunit gene

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDN305

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806275%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806275%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference