Bifunctional antisense oligonucleotides provide a trans-acting splicing enhancer that stimulates SMN2 gene expression in patient fibroblasts (Q34921907)

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scholarly article

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English	Bifunctional antisense oligonucleotides provide a trans-acting splicing enhancer that stimulates SMN2 gene expression in patient fibroblasts	scholarly article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Bifunctional antisense oligonucleotides provide a trans-acting splicing enhancer that stimulates SMN2 gene expression in patient fibroblasts (English)

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Europe PubMed Central

PubMed publication ID

5 August 2017

1 reference

based on heuristic

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object named as

Ian C Eperon

4

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author name string

Leigh A Skordis

1

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Matthew G Dunckley

2

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Baigong Yue

3

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Europe PubMed Central

PubMed publication ID

5 August 2017

Francesco Muntoni

5

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Europe PubMed Central

PubMed publication ID

5 August 2017

language of work or name

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publication date

17 March 2003

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Europe PubMed Central

PubMed publication ID

5 August 2017

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

PubMed publication ID

5 August 2017

100

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Europe PubMed Central

PubMed publication ID

5 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

4114-4119

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

describes a project that uses

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC153057/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Modification of alternative splicing by antisense oligonucleotides as a potential chemotherapy for cancer and other diseases

1 reference

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8 July 2018

Predictive identification of exonic splicing enhancers in human genes

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Listening to silence and understanding nonsense: exonic mutations that affect splicing

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

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Exon Identity Established through Differential Antagonism between Exonic Splicing Silencer-Bound hnRNP A1 and Enhancer-Bound SR Proteins

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Aclarubicin treatment restores SMN levels to cells derived from type I spinal muscular atrophy patients

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Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases

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A mouse model for spinal muscular atrophy

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Antisense oligonucleotides as therapeutic agents

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A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.

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A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

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hnRNP A1 recruited to an exon in vivo can function as an exon splicing silencer

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Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number.

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Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins

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Ribonucleoprotein assembly: clues from spinal muscular atrophy

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Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous system

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Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

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The survival motor neuron protein in spinal muscular atrophy

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Directing alternative splicing: cast and scenarios

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A novel nuclear structure containing the survival of motor neurons protein

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The Relationship between SMN, the Spinal Muscular Atrophy Protein, and Nuclear Coiled Bodies in Differentiated Tissues and Cultured Cells

1 reference

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Activation of c-src neuron-specific splicing by an unusual RNA element in vivo and in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/12642665

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based on heuristic

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hnRNP A1 selectively interacts through its Gly-rich domain with different RNA-binding proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/12642665

12 December 2020

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inferred from PubMed ID database lookup

Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/12642665

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based on heuristic

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Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III

1 reference

https://pubmed.ncbi.nlm.nih.gov/12642665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0633863100

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

2003PNAS..100.4114S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

ResearchGate publication ID

0 references

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