Oligonucleotide-mediated survival of motor neuron protein expression in CNS improves phenotype in a mouse model of spinal muscular atrophy. (Q48565771)

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31 January 2020

title

Oligonucleotide-mediated survival of motor neuron protein expression in CNS improves phenotype in a mouse model of spinal muscular atrophy (English)

1 reference

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31 January 2020

main subject

spinal muscular atrophy

1 reference

1 reference

Jason H Williams

1

1 reference

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31 January 2020

Rebecca C Schray

2

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31 January 2020

Carlyn A Patterson

3

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31 January 2020

Semira O Ayitey

4

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31 January 2020

Melanie K Tallent

5

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31 January 2020

Gordon J Lutz

6

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31 January 2020

language of work or name

English

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publication date

1 June 2009

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31 January 2020

published in

Journal of Neuroscience

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31 January 2020

volume

29

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31 January 2020

issue

24

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31 January 2020

page(s)

7633-7638

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The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy

31 January 2020

cites work

1 reference

12 December 2020

Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1

1 reference

12 December 2020

Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy

1 reference

12 December 2020

SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN

1 reference

12 December 2020

Splicing of a critical exon of human Survival Motor Neuron is regulated by a unique silencer element located in the last intron

1 reference

12 December 2020

Antisense oligonucleotide therapy for neurodegenerative disease.

1 reference

12 December 2020

Spinal muscular atrophy: from gene to therapy

1 reference

12 December 2020

Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy

1 reference

12 December 2020

Enhancement of SMN2 exon 7 inclusion by antisense oligonucleotides targeting the exon

1 reference

12 December 2020

Antisense masking of an hnRNP A1/A2 intronic splicing silencer corrects SMN2 splicing in transgenic mice

1 reference

12 December 2020

Sustained improvement of spinal muscular atrophy mice treated with trichostatin A plus nutrition

1 reference

12 December 2020

Spinal muscular atrophy: advances in research and consensus on care of patients

1 reference

12 December 2020

Delivery of bifunctional RNAs that target an intronic repressor and increase SMN levels in an animal model of spinal muscular atrophy

1 reference

12 December 2020

A negatively acting bifunctional RNA increases survival motor neuron both in vitro and in vivo

1 reference

12 December 2020

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

12 December 2020

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

1 reference

12 December 2020

SMN oligomerization defect correlates with spinal muscular atrophy severity

1 reference

12 December 2020

10.1523/JNEUROSCI.0950-09.2009

Identifiers

DOI

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31 January 2020

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31 January 2020

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