Plastin 3 Expression Does Not Modify Spinal Muscular Atrophy Severity in the ∆7 SMA Mouse (Q35680796)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26134627 AND SRC:MED&resulttype=core&format=json

18 February 2020

title

Plastin 3 Expression Does Not Modify Spinal Muscular Atrophy Severity in the ∆7 SMA Mouse (English)

1 reference

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18 February 2020

main subject

spinal muscular atrophy

1 reference

Survival of motor neuron 1, telomeric

inferred from title

1 reference

GOA release 2020-03-11

1 reference

8

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18 February 2020

author name string

Vicki L McGovern

1

1 reference

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18 February 2020

Aurélie Massoni-Laporte

2

1 reference

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18 February 2020

Xueyong Wang

3

1 reference

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18 February 2020

Thanh T Le

4

1 reference

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18 February 2020

Hao T Le

5

1 reference

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18 February 2020

Christine E Beattie

6

1 reference

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18 February 2020

Mark M Rich

7

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18 February 2020

language of work or name

English

0 references

publication date

2 July 2015

1 reference

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18 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26134627 AND SRC:MED&resulttype=core&format=json

18 February 2020

volume

10

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18 February 2020

issue

7

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18 February 2020

page(s)

e0132364

1 reference

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Creative Commons Attribution 4.0 International

18 February 2020

copyright license

start time

2 July 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4489873/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY

25 September 2018

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25 September 2018

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Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion pattern

25 September 2018

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Crossref

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0132364

The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

21 January 2018

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12 December 2020

Therapeutic benefits of cardiotrophin-1 gene transfer in a mouse model of spinal muscular atrophy

1 reference

12 December 2020

SMN oligomerization defect correlates with spinal muscular atrophy severity

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

A rare SMN2 variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy

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12 December 2020

Deletion and conversion in spinal muscular atrophy patients: is there a relationship to severity?

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12 December 2020

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

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12 December 2020

Linkage mapping of the spinal muscular atrophy gene

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12 December 2020

[Study of the clinical aspects of infantile spinal progressive muscular atrophy of the Werdnig-Hoffman type.]

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12 December 2020

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals

1 reference

12 December 2020

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0132364

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26134627 AND SRC:MED&resulttype=core&format=json

18 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26134627 AND SRC:MED&resulttype=core&format=json

18 February 2020

PubMed publication ID

26134627

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26134627 AND SRC:MED&resulttype=core&format=json