Loss of Drosophila melanogaster p21-activated kinase 3 Suppresses Defects in Synapse Structure and Function Caused by spastin Mutations (Q35221529)

7 August 2017

title

Loss of Drosophila melanogaster p21-activated kinase 3 suppresses defects in synapse structure and function caused by spastin mutations (English)

1 reference

7 August 2017

Loss of Drosophila melanogaster p21-activated kinase 3 Suppresses Defects in Synapse Structure and Function Caused by spastin Mutations (English)

1 reference

10.1534/GENETICS.111.130831

Crossref

DOI

https://api.crossref.org/works/10.1534/GENETICS.111.130831

5 December 2024

main subject

Drosophila melanogaster

0 references

author name string

Sophia Gayle

2

1 reference

7 August 2017

Hong Bao

3

1 reference

7 August 2017

Bing Zhang

4

1 reference

7 August 2017

Emily F. Ozdowski

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21705760

5 December 2024

Nina T. Sherwood

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21705760

5 December 2024

language of work or name

English

0 references

publication date

29 July 2011

1 reference

7 August 2017

number of pages

13

1 reference

full work available at URL

inferred from page(s)

http://www.genetics.org/content/189/1/123.full.pdf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21705760

https://europepmc.org/articles/PMC3176117

5 December 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21705760

https://europepmc.org/articles/PMC3176117?pdf=render

5 December 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21705760

https://doi.org/10.1534/genetics.111.130831

5 December 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21705760

https://academic.oup.com/genetics/article-pdf/189/1/123/46857631/genetics0123.pdf

5 December 2024

1 reference

10.1534/GENETICS.111.130831

https://api.crossref.org/works/10.1534/GENETICS.111.130831

5 December 2024

1 reference

7 August 2017

volume

189

1 reference

7 August 2017

issue

1

1 reference

7 August 2017

page(s)

123-135

1 reference

describes a project that uses

7 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3176117/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene

26 September 2018

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12 December 2020

Clinical features of hereditary spastic paraplegia due to spastin mutation

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12 December 2020

Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon

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12 December 2020

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12 December 2020

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12 December 2020

10.1534/GENETICS.111.130831

Identifiers

DOI

1 reference

7 August 2017

1 reference

7 August 2017

1 reference