(Q28587035)

English

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

scientific journal article

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scholarly article

2 references

31 January 2017

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients (English)

2 references

31 January 2017

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

0 references

1 reference

GOA release 2020-03-11

hereditary spastic paraplegia

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Ellen J Bennett

5

1 reference

Europe PubMed Central

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28 January 2020

Christopher C. Miller

10

1 reference

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28 January 2020

11

1 reference

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28 January 2020

Andrew Grierson

12

1 reference

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28 January 2020

author name string

Catherine Manser

4

2 references

31 January 2017

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Megan Bingley

6

2 references

31 January 2017

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Roy Milner

8

2 references

31 January 2017

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Stephen B Wharton

3

1 reference

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28 January 2020

Jonathan D Wood

7

1 reference

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28 January 2020

Christopher J McDermott

9

1 reference

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28 January 2020

language of work or name

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publication date

22 April 2009

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28 January 2020

Journal of Neurochemistry

2 references

31 January 2017

Europe PubMed Central

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28 January 2020

110

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31 January 2017

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28 January 2020

1

2 references

31 January 2017

Europe PubMed Central

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28 January 2020

34-44

1 reference

Europe PubMed Central

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28 January 2020

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2009.06104.X

21 January 2018

Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2009.06104.X

21 January 2018

Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2009.06104.X

21 January 2018

Identifiers

10.1111/J.1471-4159.2009.06104.X

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19453301%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

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