(Q46987553)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Translated mutation in the Nurr1 gene as a cause for Parkinson's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

4

1 reference

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17 January 2020

Dennis E Bulman

8

1 reference

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17 January 2020

author name string

David A Grimes

1

1 reference

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17 January 2020

Fabin Han

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Michel Panisset

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Fengxia Xiao

5

1 reference

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17 January 2020

Ruobing Zou

6

1 reference

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17 January 2020

Kelly Westaff

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

language of work or name

English

0 references

publication date

1 July 2006

1 reference

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17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

21

1 reference

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17 January 2020

issue

7

1 reference

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17 January 2020

page(s)

906-909

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16532445%20AND%20SRC:MED&resulttype=core&format=json

Cellular expression of the immediate early transcription factors Nurr1 and NGFI-B suggests a gene regulatory role in several brain regions including the nigrostriatal dopamine system

17 January 2020

cites work

1 reference

A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.

21 January 2018

1 reference

Assessment of Nurr1 nucleotide variations in familial Parkinson's disease.

21 January 2018

1 reference

NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.

21 January 2018

1 reference

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease

21 January 2018

1 reference

Mutations in NR4A2 associated with familial Parkinson disease

21 January 2018

1 reference

Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease

21 January 2018

1 reference

Nurr1 mutational screen in Parkinson's disease

21 January 2018

1 reference

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

Activity of the Nurr1 Carboxyl-terminal Domain Depends on Cell Type and Integrity of the Activation Function 2

21 January 2018

1 reference

Defining an N-terminal activation domain of the orphan nuclear receptor Nurr1.

21 January 2018

1 reference