(Q35160047)

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Rare autism-associated variants implicate syntaxin 1 (STX1 R26Q) phosphorylation and the dopamine transporter (hDAT R51W) in dopamine neurotransmission and behaviors

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Europe PubMed Central

PubMed publication ID

6 August 2017

Rare autism-associated variants implicate syntaxin 1 (STX1 R26Q) phosphorylation and the dopamine transporter (hDAT R51W) in dopamine neurotransmission and behaviors (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Aparna Shekar

4

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James S. Sutcliffe

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James S Sutcliffe

10

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Ulrik Gether

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Jeremy Veenstra-VanderWeele

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Jeremy Veenstra-Vanderweele

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Europe PubMed Central

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6 August 2017

author name string

Etienne Cartier

1

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6 August 2017

Peter J Hamilton

2

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6 August 2017

Andrea N Belovich

3

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6 August 2017

Nicholas G Campbell

5

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6 August 2017

Christine Saunders

6

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6 August 2017

Thorvald F Andreassen

7

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6 August 2017

Paula G Ulery-Reynolds

11

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6 August 2017

Kevin Erreger

12

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6 August 2017

Heinrich J G Matthies

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6 August 2017

Aurelio Galli

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6 August 2017

publication date

1 February 2015

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6 August 2017

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6 August 2017

2

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Europe PubMed Central

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6 August 2017

2

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Europe PubMed Central

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6 August 2017

135-146

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Europe PubMed Central

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6 August 2017

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4353922/fullTextXML

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1 reference

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1 reference

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SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.

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Syntaxin 1A interaction with the dopamine transporter promotes amphetamine-induced dopamine efflux

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Identifiers

10.1016/J.EBIOM.2015.01.007

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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