A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE. (Q30090177)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26797119%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

title

A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE (English)

1 reference

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Proline-rich transmembrane protein 2

5 March 2020

main subject

transmembrane protein

0 references

1 reference

GOA release 2020-03-11

author

Bruno Sterlini

2

1 reference

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5 March 2020

Enrico Castroflorio

3

1 reference

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5 March 2020

Flavia Valtorta

6

1 reference

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5 March 2020

Luca Maragliano

7

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5 March 2020

author name string

Pia Rossi

1

1 reference

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5 March 2020

Antonella Marte

4

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5 March 2020

Franco Onofri

5

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5 March 2020

Anna Corradi

8

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5 March 2020

Fabio Benfenati

9

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5 March 2020

language of work or name

English

0 references

publication date

21 January 2016

1 reference

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Journal of Biological Chemistry

5 March 2020

published in

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5 March 2020

volume

291

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5 March 2020

issue

12

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5 March 2020

page(s)

6111-6123

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PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling

5 March 2020

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PRRT2 truncated mutations lead to nonsense-mediated mRNA decay in Paroxysmal Kinesigenic Dyskinesia

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Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy.

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PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.

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PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

20 June 2018

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PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures

20 June 2018

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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

20 June 2018

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Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

20 June 2018

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20 June 2018

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High-resolution proteomics unravel architecture and molecular diversity of native AMPA receptor complexes

20 June 2018

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The dispanins: a novel gene family of ancient origin that contains 14 human members

20 June 2018

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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

20 June 2018

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Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

20 June 2018

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Cadherin-catenin adhesion complexes at the synapse

20 June 2018

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20 June 2018

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The dual role of the extracellular matrix in synaptic plasticity and homeostasis

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1074%2FJBC.M115.683888

Numerical integration of the cartesian equations of motion of a system with constraints: molecular dynamics of n-alkanes

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1074%2FJBC.M115.683888

PRRT2 mutation causes benign familial infantile convulsions

21 January 2018

1 reference

12 December 2020

Genetics: expanding the spectrum of neurological disorders associated with PRRT2 mutations

1 reference

12 December 2020

PRRT2 mutations cause hemiplegic migraine

1 reference

12 December 2020

Paroxysmal disorders associated with PRRT2 mutations shake up expectations on ion channel genes

1 reference

12 December 2020

Identifiers

DOI

10.1074/JBC.M115.683888

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26797119%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26797119%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

PubMed publication ID

26797119

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26797119%20AND%20SRC:MED&resulttype=core&format=json