Literature DB >> 28684951

The Role of PRRT2 in Synaptic Transmission May Not Be So Benign.

Matthew C Weston.   

Abstract

Entities:  

Year:  2017        PMID: 28684951      PMCID: PMC5486426          DOI: 10.5698/1535-7511.17.3.165

Source DB:  PubMed          Journal:  Epilepsy Curr        ISSN: 1535-7511            Impact factor:   7.500


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  7 in total

1.  Quantal components of the end-plate potential.

Authors:  J DEL CASTILLO; B KATZ
Journal:  J Physiol       Date:  1954-06-28       Impact factor: 5.182

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

Authors:  Sarah E Heron; Bronwyn E Grinton; Sara Kivity; Zaid Afawi; Sameer M Zuberi; James N Hughes; Clair Pridmore; Bree L Hodgson; Xenia Iona; Lynette G Sadleir; James Pelekanos; Eric Herlenius; Hadassa Goldberg-Stern; Haim Bassan; Eric Haan; Amos D Korczyn; Alison E Gardner; Mark A Corbett; Jozef Gécz; Paul Q Thomas; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

Review 3.  The evolving spectrum of PRRT2-associated paroxysmal diseases.

Authors:  Darius Ebrahimi-Fakhari; Afshin Saffari; Ana Westenberger; Christine Klein
Journal:  Brain       Date:  2015-11-23       Impact factor: 13.501

4.  Differential abilities of SNAP-25 homologs to support neuronal function.

Authors:  Ignacio Delgado-Martínez; Ralf B Nehring; Jakob B Sørensen
Journal:  J Neurosci       Date:  2007-08-29       Impact factor: 6.167

5.  PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery.

Authors:  Pierluigi Valente; Enrico Castroflorio; Pia Rossi; Manuela Fadda; Bruno Sterlini; Romina Ines Cervigni; Cosimo Prestigio; Silvia Giovedì; Franco Onofri; Elisa Mura; Fabrizia C Guarnieri; Antonella Marte; Marta Orlando; Federico Zara; Anna Fassio; Flavia Valtorta; Pietro Baldelli; Anna Corradi; Fabio Benfenati
Journal:  Cell Rep       Date:  2016-03-24       Impact factor: 9.423

6.  The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations.

Authors:  Caterina Michetti; Enrico Castroflorio; Ivan Marchionni; Nicola Forte; Bruno Sterlini; Francesca Binda; Floriana Fruscione; Pietro Baldelli; Flavia Valtorta; Federico Zara; Anna Corradi; Fabio Benfenati
Journal:  Neurobiol Dis       Date:  2016-12-20       Impact factor: 5.996

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

Authors:  Hsien-Yang Lee; Yong Huang; Nadine Bruneau; Patrice Roll; Elisha D O Roberson; Mark Hermann; Emily Quinn; James Maas; Robert Edwards; Tetsuo Ashizawa; Betul Baykan; Kailash Bhatia; Susan Bressman; Michiko K Bruno; Ewout R Brunt; Roberto Caraballo; Bernard Echenne; Natalio Fejerman; Steve Frucht; Christina A Gurnett; Edouard Hirsch; Henry Houlden; Joseph Jankovic; Wei-Ling Lee; David R Lynch; Shehla Mohammed; Ulrich Müller; Mark P Nespeca; David Renner; Jacques Rochette; Gabrielle Rudolf; Shinji Saiki; Bing-Wen Soong; Kathryn J Swoboda; Sam Tucker; Nicholas Wood; Michael Hanna; Anne M Bowcock; Pierre Szepetowski; Ying-Hui Fu; Louis J Ptáček
Journal:  Cell Rep       Date:  2011-12-15       Impact factor: 9.423

  7 in total

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