标题
A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2)
作者
关键词
-
出版物
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 291, Issue 12, Pages 6111-6123
出版商
American Society for Biochemistry & Molecular Biology (ASBMB)
发表日期
2016-01-22
DOI
10.1074/jbc.m115.683888
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling
- (2015) Ming Li et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- PRRT2 truncated mutations lead to nonsense-mediated mRNA decay in Paroxysmal Kinesigenic Dyskinesia
- (2014) Li Wu et al. PARKINSONISM & RELATED DISORDERS
- A Membrane Topology Model for Human Interferon Inducible Transmembrane Protein 1
- (2014) Stuart Weston et al. PLoS One
- PRRT2mutations and paroxysmal disorders
- (2013) A. Méneret et al. EUROPEAN JOURNAL OF NEUROLOGY
- SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth
- (2013) Anna Corradi et al. HUMAN MOLECULAR GENETICS
- Interferon-induced Transmembrane Protein 3 Is a Type II Transmembrane Protein
- (2013) Charles C. Bailey et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Role ofPRRT2in common paroxysmal neurological disorders: a gene with remarkable pleiotropy
- (2013) Sarah E Heron et al. JOURNAL OF MEDICAL GENETICS
- PRRT2-related disorders: further PKD and ICCA cases and review of the literature
- (2013) Felicitas Becker et al. JOURNAL OF NEUROLOGY
- PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
- (2012) Sarah E. Heron et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Molecular machines governing exocytosis of synaptic vesicles
- (2012) Reinhard Jahn et al. NATURE
- Expanding the spectrum of neurological disorders associated with PRRT2 mutations
- (2012) Heather Wood Nature Reviews Neurology
- PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures
- (2012) I. E. Scheffer et al. NEUROLOGY
- Paroxysmal disorders associated with PRRT2 mutations shake up expectations on ion channel genes
- (2012) R. Guerrini et al. NEUROLOGY
- PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine
- (2012) C. Marini et al. NEUROLOGY
- PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
- (2012) R. Cloarec et al. NEUROLOGY
- PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine
- (2012) A. R. Gardiner et al. NEUROLOGY
- PRRT2 mutation causes benign familial infantile convulsions
- (2012) B. de Vries et al. NEUROLOGY
- PRRT2 mutations cause hemiplegic migraine
- (2012) F. Riant et al. NEUROLOGY
- High-Resolution Proteomics Unravel Architecture and Molecular Diversity of Native AMPA Receptor Complexes
- (2012) Jochen Schwenk et al. NEURON
- The Dispanins: A Novel Gene Family of Ancient Origin That Contains 14 Human Members
- (2012) Markus Sällman Almén et al. PLoS One
- Synaptic Vesicle Endocytosis
- (2012) Y. Saheki et al. Cold Spring Harbor Perspectives in Biology
- Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
- (2012) Hsien-Yang Lee et al. Cell Reports
- Cadherin-catenin adhesion complexes at the synapse
- (2011) G Stefano Brigidi et al. CURRENT OPINION IN NEUROBIOLOGY
- Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
- (2011) Wan-Jin Chen et al. NATURE GENETICS
- The dual role of the extracellular matrix in synaptic plasticity and homeostasis
- (2010) Alexander Dityatev et al. NATURE REVIEWS NEUROSCIENCE
- CHARMM: The biomolecular simulation program
- (2009) B. R. Brooks et al. JOURNAL OF COMPUTATIONAL CHEMISTRY
- Neuroligins and neurexins link synaptic function to cognitive disease
- (2008) Thomas C. Südhof NATURE
- QMEAN: A comprehensive scoring function for model quality assessment
- (2007) Pascal Benkert et al. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now