标题
RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
作者
关键词
-
出版物
PLoS One
Volume 8, Issue 9, Pages e73323
出版商
Public Library of Science (PLoS)
发表日期
2013-09-07
DOI
10.1371/journal.pone.0073323
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。- Rare exonic deletions of theRBFOX1gene increase risk of idiopathic generalized epilepsy
- (2013) Dennis Lal et al. EPILEPSIA
- Rare inheritedA2BP1deletion in a proband with autism and developmental hemiparesis
- (2012) L.K. Davis et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes
- (2012) Danya F. Vears et al. EPILEPSIA
- RBFOX1 regulates both splicing and transcriptional networks in human neuronal development
- (2012) Brent L. Fogel et al. HUMAN MOLECULAR GENETICS
- Epilepsy and neurodevelopmental disorders of language
- (2011) Deb K Pal CURRENT OPINION IN NEUROLOGY
- Rbfox proteins regulate alternative splicing of neuronal sodium channel SCN8A
- (2011) Janelle E. O'Brien et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
- (2011) Josephine Elia et al. NATURE GENETICS
- The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain
- (2011) Lauren T Gehman et al. NATURE GENETICS
- NeuN/Rbfox3 Nuclear and Cytoplasmic Isoforms Differentially Regulate Alternative Splicing and Nonsense-Mediated Decay of Rbfox2
- (2011) B. Kate Dredge et al. PLoS One
- Mechanisms of activation and repression by the alternative splicing factors RBFOX1/2
- (2011) S. Sun et al. RNA
- Atypical Benign Partial Epilepsy of Childhood
- (2010) J. Aicardi et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
- (2010) Anne T. Berg et al. EPILEPSIA
- Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
- (2010) Sabine Endele et al. NATURE GENETICS
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)
- (2009) Lisa J Strug et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- An inducible change in Fox-1/A2BP1 splicing modulates the alternative splicing of downstream neuronal target exons
- (2009) J.-A. Lee et al. GENES & DEVELOPMENT
- Autoregulation of Fox protein expression to produce dominant negative splicing factors
- (2009) A. Damianov et al. RNA
- KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
- (2008) B. A. Neubauer et al. NEUROLOGY
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started