Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus
Epilepsy has many causes and comorbidities affecting as many as 4% of people in their lifetime. Both idiopathic and symptomatic epilepsies are highly heritable, but genetic factors are difficult to characterize among humans due to complex disease etiologies. Rodent genetic studies have been critical...
Main Authors: | Russell J. Ferland, Jason Smith, Dominick Papandrea, Jessica Gracias, Leah Hains, Sridhar B. Kadiyala, Brittany O’Brien, Eun Yong Kang, Barbara S. Beyer, Bruce J. Herron |
---|---|
Format: | Article |
Language: | English |
Published: |
Oxford University Press
2017-08-01
|
Series: | G3: Genes, Genomes, Genetics |
Subjects: | |
Online Access: | http://g3journal.org/lookup/doi/10.1534/g3.117.042234 |
Similar Items
-
Segregation of seizure traits in C57 black mouse substrains using the repeated-flurothyl model.
by: Sridhar B Kadiyala, et al.
Published: (2014-01-01) -
Immune Challenges and Seizures: How Do Early Life Insults Influence Epileptogenesis?
by: Bridgette D. Semple, et al.
Published: (2020-02-01) -
Neonatal Seizure Models to Study Epileptogenesis
by: Yuka Kasahara, et al.
Published: (2018-04-01) -
Protease-activated receptor-2 regulates trypsin expression in the brain and protects against seizures and epileptogenesis
by: Rink-Jan Lohman, et al.
Published: (2008-04-01) -
Ionic and synaptic mechanisms of seizure generation and epileptogenesis
by: Oscar C. González, et al.
Published: (2019-10-01)