|  Help  |  About  |  Contact Us

Publication : Ceruloplasmin gene defect associated with epilepsy in EL mice.

First Author  Garey CE Year  1994
Journal  Nat Genet Volume  6
Issue  4 Pages  426-31
PubMed ID  7914452 Mgi Jnum  J:17497
Mgi Id  MGI:65534 Doi  10.1038/ng0494-426
Citation  Garey CE, et al. (1994) Ceruloplasmin gene defect associated with epilepsy in EL mice. (Retraction Nat Genet 1995;11:104). Nat Genet 6(4):426-31
abstractText  Epilepsy is a dominant trait in EL mice, a model for human complex partial seizures. We recently mapped the major gene, El-1, to chromosome 9 near the predicted location for the ceruloplasmin (Cp) gene. We now present evidence for a partial duplication in the Cp gene in EL mice. This Cp duplication is coinherited with seizures in backcross generations and is associated with enhanced expression of Cp mRNA and increased Cp oxidase activity. Moreover, the duplication is associated with an enhanced frequency of double recombinants, simulating negative interference. The findings are relevant to the basic mechanisms of epilepsy and to theories of genetic recombination and gene mapping.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

0 Bio Entities

0 Expression