One of the putative causative genes for juvenile myoclonic epilepsy (JME) is EFHC1. We report here the expression profile and distribution of Efhc1 messenger RNA (mRNA) during mouse and rat brain development. Real-time polymerase chain reaction revealed that there is no difference in the expression of Efhc1 mRNA between right and left hemispheres in both species. In addition, the highest levels of Efhc1 mRNA were found at intra-uterine stages in mouse and in adulthood in rat. In common, there was a progressive decrease in Efhc1 expression from 1-day-old neonates to 14-day-old animals in both species. In situ hybridization studies showed that rat and mouse Efhc1 mRNAs are expressed in ependymal cells of ventricle walls. Our findings suggest ...
Neurons throughout the mammalian brain possess non-motile cilia, organelles with varied functions in...
Audiogenic epilepsy (AE), developing in rodent strains in response to sound, is widely used as the m...
Differential mRNA display was carried out to find genes that are differentially regulated in the bra...
One of the putative causative genes for juvenile myoclonic epilepsy (JME) is EFHC1. We report here t...
One of the putative causative genes for juvenile myoclonic epilepsy (JME) is EFHC1. We report here t...
EFHC1 gene mutations have been described in patients with juvenile myoclonic epilepsy (JME) and othe...
peer reviewedMutations in the EFHC1 gene are linked to juvenile myoclonic epilepsy (JME), one of the...
g.oxfordjournals.org/ D ow nloaded from 2 Heterozygous mutations in Myoclonin1/EFHC1 cause juvenile ...
A novel gene, EFHC1, mutated in juvenile myoclonic epilepsy (JME) encodes a protein with three DM10 ...
AbstractThe gene product of EFHC1 recently implicated in juvenile myoclonic epilepsy (JME) was found...
The molecular basis of epileptogenesis is poorly characterized. Studies in humans and animal models ...
Rationale: Juvenile myoclonic epilepsies (JME) are one of the most common forms of genetic generaliz...
<p><i>A, B.</i> Representative coronal section of the brain from wild type (<i>A</i>) and <i>EfnB1</...
to the ribosome. We recently reported that a R132H mutation in the catalytic subunit of this GEF, c...
EFHC1 encodes a ciliary protein that has been linked to Juvenile Myoclonic Epilepsy. In ectodermal e...
Neurons throughout the mammalian brain possess non-motile cilia, organelles with varied functions in...
Audiogenic epilepsy (AE), developing in rodent strains in response to sound, is widely used as the m...
Differential mRNA display was carried out to find genes that are differentially regulated in the bra...
One of the putative causative genes for juvenile myoclonic epilepsy (JME) is EFHC1. We report here t...
One of the putative causative genes for juvenile myoclonic epilepsy (JME) is EFHC1. We report here t...
EFHC1 gene mutations have been described in patients with juvenile myoclonic epilepsy (JME) and othe...
peer reviewedMutations in the EFHC1 gene are linked to juvenile myoclonic epilepsy (JME), one of the...
g.oxfordjournals.org/ D ow nloaded from 2 Heterozygous mutations in Myoclonin1/EFHC1 cause juvenile ...
A novel gene, EFHC1, mutated in juvenile myoclonic epilepsy (JME) encodes a protein with three DM10 ...
AbstractThe gene product of EFHC1 recently implicated in juvenile myoclonic epilepsy (JME) was found...
The molecular basis of epileptogenesis is poorly characterized. Studies in humans and animal models ...
Rationale: Juvenile myoclonic epilepsies (JME) are one of the most common forms of genetic generaliz...
<p><i>A, B.</i> Representative coronal section of the brain from wild type (<i>A</i>) and <i>EfnB1</...
to the ribosome. We recently reported that a R132H mutation in the catalytic subunit of this GEF, c...
EFHC1 encodes a ciliary protein that has been linked to Juvenile Myoclonic Epilepsy. In ectodermal e...
Neurons throughout the mammalian brain possess non-motile cilia, organelles with varied functions in...
Audiogenic epilepsy (AE), developing in rodent strains in response to sound, is widely used as the m...
Differential mRNA display was carried out to find genes that are differentially regulated in the bra...