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EFHC1, a protein mutated in juvenile myoclonic epilepsy, associates with the mitotic spindle through its N-terminus.
A novel gene, EFHC1, mutated in juvenile myoclonic epilepsy (JME) encodes a protein with three DM10 domains of unknown function and one putative EF-hand motif. To study the properties of EFHC1, weExpand
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Human immune cells express ppMCH mRNA and functional MCHR1 receptor
Melanin‐concentrating hormone (MCH) is highly expressed in the brain and modulates feeding behavior. It is also expressed in some peripheral tissues where its role remains unknown. We haveExpand
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Neuronal localization of the 25-kDa specific thiamine triphosphatase in rodent brain
Thiamine triphosphate (ThTP) is found in small amounts in most organisms from bacteria to mammals, but little is known about its physiological role. In vertebrate tissues, ThTP may act as a phosphateExpand
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Regulation of nestin expression by thrombin and cell density in cultures of bone mesenchymal stem cells and radial glial cells
BackgroundBone marrow stromal cells and radial glia are two stem cell types with neural phenotypic plasticity. Bone marrow mesenchymal stem cells can differentiate into osteocytes, chondrocytes andExpand
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Distribution of EFHC1 or Myoclonin 1 in mouse neural structures
EFHC1, a gene mutated in juvenile myoclonic epilepsy, encodes EFHC1, a protein with three DM10 domains and one EF-hand motif. We recently demonstrated that this molecule is a microtubule-associatedExpand
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