Abstract Mutation of the protein spartin is a cause of one form of spastic paraplegia. Spartin interacts with ubiquitin ligases of the Nedd4 family, and a recent report in BMC Biology now shows that it acts as an adaptor to recruit and activate the ubiquitin ligase AIP4 onto lipid droplets, leading to the ubiquitination and degradation of droplet-associated proteins. A deficiency of spartin apparently causes lipid droplets to accumulate. See research article: http://www.biomedcentral.com/1741-7007/8/72
Lipid droplets are the intracellular sites for neutral lipid storage. They are critical for lipid me...
Abstract Background Spastin significantly influences microtubule regulation in neurons and is implic...
Deleterious mutations in the serine lipase DDHD2 are a causative basis of complex hereditary spastic...
Abstract Mutation of the protein spartin is a cause of one form of spastic paraplegia....
Abstract Background Spartin protein is involved in degradation of epidermal growth factor receptor a...
SummaryHere, we used mRNA display to search for proteins that bind to FK506, a potent immunosuppress...
Lipid droplets (LD) are affected in multiple human disorders. These highly dynamic organelles are in...
The HSPs (hereditary spastic paraplegias) are genetic conditions in which there is distal degenerati...
<div><p>Mutations in <i>SPAST</i>, encoding spastin, are the most common cause of autosomal dominant...
Mutations in SPAST, encoding spastin, are the most common cause of autosomal dominant hereditary spa...
This thesis has focused on the protein spartin, which is mutated in a form of autosomal recessive he...
Troyer syndrome is a hereditary spastic paraplegia caused by a mutation that leads to a complete los...
Mutations in the SPG4 gene (Spastin), SPG31 gene (REEP1) and SPG3A gene (Atlastin) are the most comm...
Hereditary spastic paraplegias (HSPs, SPG1-46) are inherited neurological disorders characterized by...
Mutations of various genes cause hereditary spastic paraplegia (HSP), a neurological disease involvi...
Lipid droplets are the intracellular sites for neutral lipid storage. They are critical for lipid me...
Abstract Background Spastin significantly influences microtubule regulation in neurons and is implic...
Deleterious mutations in the serine lipase DDHD2 are a causative basis of complex hereditary spastic...
Abstract Mutation of the protein spartin is a cause of one form of spastic paraplegia....
Abstract Background Spartin protein is involved in degradation of epidermal growth factor receptor a...
SummaryHere, we used mRNA display to search for proteins that bind to FK506, a potent immunosuppress...
Lipid droplets (LD) are affected in multiple human disorders. These highly dynamic organelles are in...
The HSPs (hereditary spastic paraplegias) are genetic conditions in which there is distal degenerati...
<div><p>Mutations in <i>SPAST</i>, encoding spastin, are the most common cause of autosomal dominant...
Mutations in SPAST, encoding spastin, are the most common cause of autosomal dominant hereditary spa...
This thesis has focused on the protein spartin, which is mutated in a form of autosomal recessive he...
Troyer syndrome is a hereditary spastic paraplegia caused by a mutation that leads to a complete los...
Mutations in the SPG4 gene (Spastin), SPG31 gene (REEP1) and SPG3A gene (Atlastin) are the most comm...
Hereditary spastic paraplegias (HSPs, SPG1-46) are inherited neurological disorders characterized by...
Mutations of various genes cause hereditary spastic paraplegia (HSP), a neurological disease involvi...
Lipid droplets are the intracellular sites for neutral lipid storage. They are critical for lipid me...
Abstract Background Spastin significantly influences microtubule regulation in neurons and is implic...
Deleterious mutations in the serine lipase DDHD2 are a causative basis of complex hereditary spastic...