SCRAPPER, an F-box protein coded by FBXL20, is a subunit of SCF type E3 ubiquitin ligase. SCRAPPER localizes synapses and directly binds to Rab3-interacting molecule 1 (RIM1), an essential factor for synaptic vesicle release, thus it regulates neural transmission via RIM1 degradation. A defect in SCRAPPER leads to neurotransmission abnormalities, which could subsequently result in neurodegenerative phenotypes. Because it is likely that the alteration of neural transmission in Scrapper mutant mice affect their systemic condition, we have analyzed the behavioral phenotypes of mice with decreased or increased the amount of SCRAPPER. We carried out a series of behavioral test batteries for Scrapper mutant mice. Scrapper transgenic mice overexpr...
The genetic and molecular basis underlying fear memory formation is a key theme in anxiety disorder ...
<div><p>Extinction is an integral part of normal healthy fear responses, while it is compromised in ...
Fragile X syndrome is the most common inherited form of mental retardation. It is a neurodevelopmen...
SCRAPPER, an F-box protein coded by FBXL20, is a subunit of SCF type E3 ubiquitin ligase. SCRAPPER l...
SCRAPPER, which is an F-box protein encoded by FBXL20, regulates the frequency of the miniature exci...
SummaryLittle is known about how synaptic activity is modulated in the central nervous system. We ha...
The presynaptic scaffold molecule RIM1α is important for regulating neurotransmitter release. In thi...
Neurodegenerative disorders are growing burdens in modern societies because of increased life expect...
Recent advances in techniques for manipulating genomes have allowed the generation of transgenic ani...
Neurodevelopmental and neuropsychiatric disorders are a significant and expanding global health cris...
Background Cellular prion protein (PrP(C)) is a cell surface GPI-anchored protein, usually known for...
Neurodegenerative disorders are growing burdens in modern societies because of increased life expect...
Synapse-specific local protein synthesis is thought to be important for neurodevelopment and plastic...
Fragile X syndrome (FXS), the most common form of hereditary mental retardation, is caused by a loss...
Background: Copy number variation (CNV) at the 15q11.2 region, which includes a gene that codes for ...
The genetic and molecular basis underlying fear memory formation is a key theme in anxiety disorder ...
<div><p>Extinction is an integral part of normal healthy fear responses, while it is compromised in ...
Fragile X syndrome is the most common inherited form of mental retardation. It is a neurodevelopmen...
SCRAPPER, an F-box protein coded by FBXL20, is a subunit of SCF type E3 ubiquitin ligase. SCRAPPER l...
SCRAPPER, which is an F-box protein encoded by FBXL20, regulates the frequency of the miniature exci...
SummaryLittle is known about how synaptic activity is modulated in the central nervous system. We ha...
The presynaptic scaffold molecule RIM1α is important for regulating neurotransmitter release. In thi...
Neurodegenerative disorders are growing burdens in modern societies because of increased life expect...
Recent advances in techniques for manipulating genomes have allowed the generation of transgenic ani...
Neurodevelopmental and neuropsychiatric disorders are a significant and expanding global health cris...
Background Cellular prion protein (PrP(C)) is a cell surface GPI-anchored protein, usually known for...
Neurodegenerative disorders are growing burdens in modern societies because of increased life expect...
Synapse-specific local protein synthesis is thought to be important for neurodevelopment and plastic...
Fragile X syndrome (FXS), the most common form of hereditary mental retardation, is caused by a loss...
Background: Copy number variation (CNV) at the 15q11.2 region, which includes a gene that codes for ...
The genetic and molecular basis underlying fear memory formation is a key theme in anxiety disorder ...
<div><p>Extinction is an integral part of normal healthy fear responses, while it is compromised in ...
Fragile X syndrome is the most common inherited form of mental retardation. It is a neurodevelopmen...