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Spectrum: Autism Research News

Tag: mouse models

March 2012

Autism mutations lead to scores of symptoms in rodents

by  /  14 March 2012

Mutations in more than 100 autism-associated genes lead to shared neurobiological deficits in mice, including alterations in the shape of their brains and changes to the electrical properties of neurons, according to a study published 20 February in Molecular Autism.

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RAS pathway, a potentially unifying theory of autism

by  /  13 March 2012

Dysregulation of the intracellular signaling pathway RAS, a risk factor for idiopathic autism, may provide a unifying theory of the disorder. Although this is not an altogether new hypothesis, several new findings have strengthened the evidence for it considerably.

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February 2012

Cognition and behavior: Contaminant acts with autism gene

by  /  28 February 2012

A commonly used flame retardant may lead to deficits in sociability, learning and memory in healthy female mice and those that model Rett syndrome, according to a study published 15 February in Human Molecular Genetics. The effects are different in Rett syndrome models compared with healthy mice, suggesting gene-environment interactions.

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Molecular mechanisms: Study reveals new fragile X drug target

by  /  22 February 2012

Researchers have identified a new mechanism that may underlie a runaway cell signaling pathway in fragile X syndrome. The results were published 22 January in Nature Neuroscience.  

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Molecular mechanisms: Excess MeCP2 leads to anxiety in mice

by  /  14 February 2012

Two genes may be responsible for autism symptoms in mice with extra copies of the Rett syndrome gene, according to a study published 8 January in Nature Genetics.

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SHANK2 study bolsters ‘multi-hit’ gene model of autism

by  /  13 February 2012

By screening the genomes of hundreds of people with autism and analyzing the effects of newly identified mutations in cultured neurons, researchers have clarified the disorder’s link to the SHANK2 gene.

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Clinical research: Mice model Rett syndrome’s heart symptoms

by  /  10 February 2012

Mice engineered to carry a Rett syndrome mutation only in neurons are prone to an irregular heartbeat that can lead to sudden death, according to a study published 14 December in Science Translational Medicine.

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Microscope reveals nanoscale detail in live mouse brains

by  /  8 February 2012

A new microscope allows researchers to capture the movement of tiny signal-receiving branches in the brains of adult mice at the nanoscale level. The results were published 3 February in Science.

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Molecular mechanisms: Lithium treats fragile X in mice

by  /  3 February 2012

Lithium alleviates the symptoms of fragile X syndrome in mice in part by normalizing protein synthesis in the brain, according to a study published 29 December in Neurobiology of Disease.

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New machine takes rapid, reliable pictures of brains

by  /  1 February 2012

An automated instrument can reconstruct fluorescently labeled mouse brains in less than a day, researchers reported 15 January in Nature Methods.

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