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Spectrum: Autism Research News

Tag: MECP2

June 2011

Rett protein needed for adult brain function

by  /  20 June 2011

A new study calls into question the assumption that Rett syndrome is exclusively a neurodevelopmental disorder caused by the lack of a critical protein in utero.

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May 2011

Rett protein alters visual circuits in mice

by  /  23 May 2011

MeCP2, the protein that’s missing or mutated in Rett syndrome, is crucial for remodeling neural circuits in response to vision, according to a study published in April in Neuron.

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April 2011

Maternal stress alters behavior of generations

by  /  18 April 2011

Early trauma alters both behavior and gene expression in three generations of mice, suggesting that epigenetic changes may contribute to ‘hidden heritability’ in neuropsychiatric disorders.

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December 2010

Jumping genes implicated in Rett syndrome

by  /  27 December 2010

The neurons of people with Rett syndrome contain an overabundance of retrotransposons — DNA sequences that copy and insert themselves into new spots throughout the genome — during early development, according to a study published 18 November in Nature.

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Calming neurons may ease apnea in Rett syndrome

by  /  9 December 2010

A controversial new approach that quiets the activity of certain neurons in the brain alleviates breathing difficulties in a mouse model of Rett syndrome, according to a study published 4 October in the Proceedings of the National Academy of Sciences.

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November 2010

Stem cell assay reveals early development of Rett neurons

by  /  16 November 2010

Researchers have developed the first stem cell system that makes it possible to study the early development of neurons from people with Rett syndrome, a rare disorder on the autism spectrum.

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Rett gene needed to stabilize synaptic strength

by  /  16 November 2010

Blocking the expression of the MeCP2 gene decreases the number of synapses, the junctions between neurons. It also prevents synapses from scaling up their activity to make up for the loss, according to unpublished data shown yesterday at the Society for Neuroscience annual meeting in San Diego.

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Researchers debut new mouse model for Rett syndrome

by  /  11 November 2010

A new mouse model for Rett syndrome shows that disrupting a single brain messenger can produce nearly all of the characteristic features of the syndrome, researchers report today in Nature.

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October 2010

Crossover potential?

by  /  18 October 2010

“I don’t know anything about Williams syndrome”: That isn’t exactly how you’d expect a talk at a meeting on the syndrome to begin, but it happened more than once at a symposium on the disorder last week. Could scientific interchange between Williams syndrome and autism researchers benefit people with either condition?

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September 2010

Molecular mechanisms: Autism brains show ‘angry’ microglia

by  /  27 September 2010

A study of postmortem tissue shows that microglia, cells that provide immune protection to the brain, are altered in the brains of individuals with autism.

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