Skip to main content

Spectrum: Autism Research News

Tag: synapses

May 2012

Molecular mechanisms: Mutant mice show signs of autism

by  /  25 May 2012

Mice that are unable to produce a carbohydrate molecule that regulates cell growth show behaviors that resemble the core deficits of autism, according to a study published 27 March in the Proceedings of the National Academy of Sciences.

Comments

Rinse and repeat

by  /  22 May 2012

Researchers typically use only one ‘cohort,’ a group of about three dozen mice, for a given set of experiments. When others repeat the experiments with a different set of animals, sometimes the results hold up, and sometimes they don’t.

Comments

Genetics: Mutations at neuronal junctions linked to autism

by  /  22 May 2012

Researchers have identified four new mutations in the autism-linked gene neurexin-1 in individuals who have autism and severe intellectual disability, they reported 3 April in Neurobiology of Disease.

Comments

Early data suggest antibiotic helps treat fragile X syndrome

by  /  19 May 2012

Preliminary results from a placebo-controlled trial of the antibiotic minocycline in children with fragile X syndrome suggest the drug alleviates some aspects of the disorder, according to research presented Friday at the International Meeting for Autism Research in Toronto.

Comments

Molecular mechanisms: SHANK2, SHANK3 mouse brains differ

by  /  16 May 2012

Mice lacking the autism-associated gene SHANK2 show autism-like behaviors similar to those seen in mice lacking SHANK3, another member of the same gene family. But SHANK2 and SHANK3 mice have distinct alterations at neuronal junctions, according to a report published 29 April in Nature.

Comments

Personalizing medicine

by  /  15 May 2012

A pilot project highlights how adult stem cells could be used to test and select personalized therapies.

Comments

Genetics: SHANK1 mutations found in men with autism

by  /  11 May 2012

Researchers have identified deletions in SHANK1 — the third member of a gene family that is closely linked to autism — in five men with the disorder, they reported 4 May in the American Journal of Human Genetics. This is the first study linking SHANK1 mutations to people with autism.

Comments

Complex case

by  /  4 May 2012

Multiple levels of complexity make it challenging to develop drugs to treat autism.

Comments

Genetics: Study further implicates rare CNVs in autism

by  /  2 May 2012

Individuals with autism are more likely than controls to have small, rare duplications or deletions of stretches of DNA in genes that play a role in dampening signals in the brain, according to a study published 2 April in Molecular Autism.

Comments
April 2012

Studies highlight promise of fragile X treatment

by  /  30 April 2012

A promising approach to treating fragile X syndrome could benefit people even after the critical window of early brain development, and alleviate core symptoms of autism, according to two studies published this month.

Comments