SALK 2013

Recent articles

Network of protein variants suggests new autism genes

Researchers have created a network of various forms of many proteins linked to autism, revealing new molecular interactions that may play a role in the disorder. The unpublished work was presented in a poster last week at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California.

By Sarah DeWeerdt
25 January 2013 | 3 min read

Fragile X mice show brain-wave abnormalities during sleep

Neurons in mice that model fragile X syndrome show immature, overexcitable firing patterns, particularly during sleep, according to unpublished research presented last week at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California.

By Sarah DeWeerdt
25 January 2013 | 3 min read

Eye movement, motor difficulties linked in autism

Problems with eye movements in people with autism are part of their motor difficulties and may contribute to the social deficits characteristic of the disorder, according to unpublished research presented last week at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California.

By Sarah DeWeerdt
24 January 2013 | 3 min read

Autism-linked protein differs in male and female brains

The autism-linked protein MET is expressed at lower levels in the brains of men with autism than in control brains, according to unpublished research presented Thursday at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California. Women with autism do not differ from healthy controls, however.

By Sarah DeWeerdt
24 January 2013 | 4 min read

Alzheimer’s drug aids autism mouse model

Memantine, a drug used to treat Alzheimer’s disease, can reverse autism-like features in mice lacking one copy of the MEF2C gene, according to a poster presented last week at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California.

By Sarah DeWeerdt
23 January 2013 | 2 min read

Childhood-onset schizophrenia, autism share genetic links

Individuals who have childhood-onset schizophrenia carry more DNA deletions and duplications associated with other disorders, such as autism, than their unaffected siblings do. The unpublished research was presented 16 January at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California.

By Sarah DeWeerdt
23 January 2013 | 4 min read

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