| pubmed-article:16675393 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16675393 | lifeskim:mentions | umls-concept:C0037420 | lld:lifeskim |
| pubmed-article:16675393 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
| pubmed-article:16675393 | lifeskim:mentions | umls-concept:C0521390 | lld:lifeskim |
| pubmed-article:16675393 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
| pubmed-article:16675393 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:16675393 | pubmed:dateCreated | 2006-5-5 | lld:pubmed |
| pubmed-article:16675393 | pubmed:abstractText | CNS deletion of Pten in the mouse has revealed its roles in controlling cell size and number, thus providing compelling etiology for macrocephaly and Lhermitte-Duclos disease. PTEN mutations in individuals with autism spectrum disorders (ASD) have also been reported, although a causal link between PTEN and ASD remains unclear. In the present study, we deleted Pten in limited differentiated neuronal populations in the cerebral cortex and hippocampus of mice. Resulting mutant mice showed abnormal social interaction and exaggerated responses to sensory stimuli. We observed macrocephaly and neuronal hypertrophy, including hypertrophic and ectopic dendrites and axonal tracts with increased synapses. This abnormal morphology was associated with activation of the Akt/mTor/S6k pathway and inactivation of Gsk3beta. Thus, our data suggest that abnormal activation of the PI3K/AKT pathway in specific neuronal populations can underlie macrocephaly and behavioral abnormalities reminiscent of certain features of human ASD. | lld:pubmed |
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| pubmed-article:16675393 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:16675393 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:16675393 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16675393 | pubmed:month | May | lld:pubmed |
| pubmed-article:16675393 | pubmed:issn | 0896-6273 | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:ZhangWeiW | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:ZhouJingJ | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:ParadaLuis... | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:BakerSuzanne... | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:KwonChang-Hyu... | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:MathenySharon... | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:PowellCraig... | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:LuikartBryan... | lld:pubmed |
| pubmed-article:16675393 | pubmed:author | pubmed-author:LiYanjiaoY | lld:pubmed |
| pubmed-article:16675393 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16675393 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:16675393 | pubmed:volume | 50 | lld:pubmed |
| pubmed-article:16675393 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16675393 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16675393 | pubmed:pagination | 377-88 | lld:pubmed |
| pubmed-article:16675393 | pubmed:dateRevised | 2011-11-2 | lld:pubmed |
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| pubmed-article:16675393 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16675393 | pubmed:articleTitle | Pten regulates neuronal arborization and social interaction in mice. | lld:pubmed |
| pubmed-article:16675393 | pubmed:affiliation | Kent Waldrep Foundation Center for Basic Neuroscience Research on Nerve Growth and Regeneration, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA. | lld:pubmed |
| pubmed-article:16675393 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16675393 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:16675393 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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