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1
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.
Proc Natl Acad Sci U S A. 2010 Apr 27;107(17):7863-8. doi: 10.1073/pnas.0906232107. Epub 2010 Apr 12.
2
Novel de novo SHANK3 mutation in autistic patients.
Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):421-4. doi: 10.1002/ajmg.b.30822.
5
Contribution of SHANK3 mutations to autism spectrum disorder.
Am J Hum Genet. 2007 Dec;81(6):1289-97. doi: 10.1086/522590. Epub 2007 Oct 16.
7
Mice with Shank3 Mutations Associated with ASD and Schizophrenia Display Both Shared and Distinct Defects.
Neuron. 2016 Jan 6;89(1):147-62. doi: 10.1016/j.neuron.2015.11.023. Epub 2015 Dec 10.
8
Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders.
Am J Med Genet A. 2018 Dec;176(12):2668-2676. doi: 10.1002/ajmg.a.40666. Epub 2018 Dec 9.
9
The PSD protein ProSAP2/Shank3 displays synapto-nuclear shuttling which is deregulated in a schizophrenia-associated mutation.
Exp Neurol. 2014 Mar;253:126-37. doi: 10.1016/j.expneurol.2013.12.015. Epub 2013 Dec 29.

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Zebrafish in neurodevelopmental disorders studies: Genetic models and pathological involvement of microglia.
Dev Med Child Neurol. 2025 Oct;67(10):1257-1265. doi: 10.1111/dmcn.16317. Epub 2025 Mar 28.
6
Inhibition of HCN1 currents by norquetiapine, an active metabolite of the atypical anti-psychotic drug quetiapine.
Front Pharmacol. 2024 Oct 7;15:1445509. doi: 10.3389/fphar.2024.1445509. eCollection 2024.
10
Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing.
Front Genet. 2024 Aug 30;15:1352480. doi: 10.3389/fgene.2024.1352480. eCollection 2024.

本文引用的文献

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Pre-morbid IQ in mental disorders: a Danish draft-board study of 7486 psychiatric patients.
Psychol Med. 2010 Apr;40(4):547-56. doi: 10.1017/S0033291709990754. Epub 2009 Aug 6.
2
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders.
Trends Neurosci. 2009 Jul;32(7):402-12. doi: 10.1016/j.tins.2009.04.003. Epub 2009 Jun 21.
3
SNAP predicts effect of mutations on protein function.
Bioinformatics. 2008 Oct 15;24(20):2397-8. doi: 10.1093/bioinformatics/btn435. Epub 2008 Aug 30.
4
Large recurrent microdeletions associated with schizophrenia.
Nature. 2008 Sep 11;455(7210):232-6. doi: 10.1038/nature07229.
5
Novel de novo SHANK3 mutation in autistic patients.
Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):421-4. doi: 10.1002/ajmg.b.30822.
6
Strong association of de novo copy number mutations with sporadic schizophrenia.
Nat Genet. 2008 Jul;40(7):880-5. doi: 10.1038/ng.162. Epub 2008 May 30.
7
Premorbid IQ in schizophrenia: a meta-analytic review.
Am J Psychiatry. 2008 May;165(5):579-87. doi: 10.1176/appi.ajp.2008.07081242. Epub 2008 Apr 15.
8
Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.
J Neurosci. 2008 Feb 13;28(7):1697-708. doi: 10.1523/JNEUROSCI.3032-07.2008.
9
Contribution of SHANK3 mutations to autism spectrum disorder.
Am J Hum Genet. 2007 Dec;81(6):1289-97. doi: 10.1086/522590. Epub 2007 Oct 16.
10
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
Hum Mol Genet. 2008 Feb 1;17(3):458-65. doi: 10.1093/hmg/ddm323. Epub 2007 Nov 6.

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