关于表观遗传机制在自闭症谱系及相关神经发育障碍中导致基因沉默的有力且明确的证据。 - Suppr

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超能文献

Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.

作者信息

Lopez-Rangel E, Lewis M E S

机构信息

Department of Medical Genetics, B.C. Children and Women's Health Center, Vancouver, BC, Canada V6H 3N1.

出版信息

Clin Genet. 2006 Jan;69(1):21-2. doi: 10.1111/j.1399-0004.2006.00543a.x.

DOI:10.1111/j.1399-0004.2006.00543a.x

PMID:16451129

Abstract

摘要

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Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.

作者信息

Lopez-Rangel E, Lewis M E S

机构信息

Department of Medical Genetics, B.C. Children and Women's Health Center, Vancouver, BC, Canada V6H 3N1.

出版信息

Clin Genet. 2006 Jan;69(1):21-2. doi: 10.1111/j.1399-0004.2006.00543a.x.

DOI:10.1111/j.1399-0004.2006.00543a.x

PMID:16451129

Abstract

摘要

相似文献

Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.

Clin Genet. 2006 Jan;69(1):21-2. doi: 10.1111/j.1399-0004.2006.00543a.x.

Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.

J Child Neurol. 2009 Jun;24(6):772-4. doi: 10.1177/0883073808327834. Epub 2009 Feb 2.

Autism spectrum disorders and epigenetics.

J Am Acad Child Adolesc Psychiatry. 2010 Aug;49(8):794-809. doi: 10.1016/j.jaac.2010.05.005. Epub 2010 Jul 3.

Epigenetics of autism spectrum disorders.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R138-50. doi: 10.1093/hmg/ddl213.

Reversing symptoms in autistic disorder.

Biotechnol J. 2007 Apr;2(4):406. doi: 10.1002/biot.200790041.

[Autism and epigenetics. A model of explanation for the understanding of the genesis in autism spectrum disorders].

Medicina (B Aires). 2013;73 Suppl 1:20-9.

Advances in behavioral genetics: mouse models of autism.

Mol Psychiatry. 2008 Jan;13(1):4-26. doi: 10.1038/sj.mp.4002082. Epub 2007 Sep 11.

The role of MeCP2 in brain development and neurodevelopmental disorders.

Curr Psychiatry Rep. 2010 Apr;12(2):127-34. doi: 10.1007/s11920-010-0097-7.

MeCP2 dysfunction in Rett syndrome and related disorders.

Curr Opin Genet Dev. 2006 Jun;16(3):276-81. doi: 10.1016/j.gde.2006.04.009. Epub 2006 May 2.

Genomic imprinting in the development and evolution of psychotic spectrum conditions.

Biol Rev Camb Philos Soc. 2008 Nov;83(4):441-93. doi: 10.1111/j.1469-185X.2008.00050.x. Epub 2008 Sep 9.

引用本文的文献

Assessing the impact of medically assisted reproduction on autism spectrum disorder risk.

J Assist Reprod Genet. 2024 Oct;41(10):2607-2613. doi: 10.1007/s10815-024-03180-z. Epub 2024 Jun 26.

A Spectrum of Solutions: Unveiling Non-Pharmacological Approaches to Manage Autism Spectrum Disorder.

Medicina (Kaunas). 2023 Aug 31;59(9):1584. doi: 10.3390/medicina59091584.

Hearing Loss in Neurological Disorders.

Front Cell Dev Biol. 2021 Aug 11;9:716300. doi: 10.3389/fcell.2021.716300. eCollection 2021.

MLPA analysis in a cohort of patients with autism.

Mol Cytogenet. 2017 Feb 4;10:2. doi: 10.1186/s13039-017-0302-z. eCollection 2017.

Complex epigenetic regulation of engrailed-2 (EN-2) homeobox gene in the autism cerebellum.

Transl Psychiatry. 2013 Feb 19;3(2):e232. doi: 10.1038/tp.2013.8.

Early medical and behavioral characteristics of NICU infants later classified with ASD.

Pediatrics. 2010 Sep;126(3):457-67. doi: 10.1542/peds.2009-2680. Epub 2010 Aug 2.

FASEB J. 2010 Aug;24(8):3036-51. doi: 10.1096/fj.10-154484. Epub 2010 Apr 7.

Abnormal transmethylation/transsulfuration metabolism and DNA hypomethylation among parents of children with autism.

J Autism Dev Disord. 2008 Nov;38(10):1966-75. doi: 10.1007/s10803-008-0591-5. Epub 2008 May 30.