MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro-Reference-Cited by-同舟云学术

MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro

Published:2018-03-08 Issue:5 Volume:39 Page:717-728
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Sheikh Taimoor I.¹²,Harripaul Ricardo¹²,Ayub Muhammad³⁴,Vincent John B.¹²⁵^ORCID

Affiliation:

1. Molecular Neuropsychiatry & Development (MiND) Lab; Campbell Family Mental Health Research Institute; Centre for Addiction and Mental Health; Toronto Ontario Canada

2. Institute of Medical Science; University of Toronto; Toronto Ontario Canada

3. Lahore Institute of Research & Development; Lahore Pakistan

4. Department of Psychiatry; Queen's University; Kingston Ontario Canada

5. Department of Psychiatry; University of Toronto; Toronto Ontario Canada

Funder

Ontario Rett Syndrome Association (ORSA)

Centre for Addiction and Mental Health Foundation

University of Toronto

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference57 articles.

1. MeCP2 Rett mutations affect large scale chromatin organization;Agarwal;Human Molecular Genetics,2011

2. Application of carrier testing to genetic counseling for X-linked agammaglobulinemia;Allen;American Journal of Human Genetics,1994

3. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;American Journal of Human Genetics,1992

4. Prevalence of nonaffective psychosis in intellectually disabled clients: Systematic review and meta-analysis;Aman;Psychiatric Genetics,2016

5. AT-hook motifs identified in a wide variety of DNA-binding proteins;Aravind;Nucleic Acids Research,1998

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