文献检索文档翻译深度研究

邀请有礼套餐&价格历史记录

新学期，新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

不再提醒

插件&应用

Zotero 插件浏览器插件 Mac 客户端 Windows 客户端微信小程序

高级版

套餐订阅购买积分包

AI 工具

文献检索文档翻译深度研究

关于我们

关于 Suppr 公司介绍联系我们用户协议隐私条款

关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究

粤ICP备2023148730 号-1Suppr @ 2025

Association of a functional Claudin-5 variant with schizophrenia in female patients with the 22q11.2 deletion syndrome.

作者信息

Guo Yiran, Singh Larry N, Zhu Yuankun, Gur Raquel E, Resnick Adam, Anderson Stewart A, Alvarez Jorge I

机构信息

Center for Data Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, United States.

Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, United States.

出版信息

Schizophr Res. 2020 Jan;215:451-452. doi: 10.1016/j.schres.2019.09.014. Epub 2019 Oct 23.

DOI:10.1016/j.schres.2019.09.014

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7365141/

Abstract

摘要

相似文献

[1]

Association of a functional Claudin-5 variant with schizophrenia in female patients with the 22q11.2 deletion syndrome.

Schizophr Res. 2020-1

[2]

[22q11.2DS Syndrome as a Genetic Subtype of Schizophrenia].

Rev Colomb Psiquiatr. 2015

[3]

Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia.

Curr Opin Psychiatry. 2017-5

[4]

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.

Hum Mol Genet. 2008-12-15

[5]

Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study.

Schizophr Res. 2007-11

[6]

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Dev Disabil Res Rev. 2008

[7]

Subthreshold social cognitive deficits may be a key to distinguish 22q11.2DS from schizophrenia.

Early Interv Psychiatry. 2019-4

[8]

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.

J Psychiatr Res. 2014-9

[9]

Cognitive behavioral therapy in 22q11.2 microdeletion with psychotic symptoms: What do we learn from schizophrenia?

Eur J Med Genet. 2016-11

[10]

Neurocognitive Functioning in Patients with 22q11.2 Deletion Syndrome: A Meta-Analytic Review.

Behav Genet. 2018-6-19

引用本文的文献

[1]

Pumilio-1 mediated translational control of claudin-5 at the blood-brain barrier.

Fluids Barriers CNS. 2024-6-19

[2]

22q11.2 Deletion-Associated Blood-Brain Barrier Permeability Potentiates Systemic Capillary Leak Syndrome Neurologic Features.

J Clin Immunol. 2024-4-5

[3]

Serum Zonula Occludens-1 and Claudin-5 Levels in Patients with Insomnia Disorder: A Pilot Study.

Nat Sci Sleep. 2023-10-31

[4]

22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders.

Mol Syndromol. 2023-2

[5]

Interrogating the Human Diplome: Computational Methods, Emerging Applications, and Challenges.

Methods Mol Biol. 2023

[6]

From Neurodevelopmental to Neurodegenerative Disorders: The Vascular Continuum.

Front Aging Neurosci. 2021-10-20

[7]

Disruption of the blood-brain barrier in 22q11.2 deletion syndrome.

Brain. 2021-6-22

[8]

This was the year that was: brain barriers and brain fluid research in 2019.

Fluids Barriers CNS. 2020-3-5

本文引用的文献

[1]

The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.

Nucleic Acids Res. 2019-1-8

[2]

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.

Mol Psychiatry. 2020-8

[3]

Inflammation in Schizophrenia: Pathogenetic Aspects and Therapeutic Considerations.

Schizophr Bull. 2018-8-20

[4]

Elevated Proinflammatory Markers in 22q11.2 Deletion Syndrome Are Associated With Psychosis and Cognitive Deficits.

J Clin Psychiatry. 2017

[5]

Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia.

Mol Psychiatry. 2017-10-10

[6]

Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia.

Curr Opin Psychiatry. 2017-5

[7]

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.

JAMA Psychiatry. 2017-3-1

[8]

Multifaceted interactions between adaptive immunity and the central nervous system.

Science. 2016-8-19

[9]

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.

Hum Genet. 2016-3

[10]

Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register Study.

Schizophr Bull. 2016-5

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

推荐工具

医学文档翻译智能文献检索