A comprehensive analysis of 22q11 gene expression in the developing and adult brain
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference42 articles.
1. 22q11 deletion syndrome: a genetic subtype of schizophrenia
2. Structural brain abnormalities associated with deletion at chromosome 22q11
3. Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients
4. Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene
Cited by 132 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Robust and replicable functional brain signatures of 22q11.2 deletion syndrome and associated psychosis: a deep neural network-based multi-cohort study;Molecular Psychiatry;2024-04-12
2. Tbx1 haploinsufficiency causes brain metabolic and behavioral anomalies in adult mice which are corrected by vitamin B12 treatment;2024-02-01
3. Dysfunctional parvalbumin interneurons in a genetic mouse model of schizophrenia;2023-09-10
4. Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder;Developmental Neuroscience;2023-05-10
5. Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome;Biomolecules;2023-04-27
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3