Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference28 articles.
1. Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic density;Boeckers;J Neurosci,1999
2. Proline-rich synapse-associated proteins ProSAP1 and ProSAP2 interact with synaptic proteins of the SAPAP/GKAP family;Boeckers;Biochem Biophys Res Commun,1999
3. Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation;Chelly;Hum Mol Genet,1999
4. A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3;Chong;Hum Mol Genet,1997
5. Genomic sequencing;Church;Proc Natl Acad Sci USA,1984
Cited by 249 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. Disrupted extracellular matrix and cell cycle genes in autism-associated Shank3 deficiency are targeted by lithium;Molecular Psychiatry;2023-12-20
2. Description of a patient with developmental delay and dysmorphic features caused by a novel SHANK2 deletion;Egyptian Journal of Medical Human Genetics;2023-12-13
3. Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes;Nature Reviews Neurology;2023-11-24
4. Expression profiles of the autism-related SHANK proteins in the human brain;BMC Biology;2023-11-13
5. Dual-Hit: Glyphosate exposure at NOAEL level negatively impacts birth and glia-behavioural measures in heterozygous shank3 mutants;Environment International;2023-10
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