A reeler mutant mouse with a new, spontaneous mutation in the reelin gene
Author:
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Molecular Biology
Reference20 articles.
1. A YAC contig containing the reeler locus with preliminary characterization of candidate gene fragments;Bar;Genomics,1995
2. Decoding the reelin signal;Bar;Nature,1999
3. The reeler malformation. Implications for neocortical histogenesis;Caviness,1988
4. Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality;Chae;Neuron,1997
5. A protein related to extracellular matrix proteins deleted in the mouse mutant reeler;D’Arcangelo;Nature,1995
Cited by 17 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. The genetics of gaits in Icelandic horses goes beyond DMRT3, with RELN and STAU2 identified as two new candidate genes;Genetics Selection Evolution;2023-12-11
2. Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders;Brain;2022-06-30
3. The Reeler Mouse: A Translational Model of Human Neurological Conditions, or Simply a Good Tool for Better Understanding Neurodevelopment?;Journal of Clinical Medicine;2019-12-01
4. Decreased Expression of Synaptophysin 1 (SYP1 Major Synaptic Vesicle Protein p38) and Contactin 6 (CNTN6/NB3) in the Cerebellar Vermis of reln Haplodeficient Mice;Cellular and Molecular Neurobiology;2019-05-16
5. The number of Purkinje neurons and their topology in the cerebellar vermis of normal and reln haplodeficient mouse;Annals of Anatomy - Anatomischer Anzeiger;2016-09
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